Pulmonary arterial hypertension in scleroderma: care gaps in screening.

Abstract:

:One in six patients with systemic sclerosis will develop pulmonary arterial hypertension (PAH). Screening with echocardiography and possibly pulmonary function testing (to determine the diffusing capacity of carbon monoxide) is recommended to detect PAH at a less severe stage. However, real-world screening programs have problems. Registries where echocardiograms are to be performed annually should have the best-case scenario of nearly perfect screening and referral for right heart catheterization of those highly suspect for PAH. However, registries demonstrate care gaps where patients are not referred for appropriate confirmatory testing when PAH is suspected.

journal_name

Arthritis Res Ther

authors

Pope JE

doi

10.1186/s13075-017-1347-4

subject

Has Abstract

pub_date

2017-06-06 00:00:00

pages

128

issue

1

eissn

1478-6354

issn

1478-6362

pii

10.1186/s13075-017-1347-4

journal_volume

19

pub_type

社论
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