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经皮腔内冠状动脉成形术期间对缺血心肌的保护

Protection of the ischemic myocardium during percutaneous transluminal coronary angioplasty.

作者信息

Zalewski A, Savage M, Goldberg S

机构信息

Department of Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania.

出版信息

Am J Cardiol. 1988 May 9;61(14):54G-60G. doi: 10.1016/s0002-9149(88)80033-x.

DOI:10.1016/s0002-9149(88)80033-x
PMID:2896457
Abstract

Therapeutic balloon coronary angioplasty provides a useful model for studying the effects of epicardial coronary artery occlusion in conscious humans. In addition, it is a potent model in which the effectiveness of interventions designed to ameliorate ischemia can be evaluated. Whereas intravenous beta-adrenergic blocking drugs and nitrates appear to have a limited protective effect, the regional (i.e., intracoronary) use of beta-adrenergic blocking drugs and calcium antagonists seem more potent. Currently, coronary venous retroperfusion with arterial blood does not appear practical, and the intraaortic balloon is a useful adjunctive measure in relatively few patients undergoing percutaneous transluminal coronary angioplasty. In contrast, the direct anterograde delivery of oxygen-rich blood or fluorocarbons holds promise as a reliable means of providing local myocardial protection. If ischemia could be markedly reduced, percutaneous transluminal coronary angioplasty might be applied safely in more high-risk clinical settings. In addition, if prolonged balloon inflation could be performed, there might be an increase in primary success rate and possibly a reduction in restenosis rate.

摘要

治疗性球囊冠状动脉成形术为研究清醒人体心外膜冠状动脉闭塞的影响提供了一个有用的模型。此外,它还是一个有力的模型,在该模型中可以评估旨在改善缺血的干预措施的有效性。虽然静脉注射β-肾上腺素能阻滞剂和硝酸盐似乎具有有限的保护作用,但局部(即冠状动脉内)使用β-肾上腺素能阻滞剂和钙拮抗剂似乎更有效。目前,用动脉血进行冠状静脉逆行灌注似乎不切实际,主动脉内球囊在接受经皮腔内冠状动脉成形术的相对较少患者中是一种有用的辅助措施。相比之下,直接顺行输送富氧血液或氟碳化合物有望成为提供局部心肌保护的可靠手段。如果缺血能够显著减少,经皮腔内冠状动脉成形术可能可以在更多高风险临床情况下安全应用。此外,如果能够进行长时间的球囊充盈,可能会提高一次成功率,并有可能降低再狭窄率。

相似文献

1
Protection of the ischemic myocardium during percutaneous transluminal coronary angioplasty.经皮腔内冠状动脉成形术期间对缺血心肌的保护
Am J Cardiol. 1988 May 9;61(14):54G-60G. doi: 10.1016/s0002-9149(88)80033-x.
2
Prevention of ischemia during percutaneous transluminal coronary angioplasty by transcatheter infusion of oxygenated Fluosol DA 20%.经导管输注20%氧合全氟三丙胺乳剂预防经皮腔内冠状动脉成形术期间的局部缺血。
Circulation. 1986 Sep;74(3):555-62. doi: 10.1161/01.cir.74.3.555.
3
Distal coronary artery perfusion during percutaneous transluminal coronary angioplasty.经皮腔内冠状动脉成形术期间的冠状动脉远端灌注。
Am Heart J. 1985 Oct;110(4):720-6. doi: 10.1016/0002-8703(85)90448-x.
4
Reduction of myocardial ischemia during percutaneous transluminal coronary angioplasty with oxygenated Fluosol.使用含氧全氟三丙胺在经皮腔内冠状动脉成形术期间减少心肌缺血
Am J Cardiol. 1990 Aug 1;66(3):279-84. doi: 10.1016/0002-9149(90)90836-p.
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Effects of intracoronary infusion of arterial blood or Fluosol-DA 20% on regional myocardial metabolism and function during brief coronary artery occlusions.冠状动脉内输注动脉血或20%氟碳化合物对短暂冠状动脉闭塞期间局部心肌代谢和功能的影响。
Circulation. 1987 Feb;75(2):473-81. doi: 10.1161/01.cir.75.2.473.
6
Protection against ischemia during prolonged balloon inflation by distal coronary perfusion with use of an autoperfusion catheter or Fluosol.
J Am Coll Cardiol. 1992 Nov 15;20(6):1378-84. doi: 10.1016/0735-1097(92)90251-h.
7
[Protection against ischemic damage during percutaneous coronary angioplasty].经皮冠状动脉腔内血管成形术期间对缺血性损伤的防护
Cardiologia. 1991 Dec;36(12 Suppl 1):215-20.
8
Preservation of left ventricular ejection fraction during percutaneous transluminal coronary angioplasty by distal transcatheter coronary perfusion of oxygenated Fluosol DA 20%.通过经导管向冠状动脉远端灌注20%含氧全氟三丙胺乳剂,在经皮腔内冠状动脉成形术期间保存左心室射血分数。
Am Heart J. 1988 Jun;115(6):1156-64. doi: 10.1016/0002-8703(88)90002-6.
9
Does intracoronary infusion of Fluosol-DA 20% prevent left ventricular diastolic dysfunction during coronary balloon angioplasty?冠状动脉内输注20%全氟萘烷能否预防冠状动脉球囊血管成形术期间的左心室舒张功能障碍?
J Am Coll Cardiol. 1990 Oct;16(4):959-66. doi: 10.1016/s0735-1097(10)80349-3.
10
Arterial blood infusion for myocardial protection during percutaneous transluminal coronary angioplasty.经皮腔内冠状动脉成形术期间用于心肌保护的动脉血灌注
Eur Heart J. 1987 Apr;8(4):340-6. doi: 10.1093/oxfordjournals.eurheartj.a062283.