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European Heart Journal 1989 10(Supplement H):61-70; doi:10.1093/eurheartj/10.suppl_H.61
Copyright © 1989 by the European Society of Cardiology.
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© 1989 The European Society of Cardiology

Bilateral mammary artery surgery or percutaneous transluminal coronary angioplasty for multivessel coronary artery disease? An analysis of effects and Costs

E. Berreklouw, J. Hoogsteen*, R. van Wandelen, M. Verkroost, J. Schonberger, H. Bavinck, R. Michels*, H. Bonnier*, M. El Deeb*, M. El Gamal*, J. Wijnen**, M. Netelbeek{dagger}, G. Haan{dagger} and J. Vos{ddagger}

Catharina Hospital, Department of Cardiopulmonary surgery Eindhoven
* Catharina Hospital, Department of Cardiology Eindhoven
** Technical University Eindhoven, Department of Statistics Eindhoven
{dagger} University Maastricht, Department of Health Economics Maastricht
{ddagger} Erasmus University Rotterdam, Department of Clinical Epidemiology, Rotterdam The Netherlands

Address for correspondence: E. Berreklouw MD, Catharina Hospital, Department of Cardiopulmonary Surgery, Michelangelolaan 2, 5602 ZA Eindhoven, The Netherlands

Seventy-two patients with stable or unstable angina treated since 1983 by multivessel-PTCA(MVP) were retrospectively compared with 44 similar patients that were suitable for MVP, but who had undergone bilateral mammary artery (BIMA) surgery (and additional vein grafts in 60·5% of the patients) since 1986. Both groups were comparable (P = not significant [NS])for gender, age, most risk factors, objective ischaemia and left ventricular function; however, in the BIMA group there were more previous infarctions (P = 0·02), hypertension (P = 0·03), three-vessel disease (P = 0·0001), and less severe angina (P = 0·007). In the BIMA group, a mean of 3·1 (range 2-5) vessels were treated and in the MVP group 2·0 (range 2–3) vessels (P = 00001). Both groups were almost completely revascularized (NS). In 39·5% of the BIMA group, no veins were used and in 20·9% the BIMAs were used as sequential grafts. In-hospital mortality was comparable: 2·3% for BIMA and 1·4% for MVP, so were periprocedural infarctions (13·6% vs 8·3%), rethoracotomies (9·1% vs 0% ), emergency procedures (0% vs 5·7% ), low cardiac output (2·3% vs 5·6%) and other complications (18·2% vs 9·2%). The mean stay (days) on the ICU/CCU for BIMA was 2·3 and for MVP 1·6 (P = 0·005) and the mean hospital stay for BIMA 12·3 and for MVP 6·6 (P = 00001). The maximum and mean follow-up (months) of43 BIMA and 71 MVP hospital survivors was 35 vs 72 and9·5 vs 22·3 (P = 00001) with a late mortality of 0% and 4·2% (NS). MVP patients, including 12 with re-procedures, had more recurrent angina (17·7% vs 4·7%, P<005) and more often used anti-anginal medications (62·0% vs 18·6%, P<0000I). Late complications (excluding re-procedures) were comparable for MVP and BIMA (20% vs 9·3%, 4·4% vs 0%, 9·2% vs 14%). MVP patients had more re-hospitalizations (34 vs 5, P<0·0001), re-catheterizations (33% vs 2·3%, P<0·0001) and cardiac re-procedures (16 vs 0, P = 0·0006) than BIMA patients. Recurrent-angina-free survival at 1 year was 96% after BIMA and 64% after MVP (P<001). Event-free survival at 1 year was 86% after BIMA and 58% after MVP (P < 0·05).

Cost analysis revealed that MVP can initially be performed at half of the costs of BIMA, but the cost of M VP rises within 2 years to 67% of the cost of BIMA, due to re-procedures and the continued use of anti-anginal medications. Thus, the relationship between effects and costs of M VP might become equal to that of BIMA within 2 years, after which the results will probably be in favour of BIMA.

Key Words: Coronary bypass surgery • internal mammary artery • bilateral mammary artery bypass surgery • percutaneous transluminal coronary angioplasty • multivessel percutaneous transluminal coronary angioplasty • cost


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