Title
A systematic review and meta-analysis of randomized controlled trials evaluating pharmacologic therapies for acute and recurrent pericarditis
Date Issued
01 January 2022
Access level
metadata only access
Resource Type
review
Author(s)
Melendo-Viu M.
Marchán-Lopez Á.
Guarch C.J.L.
Roubín S.R.
Abu-Assi E.
Meneses R.T.
Ynsaurriaga F.A.
Bueno H.
University of Connecticut School of Pharmacy
Publisher(s)
Elsevier Inc.
Abstract
Acute idiopathic pericarditis (AIP) is a benign inflammatory condition associated with high recurrence rates. Non-steroidal anti-inflammatory drug (NSAIDs) and colchicine are the recommended therapies. Our objective was to systematically assess effects of pharmacological therapies on recurrences or treatment failure in patients with first and subsequent AIP episodes. PubMed, BioMedCentral, Cochrane, Clinicaltrials.gov, Google Scholar and EMBASE (Ovid) were searched up to April 2020 for randomized controlled trials (RCT) evaluating NSAIDs, indomethacin, colchicine, steroids, intravenous immunoglobulins, immunomodulators, or interleukin receptor antagonists in adult patients with acute episode of idiopathic pericarditis. Mantel-Haenzel random effects models were used for meta-analyses, and effects were reported as odds ratios (ORs) and their 95% confidence intervals (CI). Six RCTs of colchicine plus NSAIDs (n=914 patients) and one RCT of anakinra (n=21) were found. No RCTs testing NSAIDs or corticosteroids were identified. Colchicine plus NSAIDs and anakinra significantly reduced recurrence (OR 0.37; 95%CI 0.27-0.51; and OR 0.02; 95%CI, 0.00-0.32, respectively). Colchicine plus NSAIDs also reduced treatment failure (OR 0.29; 95%CI 0.21-0.41). No differences in adverse events between colchicine and placebo were found (OR 1.16; 95%CI 0.72 to 1.86). In conclusion, Colchicine plus NSAIDS and anakinra are efficacious for preventing AIP recurrences. Colchicine reduces treatment failure as well. Although its use is supported by clinical experience, no solid evidence is currently available for the role of NSAIDs or steroids in the treatment of AIP.
Language
English
OCDE Knowledge area
Sistema cardiaco, Sistema cardiovascular
Subjects
Scopus EID
2-s2.0-85124326448
PubMed ID
Source
Trends in Cardiovascular Medicine
ISSN of the container
10501738
Sponsor(s)
Dr. Bueno receives research funding from the Instituto de Salud Carlos III, Spain (PIE16/00021 & PI17/01799), Astra-Zeneca, BMS, Janssen and Novartis; has received consulting fees from Astra-Zeneca, Bayer, BMS-Pfizer, Novartis; and speaking fees or support for attending scientific meetings from Amgen, Astra-Zeneca, Bayer, BMS-Pfizer, Novartis, and MEDSCAPE-the heart.org. Dr. Tello receives speaking fees or support for attending scientific meetings from Bayer, Novartis and Novo-Nordisk. Dr. Jimenez receives speaking fees from Philips. Dr. Hernandez is funded by the Agency for Health Care Research and Quality (AHRQ) (contract HHSA290-2015- 00012I). Other authors have no conflict of interest to disclose.
Sources of information:
Directorio de Producción Científica
Scopus