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Clinical Science  |   February 1997
Perioperative Sympatholysis: Beneficial Effects of the alpha2-Adrenoceptor Agonist Mivazerol on Hemodynamic Stability and Myocardial Ischemia
Author Notes
  • McSPI-Europe Research Group*.
  • *See Appendix 1 for participating European centers and investigators, and Appendix 2 for other analysis investigators.
  • Received from the Departments of Anesthesiology, Cardiology, Surgery, Medicine, and Epidemiology and Biostatistics of the member centers of the McSPI-Europe Research Group, the Ischemia Research and Education Foundation (IREF), the San Francisco Veterans Affairs Medical Center, and the University of California, San Francisco, and Stanford University, Palo Alto, California. Submitted for publication December 8, 1995. Accepted for publication November 1, 1996. Supported by grants from UCB Pharma, Belgium, and the Ischemia Research and Education Foundation.
  • Dr. Mangano, as director of McSPI, assumes full responsibility for the integrity of the data and analyses.
  • Address reprint requests to Dr. Mangano: c/o McSPI-Europe, 250 Executive Park Boulevard, Suite 3400, San Francisco, California 94134.
Article Information
Clinical Science
Clinical Science   |   February 1997
Perioperative Sympatholysis: Beneficial Effects of the alpha2-Adrenoceptor Agonist Mivazerol on Hemodynamic Stability and Myocardial Ischemia
Anesthesiology 2 1997, Vol.86, 346-363. doi:
Anesthesiology 2 1997, Vol.86, 346-363. doi:
Of the 60 million patients a year who undergo noncardiac surgery in the United States, Canada, Europe, Australia, New Zealand, and Japan, [1,2] approximately 30% have, or are at risk of, coronary artery disease (CAD). Of these, 3 million have a serious adverse perioperative cardiac outcome-myocardial infarction (MI), cardiac death, unstable angina, heart failure, or life-threatening dysrhythmias. [1] These complications add approximately $40 billion annually to worldwide surgical health care costs. [3] 
Mangano DT, and colleagues [4] demonstrated that the single most important predictor of such adverse cardiac outcome is the occurrence of myocardial ischemia soon after surgery (i.e., within 48 h). Occurring in 41% of patients undergoing elective noncardiac surgery, ischemia is associated with a ninefold increase in the odds of having in-hospital cardiac death, nonfatal MI, or unstable angina. In addition, the risk of long-term (up to 2 yr) adverse cardiac outcomes increases twofold in patients with postoperative ischemia alone, and 14- to 20-fold in patients with postoperative MI or unstable angina. [5] 
The entire perioperative period is known to be stressful, characterized by complex and rapidly changing physiologic responses that may be poorly tolerated by patients with compromised circulation or poor left ventricular function. During, and particularly after, anesthesia and surgery, hypertension, tachycardia, and increased sympathetic activity are common occurrences. [1,6] These hyperdynamic cardiovascular responses adversely affect the balance between myocardial oxygen supply and demand, predisposing the vulnerable myocardium to ischemia.
Compounds with alpha-2 adrenoceptor agonist activity are reported to have sympatholytic, sedative, analgesic, and anxiolytic effects and attenuate the catecholamine response to perioperative stress. Therefore, alpha2-adrenoceptor agonists may prevent perioperative hyperdynamic changes, mitigating imbalances between myocardial oxygen supply and demand, and possibly reduce the incidence of myocardial ischemia. [7–9] 
Mivazerol (2-hydroxy-3 [1H-imidazole-4-methyl] benzamide hydrochloride) is a new alpha2-adrenoceptor agonist with a high affinity and a marked specificity for alpha2-adrenergic receptors. In animal studies, mivazerol blunts the surge in heart rate during emergence from halothane anesthesia, decreases basal norepinephrine concentrations, and reduces ischemia in animal models of coronary occlusion.* In clinical pharmacology studies, mivazerol decreases basal plasma levels of norepinephrine and, at higher doses, produces mild bradycardia, negative inotropic effects, and an early and transient increase in afterload.** In patients with stable angina undergoing a treadmill exercise tolerance test, mivazerol reduced ischemia and angina. [10] Most recently, in high-risk patients undergoing noncardiac surgery, a 24-patient dose-response trial demonstrated safety and tolerability.***
Based on the above, we conducted a multicenter phase II trial to investigate whether mivazerol could reduce the incidence of, and treatment for, tachycardia and hypertension in patients with, or at risk for, CAD who were undergoing vascular surgery and general anesthesia. We also determined the effect of mivazerol on the incidence and severity of perioperative myocardial ischemia, adverse clinical events, and anesthetic and analgesic requirements.
Materials and Methods
General Study Design
After institutional approval and informed consent were obtained, we enrolled 317 patients from 23 medical centers in 7 European countries (Table 8Appendix 1) between March and December 1993; analysis for the current study was completed in March 1996. The study was placebo-controlled, double-blind, and randomized with parallel groups using block randomization within each center to assign placebo or one of two doses of mivazerol to patients. For inclusion in the study, patients were required to be at least 21 yr old, to have CAD and normal renal function, and to be undergoing vascular surgery (excluding aortic surgery) that required general anesthesia for at least 1 h. Coronary artery disease was confirmed by the existence of any of the following conditions:(1) a history of either typical angina pectoris (as defined by the Canadian Heart Classification system [11]) or atypical angina with an ischemic (electrocardiographic, echocardiographic) response to exercise testing, or with scintigraphic evidence of myocardial perfusion defect;(2) a history of MI;(3) new Q wave on electrocardiogram typical of MI, with no history of MI; or (4) angiographic evidence of CAD. Patients were excluded from study if they:(1) had been taking alpha-methyl dopa, alpha2-agonists, or tricyclic antidepressants;(2) were in cardiogenic shock and had clinical signs of congestive heart failure or required chronic inotropic support for ventricular dysfunction;(3) had unstable angina or treated, uncontrolled hypertension;(4) had conduction defects that precluded electrocardiographic analysis of the ST segment;(5) were pregnant or of childbearing potential but not using reliable contraception; or (6) were American Society of Anesthesiologists physical status V.
Table 8. Appendix 1. Participating McSPI-EUROPE Medical Centers and Investigators
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Table 8. Appendix 1. Participating McSPI-EUROPE Medical Centers and Investigators
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The primary measures used to judge the efficacy of mivazerol and placebo were hemodynamic instability (tachycardia, hypertension) and the need for cardiovascular medications to treat instability in the first 24 h after surgery, and secondarily for the intraoperative and 24- to 72-h postoperative periods. Other secondary measures consisted of the incidence and severity of myocardial ischemia and the need for medications to treat ischemia. Safety was assessed by the occurrence of adverse clinical events and hemodynamic abnormalities (bradycardia, hypotension), and by the use of cardiovascular medications to treat these hemodynamic abnormalities.
Study Procedures
Preoperative Procedures.
The investigators gathered demographic and clinical data by taking a complete history and physical examination that included a neurologic examination and gathering information on previous and concurrent medications. Research data were obtained from measurement of hemodynamic variables and cardiac enzymes, and from ambulatory (Holter) and 12-lead electrocardiography. Preoperative cardiac medications were continued until the day of surgery. Premedication consisted of 5 mg diazepam given orally on the day of surgery.
