医院获得性常见呼吸道病毒感染的发生率、危险因素和结果

Joshua Petrie, Riley Moore, Adam Lauring, Keith Kaye
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引用次数: 0

摘要

背景:我们估计了不同病毒种类的医院获得性呼吸道病毒感染(HARVIs)的发生率,并确定了HARVIs的危险因素和结局。方法:我们确定了密歇根大学医院在3个研究年(2017-2018、2018-2019和2019-2020)住院≥24小时的所有患者的队列。HARVIs被定义为在病毒特异性潜伏期的第95个百分位之后,在临床试验中进行初始呼吸道病毒检测(腺病毒、冠状病毒、人中肺病毒、甲型和乙型流感病毒、副流感病毒、呼吸道合胞病毒或鼻病毒-肠病毒)。发生率计算为每10,000名患者入院日中接受HARVIs治疗的人数。患者人口统计学和临床特征被评估为HARVI的危险因素,在HARVI和出院的竞争结果的Cox比例风险模型中。在协变量校正cox比例风险模型中估计随时间变化的HARVI状态与出院和院内死亡的竞争结果之间的关系。所有分析分别对成人患者(≥18岁)和儿科患者(≥18岁)进行。结果:儿童和成人患者HARVI的总发生率分别为8.5和3.0 / 10000入院日。鼻病毒是儿童和成人患者中最常见的HARVI,发病率分别为每10,000入院日5.1和1.1。除甲型流感外,儿童患者的HARVI发生率高于所有病毒种类的成人患者。对于成人,充血性心力衰竭、肾脏疾病和癌症都增加了HARVI风险,与延长住院时间无关。9月至6月入院的患者发生HARVI的风险也高于7月入院的患者。对于儿科患者,慢性心血管和呼吸系统疾病、癌症、医疗器械依赖和12月入院增加了HARVI的风险。年龄、性别和种族与儿童或成人发生HARVI的风险无关。患有HARVI的成年人的住院时间比没有的更长(病毒特异性风险比范围,0.48 - 0.77)。然而,估计的效应对人偏肺病毒、副流感病毒或腺病毒没有统计学意义。只有甲型流感与成人感染后30天内住院死亡风险增加有关。无HARVIs与儿科患者住院时间或死亡风险增加相关。结论:HARVI的发病率因病毒种类而异,在儿科患者中较高。HARVIs增加了成人的住院时间,但没有增加儿科患者的住院时间。披露:没有
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Incidence, risk factors, and outcomes of hospital-acquired infections with common respiratory viruses
Background: We estimated the incidence of hospital-acquired respiratory virus infections (HARVIs) by viral species, and we identified risk factors for and outcomes of HARVIs. Methods: We identified a cohort of all inpatient admissions of ≥24 hours duration to University of Michigan hospitals during 3 study years (2017–2018, 2018–2019, and 2019–2020). HARVIs were defined as initial respiratory virus detection (adenovirus, coronaviruses, human metapneumovirus, influenza A and B, parainfluenza viruses, respiratory syncytial virus, or rhinovirus-enterovirus) in a clinical test ordered after the 95th percentile of the virus-specific incubation period. Incidence was calculated as the number of HARVIs per 10,000 patient admission days. Patient demographic and clinical characteristics were assessed as risk factors for HARVI in Cox proportional hazards models of the competing outcomes of HARVIs and hospital discharge. The association between time-varying HARVI status and the competing outcomes of discharge and in-hospital death was estimated in covariate-adjusted Cox-proportional hazards models. All analyses were performed separately for adult patients (aged ≥18 years) and pediatric patients (aged <18 years). Results: The overall incidences of HARVI were 8.5 and 3.0 per 10,000 admission days for pediatric and adult patients, respectively. Rhinovirus was the most common HARVI in both pediatric and adult patients, with incidences of 5.1 and 1.1 infections per 10,000 admission days, respectively. With the exception of influenza A, the incidence of HARVI was higher in pediatric patients than adult patients for all viral species. For adults, congestive heart failure, renal disease, and cancer all increased HARVI risk independent of their associations with extended hospital stays. Risk of HARVI was also elevated for patients admitted September through June relative to July admissions. For pediatric patients, chronic cardiovascular and respiratory conditions, cancer, medical-device dependence, and December admission increased risk of HARVI. Age, sex, and race were not associated with risk of HARVI for children or adults. Inpatient lengths of stay were longer for adults with HARVI compared to those without (range of virus-specific hazard ratios, 0.48– 0.77). However, estimated effects were not statistically significant for human metapneuomovirus, parainfluenza, or adenovirus. Only influenza A was associated with an increased risk of in-hospital death within 30 days of infection for adults. No HARVIs were associated with increased length of stay or risk of death for pediatric patients. Conclusions: The incidence of HARVI varied by viral species and was higher among pediatric patients. HARVIs increased the length of hospital stays for adults but not for pediatric patients. Disclosures: None
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