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doi: 10.1097/ALN.0b013e31829bd883
Perioperative Medicine

The Anesthesia in Abdominal Aortic Surgery (ABSENT) Study: A Prospective, Randomized, Controlled Trial Comparing Troponin T Release with Fentanyl–Sevoflurane and Propofol–Remifentanil Anesthesia in Major Vascular Surgery

Lindholm, Espen E. M.D.*; Aune, Erlend M.D., Ph.D.; Norén, Camilla B.; Seljeflot, Ingebjørg Ph.D.§; Hayes, Thomas M.D.; Otterstad, Jan E. M.D., Ph.D.#; Kirkeboen, Knut A. M.D., Ph.D.**

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Background: On the basis of data indicating that volatile anesthetics induce cardioprotection in cardiac surgery, current guidelines recommend volatile anesthetics for maintenance of general anesthesia during noncardiac surgery in hemodynamic stable patients at risk for perioperative myocardial ischemia. The aim of the current study was to compare increased troponin T (TnT) values in patients receiving sevoflurane-based anesthesia or total intravenous anesthesia in elective abdominal aortic surgery.
Methods: A prospective, randomized, open, parallel-group trial comparing sevoflurane-based anesthesia (group S) and total intravenous anesthesia (group T) with regard to cardioprotection in 193 patients scheduled for elective abdominal aortic surgery. Increased TnT level on the first postoperative day was the primary endpoint. Secondary endpoints were postoperative complications, nonfatal coronary events and mortality.
Results: On the first postoperative day increased TnT values (>13 ng/l) were found in 43 (44%) patients in group S versus 41 (43%) in group T (P = 0.999), with no significant differences in TnT levels between the groups at any time point. Although underpowered, the authors found no differences in postoperative complications, nonfatal coronary events or mortality between the groups.
Conclusions: In elective abdominal aortic surgery sevoflurane-based anesthesia did not reduce myocardial injury, evaluated by TnT release, compared with total intravenous anesthesia. These data indicate that potential cardioprotective effects of volatile anesthetics found in cardiac surgery are less obvious in major vascular surgery.
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What We Already Know about This Topic

* Previous studies have demonstrated that volatile anesthetics may induce cardioprotection during cardiac surgery
* This study compared troponin T values in patients receiving volatile versus total intravenous anesthesia during elective abdominal aortic surgery
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What This Article Tells Us That Is New

* No significant differences in troponin levels were observed between patients receiving volatile versus total intravenous anesthesia after elective abdominal aortic surgery
* These prospective randomized data suggest that volatile anesthesia is no more protective than total intravenous anesthesia
MYOCARDIAL ischemia and myocardial infarction (MI) are serious complications in cardiac and major noncardiac surgery.1 Cardiac troponins have high tissue specificity and are sensitive markers of myocardial necrosis.2 Troponin increase relates directly to magnitude of injury3,4 and predicts short- and long-term outcomes after major surgery.5,6 In cardiac surgery there are studies supporting that volatile anesthetics reduce postoperative complications including MI and mortality.7–11 There is increased use of total intravenous anesthesia (TIVA) in major surgery12,13 and propofol has been suggested to be cardioprotective in cardiac surgery.13 The American College of Cardiology/American Heart Association 2007 guidelines14 recommend the use of volatile anesthetics for maintenance of general anesthesia during noncardiac surgery in hemodynamic stable patients at risk for perioperative myocardial ischemia. Presently, there are limited data on cardioprotection by volatile anesthetics in major noncardiac surgery, and the recommendation is solely based on data from cardiac surgery.
Abdominal aortic aneurysm (AAA) is a common disease. Depending on aneurysm size and other factors,15 untreated annual mortality rate varies from 0 to 50%. Patients with atherosclerosis in lower extremities often have coexisting coronary and cerebrovascular diseases and increased risk of MI, stroke, and cardiovascular death.16 In this study (the ABSENT study: Anesthesia in abdominal aortic surgery) consecutive patients with AAA and/or arteriosclerosis obliterans scheduled for elective surgery were included. We hypothesized that sevoflurane-based anesthesia is cardioprotective compared with TIVA also in elective abdominal aortic surgery. Cardioprotection is often primarily related to troponin levels.17 Increased TnT level on the first postoperative day was the primary endpoint as a marker of myocardial damage. Secondary endpoints were postoperative complications, nonfatal coronary events, and mortality.
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Materials and Methods

