Free
Perioperative Medicine  |   December 2015
Nitrous Oxide and Serious Long-term Morbidity and Mortality in the Evaluation of Nitrous Oxide in the Gas Mixture for Anaesthesia (ENIGMA)-II Trial
Author Notes
  • From the Department of Anaesthesia and Pain Management, Royal Melbourne Hospital, and Anaesthesia, Perioperative and Pain Medicine Unit, and Department of Pharmacology and Therapeutics, University of Melbourne, and Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Australia (K.L.); Department of Anaesthesia and Perioperative Medicine, The Alfred Hospital, and Academic Board of Anaesthesia and Perioperative Medicine, and Department of Epidemiology and Preventive Medicine, Monash University, and National Health and Medical Research Council Practitioner Fellow, Melbourne, Australia (P.S.M.); Department of Epidemiology and Preventive Medicine (J.K., A.F.), Monash University, Melbourne, Australia; Department of Anaesthesia, Austin Hospital, and Department of Surgery, University of Melbourne, Melbourne, Australia (P.J.P.); Department of Anaesthesia, Chinese University of Hong Kong, Hong Kong Special Administrative Region, People’s Republic of China (M.T.V.C.); Department of Anaesthesia and Pain Medicine, Royal Perth Hospital, Perth, Australia, and School of Medicine and Pharmacology, University of Western Australia, Perth, Western Australia, Australia (M.J.P.); Department of Outcomes Research, Cleveland Clinic, Cleveland, Ohio (D.I.S.); Department of Anesthesia, University of Toronto, and Department of Anaesthesia, Toronto General Hospital, Toronto, Ontario, Canada (W.S.B.); Population Health Research Institute, Hamilton Health Sciences and McMaster University, and Departments of Medicine, Clinical Epidemiology, and Biostatistics, McMaster University, Hamilton, Ontario, Canada (P.J.D.); and Department of Anaesthesia and Perioperative Medicine, Alfred Hospital, and Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Australia (S.W.).
  • This article has been selected for the Anesthesiology CME Program. Learning objectives and disclosure and ordering information can be found in the CME section at the front of this issue.
    This article has been selected for the Anesthesiology CME Program. Learning objectives and disclosure and ordering information can be found in the CME section at the front of this issue.×
  • This article is featured in “This Month in Anesthesiology,” page 3A.
    This article is featured in “This Month in Anesthesiology,” page 3A.×
  • Corresponding article on page 1229.
    Corresponding article on page 1229.×
  • Supplemental Digital Content is available for this article. Direct URL citations appear in the printed text and are available in both the HTML and PDF versions of this article. Links to the digital files are provided in the HTML text of this article on the Journal’s Web site (www.anesthesiology.org).
    Supplemental Digital Content is available for this article. Direct URL citations appear in the printed text and are available in both the HTML and PDF versions of this article. Links to the digital files are provided in the HTML text of this article on the Journal’s Web site (www.anesthesiology.org).×
  • Submitted for publication May 18, 2015. Accepted for publication July 16, 2015.
    Submitted for publication May 18, 2015. Accepted for publication July 16, 2015.×
  • Address correspondence to Prof. Leslie: Department of Anaesthesia and Pain Management, Royal Melbourne Hospital, Parkville, Victoria 3050, Australia. kate.leslie@mh.org.au. This article may be accessed for personal use at no charge through the Journal Web site, www.anesthesiology.org.
Article Information
Perioperative Medicine / Clinical Science / Cardiovascular Anesthesia / Ethics / Medicolegal Issues
Perioperative Medicine   |   December 2015
Nitrous Oxide and Serious Long-term Morbidity and Mortality in the Evaluation of Nitrous Oxide in the Gas Mixture for Anaesthesia (ENIGMA)-II Trial
Anesthesiology 12 2015, Vol.123, 1267-1280. doi:10.1097/ALN.0000000000000908
Anesthesiology 12 2015, Vol.123, 1267-1280. doi:10.1097/ALN.0000000000000908
Abstract

Background: The Evaluation of Nitrous Oxide in the Gas Mixture for Anaesthesia (ENIGMA)-II trial randomly assigned 7,112 noncardiac surgery patients at risk of perioperative cardiovascular events to 70% N2O or 70% N2 groups. The aim of this follow-up study was to determine the effect of nitrous oxide on a composite primary outcome of death and major cardiovascular events at 1 yr after surgery.

