Children with pulmonary arterial hypertension and prostanoid therapy: Long-term hemodynamics

被引:52
|
作者
Siehr, Stephanie L. [1 ]
Ivy, D. Dunbar [2 ]
Miller-Reed, Kathleen [2 ]
Ogawa, Michelle [1 ]
Rosenthal, David N. [1 ]
Feinstein, Jeffrey A. [1 ]
机构
[1] Stanford Univ, Dept Pediat, Div Pediat Cardiol, Palo Alto, CA 94304 USA
[2] Univ Colorado, Dept Pediat, Div Pediat Cardiol, Aurora, CO USA
来源
基金
美国国家卫生研究院;
关键词
pediatric patients; pulmonary arterial hypertension; epoprostenol; treprostinil; hemodynamics; INTRAVENOUS EPOPROSTENOL; SUBCUTANEOUS TREPROSTINIL; PEDIATRIC-PATIENTS; PROSTACYCLIN; SURVIVAL; EFFICACY; BOSENTAN; SAFETY;
D O I
10.1016/j.healun.2013.01.1055
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Pediatric patients with severe pulmonary arterial hypertension (PAH) are treated with intravenous epoprostenol or intravenous or subcutaneous treprostinil. Little is known about longitudinal hemodynamics and outcomes of epoprostenol, treprostinil, and transitions from epoprostenol to treprostinil. METHODS: This was retrospective study of 77 pediatric patients (47 idiopathic PAH, 24 congenital heart disease-PAH) receiving epoprostenol or treprostinil from 1992 to 2010 at 2 centers. Outcomes were defined as living vs dead/transplant. RESULTS: Mean age at baseline was 7.7 +/- 5.2 years, with follow-up of 4.3 +/- 3.4 years. Thirty-seven patients were treated with epoprostenol, 20 with treprostinil, and 20 were transitioned from epoprostenol to treprostinil. Mean pulmonary-to-systemic vascular resistance ratio (Rp/Rs) for epoprostenol was 1.0 +/- 0.4, 0.8 +/- 0.4, 0.8 +/- 0.4, 1.0 +/- 0.4, and 1.2 +/- 0.4, respectively, at baseline, 1, 2, 3, and 4 years. For treprostinil, Rp/Rs was 0.9 +/- 0.3, 0.7 +/- 0.3, 0.5 +/- 0.2, (p < 0.01 vs baseline), and 1.1 +/- 0.2, respectively, at baseline, 1, 2, and 3 to 4 years, respectively. There were similar changes in mean pulmonary artery pressure and pulmonary vascular resistance index. The Rp/Rs 1 year after epoprostenol to treprostinil transition increased from 0.6 to 0.8 (n = 7). Changes not statistically significant unless noted. Eight patients died or received a transplant within 2 years of baseline; compared with the rest of the cohort, mean baseline Rp/Rs, right atrial pressure, and pulmonary vascular resistance index were significantly worse in this group. Thirty-nine patients remain on prostanoids, 17 are off, 16 died, and 5 received heart-lung transplant. Kaplan-Meier 5-year transplant-free survival was 70% (95% confidence interval, 56%-80%). CONCLUSION: There was improvement in Rp/Rs on both therapies at 1 to 2 years that was not sustained. The 5-year transplant-free survival was better than in similar adult studies. J Heart Lung Transplant 2013;32:546-552 (C) 2013 International Society for Heart and Lung Transplantation. All rights reserved.
引用
收藏
页码:546 / 552
页数:7
相关论文
共 50 条
  • [1] Prostanoid therapy for pulmonary arterial hypertension
    Strauss, Wayne L.
    Edelman, Jeffrey D.
    [J]. CLINICS IN CHEST MEDICINE, 2007, 28 (01) : 127 - +
  • [2] Prostanoid therapy for pulmonary arterial hypertension
    Badesch, DB
    McLaughlin, VV
    Delcroix, M
    Vizza, CD
    Olschewski, H
    Sitbon, O
    Barst, RJ
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2004, 43 (12) : 56S - 61S
  • [3] Long-term vardenafil therapy improves hemodynamics in patients with pulmonary hypertension
    Aizawa, K
    Hanaoka, T
    Kasai, H
    Kogashi, K
    Kumazaki, S
    Koyama, J
    Tsutsui, H
    Yazaki, Y
    Watanabe, N
    Kinoshita, O
    Ikeda, U
    [J]. HYPERTENSION RESEARCH, 2006, 29 (02) : 123 - 128
  • [4] Long-Term Vardenafil Therapy Improves Hemodynamics in Patients with Pulmonary Hypertension
    Kazunori Aizawa
    Takeshi Hanaoka
    Hiroki Kasai
    Kaoru Kogashi
    Setsuo Kumazaki
    Jun Koyama
    Hiroshi Tsutsui
    Yoshikazu Yazaki
    Noboru Watanabe
    Osamu Kinoshita
    Uichi Ikeda
    [J]. Hypertension Research, 2006, 29 : 123 - 128
  • [5] Long-term bosentan treatment in children with pulmonary arterial hypertension
    Standing, JF
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2006, 47 (09) : 1914 - 1915
  • [6] Effects of long-term bosentan in children with pulmonary arterial hypertension
    Rosenzweig, EB
    Ivy, DD
    Widlitz, A
    Doran, A
    Claussen, LR
    Yung, D
    Abman, SH
    Morganti, A
    Nguyen, N
    Barst, RJ
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2005, 46 (04) : 697 - 704
  • [7] Long-term sitaxsentan therapy in Pulmonary Arterial Hypertension (PAH)
    Horn, E
    Langleben, D
    Frost, A
    Hill, N
    McLaughlin, V
    Oudiz, R
    Dixon, RAF
    Barst, RJ
    [J]. EUROPEAN HEART JOURNAL, 2004, 25 : 466 - 466
  • [8] Long-Term Ambrisentan Therapy for the Treatment of Pulmonary Arterial Hypertension
    Oudiz, Ronald J.
    Galie, Nazzareno
    Olschewski, Horst
    Torres, Fernando
    Frost, Adaani
    Ghofrani, Hossein A.
    Badesch, David B.
    McGoon, Michael D.
    McLaughlin, Vallerie V.
    Roecker, Ellen B.
    Harrison, Brooke C.
    Despain, Darrin
    Dufton, Christopher
    Rubin, Lewis J.
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2009, 54 (21) : 1971 - 1981
  • [9] Plasma proteomics of differential outcome to long-term therapy in children with idiopathic pulmonary arterial hypertension
    Yeager, Michael E.
    Colvin, Kelley L.
    Everett, Allen D.
    Stenmark, Kurt R.
    Ivy, D. Dunbar
    [J]. PROTEOMICS CLINICAL APPLICATIONS, 2012, 6 (5-6) : 257 - 267
  • [10] Short- and long-term effects of inhaled iloprost therapy in children with pulmonary arterial hypertension
    Ivy, D. Dunbar
    Doran, Aimee K.
    Smith, Kelly J.
    Mallory, George B.
    Beghetti, Maurice
    Barst, Robyn J.
    Brady, Danicla
    Law, Yuk
    Parker, Donna
    Claussen, Lori
    Abman, Steven H.
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2008, 51 (02) : 161 - 169