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Clinical Examination of Farm Animals - CYF MEDICAL DISTRIBUTION

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<strong>Clinical</strong> <strong>Examination</strong> <strong>of</strong> the Gastrointestinal System<br />

tube into the ventral meatus. The tube is advanced to<br />

the larynx. The tube is further advanced at the pause<br />

following expiration. On passage through the larynx<br />

the animal is usually observed to swallow. If there is<br />

coughing and breathing sounds are detected at the<br />

end <strong>of</strong> the tube, it should be withdrawn into the nostril<br />

and advanced again. If the tube passes down the<br />

oesophagus into the rumen, gas may escape which<br />

has a characteristic odour if the end <strong>of</strong> the tube is<br />

smelled. To confirm that the tube is in the rumen, an<br />

assistant should blow forcefully down the tube and<br />

the veterinary surgeon should auscultate the rumen<br />

at the left sublumbar fossa for bubbling sounds as the<br />

gas penetrates the rumen fluid. To obtain a sample <strong>of</strong><br />

rumen fluid negative pressure is applied to the end <strong>of</strong><br />

the tube with a stirrup pump or by sucking the end <strong>of</strong><br />

the tube. Free fluid may flow through the tube and be<br />

collected. If this fails, the tube should be bent and<br />

withdrawn and a sample decanted from the rumen<br />

fluid in its distal end. Asample can be collected into a<br />

universal sample pot. The only difference between<br />

using a stomach tube and a nasogastric tube is that the<br />

tube is advanced through the gagged mouth to the<br />

larynx.<br />

The equipment required to perform a rumenocentesis<br />

includes clippers, surgical antiseptic, alcohol and<br />

a 9 cm 18 BWG (1.20 mm) spinal needle with a stylet.<br />

The rumen contains a dorsal gas cap, a fibrous raft<br />

and fluid in the ventral sac. Asmall area <strong>of</strong> skin in the<br />

left ventral quadrant <strong>of</strong> abdomen is surgically prepared.<br />

To protect the operator, a tail kinch or an antikick<br />

bar can be applied. The lumbar spinal needle is<br />

thrust up to the hilt through the skin <strong>of</strong> the prepared<br />

site into the fluid contained within the ventral sac. A<br />

syringe is attached to the needle and a sample withdrawn.<br />

Sometimes the needle can get blocked by<br />

solid material and may have to be cleared by injecting<br />

air. Once a sample has been obtained the needle is<br />

withdrawn.<br />

Rumen fluid analysis<br />

Care with sampling is required as saliva contamination<br />

increases the pH <strong>of</strong> the rumen sample. The sample<br />

should be evaluated as soon as possible because<br />

cooling and exposure to air alter protozoan and bacterial<br />

activity.<br />

Colour<br />

Normal rumen fluid is usually olive green or greenish<br />

brown. In ruminal acidosis the fluid may appear<br />

milky grey.<br />

pH<br />

The rumen fluid pH can be measured in the field<br />

by using pH papers with a range <strong>of</strong> 3.0 to 9.0. The<br />

rumen fluid pH is normally 6.0 to 7.0 in cattle on a<br />

roughage-based diet and 5.5 to 6.5 in cattle on a<br />

concentrate-based diet. In ruminal acidosis (carbohydrate<br />

engorgement) the pH will be 5.0 or less. In<br />

anorexic cattle, because <strong>of</strong> the constant production<br />

<strong>of</strong> saliva which has an alkaline pH and a lack <strong>of</strong> substrate<br />

for the rumen flora to produce volatile fatty<br />

acids, the pH will be alkaline and usually in the range<br />

7.5 to 8.0. Higher pH values can occur with urea<br />

poisoning.<br />

Sedimentation/flotation<br />

This test is an indirect measure <strong>of</strong> the activity <strong>of</strong><br />

the micr<strong>of</strong>lora; it must be performed within a short<br />

time following collection <strong>of</strong> the sample otherwise<br />

it may not be an accurate measure <strong>of</strong> their activity<br />

within the rumen. The sample <strong>of</strong> rumen fluid is<br />

placed in a measuring cylinder. The time is measured<br />

for complete sedimentation and flotation <strong>of</strong> solid<br />

particles. The finer particles sink and the coarser particles<br />

float supported by gas bubbles <strong>of</strong> fermentation.<br />

In healthy cattle the normal time for sedimentation<br />

and floatation is 4 to 8 minutes. Inactive micr<strong>of</strong>lora<br />

results in rapid sedimentation with little floating<br />

material. Chronically anorexic cattle would give this<br />

result.<br />

Redox potential (methylene blue<br />

reduction time)<br />

This test is a measure <strong>of</strong> the reduction–oxidation<br />

activity <strong>of</strong> the ruminal micr<strong>of</strong>lora and reflects anaerobic<br />

fermentation by rumen bacteria. It must be<br />

performed within a short time following collection <strong>of</strong><br />

the sample to produce an accurate result. One ml <strong>of</strong><br />

0.03% methylene blue is mixed with 20 ml <strong>of</strong> rumen<br />

fluid and the colour compared with a control <strong>of</strong><br />

rumen fluid only. The time taken to decolourise the<br />

methylene blue is measured. Rumen fluid from<br />

healthy cattle on a concentrate and hay diet will de-<br />

105

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