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PAC use in cardiogenic shock associated with lower mortality but higher sepsis risk in meta-analysisCan a heart monitor help people survive cardiogenic shock?

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Key Takeaway
Interpret PAC-associated mortality benefit in cardiogenic shock cautiously given observational data and sepsis risk.

This systematic review and meta-analysis examined the association between pulmonary artery catheterization (PAC) use and clinical outcomes in adults with cardiogenic shock. The analysis included 14 observational and registry studies with 789,553 patients, comparing outcomes between those who received PAC versus no PAC. The primary outcome was in-hospital or 30-day mortality.

PAC use was associated with lower mortality (odds ratio 0.70, 95% CI 0.63-0.78, P < 0.001; hazard ratio 0.68, 95% CI 0.60-0.77). Overall mortality averaged 34%, representing 271,305 deaths across studies. PAC use was also associated with higher mechanical circulatory support initiation (OR 2.76, 95% CI 1.82-4.20, P < 0.001) but increased sepsis risk (OR 1.83, 95% CI 1.42-2.35).

Safety data on adverse events, serious adverse events, and discontinuations were not reported. Key limitations include substantial heterogeneity (I² > 90% for mortality), evidence of publication bias for the MCS outcome (Egger P = 0.0057), and inconsistent phenotypic and outcome reporting across studies. Funding and conflicts of interest were not reported.

These observational findings suggest PAC use may be associated with mortality benefit in cardiogenic shock but also with increased sepsis risk and greater MCS utilization. The substantial heterogeneity and potential for confounding limit causal inference. The authors suggest these findings should inform protocol development and future randomized trial design rather than dictate immediate practice changes.

Cardiogenic shock is a medical emergency where the heart can't pump enough blood, and it's incredibly dangerous. Doctors have long debated whether to use a pulmonary artery catheter—a thin tube threaded into the heart to measure pressures—to guide treatment. This analysis looked back at data from nearly 790,000 adults who experienced this shock. It found that patients who had this catheter placed were less likely to die in the hospital. However, they were also more likely to develop a serious bloodstream infection (sepsis) and to be placed on powerful mechanical heart pumps. It's crucial to understand this is a look at past patterns, not a controlled experiment. The data came from many different studies that didn't all measure things the same way, and there are signs that studies with certain results might have been more likely to be published. So, while the findings strongly suggest this monitoring tool might help save lives, they also highlight a real risk and the urgent need for better, more consistent research to know for sure.

What this means for you:
A heart monitor is linked to better survival in shock, but also to more infections.

Study Details

Study typeMeta analysis
Sample sizen = 789,553
EvidenceLevel 1
PublishedApr 2026
View Original Abstract ↓
INTRODUCTION: The role of pulmonary artery catheterization (PAC) in cardiogenic shock (CS) remains debated: prior intensive care unit trials showed no benefit, but contemporary observational registries suggest improved outcomes. However, the overall evidence remains fragmented, with inconsistent phenotypic and outcome reporting. Our objective was to assess the association between PAC use and clinical outcomes in CS. METHODS: We systematically searched MEDLINE, Cochrane, and Scopus (2015-2025) for observational and registry studies in adult CS. Outcomes included in-hospital/30-day mortality, mechanical circulatory support (MCS), and sepsis. Pooled odds ratios (OR) and hazard ratios were estimated using random-effects models. Subgroup, meta-regression, and trial sequential analysis were performed. RESULTS: Fourteen observational studies (n = 789,553; 271,305 deaths) were included. Overall mortality averaged 34%. PAC use was associated with lower mortality (OR 0.70, 95% confidence interval [CI] 0.63-0.78; P < 0.001) with consistent benefit across CS phenotypes, although substantial heterogeneity was present (I² > 90%). Time-to-event analyses (7 studies, n = 5,142) confirmed a 32% relative hazard ratio (0.68, 95% CI 0.60-0.77; I² = 34%). PAC use was also linked to higher MCS initiation (OR 2.76, 95% CI 1.82-4.20; P < 0.001), with evidence of publication bias (Egger P = 0.0057) and an adjusted OR 3.98 after trim-and-fill. In addition, PAC was associated with increased sepsis risk (OR 1.83, 95% CI 1.42-2.35; I² = 61%). CONCLUSIONS: PAC use was consistently associated with improved survival across CS, and higher MCS use was associated with increased sepsis risk. Our findings support systematic PAC use as a therapeutic enabler in CS and should inform protocols and future randomized clinical trials design.
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