Literature DB >> 8222098

Excimer laser coronary angioplasty of aorto-ostial stenoses. Results of the excimer laser coronary angioplasty (ELCA) registry in the first 200 patients.

N L Eigler1, B Weinstock, J S Douglas, T Goldenberg, G Hartzler, D Holmes, M Leon, J Margolis, M Nobuyoshi, W O'Neill.   

Abstract

BACKGROUND: Percutaneous transluminal coronary angioplasty (PTCA) of aorto-ostial stenosis has been associated with a lower rate of acute success, a high risk of vessel closure, and late restenosis. The purpose of this report is to document a prospective multicenter trial of excimer laser coronary angioplasty (ELCA) of aorto-ostial stenosis involving the coronary arteries and saphenous vein grafts. METHODS AND
RESULTS: Between December 1989 and May 1992, 206 aorto-ostial ELCA procedures were performed on 209 stenoses in 200 patients. Canadian Cardiovascular Society class III or IV angina was present in 76%. The distribution of stenosis locations was left main coronary (LM) in 26 (12%), right coronary (RCA) in 124 (59%), and vein grafts (VG) in 59 (28%). Adjunctive PTCA was performed in 72%. Procedure success defined as < or = 50% diameter stenosis without major complications was achieved in 90% (LM, 92%; RCA, 89%, VG, 90%). Quantitative angiographic analysis documented an improvement in stenosis diameter from 0.8 +/- 0.5 mm or 76 +/- 14% at baseline to 2.1 +/- 0.6 mm or 36 +/- 15% at completion (P < .01). The majority of the acute gain in diameter (1.0 +/- 0.6 mm) resulted from ELCA. A major complication during hospitalization occurred in 3.9% (death, 0%; Q-wave myocardial infarction, 0.5%; bypass surgery, 3.4%). The only logistic regression univariate and multivariate predictor of procedure failure was female gender. Six-month angiographic follow-up, available in 51% of eligible patients, documented an average lumen diameter of 1.7 +/- 1.0 mm and mean diameter stenosis of 46 +/- 26%. Restenosis (> 50% diameter stenosis) occurred in 39% (LM, 64%; RCA, 35%; VG, 35%). Restenosis was less likely when residual stenosis was < or = 35% (28% versus 53%, P < .05). Clinical events at follow-up were death, 2.7%; bypass surgery, 6.5%; myocardial infarction, 2.2%; and repeat angioplasty, 16.2%. Of the remainder, 78% were asymptomatic, class I or II for anginal symptoms. An adverse event during follow-up was more than twice as likely in the group with LM (50.0% versus 21.1%, P < .02).
CONCLUSIONS: ELCA is acutely effective and safe therapy in patients with aorto-ostial stenosis. Six-month restenosis, adverse-event rates were higher and functional status was poorer in the group with LM stenosis. ELCA may be considered as an alternative to bypass surgery in carefully selected patients with isolated aorto-ostial stenosis of the RCA and saphenous vein grafts.

Entities:  

Mesh:

Year:  1993        PMID: 8222098     DOI: 10.1161/01.cir.88.5.2049

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  5 in total

1.  Clinical impact of the gap-angle ratio in patients with ostial lesions of the right coronary artery undergoing percutaneous coronary intervention.

Authors:  Koichi Ohashi; Daisuke Abe; Norihiro Kuroki; Takao Yuba; Kou Suzuki
Journal:  Heart Vessels       Date:  2019-04-26       Impact factor: 2.037

Review 2.  Recent advances in cardiology.

Authors:  C S Lawson; D J Coltart
Journal:  Postgrad Med J       Date:  1994-04       Impact factor: 2.401

3.  Cutting balloon angioplasty and stenting for aorto-ostial lesions.

Authors:  A S Kurbaan; P A Kelly; U Sigwart
Journal:  Heart       Date:  1997-04       Impact factor: 5.994

4.  Excimer laser debulking for percutaneous coronary intervention in left main coronary artery disease.

Authors:  On Topaz; Pritam R Polkampally; Pramod K Mohanty; Maged Rizk; Julie Bangs; Nelson L Bernardo
Journal:  Lasers Med Sci       Date:  2009-02-24       Impact factor: 3.161

Review 5.  The invasive management of angina: issues for consumers and commissioners.

Authors:  D Gunnell; I Harvey; L Smith
Journal:  J Epidemiol Community Health       Date:  1995-08       Impact factor: 3.710

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.