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Recommendations for Screening and Detection of Connective Tissue Disease-Associated Pulmonary Arterial Hypertension

期刊

ARTHRITIS AND RHEUMATISM
卷 65, 期 12, 页码 3194-3201

出版社

WILEY
DOI: 10.1002/art.38172

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资金

  1. Scleroderma Foundation
  2. Actelion
  3. Gilead
  4. United Therapeutics
  5. NIH (National Institute of Arthritis and Musculoskeletal and Skin Diseases) [K24-AR-063120-02]
  6. Scleroderma Research Foundation
  7. NIH
  8. Pulmonary Hypertension Association
  9. National Heart, Lung, and Blood Institute [K23-HL-093387]
  10. Roche
  11. Bristol-Myers Squibb
  12. Pfizer
  13. Digna Biotech
  14. Impact Pharmaceutical Services
  15. Bayer
  16. ErgoNex
  17. Sanofi-Aventis
  18. Sinoxa
  19. United BioSource
  20. Medac
  21. Swedish Orphan Biovitrum
  22. Boehringer Ingelheim Pharma
  23. Novartis
  24. Active Biotech
  25. 4D Science
  26. Lilly
  27. GlaxoSmithKline
  28. Aires Pharmaceuticals
  29. Bayer Healthcare
  30. Merck

向作者/读者索取更多资源

ObjectivePulmonary arterial hypertension (PAH) affects up to 15% of patients with connective tissue diseases (CTDs). Previous recommendations developed as part of larger efforts in PAH did not include detailed recommendations for patients with CTD-associated PAH. Therefore, we sought to develop recommendations for screening and early detection of CTD-associated PAH. MethodsWe performed a systematic review of the literature on the screening and diagnosis of PAH in CTD. Using the RAND/University of California, Los Angeles consensus methodology, we developed case scenarios followed by 2 stages of voting. First, international experts from a variety of specialties voted anonymously on the appropriateness of each case scenario. The experts then met face-to-face to discuss and resolve discrepant votes to arrive at consensus recommendations. ResultsThe key recommendation stated that all patients with systemic sclerosis (SSc) should be screened for PAH. In addition, patients with mixed connective tissue disease or other CTDs with scleroderma features (scleroderma spectrum disorders) should be screened for PAH. It was recommended that screening pulmonary function tests (PFTs) with single-breath diffusing capacity for carbon monoxide, transthoracic echocardiogram, and measurement of N-terminal pro-brain natriuretic peptide (NT-proBNP) be performed in all patients with SSc and scleroderma spectrum disorders. In patients with SSc and scleroderma spectrum disorders, transthoracic echocardiogram and PFTs should be performed annually. The full screening panel (transthoracic echocardiogram, PFTs, and measurement of NT-proBNP) should be performed as soon as any new signs or symptoms are present. ConclusionWe provide consensus-based, evidence-driven recommendations for screening and early detection of CTD-associated PAH. It is our hope that these recommendations will lead to earlier detection of CTD-associated PAH and ultimately improve patient outcomes.

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