Intraoperative Procedures and Administration of Mivazerol.
Anesthesia was induced by intravenous administration of sodium thiopental (as much as 5 mg/kg) and fentanyl (as much as 2 micro gram/kg). Anesthesia was maintained by continuous intravenous infusion of fentanyl (1 micro gram [center dot] kg-1[center dot] h-1) and isoflurane (end-tidal concentration of up to 2.0%). Vecuronium provided muscle relaxation. Systolic blood pressure (SBP) and heart rate (HR) were kept within 20% of preoperative baseline values by the use of cardiovascular drugs and prespecified changes in the anesthetic. The anesthetic concentration was first altered if necessary to treat hemodynamic abnormalities. After this, tachycardia with concomitant hypertension was to be treated with a beta blocker. Hypertension was to be treated with hydralazine or sodium nitroprusside. Bradycardia was to be treated with atropine or, when necessary, isoproterenol. Hypotension was treated with phenylephrine, methoxamine, or norepinephrine. Intravenous fluids were used, as was dopamine, when necessary. Prophylactic use of nitrates, calcium-channel blockers, or beta-adrenergic blocking drugs to prevent ischemia was specifically prohibited; nitroglycerin was used only to treat documented myocardial ischemia (as demonstrated by ST-segment changes on the clinical monitor).
The “low-dose” group was given 2 micro gram/kg mivazerol for 20 min before induction of anesthesia, followed by 0.75 micro gram [center dot] kg-1[center dot] h-1intraoperatively and for as long as 72 h postoperatively. The “high-dose” group was given 4 micro gram/kg and then 1.5 micro gram [center dot] kg-1[center dot] h-1, following the same protocol. These doses were selected to produce plasma levels of mivazerol of approximately 1.0 ng/ml in the low-dose group and 2.0 ng/ml in the high-dose group during surgery and for as long as 72 h after surgery.
Postoperative Procedures.
Heart rate was to be kept between 40 and 100 beats/min, and SBP between 90 and 180 mmHg, during the 96-h postoperative period, using prespecified analgesic, sedative, and cardiac adjuvant therapies. Morphine sulfate was administered intravenously or by patient-controlled analgesia, and midazolam was given for anxiety.
Clinical Care.
Routine clinical monitoring included continuous five-lead electrocardiography, measurement of radial artery pressure and arterial blood oxygen saturation, and assessment of inspired concentrations of isoflurane and oxygen. In parallel with clinical monitors, research monitors included three-channel, seven-lead Holter electrocardiography, continuous measurement of HR and blood pressure, 12-lead electrocardiography, and assays of cardiac enzymes. Clinical decisions were not controlled by study protocol, and clinicians caring for the patients had no knowledge of any research data.
Determination of Hemodynamic Variables.
Baseline HR and blood pressure were determined by averaging 3 readings obtained 5 min apart before induction of anesthesia. Intraoperatively and for as long as 96 h after surgery, HR, SBP, diastolic blood pressure, and mean arterial pressure were measured every 10 s and stored by portable patient monitor (McSPI/Ischemia Research and Education Foundation-(IREF) Patient Monitor System) until the arterial line was removed, and then an automated blood pressure cuff recorded pressures, which also were stored in the computer. Heart rate continued to be recorded every 10 s throughout all periods. The HR and blood pressure data were compressed into 1-min data samples and were then reviewed to eliminate artifacts (such as those associated with drawing of blood or flushing of the catheter). Median values for these data were calculated, and each value was evaluated for out-of-bounds conditions, which were annotated. The occurrence of episodes of hemodynamic instability was determined, and the frequency distribution and characteristics of these episodes were derived for the intraoperative and postoperative periods. (Table 9)
Table 9. Appendix 2. Analysis Group/Ischemia Research and Education Foundation
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Table 9. Appendix 2. Analysis Group/Ischemia Research and Education Foundation
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For the intraoperative period, a hemodynamic episode was said to have occurred if:(1) HR increased at least 20% from baseline or was 40 beats/min or less;(2) SBP increased or decreased 20% or more from baseline; and (3) the episode lasted at least 5 min. For the postoperative period, episodes were said to have occurred if:(1) HR decreased to 40 beats/min or less, or increased to 100 beats/min or more;(2) SBP decreased to 90 mmHg or less, or increased to 180 mmHg or more. In addition, treatment for hemodynamic changes (tachycardia, bradycardia, hypertension, hypotension) were recorded and characterized. To evaluate hemodynamic rebound, the incidence of, and treatment for, either tachycardia or hypertension during the 12-h post-infusion period (> 72 h) was compared between the placebo and mivazerol groups.
Two independent, blinded clinicians individually scanned the annotated hemodynamic files, located the out-of-bounds conditions, and reviewed the annotated data to determine whether the hemodynamic abnormalities were real or artifact. A computerized report that described all episodes identified by the two clinicians and any discrepancies between the two clinicians was generated after both primary readers completed their analyses. A third independent reviewer reviewed the generated report and validated all previous readings and resolved any discrepancies. To assess concordance of the hemodynamic analysis, a concordance plan was pre-specified, and 20% of the patient population was randomly selected and reanalyzed for hemodynamic events. All analysis individuals (IREF) were blinded to previous results, patient identification, clinical events, and other outcome events. The results of this analysis, which occurred after completion of the main analysis, were compared statistically as described earlier.
Electrocardiographic Monitoring.
Patients were monitored with a three-channel AM Holter electrocardiogram recorder (series 8500; Marquette Electronics, Milwaukee, WI), commencing at least 8 h before surgery and continuing up to the 96th postoperative hour. Bipolar leads (CC5, CM5, ML) were used. Each complete electrocardiographic recording was scanned using an electrocardiographic analysis system (Marquette Series Laser Holter SXP); all abnormal QRS complexes (i.e., ventricular ectopic beats, conduction abnormalities) were excluded, and a continuous three-lead ST-segment trend was generated, as described elsewhere. [4] ST deviation values were determined at 60 msec past the J point, in each of the three channels, unless that point fell within the T wave, in which case the measurement point of ST segment depression was shortened to a minimum of J + 40 msec. Electrocardiographic episodes of ischemia were defined as:(1) horizontal or downsloping ST segment depression from baseline of greater or equal to 1 mm lasting at least 1 min and separated from other episodes by greater or equal to 1 min;(2) ST segment evaluation from baseline greater or equal to 2 mm measured at the J point lasting at least 1 min and separated from other episodes by greater or equal to 1 min. The reversal of an ischemic episode was defined by the return of the ST segment to baseline for at least 1 min. Each episode was assessed for duration, magnitude, severity (area under the curve), as well as for “ischemic burden”(minutes of ischemia/hours monitored). Results of Holter scanner interpretation were recorded on data sheets by the first electrocardiographer. A second electrocardiographer reviewed these results. A third-level electrocardiographer also reviewed all the results and resolved all differences.
The intraoperative results also were analyzed by dividing the period into the nonemergence period and the emergence from anesthesia period, with emergence being defined as the 30-min period before leaving the operating room. The period definitions were arbitrary, but were specified before unblinding.
