Blood

518-123 NSN 7540-00-634-4158
MEDICAL RECORD BLOOD OR BLOOD COMPONENT TRANSFUSION

SECTION I - REQUISITION
COMPONENT REQUESTED (Check one) TYPE OF REQUEST (Check ONLY if Red Blood Cell REQUESTING PHYSICIAN (Print)
Products are requested.)
RED BLOOD CELLS
TYPE AND SCREEN DIAGNOSIS OR OPERATIVE PROCEDURE
FRESH FROZEN PLASMA
CROSSMATCH
PLATELETS (Pool of units)
CRYOPRECIPITATE (Pool of units) DATE REQUESTED

I have collected a blood specimen on the below named
Rh IMMUNE GLOBULIN patient, verified the name and ID No. of the patient and
DATE AND HOUR REQUIRED verified the specimen tube label to be correct.
OTHER (Specify)
VOLUME REQUESTED (If applicable) KNOWN ANTIBODY FORMATION/TRANSFUSION SIGNATURE OF VERIFIER

REACTION (Specify)
ML
REMARKS: IF PATIENT IS FEMALE, IS THERE HISTORY OF: DATE VERIFIED
RhIG TREATMENT? DATE GIVEN:

TIME VERIFIED
HEMOLYTIC DISEASE OF NEWBORN?
SECTION II - PRE-TRANSFUSION TESTING

UNIT NO. TRANSFUSION NO. TEST INTERPRETATION PREVIOUS RECORD CHECK:
ANTIBODY SCREEN CROSSMATCH RECORD NO RECORD
PATIENT NO. SIGNATURE OR PERSON PERFORMING TEST
DONOR RECIPIENT
CROSSMATCH NOT REQUIRED FOR THE COMPONENT REQUESTED DATE
ABO ABO REMARKS:
Rh Rh
SECTION III - RECORD OF TRANSFUSION

PRE-TRANSFUSION DATA POST-TRANSFUSION DATA
INSPECTED AND ISSUED BY (Signature) AMOUNT GIVEN TIME/DATE COMPLETED/INTERRUPTED
REACTION TEMPERATURE PULSE BLOOD PRESSURE

AT (Hour) ON (Date) NONE SUSPECTED
IDENTIFICATION If reaction is suspected – IMMEDIATELY:
I have examined the Blood Component container label and this form and I find all 1. Discontinue transfusion, treat shock if present, keep intravenous line open.
information identifying the container with the intended recipient matches item by item. 2. Notify Physician and Transfusion Service.
The recipient is the same person named on this Blood Component Transfusion Form 3. Follow Transfusion Reaction Procedures.
and on the patient identification tag. 4. Do NOT discard unit. Return Blood Bag, Filter Set, and I.V. Solutions to the Blood Bank.
1st VERIFIER (Signature) DESCRIPTION OF REACTION
URTICARIA CHILL FEVER PAIN
2nd VERIFIER (Signature) OTHER (Specify)
OTHER DIFFICULTIES (Equipment, clots, etc.)

PRE-TRANSFUSION
NO YES (Specify)
TEMP. PULSE BP SIGNATURE OF PERSON NOTING ABOVE
DATE OF TRANSFUSION TIME STARTED
PATIENT IDENTIFICATION – USE EMBOSSER (For typed or written entries give: Name–Last, first, middle; grade; rank; SEX WARD
rate; hospital or medical facility)
BLOOD OR BLOOD COMPONENT TRANSFUSION

Medical Record
STANDARD FORM 518 (REV. 9-92)

Prescribed by GSA/ICMR, FIRMR (41 CFR) 201-9.202-1
INSTRUCTIONS FOR NON SELF-EXPLANATORY ITEMS
SECTION I – REQUISITION
Component Requested
"Other (Specify)" – List any whole blood or blood product not on menu, i.e., washed RBC's deglycerolized RBC's, etc.
"Volume Requested (If applicable)" – Use only when different from standard amount, i.e., exchange transfusion 50 ml.
"Known Antibody Formation/Transfusion Reaction" – Check Medical Records. Annotate N/A if appropriate.
"If Patient is Female, Is There History Of" – Check medical records. Annotate N/A if appropriate.
SECTION II – PRE-TRANSFUSION TESTING
"Transfusion Number/Patient Number" – List either based on local procedures.
"Previous Record Check" – Current tests should be compared with prior records for ABO and Rh type, difficulty in blood typing,
clinically significant unexpected antibodies, and severe adverse reactions.
"Test Interpretation" – Use the following standard notations. "NEG or "POS" for antibody screen block. "COMPAT" or "INCOMPAT"
for crossmatch block.
SECTION III – RECORD OF TRANSFUSION
"Pre-Transfusion Data"
"Inspected and Issued by at on ."

(Signature) (Hour) (Date)
This statement is to be completed by the issuing laboratory person once he/she has inspected the blood immediately before issue
from the laboratory. The blood must not be abnormal in color or appearance or expired, and if any of these conditions exist the
blood will not be used for transfusion.
"Signature" blank must contain the signature, as opposed to name, of issuing laboratory person.
"Hour" and "Date" are as of actual issue.
The issuing laboratory person will secure this form to the blood bag by string, rubberband, or tie knotted to the tag and the blood
container before issuing the blood.
"Post-Transfusion Data" – Completed by transfusionist.
"Amount Given ml" – Visual approximation.
"Description of Reaction" – Check appropriate reaction or describe "other" on separate sheet, if necessary, and
attach to SF 518.
"Other Difficulties"– Check item or describe on separate sheet and attach to SF 518.
STANDARD FORM 518 BACK (REV. 9-92)

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518-123 NSN 7540-00-634-4158

MEDICAL RECORD BLOOD OR BLOOD COMPONENT TRANSFUSION

CRYOPRECIPITATE (Pool of units) DATE REQUESTED

VOLUME REQUESTED (If applicable) KNOWN ANTIBODY FORMATION/TRANSFUSION SIGNATURE OF VERIFIER

REMARKS: IF PATIENT IS FEMALE, IS THERE HISTORY OF: DATE VERIFIED

RhIG TREATMENT? DATE GIVEN:

SECTION II - PRE-TRANSFUSION TESTING

PATIENT NO. SIGNATURE OR PERSON PERFORMING TEST

SECTION III - RECORD OF TRANSFUSION

REACTION TEMPERATURE PULSE BLOOD PRESSURE

2nd VERIFIER (Signature) OTHER (Specify)

OTHER DIFFICULTIES (Equipment, clots, etc.)

BLOOD OR BLOOD COMPONENT TRANSFUSION

STANDARD FORM 518 (REV. 9-92)

SECTION II – PRE-TRANSFUSION TESTING

"Transfusion Number/Patient Number" – List either based on local procedures.

SECTION III – RECORD OF TRANSFUSION

"Inspected and Issued by at on ."

"Hour" and "Date" are as of actual issue.

"Post-Transfusion Data" – Completed by transfusionist.

"Amount Given ml" – Visual approximation.

STANDARD FORM 518 BACK (REV. 9-92)

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