• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[治疗肺动脉高压的特效药物——现状]

[Specific drugs for the treatment of pulmonary arterial hypertension - current status].

作者信息

Stähler G

机构信息

Medizinische Klinik I Pneumologie, Klinik Löwenstein.

出版信息

Dtsch Med Wochenschr. 2008 Oct;133 Suppl 6:S183-6. doi: 10.1055/s-0028-1091234. Epub 2008 Sep 23.

DOI:10.1055/s-0028-1091234
PMID:18814092
Abstract

For some years drugs of several different classes have been available in Germany for the treatment of pulmonary arterial hypertension (PHT): prostanoids, endothelin-receptor antagonists and phosphodiesterase inhibitors. To-date all relevant studies have consistently shown improvement in the 6-minute walking test (Iloprost, Treprostinil, Bosentan, Sitaxentan, Ambrisentan, Sildenafil). Results have not been consistent when the end-point has been an improvement in New York Heart Association (NYHA) class III or in the time to clinical worsening. Despite the good safety data for all drugs approved in Germany in the treatment of PHT, there are some clinically relevant interactions and significant contraindications. The availability of several options demands a detailed knowledge of studies to optimize safety and success in the treatment of PHT. Placebo-control mortality studies are not available for ethical reasons for those drugs that have been approved in Germany. But cohort analyses using historical survival rates have demonstrated a impressive improvement in survival of patients with PHT. Although there has been great progress in the treatment of PHT, a cure of this grave disease is not yet possible.

摘要

多年来,德国已有几种不同类别的药物可用于治疗肺动脉高压(PHT):前列环素类、内皮素受体拮抗剂和磷酸二酯酶抑制剂。迄今为止,所有相关研究均一致表明6分钟步行试验有改善(依洛前列素、曲前列尼尔、波生坦、西他生坦、安立生坦、西地那非)。当终点为纽约心脏协会(NYHA)III级改善或临床恶化时间改善时,结果并不一致。尽管德国批准用于治疗PHT的所有药物都有良好的安全性数据,但仍存在一些临床相关的相互作用和重大禁忌证。有多种选择需要详细了解研究情况,以优化PHT治疗的安全性和成功率。由于伦理原因,德国已批准的那些药物没有安慰剂对照死亡率研究。但使用历史生存率的队列分析显示,PHT患者的生存率有显著提高。尽管PHT治疗取得了很大进展,但这种严重疾病仍无法治愈。

相似文献

1
[Specific drugs for the treatment of pulmonary arterial hypertension - current status].[治疗肺动脉高压的特效药物——现状]
Dtsch Med Wochenschr. 2008 Oct;133 Suppl 6:S183-6. doi: 10.1055/s-0028-1091234. Epub 2008 Sep 23.
2
[Endothelin receptor antagonists in the new European guidelines on pulmonary hypertension].[内皮素受体拮抗剂在欧洲肺动脉高压新指南中的应用]
Rev Mal Respir. 2010 Feb;27(2):103-5. doi: 10.1016/j.rmr.2009.12.007. Epub 2010 Jan 25.
3
Clinical and cost-effectiveness of epoprostenol, iloprost, bosentan, sitaxentan and sildenafil for pulmonary arterial hypertension within their licensed indications: a systematic review and economic evaluation.在其许可适应症范围内,依前列醇、伊洛前列素、波生坦、西他生坦和西地那非治疗肺动脉高压的临床和成本效益:系统评价和经济评估。
Health Technol Assess. 2009 Oct;13(49):1-320. doi: 10.3310/hta13490.
4
[Treatment of pulmonary arterial hypertension: endothelin-receptor antagonists].[肺动脉高压的治疗:内皮素受体拮抗剂]
Dtsch Med Wochenschr. 2006 Dec 8;131(49 Suppl 9):S308-10. doi: 10.1055/s-2006-957198.
5
An evidence-based approach to the management of pulmonary arterial hypertension.一种基于证据的肺动脉高压管理方法。
Curr Opin Cardiol. 2006 Jul;21(4):385-92. doi: 10.1097/01.hco.0000231410.07426.9b.
6
Ironic case of hepatic dysfunction following the global withdrawal of sitaxentan.西他生坦全球撤市后肝功能异常的罕见病例报告。
Intern Med J. 2012 Dec;42(12):1351-4. doi: 10.1111/imj.12007.
7
[Drug combination treatment for pulmonary arterial hypertension].[肺动脉高压的联合药物治疗]
Dtsch Med Wochenschr. 2006 Dec 8;131(49 Suppl 9):S330-3. doi: 10.1055/s-2006-957205.
8
[The treatment of idiopathic pulmonary artery hypertension and its relation to systemic scleroderma].[特发性肺动脉高压的治疗及其与系统性硬化症的关系]
Rev Med Interne. 2007 Dec;28 Suppl 4:S273-6. doi: 10.1016/j.revmed.2007.09.012. Epub 2007 Oct 8.
9
An evidence-based approach to the management of pulmonary arterial hypertension.
Curr Opin Cardiol. 2006 Sep;21(5):526; author reply 526-7. doi: 10.1097/01.hco.0000240592.44957.4b.
10
Oral therapies for the treatment of pulmonary arterial hypertension: a population-based cost-minimization analysis.用于治疗肺动脉高压的口服疗法:一项基于人群的成本最小化分析。
Appl Health Econ Health Policy. 2009;7(1):43-59. doi: 10.1007/BF03256141.

引用本文的文献

1
Perioperative management of patients with severe pulmonary hypertension in major orthopedic surgery: experience-based recommendations.重大骨科手术中重度肺动脉高压患者的围手术期管理:基于经验的建议
GMS Interdiscip Plast Reconstr Surg DGPW. 2015 Jan 14;4:Doc03. doi: 10.3205/iprs000062. eCollection 2015.
2
[Therapy of mild, but symptomatic pulmonary hypertension].[轻度但有症状的肺动脉高压的治疗]
Internist (Berl). 2009 Mar;50(3):374-6. doi: 10.1007/s00108-009-2333-y.