Department of Microbiology and Infectious Diseases, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
Hôpital Maisonneuve-Rosemont, Montréal, Quebec, Canada.
PLoS One. 2018 Oct 23;13(10):e0206289. doi: 10.1371/journal.pone.0206289. eCollection 2018.
To examine secular changes in the incidence of invasive beta-hemolytic streptococcal infections, and to assess the efficacy of immunoglobulins and clindamycin as adjunctive therapies in the management of Streptococcus pyogenes infections.
Retrospective cohort study of all cases of invasive group A (GAS), B (GBS), C or G (GCGS) streptococcal infections managed in a Canadian tertiary center from 1996-2016. Population incidence was measured for diabetics and non-diabetics. Adjusted odds ratios (AOR) and their 95% confidence intervals (CI) were calculated by logistic regression.
741 cases were identified (GAS: 249; GBS: 304; GCGS: 188). While the incidence of invasive GAS infections fluctuated with no clear trend, incidence of invasive GBS and GCGS increased over time and were 8.4 and 6.3 times higher in diabetics. Mortality of invasive GAS infections decreased from 16% (6/37) in 1996-2001 to 4% (4/97) in 2011-15. Among patients with GAS infections, clindamycin administered concomitantly with a beta-lactam within 24 hours of admission decreased mortality (AOR: 0.04, 95%CI: 0.003-0.55, P = 0.02. Immunoglobulins had no such effect (AOR: 1.66, 95%CI: 0.16-17.36, P = 0.67). The protective effect of clindamycin was similar in patients with pneumonia/empyema compared to all others.
Incidence of GBS and GCGS infections increased due to an expansion of the high-risk population (elderly diabetics), but also rose in non-diabetics. No such secular change was seen for invasive GAS infections. The decrease in mortality in patients with invasive GAS infections presumably reflects better case-management. Adjunctive clindamycin reduced mortality in invasive GAS infections; immunoglobulins did not, but power was limited. The highest mortality was seen in patients with GAS pneumonia/empyema, for whom clindamycin was protective but underused.
研究β-溶血性链球菌侵袭性感染发病率的季节性变化,并评估免疫球蛋白和克林霉素作为辅助治疗链球菌性咽炎感染的疗效。
回顾性分析了 1996 年至 2016 年在加拿大一家三级中心治疗的所有 A 组(GAS)、B 组(GBS)、C 或 G 组(GCGS)侵袭性链球菌感染病例。测量了糖尿病患者和非糖尿病患者的人群发病率。通过逻辑回归计算调整后的优势比(AOR)及其 95%置信区间(CI)。
共发现 741 例病例(GAS:249 例;GBS:304 例;GCGS:188 例)。虽然侵袭性 GAS 感染的发病率波动不定,没有明显的趋势,但侵袭性 GBS 和 GCGS 的发病率随时间推移而增加,在糖尿病患者中分别高出 8.4 倍和 6.3 倍。侵袭性 GAS 感染的死亡率从 1996 年至 2001 年的 16%(6/37)降至 2011 年至 2015 年的 4%(4/97)。在 GAS 感染患者中,入院 24 小时内同时使用β-内酰胺类药物和克林霉素可降低死亡率(AOR:0.04,95%CI:0.003-0.55,P=0.02)。免疫球蛋白没有这种效果(AOR:1.66,95%CI:0.16-17.36,P=0.67)。克林霉素在肺炎/脓胸患者中的保护作用与其他患者相似。
由于高危人群(老年糖尿病患者)的扩大,GBS 和 GCGS 感染的发病率增加,但在非糖尿病患者中也有所增加。侵袭性 GAS 感染没有这种季节性变化。侵袭性 GAS 感染患者死亡率的下降可能反映了更好的病例管理。辅助克林霉素降低了侵袭性 GAS 感染患者的死亡率;免疫球蛋白没有,但效力有限。死亡率最高的是 GAS 肺炎/脓胸患者,克林霉素对此有保护作用,但使用不足。