Clinical Medicine

Read e-book online A Clinician's Guide to Pulmonary Arterial Hypertension: PDF

By Stewart Simon

ISBN-10: 1439802041

ISBN-13: 9781439802045

ISBN-10: 1841846651

ISBN-13: 9781841846651

A Clinician's advisor to Pulmonary Arterial high blood pressure, moment version complements the general 'PAH know-how' of the broader medical neighborhood, and descriptions the necessity for screening, potent prognosis and useful remedy. themes contain:

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Extra resources for A Clinician's Guide to Pulmonary Arterial Hypertension: Pocketbook, 2nd edition

Example text

62. MacGregor AJ, Canavan R, Knight C et al. Pulmonary hypertension in systemic sclerosis: risk factors for progression and consequences for survival. Rheumatology 2001; 40: 453–9. 63. Fuster V, Steele PM, Edwards WD et al. Primary pulmonary hypertension: natural history and the importance of thrombosis. Circulation 1984; 70: 580–7. qxd 11/26/2007 2:16 PM Page 53 64. Kanemoto N. Natural history of pulmonary hemodynamics in primary pulmonary hypertension. Am Heart J 1987; 114: 407–13. 65. Eysmann SB, Palevsky HI, Reichek N et al.

101. Keogh AM, McNeil KD, Wlodarczyk J, Gabbay E, Williams TJ. Quality of life in pulmonary arterial hypertension: improvement and maintenance with bosentan. J Heart Lung Transplant 2007; 26(2): 181–7. 102. Denton CP, Humbert M, Rubin L, Black CM. Bosentan treatment for pulmonary arterial hypertension related to connective tissue disease: a subgroup analysis of the pivotal clinical trials and their open-label extensions. Ann Rheum Dis 2006; 65(10): 1336–40. 103. Provencher S, Sitbon O, Humbert M et al.

WHO functional class As worsening dyspnoea on exertion is the most obvious and probably most sensitive marker of the underlying disease progression associated with PAH, it has proven to be the most practical means of delineating the clinical status of affected patients. 1). Patients whose clinical profile is consistent with WHO Class IV usually have signs of advanced right heart failure and there is little doubt that the progression from WHO Class I to IV mirrors the evolution/progression of right-sided heart failure secondary to the underlying PAH.

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A Clinician's Guide to Pulmonary Arterial Hypertension: Pocketbook, 2nd edition by Stewart Simon


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