Yek Christina, Mancera Alex G, Diao Guoqing, Walker Morgan, Neupane Maniraj, Chishti Emad A, Amirahmadi Roxana, Richert Mary E, Rhee Chanu, Klompas Michael, Swihart Bruce, Warner Sarah R, Kadri Sameer S
Critical Care Medicine Department, National Institutes of Health Clinical Center, Bethesda, Critical Care Medicine Branch, National Heart, Lung, and Blood Institute, Bethesda, and Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, Rockville, Maryland (C.Y.).
Critical Care Medicine Department, National Institutes of Health Clinical Center, and Critical Care Medicine Branch, National Heart, Lung, and Blood Institute, Bethesda, Maryland (A.G.M., M.W., M.N., E.A.C., R.A., M.E.R., B.S., S.R.W., S.S.K.).
Ann Intern Med. 2025 Jun;178(6):796-807. doi: 10.7326/ANNALS-24-03078. Epub 2025 Apr 29.
In 2022, the U.S. Centers for Disease Control and Prevention reported increases in antimicrobial resistance (AMR) across U.S. hospitals during the COVID-19 pandemic. The key drivers and lasting effects of this phenomenon remain unexplored.
To determine the incidence of AMR infections in U.S. hospitals during and beyond the pandemic and identify factors contributing to AMR.
Retrospective cohort study.
243 U.S. hospitals.
Adult hospitalizations, excluding inpatient transfers.
Prepandemic (January 2018 to December 2019), peak pandemic (March 2020 to February 2022), and waning pandemic (March to December 2022).
Incidence of methicillin-resistant ; vancomycin-resistant ; extended-spectrum cephalosporin-resistant Enterobacterales; and carbapenem-resistant Enterobacterales, , and infections was evaluated among 120 continuously reporting hospitals. Infections detected more than 3 days after admission were classified as hospital-onset. Antibiotic exposure was estimated using a duration- and spectrum-weighted index. A competing risks analysis was done in 243 hospitals to identify risk factors for resistance.
During the peak of the COVID-19 pandemic, AMR infections increased from 182 to 193 per 10 000 hospitalizations (6.5% [95% CI, 5.1% to 8.0%]). Hospital-onset AMR infections increased from 28.9 to 38.0 per 10 000 hospitalizations (31.5% [CI, 27.3% to 35.8%]). Factors associated with hospital-onset AMR included illness severity (intensive care unit admission, mechanical ventilation, vasopressors, COVID-19 diagnosis), comorbidities (Elixhauser Comorbidity Index), and prior exposure to antibiotics, but not hospital factors. Prevalence of AMR returned to prepandemic levels as the pandemic waned (182 to 182 per 10 000 hospitalizations; 0.4% [CI, -1.4% to 2.2%]), however, hospital-onset AMR remained above baseline (28.9 to 32.3 per 10 000 hospitalizations; 11.6% [CI, 6.8% to 16.7%]).
Residual confounding; unknown appropriateness of antibiotics.
Sustained increases in hospital-onset AMR infections occurred in U.S. hospitals during the pandemic and were strongly associated with antibiotic exposure.
National Institutes of Health Clinical Center; National Heart, Lung, and Blood Institute; and National Institute of Allergy and Infectious Diseases Intramural Research Programs.
2022年,美国疾病控制与预防中心报告称,在新冠疫情期间,美国各医院的抗菌药物耐药性(AMR)有所增加。这一现象的关键驱动因素和长期影响仍未得到探索。
确定疫情期间及之后美国医院AMR感染的发生率,并确定导致AMR的因素。
回顾性队列研究。
243家美国医院。
成年住院患者,不包括住院期间的转科患者。
疫情前(2018年1月至2019年12月)、疫情高峰期(2020年3月至2022年2月)和疫情消退期(2022年3月至12月)。
在120家持续报告的医院中评估耐甲氧西林金黄色葡萄球菌、耐万古霉素肠球菌、对超广谱头孢菌素耐药的肠杆菌科细菌以及耐碳青霉烯类肠杆菌科细菌、金黄色葡萄球菌和肠球菌感染的发生率。入院3天以上检测到的感染被分类为医院获得性感染。使用持续时间和谱加权指数估计抗生素暴露情况。在243家医院进行了竞争风险分析,以确定耐药的危险因素。
在新冠疫情高峰期,每10000例住院患者中AMR感染从182例增加到193例(6.5%[95%CI,5.1%至8.0%])。每10000例住院患者中医院获得性AMR感染从28.9例增加到38.0例(31.5%[CI,27.3%至35.8%])。与医院获得性AMR相关的因素包括疾病严重程度(入住重症监护病房、机械通气、使用血管活性药物、新冠诊断)、合并症(埃利克斯豪泽合并症指数)和既往抗生素暴露,但不包括医院因素。随着疫情消退,AMR的患病率恢复到疫情前水平(每10000例住院患者中182例至182例;0.4%[CI,-1.4%至2.2%]),然而,医院获得性AMR仍高于基线水平(每10000例住院患者中28.9例至32.3例;11.6%[CI,6.8%至16.7%])。
残余混杂因素;抗生素使用的适宜性未知。
疫情期间美国医院医院获得性AMR感染持续增加,且与抗生素暴露密切相关。
美国国立卫生研究院临床中心;美国国立心肺血液研究所;以及美国国立过敏与传染病研究所内部研究项目。