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Surgery and Healing in the Developing World - Dartmouth-Hitchcock

Surgery and Healing in the Developing World - Dartmouth-Hitchcock

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8<br />

62 <strong>Surgery</strong> <strong>and</strong> <strong>Heal<strong>in</strong>g</strong> <strong>in</strong> <strong>the</strong> Develop<strong>in</strong>g <strong>World</strong><br />

<strong>and</strong> donor if a transfusion is necessary immediately. Once a match is made, obta<strong>in</strong><br />

<strong>the</strong> necessary blood <strong>and</strong> transfuse <strong>the</strong> patient <strong>in</strong> a timely fashion. The use of blood<br />

typ<strong>in</strong>g agglut<strong>in</strong>ation kits purchased <strong>and</strong> carried <strong>in</strong> <strong>the</strong> suitcase will allow for rapid<br />

typ<strong>in</strong>g. Follow <strong>in</strong>structions on <strong>the</strong> kit. Agglut<strong>in</strong>ation (clump<strong>in</strong>g) of sample <strong>in</strong>dicates<br />

blood type. If matched, isolate <strong>the</strong> blood us<strong>in</strong>g 16G or 18G sterile needles <strong>and</strong><br />

prepackaged blood transfusion bags conta<strong>in</strong><strong>in</strong>g citrate to prevent coagulation.<br />

Hematology <strong>and</strong> Serum Chemistry<br />

A few tests have been chosen which are deemed essential to basic patient care.<br />

Basic Blood Tests<br />

Differential <strong>and</strong> TLC<br />

These blood tests can be performed easily. After obta<strong>in</strong><strong>in</strong>g <strong>the</strong> anticoagulated<br />

blood specimen (mix 4.5 ml blood with 0.5 ml sodium citrate) from <strong>the</strong> patient<br />

blood films on a glass slide are made. This can be done by first putt<strong>in</strong>g a small drop<br />

of blood on one end of <strong>the</strong> slide <strong>and</strong> <strong>the</strong>n, us<strong>in</strong>g ano<strong>the</strong>r slide, smear <strong>the</strong> drop with<br />

<strong>the</strong> edge.<br />

Leishman Sta<strong>in</strong><br />

This sta<strong>in</strong><strong>in</strong>g procedure is widely used for dist<strong>in</strong>guish<strong>in</strong>g between different types<br />

of normal blood cells. Each cell sta<strong>in</strong>s <strong>in</strong> a different pattern when viewed under <strong>the</strong><br />

microscope <strong>and</strong> will allow for easy identification. Note: The sta<strong>in</strong>s described will<br />

sta<strong>in</strong> h<strong>and</strong>s <strong>and</strong> cloth<strong>in</strong>g as well as bacteria. Do not wear good clo<strong>the</strong>s <strong>in</strong> <strong>the</strong> laboratory,<br />

wear gloves when sta<strong>in</strong><strong>in</strong>g, <strong>and</strong> keep <strong>in</strong> m<strong>in</strong>d that all sta<strong>in</strong>s are assumed to be<br />

toxic unless o<strong>the</strong>rwise stated.<br />

Leishman Sta<strong>in</strong> Procedure<br />

1. Prepare blood film.<br />

2. Allow <strong>the</strong> sample to air dry for a few m<strong>in</strong>utes.<br />

3. Once dry, cover film with 10 drops of Leishman sta<strong>in</strong> us<strong>in</strong>g an eyedropper<br />

<strong>and</strong> allow to sit for 30 sec.<br />

4. Add 20 drops of water <strong>and</strong> let sit for 15 m<strong>in</strong>.<br />

5. Pick up slide with forceps <strong>and</strong> r<strong>in</strong>se <strong>in</strong> fast runn<strong>in</strong>g tap water for 1 sec.<br />

6. Allow to dry.<br />

7. Exam<strong>in</strong>e under microscope us<strong>in</strong>g an oil immersion lens.<br />

Microscopic Observation of a Leishman Sta<strong>in</strong><br />

Differential: A good approach to observ<strong>in</strong>g any smear is to exam<strong>in</strong>e it under low<br />

power (10X) <strong>in</strong> a bright field for orientation. After focus<strong>in</strong>g, work up to 40X <strong>and</strong><br />

f<strong>in</strong>ally 100X. Be sure that <strong>the</strong> smear is not upside down, or focus<strong>in</strong>g will not be<br />

possible. When do<strong>in</strong>g a differential, count 100 cells <strong>in</strong> <strong>the</strong> follow<strong>in</strong>g way to obta<strong>in</strong><br />

<strong>the</strong> percentage of white cells (Fig. 3).<br />

TLC: A TLC can be done by sta<strong>in</strong><strong>in</strong>g with Leishman’s on a hemocytometer as<br />

opposed to a simple glass slide. The hemocytometer has grids on <strong>the</strong> slide which will<br />

allow for organized count<strong>in</strong>g of cells. Though not as accurate as a mach<strong>in</strong>e, it will be<br />

more accurate than count<strong>in</strong>g without <strong>the</strong> grid.<br />

Erythrocyte Sedimentation Rate (ESR)<br />

The ESR is a nonspecific <strong>in</strong>dicator of disease that measures <strong>the</strong> rate of sedimentation<br />

of erythrocytes <strong>in</strong> anticoagulated blood over 1 hour. If various prote<strong>in</strong>s coat

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