National Institute for Antibiotic Resistance and Infection Control, Tel Aviv, Israel.
National Institute for Antibiotic Resistance and Infection Control and Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Clin Infect Dis. 2024 Jul 19;79(1):22-29. doi: 10.1093/cid/ciae110.
Little is known about the risk of progression from carbapenemase-producing Enterobacterales (CPE) carriage to CPE bloodstream infection (BSI) outside of high-risk settings. We aimed to determine the incidence of CPE BSI among CPE carriers and to assess whether the incidence differs by carbapenemase, species, and setting.
We conducted a nationwide population-based retrospective cohort study using national databases. The cohort consisted of all patients in Israel with CPE detected by screening from 1 January 2020 to 10 October 2022. We calculated the cumulative incidence of CPE BSI within 1 year among CPE carriers. We used a competing-risks model with BSI as the outcome and death as the competing risk.
The study included 6828 CPE carriers. The cumulative incidence of CPE BSI was 2.4% (95% confidence interval [CI], 2.1-2.8). Compared with Klebsiella pneumoniae carbapenemase (KPC), the subhazard of BSI was lower for New Delhi metallo-β-lactamase (NDM) (adjusted subhazard ratio [aSHR], 0.72; 95% CI, .49-1.05) and oxacillinase-48-like (OXA-48-like) (aSHR, 0.60; 95% CI, .32-1.12) but these differences did not reach statistical significance. Compared with K. pneumoniae, the subhazard of BSI was lower for carriers of carbapenemase-producing Escherichia coli (aSHR, 0.33; 95% CI, .21-.52). The subhazard of BSI was higher among patients with CPE carriage first detected in intensive care units (aSHR, 2.10; 95% CI, 1.27-3.49) or oncology/hematology wards (aSHR, 3.95; 95% CI, 2.51-6.22) compared with medical wards.
The risk of CPE BSI among CPE carriers is lower than previously reported in studies that focused on high-risk patients and settings. The risk of BSI differs significantly by bacterial species and setting, but not by carbapenemase.
在高风险环境之外,关于产碳青霉烯酶肠杆菌科(CPE)定植者进展为 CPE 血流感染(BSI)的风险知之甚少。我们旨在确定 CPE 定植者中 CPE BSI 的发生率,并评估碳青霉烯酶、物种和环境是否会影响发生率。
我们使用国家数据库进行了一项全国性基于人群的回顾性队列研究。该队列包括 2020 年 1 月 1 日至 2022 年 10 月 10 日期间通过筛查在以色列发现的所有 CPE 患者。我们计算了 CPE 定植者在 1 年内发生 CPE BSI 的累积发生率。我们使用以 BSI 为结局、死亡为竞争风险的竞争风险模型。
该研究纳入了 6828 名 CPE 定植者。CPE BSI 的累积发生率为 2.4%(95%置信区间[CI],2.1%-2.8%)。与产 KPC 肠杆菌科细菌相比,NDM(调整后的亚危险比[aSHR],0.72;95%CI,0.49-1.05)和产 OXA-48 样酶肠杆菌科细菌(aSHR,0.60;95%CI,0.32-1.12)的 BSI 亚危险比较低,但这些差异无统计学意义。与产 K. pneumoniae 的 CPE 定植者相比,产 CPE 大肠埃希菌的定植者的 BSI 亚危险比较低(aSHR,0.33;95%CI,0.21-0.52)。与内科病房相比,首次在重症监护病房(aSHR,2.10;95%CI,1.27-3.49)或肿瘤/血液病房(aSHR,3.95;95%CI,2.51-6.22)发现 CPE 定植的患者发生 CPE BSI 的亚危险比更高。
与侧重于高危患者和环境的研究相比,CPE 定植者中 CPE BSI 的风险较低。BSI 的风险因细菌种类和环境而异,但与碳青霉烯酶无关。