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Amphotericin B in resistant kala-azar in Bihar.
Natl Med J India. 1993 Mar-Apr; 6(2):57-60.NM

Abstract

BACKGROUND

During the recent epidemic of kala-azar in Bihar, we identified a group of patients who were unresponsive to the two commonly used drugs--sodium stibogluconate and pentamidine. We evaluated the use of amphotericin B in these patients because it has been shown to be active in experimental animals against amastigotes and promastigotes, it has been found to be useful in South American patients and is now recommended by the World Health Organization as a second line drug.

METHODS

We selected 300 patients who were unresponsive to sodium stibogluconate and pentamidine (out of 500 patients with kala-azar confirmed by demonstration of Leishmania donovani bodies in their splenic aspirates). Amphotericin B was given in a dose of 1 mg/kg body weight on alternate days starting with 0.05 mg/kg body weight with daily increments till a 1 mg dose was reached. A total dose of 20 mg/kg was given initially and repeated if the parasites persisted. The investigations done before and after treatment were splenic or bone marrow aspiration, measurement of the spleen and liver size, body weight, total and differential white cell counts, haemoglobin level, total serum protein, blood urea, serum creatinine, serum potassium, blood sugar, serum alanine and aspartate transaminase, electrocardiography and a chest X-ray. The efficacy of treatment was assessed at the end of treatment and after 6 months of follow up.

RESULTS

After treatment with amphotericin B, 298 (99%) of the patients had been cured of their disease as evidenced by the disappearance of fever, reduction of hepatosplenomegaly, clearance of the parasites from the spleen and bone marrow and an absence of relapse on 6 months of follow up. Two hundred and sixty-eight (89%) patients required 1 g of the drug, 24 (8%) required 1.5 g and 6 (2%) required 2 g. All patients had shivering and fever during the infusion. Two had a cardiac arrest from which they could not be revived. Other complications included anorexia, stomatitis, jaundice, hypokalaemia and a rise in blood urea. However, these were only mild and improved after treatment was stopped.

CONCLUSION

Amphotericin B is an effective drug for patients with kala-azar unresponsive to treatment with sodium stibogluconate and pentamidine, but it should be administered under close medical supervision.

Authors+Show Affiliations

Patna Medical College and Hospital, Bihar, India.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

8477209

Citation

Thakur, C P., et al. "Amphotericin B in Resistant Kala-azar in Bihar." The National Medical Journal of India, vol. 6, no. 2, 1993, pp. 57-60.
Thakur CP, Sinha GP, Pandey AK, et al. Amphotericin B in resistant kala-azar in Bihar. Natl Med J India. 1993;6(2):57-60.
Thakur, C. P., Sinha, G. P., Pandey, A. K., Barat, D., & Sinha, P. K. (1993). Amphotericin B in resistant kala-azar in Bihar. The National Medical Journal of India, 6(2), 57-60.
Thakur CP, et al. Amphotericin B in Resistant Kala-azar in Bihar. Natl Med J India. 1993 Mar-Apr;6(2):57-60. PubMed PMID: 8477209.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Amphotericin B in resistant kala-azar in Bihar. AU - Thakur,C P, AU - Sinha,G P, AU - Pandey,A K, AU - Barat,D, AU - Sinha,P K, PY - 1993/3/1/pubmed PY - 1993/3/1/medline PY - 1993/3/1/entrez SP - 57 EP - 60 JF - The National medical journal of India JO - Natl Med J India VL - 6 IS - 2 N2 - BACKGROUND: During the recent epidemic of kala-azar in Bihar, we identified a group of patients who were unresponsive to the two commonly used drugs--sodium stibogluconate and pentamidine. We evaluated the use of amphotericin B in these patients because it has been shown to be active in experimental animals against amastigotes and promastigotes, it has been found to be useful in South American patients and is now recommended by the World Health Organization as a second line drug. METHODS: We selected 300 patients who were unresponsive to sodium stibogluconate and pentamidine (out of 500 patients with kala-azar confirmed by demonstration of Leishmania donovani bodies in their splenic aspirates). Amphotericin B was given in a dose of 1 mg/kg body weight on alternate days starting with 0.05 mg/kg body weight with daily increments till a 1 mg dose was reached. A total dose of 20 mg/kg was given initially and repeated if the parasites persisted. The investigations done before and after treatment were splenic or bone marrow aspiration, measurement of the spleen and liver size, body weight, total and differential white cell counts, haemoglobin level, total serum protein, blood urea, serum creatinine, serum potassium, blood sugar, serum alanine and aspartate transaminase, electrocardiography and a chest X-ray. The efficacy of treatment was assessed at the end of treatment and after 6 months of follow up. RESULTS: After treatment with amphotericin B, 298 (99%) of the patients had been cured of their disease as evidenced by the disappearance of fever, reduction of hepatosplenomegaly, clearance of the parasites from the spleen and bone marrow and an absence of relapse on 6 months of follow up. Two hundred and sixty-eight (89%) patients required 1 g of the drug, 24 (8%) required 1.5 g and 6 (2%) required 2 g. All patients had shivering and fever during the infusion. Two had a cardiac arrest from which they could not be revived. Other complications included anorexia, stomatitis, jaundice, hypokalaemia and a rise in blood urea. However, these were only mild and improved after treatment was stopped. CONCLUSION: Amphotericin B is an effective drug for patients with kala-azar unresponsive to treatment with sodium stibogluconate and pentamidine, but it should be administered under close medical supervision. SN - 0970-258X UR - https://www.unboundmedicine.com/medline/citation/8477209/Amphotericin_B_in_resistant_kala_azar_in_Bihar_ L2 - http://archive.nmji.in/approval/archive/Volume-6/issue-2/original-articles-1.pdf DB - PRIME DP - Unbound Medicine ER -