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新型医学疗法时代小儿肺动脉高压患者的转归。

Outcome of pediatric patients with pulmonary arterial hypertension in the era of new medical therapies.

机构信息

Department of Pediatric Cardiology, University Medical Center Groningen, Groningen, The Netherlands.

出版信息

Am J Cardiol. 2010 Jul 1;106(1):117-24. doi: 10.1016/j.amjcard.2010.02.023.

Abstract

Little is known about the effects of "second-generation drugs" (prostanoids, endothelin receptor antagonists, 5-phosphodiesterase inhibitors) in children with pulmonary arterial hypertension (PAH). This study describes the outcome of a national cohort of children with PAH in an era when these drugs became available. From 1993 to 2008, 52 consecutive children with idiopathic PAH (n = 29) or systemic-to-pulmonary shunt-associated PAH (n = 23) underwent baseline and follow-up assessments. Treatment was initiated depending on functional class, acute pulmonary vasoreactivity response, and drug availability. Observed survival was evaluated depending on time of diagnosis in relation to second-generation drug availability and subsequently compared to calculated predicted survival. Children for whom second-generation drugs were available had improved survival compared to their predicted survival (1-, 3-, and 5-year survival rates 93%, 83%, and 66% vs 79%, 61%, and 50%, respectively). However, this improved survival was observed only in patients for whom second-generation drugs became available during their disease course. No improved survival was observed in patients for whom drugs were available already at diagnosis. Baseline variables associated with decreased survival included higher functional class, higher pulmonary-to-systemic arterial pressure ratio, lower cardiac index, and higher serum levels of N-terminal pro-brain natriuretic peptide and uric acid. After start of second-generation drugs, functional class, 6-minute walking distance, and N-terminal pro-brain natriuretic peptide improved but gradually decreased after longer follow-up. In conclusion, survival of pediatric PAH seemed improved since the introduction of second-generation drugs only in selected patients for whom these drugs became available during their disease course. Start of second-generation drugs initially induced clinical improvements, but these effects decreased after longer follow-up.

摘要

关于“第二代药物”(前列腺素、内皮素受体拮抗剂、5-磷酸二酯酶抑制剂)在肺动脉高压(PAH)儿童中的作用知之甚少。本研究描述了这些药物问世后,一个全国性 PAH 患儿队列的结局。1993 年至 2008 年,52 例特发性 PAH(n = 29)或体肺分流相关性 PAH(n = 23)患儿连续进行了基线和随访评估。根据功能分类、急性肺血管反应性和药物可及性开始治疗。观察到的生存率根据诊断时间与第二代药物可及性的关系进行评估,并与计算的预测生存率进行比较。有第二代药物可用的患儿的生存率较预测生存率有所提高(1、3、5 年生存率分别为 93%、83%和 66%,而预测生存率分别为 79%、61%和 50%)。然而,这种生存改善仅见于疾病过程中可用第二代药物的患者。在诊断时就有药物可用的患者未观察到生存改善。与生存率降低相关的基线变量包括更高的功能分类、更高的肺动脉压/体动脉压比值、更低的心指数以及更高的 N 末端脑钠肽前体和尿酸血清水平。开始使用第二代药物后,功能分类、6 分钟步行距离和 N 末端脑钠肽前体得到改善,但在更长的随访后逐渐下降。总之,自第二代药物问世以来,只有在疾病过程中可用这些药物的选定患者中,儿童 PAH 的生存率似乎有所提高。开始使用第二代药物会引起临床改善,但在更长的随访后这些效果会下降。

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