Clinically Significant Pericardial Effusion Requiring Drainage in Patients With Cancer
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Min-Ha Jeong1, Chan Soon Park2, Jaewon Choi3
1Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea; Division of Cardiology, Cardiovascular Center, Seoul National University Hospital, Seoul, Republic of Korea.
Background:
The incidence and prognostic implications of clinically significant pericardial effusion requiring drainage among patients with cancer remain incompletely characterized.
Objectives:
The authors aimed to investigate the incidence, cancer-specific risk, and prognostic implications of clinically significant pericardial effusion among patients with cancer.
Methods:
We analyzed 2 population-based cohorts (Korean National Health Insurance Service and UK Biobank), comparing adults with incident cancer and age- and sex-matched noncancer controls. Among patients with cancer, drainage-date-anchored matched analyses evaluated subsequent mortality, new-onset atrial fibrillation (NOAF), and heart failure (HF) using Cox and Fine-Gray models, with landmark and restricted mean time analyses.
Results:
Over a median follow-up of 7.7 years (Q1-Q3: 6.3-9.2) in the Korean National Health Insurance Service and 5.2 years (1.8-8.2) in the UK Biobank, clinically significant pericardial effusion occurred in 1,088 of 499,127 patients with cancer vs 320 of 390,260 controls (33.66 [95% CI: 31.7-35.7] vs 10.32 [9.2-11.5] per 100,000 person-years). Risk was greatest for cancers anatomically adjacent to the heart. Pericardial effusion was associated with higher all-cause mortality (adjusted HR: 13.29; 95% CI: 12.21-14.46) and with increased risks of NOAF and HF. Excess mortality persisted among patients surviving beyond 30 days and beyond 1 year, whereas associations with nonfatal outcomes were attenuated after accounting for competing mortality.
Conclusions:
Cancer was associated with a higher incidence of clinically significant pericardial effusion. Among patients with cancer, this phenotype identified a substantially higher risk of death and increased risks of NOAF and HF, and the excess risk was not explained by early periprocedural mortality alone.
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