住院时间的竞争风险模型增强了病人护理的风险分层:应用于马拉维住院的五岁以下儿童

Christopher C. Stanley, Madalitso Zulu, Harrison Msuku, Vincent S. Phiri, Lawrence N. Kazembe, Jobiba Chinkhumba, Tisungane Mvalo, Don P. Mathanga
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Methods This study analyzed data from ongoing safety surveillance of the malaria vaccine implementation program in Malawi's four district hospitals of Balaka, Machinga, Mchinji, and Ntchisi. Children aged 1–59 months who were hospitalized (spending at least one night in hospital) with a medical illness were consecutively enrolled between 1 November 2019 and 31 July 2021. Sub-distribution-hazard (SDH) ratios for the cumulative incidence of discharge were estimated using the Fine-Gray competing risk model. Results Among the 15,463 children hospitalized, 8,607 (55.7%) were male and 6,856 (44.3%) were female. The median age was 22 months [interquartile range (IQR): 12–33 months]. The cumulative incidence of discharge was 40% lower among HIV-positive children compared to HIV-negative (sub-distribution-hazard ratio [SDHR]: 0.60; [95% CI: 0.46–0.76]; P < 0.001); lower among children with severe and cerebral malaria [SDHR: 0.94; (95% CI: 0.86–0.97); P = 0.04], sepsis or septicemia [SDHR: 0.90; (95% CI: 0.82–0.98); P = 0.027], severe anemia related to malaria [SDHR: 0.54; (95% CI: 0.48–0.61); P < 0.001], and meningitis [SDHR: 0.18; (95% CI: 0.09–0.37); P < 0.001] when compared to non-severe malaria; and also 39% lower among malnourished children compared to those that were well-nourished [SDHR: 0.61; (95% CI: 0.55–0.68); P < 0.001]. Conclusions This study applied the Fine-Gray competing risk approach to more accurately model LOS as the time to discharge when there were significant rates of in-hospital mortality, referrals, and abscondment. 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引用次数: 0

摘要

住院时间(LOS),定义为从住院到出院、死亡、转诊或潜逃的时间,是患者护理质量的关键指标之一。降低LOS可降低医疗保健支出并最大限度地减少院内获得性感染的机会。估计LOS的传统方法,如Kaplan-Meier生存曲线和Cox出院时间比例风险回归,不能解释诸如死亡、转诊和潜逃等竞争风险。本研究应用竞争风险方法探讨基于LOS的患者风险分层的重要因素,以加强患者护理。方法本研究分析了马拉维Balaka、Machinga、Mchinji和Ntchisi四个区医院正在进行的疟疾疫苗实施计划的安全监测数据。在2019年11月1日至2021年7月31日期间连续登记因医疗疾病住院(至少住院一晚)的1 - 59个月儿童。使用Fine-Gray竞争风险模型估计累积排放发生率的亚分布风险(SDH)比率。结果15463例住院患儿中,男性8607例(55.7%),女性6856例(44.3%)。中位年龄为22个月[四分位间距(IQR): 12-33个月]。hiv阳性儿童的累计出院发生率比hiv阴性儿童低40%(亚分布-风险比[SDHR]: 0.60;[95% ci: 0.46-0.76];P, lt;0.001);重度疟疾和脑型疟疾患儿的发病率较低[SDHR: 0.94;(95% ci: 0.86-0.97);P = 0.04],败血症或败血症[SDHR: 0.90;(95% ci: 0.82-0.98);P = 0.027],与疟疾相关的严重贫血[SDHR: 0.54;(95% ci: 0.48-0.61);P, lt;0.001],脑膜炎[SDHR: 0.18;(95% ci: 0.09-0.37);P, lt;0.001]与非严重疟疾相比;与营养良好的儿童相比,营养不良儿童的死亡率也低39% [SDHR: 0.61;(95% ci: 0.55-0.68);P, lt;0.001]。本研究应用Fine-Gray竞争风险方法更准确地模拟了当住院死亡率、转诊率和潜逃率显著时的LOS作为出院时间。通过基于儿童年龄、艾滋病毒状况、诊断和营养状况的LOS风险分层,可以加强患者护理。
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Competing risks modeling of length of hospital stay enhances risk-stratification of patient care: application to under-five children hospitalized in Malawi
Introduction Length of hospital stay (LOS), defined as the time from inpatient admission to discharge, death, referral, or abscondment, is one of the key indicators of quality in patient care. Reduced LOS lowers health care expenditure and minimizes the chance of in-hospital acquired infections. Conventional methods for estimating LOS such as the Kaplan-Meier survival curve and the Cox proportional hazards regression for time to discharge cannot account for competing risks such as death, referral, and abscondment. This study applied competing risk methods to investigate factors important for risk-stratifying patients based on LOS in order to enhance patient care. Methods This study analyzed data from ongoing safety surveillance of the malaria vaccine implementation program in Malawi's four district hospitals of Balaka, Machinga, Mchinji, and Ntchisi. Children aged 1–59 months who were hospitalized (spending at least one night in hospital) with a medical illness were consecutively enrolled between 1 November 2019 and 31 July 2021. Sub-distribution-hazard (SDH) ratios for the cumulative incidence of discharge were estimated using the Fine-Gray competing risk model. Results Among the 15,463 children hospitalized, 8,607 (55.7%) were male and 6,856 (44.3%) were female. The median age was 22 months [interquartile range (IQR): 12–33 months]. The cumulative incidence of discharge was 40% lower among HIV-positive children compared to HIV-negative (sub-distribution-hazard ratio [SDHR]: 0.60; [95% CI: 0.46–0.76]; P < 0.001); lower among children with severe and cerebral malaria [SDHR: 0.94; (95% CI: 0.86–0.97); P = 0.04], sepsis or septicemia [SDHR: 0.90; (95% CI: 0.82–0.98); P = 0.027], severe anemia related to malaria [SDHR: 0.54; (95% CI: 0.48–0.61); P < 0.001], and meningitis [SDHR: 0.18; (95% CI: 0.09–0.37); P < 0.001] when compared to non-severe malaria; and also 39% lower among malnourished children compared to those that were well-nourished [SDHR: 0.61; (95% CI: 0.55–0.68); P < 0.001]. Conclusions This study applied the Fine-Gray competing risk approach to more accurately model LOS as the time to discharge when there were significant rates of in-hospital mortality, referrals, and abscondment. Patient care can be enhanced by risk-stratifying by LOS based on children's age, HIV status, diagnosis, and nutritional status.
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