Study Design
Fig. 1
Fig. 1
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Table 1
Table 1
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This prospective, randomized, open, parallel-group trial was conducted at a central hospital in Norway, from February 2008 to February 2012, according to the Declaration of Helsinki principles. The necessary health authorities in Norway and at the hospital accepted initiation of the study, which was registered in Clinical (NCT00538421). Consecutive patients with AAA and/or aortic arteriosclerosis obliterans scheduled for open abdominal aortic surgery were screened for exclusion criteria (table 1). One hundred ninety-three patients were included and randomized (1:1) to sevoflurane-based anesthesia (group S) or TIVA (group T), illustrated in figure 1. After informed consent was given, patients selected a blank envelope with the randomization code inside from a box containing envelopes for all remaining patients to be included. Time from informed consent to surgery was 7 (2–9) days. Biochemical analysis and postoperative care were blinded with regard to randomization. A preoperative cardiological examination was performed by a doctor not involved in the ABSENT study. At time of inclusion, all patients were in a stable clinical condition, without evidence of acute coronary syndrome, uncontrolled heart failure, arrhythmia, or severe valvular disease.
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Medication, Anesthesia, and Monitoring
Premedication was paracetamol (1.5 g <60 and 2.0 g >60 kg body weight). Concurrent medication like β-blockers, aspirin, and statins were continued through the perioperative period. Patients discontinued sulfonylurea, nonsteroid antiinflammatory drugs, xanthine derivatives, angiotensin-converting enzyme inhibitor, angiotensin II receptor antagonists, and cyclooxygenase 2 inhibitors at least 24 h before surgery.
Fig. 2
Fig. 2
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Patients were intra- and postoperatively monitored by a 5-lead electrocardiogram. A 12-lead electrocardiogram was recorded preoperatively, 30 min postoperatively, first-, second- and 30th-postoperative day, and more frequently if indicated. Invasive systemic blood pressure, central venous pressure, peripheral arterial oxygen saturation, and cardiac output (Vigileo/FloTrac system, Edwards Lifescience, Irvine, CA) were monitored. Patients were treated according to goal-directed hemodynamic management and fluid optimization (fig. 2). After hemodynamic measurements with volume adjustments, dopamine (1–10 μg·kg−1·min−1) or noradrenaline (0.01–0.3 μg·kg−1·min−1) was given intravenously (iv) at the discretion of the attending anesthesiologist to maintain a mean arterial blood pressure (MAP) of 65–90 mmHg. Transfusions were given at hemoglobin level less than 8.0 g/dl. Before induction of anesthesia an epidural catheter was introduced (thoracic level 6–10). Epidural analgesia started after opening of the aortic cross-clamp. An arterial line (a. radialis) and a 2–3 lumen venous catheter (v. jugularis int.) were introduced after induction of anesthesia.
All patients received general anesthesia and were ventilated by volume-controlled ventilation with tidal volume of approximately 8 ml/kg predicted body weight and respiratory frequency 10–18 beats/min. Predicted body weight was estimated as follows: men: predicted body weight (kg) = 50 + 0.91 (height [cm] − 152.2); women: predicted body weight (kg) = 45.5 + 0.91 (height [cm] – 152.2). Bispectral index (Philips Medical Systems, Eindhoven, The Netherlands) was used to monitor depth of anesthesia (level: 40–60). Group S (n = 97) received a balanced anesthesia with sevoflurane at 0.7–1.5 minimal alveolar concentration and repeated doses of fentanyl 0.05–0.1 mg iv. Group T (n = 96) received TIVA with propofol 1–10 mg·kg−1·h−1 iv and remifentanil 0.1–0.7 μg·kg−1·min−1 iv. For induction of anesthesia, fentanyl 0.1–0.3 mg iv and thiopental sodium 3–6 mg/kg iv were given in group S, and fentanyl 0.1–0.3 mg iv and propofol 1–2 mg/kg iv in group T. Vecuronium 0.1 mg/kg iv was used for neuromuscular blockade, and 0.01–0.02 mg/kg was given based on train-of-four (TOF Watch S acceleromyograph; Organon Ltd., Dublin, Ireland). Patients were not extubated if train-of-four was less than 90%. Maintenance of anesthesia was adjusted according to bispectral index and MAP values. If bispectral index was less than 40, the propofol infusion was reduced in group T and the inspiratory sevoflurane concentration lowered in group S. If MAP was less than 65 mmHg and hypovolemia could be excluded, the remifentanil infusion was reduced in group T and planned injections of fentanyl temporarily postponed in group S. Opposite alterations were performed if bispectral index was more than 60 or MAP was more than 90 mmHg.
Postoperative analgesia consisted of oral paracetamol 1 g four times a day combined with epidural analgesia 3–12 ml/h (bupivacaine 1 mg/ml, fentanyl 2 μg/ml, and adrenaline 2 μg/ml). Morphine hydrochloride 1–10 mg iv was used as rescue pain medication.
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Data Collection and Blood Samples
The primary endpoint was increased troponin T (TnT) levels (>13 ng/l) on the first postoperative day. Absolute values of TnT were also evaluated. Secondary endpoints were postoperative complications, nonfatal coronary events including postoperative acute MI, nonthrombotic troponin increase (NTTE), and mortality. Use of inotropic-, vasodilator-, and anesthetic drugs, bleeding, urine output, tachycardia (heart rate [HR] >20 beats/min above preoperative value lasting >2 min), and bradycardia episodes (HR <40 beats/min lasting >2 min), hypotensive (MAP <65 mmHg or <15 mmHg of preoperative value lasting >2 min), and hypertensive episodes (MAP >15 mmHg of preoperative value lasting >2 min) during surgery, ischemic events and arrhythmias, fluids and transfusions administered, postoperative pain (Visual Analog Pain Score), and postoperative nausea and vomiting 24 h after surgery were registered. Sequential Organ Failure Assessment score was recorded 8 h, on the first (8:00 AM) and second (8:00 AM) days after surgery if the patient was still in the postoperative ward.
