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We were, of course, very interested to read the manuscript by Saggar et al,1 and the accompanying editorial by Nathan2 relating to the use of parenteral treprostinil therapy in patients referred for lung transplantation with pulmonary hypertension (PH) in association with pulmonary fibrosis (PF).
It is good that there is continued interest in finding a clinical phenotype of patient with PF who may benefit on both symptomatic and prognostic grounds from targeted PH therapy. It is also good because there is a great clinical need to help this group of desperate …
Footnotes
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Contributors PAC conceived the idea and drafted the first version. SS and LT made statistical contribution and amendments to the letter. All authors approved the final version.
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Competing interests PAC has received support from GSK, Bayer and Actelion for advisory boards and educational meetings. The Newcastle Pulmonary Vascular Service has received grant support from Bayer.
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Provenance and peer review Not commissioned; externally peer reviewed.