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DOI 10.1136/bcr-2023-255242

Медицинская библиотека · BMJ case reports · 2024

Polymyxin B-induced Bartter syndrome.

Mohan Lal Bhavesh, Musthafa Hafeesa Nimisha, Vikram Naval Kishore, Ray Animesh

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Аннотация

Bartter syndrome is a genetic disorder characterised by chloride-unresponsive metabolic alkalosis, hypokalaemia, hypomagnesaemia and hypercalciuria. While it commonly presents antenatally or in early infancy, sometimes, drugs can induce a state similar to Bartter syndrome in any age group, called acquired Bartter syndrome. Polymyxins and aminoglycosides are the most commonly implicated drugs. Polymyxin B and polymyxin E (popularly known as colistin) are the two chemically similar polymyxins that are commonly used clinically. While colistin is frequently associated with nephrotoxicity, polymyxin B is generally considered less nephrotoxic. This difference is due to the way these two drugs are handled by the kidneys. In this case report, we discuss a middle-aged male who developed Bartter syndrome due to polymyxin B, which resolved on discontinuation of the drug, and re-appeared after its re-introduction later. This case exemplifies the nephrotoxicity caused by polymyxin B and the need for vigilance when using this drug.

Для цитирования: Mohan Lal Bhavesh, Musthafa Hafeesa Nimisha, Vikram Naval Kishore, Ray Animesh. Polymyxin B-induced Bartter syndrome.. BMJ case reports. 2024. DOI: 10.1136/bcr-2023-255242.

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