Length of postoperative ward/intensive care unit and hospital stay, complications and mortality were recorded at a follow-up visit 30 days after surgery. Discharge criteria from postoperative ward/intensive care unit were: adequate communication/obey commands, respiratory rate of 10 min−1 or more, peripheral arterial oxygen saturation of 93% or more without supplemental oxygen for minimum 5 min, no diaphoresis, HR less than 100 beats/min, adequate pain relief with Visual Analog Pain Scale less than 5. Values were accepted if equivalent to preoperative status. Data on long-term mortality were collected from the Norwegian National Population Register (vital status per September 7, 2012 for all patients included). Due to regulatory restrictions, cause of death was not available.
A high-sensitivity fifth-generation immunoassay to measure serum TnT was used (Cobas e411; Roche Diagnostics GmbH, Mannheim, Germany) with a variation coefficient less than 10% at a TnT value of 10. Plasma was kept frozen at −80°C and analyzed after completion of the study. A value more than 13 ng/l was considered abnormal.18
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Diagnostic Criteria
Preoperative Coronary Artery Disease.
A diagnosis of preexisting coronary artery disease (CAD) was based on one or more of the following: sustained acute MI verified from hospital records, previous percutaneous coronary intervention and/or coronary artery bypass grafting, angiographically verified coronary artery stenosis of 50% or more or a positive exercise test combined with a history of typical angina pectoris, as in the ACTION study.19
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History of Stroke/Transient Ischemic Attack.
Diagnosis verified by hospital records including findings of computer tomography and/or magnetic resonance imaging.
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Peripheral Artery Disease.
Diagnosis verified by angiographic findings of one or more significant stenoses (≥50%) of aortoiliac and infrainguinal arteries.
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Carotid Artery Stenosis.
Angiographic or ultrasonographic evidence of one or more significant stenosis (≥50%).
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Atherosclerotic Disease.
Presence of one or more of the diagnoses listed above.
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Postoperative MI.
To diagnose an acute MI a rise in TnT to more than 30 ng/l postoperatively and at least one of the following additional criteria had to be fulfilled20: symptoms of ischemia, new electrocardiogram changes indicative of ischemia (ST and/or T changes or left bundle branch block presumed to be of recent onset), development of pathological Q waves in the electrocardiogram. In absence of any of these concomitant criteria, the patient was categorized as having NTTE.21
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Statistical Analysis
All tests were two-sided, with a 5% significance level. Continuous data, if near normally distributed, are expressed as mean and SD and analyzed with independent and paired samples t tests. The Kolmogorov–Smirnov test was used to test normality. Categorical data are presented as proportions, n (%), and analyzed with Fisher exact test. Data with skewed distributions, which included our primary endpoint TnT, are presented as median (25, 75% percentile) and analyzed with the Mann–Whitney U test or the Wilcoxon signed-rank test. To compare biochemical variables in blood samples pre-, intra-, and postoperatively we used the Friedman test. All analyses were performed by using SPSS 17 (SPSS Inc., Chicago, IL).
The current study included 193 patients scheduled for elective abdominal aortic surgery. To our knowledge, the only data on troponin release in patients anesthetized with volatile anesthetics or TIVA in elective open abdominal aortic surgery, which existed when the ABSENT study was planned and designed were data in an Abstract presented at the American Society of Anesthesiologist congress in 2004. Prestudy sample size calculations were based on these preliminary data from the study by De Hert et al. where they found increased postoperative troponin I levels in 27.9% of patients in the TIVA group, compared with 10.9% in the sevoflurane group (approximately 60% relative risk reduction). To be able to detect the same relative risk reduction (approximately 60%) for increased postoperative TnT levels, assuming 28% of patients with increased TnT levels in group T, α of 0.05 and power of 80%, 96 patients had to be randomized to each group. No power calculations were performed for comparison of secondary outcomes.
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Preoperative Characteristics and Baseline Demographics
Table 2
Table 2
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Table 3
Table 3
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Preoperative characteristics and baseline demographics are given in table 2. Mean age of the study population was 68 (range 43–84) yr. The study included 123 patients (64%) in American Society of Anesthesiologist class 3 and 4. Coexistent CAD was present in 70 patients (36%). Except for slightly higher HR and lower use of aspirin in group S, the groups were well balanced for all remaining variables. In group S, 76 patients (78%) were subjected to AAA surgery versus 74 (77%) in group T. Remaining patients had to undergo surgery for other conditions in the infrarenal aorta or iliac arteries, requiring abdominal aortic surgery either with a tube graft or bifurcated graft (table 3).
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TnT Release
There were no significant group differences between the two groups in TnT levels pre- or postoperatively. In group S, 22 patients (23%) had preoperative TnT values more than 13 ng/l versus 15 (16%) in group T (P = 0.202). Preoperative median TnT value was less than 10 ng/l (<10, 13) in group S versus less than 10 (<10, 10) in group T (P = 0.345). On the first postoperative day TnT values were more than 13 ng/l in 43 patients (44%) in group S versus 41 (43%) in group T (P = 0.999). In group S, 19 patients (20%) had a rise of TnT to more than 30 ng/l versus 15 (16%) in group T (P = 0.579). Median TnT value on the first postoperative day was 12 ng/l (<10, 26) in group S versus 12 (<10, 22) in group T (P = 0.662).
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Intra- and Postoperative Characteristics
Table 4
Table 4
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There were no significant differences between the two groups regarding intra- and postoperative characteristics (table 4), except that more patients in group T were bleeding the first day after surgery (P = 0.037) and patients in group T had higher intraoperative diuresis (P = 0.002) compared with group S. More patients were given dopamine in group T compared with group S (P = 0.003). On the basis of post hoc analysis of paper anesthesia records there were no differences between the two groups in number of episodes of brady-/tachycardia and hyper-/hypotension lasting more than 2 min (table 4). Two patients did not receive an epidural catheter (one in each group). The first postoperative day at 8:00 AM, 11 patients (7 in group S and 4 in group T) had epidural analgesia that was not optimal.
