Copyright © 2006, The European Society of Cardiology
Reply to the letter to the editor
Cardiovascular Unit, John Hunter Hospital, Lookout Rd, New Lambton, NSW 2305, Australia
Received 19 March 2006; accepted after revision 19 March 2006.
* Tel.: +1 416 726 9452. nandl_collins@yahoo.com.au
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Dr Callejas Rubio contends that the prevalence of mild pulmonary arterial hypertension (PAH) in patients with autoimmune disease (PAH) is excessively high based on the parameters used in our assessment.
Assessment of pulmonary artery pressure (PAP) remains an emerging utility