Treatment of patients with pulmonary arterial hypertension at the time of death or deterioration to functional class IV: Insights from the REVEAL Registry

被引:75
作者
Farber, Harrison W. [1 ]
Miller, Dave P. [2 ]
Meltzer, Leslie A. [3 ]
McGoon, Michael D. [4 ]
机构
[1] Boston Univ, Sch Med, Ctr Pulm, Boston, MA 02118 USA
[2] ICON Late Phase & Outcomes Res, San Francisco, CA USA
[3] Actelion Pharmaceut US Inc, San Francisco, CA USA
[4] Mayo Clin, Dept Cardiovasc Dis, Rochester, MN USA
关键词
pharmacology; prognosis; pulmonary hypertension; registries; survival; CONTINUOUS INTRAVENOUS EPOPROSTENOL; INHALED ILOPROST; COMBINATION THERAPY; MEDICAL THERAPY; DOUBLE-BLIND; TASK-FORCE; BOSENTAN; SILDENAFIL; PROSTACYCLIN; SURVIVAL;
D O I
10.1016/j.healun.2013.08.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Current guidelines recommend intravenous prostacyclin as first-line therapy for patients with pulmonary arterial hypertension (PAH) in New York Heart Association/World Health Organization functional class (FC) IV, or combination therapy for patients in any FC who do not respond to monotherapy. We investigated the aggressiveness of therapy in patients enrolled in the REVEAL (Registry to Evaluate Early and Long-Term PAH Disease Management) Registry who deteriorated to FC IV or died. METHODS: Among 3,515 patients (age >= 18 years) in REVEAL with a mean pulmonary artery pressure >= 25 mm Hg and pulmonary capillary wedge pressure <= 15 mm Hg, we examined three sub-sets: the 487 patients who had a PAH-related death, the larger set of 908 patients who died from any cause (PAH-related, not PAH-related, or unknown), and the 294 patients who were FC I, II, or III at enrollment and later assessed as FC IV. RESULTS: Among patients who died, 56% (n = 272 of 487) and 43% (n = 391 of 908) were receiving intravenous prostacyclin before death in the PAH-related death and all-cause death cohorts, respectively. In the PAH-related death cohort, 60% and 16% of patients were most recently assessed as FC III and IV, respectively; among those assessed as FC IV within 6 months of death, 57.7% (n = 15 of 26) had received intravenous prostacyclin. Because many patients died without an observed assessment of worsening to FC IV, we also evaluated medication use among the cohort of patients who worsened to FC IV during the study. One day before worsening to PC IV, 150 of 294 patients were not receiving intravenous prostacyclin and 70 were receiving only PAH-specific monotherapy; of these, 61% and 67%, respectively, received no additional therapy 90 days later. CONCLUSIONS: Intravenous prostacyclin and combination therapy are not consistently used in the most seriously ill patients enrolled in REVEAL after being assessed as FC IV or at the time of death. (C) 2013 International Society for Heart and Lung Transplantation. All rights reserved.
引用
收藏
页码:1114 / 1122
页数:9
相关论文
共 39 条
[11]   Management of pulmonary arterial hypertension with a focus on combination therapies [J].
Benza, Raymond L. ;
Park, Myung H. ;
Keogh, Anne ;
Girgis, Reda E. .
JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2007, 26 (05) :437-446
[12]   Effects of the dual endothelin-receptor antagonist bosentan in patients with pulmonary hypertension: a randomised placebo-controlled study [J].
Channick, RN ;
Simonneau, G ;
Sitbon, O ;
Robbins, IM ;
Frost, A ;
Tapson, VF ;
Badesch, DB ;
Roux, S ;
Rainisio, M ;
Bodin, F ;
Rubin, LJ .
LANCET, 2001, 358 (9288) :1119-1123
[13]   SURVIVAL IN PATIENTS WITH PRIMARY PULMONARY-HYPERTENSION - RESULTS FROM A NATIONAL PROSPECTIVE REGISTRY [J].
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 .
ANNALS OF INTERNAL MEDICINE, 1991, 115 (05) :343-349
[14]   The Changing Picture of Patients With Pulmonary Arterial Hypertension in the United States How REVEAL Differs From Historic and Non-US Contemporary Registries [J].
Frost, Adaani E. ;
Badesch, David B. ;
Barst, Robyn J. ;
Benza, Raymond L. ;
Elliott, Gregory ;
Farber, Harrison W. ;
Krichman, Abby ;
Liou, Theodore G. ;
Raskob, Gary E. ;
Wason, Prieya ;
Feldkircher, Kathleen ;
Turner, Michelle ;
McGoon, Michael D. .
CHEST, 2011, 139 (01) :128-137
[15]   Ambrisentan therapy for pulmonary arterial hypertension [J].
Galié, N ;
Badesch, D ;
Oudiz, R ;
Simonneau, G ;
McGoon, MD ;
Keogh, AM ;
Frost, AE ;
Zwicke, D ;
Naeije, R ;
Shapiro, S ;
Olschewski, H ;
Rubin, LJ .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2005, 46 (03) :529-535
[16]   Guidelines on diagnosis and treatment of pulmonary arterial hypertension -: The Task Force on Diagnosis and Treatment of Pulmonary Arterial Hypertension of the European Society of Cardiology [J].
Galiè, N ;
Torbicki, A ;
Barst, R ;
Dartevelle, P ;
Haworth, S ;
Higenbottam, T ;
Olschewski, H ;
Peacock, A ;
Pietra, G ;
Rubin, LJ ;
Simonneau, G .
EUROPEAN HEART JOURNAL, 2004, 25 (24) :2243-2278
[17]   Guidelines for the diagnosis and treatment of pulmonary hypertension [J].
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 .
EUROPEAN HEART JOURNAL, 2009, 30 (20) :2493-2537
[18]   Combination therapy with oral sildenafil and inhaled iloprost for severe pulmonary hypertension [J].
Ghofrani, HA ;
Wiedemann, R ;
Rose, F ;
Olschewski, H ;
Schermuly, RT ;
Weissmann, N ;
Seeger, W ;
Grimminger, F .
ANNALS OF INTERNAL MEDICINE, 2002, 136 (07) :515-522
[19]   Pulmonary arterial hypertension [J].
Highland, Kristin B. .
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2008, 335 (01) :40-45
[20]   Combining inhaled iloprost with bosentan in patients with idiopathic pulmonary arterial hypertension [J].
Hoeper, M. M. ;
Leuchte, H. ;
Halank, M. ;
Wilkens, H. ;
Meyer, F. J. ;
Seyfarth, H. J. ;
Wensel, R. ;
Ripken, F. ;
Bremer, H. ;
Kluge, S. ;
Hoeffken, G. ;
Behr, J. .
EUROPEAN RESPIRATORY JOURNAL, 2006, 28 (04) :691-694