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Postoperative Complications
Table 5
Table 5
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Postoperative complications assessed from end of surgery to 30 days follow-up are given in table 5. Six of 34 patients with a rise in TnT to more than 30 ng/l on the first postoperative day qualified for a diagnosis of acute MI. Another two patients had acute MI (one with normal TnT the first postoperative day) with a rise in TnT to more than 30 ng/l at a later stage during hospitalization. Total incidence of postoperative acute MI was 8 (4.1%); 5 (5.2%) in group S versus 3 (3.1%) in group T. All patients with acute MI were categorized to have non-ST segment increase MI and none of them had evidence of new left ventricular dysfunction, as shown by a postoperative echocardiogram.
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Mortality Rates
Fig. 3
Fig. 3
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Total 30-day mortality was 8/193 (4.1%), 6/84 (7%) in patients with increased TnT more than 13 ng/l versus 2/109 (2%) among patients with normal TnT. The mortality rate was 3/8 (37.5%) in patients with acute MI versus 2/27 (7.4%) in the NTTE group. Total study group mortality rates were 11 (5.7%) at 3 months and 12 (6.2%) at 6 months (fig. 3). Median long-term follow-up was 1,064 (range 221–1,649) days. During this period 23 patients (11.9%) died, 10 in group S (10.3%) versus 13 (13.5%) in group T.
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Time of Hospitalization
Median hours of stay at the postoperative ward/intensive care unit were 28 (25, 62) in group S versus 27 (25, 50) in group T, and median days of hospital stay were 9 (8, 12) in group S versus 9 (8, 12) in group T.
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In elective abdominal aortic surgery we found no significant differences between patients receiving sevoflurane-based anesthesia compared with TIVA in increased TnT levels (>13 ng/l) on the first postoperative day or in TnT levels at any time.
In different models and species it has been shown that volatile anesthetics and opioids can induce cardioprotection.22–26 Data from cardiac surgery have shown a cardioprotective effect of volatile anesthetics8–11 and is supported by two meta-analyses.7,27 Also, propofol has been suggested to have protective effects28,29 and has been indicated in clinical studies.13,30
There are limited data on cardioprotection by volatile anesthetics in noncardiac surgery. In a retrospective, nonrandomized study, De Hert et al.31 found a nonsignificant trend toward lower troponin I release with volatile agents versus nonvolatile anesthetic regimen in patients undergoing aortic surgery. To the best of our knowledge, there are only two prospective randomized studies comparing volatile anesthetics and TIVA with regard to cardioprotection in major noncardiac surgery.32,33 Zangrillo et al.32 randomized 88 patients to sevoflurane-based anesthesia or TIVA. They found no significant difference in number of patients with troponin release after surgery and no differences in complications between the two groups. On the basis of American Society of Anesthesiologist classification, the populations in the two studies seem to be quite similar. In both studies coexistent CAD was present in 36% of the patients. An important aspect separating the two studies is that peripheral vascular surgery was included in the study by Zangrillo et al.,32 as opposed to open abdominal aortic surgery. In the study by Zangrillo et al.32 no perioperative MI or ischemia occurred after 30 days, and the incidence of cardiac events after 1 yr was limited, reflecting that their heterogeneous study population was not optimal for detecting cardioprotection. Additionally, intraoperative hemodynamic assessment and management were not described in their study.
In a study by Lurati Buse et al.,33 385 patients subjected to noncardiac surgery were randomized to sevoflurane or propofol. The sample-size calculation in their study was based on myocardial ischemia on a 3-lead electrocardiogram and not on TnT increase. The primary endpoint was a composite of any ischemic episode, detected by 3-lead electrocardiogram and/or by TnT increase. They found that sevoflurane did not reduce the incidence of ischemia compared with propofol. Details regarding intraoperative hemodynamic management were not given. Only 58% of their patients were subjected to major vascular surgery. The study population had either established CAD or two or more risk factors for CAD, resulting in a higher prevalence of CAD and ongoing chronic β-blockade than in our study. β-Blockade could theoretically diminish potential cardioprotective effects of anesthetic drugs. TnT increase in their study was based on two assays with different cutoff values, with the majority based at more than 30 ng/l. This may explain why the incidence of TnT increase in the two groups was lower compared with that in our study.
In a large-cohort study of patients aged more than 65 yr, Newman et al.34 found that AAA patients had increased risk for other cardiovascular diseases and cardiovascular death, and the risk increased with size of the aneurism. In that survey 41% of individuals with AAA had a history of cardiovascular disease, compared with 36% in the current study. These aspects may explain the relative high incidence of cardiovascular complications in the current study.
The incidence of acute MI is comparable with that in other studies.35,36 Although this study was not powered to evaluate mortality or other secondary outcomes, mortality in patients with acute MI tended to be higher than in patients with NTTE. This is contradictory to mortality in patients hospitalized with chest pain and troponin increase.21 All patients with acute MI in our study were without ST-segment increase. We found no significant difference in TnT levels among patients with acute MI versus NTTE.
