Division of Pulmonary and Critical Care Medicine, University of Utah, Salt Lake City.
VA Salt Lake City Health Care System, Salt Lake City, Utah.
JAMA Netw Open. 2023 May 1;6(5):e2314185. doi: 10.1001/jamanetworkopen.2023.14185.
Non-ventilator-associated hospital-acquired pneumonia (NV-HAP) is a common and deadly hospital-acquired infection. However, inconsistent surveillance methods and unclear estimates of attributable mortality challenge prevention.
To estimate the incidence, variability, outcomes, and population attributable mortality of NV-HAP.
DESIGN, SETTING, AND PARTICIPANTS: This cohort study retrospectively applied clinical surveillance criteria for NV-HAP to electronic health record data from 284 US hospitals. Adult patients admitted to the Veterans Health Administration hospital from 2015 to 2020 and HCA Healthcare hospitals from 2018 to 2020 were included. The medical records of 250 patients who met the surveillance criteria were reviewed for accuracy.
NV-HAP, defined as sustained deterioration in oxygenation for 2 or more days in a patient who was not ventilated concurrent with abnormal temperature or white blood cell count, performance of chest imaging, and 3 or more days of new antibiotics.
NV-HAP incidence, length-of-stay, and crude inpatient mortality. Attributable inpatient mortality by 60 days follow-up was estimated using inverse probability weighting, accounting for both baseline and time-varying confounding.
Among 6 022 185 hospitalizations (median [IQR] age, 66 [54-75] years; 1 829 475 [26.1%] female), there were 32 797 NV-HAP events (0.55 per 100 admissions [95% CI, 0.54-0.55] per 100 admissions and 0.96 per 1000 patient-days [95% CI, 0.95-0.97] per 1000 patient-days). Patients with NV-HAP had multiple comorbidities (median [IQR], 6 [4-7]), including congestive heart failure (9680 [29.5%]), neurologic conditions (8255 [25.2%]), chronic lung disease (6439 [19.6%]), and cancer (5,467 [16.7%]); 24 568 cases (74.9%) occurred outside intensive care units. Crude inpatient mortality was 22.4% (7361 of 32 797) for NV-HAP vs 1.9% (115 530 of 6 022 185) for all hospitalizations; 12 449 (8.0%) were discharged to hospice. Median [IQR] length-of-stay was 16 (11-26) days vs 4 (3-6) days. On medical record review, pneumonia was confirmed by reviewers or bedside clinicians in 202 of 250 patients (81%). It was estimated that NV-HAP accounted for 7.3% (95% CI, 7.1%-7.5%) of all hospital deaths (total hospital population inpatient death risk of 1.87% with NV-HAP events included vs 1.73% with NV-HAP events excluded; risk ratio, 0.927; 95% CI, 0.925-0.929).
In this cohort study, NV-HAP, which was defined using electronic surveillance criteria, was present in approximately 1 in 200 hospitalizations, of whom 1 in 5 died in the hospital. NV-HAP may account for up to 7% of all hospital deaths. These findings underscore the need to systematically monitor NV-HAP, define best practices for prevention, and track their impact.
非呼吸机相关性医院获得性肺炎(NV-HAP)是一种常见且致命的医院获得性感染。然而,不一致的监测方法和不清楚的归因死亡率挑战了预防措施。
估计 NV-HAP 的发病率、变异性、结局和人群归因死亡率。
设计、地点和参与者:本队列研究回顾性地将 NV-HAP 的临床监测标准应用于来自 284 家美国医院的电子健康记录数据。纳入 2015 年至 2020 年退伍军人健康管理局医院和 2018 年至 2020 年 HCA 医疗保健医院住院的成年患者。对符合监测标准的 250 名患者的病历进行了回顾性准确性审查。
NV-HAP,定义为未同时进行通气的患者在 2 天或以上的时间内持续恶化氧合,同时出现异常体温或白细胞计数、进行胸部成像和 3 天或以上的新抗生素治疗。
NV-HAP 的发病率、住院时间和住院死亡率。使用逆概率加权法估计 60 天随访时的归因住院死亡率,同时考虑基线和随时间变化的混杂因素。
在 6022185 例住院治疗中(中位数[IQR]年龄,66[54-75]岁;1829475[26.1%]女性),有 32797 例 NV-HAP 事件(每 100 例入院 0.55[95%CI,0.54-0.55],每 1000 例患者日 0.96[95%CI,0.95-0.97])。患有 NV-HAP 的患者有多种合并症(中位数[IQR],6[4-7]),包括充血性心力衰竭(9680[29.5%])、神经系统疾病(8255[25.2%])、慢性肺部疾病(6439[19.6%])和癌症(5467[16.7%]);24568 例(74.9%)发生在重症监护病房外。NV-HAP 的住院死亡率为 22.4%(7361 例),而所有住院治疗的死亡率为 1.9%(115530 例);12449 例(8.0%)出院至临终关怀。中位[IQR]住院时间为 16(11-26)天,而所有住院治疗为 4(3-6)天。在病历回顾中,250 名患者中有 202 名(81%)经审查者或床边临床医生确诊为肺炎。据估计,NV-HAP 占所有医院死亡人数的 7.3%(95%CI,7.1%-7.5%)(包括 NV-HAP 事件的医院总人群住院死亡风险为 1.87%,不包括 NV-HAP 事件的风险为 1.73%;风险比,0.927;95%CI,0.925-0.929)。
在这项队列研究中,使用电子监测标准定义的 NV-HAP 在大约每 200 例住院治疗中出现 1 例,其中 1/5 在医院死亡。NV-HAP 可能占所有医院死亡人数的 7%。这些发现强调了需要系统监测 NV-HAP、定义预防的最佳实践并跟踪其影响。