1,121
Views
1
CrossRef citations to date
0
Altmetric
Original research

Effect of ambrisentan on echocardiographic and Doppler measures from patients in China with pulmonary arterial hypertension

, , , , , , , , , , & ORCID Icon show all
Pages 643-649 | Received 05 Mar 2020, Accepted 06 Aug 2020, Published online: 29 Sep 2020

References

  • Galiè N, McLaughlin VV, Rubin LJ, et al. An overview of the 6th world symposium on pulmonary hypertension. Eur Respir J. 2018. DOI:https://doi.org/10.1183/13993003.02148-2018
  • Wilkins MR. Pulmonary hypertension: the science behind the disease spectrum. Eur Respir Rev. 2012;21(123):19–26.
  • Galiè N, Barberà JA, Frost AE, et al. Initial use of ambrisentan plus tadalafil in pulmonary arterial hypertension. N Engl J Med. 2015;373(9):834–844.
  • Zhang R, Dai LZ, Xie WP, et al. Survival of Chinese patients with pulmonary arterial hypertension in the modern treatment era. Chest. 2011;140(2):301–309.
  • Galiè N, Horst O, Ronald J, et al., Ambrisentan for the treatment of pulmonary arterial hypertension: results of the ambrisentan in pulmonary arterial hypertension, randomized, double-blind, placebo-controlled, multicenter, efficacy (ARIES) study 1 and 2. Circulation. 2008;117(23): 3010–3019.
  • Huo Y, Jing ZC, Zeng XF, et al., Evaluation of efficacy, safety and tolerability of ambrisentan in Chinese adults with pulmonary arterial hypertension: a prospective open label cohort study. BMC Cardiovasc Disord. 2016;16(1): 201.
  • Yoshida S, Shirato K, Shimamura R, et al. Long term safety and efficacy of ambrisentan in Japanese adults with pulmonary arterial hypertension. Curr Med Res Opin. 2012;28(6):1069–1076.
  • Coghlan JG, Galiè N, Barberà JA, et al. Initial combination therapy with ambrisentan and tadalafil in connective tissue disease-associated pulmonary arterial hypertension (CTD-PAH): subgroup analysis from the AMBITION trial. Ann Rheum Dis. 2017;76(7):1219–1227.
  • Chen FD, Zhou DX, Di RM, et al. Efficacy and safety of ambrisentan therapy in Chinese patients with pulmonary hypertension. Zhonghua Yi Xue Za Zhi. 2013;93(34):2736–2738.
  • He J, Wen L, Jiang R, et al. Effects of ambrisentan in treatment of pulmonary arterial hypertension: a pilot study with 15 patients. Zhonghua Xin Xue Guan Bing Za Zhi. 2013;41(6):493–496.
  • Galiè N, Humbert M, Vachiery JL, et al. 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. 2016;37(1):67–119.
  • Maron BA, Galiè N. Diagnosis, treatment, and clinical management of pulmonary arterial hypertension in the contemporary era: a review. JAMA Cardiol. 2016;1;1(9):1056–1065.
  • Austin C, Alassas K, Burger C. Echocardiographic assessment of estimated right atrial pressure and size predicts mortality in pulmonary arterial hypertension. Chest. 2015;147(1):198–208.
  • Argula RG, Karwa A, Lauer A, et al., Differences in right ventricular functional changes during treatment between systemic sclerosis–associated pulmonary arterial hypertension and idiopathic pulmonary arterial hypertension. Ann Am Thorac Soc. 2017;14(5): 682–689.
  • Bhave NM, Visovatti SH, Kulick B, et al., Right atrial strain is predictive of clinical outcomes and invasive hemodynamic data in group 1 pulmonary arterial hypertension. Int J Cardiovasc Imaging. 2017;33(6): 847–855.
  • Nagueh SF, Smiseth OA, Christopher P, et al. Recommendations for the evaluation of left ventricular diastolic function by echocardiography: an update from the American society of echocardiography and the European association of cardiovascular imaging. J Am Soc Echocardiogr. 2016;29(4):277–314.
  • Galiè N, Hinderliter AL, Torbicki A, et al. Effects of the oral endothelin-receptor antagonist bosentan on echocardiographic and doppler measures in patients with pulmonary arterial hypertension. J Am Coll Cardiol. 2003;41(8):1380–1386.
  • Moles VM, McLaughlin VV. Pulmonary hypertension in women: what does the cardiologist need to know? Curr Cardiovasc Risk Rep. 2017;11:10.
  • Pugh ME, Hemnes AR. Pulmonary hypertension in women. Expert Rev Cardiovasc Ther. 2010;8(11):1549–1558.
  • White RJ. Estrogen: friend or foe in pulmonary hypertension? Am J Respir Crit Care Med. 2016;193(10):1084–1086.
  • Hassoun PM, Zamanian RT, Damico R, et al., Ambrisentan and tadalafil up-front combination therapy in scleroderma-associated pulmonary arterial hypertension. Am J Respir Crit Care Med. 2015;192(9): 1102–1110.
  • Li X-Q, Li Y-J, Wang Y. Ambrisentan may improve exercise tolerance and cardiac function in patients with pulmonary hypertension. Clin Ther. 2015;37(6):1270–1279.
  • Ryan T, Petrovic O, Dillon JC. An echocardiographic index for separation of right ventricular volume and pressure overload. J Am Coll Cardiol. 1985;5(4):918–924.
  • Jia J, Han Q, Leng N, et al. Characteristics of connective tissue disease-associated pulmonary arterial hypertension: a retrospective cohort study. Int J Clin Exp Med. 2017;10(12):16254–16263.
  • Mitter SS, Shah SJ, Thomas JD. E/A and E/e’ to assess diastolic dysfunction and LV filling pressure. J Am Coll Cardiol. 2017;69(11):1451–1464.