When we initiated inclusion, the only data that existed on troponin release in patients anesthetized with volatile anesthetics or TIVA in elective open-abdominal aortic surgery was an Abstract presented at the American Society of Anesthesiologist annual meeting in 2004. We used these data for our prestudy sample-size analysis. Calculations regarding the primary endpoint assumed an approximately 60% relative risk reduction. We cannot exclude that smaller differences in TnT release do exist between the two groups. Another assumption was that increased TnT levels occurred in minimum 28% of patients anesthetized with TIVA. We observed increased TnT levels in 43% of the patients, a fact that further increases power of the primary endpoint of the study. With the relatively high number of NTTE and noncardiac complications observed, it seems unlikely that one anesthetic method is associated with substantial clinical benefit versus the other. To evaluate myocardial injury based on the rise of troponins, the cutoff values applied are essential. Different results may occur by using different cutoff values. Differences between the two anesthetic regimens were not detectable using either TnT more than 13 ng/l or more than 30 ng/l as cutoff values. When TnT of more than 13 ng/l was used, a higher number of patients inevitably had TnT increase, representing a higher power to detect possible differences. We did not observe any differences between the groups in postoperative complications, length of stay at intensive care unit/hospital, or mortality. These observations, however, must be interpreted with caution because the study was not powered to detect a difference in these secondary outcomes.
For induction of anesthesia thiopental was used in group S and propofol in group T. Cardioprotective effect of thiopental is controversial.37,38 In the current study fentanyl was used for induction of anesthesia in both groups. Thereafter, fentanyl was used to potentiate sevoflurane anesthesia in group S, whereas remifentanil was used in group T. It has been shown that opioids, especially remifentanil, have cardioprotective effects.39 Thus, the use of opioids and choice of induction agents might have influenced the results and made the results harder to interpret. Another important aspect is that minimum alveolar concentration of sevoflurane used in the current study should be high enough to achieve cardioprotection.40,41
Before accepting our results it is mandatory to exclude potential differences between the two groups. We used goal-directed hemodynamic management intra- and postoperatively. The protocol was followed rigorously. There was no difference in amount of iv fluid, hemodynamic alterations, or use of epidural analgesia perioperatively between the two groups. The groups were well balanced for coexisting CAD and other important prognostic variables. However, significantly more patients used aspirin in group T compared with group S. Aspirin has shown to be protective during surgery.42 Thus, this could have improved the results in group T. Patients in group S also had slightly higher resting HR than in group T. We also found a higher urine output during surgery in group T, which might be explained by more use of dopamine in this group. We consider these differences too small to explain the neutral finding in our study.
Another possible confounder may be a selection bias in patients with too few complications to detect differences in cardioprotection. The prevalence of preexisting CAD, however, was identical to that reported by Young et al.43 and increase of TnT above the discriminator level for myocardial necrosis was comparable with that in a study by Abraham et al.44 Thirty-day mortality for elective AAA surgery has been reported from 1.6 to 7.8%,45,46 indicating that our study group did not represent a low-risk group, as reflected from the 30-day and 6-month mortality rates of 4.1% and 6.2% respectively. Although we did not include predefined high-risk cardiovascular patients, included patients had substantial morbidity and mortality. Due to regulatory rules, data on long-term total mortality could only be obtained without the possibility of subdividing between cardiovascular and noncardiovascular death. Therefore, it cannot be excluded that the number of deaths unrelated to the surgically treated aortic disease may have been different in the two groups.
A factor that could diminish differences between the groups is remote ischemic preconditioning.47,48 During abdominal aortic surgery, aorta is cross-clamped and both limbs made ischemic. We found no significant difference in cross-clamp time (P = 0.218) between the groups, but cannot exclude that remote protection may have masked anesthetic cardioprotective differences.
The proportion of increased TnT is considerably higher than in previous reports and is probably related to the use of highly sensitive assay with low levels for normality. The value of 13 ng/l was chosen as cutoff point because even small postoperative TnT increases are associated with higher long-term risks of subsequent cardiovascular events and all-cause mortality.6,49,50
Current guidelines14 recommend use of volatile anesthetics during noncardiac surgery in high-risk patients for the maintenance of general anesthesia in hemodynamically stable patients at risk for perioperative myocardial ischemia. Data from the ABSENT study together with data from the studies by Zangrillo et al.32 and Lurati Buse et al.33 do not support these recommendations.
We conclude that there were no differences in number of patients and levels of increased postoperative TnT values between the two anesthetic regimens. Our data indicate that cardioprotective effects of volatile anesthetics found in cardiac surgery are less obvious in unselected patients undergoing elective major vascular abdominal surgery. Further larger-scaled studies are needed to clarify potential anesthetic cardioprotection in different types of noncardiac surgery.
The authors thank Marit Eide, Study Nurse, Department of Anesthesiology, Vestfold Hospital Trust, Tønsberg, Norway; Tone Næss, Study Nurse, Department of Anesthesiology, Vestfold Hospital Trust; Else-Marie Ringvold, M.D., present Head of Department of Anesthesiology, Vestfold Hospital Trust; Odd Helmers, M.D., former Head of Department of Anesthesiology, Vestfold Hospital Trust; Erna Engelstad, Laboratory Assistant, Central Laboratory, Vestfold Hospital Trust; and Matthew McGee, Proofreader, The Morbid Obesity Centre, Vestfold Hospital Trust for their invaluable support.
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1. Mangano DT, Browner WS, Hollenberg M, Li J, Tateo IM. Long-term cardiac prognosis following noncardiac surgery. The Study of Perioperative Ischemia Research Group. JAMA. 1992;268:233–9

