# Community-based prediction models of cardiovascular events, acute exacerbations and all-cause mortality in individuals with chronic obstructive pulmonary disease: a systematic review and meta-analysis on behalf of the International Cardiovascular and Respiratory Alliance

**Authors:** Tobin Joseph, Keerthenan Raveendra, Mohammad Haris, Jasmin Kirupananthan, Amaan Aslam, Alexandra Mircescu, Ashmit Bhardwaj, Aidan Wong, Ramesh Nadarajah, David B Price, Mohit Bhutani, Chris Gale

PMC · DOI: 10.1136/bmjresp-2025-003752 · BMJ Open Respiratory Research · 2026-02-27

## TL;DR

This study reviews existing models for predicting cardiovascular events and COPD exacerbations in community settings but finds no suitable models for these outcomes.

## Contribution

The study identifies a gap in community-based prediction models for cardiopulmonary events in COPD patients.

## Key findings

- No models predicted cardiopulmonary events in COPD using community-based data.
- ADO-SQ and BODE models showed good prediction performance for all-cause mortality.
- Most studies had a high risk of bias and lacked evaluation of clinical utility.

## Abstract

Preventable morbidity and mortality from chronic obstructive pulmonary disease (COPD) accrue from major adverse cardiovascular events (MACEs) and acute exacerbations of COPD (AECOPD). The study aims to summarise models for the prediction of these cardiopulmonary events in community-based settings.

We searched for studies of multivariable models derived, validated or augmented for the prediction of cardiopulmonary events in COPD and used community-based data sources using MEDLINE and Embase from inception through 10 April 2025. Discrimination measures for the model with C-statistic data from ≥3 cohorts were pooled by Bayesian meta-analysis, and heterogeneity and risk of bias assessments were undertaken.

No models were identified that predicted cardiopulmonary events in COPD using community-based data. Of the 71 models included, 5 predicted cardiovascular events, 32 predicted AECOPD and 30 predicted all-cause mortality. None were eligible for meta-analysis for the prediction of cardiovascular events or AECOPD. For all-cause mortality, age, dyspnoea and airflow obstruction—surprise question (ADO-SQ) (0.763, 95% CI 0.533 to 0.942) and body mass index, airflow obstruction, dyspnoea score and exercise capacity (BODE) (0.753, 95% CI 0.583 to 0.907) demonstrated good prediction performance, while ADO (0.638, 95% CI 0.443 to 0.827) demonstrated adequate prediction performance. The risk of bias was high for 57.9% of studies, and none had clinical utility evaluated.

Despite the high burden of MACE and AECOPD, there is an absence of community-based models that predict this composite outcome. Models to identify individuals with COPD at high risk of cardiopulmonary events could enable targeted clinical intervention.

CRD420251026275.

## Linked entities

- **Diseases:** chronic obstructive pulmonary disease (MONDO:0005002)

## Full-text entities

- **Diseases:** ventricular tachycardia (MESH:D017180), ventricular fibrillation (MESH:D014693), ischaemic heart disease (MESH:D006331), heart failure (MESH:D006333), ADO (MESH:D019588), atrial fibrillation (MESH:D001281), myocardial infarction (MESH:D009203), Cardiovascular disease (MESH:D002318), death (MESH:D003643), atrial flutter (MESH:D001282), acute exacerbations of (MESH:D000208), Dyspnoea, Obstruction (MESH:D000402), stroke (MESH:D020521), COPD (MESH:D029424), arrhythmias (MESH:D001145), DM (MESH:D009223), diabetes mellitus (MESH:D003920)
- **Chemicals:** ADO (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12958919/full.md

## References

56 references — full list in the complete paper: https://tomesphere.com/paper/PMC12958919/full.md

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Source: https://tomesphere.com/paper/PMC12958919