Assessment of Myocardial Infarction.
Twelve-lead electrocardiograms were obtained at the time of patient screening, on arrival at the intensive care unit, daily on postoperative days 1 to 5, on postoperative day 7, and at hospital discharge. Creatine kinase myocardial band (CK-MB) isoenzyme levels were obtained preoperatively; on arrival at the intensive care unit; and at 4, 8, 12, 16, 20, 24, 32, 40, 48, 60, 72, 84, and 96 h after surgery. The occurrence of perioperative MI was assessed for the period from induction of anesthesia to hospital discharge. Myocardial infarction was diagnosed if any of the following occurred:(1) new Q wave on a postoperative 12-lead electrocardiogram, as determined by application of the Minnesota Code criteria [12] (1–1 to 1–3) and analysis panel validation; or (2) an elevation in CK-MB levels to greater or equal to 100 ng/ml at any time after surgery, or to greater or equal to 70 ng/ml within 12 h after surgery; or (3) diagnosis of acute MI made during autopsy.
Two blinded investigators applied the Minnesota Code criteria, as modified by Chaitman et al., [13] to code the 12-lead electrocardiograms. If disagreements arose between the two investigators regarding coding or diagnosis, a third investigator reviewed the set of electrocardiograms, and, along with the original two investigators, a final diagnosis was achieved by consensus.
Determinations of CK-MB levels were performed centrally by the Bioanalytical Research Corporation (BARC, Gent, Belgium) using an immunoenzymetric assay (Hybritech Tandem-E CK-MB). Diagnosis of MI by autopsy was made by the pathologist at the participating center.
Blood Sampling.
Blood samples for clinical chemistry and for determination of plasma mivazerol concentrations were performed at predetermined times.
Assessment of Adverse Events.
Adverse events and serious adverse events were ascertained by site investigators and reported on Case Report Forms using the system organ classification of the World Health Organization. [14] 
Data and Statistical Analyses
All research data (Holter electrocardiogram, hemodynamic data, 12-lead electrocardiographic data) were analyzed at the coordinating center (IREF, San Francisco, CA) in a blinded fashion to ensure that uniform criteria for data analysis were used. Because block randomization was performed at each of the 23 centers, the analyses presented herein include an adjustment for any effect associated with individual centers.
For the analysis of the incidence of hemodynamic or ischemic episodes, when the outcome variable was binary and the explanatory variable was treatment, the two-by-three contingency Table analysiswas controlled for center effect using the Cochran-Mantel-Haenszel general association chi-square statistic. For the high-dose versus placebo comparison, the same technique was performed using data for the high-dose and placebo groups. These analyses were performed using PROC FREQ of the Statistical Analysis System (SAS, SAS Institute, Cary, NC). For a continuous response variable, a general linear model was used and included center and treatment-by-center effects, to derive the adjustment treatment effect.
The treatment-by-center effect was included in all models, regardless of whether the effect was statistically significant (at the 5% level), because the sample size per center was not sufficiently large to assess adequately whether there was treatment-by-center effect, and because randomization was carried out at each center. In addition, in most of the models, the center effect was significant, suggesting a high level of heterogeneity in the least-squares estimated means of the response variable across the 23 centers. PROC GLM (General Linear Model) was used to fit these models and to obtain the adjusted estimated treatment effect. The comparison between high-dose mivazerol and placebo was carried out using data from the high-dose and placebo groups, and the same technique as described was used.
The secondary efficacy variables included myocardial ischemia, anesthetic and analgesic requirements, and adverse clinical outcomes. For these endpoints, incidence was compared using either chi-square or Fisher's exact test. Analysis of variance or the Kruskal-Wallis test was used to analyze characteristics of hemodynamic and ischemic abnormalities. For analysis of area under the CK-MB curve and the maximum CK-MB, the data window was taken to be 4–96 h after surgery, a period that encompassed 14 measurements of CK-MB. Values for area under the CK-MB curves and maximum CK-MB were compared across treatment groups using analysis of variance techniques. Missing data were considered unevaluable and therefore excluded from analysis. However, because the values were missing, at random, across study groups, the statistical inferences were still able to be generalized for the whole sample size.
The statistical methods for the concordance analysis of the primary outcome variable, hemodynamic stability, includes the incidence, frequency, and severity of hemodynamic abnormality (tachycardia, bradycardia, hypertension, or hypotension) during each of the study periods. Twenty percent (60 patients) were selected randomly from the 300-patient population, and hemodynamics were reanalyzed using the same methods as for the original analysis, with all patient identifiers blinded to the investigators. Concordance between the original analysis results and the reanalysis results was first determined for the incidence of each of four types of hemodynamic abnormality during the primary outcome period, as well as all other time periods. The concordance was evaluated using the Kappa statistic, [15] with an acceptance threshold prespecified to equal 0.60, which is considered to indicate substantial agreement. [16] The second part of the analysis assesses the concordance of the frequency and severity of hemodynamic episodes during each of the study periods. Frequency was defined as the number of hemodynamic episodes (tachycardia, bradycardia, hypertension, or hypotension) per patient for each period. Hemodynamic severity parameters were defined as:(1) the mean of all episodes' durations for each patient; and (2) the mean of all episodes' area under the curve for each patient. The concordance for frequency and severity was evaluated by the method described by Dunn, [17] which uses the traditional method in which the coefficient of correlation serves as the reliability coefficient; for the purposes of this analysis, a threshold greater or equal to 0.6 was prespecified before analysis, and is considered good agreement.
Data Management
All patient case report forms were entered (double-data entry) into a PC/MS-DOS SAS database by the sponsor. The data were backed up daily onto a Vax computer. A copy of the database that consisted of all the information from the case report forms was sent every month to the coordinating and analysis center in San Francisco in a PC/SAS 6.04 format. The technology data that included the Holter and 12-lead electrocardiographic data were double-data entered into a PC/MS-DOS database at the analysis center in San Francisco (IREF)-where error-checking and data validation were done individually by research investigators using SAS error-checking programs. The continuous hemodynamic data were sent by the centers to IREF and were converted to SAS formats. The laboratory data were sent from BARC (Gent, Belgium) to IREF on a DOS diskette, in a flat ASCII file, and then were converted to PC/SAS 6.04 format. All data management tasks were carried out using the PC/SAS 6.04 system. The final database was then converted to UNIX SAS 6.09, and all data analyses were performed using this system.
Results
Of the 317 patients enrolled in the study, 17 were not assigned to a study group, because of ineligibility (7), patient refusal (3), or technical reasons (7). Of the remaining 300 patients, 103 were given placebo; 99, low-dose mivazerol; and 98, high-dose mivazerol. Table 1shows that demographic data and preoperative cardiac medications were similar for the three groups. Generally, patients were older and hypertensive and were taking a number of cardiovascular medications. Exposure to the study drug did not differ (P = 0.082) for the three groups (placebo, 75.3 h; low-dose, 75.3 h; high-dose, 75.7 h, all medians).
Table 1. Comparison of Study Groups Undergoing Vascular Surgery and Administration of Placebo or Mivazerol
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Table 1. Comparison of Study Groups Undergoing Vascular Surgery and Administration of Placebo or Mivazerol
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Hemodynamic Variability
General Hemodynamic Response.