2. Twerenbold R, Jaffe A, Reichlin T, Reiter M, Mueller C. High-sensitive troponin T measurements: What do we gain and what are the challenges? Eur Heart J. 2012;33:579–86

3. Panteghini M, Cuccia C, Bonetti G, Giubbini R, Pagani F, Bonini E. Single-point cardiac troponin T at coronary care unit discharge after myocardial infarction correlates with infarct size and ejection fraction. Clin Chem. 2002;48:1432–6

4. Licka M, Zimmermann R, Zehelein J, Dengler TJ, Katus HA, Kübler W. Troponin T concentrations 72 hours after myocardial infarction as a serological estimate of infarct size. Heart. 2002;87:520–4

5. Redfern G, Rodseth RN, Biccard BM. Outcomes in vascular surgical patients with isolated postoperative troponin leak: A meta-analysis. Anaesthesia. 2011;66:604–10

6. Landesberg G, Shatz V, Akopnik I, Wolf YG, Mayer M, Berlatzky Y, Weissman C, Mosseri M. Association of cardiac troponin, CK-MB, and postoperative myocardial ischemia with long-term survival after major vascular surgery. J Am Coll Cardiol. 2003;42:1547–54

7. Landoni G, Biondi-Zoccai GG, Zangrillo A, Bignami E, D’Avolio S, Marchetti C, Calabrò MG, Fochi O, Guarracino F, Tritapepe L, De Hert S, Torri G. Desflurane and sevoflurane in cardiac surgery: A meta-analysis of randomized clinical trials. J Cardiothorac Vasc Anesth. 2007;21:502–11

8. Conzen PF, Fischer S, Detter C, Peter K. Sevoflurane provides greater protection of the myocardium than propofol in patients undergoing off-pump coronary artery bypass surgery. Anesthesiology. 2003;99:826–33

9. Tritapepe L, Landoni G, Guarracino F, Pompei F, Crivellari M, Maselli D, De Luca M, Fochi O, D’Avolio S, Bignami E, Calabrò MG, Zangrillo A. Cardiac protection by volatile anaesthetics: A multicentre randomized controlled study in patients undergoing coronary artery bypass grafting with cardiopulmonary bypass. Eur J Anaesthesiol. 2007;24:323–31

10. De Hert SG, Van der Linden PJ, Cromheecke S, Meeus R, ten Broecke PW, De Blier IG, Stockman BA, Rodrigus IE. Choice of primary anesthetic regimen can influence intensive care unit length of stay after coronary surgery with cardiopulmonary bypass. Anesthesiology. 2004;101:9–20

11. De Hert SG, Van der Linden PJ, Cromheecke S, Meeus R, Nelis A, Van Reeth V, ten Broecke PW, De Blier IG, Stockman BA, Rodrigus IE. Cardioprotective properties of sevoflurane in patients undergoing coronary surgery with cardiopulmonary bypass are related to the modalities of its administration. Anesthesiology. 2004;101:299–10

12. Höcker J, Tonner PH, Böllert P, Paris A, Scholz J, Meier-Paika C, Bein B. Propofol/remifentanil vs sevoflurane/remifentanil for long lasting surgical procedures: A randomised controlled trial. Anaesthesia. 2006;61:752–7

13. Jakobsen CJ, Berg H, Hindsholm KB, Faddy N, Sloth E. The influence of propofol versus sevoflurane anesthesia on outcome in 10,535 cardiac surgical procedures. J Cardiothorac Vasc Anesth. 2007;21:664–71

14. Fleisher LA, Beckman JA, Brown KA, Calkins H, Chaikof E, Fleischmann KE, Freeman WK, Froehlich JB, Kasper EK, Kersten JR, Riegel B, Robb JF, Smith SC Jr, Jacobs AK, Adams CD, Anderson JL, Antman EM, Buller CE, Creager MA, Ettinger SM, Faxon DP, Fuster V, Halperin JL, Hiratzka LF, Hunt SA, Lytle BW, Nishimura R, Ornato JP, Page RL, Riegel B, Tarkington LG, Yancy CWACC/AHA Task Force Members. . ACC/AHA 2007 Guidelines on Perioperative Cardiovascular Evaluation and Care for Noncardiac Surgery: Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to Revise the 2002 Guidelines on Perioperative Cardiovascular Evaluation for Noncardiac Surgery): Developed in Collaboration With the American Society of Echocardiography, American Society of Nuclear Cardiology, Heart Rhythm Society, Society of Cardiovascular Anesthesiologists, Society for Cardiovascular Angiography and Interventions, Society for Vascular Medicine and Biology, and Society for Vascular Surgery. Circulation. 2007;116:1971–96

15. Brewster DC, Cronenwett JL, Hallett JW Jr, Johnston KW, Krupski WC, Matsumura JS. Guidelines for the treatment of abdominal aortic aneurysms: Report of a subcommittee of the Joint Council of the American Association for Vascular Surgery and Society for Vascular Surgery. J Vasc Surg. 2003;37:1106–17

