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首页> 外文期刊>Circulation: An Official Journal of the American Heart Association >Anticoagulation and survival in pulmonary arterial hypertension: Results from the comparative, prospective registry of newly initiated therapies for pulmonary hypertension (COMPERA)
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Anticoagulation and survival in pulmonary arterial hypertension: Results from the comparative, prospective registry of newly initiated therapies for pulmonary hypertension (COMPERA)

机译:肺动脉高压的抗凝治疗和生存:新近开始的肺动脉高压疗法(COMPERA)的比较,前瞻性研究结果

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摘要

BACKGROUND-: For almost 30 years, anticoagulation has been recommended for patients with idiopathic pulmonary arterial hypertension (IPAH). Supporting evidence, however, is limited, and it is unclear whether this recommendation is still justified in the modern management era and whether it should be extended to patients with other forms of pulmonary arterial hypertension (PAH). METHODS AND RESULTS-: We analyzed data from Comparative, Prospective Registry of Newly Initiated Therapies for Pulmonary Hypertension (COMPERA), an ongoing European pulmonary hypertension registry. Survival rates of patients with IPAH and other forms of PAH were compared by the use of anticoagulation. The sample consisted of 1283 consecutively enrolled patients with newly diagnosed PAH. Anticoagulation was used in 66% of 800 patients with IPAH and in 43% of 483 patients with other forms of PAH. In patients with IPAH, there was a significantly better 3-year survival (P=0.006) in patients on anticoagulation compared with patients who never received anticoagulation, albeit the patients in the anticoagulation group had more severe disease at baseline. The survival difference at 3 years remained statistically significant (P=0.017) in a matched-pair analysis of n=336 IPAH patients. The beneficial effect of anticoagulation on survival of IPAH patients was confirmed by Cox multivariable regression analysis (hazard ratio, 0.79; 95% confidence interval, 0.66-0.94). In contrast, the use of anticoagulants was not associated with a survival benefit in patients with other forms of PAH. CONCLUSIONS-: The present data suggest that the use of anticoagulation is associated with a survival benefit in patients with IPAH, supporting current treatment recommendations. The evidence remains inconclusive for other forms of PAH. CLINICAL TRIAL REGISTRATION-: URL: http://www.clinicaltrials.gov. Unique identifier: NCT01347216.
机译:背景技术:近30年以来,特发性肺动脉高压(IPAH)患者被推荐抗凝治疗。但是,支持证据有限,目前尚不清楚该建议在现代管理时代是否仍然合理,是否应将其扩展至其他形式的肺动脉高压(PAH)患者。方法和结果-:我们分析了新近开展的欧洲肺动脉高压注册肺动脉高压疗法(COMPERA)的比较性,前瞻性注册数据。通过使用抗凝剂比较了IPAH和其他形式的PAH患者的生存率。该样本由1283名连续入组的新诊断为PAH的患者组成。 800例IPAH患者中有66%使用抗凝治疗,483例其他形式的PAH患者中有43%使用抗凝治疗。与从未接受抗凝治疗的患者相比,接受抗凝治疗的IPAH患者的3年生存率(P = 0.006)明显更高,尽管抗凝治疗组的患者在基线时的病情更为严重。在n = 336 IPAH患者的配对研究中,3年生存率差异具有统计学意义(P = 0.017)。 Cox多变量回归分析证实了抗凝治疗对IPAH患者生存的有益作用(危险比0.79; 95%置信区间0.66-0.94)。相反,抗凝剂的使用与其他形式的PAH患者的生存获益无关。结论-:目前的数据表明,抗凝药物的使用与IPAH患者的生存获益相关,支持当前的治疗建议。对于其他形式的PAH,证据尚无定论。临床试验注册-:URL:http://www.clinicaltrials.gov。唯一标识符:NCT01347216。

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