PMID- 33765691 OWN - NLM STAT- MEDLINE DCOM- 20210408 LR - 20220401 IS - 1469-493X (Electronic) IS - 1361-6137 (Linking) VI - 3 IP - 3 DP - 2021 Mar 26 TI - Endothelin receptor antagonists for pulmonary arterial hypertension. PG - CD004434 LID - 10.1002/14651858.CD004434.pub6 [doi] LID - CD004434 AB - BACKGROUND: Pulmonary arterial hypertension is a devastating disease that leads to right heart failure and premature death. Endothelin receptor antagonists have shown efficacy in the treatment of pulmonary arterial hypertension. OBJECTIVES: To evaluate the efficacy of endothelin receptor antagonists (ERAs) in pulmonary arterial hypertension. SEARCH METHODS: We searched the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, Embase, and the reference sections of retrieved articles. The searches are current as of 4 November 2020. SELECTION CRITERIA: We included randomised trials and quasi-randomised trials involving participants with pulmonary arterial hypertension. DATA COLLECTION AND ANALYSIS: Two of five review authors selected studies, extracted data and assessed study quality according to established criteria. We used standard methods expected by Cochrane. The primary outcomes were exercise capacity (six-minute walk distance, 6MWD), World Health Organization (WHO) or New York Heart Association (NYHA) functional class, Borg dyspnoea scores and dyspnoea-fatigue ratings, and mortality. MAIN RESULTS: We included 17 randomised controlled trials involving a total of 3322 participants. Most trials were of relatively short duration (12 weeks to six months). Sixteen trials were placebo-controlled, and of these nine investigated a non-selective ERA and seven a selective ERA. We evaluated two comparisons in the review: ERA versus placebo and ERA versus phosphodiesterase type 5 (PDE5) inhibitor. The abstract focuses on the placebo-controlled trials only and presents the pooled results of selective and non-selective ERAs. After treatment, participants receiving ERAs could probably walk on average 25.06 m (95% confidence interval (CI) 17.13 to 32.99 m; 2739 participants; 14 studies; I(2) = 34%, moderate-certainty evidence) further than those receiving placebo in a 6MWD. Endothelin receptor antagonists probably improved more participants' WHO functional class (odds ratio (OR) 1.41, 95% CI 1.16 to 1.70; participants = 3060; studies = 15; I(2) = 5%, moderate-certainty evidence) and probably lowered the odds of functional class deterioration (OR 0.43, 95% CI 0.26 to 0.72; participants = 2347; studies = 13; I(2) = 40%, moderate-certainty evidence) compared with placebo. There may be a reduction in mortality with ERAs (OR 0.78, 95% CI 0.58, 1.07; 2889 participants; 12 studies; I(2) = 0%, low-certainty evidence), and pooled data suggest that ERAs probably improve cardiopulmonary haemodynamics and may reduce Borg dyspnoea score in symptomatic patients. Hepatic toxicity was not common, but may be increased by ERA treatment from 37 to 67 (95% CI 34 to 130) per 1000 over 25 weeks of treatment (OR 1.88, 95% CI 0.91 to 3.90; moderate-certainty evidence). Although ERAs were well tolerated in this population, several cases of irreversible liver failure caused by sitaxsentan have been reported, which led the licence holder for sitaxsentan to withdraw the product from all markets worldwide. As planned, we performed subgroup analyses comparing selective and non-selective ERAs, and with the exception of mean pulmonary artery pressure, did not detect any clear subgroup differences for any outcome. AUTHORS' CONCLUSIONS: For people with pulmonary arterial hypertension with WHO functional class II and III, endothelin receptor antagonists probably increase exercise capacity, improve WHO functional class, prevent WHO functional class deterioration, result in favourable changes in cardiopulmonary haemodynamic variables compared with placebo. However, they are less effective in reducing dyspnoea and mortality. The efficacy data were strongest in those with idiopathic pulmonary hypertension. The irreversible liver failure caused by sitaxsentan and its withdrawal from global markets emphasise the importance of hepatic monitoring in people treated with ERAs. The question of the effects of ERAs on pulmonary arterial hypertension has now likely been answered.. The combined use of ERAs and phosphodiesterase inhibitors may provide more benefit in pulmonary arterial hypertension; however, this needs to be confirmed in future studies. CI - Copyright (c) 2021 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd. FAU - Liu, Chao AU - Liu C AD - Division of Cardiology, The First Hospital of Hebei Medical University, Shijiazhuang, China. FAU - Chen, Junmin AU - Chen J AD - Department of Haematology and Rheumatology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China. FAU - Gao, Yanqiu AU - Gao Y AD - The First Hospital of Hebei Medical University, Shijiazhuang, China. FAU - Deng, Bao AU - Deng B AD - The First Hospital of Hebei Medical University, Shijiazhuang, China. FAU - Liu, Kunshen AU - Liu K AD - The First Hospital of Hebei Medical University, Shijiazhuang, China. LA - eng SI - ClinicalTrials.gov/NCT00070590 SI - ClinicalTrials.gov/NCT00077584 PT - Journal Article PT - Meta-Analysis PT - Research Support, Non-U.S. Gov't PT - Systematic Review DEP - 20210326 PL - England TA - Cochrane Database Syst Rev JT - The Cochrane database of systematic reviews JID - 100909747 RN - 0 (Antihypertensive Agents) RN - 0 (Endothelin Receptor Antagonists) RN - 0 (Phosphodiesterase 5 Inhibitors) SB - IM UOF - Cochrane Database Syst Rev. 2013 Feb 28;(2):CD004434. PMID: 23450552 MH - Antihypertensive Agents/*therapeutic use MH - Bias MH - Endothelin Receptor Antagonists/*therapeutic use MH - Humans MH - Hypertension, Pulmonary/*drug therapy/mortality MH - Phosphodiesterase 5 Inhibitors/therapeutic use MH - Randomized Controlled Trials as Topic MH - Walk Test PMC - PMC8094512 COIS- This systematic review was supported by a grant from the World Health Organization whilst CL was in residence at the Australasian Cochrane Centre. Dr Chao Liu participated in training from the Australasian Cochrane Centre (including the Cochrane Review Completion Program) whilst in Australia. Chao Liu: none known
Junmin Chen: none known
Yanqiu Gao: none known
Bao Deng: none known
Kunshen Liu: none known EDAT- 2021/03/26 06:00 MHDA- 2021/04/10 06:00 PMCR- 2022/03/25 CRDT- 2021/03/25 20:26 PHST- 2021/03/25 20:26 [entrez] PHST- 2021/03/26 06:00 [pubmed] PHST- 2021/04/10 06:00 [medline] PHST- 2022/03/25 00:00 [pmc-release] AID - CD004434.pub6 [pii] AID - 10.1002/14651858.CD004434.pub6 [doi] PST - epublish SO - Cochrane Database Syst Rev. 2021 Mar 26;3(3):CD004434. doi: 10.1002/14651858.CD004434.pub6.