H3 A5

H3-A5
Vol. 23 No. 32
Replaces H3-A4
Vol. 18 No. 7
Procedures for the Collection of Diagnostic

Blood Specimens by Venipuncture;
Approved StandardFifth Edition
This document provides procedures for the collection of diagnostic specimens by

venipuncture, including line draws, blood culture collection, and venipuncture in
children.
A standard for global application developed through the NCCLS consensus process.
NCCLS...
Serving the Worlds Medical Science Community Through Voluntary Consensus
NCCLS is an international, interdisciplinary, nonprofit,
standards-developing, and educational organization that
promotes the development and use of voluntary
consensus standards and guidelines within the healthcare
community. It is recognized worldwide for the
application of its unique consensus process in the
development of standards and guidelines for patient
testing and related healthcare issues. NCCLS is based on
the principle that consensus is an effective and costeffective way to improve patient testing and healthcare
services.
In addition to developing and promoting the use of
voluntary consensus standards and guidelines, NCCLS
provides an open and unbiased forum to address critical
issues affecting the quality of patient testing and health
care.
PUBLICATIONS
An NCCLS document is published as a standard,
guideline, or committee report.
Standard A document developed through the consensus
process that clearly identifies specific, essential
requirements for materials, methods, or practices for use
in an unmodified form. A standard may, in addition,
contain discretionary elements, which are clearly
identified.
Guideline
A document developed through the
consensus process describing criteria for a general
operating practice, procedure, or material for voluntary
use. A guideline may be used as written or modified by
the user to fit specific needs.
Report A document that has not been subjected to
consensus review and is released by the Board of
Directors.
CONSENSUS PROCESS
The NCCLS voluntary consensus process is a protocol
establishing formal criteria for:
the authorization of a project
the development and open review of documents
the revision of documents in response to comments

by users
the acceptance of a document as a consensus

standard or guideline.
Most NCCLS documents are subject to two levels of

consensusproposed and approved. Depending on
the need for field evaluation or data collection, documents

may also be made available for review at an intermediate
(i.e., tentative) consensus level.
Proposed An NCCLS consensus document undergoes the
first stage of review by the healthcare community as a
proposed standard or guideline. The document should
receive a wide and thorough technical review, including an
overall review of its scope, approach, and utility, and a lineby-line review of its technical and editorial content.
Tentative A tentative standard or guideline is made
available for review and comment only when a
recommended method has a well-defined need for a field
evaluation or when a recommended protocol requires that
specific data be collected. It should be reviewed to ensure its
utility.
Approved An approved standard or guideline has achieved
consensus within the healthcare community. It should be
reviewed to assess the utility of the final document, to
ensure attainment of consensus (i.e., that comments on
earlier versions have been satisfactorily addressed), and to
identify the need for additional consensus documents.
NCCLS standards and guidelines represent a consensus
opinion on good practices and reflect the substantial
agreement by materially affected, competent, and interested
parties obtained by following NCCLSs established
consensus procedures. Provisions in NCCLS standards and
guidelines may be more or less stringent than applicable
regulations. Consequently, conformance to this voluntary
consensus document does not relieve the user of
responsibility for compliance with applicable regulations.
COMMENTS
The comments of users are essential to the consensus
process. Anyone may submit a comment, and all comments
are addressed, according to the consensus process, by the
NCCLS committee that wrote the document. All comments,
including those that result in a change to the document when
published at the next consensus level and those that do not
result in a change, are responded to by the committee in an
appendix to the document. Readers are strongly encouraged
to comment in any form and at any time on any NCCLS
document. Address comments to the NCCLS Executive
Offices, 940 West Valley Road, Suite 1400, Wayne, PA
19087, USA.
VOLUNTEER PARTICIPATION
Healthcare professionals in all specialties are urged to
volunteer for participation in NCCLS projects. Please
contact the NCCLS Executive Offices for additional
information on committee participation.
Volume 23 Number 32
H3-A5
ISBN 1-56238-515-1
ISSN 0273-3099
Procedures for the Collection of Diagnostic Blood Specimens by

Venipuncture; Approved StandardFifth Edition
Charles F. Arkin, M.D.
J. David Bessman, M.D.
Roger R. Calam, Ph.D., DABCC
Dennis J Ernst, M.T.(ASCP)
Gary T. Parish
Diane I. Szamosi, M.A., M.T.(ASCP), SH
David J. Warunek, Ph.D.
Joan D. Wiseman, M.T.(ASCP)CT
Abstract
H3-A5Procedures for the Collection of Diagnostic Blood Specimens by Venipuncture; Approved StandardFifth Edition
provides a descriptive, stepwise procedure for the collection of diagnostic blood specimens by venipuncture. Special
considerations for venipuncture in children, line draws, blood culture collection, and venipuncture in isolation situations are
included.
NCCLS. Procedures for the Collection of Diagnostic Blood Specimens by Venipuncture; Approved StandardFifth Edition.
NCCLS document H3-A5 (ISBN 1-56238-515-1). NCCLS, 940 West Valley Road, Suite 1400, Wayne, Pennsylvania 190871898 USA, 2003.
THE NCCLS consensus process, which is the mechanism for moving a document through two or more levels of review by the
healthcare community, is an ongoing process. Users should expect revised editions of any given document. Because rapid
changes in technology may affect the procedures, methods, and protocols in a standard or guideline, users should replace
outdated editions with the current editions of NCCLS documents. Current editions are listed in the NCCLS Catalog, which is
distributed to member organizations, and to nonmembers on request. If your organization is not a member and would like to
become one, and to request a copy of the NCCLS Catalog, contact the NCCLS Executive Offices. Telephone: 610.688.0100;
Fax: 610.688.0700; E-Mail: [email protected]; Website: www.nccls.org
Number 32
NCCLS
This publication is protected by copyright. No part of it may be reproduced, stored in a retrieval system,
transmitted, or made available in any form or by any means (electronic, mechanical, photocopying,
recording, or otherwise) without prior written permission from NCCLS, except as stated below.
NCCLS hereby grants permission to reproduce limited portions of this publication for use in laboratory
procedure manuals at a single site, for interlibrary loan, or for use in educational programs provided that
multiple copies of such reproduction shall include the following notice, be distributed without charge,
and, in no event, contain more than 20% of the documents text.
Reproduced with permission, from NCCLS publication H3-A5Procedures for the
Collection of Diagnostic Blood Specimens by Venipuncture; Approved StandardFifth
Edition (ISBN 1-56238-515-1). Copies of the current edition may be obtained from
NCCLS, 940 West Valley Road, Suite 1400, Wayne, Pennsylvania 19087-1898, USA.
Permission to reproduce or otherwise use the text of this document to an extent that exceeds the
exemptions granted here or under the Copyright Law must be obtained from NCCLS by written request.
To request such permission, address inquiries to the Executive Director, NCCLS, 940 West Valley Road,
Suite 1400, Wayne, Pennsylvania 19087-1898, USA.
Copyright 2003. The National Committee for Clinical Laboratory Standards.
Suggested Citation
(NCCLS. Procedures for the Collection of Diagnostic Blood Specimens by Venipuncture; Approved
StandardFifth Edition. NCCLS document H3-A5 [ISBN 1-56238-515-1]. NCCLS, 940 West Valley
Road, Suite 1400, Wayne, Pennsylvania 19087-1898 USA, 2003.)
Proposed Standard
Approved StandardFourth Edition
August 1977
June 1998
Tentative Standard
Approved StandardFifth Edition
February 1979
December 2003
Approved Standard
March 1980
Approved StandardSecond Edition

April 1984
Approved StandardThird Edition

July 1991
ISBN 1-56238-515-1
ISSN 0273-3099
ii
Volume 23
H3-A5
Committee Membership
Area Committee on Hematology
Chairholder
Lahey Clinic
Burlington, Massachusetts
Bruce H. Davis, M.D.
Vice-Chairholder
Maine Medical Center Research
Institute
Scarborough, Maine
University of Texas Medical Branch
Galveston, Texas
Berend Houwen, M.D., Ph.D.
Beckman Coulter, Inc.
Brea, California
Frank M. LaDuca, Ph.D.
International Technidyne
Corporation
Edison, New Jersey
Ginette Y. Michaud, M.D.
FDA Center for Devices/Rad.
Health
Rockville, Maryland
Onno W. van Assendelft, M.D.,
Ph.D.
Centers for Disease Control and
Prevention
Atlanta, Georgia
Advisors
Dorothy M. Adcock, M.D.
Esoterix Coagulation
Aurora, Colorado
Richard A. Marlar, Ph.D.

Denver VA Medical Center
Denver, Colorado
Sheila Clover, CPT (ASCP) (NCA)

Phlebotomy West
Brentwood, California
Diane L. Szamosi,
M.A.,M.T.(ASCP)SH
Greiner Bio-One, VACUETTE
North America, Inc.
Monroe, North Carolina
Dennis J. Ernst, M.T.(ASCP)

Center for Phlebotomy Education
Ramsey, Indiana
Luc Van Hove, M.D., Ph.D.

Abbott Laboratories
Abbott Park, Illinois
J. Heinrich Joist, M.D., Ph.D.

St. Louis University Health Science
Center
St. Louis, Missouri
Staff
John A. Koepke, M.D.

Durham, North Carolina
Francis Lacombe, M.D., Ph.D.
Laboratoire dHematologie
Pessac, France
Samuel J. Machin, MB, Ch.B,
FRCPath
The University College London
Hospital
London, United Kingdom
Tracy A. Dooley, M.L.T.(ASCP)

Staff Liaison
NCCLS
Wayne, Pennsylvania
David E. Sterry, M.T.(ASCP)
Project Manager
NCCLS
Wayne, Pennsylvania
Donna M. Wilhelm
Editor
NCCLS
Wayne, Pennsylvania
Melissa A. Lewis
Assistant Editor
NCCLS
Wayne, Pennsylvania
Acknowledgement
NCCLS gratefully acknowledges the working group for their help in preparing the approved-level, fifth
edition of this standard.
Lahey Clinic
Dennis J. Ernst, M.T.(ASCP)

Center for Phlebotomy Education

University of Texas Medical Branch
Gary T. Parish
Sarstedt, Inc.
Roger R. Calam, Ph.D., DABCC

St. John Hospital
Diane I. Szamosi, M.A.,

M.T.(ASCP), SH
Greiner Bio-One, VACUETTE
North America, Inc.
David J. Warunek, Ph.D., M.B.A.
BD VACUTAINER Systems
Joan D. Wiseman, M.T.(ASCP), CT
Consultant
Bernardsville, New Jersey
iii
Number 32
iv
NCCLS
Volume 23
H3-A5
Contents
Abstract ....................................................................................................................................................i
Committee Membership........................................................................................................................ iii
Foreword .............................................................................................................................................. vii
1
Scope..........................................................................................................................................1
Introduction................................................................................................................................1
Standard Precautions..................................................................................................................1
Definitions .................................................................................................................................1
Factors That Affect Laboratory Values .....................................................................................2
Facilities.....................................................................................................................................2
6.1
6.2
Supplies......................................................................................................................................3
7.1
7.2
7.3
7.4
7.5
7.6
7.7
7.8
7.9
7.10
7.11
7.12
7.13
7.14
Venipuncture Chairs ......................................................................................................2

Hospital Area.................................................................................................................3
Utility Carts ...................................................................................................................3
Blood Collecting Trays..................................................................................................3
Gloves............................................................................................................................3
Needles and Holders......................................................................................................4
Sterile Syringes..............................................................................................................4
Venous Blood Collection Tubes....................................................................................4
Tourniquets....................................................................................................................4
Antiseptics .....................................................................................................................5
Gauze Pads ....................................................................................................................5
Puncture-Resistant Disposal Container .........................................................................5
Ice ..................................................................................................................................5
Adhesive Bandages........................................................................................................5
Warming Devices ..........................................................................................................5
Test Reference Manual..................................................................................................5
Venipuncture Procedure.............................................................................................................5
8.1
8.2
8.3
8.4
8.5
8.6
8.7
8.8
8.9
8.10
8.11
8.12
8.13
8.14
Step 1: Prepare Accession Order ..................................................................................6

Step 2: Approach and Identify the Patient....................................................................6
Step 3: Verify Patient Diet Restrictions and Latex Sensitivity.....................................8
Step 4: Assemble Supplies ...........................................................................................8
Step 5: Position Patient.................................................................................................9
Step 6: Apply Tourniquet ...........................................................................................10
Step 7: Put on Gloves .................................................................................................13
Step 8: Cleanse Venipuncture Site .............................................................................13
Step 9: Perform Venipuncture ....................................................................................13
Step 10: Order of Draw ..............................................................................................17
Step 11: Release the Tourniquet .................................................................................17
Step 12: Place the Gauze Pad .....................................................................................17
Step 13: Remove and Dispose of the Needle..............................................................18
Step 14: Bandage the Arm..........................................................................................18
v
Number 32
NCCLS
Contents (Continued)
8.15
8.16
8.17
9
Venipuncture in Children and Difficult Collections ................................................................19

9.1
9.2
10
Procedure.....................................................................................................................19
Equipment....................................................................................................................19
Additional Considerations .......................................................................................................19

10.1
10.2
10.3
11
Step 15: Label Blood Collection Tubes and Record Time of Collection ...................18
Step 16: Chill the Specimen .......................................................................................19
Step 17: Send Blood Collection Tubes to the Proper Laboratories ............................19
Monitoring Blood Volume Collected ..........................................................................19

