Cargando…

Unusual Complication of Multidrug Resistant Tuberculosis

INTRODUCTION: Capreomycin is a second-line drug often used for multidrug-resistant tuberculosis which can result in nephrotoxic effects similar to other aminoglycosides. We describe a case of capreomycin induced Bartter-like syndrome with hypocalcemic tetany. CASE REPORT: 23-year-old female patient...

Descripción completa

Detalles Bibliográficos
Autores principales: Sharma, Prerna, Sahay, Ravindra Nath
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5624136/
https://www.ncbi.nlm.nih.gov/pubmed/29075541
http://dx.doi.org/10.1155/2017/6835813
_version_ 1783268196420157440
author Sharma, Prerna
Sahay, Ravindra Nath
author_facet Sharma, Prerna
Sahay, Ravindra Nath
author_sort Sharma, Prerna
collection PubMed
description INTRODUCTION: Capreomycin is a second-line drug often used for multidrug-resistant tuberculosis which can result in nephrotoxic effects similar to other aminoglycosides. We describe a case of capreomycin induced Bartter-like syndrome with hypocalcemic tetany. CASE REPORT: 23-year-old female patient presented with carpopedal spasms and tingling sensations in hands. Patient was being treated with capreomycin for two months for tuberculosis. On further investigation, hypocalcemia, hyponatremia, hypomagnesemia, hypokalemia, and hypochloremic metabolic alkalosis were noted. Vitamin D and serum PTH levels were within normal limits. Hypercalciuria was confirmed by urine calcium/creatinine ratio. Calcium, potassium, and magnesium supplementation was given and capreomycin was discontinued. Electrolytes normalized in two days after cessation of capreomycin with no further abnormalities on repeat investigations. DISCUSSION: Aminoglycosides can result in renal tubular dysfunction leading to Fanconi syndrome, Bartter syndrome, and distal tubular acidosis. Impaired mitochondrial function in the tubular cells has been hypothesized as the possible cause of these tubulopathies. Acquired Bartter-like syndrome phenotypically resembles autosomal dominant type 5 Bartter syndrome. Treatment consists of correction of electrolyte abnormalities, indomethacin, and potassium-sparing diuretics. Prompt diagnosis and treatment of severe dyselectrolytemia are warranted in patients on aminoglycoside therapy.
format Online
Article
Text
id pubmed-5624136
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-56241362017-10-26 Unusual Complication of Multidrug Resistant Tuberculosis Sharma, Prerna Sahay, Ravindra Nath Case Rep Nephrol Case Report INTRODUCTION: Capreomycin is a second-line drug often used for multidrug-resistant tuberculosis which can result in nephrotoxic effects similar to other aminoglycosides. We describe a case of capreomycin induced Bartter-like syndrome with hypocalcemic tetany. CASE REPORT: 23-year-old female patient presented with carpopedal spasms and tingling sensations in hands. Patient was being treated with capreomycin for two months for tuberculosis. On further investigation, hypocalcemia, hyponatremia, hypomagnesemia, hypokalemia, and hypochloremic metabolic alkalosis were noted. Vitamin D and serum PTH levels were within normal limits. Hypercalciuria was confirmed by urine calcium/creatinine ratio. Calcium, potassium, and magnesium supplementation was given and capreomycin was discontinued. Electrolytes normalized in two days after cessation of capreomycin with no further abnormalities on repeat investigations. DISCUSSION: Aminoglycosides can result in renal tubular dysfunction leading to Fanconi syndrome, Bartter syndrome, and distal tubular acidosis. Impaired mitochondrial function in the tubular cells has been hypothesized as the possible cause of these tubulopathies. Acquired Bartter-like syndrome phenotypically resembles autosomal dominant type 5 Bartter syndrome. Treatment consists of correction of electrolyte abnormalities, indomethacin, and potassium-sparing diuretics. Prompt diagnosis and treatment of severe dyselectrolytemia are warranted in patients on aminoglycoside therapy. Hindawi 2017 2017-09-18 /pmc/articles/PMC5624136/ /pubmed/29075541 http://dx.doi.org/10.1155/2017/6835813 Text en Copyright © 2017 Prerna Sharma and Ravindra Nath Sahay. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Sharma, Prerna
Sahay, Ravindra Nath
Unusual Complication of Multidrug Resistant Tuberculosis
title Unusual Complication of Multidrug Resistant Tuberculosis
title_full Unusual Complication of Multidrug Resistant Tuberculosis
title_fullStr Unusual Complication of Multidrug Resistant Tuberculosis
title_full_unstemmed Unusual Complication of Multidrug Resistant Tuberculosis
title_short Unusual Complication of Multidrug Resistant Tuberculosis
title_sort unusual complication of multidrug resistant tuberculosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5624136/
https://www.ncbi.nlm.nih.gov/pubmed/29075541
http://dx.doi.org/10.1155/2017/6835813
work_keys_str_mv AT sharmaprerna unusualcomplicationofmultidrugresistanttuberculosis
AT sahayravindranath unusualcomplicationofmultidrugresistanttuberculosis