Methods: One-year follow-up was conducted via a medical record review and telephone interview. Disability was defined as a Katz index of independence in activities of daily living score less than 8. Adjusted odds ratios and hazard ratios were calculated as appropriate for primary and secondary outcomes.

Results: Among 5,844 patients evaluated at 1 yr, 435 (7.4%) had died, 206 (3.5%) had disability, 514 (8.8%) had a fatal or nonfatal myocardial infarction, and 111 (1.9%) had a fatal or nonfatal stroke during the 1-yr follow-up period. Exposure to nitrous oxide did not increase the risk of the primary outcome (odds ratio, 1.08; 95% CI, 0.94 to 1.25; P = 0.27), disability or death (odds ratio, 1.07; 95% CI, 0.90 to 1.27; P = 0.44), death (hazard ratio, 1.17; 95% CI, 0.97 to 1.43; P = 0.10), myocardial infarction (odds ratio, 0.97; 95% CI, 0.81 to 1.17; P = 0.78), or stroke (odds ratio, 1.08; 95% CI, 0.74 to 1.58; P = 0.70).

Conclusion: These results support the long-term safety of nitrous oxide administration in noncardiac surgical patients with known or suspected cardiovascular disease.

Abstract

Nitrous oxide did not increase the risk of a composite primary outcome of death and major cardiovascular events at 1 yr in 5,844 patients with cardiovascular disease recruited to the Evaluation of Nitrous Oxide in the Gas Mixture for Anaesthesia (ENIGMA)-II trial. These results support the long-term safety of nitrous oxide administration in noncardiac surgical patients with known or suspected cardiovascular disease.

Supplemental Digital Content is available in the text.

What We Already Know about This Topic
  • The pathophysiological effects of nitrous oxide might lead to major cardiovascular events after noncardiac surgery

  • Nitrous oxide increased the risk of myocardial infarction in the long-term follow-up of the Evaluation of Nitrous Oxide in the Gas Mixture for Anaesthesia (ENIGMA) trial but that trial did not specifically recruit patients at risk of cardiovascular events

What This Article Tells Us That Is New
  • Nitrous oxide did not increase the risk of a composite primary outcome of death and major cardiovascular events at 1 yr in 5,844 patients with cardiovascular disease recruited to the Evaluation of Nitrous Oxide in the Gas Mixture for Anaesthesia (ENIGMA)-II trial

  • These results support the long-term safety of nitrous oxide administration in noncardiac surgical patients with known or suspected cardiovascular disease

HEALTHCARE research is increasingly focused on longer-term outcomes that are important to patients and the community.1  For example, the long-term follow-up of the Evaluation of Nitrous Oxide in the Gas Mixture for Anaesthesia (ENIGMA) trial revealed that nitrous oxide increased risk of myocardial infarction in noncardiac surgery patients (odds ratio [OR], 1.59; 95% CI, 1.01 to 2.51; P = 0.04).2  This effect had not been evident at the 30-day follow-up (OR, 0.58; 95% CI, 0.22 to 1.50; P = 0.26).3  However, because the patients in the ENIGMA trial were not selected on the basis of the risk for cardiovascular events and because the event rates were low, both the 30-day and long-term results required confirmation in suitably powered studies.
Therefore, we conducted the ENIGMA-II trial to explore the risks and benefits of nitrous oxide in noncardiac surgery patients with known or suspected cardiovascular disease.4  There were no significant differences between patients receiving and not receiving nitrous oxide in terms of their 30-day risk of a composite primary outcome of death or major cardiovascular events.5  The aim of the current study was to determine the effect of nitrous oxide administration on the composite primary outcome and secondary outcomes (death, disability, myocardial infarction, and stroke) at 1 yr after surgery in the ENIGMA-II patients.
Materials and Methods
The ENIGMA-II trial was an international, parallel-group, patient- and observer-blinded, randomized trial. A total of 7,112 noncardiac surgery patients, older than 45 yr and at risk of perioperative cardiovascular complications, were enrolled. ENIGMA-II was registered at ClinicalTrials.gov (number: NCT00430989; principal investigator: P.S.M.; date of registration: January 31, 2007). The protocol4  and results5  of the 30-day follow-up have been published. The trial steering committee prospectively approved the protocol for the 1-yr follow-up, including the detailed statistical analysis plan. Ethics committee approval for the 1-yr follow-up study was obtained at 39 of the 45 participating sites, and patients at these 39 sites consented to the 30-day and 1-yr follow-ups before randomization. Participating sites, investigators, and names and locations of ethics committees are listed in the appendix.