(Figure 1and Figure 2) show the median HR and SBP for various time periods. For all time periods, HR was significantly lower with high-dose mivazerol than with placebo. Systolic blood pressure was significantly lower in the high-dose group at 8, 16, and 24 h after leaving the operating room.
Figure 1. Heart rate response-Median heart rate for various time periods for three study groups of vascular surgery patients given low-dose (0.75 micro gram [center dot] kg-1[center dot] h-1) or high-dose (1.5 micro gram [center dot] kg-1[center dot] h-1) mivazerol, or placebo. For each patient of a group, the median heart rate for that period was calculated, and then, for the group, the median for all patients was calculated. The postoperative periods (+8, +16, etc.) indicate 0–8 h post-operatively, 8–16 h, etc. Differences were significant (P < 0.05) between the high-dose and placebo groups and are indicated by asterisks. The number of patients per group for each study period is presented in Table 2.
Figure 1. Heart rate response-Median heart rate for various time periods for three study groups of vascular surgery patients given low-dose (0.75 micro gram [center dot] kg-1[center dot] h-1) or high-dose (1.5 micro gram [center dot] kg-1[center dot] h-1) mivazerol, or placebo. For each patient of a group, the median heart rate for that period was calculated, and then, for the group, the median for all patients was calculated. The postoperative periods (+8, +16, etc.) indicate 0–8 h post-operatively, 8–16 h, etc. Differences were significant (P < 0.05) between the high-dose and placebo groups and are indicated by asterisks. The number of patients per group for each study period is presented in Table 2.
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Figure 1. Heart rate response-Median heart rate for various time periods for three study groups of vascular surgery patients given low-dose (0.75 micro gram [center dot] kg-1[center dot] h-1) or high-dose (1.5 micro gram [center dot] kg-1[center dot] h-1) mivazerol, or placebo. For each patient of a group, the median heart rate for that period was calculated, and then, for the group, the median for all patients was calculated. The postoperative periods (+8, +16, etc.) indicate 0–8 h post-operatively, 8–16 h, etc. Differences were significant (P < 0.05) between the high-dose and placebo groups and are indicated by asterisks. The number of patients per group for each study period is presented in Table 2.
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Table 2. Incidence of Hemodynamic Responses to Placebo or Mivazerol in Patients Undergoing Vascular Surgery
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Table 2. Incidence of Hemodynamic Responses to Placebo or Mivazerol in Patients Undergoing Vascular Surgery
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Figure 2. Blood pressure response-Median systolic blood pressure for various time periods for three study of groups of vascular surgery patients given low-dose (0.75 micro gram [center dot] kg-1[center dot] h-1) or high-dose (1.5 micro gram [center dot] kg-1[center dot] h-1) mivazerol or placebo. For each patient of a group, the median blood pressure for that period was calculated, and then, for the group, the median for all patients was calculated. The asterisks indicate which differences between the high-dose and placebo groups were statistically significant (P < 0.05). The number of patients per group for each study period is presented in Table 2.
Figure 2. Blood pressure response-Median systolic blood pressure for various time periods for three study of groups of vascular surgery patients given low-dose (0.75 micro gram [center dot] kg-1[center dot] h-1) or high-dose (1.5 micro gram [center dot] kg-1[center dot] h-1) mivazerol or placebo. For each patient of a group, the median blood pressure for that period was calculated, and then, for the group, the median for all patients was calculated. The asterisks indicate which differences between the high-dose and placebo groups were statistically significant (P < 0.05). The number of patients per group for each study period is presented in Table 2.
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Figure 2. Blood pressure response-Median systolic blood pressure for various time periods for three study of groups of vascular surgery patients given low-dose (0.75 micro gram [center dot] kg-1[center dot] h-1) or high-dose (1.5 micro gram [center dot] kg-1[center dot] h-1) mivazerol or placebo. For each patient of a group, the median blood pressure for that period was calculated, and then, for the group, the median for all patients was calculated. The asterisks indicate which differences between the high-dose and placebo groups were statistically significant (P < 0.05). The number of patients per group for each study period is presented in Table 2.
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Tachycardia and Hypertension-Efficacy Outcomes.
(Table 2) shows the incidence of hemodynamic changes, and Table 3shows the therapeutic interventions to treat those changes. Before administration of mivazerol, the incidence of tachycardia tended to be higher in the high-dose group. However, during drug administration (i.e., during the intraoperative, early postoperative, and late postoperative periods), the incidence of tachycardia was significantly lower in the high-dose group (Table 2). For the low-dose group, the incidence of tachycardia during the intraoperative period was 38% versus 51% for placebo (P = 0.064), and was significantly reduced during the late postoperative period (54% vs. 70%, P = 0.031). The incidence of hypertension was significantly decreased with low-dose or high-dose mivazerol for the intraoperative period only (Table 2). For all time periods, the incidence of either tachycardia or hypertension was significantly less with mivazerol (at either dose level) than with placebo. Specifically, the incidences for the three groups during the various time periods were as follows: for the intraoperative period, 65%(high dose) and 64%(low dose), versus 80%(placebo)(P = 0.015); for the early postoperative period, 55% and 70%, versus 69%(P = 0.029); and for the late postoperative period, 63% and 66%, versus 82%(P = 0.011). An effect also was observed after discontinuation of the infusion of mivazerol: 85% and 85%, versus 96%(P = 0.015).
Table 3. Number of Patients Given Placebo or Mivazerol Who Were Treated for Hemodynamic Instability during and after Vascular Surgery
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Table 3. Number of Patients Given Placebo or Mivazerol Who Were Treated for Hemodynamic Instability during and after Vascular Surgery
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The need for treatment of tachycardia was significantly lower with high-dose mivazerol for the early and late postoperative periods (Table 3). The need for treatment of hypertension was similar in the high-dose, placebo, and low-dose groups (Table 3). The low-dose group did not differ from the placebo group regarding treatment for tachycardia or hypertension, except for the intraoperative period (34% vs. 46%, P = 0.028). After discontinuation of mivazerol, treatment for tachycardia or hypertension did not differ between groups.
Bradycardia and Hypotension-Safety Outcomes.
Episodes of bradycardia occurred in both mivazerol groups during all time periods of drug administration and even after discontinuation of the drug; the incidence was significantly higher than that with placebo (Table 2). However, treatment for bradycardia did not differ significantly across groups during any period. The groups did not differ in the incidence of hypotension, except during the intra-operative period, at which time the low-dose group had a higher incidence than the placebo group (87% vs. 77%, P = 0.028). There was no difference in the incidence of either bradycardia or hypotension for any of the postoperative periods. However, for the intraoperative period, the low-dose group had a higher incidence of either bradycardia or hypotension (high-dose, 78%; low-dose, 88%; placebo, 77%; P = 0.048). Treatment for hypotension did not differ significantly between the groups during or after drug administration (Table 3).
Myocardial Ischemia
(Table 4) shows the incidence of changes in the ST segment on Holter electrocardiogram. This incidence was significantly less (50% less) for the high-dose group than for the placebo group during the intraoperative period. Post hoc analysis, derived by subdividing the intraoperative period into the emergence-from-anesthesia period (i.e., the 30 min before transport of the patient from the operating room) and the nonemergence period, revealed that the incidence was 67% less in the emergence period. For other periods, these differences were not significant (Table 4).
