Introduction of Clinical Pathology Science: Clinical Pathology Is A Subspecialty of Pathology That Deals With The Use of

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Pathological Analysises Lec.

Introduction of Clinical Pathology Science


Health care providers may be unfamiliar with the workings of the pathology
laboratory. The delivery of a specimen to the pathology laboratory initiates a
complex series of events resulting in a pathologic diagnosis/interpretation. The
following section reviews the importance and key objectives in the pathologic
evaluation of tissue and provides information on the types and members of the
pathology laboratory.
Clinical Pathology is a subspecialty of pathology that deals with the use of
laboratory methods (clinical chemistry, microbiology,
hematology and emerging subspecialties such as molecular diagnostics) for the
diagnosis and treatment of disease. This branch is devided in to:

1-Hematology : Studies the blood and blood-forming tissues to evaluate presence


of disease and assist in therapeutic interventions as clinically indicated.

2-Clinical chemistry : (also known as chemical pathology and clinical


biochemistry) is the area of clinical pathology that is generally concerned with
analysis of bodily fluids.

3-Clinical Microbiology : This encompasses five different sciences. These include


bacteriology, virology, parasitology, immunology, and mycology.

4-Genetics: is also studied along with a subspecialty known as cytogenetics.

5-Reproductive biology: Semen analysis, Sperm bank and assisted reproductive


technology.

Basic Laboratory Practices

Biosafety level guidelines recognize that facility design is important in providing a


barrier to protect persons working in the facility as well as those in the community.

The following prudent biosafety practices are recommended by the National


Academy of Sciences in the publication Biosafety in the Laboratory and in part
constitute basic good biosafety practices. Although these practices may be
considered “common sense” and overly simplistic by experienced laboratorians,
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strict adherence to these basic principles will greatly reduce the likelihood of
laboratory acquired infections.

−Biosafety Practice
 Do not mouth pipette .
 Manipulate infectious fluids carefully to avoid spills and the production of
aerosols.
 Restrict use of needles, syringes, and other sharps to those procedures for
which there are no alternatives; dispose of sharps in leak- and puncture-
proof containers.
 Use lab coats, gloves, safety eye wear, and other personal protective
equipment.
 Wash hands after all laboratory activities, following the removal of gloves,
and immediately following contact with infectious agents.
 Decontaminate work surfaces before and after use, and immediately after
spills.
 Do not eat, drink, store foods, or smoke in the laboratory.

−Biological Hazard Information: Laboratory workers must be knowledge


able of the hazards associated with the biological agents present in the laboratory,
and have hazard information available to them. The following are sources of
hazard information for biological agents.

 Security and Inventory of Biological Agents

Each biological researcher is responsible for ensuring that his or her laboratory
implements sufficient security measures and procedures to prevent unauthorized
access to biological agents. Select Agents and other higher risk microorganisms
and toxins must be stored in a locked container, and an inventory must be
maintained with sufficient detail to enable identification of missing materials.

 Prevention and Containment of Aerosols and Droplets


Handling of liquids or dry powders is likely to generate aerosols or droplets.
Procedures such as centrifuging, mixing, and pipetting that involve high energy
tend to produce respirable aerosols that stay airborne for extended periods and are

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small enough to be inhaled. Low energy procedures including opening containers


and streaking plates produce droplets that settle quickly on surfaces, skin, and
mucous membranes.

 Biological Safety Cabinets


Procedures involving infectious material should be performed inside a biological
safety cabinet (BSC) whenever possible. A properly operating will contain aerosols
and droplets generated during handling of infectious agents .

 Pipetting
Do not mouth pipette! Always use a mechanical pipetting device. Pipettes should
be drained gently with the tip against the inner wall of the receiving vessel and
liquid should not be forcibly expelled from the pipette.

 Blending

Use a safety blender that has leak proof bearings and a tight fitting lid with a
sealable gasket. Use the blender inside a cabinets when blending material
containing infectious agents.

