Sulfa Use, Dihydropteroate Synthase Mutations, and Pneumocystis jirovecii Pneumonia

A systematic review was conducted to examine the associations in Pneumocystis jirovecii pneumonia (PCP) patients between dihydropteroate synthase (DHPS) mutations and sulfa or sulfone (sulfa) prophylaxis and between DHPS mutations and sulfa treatment outcome. Selection criteria included study popula...

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Main Authors: Cheryl R. Stein, Charles Poole, Powel Kazanjian, Steven R Meshnick
Format: Article
Language:English
Published: Centers for Disease Control and Prevention 2004-10-01
Series:Emerging Infectious Diseases
Subjects:
Online Access:https://wwwnc.cdc.gov/eid/article/10/10/04-0362_article
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spelling doaj-ab1953f5e826417cb8e214677e55e5a72020-11-25T00:30:56ZengCenters for Disease Control and PreventionEmerging Infectious Diseases1080-60401080-60592004-10-0110101760176510.3201/eid1010.040362Sulfa Use, Dihydropteroate Synthase Mutations, and Pneumocystis jirovecii PneumoniaCheryl R. SteinCharles PoolePowel KazanjianSteven R MeshnickA systematic review was conducted to examine the associations in Pneumocystis jirovecii pneumonia (PCP) patients between dihydropteroate synthase (DHPS) mutations and sulfa or sulfone (sulfa) prophylaxis and between DHPS mutations and sulfa treatment outcome. Selection criteria included study populations composed entirely of PCP patients and mutation or treatment outcome results for all patients, regardless of exposure status. Based on 13 studies, the risk of developing DHPS mutations is higher for PCP patients receiving sulfa prophylaxis than for PCP patients not receiving sulfa prophylaxis (p < 0.001). Results are too heterogeneous (p < 0.001) to warrant a single summary effect estimate. Estimated effects are weaker after 1996 and stronger in studies that included multiple isolates per patient. Five studies examined treatment outcome. The effect of DHPS mutations on treatment outcome has not been well studied, and the few studies that have been conducted are inconsistent even as to the presence or absence of an association.https://wwwnc.cdc.gov/eid/article/10/10/04-0362_articledihydropteroate synthasemeta-analysisPneumocystisPneumocystis cariniitrimethoprim-sulfamethoxazole combination (sulfa drugs)treatment failure
collection DOAJ
language English
format Article
sources DOAJ
author Cheryl R. Stein
Charles Poole
Powel Kazanjian
Steven R Meshnick
spellingShingle Cheryl R. Stein
Charles Poole
Powel Kazanjian
Steven R Meshnick
Sulfa Use, Dihydropteroate Synthase Mutations, and Pneumocystis jirovecii Pneumonia
Emerging Infectious Diseases
dihydropteroate synthase
meta-analysis
Pneumocystis
Pneumocystis carinii
trimethoprim-sulfamethoxazole combination (sulfa drugs)
treatment failure
author_facet Cheryl R. Stein
Charles Poole
Powel Kazanjian
Steven R Meshnick
author_sort Cheryl R. Stein
title Sulfa Use, Dihydropteroate Synthase Mutations, and Pneumocystis jirovecii Pneumonia
title_short Sulfa Use, Dihydropteroate Synthase Mutations, and Pneumocystis jirovecii Pneumonia
title_full Sulfa Use, Dihydropteroate Synthase Mutations, and Pneumocystis jirovecii Pneumonia
title_fullStr Sulfa Use, Dihydropteroate Synthase Mutations, and Pneumocystis jirovecii Pneumonia
title_full_unstemmed Sulfa Use, Dihydropteroate Synthase Mutations, and Pneumocystis jirovecii Pneumonia
title_sort sulfa use, dihydropteroate synthase mutations, and pneumocystis jirovecii pneumonia
publisher Centers for Disease Control and Prevention
series Emerging Infectious Diseases
issn 1080-6040
1080-6059
publishDate 2004-10-01
description A systematic review was conducted to examine the associations in Pneumocystis jirovecii pneumonia (PCP) patients between dihydropteroate synthase (DHPS) mutations and sulfa or sulfone (sulfa) prophylaxis and between DHPS mutations and sulfa treatment outcome. Selection criteria included study populations composed entirely of PCP patients and mutation or treatment outcome results for all patients, regardless of exposure status. Based on 13 studies, the risk of developing DHPS mutations is higher for PCP patients receiving sulfa prophylaxis than for PCP patients not receiving sulfa prophylaxis (p < 0.001). Results are too heterogeneous (p < 0.001) to warrant a single summary effect estimate. Estimated effects are weaker after 1996 and stronger in studies that included multiple isolates per patient. Five studies examined treatment outcome. The effect of DHPS mutations on treatment outcome has not been well studied, and the few studies that have been conducted are inconsistent even as to the presence or absence of an association.
topic dihydropteroate synthase
meta-analysis
Pneumocystis
Pneumocystis carinii
trimethoprim-sulfamethoxazole combination (sulfa drugs)
treatment failure
url https://wwwnc.cdc.gov/eid/article/10/10/04-0362_article
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