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首页> 外文期刊>BMC Pulmonary Medicine >Changes in REVEAL risk score in patients with pulmonary arterial hypertension treated with macitentan in clinical practice: results from the PRACMA study
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Changes in REVEAL risk score in patients with pulmonary arterial hypertension treated with macitentan in clinical practice: results from the PRACMA study

机译:临床实践中肺动脉高血压治疗肺动脉高血压患者揭示风险评分的变化:PRACMA研究的结果

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摘要

Macitentan is a dual endothelin receptor antagonist indicated for the long-term treatment of pulmonary arterial hypertension (PAH). We evaluated the change over time in REVEAL risk score in incident and prevalent patients receiving macitentan for the first time. Retrospective, observational study including adult patients with idiopathic/heritable PAH or PAH associated with connective tissue disorders or congenital heart disease treated with macitentan for ≥6-month follow-up in Spain. The REVEAL risk score and risk strata were computed at the start of macitentan and after ≥6-month in patients with ≥7 out of 12 valid REVEAL components. Overall, 81 patients (57 for the REVEAL score) were analysed, 77.8% women. The mean age was 57.2?years and 50.6% of patients had idiopathic/heritable PAH. Prevalent patients were 59.3 and 40.7% were incident. Main therapies for PAH included macitentan monotherapy (42.0%) and macitentan in combination with phosphodiesterase type 5 inhibitor (44.4%). With a median time of macitentan treatment of 10.5?months, the mean REVEAL score was 8.7 points at baseline and was 7.2 points after ≥6-month follow-up. The mean change (95% CI) in REVEAL risk score was ??1.4 (??2.0, ??0.9) points (p??0.0001), being ??1.8 (??3.0, ??0.7) points (p?=?0.0040) and???1.2 (??1.8, ??0.5) points (p?=?0.0010), in incident and prevalent patients, respectively. The reduction was also significant by risk stratum (36.8% of patients in the high-very high risk strata at baseline versus 14.0% after ≥6-month, p??0.05) and therapy group. The REVEAL components that significantly improved were WHO functional class (FC) (63.9% FC III at macitentan initiation and 23.6% after ≥6-month, p??0.0001), 6-min walk test (mean change: 41.8?m, p??0.01), brain natriuretic peptide (BNP) or N-terminal proBNP (NT-proBNP) (mean change of ??157.6?pg/mL and???530.0?pg/mL, respectively, p??0.05 both), and pulmonary vascular resistance (PVR) (mean change: ??3.4 WU, p??0.01). In this study, treatment with macitentan improved the REVEAL risk strata and score in both incident and prevalent PAH patients, and in all patients regardless of the therapy strategy. Macitentan significantly improved some of REVEAL components including WHO FC, BNP/NT-proBNP, PVR, and 6-min walk test after at least 6-month follow-up.
机译:美西特田为肺动脉高血压(PAH)的长期治疗所指示的双重内皮素受体拮抗剂。我们评估了随着时间的推移REVEAL风险评分在事件和流行的患者接受马西首次变化。回顾性,观察性研究包括成人患者与马西治疗≥6个月随访西班牙结缔组织疾病或先天性心脏疾病有关的先天性/遗传PAH或PAH。揭密风险分数和风险阶层都在马西开始计算,并在患者≥7出12有效REVEAL组件后≥6个月。总体而言,81例(57分揭密)进行了分析,77.8%为女性。平均年龄为57.2?岁的患者50.6%有先天性/遗传PAH。普遍的患者为59.3和40.7%的事件。对于PAH主要治疗包括美西特田单一疗法(42.0%)和美西特田结合5型磷酸二酯酶抑制剂(44.4%)。 10.5?个月马西治疗的中位时间,平均得分REVEAL在基线8.7点,为≥6个月随访7.2分。在REVEAL风险得分的平均变化(95%CI)为1.4 ??(?? 2.0,?? 0.9)点(p <??0.0001),被?? 1.8(?? 3.0,?? 0.7)点(p ?=?0.0040)和??? 1.2(?? 1.8,?? 0.5)点(p =?0.0010),在入射和普遍的患者,分别。的减少是由也风险层(患者在≥6月后在基线高非常高的风险地层与14.0%36.8%,P <??0.05)和治疗组显著。的显示,显著改进组分是WHO功能类(FC)(63.9%FC III在美西特田起始和≥6个月,P <0.0001后23.6%?),6分钟步行测试(平均变化:41.8米, p'<?0.01),脑利钠肽(BNP)或N端proBNP的(NT-proBNP水平)(?? 157.6?pg / mL至??? 530.0?皮克/毫升,分别,p <?的平均变化? 0.05两者),和肺血管阻力(PVR)(平均变化:?? 3.4 WU,p <0.01)?。在这项研究中,与马西治疗好转揭密风险阶层,在这两个事件和流行PAH患者得分,并且在不考虑治疗策略的所有患者。后马西显著改善一些REVEAL组件,包括WHO FC,BNP / NT-proBNP水平,PVR,和6分钟步行试验至少6个月的随访。

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