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Surgery and Healing in the Developing World - Dartmouth-Hitchcock

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Lab <strong>in</strong> a Suitcase<br />

Figure 3. Manual count<strong>in</strong>g procedure for differential analysis.<br />

<strong>the</strong> red blood cells, <strong>the</strong>y will stick toge<strong>the</strong>r <strong>and</strong> result <strong>in</strong> a faster ESR rate. Obta<strong>in</strong><br />

<strong>the</strong> anticoagulated blood sample us<strong>in</strong>g a pipette bulb <strong>and</strong> draw <strong>the</strong> blood <strong>in</strong>to <strong>the</strong><br />

graduated ESR tube. Place <strong>in</strong> a vertical st<strong>and</strong> <strong>and</strong> set <strong>the</strong> timer for 1 hour. Measure<br />

<strong>the</strong> level of sedimentation red cells <strong>in</strong> mm after 1 hour. ESR normally rises with<br />

<strong>in</strong>creased age <strong>and</strong> anemia. Normal values can be calculated <strong>in</strong> men: (age)/2, <strong>and</strong> <strong>in</strong><br />

women: (age+10)/2.<br />

Blood Tests Requir<strong>in</strong>g Kits<br />

T3, T4, TSH, Creat<strong>in</strong><strong>in</strong>e, Amalyse, Bilirub<strong>in</strong>, PTT <strong>and</strong> PT<br />

These tests require prepackaged kits that must be refrigerated at 4˚C. All analyses<br />

can be carried out with plasma <strong>and</strong>/or serum samples.<br />

MCV, Hb, Hct, Na, K, <strong>and</strong> Ca<br />

These tests require specific reagents <strong>and</strong> a photometer. Most of <strong>the</strong> reagents need<br />

to be refrigerated at 4˚C.<br />

Glucose<br />

A glucometer is required to measure serum glucose. Do not forget that a<br />

glucometer requires batteries.<br />

Microbiology <strong>and</strong> Parasitology<br />

Prepar<strong>in</strong>g a Smear<br />

A properly prepared smear causes bacteria to adhere to a slide so that <strong>the</strong>y can be<br />

sta<strong>in</strong>ed <strong>and</strong> observed. The correct density of bacteria on <strong>the</strong> surface of <strong>the</strong> slide is<br />

essential to ensure reliable date. If too many bacteria are present <strong>and</strong> <strong>the</strong>y overlap<br />

each o<strong>the</strong>r, bacterial will not sta<strong>in</strong> properly. If too few, <strong>and</strong> <strong>the</strong>y cannot be located<br />

on <strong>the</strong> slide.<br />

1. The slide must be clean <strong>and</strong> grease-free. Clean <strong>the</strong> slide by breath<strong>in</strong>g on it<br />

repeatedly followed by rubb<strong>in</strong>g vigorously with a kimwipe or paper towel<br />

to remove <strong>the</strong> fog. When <strong>the</strong> slide de-fogs immediately after breath<strong>in</strong>g on<br />

it, it is sufficiently clean.<br />

2. To prepare a smear from a dry culture, place a very small drop of distilled<br />

water on <strong>the</strong> slide. After aseptically remov<strong>in</strong>g material from a culture, mix<br />

with <strong>the</strong> water. If <strong>the</strong> specimen is <strong>in</strong> dilute culture broth, place directly on<br />

slide. Note: very little sample is needed for a good smear.<br />

3. Allow drop to air dry.<br />

4. Pass <strong>the</strong> slide quickly through a flame three times to kill <strong>the</strong> bacterial <strong>and</strong><br />

cause <strong>the</strong>m to adhere.<br />

5. Allow <strong>the</strong> slide to cool <strong>and</strong> <strong>the</strong>n proceed with sta<strong>in</strong><strong>in</strong>g.<br />

63<br />

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