Hematoma....................................................................................................................20
Hemolysis ....................................................................................................................20
Special Situations.....................................................................................................................20
11.1
11.2
11.3
11.4
11.5
11.6
11.7
11.8
Timed Intervals............................................................................................................20
Specific Collection Techniques ...................................................................................20
Indwelling Lines or VADs ..........................................................................................21
Heparin or Saline Locks ..............................................................................................22
Fistula ..........................................................................................................................22
Intravenous Fluids .......................................................................................................22
Isolation .......................................................................................................................23
Emergency Situations ..................................................................................................24
References.............................................................................................................................................26
Summary of Comments and Subcommittee Responses........................................................................27
Summary of Delegate Comments and Working Group Responses ......................................................28
The Quality System Approach..............................................................................................................34
Related NCCLS Publications................................................................................................................35
vi
Volume 23
H3-A5
Foreword
The errors that can occur during the collection and handling of blood specimens are potentially numerous
(e.g., inaccurate identification of specimens, specimen hemolysis, the improper handling of
anticoagulants, the formation of hematomas, hemoconcentration). Standards for venipuncture can reduce
or alleviate many of these errors in much the same way that quality control standards have reduced errors
within the laboratory.
Reducing errors during blood collecting will result in biologically representative specimens that are
comparable from one institution to another. A well-planned, attractive environment in which to perform
venipunctures will reduce patient anxiety and increase the efficiency and accuracy of the phlebotomist.
Phlebotomists need a complete assortment of equipment at their fingertips so they can judiciously select
the most appropriate materials for each patient. Standards governing the processing of paperwork will
reduce errors and save time. Without question, a comprehensive training program is needed to produce
efficient, well-trained phlebotomists. Finally, standards for the actual venipuncture procedure are needed
to help eliminate the many errors that can occur during blood collection. Biologically representative
specimens for laboratory testing will be obtained if national venipuncture standards are used.
Various comments received on the previous edition of this standard have been reviewed and incorporated
where appropriate. All comments and the subcommittees responses are summarized at the end of the
document.
This document replaces the fourth edition approved standard, H3-A4, which was published in 1998.
Several changes have been made in this edition; chief among them is the revised order of draw (Section
8.10.2), which reflects the increased use of plastic blood collection tubes. This standard also contains
revised recommendations regarding collection of blood specimens in relation to intravenous sites (Section
11.6). The recommendations regarding the collection of coagulation specimens (Section 8.10.3) have
been revised for consistency with NCCLS document H21Collection, Transport, and Processing of
Blood Specimens for Coagulation Testing and General Performance of Coagulation Assays.
Key Words
Accession, blood specimen, phlebotomist, sample, venipuncture
vii
Number 32
viii
NCCLS
Volume 23
H3-A5
Procedures for the Collection of Diagnostic Blood Specimens by

Venipuncture; Approved StandardFifth Edition
1
Scopea
This document establishes criteria for the correct collection of blood specimens by venipuncture. These
procedures are intended to be a suitable model for adoption by all healthcare providers responsible for the
collection and handling of blood specimens in both outpatient and inpatient settings.
Introduction
Since 1977, NCCLS has progressively recognized the quality requirement that significant attention be
directed towards the preanalytical components of laboratory testing, specifically, the correct collection
and handling of blood specimens. Highly sophisticated testing technology cannot produce a good result
from a poor specimen. Proper specimen collection and handling are of the utmost importance because
significant errors occur in the preanalytical phase of laboratory testing.1
Preanalytical errors have the potential to be numerous: incorrect patient ID, incorrect order-of-draw,
incorrect use of additive tubes, labeling errors, incorrect timing of collection, clerical errors, etc. Standard
procedures and protocols are intended to prevent these problems and protect patient results quality.
Standard Precautions
Because it is often impossible to know what might be infectious, all human blood specimens are to be
treated as infectious and handled according to standard precautions. Standard precautions are guidelines
that combine the major features of universal precautions and body substance isolation practices.
Standard precautions cover the transmission of any pathogen and thus are more comprehensive than
universal precautions which are intended to apply only to transmission of blood-borne pathogens.
Standard precaution and universal precaution guidelines are available from the U.S. Centers for Disease
Control and Prevention (Guideline for Isolation Precautions in Hospitals. Infection Control and Hospital
Epidemiology. CDC. 1996;Vol 17;1:53-80), (MMWR 1987;36[suppl 2S]2S-18S), and (MMWR
1988;37:377-382, 387-388). For specific precautions for preventing the laboratory transmission of bloodborne infection from laboratory instruments and materials and for recommendations for the management
of blood-borne exposure, refer to the most current edition of NCCLS document M29Protection of
Laboratory Workers from Occupationally Acquired Infections.
Definitions
In the context of this publication, the terms listed below are defined as follows:
Accession The steps required to ensure that a specific patient specimen and the accompanying
documentation are unmistakably identified as referring to a specific person.
Angle of insertion The angle formed by the surface of the arm and the needle entering the arm.
a
This standard reflects recent revisions to OSHAs Blood Borne Pathogens Standard (29 CFR 1910.1030). Therefore, all
references to needles/winged blood collection sets indicate sharps with engineered safety features. This also encompasses safety
accessories used in combination with conventional needles.
An NCCLS global consensus standard. NCCLS. All rights reserved.
Number 32
NCCLS
(Patient) sample A sample taken from the patient specimen and used to obtain information by means of
a specific laboratory test.
(Patient) specimen The discrete portion of a body fluid or tissue taken for examination, study, or
analysis of one or more quantities or characteristics to determine the character of the whole.
Pre-evacuation The creation of a vacuum (in a collection tube), induced by either the manufacturer or
by the user immediately before a liquid specimen is taken.
Vascular access device (VAD) A device inserted into a vein or artery to allow access to the circulatory
system for the administration of intravenous fluids and/or medications.
Venipuncture The puncture of a vein for surgical, or therapeutic, purposes, or for collecting blood
specimens for analysis.
Factors That Affect Laboratory Values
Interpretation of laboratory data has assumed new importance and attracted increased attention with both
more frequent testing and multiple testing. The increased use of laboratories predictably yields abnormal
unsolicited data that requires interpretation and may lead to costly, unproductive, and unnecessary
sequential testing. Even when an analytical procedure has been performed correctly and precisely,
variables can affect the test result. Knowledge of these variables and standardization of laboratory testing
procedures are essential for correct interpretation and optimal use of the data.
Major causes of laboratory error can be related to nonanalytical factors such as specimen collection,
handling, and transport. Nonbiological factorssuch as patient misidentification, and biological factors
such as patient posture and the time a specimen is drawn, all contribute to the total laboratory error.
Physiological factors that influence results include age, activity, bed rest, food ingestion, alcohol
ingestion, menstrual cycle, obesity, oral contraceptives, posture, pregnancy, race, gender, smoking, and
time of day. All biological phenomena exhibit rhythms, with the circadian rhythm (the change in a 24hour period) being the most important to laboratory testing. Many factors with documented effects on
laboratory values have been published.2-6
Facilities
The venipuncture should be performed in a clean, quiet, and private environment.

soundproof rooms for pediatric patients should be considered.
Reasonably
The room should have facilities to allow the phlebotomist to wash his/her hands between patients.
Washing with soap and running water is recommended; however, any standard detergent product
acceptable to personnel may be used. In settings where water is not available, alcohol-based gels or
liquids, hand-wipe towelettes, and cleansing foams can be used.b
6.1
Venipuncture Chairs
Venipuncture chairs should be designed for the maximum comfort and safety of the patient.
Consideration should be given to the ergonomic comfort plus easy accessibility to the patient for the
phlebotomist. Both armrests of the chairs should be adjustable so that the best venipuncture position for
In the U.S., employees must wash their hands with soap and running water as soon as feasible thereafter.
Volume 23
H3-A5
each patient can be achieved. The chair should have a safety device to prevent patients from falling if
feeling faint.
6.2
Hospital Area
A central venipuncture area should be designed to include the following features.

6.2.1
Central Desk
The central desk is a location for a telephone system used to handle emergency request calls, facilities for
processing daily and future requests, and a paging system for contacting the phlebotomist who is
collecting specimens outside of the central area.
6.2.2
Cart Area
The cart area is constructed to allow easy access to the supplies.

6.2.3
Storage Area
The storage area should be large enough to accommodate the necessary supplies.
6.2.4
Counter Space
Counter space should be adequate for efficient sorting and dispatching of specimens.
6.2.5
Sampling Time Recorder
The sampling time recorder (i.e., time stampers, bar codes, or information system) should be located for
convenient time recording of venipuncture paperwork.
Supplies
The following supplies should be available at any location where venipunctures are performed routinely.
7.1
Utility Carts
Utility carts, designed to roll smoothly and silently over all types of surfaces, may be useful. The
phlebotomist may also find it very useful to have a specially designed rack on the top shelf for storing
supplies.
7.2
Blood Collecting Trays
Blood collecting trays or carts may be used. The trays should be lightweight and easy to handle with
enough space and compartments for the various supplies that are needed.
7.3
Gloves
Latex, vinyl, or nitrile gloves provide barrier protection. Disposable latex, vinyl, or nitrile gloves are
available from hospital suppliers.
Number 32
NCCLS
Some workers may develop dermatitis from wearing latex gloves for long periods of time. These workers
should experiment with nitrile, polyethylene or other gloves of various composition or gloves without
powdered lubricant or they may wear cotton gloves under latex or plastic gloves.
Severe hypersensitivity has been reported and cases of anaphylactic shock have occurred. In such
hypersensitive individuals, latex gloves must be avoided.
7.4
Needles and Holders
Needles/holders should be compatible with the tubes selected for use. For more information on venous
blood collection tubes and additives, refer to the most current edition of NCCLS document H1
Evacuated Tubes and Additives for Blood Specimen Collection.
Needles and winged blood collection sets are individually color-coded according to their respective gauge
sizes. The gauge number indicates the size of the needle. A large gauge number indicates a small needle,
while a small gauge number indicates a large needle. The sizes for venipuncture range from 19 through
23. Needles must always be sterile.
In order to prevent potential worker exposure, the needle safety feature should be activated immediately
after specimen collection and discarded without disassembly into a sharps container.c
7.5
Sterile Syringes
In general, venipuncture using a needle and syringe should be avoided for safety reasons; however, it may
be suitable under some circumstances to have sterile syringes of the appropriate size available.
7.6
Venous Blood Collection Tubes
Venous blood collection tubes are manufactured to withdraw a predetermined volume of blood. At
present, venous blood collection tubes used in venipuncture are designated sterile. It is recommended that
information regarding the venous blood collection tubes selected for general use be clearly displayed in
venipuncture areas for easy reference. Similar information should also be made available to all personnel
who collect blood. Instructions furnished in the package insert by the manufacturer of venous blood
collection tubes and needles should be available. (See also the most current version of NCCLS document
H1Evacuated Tubes and Additives for Blood Specimen Collection for information on venous blood
collection tubes.)
7.7
Tourniquets
Tourniquets or products for use as tourniquets should be available. Examples include:
Single-use disposable tourniquet, preferably latex-free.
Blood pressure cuff inflated to 40 mmHg.
Rubber/fabric-type tourniquets with closure tape, plastic clip, buckle, or similar type of fastening.
Tourniquets must be discarded immediately when contaminated with blood or body fluids or must be
discarded if contamination is suspected.
In the U.S., refer to OSHAs Bloodborne Pathogens Standard (29 CFR 1910.1030), the safe practice of phlebotomy and blood
tube holder use (CPL2-2.9 at XIII.D.5).
Volume 23
7.8
H3-A5
Antiseptics
Antiseptics for skin preparation are necessary. The following are some examples:
7.9
Isopropyl or ethyl alcohol: 70%

1 to 10% povidone-iodine as swab sticks or chlorhexidine gluconate for blood cultures7 (see Section
8.8.2).
Nonalcohol-based cleanser for blood alcohol specimens (e.g., chlorhexidine).
Gauze Pads
Small prepackaged gauze pads, (i.e., 2 x 2 in or 3 x 3 in [5.0 x 5.0 cm or 7.5 x 7.5 cm]) should be
available. Cotton balls are not recommended because of the possibility of dislodging the platelet plug at
the venipuncture site.
7.10 Puncture-Resistant Disposal Container

An approved puncture-resistant disposal container that is compliant with OSHA regulations must be
available.
7.11 Ice
Ice or refrigerant should be available.
7.12 Adhesive Bandages

Adhesive bandages and/or gauze pads should be available. Hypoallergenic adhesives should also be
available.
7.13 Warming Devices

Warming devices may be used to increase blood flow.
7.14 Test Reference Manual

A test manual which explains which tube is to be used, that also indicates minimum volume requirements,
special handling, and precautions to be taken should be consulted.
Venipuncture Procedure
The venipuncture procedure is complex and requires both knowledge and skill (refer to Sections 8.1 to
8.17 for detailed information on the procedure). When drawing a blood specimen, the trained
phlebotomist must:
Step 1.
Step 2.
Step 3.
Step 4.
Step 5.
Step 6.
Step 7.
Prepare accession order.

Approach and identify the patient.
Verify patients diet restrictions, as appropriate, and inquire if patient has a latex sensitivity.
Select appropriate gloves and tourniquet.
Assemble necessary supplies and select appropriate tubes according to test requests.
Position the patient.
Apply the tourniquet, ensure the patient's hand is closed, and select the vein site.
Put on gloves.
Number 32
Step 8.
Step 9.
Step 10.
Step 11.
Step 12.
Step 13.
Step 14.
Step 15.
Step 16.
Step 17.
8.1
NCCLS
Cleanse the venipuncture site.
Perform venipuncture; once blood flow begins, request patient to open hand.
Use the correct order of draw.
Release and remove the tourniquet.
Place the gauze pad over the puncture site.
Remove the needle, activating any safety feature according to manufacturers instructions.
Apply pressure to the site, making sure bleeding has stopped, and then bandage the arm.
Label the tubes and record the time of collection.
Chill the specimen (if required).
Send properly labeled blood collection tubes to the appropriate laboratories.
Step 1: Prepare Accession Order
Each request for a blood specimen must be accessioned to identify all paperwork and supplies associated
with each patient. An organized system will ensure prompt and accurate processing of the various forms
required when performing a venipuncture and analyzing the results. Record all information on the test
request form.
8.1.1
Information for Test Request Form
The following information should be included:
The patients name and age from identification plate

An identification number
The date and time the specimen is to be obtained
An accessioning number
The doctors name
The department or location for which the work is being done
Other information as needed (e.g., special comments: intravenous site, sampling site if other than
arm).
8.2
Step 2: Approach and Identify the Patient
The phlebotomist should identify himself or herself, establish a rapport, and gain the patients confidence.
Information given to the patient regarding the testing to be performed and specimen to be drawn must be
in accordance with institutional policy. The phlebotomist must NOT perform blood collection against the
patients or guardians consent. Instead, report the patients objections to the physicians/nurses station.
8.2.1
Identify Patient
Identification of the patient is crucial. The phlebotomist must ensure that the blood specimen is being
drawn from the individual designated on the request form. The phlebotomist must not rely on a bed tag,
or on charts or records placed on the bed, nearby tables, or equipment. The following steps are a
suggested sequence for ensuring patient identification, regardless of the clinical setting.
8.2.2
Patient Who Is Conscious
The suggested sequence of steps for a patient who is conscious:

