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

Publication date

2023-12-07

Authors

Rijk, Merijn HORCID 0000-0003-4190-2126
Platteel, Tamara N
Geersing, Geert-JanORCID 0000-0001-6976-9844
Hollander, MonikaISNI 0000000392553595
Dalmolen, Bert L G P
Little, Paul
Rutten, Frans HORCID 0000-0002-5052-7332ISNI 0000000389122794
van Smeden, MaartenORCID 0000-0002-5529-1541
Venekamp, Roderick PORCID 0000-0002-1446-9614ISNI 0000000393819260

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Abstract

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.

Keywords

Lower respiratory tract infection, Cardiovascular disease, Primary care, Electronic Health Record, Prognosis, Prediction model, Hospitalisation, Mortality, Journal Article

Citation

Rijk, M H, Platteel, T N, Geersing, G-J, Hollander, M, Dalmolen, B L G P, Little, P, Rutten, F H, van Smeden, M & Venekamp, R P 2023, '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', Diagnostic and Prognostic Research, vol. 7, no. 1, 23. https://doi.org/10.1186/s41512-023-00161-1