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Trimethoprim-sulfamethoxazole acute respiratory distress syndrome requiring lung transplantation
Matthew Donnan1, Miranda Siemienowicz2,3, Hui Sien Tay4
1Department of Respiratory Medicine Alfred Health Melbourne Victoria Australia.
Abstract:
Trimethoprim-sulfamethoxazole (TMP-SMX) acute respiratory distress syndrome (ARDS) is a rare, but severe complication of a commonly prescribed antibiotic. TMP-SMX typically affects young, otherwise well patients with a specific human leukocyte antigen type (HLA-B*07:02 and HLA-C*07:02). The condition is poorly understood with a unique pathological appearance and mechanism that remains unclear. Mortality rate is greater than one third. We describe the case of a previously well 18-year-old woman treated with a prolonged course of TMP-SMX for a complex urinary tract infection who developed rapidly progressive respiratory failure requiring prolonged intensive care admission, extra-corporeal membranous oxygenation, and eventual lung transplantation. No targeted treatment exists, further research is required to better understand disease pathogenetic mechanisms and potential therapeutic interventions.
Insights
Trimethoprim-sulfamethoxazole (TMP-SMX) can cause rare but severe acute respiratory distress syndrome (ARDS), particularly in young individuals with specific HLA types. This condition has a high mortality rate and requires further research for effective treatments.
Area of Science:
- Pharmacology
- Immunology
- Pulmonology
Background:
- Trimethoprim-sulfamethoxazole (TMP-SMX) is a widely used antibiotic.
- Acute respiratory distress syndrome (ARDS) is a severe lung condition.
- TMP-SMX-induced ARDS is a rare but serious adverse drug reaction.
Observation:
- This condition predominantly affects young, healthy patients.
- Specific human leukocyte antigen (HLA) types, namely HLA-B*07:02 and HLA-C*07:02, are associated with increased risk.
- The case presented involves an 18-year-old female with a complex urinary tract infection treated with TMP-SMX.
Findings:
- The patient developed rapid respiratory failure requiring intensive care.
- Treatment involved extracorporeal membrane oxygenation (ECMO) and ultimately lung transplantation.
- The exact pathological mechanisms and unique features of TMP-SMX-induced ARDS remain poorly understood.
Implications:
- There is currently no targeted treatment for TMP-SMX-induced ARDS.
- The high mortality rate underscores the severity of this complication.
- Further research is crucial to elucidate pathogenesis and develop therapeutic interventions.
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