(1) Ask outpatients to give full name, address, identification number, and/or birth date.
(2) Compare this information with the information on the request form.
6
Volume 23
H3-A5
(3) Ask inpatients for the same information and compare this information with the information on the
request form and the patients identification bracelet, which must be attached to the patient.
(4) Report any discrepancy, however minor, to the responsible person in the area (as determined by
institutional policy) and have the patient identified by name and identification number before drawing
any specimen.
8.2.3
Patient Who Is Semiconscious, Comatose, or Sleeping
The phlebotomist must take special care when drawing blood from semiconscious, comatose, or sleeping
patients to anticipate any unexpected movements or jerks either while introducing the needle, or while it
is in place in the arm. Sleeping patients should be awakened before drawing blood. A gauze pad should be
readily available and the tourniquet quickly released in the event the needle is violently removed or
repositioned. If the needle accidentally goes much deeper into the arm, the phlebotomist must inform the
doctors/nurses station. If unable to identify the patient, then contact the nurse or physician.
8.2.4 Patient Who Is Unconscious, Too Young, Mentally Incompetent, or Does Not Speak the
Language of the Phlebotomist
In any of these circumstances, the phlebotomist should follow this suggested sequence of steps:
(1) Ask the nurse, a relative, or a friend to identify the patient by name, address, identification number,
and/or birth date. If unable to identify the patient, then contact the nurse or physician.
(2) Compare these data with the information on the request form and the patients identification bracelet,
which must be attached to the patient.
(3) Report any discrepancy, however minor, to the responsible person in the area (as determined by
institutional policy) and have the patient identified by name and identification number before drawing
any specimen.
8.2.5
Procedure for Identifying Unidentified Emergency Patients
Identification standards established by the American Association of Blood Banks (AABB) provide clear
guidelines for unidentified emergency patients.8
The patient must be positively identified when the blood specimen is collected. The unidentified
emergency patient should be given some temporary but clear designation until positive identification can
be made. For a person who cannot be identified immediately, it is necessary to:
Assign a master identification number (temporary) to the patient in accord with institutional policy.
Select the appropriate test request forms and record with master identification number.
Complete the necessary labels either by hand or by computer and apply the labels to the test request
forms and specimens.
When a permanent identification number is assigned to the patient, make sure the temporary
identification number is cross-referenced to the permanent number to ensure correct identification and
correlation of patient and test result information.
Number 32
NCCLS
In all cases, the name and permanent or temporary identification designation must be attached to the
patients body either by wristband or some similar device. Except in the case of isolation patients, bed
labels must not be used in place of wristbands.
8.2.6
Physician Relationship
The physician has priority with the patient. The phlebotomist should not enter the room without
permission while the physician or nurse is consulting with the patient. If the order is stat or the specimen
is a timed specimen, the phlebotomist should request permission to draw the blood specimen.
8.3
Step 3: Verify Patient Diet Restrictions and Latex Sensitivity
Some tests require the patient to fast and/or eliminate certain foods from the diet before the blood is
drawn. Time and diet restrictions vary according to the test. Such restrictions are necessary to ensure
accurate test results.
The procedure for holding meals and notifying appropriate personnel that the patient has been drawn
should be according to institutional policy.
Please refer to Section 7.3 for information regarding latex sensitivity to gloves and to Section 7.7 for
tourniquets.
8.4
Step 4: Assemble Supplies
8.4.1
Suppliesd
It is important that phlebotomy devices used reflect the most current local and regional safety regulations.9
Inspect all supplies for possible defects and applicable expiration dates. The following supplies should be
available at any location where venipunctures are performed routinely:
Blood collection tubes/blood culture bottles

Needle
Single-use tube/needle holder
Syringe
Syringe transfer device
A tourniquet
Alcohol prep pads
1 to 10% povidone-iodine pads, tincture iodine, or chlorhexidine compounds if blood culture is to be
drawn
Nonalcohol-based cleanser if blood alcohol is to be drawn
Gauze pads, adhesive bandages, or tape (including hypoallergenic adhesives)
Gloves
Sharps container, consistent with OSHA regulations
8.4.2
Needles
The phlebotomist must select the appropriate needle gauge based on the physical characteristics of the
vein, location of the vein, and the volume of blood to be drawn.
d
In the U.S., OSHA mandates the use of engineering and work practice controls that eliminate occupational exposure or reduce it
to the lowest feasible extent (e.g., safety needles, shielded needle devices, etc.).
Volume 23
8.4.3
H3-A5
Syringes
The plunger must be moved within the barrel of the syringe to show syringe and needle patency and
freedom of plunger movement.
8.4.4
System
The phlebotomist must select the appropriate blood collection system according to the patients physical
characteristics.
8.4.4.1
Venous Blood Collection Systems
When venous blood collection tubes are used, the phlebotomist must:
Select the correct types and sizes of venous blood collection tubes. (Color-coded closures and labels
make it easy to perform this step.)
Apply a label to each of the necessary tubes and all test forms immediately after blood specimen has
been drawn
Refer to institutional policy.
All tubes should be labeled immediately after the blood specimen has been drawn. The completed label
must be attached to the tube before leaving the side of the patient, and there must be a mechanism to
identify the person who drew the blood.8 If preprinted labels are not available, complete patient
information can be handwritten on the tube label. This procedure eliminates the possibility of mixing up
the blood specimens.
It is recommended that blood specimens be collected by venipuncture using a blood collection system that
collects the blood directly into tubes. (For greater detail on venous blood collection tubes and additives,
refer to the most current edition of NCCLS document H1Evacuated Tubes and Additives for Blood
Specimen Collection.) If the components are from different manufacturers, they should be checked to
ensure compatibility.
8.4.4.2
Plastic Syringe
In general, the use of a syringe and needle should be avoided for safety reasons. If a syringe is used, a
safety syringe shielded transfer device should be used to transfer blood to the appropriate venous blood
collection tube.
8.4.4.3
Blood Collection Set
The blood collection set (i.e., winged blood collection set) is described in Section 9.2.
8.5
8.5.1
Step 5: Position Patient

Procedure for Seating Patient
(1) Ask the patient to be seated comfortably in a chair suitable for venipuncture. The chair should have
arms to provide support and prevent falls if the patient loses consciousness. Chairs without arms do
not provide adequate support for the arm or protect fainting patients from falls.
Number 32
NCCLS
(2) Have the patient position his/her arm on the slanting armrest and extend the arm to form a straight
line from the shoulder to the wrist. The arm should be supported firmly by the armrest and should not
be significantly bent at the elbow. A slight bend may be important in avoiding hyperextension of the
arm.
8.5.2
Procedure for Having Patient Lie Down
(1) Ask the patient to lie on his/her back in a comfortable position.

(2) If additional support is needed, place a pillow under the arm from which the specimen is being drawn.
(3) Have the patient extend his/her arm to form a straight line from the shoulder to the wrist.
8.5.3
Foreign Objects in Mouth
No food or liquid, chewing gum, or thermometer should be in the patients mouth at the time the
specimen is drawn.
8.6
Step 6: Apply Tourniquet
A tourniquet is used to increase venous filling. This makes the veins more prominent and easier to enter.
(See Section 7.7).
8.6.1
Precautions When Using a Tourniquet
Tourniquet application for preliminary vein selection should not exceed one minute as localized stasis
with hemoconcentration and infiltration of blood into tissue can occur. This may result in erroneously
high values for all protein-based analytes, packed cell volume, and other cellular elements. If the patient
has a skin problem, the tourniquet should be applied over the patients gown or a piece of gauze pad or
paper tissue should be used so that the skin is not pinched.
8.6.2
Tourniquet Location
Wrap the tourniquet around the arm 3 to 4 inches (7.5 to 10.0 cm) above the venipuncture site.
8.6.3
Blood Pressure Cuff
If a blood pressure cuff is used as a tourniquet, inflate it to 40 mm Hg.

8.6.4
Ensure Patients Hand Is Closed
The veins become more prominent and easier to enter when the patient forms a fist. There must not be
vigorous hand exercise (pumping). Vigorous hand pumping can cause changes in the concentration of
certain analytes in the blood.
10
Volume 23
H3-A5
Figure 1. Superficial Veins of the Anterior Surface of the Upper Extremity (From Ernst DJ, Ernst C.
Phlebotomy tools of the trade: Part 2Surveying the antecubital area. Home Healthcare Nurse. 2002;20:402-403. Reprinted
with permission from Lippincott Williams & Wilkins.)
8.6.5
Select Vein
Refer to Figure 1 for a description of the superficial veins of the anterior surface of the upper extremity.
8.6.5.1
Caution
It is important to select the vein carefully for blood collection because the veins also provide an avenue of
entry for transfusion, infusion, and therapeutic agents. Because the brachial artery passes through the
antecubital area, caution must be exercised to avoid the artery. If, during the procedure, arterial puncture
is suspected, direct forceful pressure must be applied to the puncture site for a minimum of five minutes
upon removal of the needle or until active bleeding has ceased. The nursing staff and physician are to be
notified immediately thereafter.
11
Number 32
8.6.6
NCCLS
Preferred Veins
Arterial punctures should not be considered as an alternative to venipuncture for difficult draws. If this
appears to be the only alternative, consult with the physician.
Although the larger and fuller median cubital and cephalic veins (see Figure 1) are used most frequently,
veins on the back of the hand are also acceptable for venipuncture. Veins on the underside of the wrist
must not be used.
Draws to the median cubital veins are preferred because they are typically closer to the surface of the
skin, more stationary, less painful upon needle insertion, and less likely to injure nerves if needle
placement is not accurate. Attempt to locate the median cubital vein on either arm before considering
alternative veins. Due to the proximity of the basilic vein to the brachial artery and the median nerve, this
vein should only be considered if no other vein is more prominent. Above all, phlebotomists should be
aware of the potential for injury associated with each vein and select the vein that brings the greatest
degree of confidence of being accessed successfully without risking nerve or arterial involvement. (See
Figure 1.)
Alternative sites such as ankles or lower extremities must not be used without the permission of the
physician because of the potential for significant medical complications (e.g., phlebitis, thrombosis, tissue
necrosis, etc.)10-12
8.6.7
8.6.7.1
Factors in Site Selection

Extensive Scarring
Healed burn areas are to be avoided.

8.6.7.2
Mastectomy
A physician must be consulted before drawing blood from the side on which a mastectomy was
performed because of the potential for complications due to lymphostasis.
8.6.7.3
Hematoma
Specimens collected through a hematoma area may cause erroneous test results. Phlebotomy must not be
performed on any size hematoma. If another vein site is not available, the specimen is collected distal to
the hematoma.
8.6.7.4
Intravenous Therapy
Preferably, specimens should not be collected from an arm with an intravenous site. (See Section 11.6).13
8.6.7.5
Cannula, Fistula, Vascular Graft
A cannulated arm is used only after consulting the attending physician.

8.6.8
8.6.8.1
Procedure for Vein Selection

Locating Veins
To locate veins, it is necessary to palpate and trace the path of veins several times with the index finger.
Unlike veins, arteries pulsate, are more elastic, and have a thick wall. Thrombosed veins lack resilience,
12
Volume 23
H3-A5
feel cord-like, roll easily, and should not be used. A tourniquet must be used to aid in the selection of a
vein site unless specific tests require tourniquets not be used (e.g., lactate). If a tourniquet must be
applied for the preliminary vein selection, it should be released and reapplied after two minutes.
8.7
Step 7: Put on Gloves
The phlebotomist must put gloves on before the venipuncture is performed, for each patient, with
consideration for latex sensitivity as discussed in Section 7.3.
8.8
Step 8: Cleanse Venipuncture Site
The puncture site must be cleansed to prevent microbiological contamination of either the patient or the
specimen.
8.8.1
Cleansing Method for Venipuncture
(1) Use a gauze pad with 70% isopropyl alcohol solution, or a commercially prepared alcohol pad.
(2) Cleanse the site with a circular motion from the center to the periphery.
(3) Allow the area to air dry to prevent hemolysis of the specimen and to prevent the patient from
experiencing a burning sensation when the venipuncture is performed.
8.8.2
For Blood Culture Collection
For blood cultures, it is necessary to carefully disinfect the venipuncture site. Chlorhexidine gluconate is
recommended for infants two months and older and patients with iodine sensitivity. Cleanse the site with
70% alcohol, then swab concentrically, starting at the middle of the site with a 1 to 10% povidone-iodine
solution (0.1 to 1% available iodine) or chlorhexidine gluconate. Allow the site to air dry, then remove the
iodine or chlorhexidine from the skin with alcohol.8
When specimens are obtained for blood cultures, disinfect the culture bottle stopper according to the
manufacturers instructions.
8.8.3
Touching the Site After Cleansing
If the venipuncture proves difficult and the vein must be touched again to draw blood, the site should be
cleansed again.
8.9
8.9.1
Step 9: Perform Venipuncture

Venipuncture Procedure When Venous Blood Collection Tubes Are Used
There are several different blood collection systems available that collect blood samples using different
principles. For example, there are evacuated tube systems and systems that have a flexible/dual collection
technique that employ either a vacuumuser evacuates the tube immediately prior to use referred to as
pre-evacuationor aspiration principle of collection. For the proper venipuncture technique using the
blood collection system selected refer to the manufacturers instructions for use.
(1)
If pre-evacuation is required, and the blood collection tubes are not evacuated by the
manufacturer, evacuate the tubes immediately prior to use according to the manufacturers
instructions.
13
Number 32
NCCLS
(2)
If not preassembled by the manufacturer, thread the appropriate needle into the holder until it is
secure.
(3)
When drawing blood for cultures, wipe the stopper with a suitable antiseptic solution. Make
certain the stopper is dry before performing the venipuncture.
(4)
Make sure the patients arm or other venipuncture site is in a downward position to prevent reflux
or backflow.
Figure 2. Proper Angle of Insertion (Figure contributed by the Center for Phlebotomy Education, Inc.)
Figure 3. Improper Angle of Insertion (Figure contributed by the Center for Phlebotomy Education, Inc.)
14
Volume 23
H3-A5
(5)
Prior to venipuncture, if required, assemble the tube to the needle/holder according to the
manufacturers instructions.
(6)
Hold the patients arm firmly distal to the intended puncture site. The phlebotomists thumb
should be used to draw the skin taut. This anchors the vein. The thumb should be 1 to 2 inches
(2.5 to 5.0 cm) below the venipuncture site.
(7)
To prepare the patient, inform him or her that the venipuncture is about to occur. NOTE: From
this point on, be prepared to react to a sudden and unexpected loss of consciousness.
(8)
With the bevel up, puncture the vein with the needle at an angle of insertion of 30 degrees or less
(See Figure 2). Keeping the needle as stable as possible in the vein, push/connect the first tube
onto the needle. Maintain the tube below the site when the needle is in the vein.
(9)
Release the tourniquet as soon as possible after the blood begins to flow. Do not change the
position of the tube until it is removed from the needle. During the collection, do not allow the
contents of the tube to contact the closure. Movement of the blood back and forth in the tube can
cause reflux into the venous system and possible adverse patient reaction.
(10)
Allow the tube to fill until the vacuum is exhausted and blood flow ceases. For tubes that contain
additives, this will ensure there is a correct ratio of blood to additive.
NOTE: For systems that collect blood using an aspiration principle of collection rather than a
vacuum, gently pull back on the piston rod until the piston reaches the base of the tube. This will
ensure there is a correct ratio of blood to additive.
(11)
When the blood ceases to flow, remove/disconnect the tube from the needle/holder. The sleeve
re-covers the needlepoint that pierces the tube closure, stopping blood flow until the next tube is
inserted/connected to the needle/holder. To obtain additional specimens, insert/connect the next
tube to the needle/holder and repeat the collection procedure. Always remove the last tube
collected from the needle/holder prior to withdrawing the needle from the vein. If only one tube
is collected this must be removed prior to withdrawing the needle from the vein.
(12)
Immediately after drawing each tube that contains an additive mix the blood gently and
thoroughly by inverting the tube five to ten times. To avoid hemolysis, do not mix vigorously.
For tubes that have been drawn using an aspiration principle, lock the piston into the base of the
tube and snap off the piston rod after mixing.
8.9.2
Venipuncture Procedure Using Needle and Syringe
In general, venipuncture using a needle and syringe should be avoided for safety reasons.
require a syringe draw, the following procedure is recommended:
If conditions
(1) Assemble the needle and syringe.

