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Risk classification of pulmonary arterial hypertension by echocardiographic combined assessment of pulmonary vascular resistance and right ventricular function

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Abstract

Which combination of clinical parameters improves the prediction of prognosis in patients with pulmonary arterial hypertension (PAH) remains unclear. We examined whether combined assessment of pulmonary vascular resistance and right ventricular function by echocardiography is useful for classifying risks in PAH. In 41 consecutive patients with PAH (mean age of 48.9 ± 17.3 years, 31 females), a 6-min walk test, pulmonary function test, and echocardiography were performed at baseline and during PAH-specific therapies. The study endpoint was defined as a composite of cardiovascular death and hospitalization for PAH and/or right ventricular failure. During a follow-up period of 9.2 ± 8.7 months, 18 patients reached the endpoint. Multivariate regression analysis showed that the ratio of tricuspid regurgitation pressure gradient to the time–velocity integral of the right ventricular outflow tract (TRPG/TVI) and tricuspid annular plane systolic excursion (TAPSE) during PAH-specific treatment were independent prognostic predictors of the endpoint. Using cutoff values indicated by receiver operating characteristic analysis, the patients were divided into four subsets. Multivariate analyses by Cox's proportional hazards model adjusted for age, sex and body mass index indicated that subset 4 (TRPG/TVI ≥ 3.89 and TAPSE ≤ 18.9 mm) had a significantly higher event risk than did subset 1 (TRPG/TVI < 3.89 and TAPSE > 18.9 mm): HR = 25.49, 95% CI 4.70–476.97, p < 0.0001. Combined assessment of TRPG/TVI and TAPSE during adequate PAH-specific therapies enables classification of risks for death and/or progressive right heart failure in PAH.

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References

  1. Ogawa A, Satoh T, Tamura Y, Fukuda K, Matsubara H (2017) Survival of Japanese patients with idiopathic/heritable pulmonary arterial hypertension. Am J Cardiol 119:1479–1484

    Article  Google Scholar 

  2. Galiè N, Humbert M, Vachiery JL, Vachiery JL, Gibbs S, Lang I, Torbicki A, Simonneau G, Peacock A, Vonk-Noordegraaf A, Beghetti M, Ghofrani A, Gomez-Sanchez MA, Hansmann G, Klepetko W, Lancellotti P, Matucci M, McDonagh T, Pierard LA, Trindade PT, Zompatori M, Hoeper M (2016) 2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: the joint task force for the diagnosis and treatment of pulmonary hypertension of the European Society of Cardiology [ESC] and the European Respiratory Society [ERS]. Eur Heart J 37:67–119

    Article  Google Scholar 

  3. Benza RL, Gomberg-Maitland M, Miller DP, Frost A, Frantz RP, Foreman AJ, Badesch DB, McGoon MD (2012) The REVEAL Registry risk score calculator in patients newly diagnosed with pulmonary arterial hypertension. Chest 141:354–362

    Article  Google Scholar 

  4. Rudski LG, Lai WW, Afilalo J, Hua L, Handschumacher MD, Chandrasekaran K, Solomon SD, Louie EK, Schiller NB (2010) Guidelines for the echocardiographic assessment of the right heart in adults: a report from the American Society of Echocardiography, endorsed by the European Association of Echocardiography, a registered branch of the European Society of Cardiology, and the Canadian Society of Echocardiography. J Am Soc Echocardiogr. 23:685–713

    Article  Google Scholar 

  5. Farber HW, Foreman AJ, Miller DP, McGoon MD (2011) REVEAL Registry: correlation of right heart catheterization and echocardiography in patients with pulmonary arterial hypertension. Congest Heart Fail. 17:56–63

    Article  Google Scholar 

  6. Wright LM, Dwyer N, Celermajer D, Kritharides L, Marwick TH (2016) Follow-up of pulmonary hypertension with echocardiography. JACC Cardiovasc Imaging 9:733–746

    Article  Google Scholar 

  7. Vonk-Noordegraaf A, Haddad F, Chin KM, Forfia PR, Kawut SM, Lumens J, Naeije R, Newman J, Oudiz RJ, Provencher S, Torbicki A, Voelkel NF, Hassoun PM (2013) Right heart adaptation to pulmonary arterial hypertension. Physiology and pathobiology. J Am Coll Cardiol 62:D22–33

    Article  Google Scholar 

  8. Kouzu H, Nakatani S, Kyotani S, Kanzaki H, Nakanishi N, Kitakaze M (2009) Noninvasive estimation of pulmonary vascular resistance by Doppler echocardiography in patients with pulmonary arterial hypertension. Am J Cardiol. 103:872–876

    Article  Google Scholar 

  9. Mazurek JA, Vaidya A, Mathai SC, Roberts JD, Forfia PR (2017) Follow-up tricuspid annular plane systolic excursion predicts survival in pulmonary arterial hypertension. Pulm Circ 7:361–371

    Article  CAS  Google Scholar 

  10. Forfia PR, Fisher MR, Mathai SC, Housten-Harris T, Hemnes AR, Borlaug BA, Chamera E, Corretti MC, Champion HC, Abraham TP, Girgis RE, Hassoun PM (2006) Tricuspid annular displacement predicts survival in pulmonary hypertension. Am J Respir Crit Care Med. 174:1034–1041

    Article  Google Scholar 

  11. Lang RM, Badano LP, Mor-Avi V, Afilalo J, Armstrong A, Ernande L, Flachskampf FA, Foster E, Goldstein SA, Kuznetsova T, Lancellotti P, Muraru D, Picard MH, Rietzschel ER, Rudski L, Spencer KT, Tsang W, Voigt JU (2015) Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. Eur Heart J Cardiovasc Imaging 16:233–271

