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波生坦治疗无法手术的慢性血栓栓塞性肺动脉高压的长期疗效。

Long-term efficacy of bosentan in inoperable chronic thromboembolic pulmonary hypertension.

机构信息

Department of Cardiology, St Antonius Hospital, Nieuwegein, the Netherlands.

出版信息

Neth Heart J. 2009 Sep;17(9):329-33. doi: 10.1007/BF03086278.

DOI:10.1007/BF03086278
PMID:19949474
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2758347/
Abstract

UNLABELLED

Background. Inoperable chronic thromboembolic pulmonary hypertension (CTEPH) is associated with a poor survival.Objectives. To evaluate the long-term response to a dual endothelin receptor antagonist in patients with inoperable CTEPH.Methods. All consecutive 18 patients (mean age 63+/-14 years) treated with bosentan for symptomatic inoperable CTEPH were included. Efficacy was evaluated by the log value of serum levels of N-terminal-pro brain natriuretic peptide (log NTpro BNP), New York Heart Association functional class (NYHA), and the six-minute walk test (6-MWT). All follow-up data (median 31 months) were compared with baseline and divided into: short-term (<12 months), mid-term (between 12 and 24 months), and long-term follow-up (>24 months).Results. At baseline, 15 patients were in NYHA class III and three in NYHA class IV, mean log NT-pro BNP level was 7.2+/-1.4 log pg/ml, and mean 6-MWT distance was 404+/-125 m. During short-term follow-up (n=18), the NYHA class improved (p=0.001), 6-MWT distance increased by 33 m (p=0.03), and log NT-pro BNP decreased to 6.9+/-1.4 log pg/ml (p=0.007). During mid-term follow-up (n=17), the NYHA class improved (p<0.001), the mean 6-MWT distance increased by 41 m (p=0.01), and log NT-pro BNP was 6.9+/-1.4 log pg/ml (p=0.31). During late followup (n=14) the NYHA class was still improved (p=0.03), the 6-MWT distance decreased by 9 m (p=0.73), and log NT-pro BNP was 7.1+/-1.5 log pg/ml (p=0.91). The overall four year survival rate was 88%.

CONCLUSION

Bosentan seems to be effective during long-term treatment in patients with inoperable CTEPH. (Neth Heart J 2009;17:329-33.).

摘要

背景

无法手术的慢性血栓栓塞性肺动脉高压(CTEPH)与较差的生存相关。

目的

评估双重内皮素受体拮抗剂在无法手术的 CTEPH 患者中的长期疗效。

方法

所有连续的 18 例因 CTEPH 症状而接受波生坦治疗的无法手术的患者(平均年龄 63+/-14 岁)均被纳入本研究。通过血清 N 末端前脑利钠肽(NTpro BNP)的对数、纽约心脏协会功能分级(NYHA)和 6 分钟步行试验(6-MWT)来评估疗效。所有随访数据(中位数 31 个月)均与基线进行比较,并分为短期(<12 个月)、中期(12-24 个月)和长期(>24 个月)随访。

结果

基线时,15 例患者为 NYHA 心功能 III 级,3 例为 NYHA 心功能 IV 级,平均 log NTpro BNP 水平为 7.2+/-1.4 log pg/ml,平均 6-MWT 距离为 404+/-125 m。在短期随访(n=18)中,NYHA 心功能分级改善(p=0.001),6-MWT 距离增加 33 m(p=0.03),log NTpro BNP 降低至 6.9+/-1.4 log pg/ml(p=0.007)。在中期随访(n=17)中,NYHA 心功能分级改善(p<0.001),6-MWT 距离增加 41 m(p=0.01),log NTpro BNP 为 6.9+/-1.4 log pg/ml(p=0.31)。在晚期随访(n=14)中,NYHA 心功能仍在改善(p=0.03),6-MWT 距离下降 9 m(p=0.73),log NTpro BNP 为 7.1+/-1.5 log pg/ml(p=0.91)。4 年总生存率为 88%。

结论

波生坦在无法手术的 CTEPH 患者的长期治疗中似乎是有效的。(荷兰心脏杂志 2009;17:329-33.)

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