# Effect Modification by Acute Coronary Syndrome Prevalence on Non-Invasive Ventilation Efficacy in Acute Cardiogenic Pulmonary Edema: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

**Authors:** Marek Tomala, Monika Durak, Magdalena Borówka, Paweł Szkarłat, Maciej Kłaczyński

PMC · DOI: 10.3390/jcdd13030135 · Journal of Cardiovascular Development and Disease · 2026-03-12

## TL;DR

This study finds that the effectiveness of non-invasive ventilation in treating acute heart-related lung failure depends on how common heart attacks are in the patient group.

## Contribution

The study introduces the novel concept that acute coronary syndrome prevalence modifies the efficacy of non-invasive ventilation in acute cardiogenic pulmonary edema.

## Key findings

- NIV significantly reduced hospital mortality and intubation rates in ACPE patients.
- ACS prevalence was strongly linked to the magnitude of NIV's mortality benefit.
- The 3CPO trial's null result may be explained by its higher ACS prevalence.

## Abstract

Non-invasive ventilation (NIV) reduces mortality in patients with acute cardiogenic pulmonary edema (ACPE). However, the 3CPO trial reported null results. Therefore, we hypothesized that the prevalence of acute coronary syndrome (ACS) would influence the effectiveness of NIV. A systematic literature review was conducted to identify randomized controlled trials (RCTs) comparing NIV and standard oxygen therapy in patients with ACPE from PubMed, CENTRAL, and Embase databases through December 2025. Random-effects meta-analysis and REML meta-regression were utilized, and evidence quality was evaluated using GRADE. (PROSPERO: CRD420251142245). Fourteen RCTs (n = 1967) were included in the analysis. NIV significantly reduced hospital mortality (RR 0.75, 95% CI 0.58–0.96; I2 = 0%) and endotracheal intubation (RR 0.49, 95% CI 0.35–0.68). Meta-regression revealed that study-level ACS prevalence was significantly associated with the magnitude of NIV’s mortality effect (β1 = −0.023 per 1% increase in ACS, p = 0.008; R2 = 46.2%). The equilibrium point occurred at an ACS prevalence of 14.1% (95% CI 5.2–23.0%). At 3CPO’s ACS prevalence of 27%, the model predicted an RR of 0.75 (95% CI 0.58–0.97). The observed 3CPO RR was 0.97 (95% CI 0.66–1.43); the confidence intervals overlap substantially, and 3CPO was underpowered for mortality as an isolated endpoint. The mortality benefit of NIV appears to be associated with the prevalence of ACS among treated patients, though this ecological finding requires confirmation at the individual-patient level.

## Linked entities

- **Diseases:** acute coronary syndrome (MONDO:0005542)

## Full-text entities

- **Genes:** ACCS (1-aminocyclopropane-1-carboxylate synthase homolog (inactive)) [NCBI Gene 84680] {aka ACS, PHACS}
- **Diseases:** injury to (MESH:D014947), cardiogenic (MESH:D013575), unstable angina (MESH:D000789), acute myocardial ischemia (MESH:D015472), ACS (MESH:D054058), cardiac deaths (MESH:D003643), pneumonia (MESH:D011014), infarction (MESH:D007238), hypotension (MESH:D007022), Type 2 MI (MESH:D003924), respiratory acidosis (MESH:D000142), cardiogenic shock (MESH:D012770), hypocapnia (MESH:D016857), acute MI (MESH:D000208), NSTEMI (MESH:D000072658), cardiac arrest (MESH:D006323), STEMI (MESH:D000072657), COPD (MESH:D029424), myocardial injury (MESH:D009202), hypercapnia (MESH:D006935), ARDS (MESH:D012128), ischemia (MESH:D007511), chest pain (MESH:D002637), AMIS (MESH:D002545), OIS (MESH:D015875), AMI (MESH:D009203), chronic coronary disease (MESH:D003327), hypoxemia (MESH:D000860), ACPE (MESH:D011654), cardiac failure (MESH:D006333), ischemic myocardium (MESH:D017682), hypertensive (MESH:D006973), hypercapnic (MESH:D012131), valvular dysfunction (MESH:D006349), Myocardial Ischemic Syndromes (MESH:D017202), hyperventilation (MESH:D006985)
- **Chemicals:** nitrates (MESH:D009566), EPAP (-), O2 (MESH:D010100), morphine (MESH:D009020), H2O (MESH:D014867)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13026454/full.md

## References

80 references — full list in the complete paper: https://tomesphere.com/paper/PMC13026454/full.md

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Source: https://tomesphere.com/paper/PMC13026454