    Article  Google Scholar 

  12. McLaughlin VV, Archer SL, Badesch DB, Barst RJ, Farber HW, Lindner JR, Mathier MA, McGoon MD, Park MH, Rosenson RS, Rubin LJ, Tapson VF, Varga J (2009) ACCF/AHA 2009 expert consensus document on pulmonary hypertension a report of the American College of Cardiology Foundation Task Force on Expert Consensus Documents and the American Heart Association developed in collaboration with the American College of Chest Physicians; American Thoracic Society, Inc.; and the Pulmonary Hypertension Association. J Am Coll Cardiol 53:1573–1619

    Article  Google Scholar 

  13. Stevens GR, Garcia-Alvarez A, Sahni S, Garcia MJ, Fuster V, Sanz J (2012) RV dysfunction in pulmonary hypertension is independently related to pulmonary artery stiffness. JACC Cardiovas Imaging 5:378–387

    Article  Google Scholar 

  14. van de Veerdonk MC, Marcus JT, Westerhof N, de Man FS, Boostra A, Heymans MW, Bogaard HJ, Vonk-Noordegraaf A (2015) Signs of right ventricular deterioration in clinically stable patient with pulmonary arterial hypertension. Chest 147:1063–1071

    Article  Google Scholar 

  15. Tedford RJ, Mudd JO, Girgis RE, Mathai SC, Zaiman AL, Housten-Harris T, Boyce D, Kelemen BW, Bacher AC, Shah AA, Hummers LK, Wigley FM, Russell SD, Saggar R, Maughan WL, Hassoun PM, Kass DA (2013) Right ventricular dysfunction in systemic sclerosis-associated pulmonary arterial hypertension. Circ Heart Failure 6:953–963

    Article  CAS  Google Scholar 

  16. Campo A, Mathai SC, Pavec JL, Zaiman AL, Hummers LK, Boyce D, Housten T, Champion HC, Lechtzin N, Wigley FM, Girgis RE, Hassoun PM (2010) Hemodynamic predictors of survival in scleroderma-related pulmonary arterial hypertension. Am J Respir Crit Care Med 182:252–260

    Article  Google Scholar 

  17. da Costa-Junior AA, Ota-Arakaki JS, Ramos RP, Uellendahl M, Mancuso FJN, Gil MA, Fischer CH, Moises VA, de Camargo-Carvalho AC, Campos O (2017) Diagnostic and prognostic value of right ventricular strain in patients with pulmonary arterial hypertension and relatively preserved functional capacity studied with echocardiography and magnetic resonance. Int J Cardiovasc Imaging 33:39–46

    Article  Google Scholar 

  18. van Kessel M, Seaton D, Chan J, Yamada A, Kermeen F, Butler T, Sabapathy S, Morris N (2016) Prognostic value of right ventricular free wall strain in pulmonary hypertension patients with pseudo-normalized tricuspid annular plane systolic excursion values. Int J Cardiovasc Imaging 32:905–912

    Article  Google Scholar 

  19. Kawut SM, Al-Naamani N, Agerstrand C, Rosenzweig EB, Rowan C, Barst RJ, Bergmann S, Horn EM (2009) Determinants of right ventricular ejection fraction in pulmonary arterial hypertension. Chest 135:752–759

    Article  Google Scholar 

  20. Szabó G, Soós P, Bährle S, Radovits T, Weigang E, Kekesi V, Merkely B, Hagi S (2006) Adaptation of the right ventricle to an increased afterload in the chronically volume overloaded heart. Ann Thorac Surg 82:989–995

    Article  Google Scholar 

  21. Shehata ML, Lossnitzer D, Skrok J, Boyce D, Lechtzin N, Mathai SC, Girgis RE, Osman N, Lima JA, Bluemke DA, Hassoun PM, Vogel-Claussen J (2011) Myocardial delayed enhancement in pulmonary hypertension: pulmonary hemodynamics, right ventricular function, and remodeling. Am J Roentgenol 196:87–94

    Article  Google Scholar 

  22. Bogaard HJ, Natarajan R, Henderson SC, Long CS, Kraskauskas D, Smithson L, Ockaili R, McCord JM, Voelkel NF (2009) Chronic pulmonary artery pressure elevation is insufficient to explain right heart failure. Circulation 120:1951–1960

    Article  Google Scholar 

  23. Grapsa J, Gibbs JS, Dawson D, Watson G, Patni R, Athanasiou T, Punjabi PP, Howard LS, Nihonyannopoulos P (2012) Morphologic and functional remodeling of the right ventricle in pulmonary hypertension by real time three dimensional echocardiography. Am J Cardiol 109:906–913

    Article  Google Scholar 

  24. Ito M, Kodama M, Kashimura T, Obata H, Mitsuma W, Hirono S, Tomita M, Ohno Y, Tanabe N, Aizawa Y (2012) Comparison of patients with pulmonary arterial hypertension with versus without right-sided mechanical alternans. Am J Cardiol 109:428–431

    Article  Google Scholar 

  25. Amano H, Toyoda S, Arikawa T, Inami S, Otani N, Nishi Y, Kitagawa Y, Taguchi I, Abe S, Inoue T (2013) Left ventricular function in pulmonary hypertension. Heart Vessels 28:505–509

    Article  Google Scholar 

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Correspondence to Akiyoshi Hashimoto.

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Kawamukai, M., Hashimoto, A., Koyama, M. et al. Risk classification of pulmonary arterial hypertension by echocardiographic combined assessment of pulmonary vascular resistance and right ventricular function. Heart Vessels 34, 1789–1800 (2019). https://doi.org/10.1007/s00380-019-01429-7

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