Protocol
Participating patients were randomly assigned to 70% N2O in 30% O2 or 70% N2 in 30% O2 groups. Perioperative care was otherwise at the discretion of the attending anesthesiologists. Patients were monitored with 12-lead electrocardiographs preoperatively and on postoperative days 1 and 3 and with cardiac biomarkers (troponin or, if unavailable, creatine kinase-myocardial band) at 6 to 12 h and 1 to 3 days after surgery. Other investigations were ordered as clinically indicated during the 1-yr follow-up period.
One-year follow-up was conducted via medical record review and telephone interview. The medical record was interrogated for the date and cause of death and the occurrence of myocardial infarction or stroke, any time between 30 days and 1 yr after surgery. The telephone interview was conducted with the patient or their relatives or doctors if the patient had died, was incapacitated, was unavailable, or was unsure about the occurrence of myocardial infarction or stroke.
The primary outcome for the 1-yr follow-up was a composite of death and cardiovascular events (nonfatal myocardial infarction, cardiac arrest, pulmonary embolism, and stroke). The main preprescribed secondary endpoint was disability or death (the inverse of disability-free survival). Disability was defined as a Katz index of independence in activities of daily living score less than 8.6 
Other secondary outcomes were death, fatal or nonfatal myocardial infarction, and fatal or nonfatal stroke. These were defined by patient, relative, or doctor report or by fulfillment of the following criteria, as recorded in the medical record: myocardial infarction was defined by an increased cardiac biomarker level plus at least one of the ischemic symptoms, pathological Q waves, electrocardiographic changes indicative of ischemia, coronary artery intervention, new wall motion abnormality on echocardiography or a fixed defect on radionucleotide scanning, or autopsy finding of new or recent myocardial infarction.7  The troponin threshold that was considered abnormal was each site’s laboratory’s 99th percentile (upper reference limit) of a healthy reference population.8  Stroke was defined as a new neurologic deficit persisting for 24 h or longer, confirmed by a neurologist or computed tomography or magnetic resonance imaging.
Statistical Analysis
The following preoperative and intraoperative characteristics were selected prospectively as covariates in the models: age, sex, body mass index (BMI), American Society of Anesthesiologists’ (ASA) physical status, good exercise capacity (≥ 4 metabolic equivalents), history of coronary artery disease, emergency surgery, vascular surgery, randomized treatment (nitrous oxide or no nitrous oxide), propofol maintenance, regional local anesthetic block, volatile anesthetic administration (minimum alveolar concentration [MAC] equivalents), bispectral index (BIS) monitoring, and duration of anesthesia.
The patients followed up at 1 yr were not necessarily a truly representative sample of the original ENIGMA-II cohort, so a logistic regression model was fitted to estimate the probability that each patient was followed up at 1 yr. For each outcome model, observations were weighted by the inverse of these probabilities. Patients who died or experienced myocardial infarction or stroke within the 30-day follow-up of ENIGMA-II were given a weight of 1. Unweighted models were fitted as sensitivity analyses.
Mortality rates were computed for each category of each covariate and were expressed as deaths per 1,000 person-years. Univariate Cox proportional hazard models were used to define hazard ratios (HRs) and 95% CIs for death. Multivariable Cox proportional hazard models for death were constructed, and assessments of proportionality of hazard functions were performed. Preoperative variables were first adjusted for each other. Then, nitrous oxide, propofol maintenance, regional local anesthetic block, and BIS monitoring were adjusted for each other and preoperative variables. Finally, volatile anesthetic administration less than the median MAC value in patients receiving volatile anesthetic maintenance and duration of anesthesia were adjusted for each other, preoperative variables, nitrous oxide, and BIS monitoring (propofol maintenance was not included because patients who received propofol for maintenance had missing data for volatile anesthetic administration).
