Tocilizumab Therapy in Gram-Positive and Gram-Negative Pediatric Septic Shock: A Comparative Pilot Study

医学 感染性休克 托珠单抗 内科学 辅助治疗 败血症 回顾性队列研究 队列 死亡率 新生儿败血症 队列研究 重症监护室 比例危险模型 生存分析 人口统计学的 外科 疾病严重程度 儿科重症监护室 重症监护
作者
Kiew-Kii Lau,Jainn-Jim Lin,Oi‐Wa Chan,Shao‐Hsuan Hsia,En‐Pei Lee
出处
期刊:Shock [Lippincott Williams & Wilkins]
卷期号:66 (2): 377-384
标识
DOI:10.1097/shk.0000000000002884
摘要

BACKGROUND: Elevated interleukin-6 (IL-6) is strongly associated with disease severity and mortality in pediatric septic shock. This study investigated whether adjunctive tocilizumab, a humanized anti-IL-6 receptor antibody, improves clinical outcomes in children with gram-positive bacteria and gram-negative bacteria (GNB) septic shock. METHODS: This retrospective cohort study included 58 children with septic shock (32 receiving adjunctive tocilizumab and 26 historical controls). We evaluated mortality rates, shock duration, and intensive care unit length of stay, with further stratification by pathogen type. RESULTS: Baseline demographics and initial disease severity were comparable between the groups. Tocilizumab administration was associated with a significantly shorter median shock duration (84 vs. 240 hours; P < 0.001), reduced intensive care unit stay (6 vs. 14 days; P = 0.002), and lower mortality (18.7% vs. 46.1%; P = 0.02) compared to controls. In subgroup analyses, tocilizumab significantly decreased mortality in GNB sepsis (23.8% vs. 56.2%; P = 0.04) and improved 28-day survival (log-rank P = 0.023). Notably, although tocilizumab-treated GNB patients had markedly higher initial IL-6 levels (median 7531 vs. 294 pg/mL; P = 0.014) and PRISM III scores than gram-positive bacteria patients, post-treatment mortality did not differ significantly between these cohorts (23.8% vs. 9.0%; P = 0.31). CONCLUSIONS: Adjunctive tocilizumab is associated with improved survival and shortened shock duration in pediatric septic shock. Targeted IL-6 blockade effectively neutralizes the hyperinflammatory surge, narrowing the clinical outcome gap typically driven by severe GNB infections.
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