Pediatric Intensive Care Department, The Edmond and Lily Safra Children's Hospital, Chaim Sheba Medical Center, Ramat-Gan, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Pediatr Crit Care Med. 2019 May;20(5):e231-e239. doi: 10.1097/PCC.0000000000001919.
Stenotrophomonas maltophilia is a gram-negative opportunistic bacterium that may cause a myriad of clinical diseases in immunocompromised individuals. We aimed to describe the clinical characteristics, risk factors, mortality, and treatment of S. maltophilia bacteremia in critically ill children, a topic on which data are sparse.
A multicenter observational retrospective study in which medical charts of critically ill children with S. maltophilia bacteremia were reviewed between 2012 and 2017.
Data were collected from each of the four largest PICUs nationwide, allocated in tertiary medical centers to which children with complex conditions are referred regularly.
A total of 68 suitable cases of S. maltophilia bacteremia were retrieved and reviewed.
The total occurrence rate of S. maltophilia isolation had increased significantly during the study period (r = 0.65; p = 0.02). The crude mortality was 42%, and the attributed mortality was 18%. Significant risk factors for mortality were a longer length of hospital stay prior to infection (33 d in nonsurvivors vs 28 in survivors; p = 0.03), a nosocomial source of infection (p = 0.02), presentation with septic shock (p < 0.001), and treatment with chemotherapy (p = 0.007) or carbapenem antibiotics (p = 0.05) prior to culture retrieval. On multivariate analysis, septic shock (odds ratio, 14.6; 95% CI, 1.45-147.05; p = 0.023) and being treated with chemotherapy prior to infection (odds ratio, 5.2; 95% CI, 1.59-17.19; p = 0.006)] were associated with mortality. The combination of ciprofloxacin, trimethoprim-sulfamethoxazole, and minocycline resulted in the longest survival time (p < 0.01).
The significant attributed mortality associated with S. maltophilia bacteremia in critically ill children calls for an aggressive therapeutic approach. The findings of this investigation favor a combination of trimethoprim-sulfamethoxazole, ciprofloxacin, and minocycline.
嗜麦芽窄食单胞菌是一种革兰氏阴性机会致病菌,可导致免疫功能低下个体发生多种临床疾病。我们旨在描述重症患儿嗜麦芽窄食单胞菌菌血症的临床特征、危险因素、死亡率和治疗方法,这方面的数据较为匮乏。
一项多中心观察性回顾性研究,对 2012 年至 2017 年期间患有嗜麦芽窄食单胞菌菌血症的重症患儿的病历进行了回顾性分析。
数据来自全国 4 家最大的 PICU 中的每一家,这些 PICU 均位于三级医疗中心,经常收治患有复杂疾病的患儿。
共检索到 68 例嗜麦芽窄食单胞菌菌血症的合适病例,并进行了回顾性分析。
研究期间,嗜麦芽窄食单胞菌分离株的总发生率显著增加(r = 0.65;p = 0.02)。粗死亡率为 42%,归因死亡率为 18%。死亡率的显著危险因素包括感染前住院时间较长(33 天 vs 幸存者 28 天;p = 0.03)、医院感染源(p = 0.02)、出现感染性休克(p < 0.001)以及在培养前接受化疗(p = 0.007)或碳青霉烯类抗生素(p = 0.05)治疗。多变量分析显示,感染性休克(比值比,14.6;95%置信区间,1.45-147.05;p = 0.023)和感染前接受化疗(比值比,5.2;95%置信区间,1.59-17.19;p = 0.006)与死亡率相关。环丙沙星、复方磺胺甲噁唑和米诺环素联合治疗的患者生存时间最长(p < 0.01)。
重症患儿嗜麦芽窄食单胞菌菌血症的显著归因死亡率需要积极的治疗方法。本研究结果支持使用复方磺胺甲噁唑、环丙沙星和米诺环素联合治疗。