Table 4. Incidence (n/N) of Ischemia after Administration of Placebo or Mivazerol in Patients Undergoing Vascular Surgery
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Table 4. Incidence (n/N) of Ischemia after Administration of Placebo or Mivazerol in Patients Undergoing Vascular Surgery
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(Table 5) shows the characteristics of ST segment changes. The high-dose group had a significantly shorter duration of ischemia and area under the curve, and less ischemic burden for the late postoperative period.
Table 5. Characteristics of Ischemic Episodes in Vascular Surgery Patients Given Placebo or Mivazerol*
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Table 5. Characteristics of Ischemic Episodes in Vascular Surgery Patients Given Placebo or Mivazerol*
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Regarding treatment of ischemia, the need for nitrates, calcium-channel blockers, or beta-blockers was significantly lower in the high-dose group for the late postoperative period, being 46% less than with placebo (high-dose, 21%; low-dose, 35%; placebo, 39%; P = 0.027). Regarding individual cardiac medications, the use of beta-blockers was significantly lower in the high-dose group in the late postoperative period (9% vs. 22% for placebo; P = 0.049).
Adverse Events
One hundred seventy-three patients (high dose, 55; low dose, 55; placebo, 63; P = 0.675) had an adverse event, as defined by the World Health Organization System Organ Classification. The incidence of serious adverse events also was not significantly different across study groups: 12%, 9%, and 13% for the high-dose, low-dose, and placebo groups, respectively. Five patients died during the study-four in the high-dose group (two from stroke after carotid surgery, one from pulmonary embolism, and one from MI and cardiogenic shock) and one in the placebo group (MI complicated by stroke and cardiogenic shock). None of these deaths was reported by the clinician (who had no knowledge of study group assignment) as probably or definitely being associated with drug therapy. Using a post hoc analysis, there was no difference in the incidence of hypertension between study groups during the acute drug infusion period before anesthetic induction (high dose, 28%; low dose, 18%; placebo, 21%; P = 0.244), nor was there any difference in the incidence of hypertension before drug infusion (high dose, 31%; low dose, 22%; placebo, 24%; P = 0.376).
Cardiac Outcomes
Myocardial infarction occurred in 6 of 103 patients given placebo, in 1 of 99 patients given low-dose mivazerol, and in 2 of 98 patients given high-dose mivazerol. The relatively small sample size limits the ability to interpret these results. The number of patients in the high-dose, low-dose, and placebo groups who had other adverse cardiac outcomes were, respectively, as follows: 0, 0, and 1 patient had unstable angina; 3, 1, and 3 patients had congestive heart failure; and 0, 0, and 1 patient had dysrhythmia. Five, six, and four patients had cerebrovascular accidents; and 1, 0, and 1 patient had cardiac death.
Anesthetic and Analgesic Requirements, and Patient Management
Anesthetic requirement was similar for all groups. For the high-dose, low-dose, and placebo groups, the mean total dose of fentanyl (micro gram) required to induce anesthesia was, respectively, 129 +/- 29, 136 +/- 35, and 136 +/- 32. The mean induction dose of thiopental (mg) was 326 +/- 71, 313 +/- 93, and 330 +/- 83; and the mean end-tidal concentration of isoflurane required (vol%) was 0.46 +/- 0.19, 0.46 +/- 0.16, and 0.48 +/- 0.15. All patients required morphine sulfate equally during the first 48 h after surgery. Midazolam requirements also were similar for the high-dose, low-dose, and placebo groups were, respectively, 3, 5, and 8 mg (early postoperative period) and 13, 15, and 17 mg (late postoperative period). The groups did not differ regarding intraoperative or postoperative oxygen saturation, intraoperative and postoperative fluid requirements, or any of the laboratory results.
Plasma Concentrations of Mivazerol
Plasma concentrations of mivazerol sampled on postoperative day 1 were not distributed normally. To normalize the plasma concentrations, we performed a logarithmic transformation of the data that resulted in a log-plasma concentration in the range defined by the mean +/- two standard deviations. The results indicate that plasma concentrations of mivazerol on postoperative day 1 approximated the target concentrations of 1 ng/ml for the low dose and 2 ng/ml for the high dose (Table 6).
Table 6. Plasma Concentrations of Mivazerol on Postoperative Day 1 in Patients Undergoing Vascular Surgery
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Table 6. Plasma Concentrations of Mivazerol on Postoperative Day 1 in Patients Undergoing Vascular Surgery
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Concordance Results
The Kappa statistic for concordance of incidence between the original reading and the 20% new reading was calculated for each period and for each type of hemodynamic episode. The Kappa statistic exceeded the threshold (0.60) in each (100%) of the 20 comparisons (four abnormality types times five measurement periods), and exceeded 0.80 for 88% of the measurements (mean 0.95: range 0.66–1.0). Regarding the frequency (number of episodes) and severity (mean duration and area under the curve) of hemodynamic episodes, the Pearson correlation coefficient exceeded the threshold (0.60) for 100% of the comparisons, and exceeded 0.80 for 96% of the comparisons (mean 0.97: range 0.67–1.0)
Discussion
Our results demonstrate the ability of mivazerol to improve hemodynamic stability perioperatively and to mitigate ischemia during emergence from anesthesia in patients with or at risk for CAD undergoing vascular surgery and general anesthesia.
Compared with placebo, high-dose mivazerol significantly decreased the incidence of tachycardia by 34–42% during all treatment periods (intraoperative, early postoperative, late postoperative) and significantly decreased the need for treatment of tachycardia for the two postoperative periods. The incidence of hypertension decreased significantly with high-dose mivazerol for the intraoperative period. Compared with placebo, low-dose mivazerol also significantly reduced the incidence of tachycardia for the late postoperative period, and the incidence of, and treatment for, hypertension for the intraoperative period. Regarding myocardial ischemia, the incidence of change in the ST segment was significantly less (40% less for the low-dose group and 67% less for the high-dose group) than for the placebo group during emergence from anesthesia. Also, for both the low-dose and high-dose groups there was a significant reduction in the use of antiischemic medications, particularly beta-blockers, in the late postoperative period.
Regarding safety, mivazerol appeared to be safe. For all time periods, an increased incidence of bradycardia episodes was observed in patients given mivazerol. However, the incidence of treatment for bradycardia did not differ between groups, nor did serious adverse events associated with bradycardia occur more frequently in the mivazerol groups. Mivazerol did not affect the incidence of, or treatment for, hypotension.
Previous Studies-Clonidine and Dexmedetomidine
Alpha-2 adrenergic agonists have received considerable attention recently as perioperative adjuvant therapy because of their salutary effects on the sympathetic nervous system and on hypertension and tachycardia, and because of their sedative, anxiolytic, and analgesic properties. Patients with CAD who undergo surgery are at increased risk of perioperative cardiac morbidity because of compromised coronary circulation or poor left ventricular function. [4] Added to these risk factors are the changes induced by surgical and postoperative stress-an increase in circulating catecholamines, hypertension tachycardia, and thermal instability, all associated with increased myocardial oxygen demand. [4,9] Coupled with an insufficient supply, increased oxygen demand may predispose patients with CAD to myocardial ischemia and adverse cardiac outcomes. Therefore, efforts to mitigate the stress response have been pursued.
