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先天性心脏病的球囊血管成形术。

Balloon angioplasty in congenital heart disease.

作者信息

Tynan M

机构信息

Department of Paediatric Cardiology, United Medical School, Guy's Hospital, London.

出版信息

Herz. 1988 Apr;13(2):59-70.

PMID:2967794
Abstract

Balloon angioplasty and valvuloplasty offer an alternative to surgery in many congenital cardiac conditions and are a useful adjunct in others. To yield optimal results, the most desirable improvement in hemodynamics with the least amount of damage to normal tissue, choice of the catheter should take into consideration the size of the balloon, type of shaft and shape of the balloon. Experience has shown that dilatation is best achieved when the size of the balloon is such that there is a combination of circumferential force, the stress exerted when the balloon is near its maximal diameter, and longitudinal force, the extent of which is directly proportional to the deformity of the balloon. If the balloon is too small, little benefit may be accrued from the procedure; if it is too large, there is a risk of danger to adjacent normal structures. A stiff shaft helps to maintain a stable position during inflation and the size of the shaft determines the caliber of the guidewire lumen and the inflation/deflation lumen. A single, circular balloon has the advantage of distributing the dilating forces uniformly during inflation; more recently introduced alternative designs with two or three balloons mounted around the shaft have the advantage of allowing some blood flow to occur even at full inflation but they also have the theoretical disadvantage of not ensuring an even distribution of circumferential force. Dilatation of pulmonary valve stenosis may be considered indicated in the presence of a pressure gradient of 40 mm Hg with a right ventricular pressure of 60 mm Hg as the lower limit. In the newborn, this may be qualified by setting the lower limit of right ventricular pressure as 10 mm Hg below systemic arterial pressure if that is 60 mm Hg or less. On choice of the proper balloon size, approximately 20 to 30 percent greater than the pulmonary root, success may be expected in 90% of the cases and, in general, the initial result appears to be that which persists. Although Doppler echocardiography frequently shows pulmonary regurgitation, this is rarely clinically evident. The procedure is safe and only few complications have been reported. Establishing the indication for aortic valvuloplasty usually requires the presence of a systolic gradient of 60 mm Hg without severe regurgitation; mild aortic regurgitation is not a contraindication to the procedure. Reports have indicated good results in both infants and children. This procedure is not without risk and deaths have been reported.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

在许多先天性心脏病中,球囊血管成形术和瓣膜成形术为手术提供了一种替代方案,在其他一些疾病中也是一种有用的辅助手段。为了获得最佳效果,即实现最理想的血流动力学改善,同时对正常组织造成的损伤最小,导管的选择应考虑球囊大小、导管杆类型和球囊形状。经验表明,当球囊大小能使圆周力(球囊接近最大直径时施加的应力)和纵向力(其程度与球囊变形直接成正比)相结合时,扩张效果最佳。如果球囊太小,该操作可能获益甚微;如果太大,则有危及相邻正常结构的风险。硬导管杆有助于在充盈过程中保持稳定位置,导管杆的大小决定了导丝腔和充放气腔的内径。单个圆形球囊的优点是在充盈时能均匀分布扩张力;最近推出的在导管杆周围安装两个或三个球囊的替代设计,其优点是即使在完全充盈时也能允许一些血流通过,但理论上也有不能确保圆周力均匀分布的缺点。当肺动脉瓣狭窄存在40毫米汞柱的压力阶差,且右心室压力下限为60毫米汞柱时,可考虑进行肺动脉瓣扩张术。在新生儿中,如果体动脉压为60毫米汞柱或更低,则将右心室压力下限设定为比体动脉压低10毫米汞柱。选择合适的球囊大小,即比肺动脉根部大约大20%至30%,90%的病例可能会成功,一般来说,初始结果似乎会持续存在。虽然多普勒超声心动图经常显示肺动脉反流,但临床上很少明显。该操作是安全的,报告的并发症很少。确定主动脉瓣成形术的指征通常需要存在60毫米汞柱的收缩期压力阶差且无严重反流;轻度主动脉反流不是该操作的禁忌证。报告表明,该操作在婴儿和儿童中均有良好效果。此操作并非没有风险,也有死亡报告。(摘要截选至400字)

相似文献

1
Balloon angioplasty in congenital heart disease.先天性心脏病的球囊血管成形术。
Herz. 1988 Apr;13(2):59-70.
2
[Catheter therapy of congenital cardiovascular defects].[先天性心血管缺陷的导管治疗]
Vestn Rentgenol Radiol. 1995 Mar-Apr(2):16-26.
3
[Angioplasty and percutaneous valvuloplasty in congenital and acquired cardiopathies. Short- and long-term results].[先天性和后天性心脏病的血管成形术及经皮瓣膜成形术。短期和长期结果]
Arch Inst Cardiol Mex. 1988 Mar-Apr;58(2):145-58.
4
Transcatheter treatment of pulmonary stenosis and coarctation of the aorta: experience with percutaneous balloon dilatation.经导管治疗肺动脉狭窄和主动脉缩窄:经皮球囊扩张术的经验
Br Heart J. 1986 Sep;56(3):250-8. doi: 10.1136/hrt.56.3.250.
5
[Transluminal balloon valvuloplasty and aortoplasty in the treatment of congenital heart defects].[经腔球囊瓣膜成形术和主动脉成形术治疗先天性心脏缺陷]
Vestn Akad Med Nauk SSSR. 1989(10):40-6.
6
[Trefoil balloon, a new instrument for percutaneous valvuloplasty].[三叶球囊,一种用于经皮瓣膜成形术的新器械]
Schweiz Med Wochenschr. 1986 Nov 15;116(46):1617-20.
7
[Therapeutic effect of Cheatham-Platinum stent implantation for vessel stenosis associated with congenital heart disease in children and adolescents].[Cheatham-Platinum支架植入术治疗儿童及青少年先天性心脏病相关血管狭窄的疗效]
Zhonghua Er Ke Za Zhi. 2009 Apr;47(4):255-9.
8
[Percutaneous transluminal balloon valvuloplasty and balloon angioplasty in congenital heart defects with left heart obstruction in childhood].
Wien Klin Wochenschr. 1990 Aug 31;102(16):479-86.
9
Balloon valvuloplasty and angioplasty in congenital heart disease.先天性心脏病的球囊瓣膜成形术和血管成形术。
Br Heart J. 1985 Sep;54(3):285-9. doi: 10.1136/hrt.54.3.285.
10
Valvuloplasty with trefoil and bifoil balloons and the long sheath technique.采用三叶和双叶球囊及长鞘技术进行瓣膜成形术。
Herz. 1988 Feb;13(1):1-13.

引用本文的文献

1
Balloon pulmonary angioplasty: are we there yet? Lessons learned and unanswered questions.球囊肺血管成形术:我们做到了吗?吸取的经验教训与未解决的问题。
Breathe (Sheff). 2022 Dec;18(4):220217. doi: 10.1183/20734735.0217-2022. Epub 2023 Jan 10.
2
Balloon pulmonary angioplasty for chronic thromboembolic pulmonary hypertension.用于慢性血栓栓塞性肺动脉高压的球囊肺动脉血管成形术。
Am J Cardiovasc Dis. 2021 Jun 15;11(3):330-347. eCollection 2021.