Survival Differences in Pediatric Pulmonary Arterial Hypertension Clues to a Better Understanding of Outcome and Optimal Treatment Strategies

被引:111
作者
Zijlstra, Willemijn M. H. [1 ]
Douwes, Johannes M. [1 ]
Rosenzweig, Erika B. [2 ]
Schokker, Sandor [1 ]
Krishnan, Usha [2 ]
Roofthooft, Marcus T. R. [1 ]
Miller-Reed, Kathleen [3 ]
Hillege, Hans L. [4 ]
Ivy, D. Dunbar [3 ]
Berger, Rolf M. F. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Beatrix Childrens Hosp, Ctr Congenital Heart Dis,Dept Pediat Cardiol, Groningen, Netherlands
[2] Columbia Univ Coll Phys & Surg, New York, NY 10032 USA
[3] Childrens Hosp Colorado, Aurora, CO USA
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen, Netherlands
关键词
pediatrics; pulmonary hypertension; survival; CALCIUM-CHANNEL BLOCKERS; CHILDREN; BOSENTAN; THERAPY; ERA;
D O I
10.1016/j.jacc.2014.02.575
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives In order to describe survival and treatment strategies in pediatric pulmonary arterial hypertension (PAH) in the current era of PAH-targeted drugs and to identify predictors of outcome, we studied uniformly defined contemporary patient cohorts at 3 major referral centers for pediatric PAH (New York [NY], Denver, and the Netherlands [NL]). Background In pediatric PAH, discrepancies exist in reported survival rates between North American and European patient cohorts, and robust data for long-term treatment effects are lacking. Methods According to uniform inclusion criteria, 275 recently diagnosed consecutive pediatric PAH patients who visited the 3 referral centers between 2000 and 2010 were included. Results Unadjusted survival rates differed between the center cohorts (1-, 3-, and 5-year transplantation-free survival rates: 100%, 96%, and 90% for NY; 95%, 87%, and 78% for Denver; and 84%, 71%, and 62% for NL, respectively; p<0.001). Based on World Health Organization (WHO) functional class and hemodynamic parameters, disease severity at diagnosis differed between the center cohorts. Adjustment for diagnosis, WHO functional class, indexed pulmonary vascular resistance, and pulmonary-to-systemic arterial pressure ratio resolved the observed survival differences. Treatment with PAH-targeted dual and triple therapy during the study period was associated with better survival than treatment with PAH-targeted monotherapy. Conclusions Survival rates of pediatric PAH patients differed between 3 major referral centers. This could be explained by differences between the center cohorts in patients' diagnoses and measures of disease severity, which were identified as important predictors of outcome. In this study, treatment with PAH-targeted combination therapy during the study period was independently associated with improved survival. (C) 2014 by the American College of Cardiology Foundation
引用
收藏
页码:2159 / 2169
页数:11
相关论文
共 27 条
  • [1] Vasodilator therapy for primary pulmonary hypertension in children
    Barst, RJ
    Maislin, G
    Fishman, AP
    [J]. CIRCULATION, 1999, 99 (09) : 1197 - 1208
  • [2] Survival in Childhood Pulmonary Arterial Hypertension Insights From the Registry to Evaluate Early and Long-Term Pulmonary Arterial Hypertension Disease Management
    Barst, Robyn J.
    McGoon, Michael D.
    Elliott, C. Gregory
    Foreman, Aimee J.
    Miller, Dave P.
    Ivy, D. Dunbar
    [J]. CIRCULATION, 2012, 125 (01) : 113 - 122
  • [3] Clinical features of paediatric pulmonary hypertension: a registry study
    Berger, Rolf M. F.
    Beghetti, Maurice
    Humpl, Tilman
    Raskob, Gary E.
    Ivy, D. Dunbar
    Jing, Zhi-Cheng
    Bonnet, Damien
    Schulze-Neick, Ingram
    Barst, Robyn J.
    [J]. LANCET, 2012, 379 (9815) : 537 - 546
  • [4] SURVIVAL IN PATIENTS WITH PRIMARY PULMONARY-HYPERTENSION - RESULTS FROM A NATIONAL PROSPECTIVE REGISTRY
    DALONZO, GE
    BARST, RJ
    AYRES, SM
    BERGOFSKY, EH
    BRUNDAGE, BH
    DETRE, KM
    FISHMAN, AP
    GOLDRING, RM
    GROVES, BM
    KERNIS, JT
    LEVY, PS
    PIETRA, GG
    REID, LM
    REEVES, JT
    RICH, S
    VREIM, CE
    WILLIAMS, GW
    WU, M
    [J]. ANNALS OF INTERNAL MEDICINE, 1991, 115 (05) : 343 - 349
  • [5] Development of a WHO growth reference for school-aged children and adolescents
    de Onis, Mercedes
    Onyango, Adelheid W.
    Borghi, Elaine
    Siyam, Amani
    Nishida, Chizuru
    Siekmann, Jonathan
    [J]. BULLETIN OF THE WORLD HEALTH ORGANIZATION, 2007, 85 (09) : 660 - 667
  • [6] Acute pulmonary vasodilator response in paediatric and adult pulmonary arterial hypertension: occurrence and prognostic value when comparing three response criteria
    Douwes, Johannes M.
    van Loon, Rosa L. E.
    Hoendermis, Elke S.
    Vonk-Noordegraaf, Anton
    Roofthooft, Marcus T. R.
    Talsma, Melle D.
    Hillege, Hans L.
    Berger, Rolf M. F.
    [J]. EUROPEAN HEART JOURNAL, 2011, 32 (24) : 3137 - 3146
  • [7] Characteristics and prospective 2-year follow-up of children with pulmonary arterial hypertension in France
    Fraisse, Alain
    Jais, Xavier
    Schleich, Jean-Marc
    di Filippo, Sylvie
    Maragnes, Pascale
    Beghetti, Maurice
    Gressing, Virginie
    Voisin, Michel
    Dauphin, Claire
    Clerson, Pierre
    Godark, Francois
    Bonnet, Damien
    [J]. ARCHIVES OF CARDIOVASCULAR DISEASES, 2010, 103 (02) : 66 - 74
  • [8] Guidelines for the diagnosis and treatment of pulmonary hypertension
    Galie, Nazzareno
    Hoeper, Marius M.
    Humbert, Marc
    Torbicki, Adam
    Vachiery, Jean-Luc
    Albert Barbera, Joan
    Beghetti, Maurice
    Corris, Paul
    Gaine, Sean
    Gibbs, J. Simon
    Angel Gomez-Sanchez, Miguel
    Jondeau, Guillaume
    Klepetko, Walter
    Opitz, Christian
    Peacock, Andrew
    Rubin, Lewis
    Zellweger, Michael
    Simonneau, Gerald
    [J]. EUROPEAN HEART JOURNAL, 2009, 30 (20) : 2493 - 2537
  • [9] Treatment and survival in children with pulmonary arterial hypertension: the UK Pulmonary Hypertension Service for Children 2001-2006
    Haworth, S. G.
    Hislop, A. A.
    [J]. HEART, 2009, 95 (04) : 312 - 317
  • [10] Goal-oriented treatment and combination therapy for pulmonary arterial hypertension
    Hoeper, MM
    Markevych, I
    Spiekerkoetter, E
    Welte, T
    Niedermeyer, J
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2005, 26 (05) : 858 - 863