Staphylococcal scalded skin syndrome: Clinical features, ancillary testing, and patient management

医学 克林霉素 养生 葡萄球菌烫伤皮肤综合征 内科学 抗生素 回顾性队列研究 金黄色葡萄球菌 重症监护医学 急诊医学 微生物学 遗传学 细菌 生物
作者
Laurel Gray,Jared Olson,Ben J. Brintz,Sarah D. Cipriano
出处
期刊:Pediatric Dermatology [Wiley]
卷期号:39 (6): 908-913 被引量:8
标识
DOI:10.1111/pde.15102
摘要

Abstract Background/Objectives The utility of ancillary testing in improving diagnostic precision or improving patient outcomes in staphylococcal scalded skin syndrome (SSSS) is unclear. Similarly, an optimal antibiotic regimen has yet to be established. Our goal was to describe clinical characteristics and ancillary work‐up of SSSS, report bacterial resistance patterns, and examine patient outcomes under varying therapeutic strategies with the aim of developing an evidence‐based management algorithm. Methods We performed a retrospective review of pediatric patients diagnosed with SSSS at Intermountain Healthcare facilities between 2010 and 2021. A Kruskal–Wallis rank sum test was used to assess median length of stay between different antibiotic regimens. Results Eighty‐five cases were identified. The most common ancillary tests obtained were a complete blood count (88%), followed by chemistry analysis (80%). Blood cultures were collected in more patients (79%) compared to aerobic cultures (60%). No blood culture was positive for Staphylococcus aureus . All S. aureus isolates were methicillin‐sensitive. Of those found resistant to clindamycin (36%), all demonstrated macrolide‐induced clindamycin resistance. None were constitutively resistant to clindamycin. There was no statistical difference between antibiotic regimen and length of stay ( p = .691). Receiving opiate medications was the only risk factor associated with prolonged hospitalization ( p = .001). Conclusions Ancillary testing does not improve diagnostic precision and can be reduced. Clindamycin does not improve patient outcomes, suggesting beta‐lactams should be considered first line. Susceptibility patterns in our cohort demonstrate inducible clindamycin resistance as opposed to constitutive.
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