Clonidine, the prototypical alpha2-agonist, and dexmedetomidine, a new highly selective alpha2-agonist, have been studied to assess their effect on catecholamines, hemodynamic stability, and ischemia. Findings have varied (Table 7). Although studies evaluating plasma catecholamines report a decrease in norepinephrine concentrations with administration of clonidine or dexmedetomidine, results for epinephrine concentrations were not consistent. [18–25],**** Regarding hemodynamic effects, clonidine and dexmedetomidine have tended to reduce anesthetic requirement, plasma catecholamine levels, and intraoperative tachycardia and hypertension. [18–20,22–25,26–36] Also, the number of interventions needed to maintain intraoperative hemodynamic stability appears lower in patients given alpha2-agonists. [27,28,36] In contrast to these findings, some studies have failed to demonstrate any hemodynamic benefits. [center dot][37],***** Regarding safety, bradycardia has been a common adverse effect observed with these agents. However, most, but not all, episodes appeared to be transient and responsive to atropine. Hypotension occurred rather consistently with dexmedetomidine, and commonly with clonidine. Early transient hypertension also has been observed with these agents. [22–25,33] 
Table 7. Reported Effects of Clonidine and Dexmedetomidine on Hemodynamic Stability and Ischemia
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Table 7. Reported Effects of Clonidine and Dexmedetomidine on Hemodynamic Stability and Ischemia
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Regarding ischemia, no large study has evaluated the antiischemic effects of alpha2-agonists throughout the entire perioperative period; however, in several studies, researchers investigated the effects of clonidine and dexmedetomidine during surgery. Findings are controversial. In several studies, researchers found a reduction in the incidence of ischemia, [20,35,38–40],***** whereas others found no difference. [27],****** Results from most of these studies were limited in applicability by small sample size.
Previous Studies-Mivazerol
Mivazerol, a new alpha2agonist, has a high affinity and specificity for alpha2receptors. [41] Mivazerol displays an alpha (2A/alpha)1selectivity ratio of 119, a value four times higher than that for clonidine (39) and 1/10 that for dexmedetomidine (1,300), and an alpha2A/I1, imidazoline selectivity ratio of 215, substantively higher than that of clonidine (16) and that of dexmedetomidine (32). [41] Regarding hemodynamic effects, researchers in animal studies report a dose-dependent decrease in HR with mivazerol and a transient increase in SBP. For example, HR decreased by 30–35% in conscious animals and by 20–40% in pentobarbital anesthetized animals; blood pressure increased 25–40% for approximately 5–10 min and then returned to baseline. Compared with clonidine and dexmedetomidine, mivazerol appears to produce a similar reduction in HR but no reduction in blood pressure in animals. These effects appear to depend, however, on the anesthetic used, because mivazerol appears not to effect either HR or SBP in halothane-anesthetized rats while blunting hemodynamic changes during emergence from anesthesia. However, in human volunteers and in clinical studies, mivazerol produced minimal decreases in HR and SBP of 10–15%(unpublished data, UCB Pharma document).
Regarding myocardial ischemia, mivazerol has produced antiischemic effects in animals. In conscious animals subjected to repeated coronary artery occlusion, mivazerol attenuated tachycardia, lactate production, and elevation of the ST segment in response to exercise treadmill testing. [42] Nonsurgical patients with stable angina who were given mivazerol had improvement of test parameters on exercise treadmill testing. The time to 1-mm depression of the ST segment, the time to angina, and the total duration of exercise all increased, without effect on HR.
In a recently completed double-blind, placebo-controlled trial in 24 patients with, or at risk for, CAD who were undergoing noncardiac surgery, mivazerol was given as a 10-min loading dose 20 min before induction of anesthesia, continuously intraoperatively, and for 72 h postoperatively.*** Three dose levels were used to obtain plasma mivazerol levels of 1, 2, and 3 ng/ml. Safety and tolerability were assessed. Although mean HR was significantly lower in the low-dose and high-dose groups for the intraoperative and postoperative periods, significant bradycardia was not observed. Mean SBP was similar for the groups, and the use of vasopressors and vasoactive medications did not differ. These findings suggested that mivazerol was safe and effective in decreasing postoperative tachycardia.
Hemodynamic Stability
The stress during, and particularly after, anesthesia and surgery is associated with increased sympathetic activity that may manifest as hemodynamic instability. Tachycardia and hypertension may result in increased myocardial oxygen demand and, at higher heart rates, reduced oxygen supply. In the presence of a compromised coronary circulation, the imbalance between supply and demand could lead to myocardial ischemia and, possibly, serious adverse outcome. In this setting, an alpha2-adrenergic agonist such as mivazerol may modulate sympathetic overactivity, thereby promoting hemodynamic stability, improving the balance between myocardial oxygen supply and demand, and perhaps mitigating ischemia.
Our results demonstrated that mivazerol (particularly the high dose) significantly decreased the incidence of tachycardia (41%) and hypertension (27%) during the intraoperative period, and the incidence of tachycardia during the early (42%) and late (34%) postoperative periods. In addition, the number of therapeutic interventions necessary to keep HR within defined limits was lower with high-dose mivazerol during the early (50%) and late (60%) postoperative periods. Treatment for hypertension was not statistically significant between groups. Similar but less substantive effects were observed with low-dose mivazerol.
Our results also allowed assessment of “hemodynamic rebound.” This complication has been reported after prolonged administration and sudden discontinuation of clonidine and is characterized by hypertension, restlessness, anxiety, tremor, headache, nausea, and vomiting. [43–45] In selected cases, angina pectoris, MI, ventricular dysrhythmia, left ventricular failure, and death also have been reported. [46] The incidence and severity of hemodynamic rebound appear to depend on the dose and duration of treatment with clonidine. We did not find evidence of hemodynamic rebound with either dose of mivazerol, as assessed by the incidence of (Table 2), or treatment for (Table 3), tachycardia or hypertension in the 12 h after infusion, even after continuous administration of mivazerol for more than 72 h.
Bradycardia was observed in 4–9% of patients given mivazerol, a significantly higher incidence than that for placebo (0–3%). However, the groups did not differ significantly in the number of treatments for bradycardia (atropine) or the reported adverse events associated with decreased HR or altered cardiac conduction. The incidence of, and treatment for, hypotension were similar among all groups. Although mivazerol appears to be safe, these findings on safety, including the potential for bradycardia, should be examined in larger trials.