 Centrifugation

The potential for contamination and infection is high if liquid and aerosol is
released during centrifugation. Sealed centrifuge buckets, or safety cups should be
used to prevent release of liquid and aerosol. Ultracentrifuges operate under
vacuum and should contain an in-line HEPA filter between the chamber and the
vacuum pump. Small bench top centrifuges can be placed inside a cabinets to
contain infectious aerosols and prevent personnel exposures.

 Inoculating Loops

Flaming inoculating loops can result in spatter and release of aerosols and droplets.
Use of an electric microincinerator will effectively control spatter resulting from
sterilization of inoculating loops.

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 Use of Absorbent Materials


Work surfaces should be covered with absorbent paper or “diaper” sheets to collect
splashes and drips, and minimize the spread of contamination. The absorbent paper
should be changed at the end of the laboratory procedure as part of the final
cleanup, or at least daily during use.

Personal Protective Equipment

Although not a substitute for use of BSCs and good laboratory practices, personal
protective equipment (PPE) is considered a primary barrier to infectious agents and
proper use will reduce the likelihood of infection. PPE is the least desirable
exposure control method because its failure results in direct exposure to the agent.
PPE is most effective when used to supplement primary control methods such as
biological safety cabinets, safety centrifuge cups, and other containment devices.

 Laboratory Coats and Gowns


Laboratory coats protect street clothes against chemical and biological spills, and
provide additional body protection. Generally, a 100% cotton lab coat is
recommended over polyester-cotton blends for general microbiological work. The
wearing of lab coats is considered to be standard microbiological practice for
laboratories.

 Gloves
Gloves are available that provide protection against a variety of hazards, including
infectious agents, chemicals, and radioactive material. Unfortunately, there is no
single glove type that provides adequate protection for all hazards (or even all
chemicals!). Always check gloves for pinholes prior to use.

−Storage and Labeling of Biological Agents


Both the primary and secondary containers must be durable and leak proof so as to
prevent accidental exposure. Primary containers must be clearly labeled to indicate
the identity of the agent and include the universal biohazard symbol (see below) as
physical space on the container permits. At a minimum, secondary (or outside)

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containers must include the universal biohazard symbol (identity of contents is also
desirable). Freezers, refrigerators, and other storage areas must also be labeled with
the biohazard symbol.

Pathogen Standard specifically requires that containers of human blood or other


potentially infectious material (OPIM), contaminated waste, and refrigerators,
freezers, and other storage containers used to store or transport blood or OPIM, be
labeled with the universal biohazard symbol (fluorescent orange or orange-red).

−General Specimen Collection:


Some of the common considerations affecting all types of specimens:

1-Please examine specimen collection and transportation supplies to be sure they


do not include expired containers.

2-Label a specimen correctly and provide all pertinent information required on the
test request form. (See Blood Specimens: Chemistry and Hematology − Blood
Collection/Transport Containers.)

3-Use the container/tube indicated in the test requirements for appropriate


specimen preservation.

4- Follow patient instructions prior to specimen collection.

5-Carefully tighten specimen container lids to avoid leakage and/or potential


contamination of specimens.

6-Maintain the specimen at the temperature indicated in the test requirements.

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−Types of Specimens:

Urine sample , Stool sample , blood sample , sputum S. , Swabs test ,and

Body fluids: Laboratory testing can be performed on many types of fluids from the
body other than blood. Often, these fluids are tested instead of blood because they
can give more direct answers to what may be going on in a particular part of the
body. Some body fluid analyses include:

 Semen Analysis
 CSF Analysis
 Synovial Fluid Analysis
 Pleural Fluid Analysis
 Pericardial Fluid Analysis
 Peritoneal Fluid Analysis

For certain body fluids, including pleural, pericardial, and peritoneal fluids, it
is important to determine through testing whether the fluid is a transudate or
an exudate because it can help diagnose the disease or condition present.

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