Because the date of outcomes other than death was sometimes imprecise or missing, logistic regression was used to compute ORs and 95% CIs for the primary composite outcome, the main secondary outcome of disability or death, and further secondary outcomes of death, myocardial infarction, and stroke. Multivariable models were constructed using the technique described in the previous paragraph. The preplanned assessment of the interaction of each variable with nitrous oxide was performed by using interaction terms in the weighted and unweighted regression models. An additional analysis for stroke was conducted that included a history of previous stroke or transient ischemic attack.
Analyses were conducted using Stata 12 (Stata Corporation, USA). All P values are two sided, and P value less than 0.05 was considered statistically significant.
Results
One-year follow-up occurred between June 2009 and October 2014, with a median follow-up time of 386 days (interquartile range, 366 to 458 days). The centers participating in the 1-yr follow-up study recruited 6,651 (95%) of the 6,992 patients who were assessed for the primary outcome at 30 days.5  Follow-up data were available for 5,844 (88%) of these patients (fig. 1).
Fig. 1.
Flow diagram.
Flow diagram.
Fig. 1.
Flow diagram.
×
A total of 435 patients (7.4%) died; 99 died before 30 days and 336 subsequently (fig. 2) (between treatment P = 0.18). The causes of death were cancer (37.5%), myocardial infarction (4.4%), stroke (4.4%), other cardiovascular death (14.3%), respiratory failure (7.8%), sepsis (13.0%), other causes (8.7%), and unknown (9.9%). In total 641 patients (10.5%) were recorded as having disability or had died (206 [3.5%] had disability), 514 patients (8.8%) were recorded as having a fatal or nonfatal myocardial infarction, and 111 patients (1.9%) were recorded as having a fatal or nonfatal stroke during the 1-yr follow-up period.
Fig. 2.
Kaplan–Meier survival curve for death for randomized treatment groups (P = 0.18).
Kaplan–Meier survival curve for death for randomized treatment groups (P = 0.18).
Fig. 2.
Kaplan–Meier survival curve for death for randomized treatment groups (P = 0.18).
×
Nitrous oxide did not increase the risk of the primary outcome (OR, 1.08; 95% CI, 0.94 to 1.25; P = 0.27) (table 1). Age, BMI, ASA physical status, exercise capacity, coronary artery disease, emergency surgery, propofol maintenance, regional local anesthetic block, and duration of anesthesia were significant predictors of the primary outcome. The adjusted ORs were largely unaffected by weighting to adjust for missing data (Supplemental Digital Content 1, http://links.lww.com/ALN/B204, table 1). The interaction between nitrous oxide and age was statistically significant (P = 0.046) in the weighted model for the primary outcome, but this did not otherwise change the main result (Supplemental Digital Content 1, http://links.lww.com/ALN/B204, table 2).
Table 1.
ORs for the Composite Primary Outcome of Death or Major Cardiovascular Events (Nonfatal Myocardial Infarction, Cardiac Arrest, Pulmonary Embolism, and Stroke)*
ORs for the Composite Primary Outcome of Death or Major Cardiovascular Events (Nonfatal Myocardial Infarction, Cardiac Arrest, Pulmonary Embolism, and Stroke)*×
ORs for the Composite Primary Outcome of Death or Major Cardiovascular Events (Nonfatal Myocardial Infarction, Cardiac Arrest, Pulmonary Embolism, and Stroke)*
Table 1.
ORs for the Composite Primary Outcome of Death or Major Cardiovascular Events (Nonfatal Myocardial Infarction, Cardiac Arrest, Pulmonary Embolism, and Stroke)*
ORs for the Composite Primary Outcome of Death or Major Cardiovascular Events (Nonfatal Myocardial Infarction, Cardiac Arrest, Pulmonary Embolism, and Stroke)*×
×
Nitrous oxide did not increase the risk of disability or death (OR, 1.07; 95% CI, 0.90 to 1.27; P = 0.44) (table 2). Age, BMI, exercise capacity, emergency surgery, and duration of anesthesia were significant predictors of death. The adjusted ORs were largely unaffected by weighting to adjust for missing data (Supplemental Digital Content 1, http://links.lww.com/ALN/B204, table 3). There was no significant interaction between nitrous oxide administration and any covariate in either the weighted or unweighted models for disability or death (Supplemental Digital Content 1, http://links.lww.com/ALN/B204, table 4).
Table 2.
ORs for Disability or Death*
ORs for Disability or Death*×
ORs for Disability or Death*
Table 2.