Myocardial Ischemia and Infarction
One of the principal objectives in maintaining hemodynamic stability in high-risk patients perioperatively is the prevention of myocardial ischemia. [9] By attenuating the release of catecholamines in response to perioperative stress, alpha2-agonists may prevent a hyperdynamic state that predisposes the vulnerable myocardium to ischemia. Our results demonstrate that high-dose mivazerol, when compared with placebo, significantly decreased the incidence of myocardial ischemia by 50% for the intraoperative period (P = 0.026). In addition, using a post hoc analysis, and dividing the intraoperative period into emergence (defined in this study as 30 min before leaving the operating room) and nonemergence periods, the reduction was even more pronounced for the emergence period (67%, P = 0.001). During the emergence period (i.e., generally, from the end of surgery to emergence from anesthesia), sympathetic stimulation increases and promotes hemodynamic lability, thermal instability, postoperative shivering, and decreased oxygen utilization. [47] The study of Udelsman et al. [48] on responses of the sympathetic nervous system, hypothalamic-pituitary axis, and renin-angiotensin axis supports this theory. Plasma levels of epinephrine, adrenocorticotropic hormone, and cortisol remained within the normal baseline ranges during induction, intubation, and surgery, but a marked elevation in plasma levels of epinephrine and cortisol occurred immediately after surgery and persisted for several days. Mangano and colleagues [4,5] showed that the incidence and severity of ischemia are greatest during this period, and that of all predictors of adverse cardiac outcome, early postoperative ischemia is the most important, conferring a ninefold increase in the risk of serious in-hospital adverse outcome, and a twofold increase in the risk of long-term (2-yr) outcome. Regarding the early and late postoperative periods, no effect on the incidence of ischemia was found, and only during the late postoperative period was an effect found for severity. There are two possible explanations. First, there is no drug effect; and second, given the relatively “low” placebo rate (16%-23%), the study was not powered to detect such difference. Resolution of this question would require approximately 250 patients per group. Tachycardia is also more frequent during the postoperative period. [49,50] Although not all postoperative ischemia is associated with increased HR, there is association between ischemia and postoperative tachycardia. Therefore, our results are particularly intriguing. We have found a significant reduction in the incidence of tachycardia during and after surgery and, in addition, a significant reduction in the incidence of ischemia during emergence. Our results, therefore, are consistent with previous reports in which researchers demonstrated the ability of alpha (2)-adrenergic agonists to reduce the incidence of intraoperative ischemia, [20,35,] *, 38* and now extend such findings to the emergence period.
Using prespecified criteria (new Q wave on electrocardiogram, elevation of CK-MB levels, or diagnosis during autopsy), we diagnosed MI in 2%, 1%, and 6%, of the high-dose, low-dose, and placebo patients, respectively. However, because of the relatively small sample size, no conclusion can be inferred.
Other Results
The groups did not differ in intraoperative anesthetic requirements, results that differed from those for clonidine and dexmedetomidine. One explanation is that we mandated strict control of hemodynamic status by use of prespecified cardiovascular adjuvants, a design that may not allow detection of differences in anesthetic requirement during the intraoperative period. Postoperatively, morphine requirements for pain were equal across groups. In contrast, patients given mivazerol required less midazolam for sedation, a finding that may be consistent with results from earlier studies on alpha2-agonists. However, it must be emphasized that this protocol was not specifically designed to detect such differences, and the results should be interpreted cautiously.
Intraoperative and postoperative fluid requirements were similar for the groups, as were blood chemistry (SMA12), hematology (hemoglobin, leukocytes), and urinalysis, suggesting safety. However, a larger-scale trial would be necessary to detect subtle differences.
There were five deaths in the study. Of the four in the high-dose group, one was assessed as cardiac death secondary to MI, two were secondary to stroke, and one was secondary to pulmonary embolism. One patient given placebo died of MI complicated by stroke. None of the deaths was attributed to the study drug. For both the mivazerol and placebo groups, the incidence of death is consistent with figures reported by previous studies on patients not given drug therapy. [4] Nevertheless, mortality and safety need to be assessed rigorously in larger-scale trials of mivazerol.
Limitations
Our study was powered to detect differences in hemodynamic stability but not differences in myocardial ischemia, MI, or adverse cardiac outcomes. For example, regarding adverse outcome, based on an 8–15% incidence of outcome, [1,51] if mivazerol were assumed to reduce the incidence rate by 40%, enrollment of 1,000–1,840 patients would be necessary to achieve an 80% chance of detecting this reduction, for a significance level (alpha) of 0.05. Therefore, such adverse outcome events cannot be assessed in the current trial but only in a large-scale trial.
Our patient population was limited to those undergoing carotid and peripheral artery revascularization. Other major noncardiac operations, such as aortic surgery, associated with more profound hemodynamic alterations, excessive blood loss, large fluid shifts, and metabolic changes, were excluded. These physiologic and metabolic aberrations, coupled with stress of the operations, may contribute to an even higher incidence of hemodynamic and ischemic events. Therefore, the efficacy of mivazerol in these patients also should be investigated.
Although plasma concentrations of mivazerol were assessed during the 3-day infusion period, technical problems made it necessary to limit the analysis of plasma levels to the first postoperative day. Therefore, we could not relate efficacy and safety data to plasma concentrations to detect a possible relation.
We infused mivazerol for as long as 72 h, because, according to the literature, [4,49,50] most episodes of myocardial ischemia and infarction occur during the first 3 days after surgery. Our results showed significant reduction in tachycardia, a trend toward less ischemia, and good tolerability. However, two studies by Mangano and colleagues, [50,52] in at-risk patients undergoing non-cardiac surgery, demonstrated the following:(1) Although postoperative myocardial ischemia is most severe within 3 days after surgery, ischemia can persist for more than a week after surgery;(2) postoperative ischemia may be related to persistently elevated heart rates during the entire first week after surgery; and (3) an association may exist between early and late postoperative ischemia and adverse cardiac outcome. Therefore, assessment of the effects of mivazerol on tachycardia or ischemia occurring beyond the third postoperative day cannot be assessed in this trial.
Summary
Continuous administration of mivazerol to patients with or at high risk for CAD during surgery and for 72 h after surgery is safe and effective in promoting perioperative hemodynamic stability. Such efficacy is demonstrated by the decreased incidence of tachycardia and hypertension intraoperatively, and by the decreased incidence of tachycardia during the early and late postoperative periods. The high dose of mivazerol (1.5 micro gram [center dot] kg-1[center dot] h-1) is more effective than the low dose (0.75 micro gram [center dot] kg-1h-1). Bradycardia did occur, but appeared amenable to therapy. Finally, high-dose mivazerol appears to attenuate intraoperative myocardial ischemia.
These results suggest the need for further study in large-scale trials that would define the effect of mivazerol on adverse cardiovascular outcome.
The authors thank Diane Beatty and Mark Riddle of IREF for their administrative/editorial assistance, and Pauline Snider for her editorial advice.
Grant support for this mivazerol study and the associated publications is provided by the Ischemia Research and Education Foundation and UCB Pharmaceuticals. There were no other financial relationships (honoraria, consulting, stocks, or ownership) between the investigators, the central analysis unit (IREF), and UCB Pharmaceuticals.
The Multicenter Study of Perioperative Ischemia (McSPI) Research Group is a consortium of investigators from approximately 150 worldwide medical centers, focusing on the problems of perioperative myocardial infarction, stroke, renal dysfunction, as well as other organ dysfunction, and the implications of such diseases for health economics. McSPI-Europe consists of 40 investigators and more than 25 centers in western Europe, and is an integral part of the McSPI Research Group. The Ischemia Research and Education Foundation is a non-profit foundation dedicated to multicenter research in these areas, and is closely affiliated with the McSPI investigators and their institutions.
