预测社区获得性下呼吸道感染成人的不良结局:开发和验证两种预测模型的方案,用于(i)全因住院和死亡率以及(ii)心血管结局。

Merijn H Rijk, Tamara N Platteel, Geert-Jan Geersing, Monika Hollander, Bert L G P Dalmolen, Paul Little, Frans H Rutten, Maarten van Smeden, Roderick P Venekamp
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引用次数: 0

摘要

背景:社区获得性下呼吸道感染(LRTI)在初级保健中很常见,并且具有特殊不良结局风险(如住院和死亡)的患者具有挑战性。LRTI还与初始感染后心血管疾病(CVD)发生率增加有关,而并发CVD可能对LRTI患者的总体预后产生负面影响。准确预测LRTI患者不良后果的风险,同时考虑与CVD的相互作用,可以帮助全科医生(GP)在临床决策过程中,并可能允许早期发现恶化。因此,本文提出了两种模型的开发设计和外部验证,用于预测患有LRTI的成年人的全因住院或死亡(模型1)和CVD短期发病率(模型2)的个体风险。方法:这两种模型都将使用来自荷兰初级和二级保健的常规电子健康记录(EHR)数据以及死亡率登记处的数据进行开发。2016年至2019年间gp诊断为LRTI的年龄≥40岁的成年人符合纳入条件。相关的患者人口统计、病史、药物使用、体征和症状、生命体征和实验室测量将被视为候选预测因素。感兴趣的结果包括30天全因住院或死亡率(模型1)和90天CVD(模型2)。多变量弹性网络回归技术将用于模型开发。在建模过程中,还将评估心血管疾病对住院或全因死亡率(模型1)的增量预测价值。这些模型将通过内部-外部交叉验证和外部验证,在初级保健LRTI患者的等效队列中进行验证。讨论:目前可用于初级保健LRTI患者的预测模型的实施受到模型性能评估有限的阻碍。在考虑CVD在LRTI预后中的作用的同时,我们的目标是开发和外部验证两个预测临床相关结果的模型,以帮助全科医生进行临床决策。我们预计的挑战包括低事件率的可能性和与EHR数据使用相关的常见问题,例如候选预测器测量和缺失,如何最好地从自由文本字段检索信息,以及结果事件的潜在错误分类。
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Predicting adverse outcomes in adults with a community-acquired lower respiratory tract infection: a protocol for the development and validation of two prediction models for (i) all-cause hospitalisation and mortality and (ii) cardiovascular outcomes.

Background: Community-acquired lower respiratory tract infections (LRTI) are common in primary care and patients at particular risk of adverse outcomes, e.g., hospitalisation and mortality, are challenging to identify. LRTIs are also linked to an increased incidence of cardiovascular diseases (CVD) following the initial infection, whereas concurrent CVD might negatively impact overall prognosis in LRTI patients. Accurate risk prediction of adverse outcomes in LRTI patients, while considering the interplay with CVD, can aid general practitioners (GP) in the clinical decision-making process, and may allow for early detection of deterioration. This paper therefore presents the design of the development and external validation of two models for predicting individual risk of all-cause hospitalisation or mortality (model 1) and short-term incidence of CVD (model 2) in adults presenting to primary care with LRTI.

Methods: Both models will be developed using linked routine electronic health records (EHR) data from Dutch primary and secondary care, and the mortality registry. Adults aged ≥ 40 years with a GP-diagnosis of LRTI between 2016 and 2019 are eligible for inclusion. Relevant patient demographics, medical history, medication use, presenting signs and symptoms, and vital and laboratory measurements will be considered as candidate predictors. Outcomes of interest include 30-day all-cause hospitalisation or mortality (model 1) and 90-day CVD (model 2). Multivariable elastic net regression techniques will be used for model development. During the modelling process, the incremental predictive value of CVD for hospitalisation or all-cause mortality (model 1) will also be assessed. The models will be validated through internal-external cross-validation and external validation in an equivalent cohort of primary care LRTI patients.

Discussion: Implementation of currently available prediction models for primary care LRTI patients is hampered by limited assessment of model performance. While considering the role of CVD in LRTI prognosis, we aim to develop and externally validate two models that predict clinically relevant outcomes to aid GPs in clinical decision-making. Challenges that we anticipate include the possibility of low event rates and common problems related to the use of EHR data, such as candidate predictor measurement and missingness, how best to retrieve information from free text fields, and potential misclassification of outcome events.

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