(2) Hold the patients arm firmly distal to the intended puncture site. The phlebotomists thumb should
be used to draw the skin taut. This anchors the vein. The phlebotomists thumb should be 1 or 2
inches (2.5 cm or 5.0 cm) below the venipuncture site.
(3) Prepare the patient by informing him or her that the venipuncture is about to occur.
(4) With the bevel up, puncture the vein with the needle at an angle of insertion of 30 degrees or less (see
Figure 2).
15
Number 32
NCCLS
(5) Keeping the needle as stable as possible in the vein, slowly withdraw the desired amount of blood.
(6) Release the tourniquet as soon as possible, after the blood begins to flow.
8.9.3
Fill the Tubes If Syringe and Needle Are Used
Syringe method of drawing venous blood is not recommended since it is much safer and easier to use a
closed, venous blood collection tube system. If it is necessary to use a syringe, proceed with the
following recommendations to transfer the blood from a syringe to a blood collection tube:
Use the same order of draw as for a venous blood collection tube system (see Section 8.10.2).
Rubber stoppers should not be removed from venous blood collection tubes to transfer blood to
multiple tubes.
To transfer the blood from the syringe to a venous blood collection tube, activate the safety feature of
the needle or winged blood collection set used to withdraw the specimen, remove and discard the
needle or winged collection set, and apply a safety transfer device.
The stopper is pierced with the needle and the tube is allowed to fill (without applying any pressure to
the plunger) until flow ceases. This technique helps to maintain the correct ratio of blood to additive
if an additive tube is being used.
Mix additive tubes by inversion.
8.9.4
Blood Specimen That Cannot Be Obtained
When a blood specimen cannot be obtained, it may be necessary to:
Change the position of the needle. If the needle has penetrated too far into the vein, pull it back a bit.
If it has not penetrated far enough, advance it farther into the vein. Rotate the needle half a turn.
Lateral needle relocation should never be attempted in an effort to access the basilic vein, since
nerves and the brachial artery are in close proximity.
Try another tube to ensure the tube selected is not defective.
Manipulation other than that recommended above is considered probing. Probing is not
recommended. Probing is painful to the patient. In most cases another puncture in a site below the
first site, or use of another vein on the other arm, is advisable.
It is not advisable to attempt a venipuncture more than twice. If possible, have another person attempt
to draw the specimen or notify the physician.
8.9.5
Ensure Patients Hand Is Open
Opening the patients hand reduces the amount of venous pressure as muscles relax. The patient must not
be allowed to pump the hand.
16
Volume 23
H3-A5
8.10 Step 10: Order of Draw

8.10.1 Additive Tubes
Gel separator tubes with clotting activators or anticoagulants are classified as additive tubes.14 (For further
information, refer to the most current edition of NCCLS document H18 Procedures for the Handling
and Processing of Blood Specimens). These tubes should be drawn after the coagulation tube (blue
stopper) and before other additive tubes (green, lavender, gray). All additive tubes should have a
complete draw (see Section 8.9.1[10]).
8.10.2 Glass and Plastic Venous Blood Collection Tubes
The following order-of-draw is recommended when drawing multiple specimens for clinical laboratory
testing during a single venipuncture. Its purpose is to avoid possible test result error due to cross
contamination from tube additives.15 This procedure should be followed for both glass and plastic venous
blood collection tubes.
(1)
(2)
(3)
(4)
(5)
(6)
Blood culture tube

Coagulation tube (e.g., blue closure)
Serum tube with or without clot activator, with or without gel (e.g., red closure)
Heparin tube with or without gel plasma separator (e.g., green closure)
EDTA (e.g., lavender closure)
Glycolytic inhibitor (e.g., gray closure)
NOTE: The order of draw has been revised to reflect the increased use of plastic blood collection tubes.
Plastic serum tubes containing a clot activator may cause interference in coagulation testing. Glass nonadditive serum tubes may be drawn before the coagulation tube.
NOTE: When using a winged blood collection set for venipuncture and a coagulation tube is the first
tube to be drawn, a discard tube should be drawn first. The discard tube must be used to fill the blood
collection tubing dead space and to assure maintenance of the proper anticoagulant/blood ratio and need
not be completely filled. The discard tube should be a nonadditive or a coagulation tube.
8.10.3 Coagulation Testing
Studies have shown that the PT (INR) and APTT results are not affected if tested on the first tube
drawn.16-18 Since it is not known whether other coagulation testing is affected, it may be advisable to draw
a second tube for other coagulation assays. When a syringe system is used and a large specimen is taken,
part of the blood from the second syringe should be used for the coagulation specimen. In the case of any
unexplained abnormal coagulation test result, a new specimen should be obtained and the test repeated. If
heparin contamination is suspected, the test should be repeated after the specimen is treated with a
method that removes or neutralizes heparin. For more detailed descriptions of collection for coagulation
testing, see the most current edition of NCCLS document H21Collection, Transport, and Processing of
Blood Specimens for Coagulation Testing and General Performance of Coagulation Assays.
8.11 Step 11: Release the Tourniquet

Release the tourniquet as soon as possible after the blood begins to flow.
8.12 Step 12: Place the Gauze Pad

A clean gauze pad should be placed lightly over the venipuncture site. Cotton balls are not recommended
because of the possibility of dislodging the platelet plug at the venipuncture site.
17
Number 32
NCCLS
8.13 Step 13: Remove and Dispose of the Needle

Remove the needle and activate the safety mechanism according to the device manufacturers
instructions. Safely dispose of the unit into an easily accessible sharps container, consistent with OSHA
regulations. Needles should not be resheathed, bent, broken, or cut, nor should they be removed from
disposable syringes unless attaching a safety transfer device prior to disposal. Phlebotomists should
anticipate a loss of consciousness and be prepared to react according to institutional policy. The use of
ammonia inhalants may be associated with untoward effects and is not recommended. (See Section
11.8.1).
8.14 Step 14: Bandage the Arm

8.14.1 Normal Conditions
Under normal conditions, the phlebotomist should:
(1) Place the gauze pad over the site, continuing mild pressure.
(2) Check that bleeding has ceased, observe for hematoma, and apply an adhesive or gauze bandage over
the venipuncture site. It is recommended that hypoallergenic adhesives be available.
(3) Tell patient to leave the bandage on for at least 15 minutes.
8.14.2 Continued Bleeding
The phlebotomist should watch for excessive bleeding. If a hematoma develops or bleeding persists
longer than five minutes, a nurse should be alerted so that the attending physician can be notified.
Pressure, applied with a gauze pad, must continue at the site as long as necessary to stop the bleeding.
Wrap a gauze bandage tightly around the arm to keep the pad in place and tell the patient to leave the
bandage on the site for at least 15 minutes.
8.15 Step 15: Label Blood Collection Tubes and Record Time of Collection
The patient and the patients blood specimen must be positively identified at the time of collection. Blood
specimens must be obtained in tubes identified with a firmly attached label bearing at least the following:
The patients first and last names

An identification number
The date
The time (as required, e.g., therapeutic drug monitoring)
The identification of the person collecting specimen.
The completed label must be attached to the tube before leaving the side of the patient, and there must be
a mechanism to identify the person who drew the blood.8 Alternatively, the manufacturers tube label can
be inscribed with the patients complete information. Blood bank specimens must be labeled according to
the standards set by the American Association of Blood Banks (AABB).
If an encoded (bar code) label is used, attach the label according to established institutional policy.
A permanent record is needed by the physician who must know exactly when each specimen was drawn
to correlate the results with any change in the patients condition. The laboratory also must document the
18
Volume 23
H3-A5
time when the specimen was collected. If unable to obtain specimens, a record of the reasons and initials
of the venipuncturist are necessary.
8.16 Step 16: Chill the Specimen (This is done only for certain specimens.)
Some tests require that blood specimens be cooled immediately following the venipuncture to slow down
metabolic processes which may alter some test results. For more information on blood specimen handling
and processing, see the most current edition of NCCLS document H18Procedures for the Handling and
Processing of Blood Specimens.
Examples of tests requiring chilling the specimen are:19
Gastrin
Ammonia
Lactic acid
Catecholamines
pH/blood gas
Parathyroid hormone (PTH).
8.17 Step 17: Send Blood Collection Tubes to the Proper Laboratories
Appropriately labeled blood collection tubes should be sent to appropriate laboratories designated to
perform the required testing procedures. (See Section 8.15 for recommendations for labeling of tubes.)
Venipuncture in Children and Difficult Collections
If a venipuncture is requested on a child younger than one year of age, the phlebotomist should consult
with the physician or follow institutional policy. For information on skin puncture blood collection, refer
to the most current edition of NCCLS document H4Procedures and Devices for the Collection of
Diagnostic Blood Specimens by Skin Puncture.
9.1
Procedure
Except where indicated below, the procedure for venipuncture of adults as described in Section 8 should
be followed for pediatric venipuncture.
9.2
Equipment
Venipunctures should be performed using equipment that can help to reduce the stress exerted on a vein
to prevent vascular collapse. Examples include a venous blood collection system with a 22- to 23-gauge
needle, or a 22- to 23-gauge (winged) blood collection set with attached tubing and venous blood
collection tube holder. For pediatric patients, through the age of 16, larger gauge needles may be
appropriate.
10 Additional Considerations
10.1 Monitoring Blood Volume Collected
It is recommended that a mechanism be in place to monitor the amount of blood drawn for pediatric and
critically ill patients to avoid phlebotomy-induced anemia.
19
Number 32
NCCLS
10.2 Hematoma
To prevent a hematoma when performing a venipuncture, the phlebotomist should:
Make sure the needle fully penetrates the uppermost wall of the vein (partial penetration may allow
blood to leak into the soft tissue surrounding the vein by way of the needle bevel).
Remove the tourniquet before removing the needle.
Use the major superficial veins.
Hold the venous blood collection assembly still while collecting the specimen.
Before bandaging, ensure that the puncture to the vein has sealed by observing for hematoma
formation after pressure is released.
Apply a small amount of pressure to the area with the gauze pad when bandaging the arm.
10.3 Hemolysis
To prevent hemolysis when performing a venipuncture, the phlebotomist should:
After cleansing, allow the venipuncture site to air dry.

Never draw blood through a hematoma.
If using a syringe, make sure the needle is fitted securely on a syringe to avoid frothing.
When using a syringe and needle, avoid drawing the plunger back too forcibly.
Gently invert the blood collection tube to mix additive specimens as recommended by the
manufacturer.
11 Special Situations
11.1 Timed Intervals
Some specimens must be drawn at timed intervals because of medications, fasting requirements, and/or
biological variations (circadian rhythm). It is important that collection of specimens for timed tests be
obtained at the precisely specified interval. Directions should be given to the venipuncture team to obtain
these specimens accurately.
11.1.1 Examples of Tests Requiring Timed Specimens
Tolerance tests (e.g., two-hour postprandial glucose and three-hour glucose tolerance test), cortisol
Therapy monitoring (e.g., prothrombin time, APTT, digoxin, and other drugs)
11.1.2 Documentation
For therapeutic drug monitoring, the dose of the medication and the time of the last dose given, as well as
the time of the specimen collection, should be recorded accurately on the request slip.
11.2 Specific Collection Techniques

11.2.1 Blood Alcohol
When drawing a blood specimen for alcohol testing, a nonalcohol-based cleanser should be used to
cleanse the venipuncture site (e.g., soap). (See the most current edition of NCCLS document T/DM6
Blood Alcohol Testing in the Clinical Laboratory for further information.)
20
Volume 23
H3-A5
11.2.2 Legal Specimens

Appropriate chain-of-custody procedure should be followed. (See NCCLS document T/DM6Blood
Alcohol Testing in the Clinical Laboratory.)
11.2.3 Blood Culture Specimens
There are time and temperature requirements to be followed in collection, transport and storage of
specimens for blood culture. In addition, there are variations in the volume of blood needed for culture.
In general, adult blood cultures require 10 to 20 mL/set and infant blood cultures are done on 1 to 2
mL/set.7 Please refer to the manufacturers instructions for specific blood volume requirements. These
requirements may vary considerably depending on the device.
11.2.4 Trace Elements
For collection of blood for trace elements testing (e.g., zinc) special, metal-free collection containers
should be used. (See the most current edition of NCCLS document C38Control of Preanalytical
Variation in Trace Element Determinations, for more information.)
11.2.5 Immunohematology Specimens
Gel separator tubes must not be used for immunohematology specimens.8 It is important to refer to
manufacturers package inserts for collection tubes and for test methods for other possible gel tube
application limitations.
11.3 Indwelling Lines or VADs

