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动脉性肺动脉高压抗凝治疗之争议 被引量:3

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摘要 肺动脉高压是临床上较为常见的疾病,其病因复杂,病情进展快,致残率和致死率较高。目前国内外指南把肺动脉高压分为5大类,其中第一大类称为动脉性肺动脉高压(PAH)。
作者 熊长明
出处 《中华医学杂志》 CAS CSCD 北大核心 2018年第2期81-83,共3页 National Medical Journal of China
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  • 1Galie N, Manes A, Negro L, et al. A recta-analysis of randomized controlled trials in pulmonary arterial hypertension. Eur Heart J, 2009, 30: 394-403.
  • 2McLaughlin VV, Shillington A, Rich S. Survival in primary pulmonary hypertension: the impact of epoprostenol therapy. Circulation, 2002, 106 : 1477-1482.
  • 3Barst RJ. Recent advances in the treatment of pediatric pulmonary artery hypertension. Pedlatr Clin North Am, 1999, 46: 331-345.
  • 4McLaughlin VV, Sithon O, Badesch DB, et al. Survival with first- line bosentan in patients with primary pulmonary hypertension. Eur Respir J, 2005, 25 : 244-249.
  • 5Galie N, Ghofrani HA, Torbicki A, et al. Sildenalil citrate therapy for pulmonary arterial hypertension. N Engl J Med, 2005, 353 : 2148-2157.
  • 6Gomberg-Maifland M, Dufton C, Oudiz RJ. Compelling evidence of long-term outcomes in pulmonary arterial hypertension? A clinical perspective. J Am Coll Cardiol, 2011,57: 1053-1061.
  • 7Macehia A, Marchioli R, Marfisi R, et al. A meta-analysis of trials of pulmonary hypertension: a clinical condition looking for drugs and research methodology. Am Heart J, 2007, 153 : 1037- 1047.
  • 8D'Alonzo GE,Barst RJ, Ayres SM, et al. Survival in patients with primary pulmonary hypertension. Results from a national prospective registry [ J]. Ann Intern Med, 1991,115 : 343-349.
  • 9McLaughlin VV, Suissa S. Prognosis of pulmonary arterial hypertension: the power of clinical registries of rare diseases [ J]. Circulation ,2010,122 : 106-108.
  • 10Simonneau G, Gatzoulis MA, Adatia I, et al. Updated clinical classification of pulmonary hypertension [ J ]. J Am Coil Cardiol, 2013,62: D34-D41.

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