'Septrin psychosis' among renal transplant patients with Pneumocystis jirovecii pneumonia

被引:14
作者
Walker, Lauren E. [2 ]
Thomas, Sherine [1 ]
McBride, Catherine [3 ]
Howse, Matthew [4 ]
Turtle, Lance C. W. [1 ]
Vivancos, Roberto [5 ]
Beeching, Nick J. [1 ]
Beadsworth, Michael B. J. [1 ]
机构
[1] Royal Liverpool Univ Hosp, Trop & Infect Dis Unit, Liverpool L7 8XP, Merseyside, England
[2] Royal Liverpool Univ Hosp, Dept Clin Pharmacol & Therapeut, Liverpool L7 8XP, Merseyside, England
[3] Royal Liverpool Univ Hosp, Dept Pharm, Liverpool L7 8XP, Merseyside, England
[4] Royal Liverpool Univ Hosp, Dept Nephrol, Liverpool L7 8XP, Merseyside, England
[5] Hlth Protect Agcy, Cheshire & Merseyside Hlth Protect Unit, Liverpool, Merseyside, England
关键词
trimethoprim/sulfamethoxazole; psychosis; adverse drug event; renal failure; ORAL TRIMETHOPRIM-SULFAMETHOXAZOLE; INTERHUMAN TRANSMISSION; RECIPIENTS; OUTBREAK;
D O I
10.1093/jac/dkr050
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: To report on the temporal relationship between administration of trimethoprim/sulfamethoxazole to medically immunosuppressed HIV-negative renal patients with Pneumocystis jirovecii pneumonia (PCP) and the development of an acute psychosis. Methods: We investigated a retrospective case series of renal transplant and immunosuppressed patients with PCP within an ongoing outbreak in the northwest of England since 2009. Four patients with PCP developed psychosis following treatment with trimethoprim/sulfamethoxazole. Results: Four of twenty patients developed acute psychoses following administration of trimethoprim/sulfamethoxazole, including one accidental re-challenge. Symptoms resolved within 24 h of changing the therapy. The striking temporal relationship between the initiation and discontinuation of the drug and the behavioural changes suggests a causal relationship. Conclusions: With increasing solid organ transplantation and the use of immunosuppressants, vigilance regarding trimethoprim/sulfamethoxazole dose modification is required and the routine use of therapeutic drug monitoring should be considered.
引用
收藏
页码:1117 / 1119
页数:3
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