A line is a piece of tubing inserted into a patients vein or artery for administering fluids and medications,
monitoring pressures, and obtaining blood samples for diagnostic tests. Without complete, thorough and
documented training, it is not recommended that phlebotomists draw blood from indwelling
cardiovascular (arterial, central venous) or umbilical lines. Institutional policy should be followed.
NOTE: Under certain circumstances, blood specimens for clinical laboratory testing may be drawn from
a vascular access device (VAD) using a blood collection system or a syringe. When obtaining a blood
specimen from a VAD, the components of the blood collection system (VAD, connecting device, syringe,
needle, and collection device) should be checked to ensure compatibility to avoid air leaks, which may
cause hemolysis and incorrect draw volumes. Collection of the blood through lines that have been
previously flushed with heparin should be avoided, if possible. If the blood must be drawn through a
VAD, possible heparin contamination and specimen dilution should be considered. The line should be
flushed with 5 mL of saline, and the first 5 mL of blood or six dead space volumes of the VAD discarded.
11.3.1 Potential Error
Obtaining blood specimens from indwelling lines or VADs may be a problem and a potential source of
test error because of incomplete flushing of collection site resulting in contamination and/or dilution of
the specimen contributing to inaccurate results.20-22
11.3.2 Flushing Lines
Because it is normal practice to flush lines with a solution to reduce the risk of thrombosis, lines must be
cleared of this fluid before blood specimens can be drawn for diagnostic testing. An adequate amount of
blood must be withdrawn from the line and discarded before drawing a specimen to ensure that the actual
specimen is not diluted or contaminated with the flush solution. Discard volume is dependent on the dead
21
Number 32
NCCLS
space volume of the particular line. Discarding two times the dead-space volume is recommended for
noncoagulation testing, and 5 mL or six times the dead-space volume for coagulation tests.20,23-25 (For
additional information, please refer to the most current edition of NCCLS document H21Collection,
Transport, and Processing of Blood Specimens for Coagulation Testing and General Performance of
Coagulation Assays.) See the NOTE in Section 11.3 for specific recommendations for coagulation
testing specimens with line draws.
11.4 Heparin or Saline Locks

An indwelling winged infusion set can be successfully left in a vein from 36 to 48 hours for intravenous
administration of medication or as a vein source to obtain a blood specimen. This procedure, known as a
heparin or saline lock, has become more common in hospitals to save veins for therapeutic use and
also to cause less trauma to the patient. With this system, it is not necessary to keep the vein open with a
continuous intravenous infusion, thus allowing the patient more comfort and mobility.
11.5 Fistula
A fistula is an artificial shunt connection done by a surgical procedure to fuse the vein and artery together.
It is used for dialysis only.
An arm with a fistula should not be used routinely for blood drawing. When possible, specimens should
be drawn from the opposite arm. Care must be taken of the fistula, as it is permanent.
11.6 Intravenous Fluids

Skin puncture is recommended when venous access is not readily available. (See the most current edition
of NCCLS document H4Procedures and Devices for the Collection of Diagnostic Blood Specimens by
Skin Puncture for more information.)
When an intravenous fluid (including transfused blood products) is being administered in a patients arm,
blood should not be drawn from that arm if at all possible. Test results from this blood may be erroneous
and thus misleading to the physician.
Satisfactory specimens may be drawn distal to the intravenous infusion site. If this is not possible, a
specimen may be obtained from a proximal site.13,26 However, it has been shown that blood drawn
proximal to the intravenous site can be contaminated with the fluid being administered. Facilities should
establish their own policy. The collection procedure is as follows:
(1) Ask the responsible caregiver for the intravenous infusion to be turned off for at least two minutes
before venipuncture. Care should be taken to ensure that the flow has been completely discontinued.
(2) Apply the tourniquet. When drawing distal to the intravenous infusion site, apply the tourniquet
between the intravenous and the intended venipuncture site.
(3) Perform the venipuncture.
It must be documented that the venipuncture was performed proximal or distal to an infusion site and
from which arm.
22
Volume 23
H3-A5
11.7 Isolation
Patients are isolated to prevent disease from spreading to other patients, visitors, or employees.27 Some
hospitals may also provide a different, protective isolation for patients who could be placed at increased
risk from outside contamination.
11.7.1 Isolation Systems
Each hospital determines the system which best provides for their particular mix of patients, visitors, and
employees. In most cases, a color-coded card placed just outside the patients room describes the type of
isolation and the precautions to be taken by those entering the room. It is important to understand and use
the appropriate precautions.
11.7.1.1 Types of Isolation
Recent guidance emphasizes two tiers of infection control precautions27:
standard, to be used for all patients, and

transmission-based.
There are three types of transmission based isolation precautions23:
airborne,
droplet, and
contact.
Hospitals have protocols for isolation procedures available through their infection control practitioner,
infection control committee, or hospital epidemiologist. The example given in Sections 11.7.1.2 through
11.7.2 is an example of such a protocol. Some hospitals may provide for disinfection, dedication or
disposal of equipment used in isolation rooms.
11.7.1.2 Clean Area
Gowns, gloves, masks, etc., are kept in a clean area. In some hospitals, a stand containing these supplies
is kept outside the room. The new modern hospital often has an anteroom which serves as the clean
area. Here, the person entering the room can gown and apply other protective barriers as necessary
before entering the patients room. Doctors suit coats, jackets, and other apparel are left here.
11.7.2 Isolation Room
11.7.2.1 Procedures to Follow Before Entering the Isolation Room
(1)
Read the isolation sign on the door. It will explain the type of isolation, protective clothing to be
worn, and the procedure to follow. Follow these instructions carefully.
(2)
Check the orders and assemble an adequate amount of necessary equipment for the patient.
NOTE: Any supplies taken into the room must be left there, or discarded.
(3)
Never take trays into the isolation room.
23
Number 32
NCCLS
11.7.2.2 Procedures to Follow in an Isolation Room

(1)
Place paper towels on the table and place the equipment on one or two towels that have been spread
open.
(2)
Wash hands.
(3)
Put on gloves.
(4)
Obtain blood specimens in the usual manner, avoiding any unnecessary contact with the patient and
bed.
(5)
After mixing, place the filled tubes on a clean paper towel.
(6)
Dispose of blood collection assembly into an easily accessible, approved puncture resistant disposal
container, consistent with OSHA regulations, according to institutional policy.
NOTE: Recapping of needle is not recommended. (See the most current edition of NCCLS
publication M29Protection of Laboratory Workers from Occupationally Acquired Infections.)
(7)
Dispose of the tourniquet in the proper container.
(8)
Remove gown and gloves and dispose of them in the proper container.
(9)
Wash hands.
(10) Turn off the faucet with a clean paper towel so that hands are not contaminated.
(11) Pick up the tubes from the paper towel and clean the outside of the tube with 1:10 dilution of
bleach. Place tubes in a secondary container, which will contain the specimen if the primary
container breaks or leaks in transit to the laboratory. A plastic bag with a sealable, leakproof
closure can be used.
(12) If blood smears were made, place the smears on two clean paper towels. When ready to leave, wrap
the smears and tubes in the top paper towel and discard the bottom paper towel and place in a
secondary container.
11.7.3 Exposure
The phlebotomist must immediately report an accidental needlestick or contamination of a break in the
skin by blood or excreta to a supervisor, and follow institutional guidelines. (See also NCCLS document
M29Protection of Laboratory Workers from Occupationally Acquired Infections.)
11.8 Emergency Situations

At least one member of available on-site healthcare personnel should have extensive first aid training,
including special training in cardiopulmonary resuscitation, so that medical attention can be given to a
needy patient while the physician on call is en route. This individual should be identified to
phlebotomists. Emergency numbers should be posted in phlebotomy drawing areas.
11.8.1 Syncope (Fainting) or Unexpected Nonresponsiveness
The procedure for dealing with a patient who has fainted or is unexpectedly nonresponsive is to:
24
Volume 23
H3-A5
(1) Notify the designated first-aid trained personnel.

(2) Where practical, lay the patient flat or lower his/her head and arms, if the patient is sitting.
(3) Loosen tight clothing.
(4) The use of ammonia inhalants may be associated with untoward effects and is not recommended.
11.8.2 Nausea
The procedure for dealing with a patient who is experiencing nausea is to:
(1) Make the patient as comfortable as possible.
(2) Instruct the patient to breathe deeply and slowly.
(3) Apply cold compresses to the patients forehead.
11.8.3 Vomiting
The procedure for dealing with a patient who vomits is to:
(1) Give the patient an emesis basin or carton, and have tissues ready.
(2) Give the patient water to rinse out his/her mouth.
11.8.4 Convulsions
The procedure for dealing with a patient who is having convulsions is to:
(1) Prevent the patient from injuring himself/herself. Do not restrain the movements of the patients
extremities completely, but try to prevent him/her from being injured.
11.8.5 Incident Reports
Incident reports should be filed according to institutional policy.
25
Number 32
NCCLS
References
1
Nevalainen D, Berte L, Kraft C, Leigh E, Morgan T. Evaluating laboratory performance on quality indicators with the six sigma scale. Arch
Pathol Lab Med. 2000;124:516-519.
Ladenson JH. Nonanalytical sources of variation. In: Gradwohl's Clinical Laboratory Methods. 8th ed. St. Louis, MO: C.V. Mosby
Co.;1980:149-193.
O'Sullivan MB. Hematology. In: Schmidt RM, ed. CRC Laboratory Hematology Procedures
Science. Boca Raton, FL: CRC Press; 1979;1:5.
Statland BE, Winkel P. Effects of preanalytical factors on the intraindividual variation of analytes in the blood of healthy subjects:
Consideration of preparation of the subject and time of venipuncture. CRC Crit Rev Clin Lab Sci. 1977;2:105-144.
Young DS. Biological variability. In: Brown SS, Mitchell FL, and Young DS, eds. Chemical Diagnosis of Diseases. Amsterdam: Elsevier,
North-Holland: Biomedical Press; 1979.
Guder WG, Narayanan S, Wisser H, Zawata B. Samples: From the patient to the laboratory. Git Verlag GMBH. 1996.
Miller JM, Holmes HT. Specimen collection, transport and storage. In: Murray PR, ed. Manual of Clinical Microbiology. 7th ed.
Washington, D.C.: ASM Press; 1999.
AABB. Technical Methods and Procedures of the American Association of Blood Banks. 12th ed. Philadelphia: J.B. Lippincott Company;
1996.
U.S. Department of Labor and Occupational Safety and Health Administration (OSHA). Enforcement Procedures for the Occupational
Exposure to Bloodborne Pathogens. Washington, DC: OSHA; Nov. 27, 2001. OSHA Instruction CPL2-2.69.
10
Kovanda B. Multiskilling: Phlebotomy Collection Procedures for the Health Care Provider. Albany, NY: Delmar; 1998.
11
Ernst C, Ernst D. Phlebotomy for Nurses and Nursing Personnel. Ramsey, IN: HealthStar Press; 2001.
12
Sommer S. Warekois R. Phlebotomy Worktext and Procedures Manual. Philadelphia, PA: W.B. Saunders; 2002.
13
Read DC, Viera H, Arkin CF. Effect of drawing blood specimens proximal to an in-place but discontinued intravenous solution: can blood
be drawn above the site of a shut-off IV. AM J Clin Path. 1988; 906:702-706.
14
Calam RR. Specimen processing separator gels: An update. J Clin Immunoassay. 1988;11:86-90.
15
Calam RR, Cooper MH. Recommended order of draw for collecting blood specimens into additive-containing tubes. Clin Chem.
1982;28:1399.
16
Gottfried EL, Adachi MM. Prothrombin time (PT) and activated partial thromboplastin time (APTT) can be performed on the first tube. Am
J Clin Pathol. 1997;107:681-683.
17
Yawn BP, Loge C, Dale JC. Prothrombin time. One tube or two? Am J Clin Pathol. 1996;105:794-797.
18
Bamberg R, Cottle J, Williams J. Effect of drawing a discard tabe on PT and APTT results in healthy adults. Clinic Lab Sci. 2003:161:1619.
19
Young DS, Bermes EW. Specimen collection and processing: Sources of biological variation. In: Tietz NS, ed. Textbook of Clinical
Chemistry. Philadelphia: WB Saunders; 1986:494.
20
Laxson CJ, Titler MG. Drawing coagulation studies from arterial lines: an integrative literature review. Am J Crit Care. 1994;1:16-24.
21
Soong WJ, Hwang B. Contamination errors when sampling blood from an aterial line. Clin Pediatr. 1993;328:501.
22
Templin K, Shively M, Riley J. Accuracy of drawing coagulation samples from heparinized arterial lines. Amer J Crit Care 2. 1993;1:88.
23
Clapham MCC, Willis N, Mapleson WW. Minimum volume of discard for valid blood sampling from indwelling arterial cannulae. Br J
Anaesth. 1987;59:232-235.
24
Molyneaux RD, Papciak B. Rorem DA. Coagulation studies and the indwelling heparinized catheter. Heart Lung 1987;16:20-23.
25
Rudisill PT, Moore LA. Relationship between arterial and venous activated partial thromboplastin time values in patients after percutaneous
transluminal coronary angioplasty. Heart Lung. 1989;18:514-519.
26
Savage R, ed. Q & A column. CAP Today. 2002:16(4):102-103.
27
Garner JS and Hospital Infection Control Practice Advisory Committee. Guidelines for Isolation Precautions in Hospitals. Atlanta, GA:
U.S. Dept of Health and Human Services, Centers for Disease Control and Prevention; 1996.
26
Handbook Series in Clinical Laboratory
Volume 23
H3-A5
NCCLS consensus procedures include an appeals process that is described in detail in Section 8 of
the Administrative Procedures. For further information, contact the Executive Offices or visit our
website at www.nccls.org.
Summary of Comments and Subcommittee Responses

H3-A4: Procedures for the Collection of Diagnostic Blood Specimens by Venipuncture; Approved
StandardFourth Edition
General
1.
NCCLS has inconsistencies in their own publications (H3 and H21) when it comes to the order of draw for coagulation
testing relative to tissue thromboplastin contamination and procurement of a discard tube. In performing intra-laboratory
studies at our institution and sister institutions, results showed no significant clinical or statistical significance on any of the
assays between each of the specimen tubes performed at each individual laboratory. Also, our results indicated that NCCLS
guidelines for obtaining a second tube when performing coagulation testing should be eliminated when the revised
document is published.
The text has been revised (see Section 8.10.2), including the order of draw, and several notes have been added to
address the use of discard tubes for coagulation test collection. The next version of H21Collection, Transport, and
Processing of Blood Specimens for Coagulation Testing and General Performance of Coagulation Assays is due to be
released by the end of 2003. The documents are now consistent.
Section 7.9.3.4, Intravenous Therapy (Now Section 8.6.7.4)

