Department of Pharmacy, Singapore General Hospital, Outram Road, Singapore, Singapore.
Department of Pharmacy, Singapore General Hospital, Outram Road, Singapore, Singapore; Saw Swee Hock School of Public Health, National University of Singapore, Singapore, Singapore.
Int J Antimicrob Agents. 2021 Jun;57(6):106340. doi: 10.1016/j.ijantimicag.2021.106340. Epub 2021 Apr 20.
In patients with a history of carbapenemase-producing, carbapenem-resistant Enterobacteriaceae (CP-CRE), the need for CP-CRE targeted treatment in subsequent sepsis episodes is unclear. This study aimed to characterise the incidence of subsequent CP-CRE infective episodes in individuals with prior CP-CRE colonisation and/or infection, and identify predictors for these subsequent CP-CRE infections.
All adult inpatients with CP-CRE detected from any site between June 2012 and May 2014 at a tertiary-care hospital were prospectively followed for two years to assess for any subsequent CP-CRE infections. Potential factors to which patients were exposed during the follow-up period were collected from medical records and analysed.
A total of 171 patients were enrolled. Of 151 patients who entered the follow-up period, 16 (10.6%) developed a subsequent CP-CRE infection. The median time to a subsequent infective episode was 24.5 days (12-105 days). The type of carbapenemase was highly conserved within index and subsequent paired episodes (16 of 17 pairs). Patients with first CP-CRE isolated from intra-abdominal or respiratory sources were ≥7 times more likely to develop a subsequent infection, while most rectal carriers remain colonised. For carriers (n = 133), Klebsiella spp. (OR 4.7) and OXA carbapenemase (OR 9.4) were significant predictors of subsequent infection. In patients with initial infection (n = 18), end-stage renal failure requiring dialysis (OR 22.0) was the only predisposing factor.
The incidence of subsequent infections in patients with prior colonisation was low. Consideration for CP-CRE targeted therapy is recommended in patients on dialysis and previous CP-CRE infections involving the bloodstream and/or respiratory tract.
在产碳青霉烯酶、耐碳青霉烯肠杆菌科细菌(CP-CRE)病史的患者中,后续败血症发作时是否需要 CP-CRE 靶向治疗尚不清楚。本研究旨在描述既往 CP-CRE 定植和/或感染患者后续 CP-CRE 感染发作的发生率,并确定这些后续 CP-CRE 感染的预测因素。
2012 年 6 月至 2014 年 5 月期间,一家三级保健医院从任何部位检测到的所有 CP-CRE 成年住院患者均前瞻性随访两年,以评估是否发生任何后续 CP-CRE 感染。从病历中收集患者在随访期间接触的潜在因素并进行分析。
共纳入 171 例患者。在进入随访期的 151 例患者中,16 例(10.6%)发生了后续 CP-CRE 感染。继发感染的中位时间为 24.5 天(12-105 天)。指数和后续配对发作中碳青霉烯酶的类型高度保守(17 对中的 16 对)。首次 CP-CRE 分离自腹腔或呼吸道来源的患者发生后续感染的可能性至少增加 7 倍,而大多数直肠携带者仍定植。对于携带者(n=133),克雷伯菌属(OR 4.7)和 OXA 碳青霉烯酶(OR 9.4)是继发感染的显著预测因子。在初始感染患者(n=18)中,需要透析的终末期肾病(OR 22.0)是唯一的易患因素。
既往定植患者继发感染的发生率较低。对于透析患者和涉及血液和/或呼吸道的既往 CP-CRE 感染患者,建议考虑 CP-CRE 靶向治疗。