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October - LRS Institute of Tuberculosis & Respiratory Diseases

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LIVER ENZYMES DURING TREATMENT WITH RESERVE REGIMEN<br />

229<br />

TABLE 8<br />

Details <strong>of</strong> cases <strong>of</strong> Clinical Jaundice<br />

Sl. Age & Hb. Weight Pre-treatment level Duration Level <strong>of</strong> Inter- Regimn resumed or<br />

No. Sex (gm%) in kg <strong>of</strong> present serum repution not<br />

LDH SGPT Serum treatment bilirubin <strong>of</strong> treat-<br />

(I.U/ (I.U/ Alk. ment<br />

litre) litre) Phos.<br />

(K.A.<br />

Unit)<br />

1. 25 F 8.5 25 200.4 8.0 7.08 9 days 12 mg% 12 days Pyrazinamide omitted,<br />

Rifampicin & Ethambutol<br />

restarted. Patient<br />

tolerated well.<br />

2. 25 F 6.8 27 300.6 20.0 16.70 10 days 12.4 mg% 16 days Pyrazinamide omitted.<br />

Rifampicin and<br />

Ethambutol restarted.<br />

Tolerated well.<br />

3. 60 F 7.5 30 300.6 8.0 3.20 12 days 10.4mg% 18 days Rifampicin +<br />

Pyrazinamide +<br />

Ethambutol resumed<br />

but patient had raised<br />

LDH, SGPT and<br />

serum bilirubin at 60<br />

days <strong>of</strong> treatment and<br />

followed subsequently<br />

without any ill effect.<br />

alkaline phosphatase at 15 and 30 days <strong>of</strong><br />

treatment whereas fall in the levels by 60th day<br />

is significant.<br />

3 (12 %) cases developed clinical jaundice during<br />

this study. Pre-treatment levels <strong>of</strong> liver<br />

enzymes, under study, are as shown in Table<br />

8. All were females and their duration <strong>of</strong> treatment<br />

was from 9 to 12 days (mean 10 days)<br />

indicating the average time for clinical jaundice.<br />

Interruption <strong>of</strong> treatment was from 12 to 18<br />

days (mean 15 days). All were severely malnourished,<br />

almost half <strong>of</strong> the average weight. One<br />

<strong>of</strong> them was severely anaemic (6.8 gm% haemoglobin)<br />

and the two others had moderate<br />

anaemia with 7.5 gm% and 8,5 gm % haemoglobin.<br />

One (4%) continued with the regimen and<br />

had raised values <strong>of</strong> LDH and SGPT and serum<br />

bilirubin at the end <strong>of</strong> 60 days <strong>of</strong> treatment and<br />

followed up subsequently without any ill effect.<br />

2(8%) had pyrazinamide omitted thinking that<br />

this drug might be responsible for damage to<br />

the liver and rifampicin and ethambutol were restarted<br />

without any ill effect. It can be concluded<br />

that this regimen should be used with<br />

great caution in those who have demonstrable<br />

hepatic dysfunction.<br />

Discussion<br />

Serum lactate dehydrogenase and serum<br />

glutamic pyruvic transaminase were used as<br />

an index <strong>of</strong> hepatocellular damage and serum<br />

alkaline phosphatase was used as an index<br />

for cholestasis. Litchman (1953) pointed out<br />

that in pulmonary tuberculosis clinical observations<br />

demonstrate a lack <strong>of</strong> parenchyma] hepatic<br />

damage contrary to the presence <strong>of</strong> such hepatic<br />

damage as revealed by sensitive hepatic tests,<br />

In our study also, none <strong>of</strong> the patients had any<br />

clinical signs <strong>of</strong> involvement <strong>of</strong> the liver or<br />

jaundice before the start <strong>of</strong> treatment though<br />

subclinical involvement <strong>of</strong> the liver was there<br />

as is revealed by the pre-treatment liver<br />

enzyme levels in the abnormal group.<br />

It can be concluded from the given data<br />

that mean enzyme activity in abnormal group<br />

start falling after treatment by 30th day onwards<br />

whereas in normal group, mean enzyme activity<br />

Ind. J. Tub., Vol. XXIX, No. 4

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