2.
The text of this section states, Optimally, specimens should not be collected from an arm with an intravenous site. If this is
impossible the attending physician should be consulted (see Section 10.3). Blood should never be collected from above any
active intravenous site (see Section 10.6). We would like a clearer definition of what is considered to be active. What
defining factors are present that would classify an active intravenous site?
The term active has been removed from the text. The text in Sections 8.6.7.4 and 11.6 has been revised to describe
the procedure for specimen collection in relation to intravenous fluids.
Section 7.13.3.3, Coagulation Testing (Now Section 8.10.3)

3.
The text of this section states, if only a coagulation tube is drawn for routine coagulation testing (APTT and PT tests) the
first tube drawn may be used for testing. This statement has raised some discussion regarding the definition of the phrase
routine coagulation testing. Does this include coumadin patient samples?
Specimens collected from patients on warfarin sodium (CoumadinTM) are considered for routine coagulation testing.
Section 10, Special Situations (Now Section 11)

4.
H3-A4 does not list recommendations for obtaining venipuncture specimens during blood transfusions. Information on this
topic would be greatly appreciated.
The directions outlined in Section 11.6 should be followed during transfusions as it is described for intravenous
fluids.
27
Number 32
NCCLS
Summary of Delegate Comments and Working Group Responses

H3-A5: Procedures for the Collection of Diagnostic Blood Specimens by Venipuncture; Approved
StandardFifth Edition
General
1.
Nothing was included about pain management (EMLA, coldspray, etc.) or age-specific consideration on developmental
stages of children. I can send you what we have if you like.
The working group recognizes the availability of pain reducing techniques. Topical sprays and treatments are
available and are used at the discretion of each institution.
Age-specific considerations are outside the scope of this document. Please refer to the current edition of NCCLS
document H4Procedures and Devices for the Collection of Diagnostic Blood Specimens by Skin Puncture.
2.
Add a Section 11.2.6, RNA Specimen. Since RNA is unstable, the whole blood should be transported to the laboratory at 2
to 25 C within six hours of collection.
References: de Gerbehaye A-I, et al. Stable hepatitis C virus RNA detection by RT-PCR during four days storage. BMC
Infectious Diseases. 2002;2:22, and Halfon P, et al. Impact of various handling and storage conditions on quantitative
defection of hepatitis C virus RNA. J Hepatol. 1996;25:307-311.
This comment is more related to specimen handling than collection and is beyond the scope of this document. This
comment will be considered during the revision of NCCLS document H18-A2Procedures for the Handling and
Processing of Blood Specimens; Approved Guideline.
Foreword
3.
Page vii should include hemolysis and clotting of samples, as these are common problems with hematology or coagulation
samples. The errors that can occur during the collection and handling of blood specimens are potentially numerous (e.g.,
inaccurate identification of specimens, the use of incorrect anticoagulant, the formation of hematomas,
hemoconcentration).
The text has been revised to include specimen hemolysis and improper handling of anticoagulants.
Section 8, Venipuncture Procedure

4.
Consider switching steps 14 and 15 so that bandaging occurs after specimens are labeled, not before. This helps assure that
specimen labeling will occur before leaving the patients side. It also accommodates situations in which the patient assists in
applying pressure while the phlebotomist labels tubes.
The working group appreciates the comment; we believe, however, that the order is correct as written. The text in
Section 8.15 emphasizes the need to label the tube before leaving the side of the patient.
5.
Between steps 5 and 6, add the following: Inquire as to patient's sensitivity to latex products. Step 7, change as follows:
Put on appropriate gloves based on patients response to Step 6.
The working group agrees with the comment. The text of step 3 has been revised as follows: Verify patient's diet
restrictions, as appropriate, and inquire if the patient has a latex sensitivity. Select appropriate gloves and
tourniquet.
6.
Modify step 6 to new step 6: Inquire on patient's allergy to latex products. Also add: Due to the prevalence of latex
sensitivity, the phlebotomist should inquire as the patients sensitivity to latex products (tourniquet and gloves.)
The text of Step 3 and Section 8.3 has been revised to include asking the patient if he/she has a latex sensitivity. The
text in Section 8.6 has been revised to refer the reader to Section 7.7.
7.
The patient should be asked to open his/her hand just when entering the vein, therefore eliminating some of the pain a tense
closed fist may cause. Also, recommend performing venipuncture using the correct order of draw.
In response to this comment, the text of step 9 has been revised as follows: Perform venipuncture; once blood flow
begins, request patient to open hand. Step 10 has been revised to recommend the use of the correct order of draw.
28
Volume 23
H3-A5
8.
Following the removal of the needle, pressure should be applied to the venipuncture site (either by the patient or
phlebotomist).
In response to this comment, the text of step 14 has been revised as follows: Apply pressure to the site, making sure
bleeding has stopped, and then bandage the arm.
Section 8.1.1, Information for Test Request Form

9.
May include should be utilized.
The working group believes that the test request form information listed should be included.
Section 8.1.2, Accessioning Blood Bank Specimens

10. Neither AABB nor CAP requires time of collection on the specimen tube label.
Time of collection is important for some specimens (e.g., therapeutic drug monitoring). The subcommittee confirmed
that AABB does not require time of collection on the specimen tube label. The text, Blood bank specimens must
be labeled according to the standards set by the American Association of Blood Banks (AABB), has been
incorporated into Section 8.15, Label Blood Collection Tubes and Record Time of Collection. The remainder of
Section 8.1.2 has been deleted.
11. This passage is more about patient identification and labeling specimens than accessioning. Passages are important, but
seem out of place. Consider moving the passage on identifying blood bank patients to Section 8.2 (Step 2: Approach and
Identify the Patient.) and the passage about labeling to Section 8.15 (Step 15: Label Blood Collection Tubes and Record
Time of Collection).
See response to comment 10.
Section 8.2.3, Patient Who Is Semiconscious, Comatose, or Sleeping

12. This passage does not address identification and is out of place. Consider moving to Section 8.5.4.
The location of this text is appropriate. Section 8.2 addresses both approaching and identifying the patient. The
following has been added to the end of the paragraph: If unable to identify the patient, then contact the nurse or
physician.
Section 8.2.4, Patient Who Is Unconscious, Too Young, Mentally Incompetent, or Does Not Speak the Language of the
Phlebotomist
13. The first bullet states, Ask the nurse, a relative, or a friend to identify the patient by name, address, and identification
number and/or birth date. This is inconsistent with Section 8.2.2, re: asking for patients address and identification number.
Suggest changing and to or for consistency with step 1 of 8.2.2.
The text in Section 8.2.4 has been revised for consistency with Section 8.2.2.
Section 8.4.1, Supplies

14. Inspect all supplies for possible defects should include inspection of expiration dates on blood collection tubes.
The text has been revised to include applicable expiration dates during inspection of supplies.
15. Supplies, sharps, or other disposal container is missing from the list (as discussed in Section 8.13). This should be available
at the bedside for safe disposal.
The following bullet point has been added to the list: Sharps container, consistent with OSHA regulations.
16. Supplies such as tubes and needles should be checked before use to ensure they are not outdated. Sterile conditions or tube
vacuum could be lost in old supplies. NCCLS document H4-A discusses tube stability and dating; H1-A4 discusses
expiration date. Therefore, this step should be added to the collection procedure.
See response to comment 13.
29
Number 32
NCCLS
Section 8.6.3, Blood Pressure Cuff

17. In Section 7.7 the blood pressure cuff is said to be inflated to 40 mmHg. However, in Section 8.6.3 it is said that a blood
pressure is taken first (an activity performed by NO phlebotomists I know) and maintained below the diastolic pressure of
the patient. I would recommend using the specific 40 mm Hg found in Section 7.7 and replace the language in Section 8.6.3
with the same.
The text has been revised as recommended. The following text has been added to replace the previous text: If a
blood pressure cuff is used as a tourniquet, inflate it to 40 mm Hg.
Section 8.6.5, Select Vein

18. Brachial is misspelled in Figure 1.
The spelling error in Figure 1 has been corrected.
Section 8.7, Step 7: Put on Gloves

19. Step 7: Add the following after the existing sentence: is performed. The type of gloves (latex, vinyl or nitrile) used for
venipuncture will depend on the patients and/or phlebotomists sensitivity to latex products. General noteAs both a
patient and laboratorian, I know the importance of covering the issue of latex sensitivity with both patients and the
phlebotomists. I highly recommend that you incorporate the information presented here into the document.
The text has been revised as follows: The phlebotomist must put gloves on before the venipuncture is performed, for
each patient, with consideration for latex sensitivity as discussed in Section 7.3.
Section 8.9.1, Venipuncture Procedure When Venous Blood Collection Tubes Are Used
20. The illustration on page 14 is very primitive and would be improved if the proper angle included a view of the needle bevel
up just as the needle enters the skin.
The illustrations (Figures 2 and 3) have been replaced with comparable photographs.
Section 8.9.3, Fill the Tubes If Syringe and Needle Are Used
21. The third bullet suggests a straight needle be applied to the syringe after removing the winged collection set. Consider
substituting attach a 19- to 21-gauge sterile needle with attach a safety transfer device.
The text of the third bullet has been revised as follows: To transfer the blood from the syringe to a venous blood
collection tube, activate the safety feature of the needle or winged blood collection set used to withdraw the specimen,
remove and discard the needle or winged collection set, and apply a safety transfer device.
22. The fourth bullet seems to define the third bullet. Consider combining the two.
The working group agrees with the comment and has deleted the fourth bullet.
23. The fifth bullet is not necessary in light of the third bullet. If standards are being followed, a transfer device protects the
user, and holding the tubes should be safe.
The fifth bullet has been deleted as suggested.
Section 8.9.4, Blood Specimen That Cannot Be Obtained

24. Consider making the passage about trying another tube into a bullet. Consider differentiating between probing and a
calculated needle relocation in an additional bullet so that the section is rewritten as follows:
30
Try another tube to ensure the tube selected is not defective.

Change the position of the needle. If the needle has penetrated too far into the vein, pull it back a bit. If it has not
penetrated far enough, advance it farther into the vein. Rotate the needle half a turn.
Lateral needle relocation should be attempted only if the phlebotomist has a high degree of confidence that so doing
will access the vein successfully without risking injury to the patient. Lateral needle relocation should never be
attempted in an effort to access the basilic vein, since nerves and the brachial artery are in close proximity.
Volume 23
H3-A5
Manipulation other than that recommended above is considered probing. Probing is not recommended. Probing is
painful to the patient. In most cases, another puncture in a site below the first site (or use of another vein on the other
arm) is advisable.
It is not advisable to attempt a venipuncture more than twice. If possible, have another person attempt to draw the
specimen or notify the physician.
The following text has been added to the first bullet point: Lateral needle relocation should never be attempted in
an effort to access the basilic vein, since nerves and the brachial artery are in close proximity.
Section 8.10.2, Glass and Plastic Venous Blood Collection Tubes

25. Consider deleting tube 4: gel serum separator tube. Since gel does not carryover, its presence or absence should not affect
the order of draw. It seems more fitting for the second italicized paragraph to immediately follow the order of draw than the
first paragraph.
Gel serum separator tube has been deleted from the fourth position on the order of draw. The third position has been
revised as follows: Serum tube with or without clot activator, with or without gel (e.g., red closure).
The italicized paragraphs have been reorganized as suggested; the note regarding the revised order of draw appears
immediately following the order of draw.
Section 8.13, Step 13: Remove and Dispose of the Needle

26. Removal of a needle (after the safety feature is activated) is necessary and acceptable to OSHA if applying a safety transfer
device. Consider modifying to read: Needles should not be resheathed, bent, broken, or cut, nor should they be removed
from disposable syringes unless attaching a safety transfer device
The text of the third sentence has been revised as follows: Needles should not be resheathed, bent, broken, or cut,
nor should they be removed from disposable syringes unless attaching a safety transfer device prior to disposal.
Section 8.14.2, Continued Bleeding

27. When a patient continues to bleed, indicates that it is inevitable. Consider revising to If a patient continues to bleed or a
hematoma develops,
The text has been revised as recommended. The first paragraph now reads as follows: If a hematoma develops or
bleeding persists longer than five minutes, a nurse should be alerted so that the attending physician can be notified.
Section 8.15, Step 15: Label Blood Collection Tubes and Record Time of Collection
28. Step 15: Consider revising the paragraph after the bullet list to accommodate handwritten identification of tubes. Suggested
revision: The label must be attached to the tube or the tube inscribed with complete information before leaving the side of
the patient .
The text has been revised as recommended. The following text has been added to the second paragraph:
Alternatively, the manufacturers tube label can be inscribed with the patients complete information.
29. Tubes should be labeled in accordance with the laboratory requirements. These may not meet all requirements for all
laboratories.
The text in this section has been revised in response to comment 9.
Section 9, Venipuncture in Children and Difficult Collections

30. Passage states, If a venipuncture is done on a child younger than one year of age, the site should be limited to superficial
veins. As opposed to what? This statement is unclear.
The first sentence has been revised for clarity. The revision is as follows: If a venipuncture is requested on a child
younger than one year of age, the phlebotomist should consult with the physician or follow institutional policy.
Section 9.2, Equipment

31. Consider modifying the range of needles to be used on pediatrics from 20-23 to 22-23 for patient comfort unless platelet
aggregation studies are required.
31
Number 32
NCCLS
The needle gauge range has been revised as suggested. The following text has also been added: For pediatric
patients, through the age of 16, larger gauge needles may be appropriate.
Section 11.6, Intravenous Fluids

32. Add the following reference: Savage R, ed. Q&A column. CAP Today. 2002:16(4):102-103.
32
The recommended reference, regarding performance of venipunctures above intravenous sites, has been added as
suggested.
Volume 23
H3-A5
NOTES
33
Number 32
NCCLS
The Quality System Approach

