Should patients with systemic sclerosis-related pulmonary arterial hypertension be anticoagulated?

dc.contributor.authorNikpour, M.
dc.contributor.authorStevens, W.
dc.contributor.authorProudman, S.
dc.contributor.authorBuchbinder, R.
dc.contributor.authorPrior, D.
dc.contributor.authorZochling, J.
dc.contributor.authorWilliams, T.
dc.contributor.authorGabbay, E.
dc.contributor.authorNandurkar, H.
dc.date.issued2013
dc.description.abstractPulmonary arterial hypertension (PAH) is a major cause of mortality in scleroderma and despite ‘advanced’ therapies confers a median survival of less than 5 years. Anticoagulation in systemic sclerosis-related PAH (SSc-PAH) is currently one of the most contentious issues in the management of patients with connective tissue disease. While some studies have shown a survival benefit with warfarin therapy in this disease, others have not. Accordingly, a state of clinical equipoise exists in relation to anticoagulation in SSc-PAH. With an over fivefold reduction in mortality demonstrated in some observational studies, the issue of anticoagulation in SSc-PAH demands resolution through a well-designed randomised controlled trial.
dc.description.statementofresponsibilityM. Nikpour, W. Stevens, S. M. Proudman, R. Buchbinder, D. Prior, J. Zochling, T. Williams, E. Gabbay and H. Nandurkar
dc.identifier.citationInternal Medicine Journal, 2013; 43(5):599-603
dc.identifier.doi10.1111/imj.12111
dc.identifier.issn1444-0903
dc.identifier.issn1445-5994
dc.identifier.orcidProudman, S. [0000-0002-3046-9884]
dc.identifier.urihttp://hdl.handle.net/2440/78667
dc.language.isoen
dc.publisherBlackwell Publishing Asia
dc.rights© 2013 The Authors
dc.source.urihttps://doi.org/10.1111/imj.12111
dc.subjectscleroderma
dc.subjectsystemic sclerosis
dc.subjectpulmonary arterial hypertension
dc.subjectanticoagulation
dc.subjectrandomised controlled trial
dc.titleShould patients with systemic sclerosis-related pulmonary arterial hypertension be anticoagulated?
dc.typeJournal article
pubs.publication-statusPublished

Files