Trimethoprim-Sulfamethoxazole for Pediatric Osteoarticular Infections

被引:3
作者
Mcdaniel, Lauren M. [1 ,4 ]
Fiawoo, Suiyini [2 ]
Tamma, Pranita D. [2 ]
Same, Rebecca G. [3 ]
机构
[1] Univ Washington, Seattle Childrens Hosp, Sch Med, Dept Pediat, Seattle, WA USA
[2] Johns Hopkins Univ, Sch Med, Dept Pediat, Johns Hopkins Childrens Ctr, Baltimore, MD USA
[3] Univ Penn, Childrens Hosp Philadelphia, Perelman Sch Med, Dept Pediat, Philadelphia, PA USA
[4] Seattle Childrens Hosp, FA 2-115,4800 Sand Point Way,NE, Seattle, WA 98105 USA
关键词
osteoarticular infection; osteomyelitis; septic arthritis; trimethoprim-sulfamethoxazole; RESISTANT STAPHYLOCOCCUS-AUREUS; METHICILLIN-RESISTANT; CHILDREN; MANAGEMENT; TRENDS;
D O I
10.1093/jpids/piad076
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background Trimethoprim-sulfamethoxazole (TMP-SMX) is active against most Staphylococcus aureus isolates but is not widely used for the treatment of pediatric osteoarticular infections.Methods This was a comparative effectiveness study of hospitalized patients <= 18 years treated with TMP-SMX vs. other antibiotic regimens for acute osteoarticular infections between 2016 and 2021 at 3 hospitals using inverse probability of treatment weighted propensity score analysis. The primary outcome was treatment failure, a composite of unanticipated emergency department (ED) or outpatient visits, hospital readmissions, extension, or change of antibiotic therapy due to inadequate clinical response, or death, all within 6 months after completing antibiotics. The secondary outcome was antibiotic-associated adverse events (AEs) within 6 months. The exposed group for the treatment failure analysis included children who received >= 7 days of TMP-SMX and did not experience treatment failure while on another antibiotic. Children receiving at least 1 dose of TMP-SMX were the exposed group for the AE analysis.Results One-hundred and sixteen patients met eligibility criteria; 26 (22.4%) patients were classified into the TMP-SMX cohort and 90 (77.6%) into the other antibiotics cohort (most commonly clindamycin, vancomycin, and cefazolin). There was no significant difference in treatment failure between TMP-SMX and other antibiotics (43% vs. 19%; 95% CI .9-10.4). More patients in the TMP-SMX cohort experienced an unplanned ED or outpatient visit (OR 4.8, 95% CI 1.3-17.8). There was no difference in hospital readmission, antibiotic change, or duration extension. Exposure to TMP-SMX was associated with more AEs (41% vs. 19%, P = .012).Conclusions Treatment with TMP-SMX was not associated with greater clinical failure but was associated with more AEs compared to alternative agents for the treatment of pediatric acute osteoarticular infections. Antibiotic resistance has prompted a re-evaluation of treatment regimens for pediatric osteoarticular infections. In a propensity score weighted cohort of 116 children with acute osteoarticular infections, trimethoprim-sulfamethoxazole was not associated with increased treatment failure but was associated with increased adverse events compared to alternative antibiotic regimens.
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收藏
页码:534 / 539
页数:6
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