• 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

法洛四联症合并肺动脉闭锁及主要体肺侧支血管的肺血管扩张剂治疗:病例系列及文献综述

Pulmonary vasodilator therapy in tetralogy of Fallot with pulmonary atresia and major aortopulmonary collaterals: case series and review of literature.

作者信息

Apostolopoulou Sotiria C, Vagenakis George, Rammos Spyridon

机构信息

Department of Pediatric Cardiology,Onassis Cardiac Surgery Center,Athens,Greece.

出版信息

Cardiol Young. 2017 Nov;27(9):1861-1864. doi: 10.1017/S1047951117001548. Epub 2017 Aug 8.

DOI:10.1017/S1047951117001548
PMID:28786367
Abstract

We present the use of pulmonary vasodilators in three adult patients with unrepaired tetralogy of Fallot, pulmonary atresia, aortopulmonary collaterals, and segmental pulmonary arterial hypertension. Patients improved by 1-2 NYHA classes with modest exercise-tolerance increase, and remained stable without side effects during 2.5, 10, and 14 years. Literature review revealed five studies with pulmonary vasodilators in heterogeneous, mostly repaired patient populations.

摘要

我们展示了肺血管扩张剂在三名患有未经修复的法洛四联症、肺动脉闭锁、主肺动脉侧支和节段性肺动脉高压的成年患者中的应用。患者的纽约心脏协会(NYHA)心功能分级改善了1 - 2级,运动耐量有适度增加,并且在2.5年、10年和14年期间保持稳定,没有出现副作用。文献综述显示,有五项关于肺血管扩张剂在异质性患者群体(大多数为已修复患者)中的研究。

相似文献

1
Pulmonary vasodilator therapy in tetralogy of Fallot with pulmonary atresia and major aortopulmonary collaterals: case series and review of literature.法洛四联症合并肺动脉闭锁及主要体肺侧支血管的肺血管扩张剂治疗:病例系列及文献综述
Cardiol Young. 2017 Nov;27(9):1861-1864. doi: 10.1017/S1047951117001548. Epub 2017 Aug 8.
2
Efficacy of bosentan therapy for segmental pulmonary artery hypertension due to major aortopulmonary collateral arteries in children.
Int J Cardiol. 2012 Nov 1;161(1):e1-3. doi: 10.1016/j.ijcard.2012.03.021. Epub 2012 Mar 28.
3
Use of Pulmonary Hypertension Medications in Patients with Tetralogy of Fallot with Pulmonary Atresia and Multiple Aortopulmonary Collaterals.肺动脉高压药物在法洛四联症合并肺动脉闭锁及多发主肺动脉侧支患者中的应用
Pediatr Cardiol. 2016 Feb;37(2):304-12. doi: 10.1007/s00246-015-1278-2. Epub 2015 Oct 28.
4
Sildenafil therapy in complex pulmonary atresia with pulmonary arterial hypertension.西地那非治疗复杂型肺动脉闭锁伴肺动脉高压。
Int J Cardiol. 2008 Oct 13;129(3):339-43. doi: 10.1016/j.ijcard.2007.08.016. Epub 2007 Nov 14.
5
Bosentan improves exercise tolerance and Tei index in patients with pulmonary hypertension and prostanoid therapy.波生坦可改善肺动脉高压患者接受前列环素治疗时的运动耐量和Tei指数。
Chest. 2005 Aug;128(2):709-13. doi: 10.1378/chest.128.2.709.
6
Treatment of segmental pulmonary artery hypertension in adults with congenital heart disease.成人先天性心脏病节段性肺动脉高压的治疗。
Int J Cardiol. 2013 Mar 20;164(1):106-10. doi: 10.1016/j.ijcard.2011.06.084. Epub 2011 Jul 18.
7
[Angiographic study of pulmonary circulation in tetralogy of Fallot with pulmonary atresia].[法洛四联症合并肺动脉闭锁的肺循环血管造影研究]
Arq Bras Cardiol. 2005 Feb;84(2):130-6. doi: 10.1590/s0066-782x2005000200007. Epub 2005 Mar 8.
8
Combination therapy with bosentan and sildenafil in idiopathic pulmonary arterial hypertension.波生坦与西地那非联合治疗特发性肺动脉高压
Eur Respir J. 2004 Dec;24(6):1007-10. doi: 10.1183/09031936.04.00051104.
9
Pulmonary reperfusion injury after the unifocalization procedure for tetralogy of Fallot, pulmonary atresia, and major aortopulmonary collateral arteries.法洛四联症、肺动脉闭锁和主肺动脉侧支血管的单灶化手术后的肺再灌注损伤。
J Thorac Cardiovasc Surg. 2012 Jul;144(1):184-9. doi: 10.1016/j.jtcvs.2011.12.030. Epub 2012 Jan 12.
10
Successful percutaneous recanalization of thrombosed major aortopulmonary collateral artery in palliated tetralogy of fallot with pulmonary atresia.成功对法洛四联症合并肺动脉闭锁姑息治疗中血栓形成的主要体肺侧支动脉进行经皮再通。
Congenit Heart Dis. 2013 Sep-Oct;8(5):E149-52. doi: 10.1111/j.1747-0803.2012.00715.x. Epub 2012 Sep 12.

