CJA
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text (PDF)
Right arrow Submit a scholarly reply
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by REVES, J. G.
Right arrow Articles by CARTER, M. R.
Right arrow Search for Related Content
PubMed
Right arrow Articles by REVES, J. G.
Right arrow Articles by CARTER, M. R.

Canadian Journal of Anesthesia, Vol 27, 238-247, Copyright © 1980 by Canadian Anesthesiologists' Society

Myocardial Damage in Coronary Artery Bypass Surgical Patients Anaesthetized with two Anaesthetic Techniques: A Random Comparison of Halothane and Enflurane

J. G. REVES 1, PAUL N. SAMUELSON 1, WILLIAM A. LELL 1, HUEY G. McDANIEL 1, NICHOLAS T. KOUCHOUKOS 1, WILLIAM J. ROGERS 1, LLOYD R. SMITH 2, and MICHAEL R. CARTER 1

1 The University of Alabama Medical Center, Birmingham, Alabama 35294
2 Clinical Cardiovascular Computer Center, The University of Alabama Medical Center, Birmingham, Alabama 35294

Fifty patients with ischaemic heart disease scheduled for coronary artery bypass surgery received either an enflurane or a halothane anaesthetic. The anaesthetic techniques were randomly assigned to the patients and consisted of induction with diazepam 0.5 mg·kg-1 and pancuronium 0.1 mg·kg-1 supplemented by nitrous oxide and oxygen (50:50). Enflurane in dosages of 0.5-1.5 volumes per cent and halothane 0.3-0.7 volumes per cent were administered to Group E (25 patients) and Group H (25 patients), respectively. The inhalation drug dosage was varied to maintain heart rate and systemic blood pressure within predetermined limits.

The two patient groups (E and H) were compared with regard to myocardial damage (determined electrocardiographically and enzymatically) as well as by haemodynamic changes and adjuvant cardiovascular drug therapy. One patient in group H sustained a postoperative infarction detected by electrocardiogram and sustained CK MB release. There was no other unequivocal electrocardiographic evidence of myocardial infarction in either group and the myocardial damage estimated from CK MB curves was remarkably low and similar in both anaesthetic groups. Myocardial damage was estimated by CK MB maximum release (CK MB MAX) of 8.1 ± 1.00 IU/1 (Group E), 7.8 ± 1.32IU/I (Group H), by area under the CK MB disappearance curve (CK MB AREA) of 144 ± 21.9 IU/1 x hr (Group E), 173 ± 32.9 IU/1 x hr (Group H), and by the accumulated CK MB or CK MB damage size (CK MB DS) of 10.5 ± 1.79 IU/1 (Group E), 10.3 ± 2.26 IU/1 (Group H). There was no release of CK MB before cardiopulmonary bypass in either group. There was no statistically significant difference between the two groups for myocardial damage, haemodynamics or adjuvant drug interventions. There was a trend toward greater use of vasodilators in Group H than in Group E.

It is concluded that enflurane and halothane are associated with equally low levels of myocardial damage when used for anaesthesia in patients with ischaemic heart disease. The release of CK MB occurred following cardiopulmonary bypass and probably represents imperfect myocardial preservation. Patients with severely impaired ventricular function were not studied, and in these patients enflurane and halothane must be used judiciously.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1980 by the Canadian Anesthesiologists' Society.