NCCLS subscribes to a quality system approach in the development of standards and guidelines, which facilitates
project management; defines a document structure via a template; and provides a process to identify needed
documents through a gap analysis. The approach is based on the model presented in the most current edition of
NCCLS HS1A Quality System Model for Health Care. The quality system approach applies a core set of quality
system essentials (QSEs), basic to any organization, to all operations in any healthcare services path of workflow.
The QSEs provide the framework for delivery of any type of product or service, serving as a managers guide. The
quality system essentials (QSEs) are:
Documents & Records
Organization
Personnel
Equipment
Purchasing & Inventory
Process Control
Information Management
Occurrence Management
Assessment
Process Improvement
Service & Satisfaction
Facilities & Safety
X
H1
X
T/DM6
Facilities &
Safety
Service &
Satisfaction
Process
Improvement
Assessment
Occurrence
Management
Information
Management
Process
Control
Purchasing &
Inventory
Equipment
Personnel
Organization
Documents
& Records
H3-A5 addresses the quality system essentials (QSEs) indicated by an X. For a description of the other NCCLS
documents listed in the grid, please refer to the Related NCCLS Publications section on the next page.
X
M29
Adapted from NCCLS document HS1 A Quality System Model for Health Care.
Path of Workflow
A path of workflow is the description of the necessary steps to deliver the particular product or service that the
organization or entity provides. For example, GP26-A2 defines a clinical laboratory path of workflow which
consists of three sequential processes: preanalytical, analytical, and postanalytical. All clinical laboratories follow
these processes to deliver the laboratorys services, namely quality laboratory information.
H3-A5 addresses the clinical laboratory path of workflow steps indicated by an X. For a description of the other
NCCLS documents listed in the grid, please refer to the Related NCCLS Publications section on the next page.
X
H18
X
T/DM6
Post-test
Specimen
Management
X
C38
H4
H11
H21
Postanalytic
Results
Report
Testing
Review
X
C38
H4
H11
H21
Laboratory
Interpretation
Specimen
Receipt
Specimen
Transport
Test Request
Analytic
Specimen
Collection
Patient
Assessment
Preanalytic
Adapted from NCCLS document HS1 A Quality System Model for Health Care.
34
Volume 23
H3-A5
Related NCCLS Publications*

C38-A
Control of Analytic Variation in Trace Element Analysis; Approved Guideline (1997). This document
provides guidelines for patient preparation, specimen collection, transport, and processing for the analysis of trace
metals in a variety of biological matrices.
H1-A4
Evacuated Tubes and Additives for Blood Specimen CollectionFourth Edition; Approved Standard
(1996). This document provides requirements for blood collection tubes and additives.
H4-A4
Procedures and Devices for the Collection of Diagnostic Blood Specimens by Skin Puncture; Approved
StandardFourth Edition (1999). A consolidation of H4-A3 and H14-A2, this standard provides detailed
descriptions and explanations of proper collection techniques, as well as hazards to patients from inappropriate
specimen collection by skin puncture procedures.
H11-A3
Procedure for the Collection of Arterial Blood Specimens; Approved StandardThird Edition (1999).
American National Standard. This standard describes principles of collecting, handling, and transporting arterial
blood specimens. The document is aimed at reducing collection hazards and ensuring integrity of the arterial
specimen.
H18-A2
Procedures for the Handling and Processing of Blood Specimens; Second EditionApproved Guideline
(1999). This guideline addresses multiple factors associated with handling and processing specimens, as well as
factors that can introduce imprecision of systematic bias into results.
H21-A3
Collection, Transport, and Processing of Blood Specimen for Coagulation Testing and General
Performance of Coagulation Assays; Approved GuidelineThird Edition (1998). This guideline contains
procedures for collecting, transporting, and storing blood; processing blood specimens; storing plasma for
coagulation testing; and provides general recommendations for performing the tests.
M29-A2
Protection of Laboratory Workers from Occupationally Acquired Infections; Approved GuidelineSecond

Edition (2001). This document provides guidance on the risk of transmission of hepatitis viruses and human
immunodeficiency viruses in any laboratory setting; specific precautions for preventing the laboratory
transmission of blood-borne infection from laboratory instruments and materials; and recommendations for the
management of blood-borne exposure.
T/DM6-A
Blood Alcohol Testing in the Clinical Laboratory; Approved Guideline (1997). This document gives
technical and administrative guidance on laboratory procedures related to blood alcohol testing.
Proposed- and tentative-level documents are being advanced through the NCCLS consensus process; therefore, readers should
refer to the most recent edition.
35
Number 32
NCCLS
NOTES
36
Volume 23
H3-A5
NOTES
37
Number 32
NCCLS
NOTES
38
Volume 23
H3-A5
NOTES
39
Active Membership
(as of 1 October 2003)
Sustaining Members
Abbott Laboratories
American Association for Clinical
Chemistry
Bayer Corporation
BD
bioMrieux, Inc.
CLMA
College of American Pathologists
GlaxoSmithKline
Ortho-Clinical Diagnostics, Inc.
Pfizer Inc
Roche Diagnostics, Inc.
Professional Members
American Academy of Family
Physicians
American Association for Clinical
Chemistry
American Association for Respiratory Care
American Chemical Society
American Medical Technologists
American Society for Clinical
Laboratory Science
American Society for Microbiology
American Society of Hematology
American Type Culture Collection,
Inc.
Asociacion Mexicana de Bioquimica
Clinica A.C.
Assn. of Public Health Laboratories
Assoc. Micro. Clinici ItalianiA.M.C.L.I.
British Society for Antimicrobial
Chemotherapy
Canadian Society for Medical
Laboratory Science - Socit
Canadienne de Science de
Laboratoire Mdical
Canadian Standards Association
Clinical Laboratory Management
Association
COLA
College of American Pathologists
College of Medical Laboratory
Technologists of Ontario
College of Physicians and Surgeons
of Saskatchewan
ESCMID
International Council for
Standardization in Haematology
International Federation of Biomedical
Laboratory Science
International Federation of Clinical
Chemistry
Italian Society of Clinical Biochemistry and
Clinical Molecular Biology
Japan Society of Clinical Chemistry
Japanese Committee for Clinical
Laboratory Standards
Joint Commission on Accreditation
of Healthcare Organizations
National Academy of Clinical
Biochemistry
National Association of Testing
Authorities - Australia
National Society for
Histotechnology, Inc.
Ontario Medical Association Quality
Management Program-Laboratory
Service
RCPA Quality Assurance Programs
PTY Limited
Sociedad Espanola de Bioquimica
Clinica y Patologia Molecular
Sociedade Brasileira de Analises
Clinicas
Taiwanese Committee for Clinical
Laboratory Standards (TCCLS)
Turkish Society of Microbiology
Government Members
Armed Forces Institute of Pathology
Association of Public Health Laboratories
BC Centre for Disease Control
Centers for Disease Control and
Prevention
Centers for Medicare & Medicaid
Services
Centers for Medicare & Medicaid
Services/CLIA Program
Chinese Committee for Clinical
Laboratory Standards
Commonwealth of Pennsylvania
Bureau of Laboratories
Department of Veterans Affairs
Medical Center
Deutsches Institut fr Normung

(DIN)
FDA Center for Devices and
Radiological Health
FDA Center for Veterinary Medicine
FDA Division of Anti-Infective
Drug Products
Iowa State Hygienic Laboratory
Massachusetts Department of Public
Health Laboratories
National Center of Infectious and
Parasitic Diseases (Bulgaria)
National Health Laboratory Service
(South Africa)
National Institute of Standards and
Technology
New York State Department of
Health
Ontario Ministry of Health
Pennsylvania Dept. of Health
Saskatchewan Health-Provincial
Laboratory
Scientific Institute of Public Health;
Belgium Ministry of Social
Affairs, Public Health and the
Environment
Swedish Institute for Infectious
Disease Control
Industry Members
AB Biodisk
Abbott Laboratories
Abbott Laboratories, MediSense
Products
Acrometrix Corporation
Alifax S.P.A.
Ammirati Regulatory Consulting
A/S ROSCO
AstraZeneca Pharmaceuticals
Aventis
Axis-Shield POC AS
Bayer Corporation - Elkhart, IN
Bayer Corporation - Tarrytown, NY
Bayer Corporation - West Haven,
CT
Bayer Medical Ltd.
BD
BD Consumer Products
BD Diagnostic Systems
BD Italia S.P.A.
BD VACUTAINER Systems
Beckman Coulter, Inc. Primary Care
Diagnostics
Beckman Coulter K.K. (Japan)
Bio-Development SRL
Bio-Inova Life Sciences
International
Biomedia Laboratories SDN BHD
bioMrieux, Inc. (MO)
Biometrology Consultants
Bio-Rad Laboratories, Inc.
Bio-Rad Laboratories, Inc. - France
Blaine Healthcare Associates, Inc.
Bristol-Myers Squibb Company
Canadian External Quality
Assessment Laboratory
Chiron Corporation
ChromaVision Medical Systems,
Inc.
The Clinical Microbiology Institute
Cognigen
Community Medical Center (NJ)
Copan Diagnostics Inc.
Cosmetic Ingredient Review
Cubist Pharmaceuticals
Dade Behring Inc. - Cupertino, CA
Dade Behring Inc. - Deerfield, IL
Dade Behring Inc. - Glasgow, DE
Dade Behring Inc. - Marburg,
Germany
Dade Behring Inc. - Sacramento, CA
Dade Behring Inc. - San Jose, CA
David G. Rhoads Associates, Inc.
Diagnostic Products Corporation
Diagnostics Consultancy
Eiken Chemical Company, Ltd.
Electa Lab s.r.l.
Enterprise Analysis Corporation
EXPERTech Associates, Inc.
F. Hoffman-La Roche AG
Fort Dodge Animal Health
General Hospital Vienna (Austria)
Gen-Probe
GlaxoSmithKline
Greiner Bio-One Inc.
IGEN Inc.
Immunicon Corporation
ImmunoSite, Inc.
Instrumentation Laboratory
International Technidyne
Corporation
I-STAT Corporation
Johnson and Johnson Pharmaceutical
Research and Development, L.L.C.
LAB-Interlink, Inc.
Laboratory Specialists, Inc.
Labtest Diagnostica S.A.
LifeScan, Inc. (a Johnson & Johnson
Company)
Lilly Research Laboratories
LUZ, Inc.
Medical Device Consultants, Inc.
Merck & Company, Inc.
Minigrip/Zip-Pak
mvi Sciences (MA)
NimbleGen Systems, Inc.
Nippon Becton Dickinson Co., Ltd.
Nissui Pharmaceutical Co., Ltd.
Norfolk Associates, Inc.
Novartis Pharmaceuticals
Corporation
Ortho-Clinical Diagnostics, Inc.
(Rochester, NY)
Ortho-McNeil Pharmaceutical
Oxoid Inc.
Paratek Pharmaceuticals
Pfizer Inc
Pfizer Inc - Kalamazoo, MI
Pfizer Italia Srl
Powers Consulting Services
Premier Inc.
Procter & Gamble Pharmaceuticals,
Inc.
QSE Consulting
Quintiles, Inc.
Radiometer America, Inc.
Radiometer Medical A/S
Replidyne
Roche Diagnostics GmbH
Roche Diagnostics, Inc.
Roche Laboratories (Div. HoffmannLa Roche Inc.)
SARL Laboratoire Carron (France)
Sarstedt, Inc.
Schering Corporation
Schleicher & Schuell, Inc.
Second Opinion
Seraphim Life Sciences Consulting
LLC
Streck Laboratories, Inc.
SYN X Pharma Inc.
Sysmex Corporation (Japan)
Sysmex Corporation (Long Grove,
IL)
Theravance Inc.
The Toledo Hospital (OH)
Transasia Engineers
Trek Diagnostic Systems, Inc.
Tyco Kendall Healthcare
Vetoquinol S.A.
Vicuron Pharmaceuticals Inc.
Vysis, Inc.
Wyeth Research
Xyletech Systems, Inc.
YD Consultant
YD Diagnostics (Seoul, Korea)
Trade Associations
AdvaMed
Japan Association Clinical
Reagents Ind. (Tokyo, Japan)
Medical Industry Association
of Australia
Associate Active Members
31st Medical Group/SGSL (APO,
AE)
67th CSH Wuerzburg, GE (NY)
121st General Hospital (CA)
Academisch Ziekenhuis -VUB
(Belgium)
Acadiana Medical Laboratories,
LTD (LA)
Akershus Central Hospital and AFA
(Norway)
Albemarle Hospital (NC)
Allina Health System (MN)
Anne Arundel Medical Center (MD)
Antwerp University Hospital
(Belgium)
Arkansas Department of Health
Armed Forces Research Institute of
Medical Science (APO, AP)
ARUP at University Hospital (UT)
Associated Regional & University
Pathologists (UT)
Atlantic Health System (NJ)

Aurora Consolidated Laboratories
(WI)
AZ Sint-Jan (Belgium)
Azienda Ospedale Di Lecco (Italy)
Baxter Regional Medical Center
(AR)
Bay Medical Center (MI)
Baystate Medical Center (MA)
Bbaguas Duzen Laboratories
(Turkey)
BC Biomedical Laboratories (Surrey,
BC, Canada)
Bermuda Hospitals Board
Bon Secours Hospital (Ireland)
Boulder Community Hospital (CO)
Brooks Air Force Base (TX)
Broward General Medical Center
(FL)
Cadham Provincial Laboratory
Calgary Laboratory Services
Cape Breton Healthcare Complex
(Nova Scotia, Canada)
Carilion Consolidated Laboratory
(VA)
Carolinas Medical Center (NC)
Cathay General Hospital (Taiwan)
Cavan General Hospital (Ireland)
Central Peninsula General Hospital
(AK)
Central Texas Veterans Health Care
System
Centro Diagnostico Italiano (Milano,
Italy)
Champlain Valley Physicians
Hospital (NY)
Chang Gung Memorial Hospital
(Taiwan)
Changi General Hospital
(Singapore)
Childrens Hospital (NE)
Childrens Hospital & Clinics (MN)
Childrens Hospital Medical Center
(Akron, OH)
Childrens Hospital of Philadelphia
(PA)
Children's Hospital of Wisconsin
Childrens Medical Center of Dallas
(TX)
CHR St. Joseph Warquignies (Belgium)
Christus St. John Hospital (TX)
Clarian Health - Methodist Hospital
(IN)
CLSI Laboratories (PA)
Community Hospital of Lancaster
(PA)
Community Hospital of the Monterey
Peninsula (CA)
CompuNet Clinical Laboratories
(OH)
Cook Childrens Medical Center (TX)
Cook County Hospital (IL)
Covance Central Laboratory
Services (IN)
Creighton University Medical Center
(NE)
Danish Veterinary Laboratory
(Denmark)
Danville Regional Medical Center
(VA)
Dean Medical Center (WI)
Department of Health & Community
Services (New Brunswick, Canada)
DesPeres Hospital (MO)
Detroit Health Department (MI)
Diagnsticos da Amrica S/A
(Brazil)
Diagnsticos da Amrica S/Z
(Brazil)
Dr. Everett Chalmers Hospital (New
Brunswick, Canada)
Doctors Hospital (Bahamas)
Duke University Medical Center
(NC)
Dwight David Eisenhower Army
Med. Ctr. (GA)
E.A. Conway Medical Center (LA)
EMH Regional Medical Center (OH)
Emory University Hospital (GA)
Fairview-University Medical Center
(MN)
Federal Medical Center (MN)
Florida Hospital East Orlando
Focus Technologies (CA)
Focus Technologies (VA)
Foothills Hospital (Calgary, AB,
Canada)
Franciscan Shared Laboratory (WI)
Fresno Community Hospital and
Medical Center
Frye Regional Medical Center (NC)

