先天性心脏病并发重度肺动脉高压介入封堵联合伐地那非的应用研究

卢荔红, 关瑞锦, 吴志勇, 等. 先天性心脏病并发重度肺动脉高压介入封堵联合伐地那非的应用研究[J]. 临床心血管病杂志, 2012, 28(7): 514-517. doi: 10.13201/j.issn.1001-1439.2012.07.003
引用本文: 卢荔红, 关瑞锦, 吴志勇, 等. 先天性心脏病并发重度肺动脉高压介入封堵联合伐地那非的应用研究[J]. 临床心血管病杂志, 2012, 28(7): 514-517. doi: 10.13201/j.issn.1001-1439.2012.07.003
LU Lihong, GUAN Ruijin, WU Zhiyong, et al. Intervention and vardenafil combination therapy in congenital heart disease with severe pulmonary hyperten[J]. J Clin Cardiol, 2012, 28(7): 514-517. doi: 10.13201/j.issn.1001-1439.2012.07.003
Citation: LU Lihong, GUAN Ruijin, WU Zhiyong, et al. Intervention and vardenafil combination therapy in congenital heart disease with severe pulmonary hyperten[J]. J Clin Cardiol, 2012, 28(7): 514-517. doi: 10.13201/j.issn.1001-1439.2012.07.003

先天性心脏病并发重度肺动脉高压介入封堵联合伐地那非的应用研究

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    通讯作者: 卢荔红,E-mail:lulihong168@163.com
  • 中图分类号: R541.1

Intervention and vardenafil combination therapy in congenital heart disease with severe pulmonary hyperten

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  • 目的:研究先天性心脏病(CHD)并发重度肺动脉高压(PAH)介入封堵联合盐酸伐地那非综合治疗的应用。方法:术前、后常规给予29例患者口服盐酸伐地那非治疗,对有介入封堵适应证的患者置入封堵器进行试验性封堵测压,若肺动脉压降低幅度为原来压力的20%或下降30mmHg(1mmHg=0.133kPa)以上后进行永久封堵,术后继续采用超声多普勒心动图随访患者肺动脉收缩压(SPAP)、肺循环、体循环收缩压比值(Pp/Ps)、右室大小(RV)、左室射血分数(LVEF)12个月。结果:本组29例患者经术前、后常规予盐酸伐地那非治疗后,27例行介入试验性封堵测压,随后有25例肺动脉压降低幅度为原来压力的20%或下降30mmHg以上。对这25例患者进行永久封堵,且5例使用带孔封堵器,随访12个月,除1例死亡外,其余心功能恢复Ⅰ级以上、动脉血氧饱和度(SaO2)均恢复在0.95以上、SPAP、Pp/Ps、LVEF、RV均有显著改善(均P<0.05)。4例无法封堵的患者除1例转心外科手术后死亡外,其余心功能由Ⅳ级恢复到Ⅲ级、SaO2在0.90以上、动脉血氧分压>60mmHg。结论:介入试验性封堵联合盐酸伐地那非综合治疗微创、简便、安全、可靠,给CHD并发重度PAH的患者带来根治的希望。
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  • [1]

    JEFFERY T K,MORRE N W.Molecular and cellular basis of pulmonary vascular remondeling in pulmonary hypertension[J].Prog Cardiol Dis,2002,45:173-202.

    [2]

    RABIONOVITCH M.Cellular and molecular patho-biology of pulmonary hypertension conference summa-ry[J].Chest,2005,128(6supp1):642S-646S.

    [3]

    SIMONNEAU G,GALIE N,RUBIN L J,et al.Clini-cal classification of pulmonary hypertension[J].J Am Coll Cardiol,2004,43:S5-S12.

    [4]

    LEWIS J R.Therapy of pulmonary hypertension:the evolution from vasodilators to antiproliferative agents[J].Am J Reapir Crit Care Med,2002,166:1308-1309.

    [5]

    AD L,BIRK E,BARAK J,et al.A one-way valved atrial septalpatch:a new surgical technique and its clinical application[J].J Thorac Cardiovasc Surg,1996,111:841-848.

    [7]

    陈若为,游昕,马游,等.先天性心脏病合并重度肺动脉高压的手术适应证探讨[J].中华胸心血管外科杂志,2006,22(5):298-300.

    [7]

    代政学,张玉顺,贾国良,等.Amplatzer封堵器试验性关闭动脉导管未闭合并重度肺动脉高压的临床意义[J].第四军医大学学报,2001,22(21):1924-1926.

    [8]

    游昕,梁勇,钱维源,等.合并重度肺动脉高压的成人先天性心脏病手术回顾及中期随访[J].实用医学杂志,2010,26(6):1022-1024.

    [9]

    HISLOP A A.Treatment and survival in children with pulmonary arterial hypertension:the UK Pulmo-nary Hypertension Service for Children2001-2006[J].Heart,2009,95:312-317.

    [10]

    JING Z C,JIANG X,WA B X,et al.Vardenafil treatment for patients with pulmonary arterial hyper-tension:a multicentre,open-label study[J].Heart,2009,95:1531-1532.

    [11]

    BARST R J,GIBBSJ S,GHOFRANI H A,et al.Updated evidence-based treatment algorithm in pul-monary arterial hypertension[J].J Am Coll Cardiol,2009,54:S78-80.

    [12]

    CLAPP L H,FINNEY P,TURCATO S,et al.Dif-ferential efects of stable prostacyclin analogues on smooth muscle proliferation and cyclic AMP genera-tion in human pulmonary artery[J].Am J Respir Cell Mol Biol,2002,26:194-201.

    [13]

    D'ALTO M,ROMEO E,ARGIENTO P,et al.Pul-monary vasoreactivity predicts long-term outcome in patients with Eisenmenger syndrome receiving bosen-tan therapy[J].Heart,2010,96:1475-1478.

    [14]

    NING Y,STEPHANIE K,JUN Y,et al.Inhaled ni-tric oxide versus aerosol ized iloprost for the treatment of pulmonary hypertension with left heart disease[J].Crit Care Med,2009,37:980-982.

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出版历程
收稿日期:  2011-11-20
修回日期:  2012-01-07

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