Baltas Ioannis, Rawson Timothy Miles, Houston Hamish, Grandjean Louis, Pollara Gabriele
Infection, Immunity & Inflammation Department, UCL Institute of Child Health, London, UK.
Department of Clinical Microbiology, University College London Hospitals NHS Foundation Trust, London, UK.
JAC Antimicrob Resist. 2024 Dec 19;6(6):dlae202. doi: 10.1093/jacamr/dlae202. eCollection 2024 Dec.
The impact of antimicrobial resistance (AMR) on death at the patient level is challenging to estimate. We aimed to characterize AMR-attributable deaths in a large UK teaching hospital.
This retrospective study investigated all deceased patients in 2022. Records of participants were independently reviewed by two investigators for cases of AMR-attributable deaths using a newly proposed patient-level definition.
In total, 758 patients met inclusion criteria. Infection was the underlying cause of death for 11.7% (89/758) and was implicated in the pathway that led to death in 41.1% (357/758) of participants. In total, 4.2% (32/758) of all deaths were AMR-attributable. Median time from index sample collection to death was 4.5 days (IQR 2-10.5 days). The majority of AMR-attributable deaths (56.3%, 18/32) were associated with intrinsic resistance mechanisms, primarily by (20.7%), Enterobacterales carrying repressed chromosomal ampicillinase Cs (AmpCs) (14.7%) and (11.8%, whereas a minority (43.7%, 14/32) had acquired resistance mechanisms, primarily derepressed chromosomal AmpCs (11.8%) and ESBLs (8.8%). The median time to effective treatment was 32 h 15 min (no difference between subgroups). Only 62.5% (20/32) of AMR-attributable deaths had infection recorded on the death certificate. AMR was not recorded as a cause of death in any of the patients.
Infection and AMR were important causes of death in our cohort, yet they were significantly underreported during death certification. In a low-incidence setting for AMR, pathogen-antimicrobial mismatch due to intrinsic resistance was an equally important contributor to AMR-attributable mortality as acquired resistance mechanisms.
抗菌药物耐药性(AMR)对患者层面死亡的影响难以估计。我们旨在描述一家大型英国教学医院中归因于AMR的死亡情况。
这项回顾性研究调查了2022年所有死亡患者。两名研究人员使用新提出的患者层面定义,对参与者的记录进行独立审查,以确定归因于AMR的死亡病例。
共有758名患者符合纳入标准。感染是11.7%(89/758)患者的潜在死亡原因,并且在41.1%(357/758)参与者导致死亡的过程中起作用。所有死亡病例中,共有4.2%(32/758)归因于AMR。从首次采样到死亡的中位时间为4.5天(四分位间距2 - 10.5天)。大多数归因于AMR的死亡(56.3%,18/32)与固有耐药机制相关,主要是 (20.7%)、携带受抑制染色体β-内酰胺酶Cs(AmpCs)的肠杆菌科细菌(14.7%)和 (11.8%),而少数(43.7%,14/32)具有获得性耐药机制,主要是去抑制染色体AmpCs(11.8%)和超广谱β-内酰胺酶(ESBLs)(8.8%)。有效治疗的中位时间为32小时15分钟(各亚组之间无差异)。死亡证明上仅记录了62.5%(20/32)归因于AMR的死亡病例存在感染。所有患者中均未将AMR记录为死亡原因。
感染和AMR是我们队列中的重要死亡原因,但在死亡证明过程中它们被严重低估。在AMR低发环境中,由于固有耐药导致的病原体 - 抗菌药物不匹配与获得性耐药机制一样,是AMR归因死亡率的重要因素。