Gambro BCT (CO)
Gamma Dynacare Medical
Laboratories (ON, Canada)
Geisinger Medical Center (PA)
General Health System (LA)
Grady Memorial Hospital (GA)
Guthrie Clinic Laboratories (PA)
Hagerstown Medical Laboratory
(MD)
Hahnemann University Hospital
(PA)
Harris Methodist Fort Worth (TX)
Hartford Hospital (CT)
Health Network Lab (PA)
Health Partners Laboratories (VA)
Highlands Regional Medical Center
(FL)
Hinsdale Hospital (IL)
Hoag Memorial Hospital
Presbyterian (CA)
Holmes Regional Medical Center
(FL)
Holy Cross Hospital (MD)
Holzer Medical Center (OH)
Hpital du Sacr-Coeur de
Montreal (Montreal, Quebec,
Canada)
Hpital Maisonneuve - Rosemont
(Montreal, Canada)
Hpital Saint-Luc (Montreal,
Quebec, Canada)
Hospital for Sick Children (Toronto,
ON, Canada)
Hospital Sousa Martins (Portugal)
Hotel Dieu Grace Hospital (Windsor,
ON, Canada)
Huddinge University Hospital
(Sweden)
Hunter Area Pathology Service
(Australia)
Hurley Medical Center (MI)
Indiana University
Innova Fairfax Hospital (VA)
Institute of Medical and Veterinary
Science (Australia)
International Health Management
Associates, Inc. (IL)
Jackson Memorial Hospital (FL)
John C. Lincoln Hospital (AZ)
John F. Kennedy Medical Center
(NJ)
Kadlec Medical Center (WA)
Kaiser Permanente (MD)
Kangnam St. Marys Hospital
(Korea)
Kantonsspital (Switzerland)
Kenora-Rainy River Regional
Laboratory Program (Ontario,
Canada)
Kimball Medical Center (NJ)
King Faisal Specialist Hospital
(Saudi Arabia)
LabCorp (NC)
Laboratoire de Sant Publique du
Quebec (Canada)
Laboratorio Dr. Echevarne (Spain)
Laboratrio Fleury S/C Ltda.
(Brazil)
Laboratory Corporation of America
(NJ)
LAC and USC Healthcare
Network (CA)
Lakeland Regional Medical Center
(FL)
Lancaster General Hospital (PA)
LeBonheur Childrens Medical
Center (TN)
Lewis-Gale Medical Center (VA)

L'Hotel-Dieu de Quebec (Canada)
Libero Instituto Univ. Campus
BioMedico (Italy)
Loma Linda Mercantile (CA)
Louisiana State University
Medical Center
Lourdes Health System (NJ)
Maccabi Medical Care and Health
Fund (Israel)
Magnolia Regional Health Center
(MS)
Maimonides Medical Center (NY)
Malcolm Grow USAF Medical
Center (MD)
Marion County Health Department
(IN)
Martin Luther King/Drew Medical
Center (CA)
Massachusetts General Hospital
(Microbiology Laboratory)
MDS Metro Laboratory Services
(Burnaby, BC, Canada)
Medical College of Virginia
Hospital
Medicare/Medicaid Certification,
State of North Carolina
Memorial Medical Center (IL)
Memorial Medical Center (LA)
Jefferson Davis Hwy
Memorial Medical Center (LA)
Napoleon Avenue
Mercy Hospital (ME)
Methodist Hospital (TX)
Michigan Department of
Community Health
Middlesex Hospital (CT)
Mississippi Baptist Medical Center
Montreal Childrens Hospital
(Canada)
Montreal General Hospital (Canada)
National University Hospital
(Singapore)
The Nebraska Medical Center
New Britain General Hospital (CT)
New England Fertility Institute (CT)
New England Medical Center (MA)
New Mexico VA Health Care
System
New York University Medical
Center
NorDx (ME)
North Carolina State Laboratory of
Public Health
North Central Medical Center (TX)
North Shore - Long Island Jewish
Health System Laboratories (NY)
North Shore University Hospital
(NY)
Northwestern Memorial Hospital
(IL)
Ochsner Clinic Foundation (LA)
O.L. Vrouwziekenhuis (Belgium)
Ordre professionnel des
technologists mdicaux du
Qubec
Ospedali Riuniti (Italy)
The Ottawa Hospital
(Ottawa, ON, Canada)
OU Medical Center (OK)
Our Lady of the Resurrection
Medical Center (IL)
Pathology Associates Medical
Laboratories (WA)
The Permanente Medical Group
(CA)
Piedmont Hospital (GA)
Pocono Medical Center (PA)
Presbyterian Hospital of Dallas

(TX)
Providence Health Care
Provincial Laboratory for Public
Health (Edmonton, AB, Canada)
Queen Elizabeth Hospital (Prince
Edward Island, Canada)
Queensland Health Pathology
Services (Australia)
Quest Diagnostics Incorporated
(CA)
Quintiles Laboratories, Ltd. (GA)
Regions Hospital
Research Medical Center (MO)
Rex Healthcare (NC)
Rhode Island Department of Health
Laboratories
Riverside Medical Center (IL)
Riyadh Armed Forces Hospital
(Saudi Arabia)
Robert Wood Johnson University
Hospital (NJ)
Royal Columbian Hospital (New
Westminster, BC, Canada)
Saad Specialist Hospital (Saudi
Arabia)
Sahlgrenska Universitetssjukhuset
(Sweden)
Saint Marys Regional Medical
Center (NV)
St. Alexius Medical Center (ND)
St. Anthony Hospital (CO)
St. Anthonys Hospital (FL)
St. Barnabas Medical Center (NJ)
St-Eustache Hospital (Quebec,
Canada)
St. Francis Medical Ctr. (CA)
St. John Hospital and Medical
Center (MI)
St. Johns Hospital & Health Center
(CA)
St. Josephs Hospital - Marshfield
Clinic (WI)
St. Joseph's Hospital & Medical
Center (AZ)
St. Jude Childrens Research
Hospital (TN)
St. Lukes Regional Medical
Center (IA)
St. Mary of the Plains Hospital
(TX)
St. Michaels Hospital (Toronto,
ON, Canada)
Ste. Justine Hospital (Montreal, PQ,
Canada)
San Francisco General Hospital
(CA)
Santa Clara Valley Medical Center
(CA)
Sentara Williamsburg Community
Hospital (VA)
Seoul Natl University Hospital
(Korea)
Shands at the University of Florida
So. California Permanente Medical
Group
South Bend Medical Foundation
(IN)
South Western Area Pathology
Service (Australia)
Southern Maine Medical Center
Southwest Texas Methodist Hospital
(TX)
Spartanburg Regional Medical
Center (SC)
Specialty Laboratories, Inc. (CA)
State of Washington Department of
Health
OFFICERS
Donna M. Meyer, Ph.D.,
President
CHRISTUS Health
Thomas L. Hearn, Ph.D.,
President Elect
Centers for Disease Control and Prevention
Emil Voelkert, Ph.D.,
Secretary
Roche Diagnostics GmbH
Gerald A. Hoeltge, M.D.,
Treasurer
The Cleveland Clinic Foundation
F. Alan Andersen, Ph.D.,
Immediate Past President
Cosmetic Ingredient Review
John V. Bergen, Ph.D.,
Executive Director
Stony Brook University Hospital

(NY)
Stormont-Vail Regional Medical
Center (KS)
Sun Health-Boswell Hospital (AZ)
Sunnybrook Health Science Center
(ON, Canada)
Swedish Medical Center Providence Campus (WA)
Temple University Hospital (PA)
Tenet Odessa Regional Hospital
(TX)
The Toledo Hospital (OH)
Touro Infirmary (LA)
Tripler Army Medical Center (HI)
Truman Medical Center (MO)
Tuenmun Hospital (Hong Kong)
UCLA Medical Center (CA)
UCSF Medical Center (CA)
UNC Hospitals (NC)
Unidad de Patologia Clinica
(Mexico)
Union Clinical Laboratory (Taiwan)
University Hospitals of Cleveland
(OH)
University of Alabama-Birmingham
Hospital
University of Chicago Hospitals
(IL)
University of Colorado Hospital
University of Debrecen Medical
Health and Science Center
(Hungary)
University of Illinois Medical Center
University of the Ryukyus (Japan)
The University of the West Indies
University of Virginia Medical
Center
University of Washington
UroCor, A Divison of Dianon
Systems, Inc. (OK)
UZ-KUL Medical Center (Belgium)
VA (Hines) Medical Center (IL)
VA (Kansas City) Medical Center
(MO)
VA (San Diego) Medical Center
(CA)
VA (Tuskegee) Medical Center
(AL)
Valley Children's Hospital (CA)
Vejle Hospital (Denmark)
Virginia Department of Health
ViroMed Laboratories (MN)
Warren Hospital (NJ)
Washington Adventist Hospital
(MD)
Washoe Medical Center
Laboratory (NV)
Waterford Regional Hospital
(Ireland)
Wellstar Health Systems (GA)
West Jefferson Medical Center (LA)
West Shore Medical Center (MI)
Wilford Hall Medical Center (TX)
William Beaumont Army Medical
Center (TX)
William Beaumont Hospital (MI)
William Osler Health Centre
(Brampton, ON, Canada)
Winn Army Community Hospital
(GA)
Winnipeg Regional Health
Authority (Winnipeg, Canada)
Wishard Memorial Hospital (IN)
Yonsei University College of
Medicine (Korea)
York Hospital (PA)
BOARD OF DIRECTORS
Susan Blonshine, RRT, RPFT, FAARC
TechEd
Carolyn D. Jones, J.D., M.P.H.

AdvaMed
Wayne Brinster
BD
J. Stephen Kroger, M.D., MACP

COLA
Kurt H. Davis, FCSMLS, CAE

Canadian Society for Medical Laboratory Science
Willie E. May, Ph.D.

National Institute of Standards and Technology
Mary Lou Gantzer, Ph.D.

Dade Behring Inc.
Gary L. Myers, Ph.D.

Centers for Disease Control and Prevention
Lillian J. Gill, M.S.

FDA Center for Devices and Radiological Health
Kiyoaki Watanabe, M.D.

Keio University School of Medicine
Robert L. Habig, Ph.D.

Abbott Laboratories
Judith A. Yost, M.A., M.T.(ASCP)

Centers for Medicare & Medicaid Services
NCCLS T 940 West Valley Road T Suite 1400 T Wayne, PA 19087 T USA T PHONE 610.688.0100
FAX 610.688.0700 T E-MAIL: [email protected] T WEBSITE: www.nccls.org T ISBN 1-56238-515-1

H3 A5

Uploaded by

Copyright:

Available Formats

H3 A5

Uploaded by

Document Information

Original Title

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

H3 A5

Uploaded by

Copyright:

Available Formats

What is NCCLS and what is its role?

What is NCCLS and what is its role?

What are the different types of NCCLS documents?

What are the different types of NCCLS documents?

H3-A5

Procedures for the Collection of Diagnostic

This document provides procedures for the collection of diagnostic specimens by

the authorization of a project

the development and open review of documents

the revision of documents in response to comments

the acceptance of a document as a consensus

Most NCCLS documents are subject to two levels of

the need for field evaluation or data collection, documents

Procedures for the Collection of Diagnostic Blood Specimens by

Approved StandardFourth Edition

Approved StandardFifth Edition

Approved StandardSecond Edition

Approved StandardThird Edition

Richard A. Marlar, Ph.D.

Sheila Clover, CPT (ASCP) (NCA)

Dennis J. Ernst, M.T.(ASCP)

Luc Van Hove, M.D., Ph.D.

J. Heinrich Joist, M.D., Ph.D.

John A. Koepke, M.D.

Tracy A. Dooley, M.L.T.(ASCP)

Dennis J. Ernst, M.T.(ASCP)

J. David Bessman, M.D.

Roger R. Calam, Ph.D., DABCC

Diane I. Szamosi, M.A.,

Factors That Affect Laboratory Values .....................................................................................2

Venipuncture Chairs ......................................................................................................2

Step 1: Prepare Accession Order ..................................................................................6

Venipuncture in Children and Difficult Collections ................................................................19

Additional Considerations .......................................................................................................19

Monitoring Blood Volume Collected ..........................................................................19

Procedures for the Collection of Diagnostic Blood Specimens by

An NCCLS global consensus standard. NCCLS. All rights reserved.

Factors That Affect Laboratory Values

The venipuncture should be performed in a clean, quiet, and private environment.

A central venipuncture area should be designed to include the following features.

The cart area is constructed to allow easy access to the supplies.

Sampling Time Recorder

Blood Collecting Trays

An NCCLS global consensus standard. NCCLS. All rights reserved.

Needles and Holders

Venous Blood Collection Tubes

Tourniquets or products for use as tourniquets should be available. Examples include:

Single-use disposable tourniquet, preferably latex-free.

Blood pressure cuff inflated to 40 mmHg.

An NCCLS global consensus standard. NCCLS. All rights reserved.

Isopropyl or ethyl alcohol: 70%

7.10 Puncture-Resistant Disposal Container

7.12 Adhesive Bandages

7.13 Warming Devices

7.14 Test Reference Manual

Prepare accession order.

An NCCLS global consensus standard. NCCLS. All rights reserved.

Step 1: Prepare Accession Order

Information for Test Request Form