Effectiveness and prognosis of initial pericardiocentesis in the primary management of malignant pericardial effusion
- PMID: 20504889
- DOI: 10.1510/icvts.2010.232546
Effectiveness and prognosis of initial pericardiocentesis in the primary management of malignant pericardial effusion
Abstract
We retrospectively reviewed the records of 100 patients with malignant disease and symptomatic pericardial effusion initially treated with pericardiocentesis at the National Cancer Institute of Mexico between 1985 and 2009. We analyzed predictive factors for recurrence of pericardial effusion by bi- and multivariate analyses. The group comprised 74 women and 26 men. Twenty patients had developed malignant pericardial effusion at the time of primary cancer diagnosis. Recurrence rate after pericardiocentesis was 33%. Progression-free survival for pericardial effusion at one year was 59% (range, 47-71%). Median overall survival (OS) after pericardiocentesis was 40.3+/-7.9 weeks (95% Confidence interval, 24.9-55.7). The sole factor that correlated with increased progression-free survival for pericardial effusion was the presence of bloody pericardial effusion. For OS, multivariate analysis yielded that female gender and presence of pericardial effusion at time of primary malignancy diagnosis were associated with higher life expectancy. Initial pericardiocentesis can provide successful management of patients with a control rate of 67%. In spite of the high effectiveness of the primary management of pericardial effusion with pericardiocentesis in oncologic patients, it might be considered for initial treatment, especially those with poor prognosis, leaving pericardial window as a secondary strategy for recurrence.
Comment in
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eComment: Pericardial sclerosis with cisplatin following pericardiocentesis. A simple and effective technique for the management of refractory malignant pericardial effusions.Interact Cardiovasc Thorac Surg. 2010 Aug;11(2):161. doi: 10.1510/icvts.2010.232546A. Interact Cardiovasc Thorac Surg. 2010. PMID: 20628020 No abstract available.
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