16. Hirsch AT, Haskal ZJ, Hertzer NR, Bakal CW, Creager MA, Halperin JL, Hiratzka LF, Murphy WR, Olin JW, Puschett JB, Rosenfield KA, Sacks D, Stanley JC, Taylor LM Jr, White CJ, White J, White RA, Antman EM, Smith SC Jr, Adams CD, Anderson JL, Faxon DP, Fuster V, Gibbons RJ, Hunt SA, Jacobs AK, Nishimura R, Ornato JP, Page RL, Riegel B. ACC/AHA 2005 Practice Guidelines for the management of patients with peripheral arterial disease (lower extremity, renal, mesenteric, and abdominal aortic): A collaborative report from the American Association for Vascular Surgery/Society for Vascular Surgery, Society for Cardiovascular Angiography and Interventions, Society for Vascular Medicine and Biology, Society of Interventional Radiology, and the ACC/AHA Task Force on Practice Guidelines (Writing Committee to Develop Guidelines for the Management of Patients With Peripheral Arterial Disease): Endorsed by the American Association of Cardiovascular and Pulmonary Rehabilitation; National Heart, Lung, and Blood Institute; Society for Vascular Nursing; TransAtlantic Inter-Society Consensus; and Vascular Disease Foundation. Circulation. 2006;113:e463–54

17. Landoni G, Bignami E, Oliviero F, Zangrillo A. Halogenated anaesthetics and cardiac protection in cardiac and non-cardiac anaesthesia. Ann Card Anaesth. 2009;12:4–9

18. Giannitsis E, Kurz K, Hallermayer K, Jarausch J, Jaffe AS, Katus HA. Analytical validation of a high-sensitivity cardiac troponin T assay. Clin Chem. 2010;56:254–61

19. Poole-Wilson PA, Lubsen J, Kirwan BA, van Dalen FJ, Wagener G, Danchin N, Just H, Fox KA, Pocock SJ, Clayton TC, Motro M, Parker JD, Bourassa MG, Dart AM, Hildebrandt P, Hjalmarson A, Kragten JA, Molhoek GP, Otterstad JE, Seabra-Gomes R, Soler-Soler J, Weber SCoronary Disease Trial Investigating Outcome with Nifedipine Gastrointestinal Therapeutic System Investigators. . Effect of long-acting nifedipine on mortality and cardiovascular morbidity in patients with stable angina requiring treatment (ACTION trial): Randomised controlled trial. Lancet. 2004;364:849–57

20. Thygesen K, Alpert JS, White HD, Jaffe AS, Apple FS, Galvani M, Katus HA, Newby LK, Ravkilde J, Chaitman B, Clemmensen PM, Dellborg M, Hod H, Porela P, Underwood R, Bax JJ, Beller GA, Bonow R, Van der Wall EE, Bassand JP, Wijns W, Ferguson TB, Steg PG, Uretsky BF, Williams DO, Armstrong PW, Antman EM, Fox KA, Hamm CW, Ohman EM, Simoons ML, Poole-Wilson PA, Gurfinkel EP, Lopez-Sendon JL, Pais P, Mendis S, Zhu JR, Wallentin LC, Fernández-Avilés F, Fox KM, Parkhomenko AN, Priori SG, Tendera M, Voipio-Pulkki LM, Vahanian A, Camm AJ, De Caterina R, Dean V, Dickstein K, Filippatos G, Funck-Brentano C, Hellemans I, Kristensen SD, McGregor K, Sechtem U, Silber S, Tendera M, Widimsky P, Zamorano JL, Morais J, Brener S, Harrington R, Morrow D, Lim M, Martinez-Rios MA, Steinhubl S, Levine GN, Gibler WB, Goff D, Tubaro M, Dudek D, Al-Attar NJoint ESC/ACCF/AHA/WHF Task Force for the Redefinition of Myocardial Infarction. . Universal definition of myocardial infarction. Circulation. 2007;116:2634–53

21. Alcalai R, Planer D, Culhaoglu A, Osman A, Pollak A, Lotan C. Acute coronary syndrome vs nonspecific troponin elevation: Clinical predictors and survival analysis. Arch Intern Med. 2007;167:276–81

22. Frässdorf J, Huhn R, Niersmann C, Weber NC, Schlack W, Preckel B, Hollmann MW. Morphine induces preconditioning via activation of mitochondrial K(Ca) channels. Can J Anaesth. 2010;57:767–73

23. Preckel B, Schlack W, Comfère T, Obal D, Barthel H, Thämer V. Effects of enflurane, isoflurane, sevoflurane and desflurane on reperfusion injury after regional myocardial ischaemia in the rabbit heart in vivo. Br J Anaesth. 1998;81:905–12

24. Toller WG, Kersten JR, Pagel PS, Hettrick DA, Warltier DC. Sevoflurane reduces myocardial infarct size and decreases the time threshold for ischemic preconditioning in dogs. Anesthesiology. 1999;91:1437–46

25. Cope DK, Impastato WK, Cohen MV, Downey JM. Volatile anesthetics protect the ischemic rabbit myocardium from infarction. Anesthesiology. 1997;86:699–9

26. Yu CK, Li YH, Wong GT, Wong TM, Irwin MG. Remifentanil preconditioning confers delayed cardioprotection in the rat. Br J Anaesth. 2007;99:632–8

27. Symons JA, Myles PS. Myocardial protection with volatile anaesthetic agents during coronary artery bypass surgery: A meta-analysis. Br J Anaesth. 2006;97:127–36

28. Kokita N, Hara A. Propofol attenuates hydrogen peroxide-induced mechanical and metabolic derangements in the isolated rat heart. Anesthesiology. 1996;84:117–27

29. Xia Z, Godin DV, Ansley DM. Application of high-dose propofol during ischemia improves postischemic function of rat hearts: Effects on tissue antioxidant capacity. Can J Physiol Pharmacol. 2004;82:919–26