ORs for Disability or Death*
ORs for Disability or Death*×
×
Nitrous oxide did not increase the risk of death (HR, 1.17; 95% CI, 0.97 to 1.43; P = 0.11) (table 3). Age, BMI, ASA physical status, exercise capacity, emergency surgery, vascular surgery, and duration of anesthesia were significant predictors of death. The adjusted HRs were largely unaffected by weighting to adjust for missing data (Supplemental Digital Content 1, http://links.lww.com/ALN/B204, table 5). The interactions between nitrous oxide and exercise capacity (P = 0.035), and nitrous oxide and MAC equivalents (P = 0.026), were statistically significant in the unweighted model for death (Supplemental Digital Content 1, http://links.lww.com/ALN/B204, table 6).
Table 3.
HRs for Death*
HRs for Death*×
HRs for Death*
Table 3.
HRs for Death*
HRs for Death*×
×
Nitrous oxide did not increase the risk of myocardial infarction (OR, 0.97; 95% CI, 0.81 to 1.17; P = 0.78) (table 4). Age, ASA physical status, exercise capacity, coronary artery disease, emergency surgery, vascular surgery, regional local anesthetic block, BIS monitoring, and duration of anesthesia were significant predictors of myocardial infarction. The adjusted ORs were largely unaffected by weighting to adjust for missing data (Supplemental Digital Content 1, http://links.lww.com/ALN/B204, table 7). The interaction between nitrous oxide and BIS monitoring was statistically significant in the weighted model for myocardial infarction (P = 0.045) (Supplemental Digital Content 1, http://links.lww.com/ALN/B204, table 8).
Table 4.
ORs for Myocardial Infarction*
ORs for Myocardial Infarction*×
ORs for Myocardial Infarction*
Table 4.
ORs for Myocardial Infarction*
ORs for Myocardial Infarction*×
×
Nitrous oxide did not increase the risk of stroke (OR, 1.08; 95% CI, 0.74 to 1.58; P = 0.70) (table 5). Age and vascular surgery were significant predictors of stroke. The adjusted ORs were largely unaffected by weighting to adjust for missing data (Supplemental Digital Content 1, http://links.lww.com/ALN/B204, table 9). There was no significant interaction between nitrous oxide administration and any covariate in either the weighted or unweighted models for stroke (Supplemental Digital Content 1, http://links.lww.com/ALN/B204, table 10). A history of previous stroke or transient ischemic attack was a significant predictor of stroke within 1 yr of surgery (adjusted OR, 2.43; 95% CI, 1.64 to 3.61; P < 0.005). Adjusted ORs for other covariates were largely unaffected by inclusion of a history of previous stroke or transient ischemic attack (results not shown).
Table 5.
ORs for Stroke*
ORs for Stroke*×
ORs for Stroke*
Table 5.
ORs for Stroke*
ORs for Stroke*×
×
Discussion
We found that nitrous oxide did not increase the incidence of a composite of death or major cardiovascular complications at 1 yr after surgery in patients enrolled in the ENIGMA-II trial. These results are consistent with our findings at 30 days postoperatively and further support the safety of nitrous oxide administration in patients with known or suspected cardiovascular disease.
The ENIGMA-II trial was established on the premise that the pathophysiological effects of nitrous oxide might lead to major cardiovascular events after noncardiac surgery.4,9  These effects include the inhibition of methionine synthase with resulting hyperhomocysteinemia10,11  and endothelial dysfunction,12,13  especially in patients with genetic14  or dietary15  predispositions. However, the recent Vitamins in Nitrous Oxide (VINO) randomized trial16  did not confirm earlier findings17  of myocardial ischemia among patients exposed to nitrous oxide or an ameliorating effect of vitamin B12 and folate administration on postoperative troponin increases. The VINO study and our ENIGMA-II analyses provide strong evidence to refute the hypothesis that the hyperhomocysteinemia associated with nitrous oxide administration leads to adverse cardiovascular outcomes.
