Department of Infection and Tropical Medicine, Royal Hallamshire Hospital, Sheffield, UK.
Department of Epidemiology and Medical Statistics, School of Health and Related Research (ScHARR), University of Sheffield, Sheffield, UK.
Clin Microbiol Infect. 2019 Jul;25(7):905.e1-905.e7. doi: 10.1016/j.cmi.2018.11.009. Epub 2018 Nov 28.
Outpatient parenteral antimicrobial therapy (OPAT) is increasingly used to treat a wide range of infections. However, there is risk of hospital readmissions. The study aim was to develop a prediction model for the risk of 30-day unplanned hospitalization in patients receiving OPAT.
Using a retrospective cohort design, we retrieved data on 1073 patients who received OPAT over 2 years (January 2015 to January 2017) at a large teaching hospital in Sheffield, UK. We developed a multivariable logistic regression model for 30-day unplanned hospitalization, assessed its discrimination and calibration abilities, and internally them validated using bootstrap resampling.
The 30-day unplanned hospitalization rate was 11% (123/1073). The main indication for hospitalization was worsening or nonresponse of infection (52/123, 42%). The final regression model consisted of age (adjusted odds ratio (aOR), 1.18 per decade; 95% confidence interval (CI), 1.04-1.34), Charlson comorbidity score (aOR, 1.11 per unit increase; 95% CI, 1.00-1.23), prior hospitalizations in past 12 months (aOR, 1.30 per admission; 95% CI, 1.17-1.45), concurrent intravenous antimicrobial therapy (aOR, 1.89; 95% CI, 1.03-3.47) and endovascular infection (aOR, 3.51; 95% CI, 1.49-8.28). Mode of OPAT treatment was retained in the model as a confounder. The model had adequate concordance (c-statistic 0.72; 95% CI 0.67-0.77) and calibration (Hosmer-Lemeshow p 0.546; calibration slope 0.99; 95% CI 0.78-1.21), and low degree of optimism (bootstrap optimism corrected c-statistic, 0.70).
We identified a set of six important predictors of unplanned hospitalization based on readily available data. The prediction model may help improve OPAT outcomes through better identification of high-risk patients and provision of tailored care.
门诊静脉输注抗菌药物治疗(OPAT)被广泛应用于多种感染的治疗。然而,OPAT 存在导致患者再次住院的风险。本研究旨在建立一个预测模型,用于预测接受 OPAT 治疗的患者在 30 天内非计划性住院的风险。
采用回顾性队列设计,我们从英国谢菲尔德一家大型教学医院的数据库中提取了 2015 年 1 月至 2017 年 1 月期间接受 OPAT 治疗的 1073 例患者的数据。我们建立了一个用于预测 30 天内非计划性住院的多变量逻辑回归模型,评估了其区分度和校准能力,并通过 bootstrap 重采样进行内部验证。
30 天内非计划性住院率为 11%(123/1073)。导致住院的主要原因为感染加重或无反应(52/123,42%)。最终的回归模型包含年龄(每十年校正优势比[aOR],1.18;95%置信区间[CI],1.04-1.34)、Charlson 合并症评分(每增加 1 分 aOR,1.11;95%CI,1.00-1.23)、过去 12 个月内的住院次数(每住院一次 aOR,1.30;95%CI,1.17-1.45)、同期静脉内使用抗菌药物治疗(aOR,1.89;95%CI,1.03-3.47)和血管内感染(aOR,3.51;95%CI,1.49-8.28)。OPAT 治疗模式作为混杂因素保留在模型中。该模型具有良好的一致性(c 统计量 0.72;95%CI,0.67-0.77)和校准度(Hosmer-Lemeshow p 值为 0.546;校准斜率为 0.99;95%CI,0.78-1.21),且具有较低的过度拟合程度(bootstrap 校正后 c 统计量为 0.70)。
我们根据易于获得的数据确定了一组 6 个重要的非计划性住院预测因子。该预测模型可通过更好地识别高危患者并提供个体化治疗,从而改善 OPAT 结局。