30. Xia Z, Huang Z, Ansley DM. Large-dose propofol during cardiopulmonary bypass decreases biochemical markers of myocardial injury in coronary surgery patients: A comparison with isoflurane. Anesth Analg. 2006;103:527–32

31. De Hert SG, Longrois D, Yang H, Fleisher LA. Does the use of a volatile anesthetic regimen attenuate the incidence of cardiac events after vascular surgery? Acta Anaesthesiol Belg. 2008;59:19–5

32. Zangrillo A, Testa V, Aldrovandi V, Tuoro A, Casiraghi G, Cavenago F, Messina M, Bignami E, Landoni G. Volatile agents for cardiac protection in noncardiac surgery: A randomized controlled study. J Cardiothorac Vasc Anesth. 2011;25:902–7

33. Lurati Buse GA, Schumacher P, Seeberger E, Studer W, Schuman RM, Fassl J, Kasper J, Filipovic M, Bolliger D, Seeberger MD. Randomized comparison of sevoflurane versus propofol to reduce perioperative myocardial ischemia in patients undergoing noncardiac surgery. Circulation. 2012;126:2696–704

34. Newman AB, Arnold AM, Burke GL, O’Leary DH, Manolio TA. Cardiovascular disease and mortality in older adults with small abdominal aortic aneurysms detected by ultrasonography: The cardiovascular health study. Ann Intern Med. 2001;134:182–90

35. Schouten O, Dunkelgrun M, Feringa HH, Kok NF, Vidakovic R, Bax JJ, Poldermans D. Myocardial damage in high-risk patients undergoing elective endovascular or open infrarenal abdominal aortic aneurysm repair. Eur J Vasc Endovasc Surg. 2007;33:544–9

36. Nathan DP, Brinster CJ, Jackson BM, Wang GJ, Carpenter JP, Fairman RM, Woo EY. Predictors of decreased short- and long-term survival following open abdominal aortic aneurysm repair. J Vasc Surg. 2011;54:1237–43

37. Zaugg M, Lucchinetti E, Spahn DR, Pasch T, Garcia C, Schaub MC. Differential effects of anesthetics on mitochondrial K(ATP) channel activity and cardiomyocyte protection. Anesthesiology. 2002;97:15–3

38. Müllenheim J, Molojavyi A, Preckel B, Thämer V, Schlack W. Thiopentone does not block ischemic preconditioning in the isolated rat heart. Can J Anaesth. 2001;48:784–9

39. Zhang Y, Irwin MG, Wong TM. Remifentanil preconditioning protects against ischemic injury in the intact rat heart. Anesthesiology. 2004;101:918–23

40. Obal D, Preckel B, Scharbatke H, Müllenheim J, Höterkes F, Thämer V, Schlack W. One MAC of sevoflurane provides protection against reperfusion injury in the rat heart in vivo. Br J Anaesth. 2001;87:905–11

41. Kehl F, Krolikowski JG, Mraovic B, Pagel PS, Warltier DC, Kersten JR. Is isoflurane-induced preconditioning dose related? Anesthesiology. 2002;96:675–80

42. Neilipovitz DT, Bryson GL, Nichol G. The effect of perioperative aspirin therapy in peripheral vascular surgery: A decision analysis. Anesth Analg. 2001;93:573–80

43. Young JR, Hertzer NR, Beven EG, Ruschhaupt WF III, Graor RA, O’Hara PJ, De Wolfe VG, Kramer JR, Simpfendorfer CC. Coronary artery disease in patients with aortic aneurysm: A classification of 302 coronary angiograms and results of surgical management. Ann Vasc Surg. 1986;1:36–2

44. Abraham N, Lemech L, Sandroussi C, Sullivan D, May J. A prospective study of subclinical myocardial damage in endovascular versus open repair of infrarenal abdominal aortic aneurysms. J Vasc Surg. 2005;41:377–80 discussion 380–1

45. Chiesa R, Tshomba Y, Psacharopulo D, Rinaldi E, Logaldo D, Marone EM, Melissano G. Open repair for infrarenal AAA: Technical aspects. J Cardiovasc Surg (Torino). 2012;53(1 suppl 1):119–31

46. Birkmeyer JD, Siewers AE, Finlayson EV, Stukel TA, Lucas FL, Batista I, Welch HG, Wennberg DE. Hospital volume and surgical mortality in the United States. N Engl J Med. 2002;346:1128–37

47. Lang SC, Elsässer A, Scheler C, Vetter S, Tiefenbacher CP, Kübler W, Katus HA, Vogt AM. Myocardial preconditioning and remote renal preconditioning—Identifying a protective factor using proteomic methods? Basic Res Cardiol. 2006;101:149–58

48. Gho BC, Schoemaker RG, van den Doel MA, Duncker DJ, Verdouw PD. Myocardial protection by brief ischemia in noncardiac tissue. Circulation. 1996;94:2193–200

49. Lopez-Jimenez F, Goldman L, Sacks DB, Thomas EJ, Johnson PA, Cook EF, Lee TH. Prognostic value of cardiac troponin T after noncardiac surgery: 6-month follow-up data. J Am Coll Cardiol. 1997;29:1241–5

50. Okmen E, Kasikcioglu H, Sanli A, Uyarel H, Cam N. Correlations between cardiac troponin I, cardiac troponin T, and creatine phosphokinase MB elevation following successful percutaneous coronary intervention and prognostic value of each marker. J Invasive Cardiol. 2005;17:63–7

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