The ENIGMA-II 1-yr follow-up results contrast with our finding in the long-term follow-up of the ENIGMA study2  of an increased long-term risk of myocardial infarction in patients who were randomly assigned to nitrous oxide group. There were important differences between ENIGMA and ENIGMA-II: (1) the inclusion criteria (unselected in ENIGMA and selected for cardiovascular risk factors in ENIGMA-II); (2) the percentage of inspired oxygen administered (30% in the nitrous oxide group and 80% in the no nitrous group in ENIGMA and 30% in both groups in ENIGMA-II); and (3) the duration of follow-up (3.5 yr [range, 0 to 5.7 yr] in ENIGMA and 1.06 yr [range, 0 to 3.89 yr] in ENIGMA-II). Most likely, though, differences in long-term outcomes simply reflect the smaller sample size of the ENIGMA follow-up (n = 1,660), leading to a spurious finding in that study.18 
The incidences of death (7.4%), disability (3.5%), myocardial infarction (8.8%), and stroke (1.9%) in this study are consistent with the inclusion criteria for ENIGMA-II and previously published studies of noncardiac surgery patients with cardiovascular disease.19–23  In relation to myocardial infarction in particular, these studies point to substantial scope for improved outcomes through primary prevention, early detection, treatment, and prevention of complications.24  Unfortunately, no primary prevention measures for perioperative myocardial infarction in noncardiac surgical patients are conclusively proven to be both effective and safe,25–28  including the omission of nitrous oxide.
The World Health Organization defines disability as “difficulties in any area of functioning as they relate to environmental and personal factors.”29  We chose to use the Katz score, which measures physical functioning, to determine the disability in the ENIGMA-II trial.6  Among the widely used scales, we now recommend the World Health Organization Disability Assessment Schedule for this purpose, as it includes cognition, interpersonal relationships, participation in society, self-care, work and household roles, and mobility.30 
Many covariates were associated with increased risk of the primary and/or secondary outcomes of this study, including increasing age,2,19,31–33  low BMI,19,31,32,34  higher ASA physical status,2,19,31–33  lower exercise capacity,35  coronary artery disease,2,32  emergency surgery,2,19,33  propofol maintenance,2  regional local anesthetic block,36  lack of BIS monitoring, and longer duration of anesthesia.2,19  Although analyses were sequentially adjusted for pre- and intraoperative factors, it is possible that some of these associations resulted from selection bias or residual confounding, in particular the interventions at the discretion of the attending anesthesiologist where the factors that impacted on the decision to use the intervention may not have been captured completely. For example, lack of BIS monitoring was associated with an increased long-term risk of myocardial infarction in this follow-up study but was not associated with major cardiovascular events in longer-term follow-up studies of patients who were randomly assigned to receive or not receive BIS-guided anesthesia.19,32  Therefore, this result should be interpreted with caution.
This study is one of the largest randomized controlled trials to follow noncardiac surgery patients with risk factors for major cardiovascular events over an extended postoperative period.2,19  Our results provide a robust estimate of the incidence of death and effect of nitrous oxide on survival after surgery. The different directions of effect on death at the 30-day5  and 1-yr follow-ups (toward a protective effect at 30 days and toward a harmful effect at 1 yr) likely arise from random error. The study is limited with respect to myocardial infarction and stroke because patients were not specifically screened for these events during the period between 30 days and 1 yr, and we relied on medical record, patient or surrogate reports. The number and scope of covariates available for adjustment in the model further limit the study. Finally, a number of centers were unable to participate in the 1-yr follow-up study due to limited resources, resulting in a 5% rate of missing 1-yr outcomes. Although we adjusted for missing 1-yr outcomes in our analyses, and results were similar in weighted and unweighted analyses, a subtle effect cannot be ruled out.
In conclusion, nitrous oxide administration did not increase the incidence of a composite of death or major cardiovascular events during a 1-yr follow-up period in patients randomly assigned to the ENIGMA-II trial. Nitrous oxide can be safely administered to patients with known or suspected cardiovascular disease undergoing noncardiac surgery.
Acknowledgments
This study was supported by Australian and New Zealand College of Anaesthetists Project Grants 10/014 and 12/008 (Melbourne, Victoria, Australia). The Evaluation of Nitrous Oxide in the Gas Mixture for Anaesthesia (ENIGMA)-II trial was supported by a National Health and Medical Research Council Project Grant (435015) (Canberra, Australian Capital Territory, Australia); a Research Grant Council General Research Fund grant (461409) (Hong Kong, Special Administrative Area, People's Repubic of China); and a Health and Research Grant Council Medical Research Fund grant (11121051) (Hong Kong, Special Administrative Area, People’s Republic of China).