*Kharkevitch T, Guyaux M, Gobert J, Wulfert E: Mivazerol, a new alpha2-adrenergic agonist with anti-ischaemic effects in animal models of myocardial ischaemia. (Presented at EACTA, 7th Annual Meeting, June 9–12, 1992), The Netherlands.
**Guyaux M, Vandevelde M, Noyer M, Grimee R, Wulfert E: Mivazerol, a novel alpha 2-adrenoceptor agonist, prevents tachycardia through activation of spinal and/or epispinal sites. Pharm Res 1995;31 [Suppl]. (Presented at the First European Congress of Pharmacology, University of Milan, Milan, Italy, June 16–19, 1995).
***Talke P, Richardson CA, Layug E, Mangano DT, SPI Research Group: Hemodynamic effects of perioperative mivazerol infusion in surgical patients. Unpublished data.
****Favre JB, Gardaz JP, Nussberger J, Chiolero RL: Clonidine does not influence anesthetic drug requirements and hemodynamic response during aortic surgery under balanced anesthesia (abstract). Anesthesiology 1991; 75:A151.
*****Kent M, Thomsen B, Cicala R: Clonidine decreases ischemic events during coronary artery surgery (abstract). Anesthesiology 1990; 73:A129.
******Lipszyc M, Engelman E: Clonidine does not prevent myocardial ischemia during noncardiac surgery (abstract). Anesthesiology 1991; 75:A93.
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Figure 1. Heart rate response-Median heart rate for various time periods for three study groups of vascular surgery patients given low-dose (0.75 micro gram [center dot] kg-1[center dot] h-1) or high-dose (1.5 micro gram [center dot] kg-1[center dot] h-1) mivazerol, or placebo. For each patient of a group, the median heart rate for that period was calculated, and then, for the group, the median for all patients was calculated. The postoperative periods (+8, +16, etc.) indicate 0–8 h post-operatively, 8–16 h, etc. Differences were significant (P < 0.05) between the high-dose and placebo groups and are indicated by asterisks. The number of patients per group for each study period is presented in Table 2.
Figure 1. Heart rate response-Median heart rate for various time periods for three study groups of vascular surgery patients given low-dose (0.75 micro gram [center dot] kg-1[center dot] h-1) or high-dose (1.5 micro gram [center dot] kg-1[center dot] h-1) mivazerol, or placebo. For each patient of a group, the median heart rate for that period was calculated, and then, for the group, the median for all patients was calculated. The postoperative periods (+8, +16, etc.) indicate 0–8 h post-operatively, 8–16 h, etc. Differences were significant (P < 0.05) between the high-dose and placebo groups and are indicated by asterisks. The number of patients per group for each study period is presented in Table 2.
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Figure 1. Heart rate response-Median heart rate for various time periods for three study groups of vascular surgery patients given low-dose (0.75 micro gram [center dot] kg-1[center dot] h-1) or high-dose (1.5 micro gram [center dot] kg-1[center dot] h-1) mivazerol, or placebo. For each patient of a group, the median heart rate for that period was calculated, and then, for the group, the median for all patients was calculated. The postoperative periods (+8, +16, etc.) indicate 0–8 h post-operatively, 8–16 h, etc. Differences were significant (P < 0.05) between the high-dose and placebo groups and are indicated by asterisks. The number of patients per group for each study period is presented in Table 2.
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Figure 2. Blood pressure response-Median systolic blood pressure for various time periods for three study of groups of vascular surgery patients given low-dose (0.75 micro gram [center dot] kg-1[center dot] h-1) or high-dose (1.5 micro gram [center dot] kg-1[center dot] h-1) mivazerol or placebo. For each patient of a group, the median blood pressure for that period was calculated, and then, for the group, the median for all patients was calculated. The asterisks indicate which differences between the high-dose and placebo groups were statistically significant (P < 0.05). The number of patients per group for each study period is presented in Table 2.
Figure 2. Blood pressure response-Median systolic blood pressure for various time periods for three study of groups of vascular surgery patients given low-dose (0.75 micro gram [center dot] kg-1[center dot] h-1) or high-dose (1.5 micro gram [center dot] kg-1[center dot] h-1) mivazerol or placebo. For each patient of a group, the median blood pressure for that period was calculated, and then, for the group, the median for all patients was calculated. The asterisks indicate which differences between the high-dose and placebo groups were statistically significant (P < 0.05). The number of patients per group for each study period is presented in Table 2.
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Figure 2. Blood pressure response-Median systolic blood pressure for various time periods for three study of groups of vascular surgery patients given low-dose (0.75 micro gram [center dot] kg-1[center dot] h-1) or high-dose (1.5 micro gram [center dot] kg-1[center dot] h-1) mivazerol or placebo. For each patient of a group, the median blood pressure for that period was calculated, and then, for the group, the median for all patients was calculated. The asterisks indicate which differences between the high-dose and placebo groups were statistically significant (P < 0.05). The number of patients per group for each study period is presented in Table 2.
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Table 8. Appendix 1. Participating McSPI-EUROPE Medical Centers and Investigators
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Table 8. Appendix 1. Participating McSPI-EUROPE Medical Centers and Investigators
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Table 9. Appendix 2. Analysis Group/Ischemia Research and Education Foundation
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Table 9. Appendix 2. Analysis Group/Ischemia Research and Education Foundation
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Table 1. Comparison of Study Groups Undergoing Vascular Surgery and Administration of Placebo or Mivazerol
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Table 1. Comparison of Study Groups Undergoing Vascular Surgery and Administration of Placebo or Mivazerol
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Table 2. Incidence of Hemodynamic Responses to Placebo or Mivazerol in Patients Undergoing Vascular Surgery
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Table 2. Incidence of Hemodynamic Responses to Placebo or Mivazerol in Patients Undergoing Vascular Surgery
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Table 3. Number of Patients Given Placebo or Mivazerol Who Were Treated for Hemodynamic Instability during and after Vascular Surgery
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Table 3. Number of Patients Given Placebo or Mivazerol Who Were Treated for Hemodynamic Instability during and after Vascular Surgery
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Table 4. Incidence (n/N) of Ischemia after Administration of Placebo or Mivazerol in Patients Undergoing Vascular Surgery
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Table 4. Incidence (n/N) of Ischemia after Administration of Placebo or Mivazerol in Patients Undergoing Vascular Surgery
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Table 5. Characteristics of Ischemic Episodes in Vascular Surgery Patients Given Placebo or Mivazerol*
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Table 5. Characteristics of Ischemic Episodes in Vascular Surgery Patients Given Placebo or Mivazerol*
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Table 6. Plasma Concentrations of Mivazerol on Postoperative Day 1 in Patients Undergoing Vascular Surgery
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Table 6. Plasma Concentrations of Mivazerol on Postoperative Day 1 in Patients Undergoing Vascular Surgery
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Table 7. Reported Effects of Clonidine and Dexmedetomidine on Hemodynamic Stability and Ischemia
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Table 7. Reported Effects of Clonidine and Dexmedetomidine on Hemodynamic Stability and Ischemia
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