Pulmonary Arterial Hypertension

被引:1
作者
Centeno, Mae M. [1 ,2 ]
机构
[1] Baylor Univ, Med Ctr, Heart Failure Program, Dallas, TX 75246 USA
[2] Baylor Univ, Med Ctr, Adv Lung Dis Ctr, Dallas, TX 75246 USA
关键词
Pulmonary hypertension; Pulmonary arterial hypertension; Classification; Medical Treatment; Pharmacologic Intervention; VASCULAR-DISEASE; THERAPY; MANIFESTATIONS; MULTICENTER; MANAGEMENT; FREQUENCY; DIAGNOSIS; EFFICACY; ILOPROST; RISK;
D O I
10.1016/j.ccell.2011.08.010
中图分类号
R47 [护理学];
学科分类号
1011 ;
摘要
Pulmonary hypertension (PH) is a rare, complex, life-threatening disorder. Most patients present with vague symptoms, making early diagnosis very difficult. Pulmonary arterial hypertension, a category of PH, is characterized by vascular proliferation and remodeling. It causes progressive increase in pulmonary vascular resistance resulting in right ventricular. failure and death. Treatment options targeting specific pathways for patients with the disease have evolved in the last 20 years to help improve quality of life and prolong their survival. The purpose of this article is to provide an insightful and helpful review of the classification of pulmonary hypertension, assessment, and treatment options.
引用
收藏
页码:645 / +
页数:16
相关论文
共 46 条
[1]   Appetite-suppressant drugs and the risk of primary pulmonary hypertension [J].
Abenhaim, L ;
Moride, Y ;
Brenot, F ;
Rich, S ;
Benichou, J ;
Kurz, X ;
Higenbottam, T ;
Oakley, C ;
Wouters, E ;
Aubier, M ;
Simonneau, G ;
Begaud, B .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (09) :609-616
[2]   Hemodynamic and functional assessment of patients with sickle cell disease and pulmonary hypertension [J].
Anthi, Anastasia ;
Machado, Roberto F. ;
Jison, Maria L. ;
Taveira-DaSilva, Angelo M. ;
Rubin, Lewis J. ;
Hunter, Lori ;
Hunter, Christian J. ;
Coles, Wynona ;
Nichols, James ;
Avila, Nilo A. ;
Sachdev, Vandana ;
Chen, Clara C. ;
Gladwin, Mark T. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2007, 175 (12) :1272-1279
[3]   Eisenmenger Syndrome A Clinical Perspective in a New Therapeutic Era of Pulmonary Arterial Hypertension [J].
Beghetti, Maurice ;
Galie, Nazzareno .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2009, 53 (09) :733-740
[4]   Frequency and clinical implications of increased pulmonary artery pressures in liver transplant patients [J].
Castro, M ;
Krowka, MJ ;
Schroeder, DR ;
Beck, KC ;
Plevak, DJ ;
Rettke, SR ;
Cortese, DA ;
Wiesner, RH .
MAYO CLINIC PROCEEDINGS, 1996, 71 (06) :543-551
[5]   Is methamphetamine use associated with idiopathic pulmonary arterial hypertension? [J].
Chin, Kelly M. ;
Channick, Richard N. ;
Rubin, Lewis J. .
CHEST, 2006, 130 (06) :1657-1663
[6]   High frequency of BMPR2 exonic deletions/duplications in familial pulmonary arterial hypertension [J].
Cogan, Joy D. ;
Pauciulo, Michael W. ;
Batchman, Amy P. ;
Prince, Melissa A. ;
Robbins, Ivan M. ;
Hedges, Lora K. ;
Stanton, Krista C. ;
Wheeler, Lisa A. ;
Phillips, John A., III ;
Loyd, James E. ;
Nichols, William C. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2006, 174 (05) :590-598
[7]   Combined pulmonary fibrosis and emphysema: a distinct underrecognised entity [J].
Cottin, V ;
Nunes, H ;
Brillet, PY ;
Delaval, P ;
Devouassoux, G ;
Tillie-Leblond, I ;
Israel-Biet, D ;
Court-Fortune, I ;
Valeyre, D ;
Cordier, JF .
EUROPEAN RESPIRATORY JOURNAL, 2005, 26 (04) :586-593
[8]   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
[9]   Current concepts: Chronic thromboembolic pulmonary hypertension [J].
Fedullo, PF ;
Auger, WR ;
Kerr, KM ;
Rubin, LJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (20) :1465-1472
[10]   Clinical classification of pulmonary hypertension [J].
Fishman, AP .
CLINICS IN CHEST MEDICINE, 2001, 22 (03) :385-+