引用本文的文献

1
Estimating pulmonary arterial remodeling via an animal-specific computational model of pulmonary artery stenosis.通过肺动脉狭窄的动物特异性计算模型评估肺动脉重塑。
Biomech Model Mechanobiol. 2024 Oct;23(5):1469-1490. doi: 10.1007/s10237-024-01850-6. Epub 2024 Jun 25.
2
Unique Pulmonary Hypertensive Vascular Diseases Associated with Heart and Lung Developmental Defects.与心肺发育缺陷相关的独特肺动脉高压性血管疾病。
J Cardiovasc Dev Dis. 2023 Aug 3;10(8):333. doi: 10.3390/jcdd10080333.
3
Macitentan in the Young-Mid-term Outcomes of Patients with Pulmonary Hypertensive Vascular Disease treated in a Pediatric Tertiary Care Center.
马西替坦治疗儿科三级护理中心肺动脉高压血管病患者的中短期疗效。
Paediatr Drugs. 2023 Jul;25(4):467-481. doi: 10.1007/s40272-023-00573-y. Epub 2023 Jun 3.
4
Long-term course of pulmonary arterial hypertension in adults with congenital heart disease under targeted therapy: a retrospective analysis of a single tertiary center.先天性心脏病成人患者在靶向治疗下肺动脉高压的长期病程:一项单中心三级医院的回顾性分析
Cardiovasc Diagn Ther. 2022 Oct;12(5):655-670. doi: 10.21037/cdt-22-266.
5
Segmental Pulmonary Hypertension in Children with Congenital Heart Disease.先天性心脏病患儿的节段性肺动脉高压
Medicina (Kaunas). 2020 Sep 24;56(10):492. doi: 10.3390/medicina56100492.
6
Association of Preoperative Mixed Venous Oxygen Saturation with Postoperative Segmental Pulmonary Hypertension in Pulmonary Atresia with Ventricular Septal Defect and Major Aortopulmonary Collaterals.室间隔缺损、主-肺动脉侧支循环的肺动脉闭锁患者术前混合静脉血氧饱和度与术后节段性肺动脉高压的相关性
Pediatr Cardiol. 2020 Dec;41(8):1689-1696. doi: 10.1007/s00246-020-02428-6. Epub 2020 Jul 24.
7
Definition and Management of Segmental Pulmonary Hypertension.节段性肺动脉高压的定义与管理
J Am Heart Assoc. 2018 Jul 4;7(14):e008587. doi: 10.1161/JAHA.118.008587.