Literature DB >> 27378592

Combination Therapy for Pulmonary Arterial Hypertension: A Systematic Review and Meta-analysis.

Benjamin D Fox1, Osnat Shtraichman2, David Langleben3, Avi Shimony4, Mordechai R Kramer5.   

Abstract

BACKGROUND: Combination therapy (CT) for patients with pulmonary arterial hypertension (PAH) has been recommended for many years, despite weak evidence of efficacy over monotherapy (MT). A previous meta-analysis comparing CT vs MT with pulmonary vasodilators failed to demonstrate a clear reduction in clinical worsening events.
METHODS: We searched for relevant articles in PubMed, EMBASE, the Cochrane Database, and clinicaltrials.gov; we also manually searched review articles and conference abstracts from 1980-December 2015. Target articles were double-blinded studies of 2 or more pulmonary vasodilators given in combination vs monotherapy for treatment of patients with PAH. The principal outcome of interest was "combined clinical worsening" (CCW) events (including but not limited to death or hospitalization). Data on physiological outcomes were also explored. Meta-analysis was performed using the DerSimonian and Laird random-effects model.
RESULTS: We extracted data from 18 randomized controlled trials (RCTs) (N = 4162). CT was associated with a significant 38% reduction of risk of CCW (15 RCTs: n = 3906; risk ratio [RR], 0.62; 95% confidence interval [CI], 0.50-0.77). This reduction in risk was driven by a reduction in nonfatal end points (12 RCTs: n = 2611; RR, 0.56; 95% CI, 0.40-0.78) and not by a reduction of mortality (12 RCTs: n = 2717; RR, 0.79; 95% CI, 0.53-1.17). CT was also associated with improvement in 6-minute walking distance (10 RCTs: n = 1553; weighted mean difference [WMD], +23.0 m; 95% CI, 15.9-30.1), improved functional class (9 RCTs: n = 1737; RR, 1.26; 95% CI, 1.05-1.51), and beneficial effects on pulmonary hemodynamics such as cardiac index (WMD, +0.35 L/min/m; 95% CI, 0.14-0.56).
CONCLUSIONS: In this highly comprehensive meta-analysis, CT reduces the risk of CCW events in patients with PAH and brings physiological improvement. Copyright Â
© 2016 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.

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Year:  2016        PMID: 27378592     DOI: 10.1016/j.cjca.2016.03.004

Source DB:  PubMed          Journal:  Can J Cardiol        ISSN: 0828-282X            Impact factor:   5.223


  19 in total

1.  Effect of Combination Therapy of Endothelin Receptor Antagonist and Phosphodiesterase-5 Inhibitor on Clinical Outcome and Pulmonary Haemodynamics in Patients with Pulmonary Arterial Hypertension: A Meta-Analysis.

Authors:  Lopamudra Kirtania; Rituparna Maiti; Anand Srinivasan; Archana Mishra
Journal:  Clin Drug Investig       Date:  2019-11       Impact factor: 2.859

2.  Inhaled combination of sildenafil and rosiglitazone improves pulmonary hemodynamics, cardiac function, and arterial remodeling.

Authors:  Jahidur Rashid; Eva Nozik-Grayck; Ivan F McMurtry; Kurt R Stenmark; Fakhrul Ahsan
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2018-10-11       Impact factor: 5.464

3.  Choice of Initial Oral Therapy for Pulmonary Arterial Hypertension: Age and Long-Term Survival.

Authors:  Gustavo A Heresi; Thomas E Love; Adriano R Tonelli; Kristin B Highland; Raed A Dweik
Journal:  Am J Respir Crit Care Med       Date:  2018-10-15       Impact factor: 21.405

4.  Fasudil and DETA NONOate, Loaded in a Peptide-Modified Liposomal Carrier, Slow PAH Progression upon Pulmonary Delivery.

Authors:  Jahidur Rashid; Kamrun Nahar; Snehal Raut; Ali Keshavarz; Fakhrul Ahsan
Journal:  Mol Pharm       Date:  2018-03-26       Impact factor: 4.939

5.  Cocktail of Superoxide Dismutase and Fasudil Encapsulated in Targeted Liposomes Slows PAH Progression at a Reduced Dosing Frequency.

Authors:  Nilesh Gupta; Jahidur Rashid; Eva Nozik-Grayck; Ivan F McMurtry; Kurt R Stenmark; Fakhrul Ahsan
Journal:  Mol Pharm       Date:  2017-02-17       Impact factor: 4.939

6.  Safety and tolerability of combination therapy with ambrisentan and tadalafil for the treatment of pulmonary arterial hypertension in children: Real-world experience.

Authors:  Azadeh Issapour; Benjamin Frank; Sarah Crook; Michelle D Hite; Michelle L Dorn; Erika B Rosenzweig; D Dunbar Ivy; Usha S Krishnan
Journal:  Pediatr Pulmonol       Date:  2022-01-03

7.  Bosentan or Macitentan Therapy in Chronic Thromboembolic Pulmonary Hypertension?

Authors:  M C J van Thor; L Ten Klooster; R J Snijder; J C Kelder; J J Mager; M C Post
Journal:  Lung       Date:  2019-10-03       Impact factor: 2.584

Review 8.  Adult congenital heart disease with pulmonary arterial hypertension: mechanisms and management.

Authors:  Michail Papamichalis; Andrew Xanthopoulos; Panagiotis Papamichalis; John Skoularigis; Filippos Triposkiadis
Journal:  Heart Fail Rev       Date:  2020-09       Impact factor: 4.214

Review 9.  The Changing Landscape of Pulmonary Arterial Hypertension in the Adult with Congenital Heart Disease.

Authors:  Alexandra C van Dissel; Barbara J M Mulder; Berto J Bouma
Journal:  J Clin Med       Date:  2017-03-30       Impact factor: 4.241

10.  Combination therapy in pulmonary arterial hypertension: recent accomplishments and future challenges.

Authors:  Annie-Christine Lajoie; Sebastien Bonnet; Steeve Provencher
Journal:  Pulm Circ       Date:  2017-05-30       Impact factor: 3.017

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