Competing Interests
The authors declare no competing interests.
Reproducible Science
Full protocol available at: kate.leslie@mh.org.au. Raw data available at: kate.leslie@mh.org.au.
References
Sessler, DI Long-term consequences of anesthetic management.. Anesthesiology. (2009). 111 1–4 [Article] [PubMed]
Leslie, K, Myles, PS, Chan, MT, Forbes, A, Paech, MJ, Peyton, P, Silbert, BS, Williamson, E Nitrous oxide and long-term morbidity and mortality in the ENIGMA trial.. Anesth Analg. (2011). 112 387–93 [Article] [PubMed]
Myles, P, Leslie, K, Chan, M, Forbes, A, Paech, M, Peyton, P, Silbert, BS, Pascoe, E ENIGMA Trial Group, Avoidance of nitrous oxide for patients undergoing major surgery: A randomized controlled trial.. Anesthesiology. (2007). 107 221–31 [Article] [PubMed]
Myles, PS, Leslie, K, Peyton, P, Paech, M, Forbes, A, Chan, MT, Sessler, D, Devereaux, PJ, Silbert, BS, Jamrozik, K, Beattie, S, Badner, N, Tomlinson, J, Wallace, S ANZCA Trials Group, Nitrous oxide and perioperative cardiac morbidity (ENIGMA-II) trial: Rationale and design.. Am Heart J. (2009). 157 488–494.e1 [Article] [PubMed]
Myles, PS, Leslie, K, Chan, MT, Forbes, A, Peyton, PJ, Paech, MJ, Beattie, WS, Sessler, DI, Devereaux, PJ, Silbert, B, Schricker, T, Wallace, S ANZCA Trials Group for the ENIGMA-II Investigators, The safety of addition of nitrous oxide to general anaesthesia in at-risk patients having major non-cardiac surgery (ENIGMA-II): A randomised, single-blind trial.. Lancet. (2014). 384 1446–54 [Article] [PubMed]
Katz, S, Ford, AB, Moskowitz, RW, Jackson, BA, Jaffe, MW Studies of illness in the aged. The index of ADL: A standardized measure of biological and psychosocial function.. JAMA. (1963). 185 914–9 [Article] [PubMed]
Thygesen, K, Alpert, JS, Jaffe, AS, Simoons, ML, Chaitman, BR, White, HD Joint ESC/ACCF/AHA/WHF Task Force for Universal Definition of Myocardial Infarction; Authors/Task Force Members Chairpersons, Thygesen, K, Alpert, JS, White, HD Biomarker Subcommittee, Jaffe, AS, Katus, HA, Apple, FS, Lindahl, B, Morrow, DA ECG Subcommittee, Chaitman, BR, Clemmensen, PM, Johanson, P, Hod, H Imaging Subcommittee, Underwood, R, Bax, JJ, Bonow, JJ, Pinto, F, Gibbons, RJ Classification Subcommittee, Fox, KA, Atar, D, Newby, LK, Galvani, M, Hamm, CW Intervention Subcommittee, Uretsky, BF, Steg, PG, Wijns, W, Bassand, JP, Menasche, P, Ravkilde, J Trials & Registries Subcommittee, Ohman, EM, Antman, EM, Wallentin, LC, Armstrong, PW, Simoons, ML Trials & Registries Subcommittee, Januzzi, JL, Nieminen, MS, Gheorghiade, M, Filippatos, G Trials & Registries Subcommittee, Luepker, RV, Fortmann, SP, Rosamond, WD, Levy, D, Wood, D Trials & Registries Subcommittee, Smith, SC, Hu, D, Lopez-Sendon, JL, Robertson, RM, Weaver, D, Tendera, M, Bove, AA, Parkhomenko, AN, Vasilieva, EJ, Mendis, S ESC Committee for Practice Guidelines (CPG); Document Reviewers, Bax, JJ, Baumgartner, H, Ceconi, C, Dean, V, Deaton, C, Fagard, R, Funck-Brentano, C, Hasdai, D, Hoes, A, Kirchhof, P, Knuuti, J, Kolh, P, McDonagh, T, Moulin, C, Popescu, BA, Reiner, Z, Sechtem, U, Sirnes, PA, Tendera, M, Torbicki, A, Vahanian, A, Windecker, S, Morais, J, Aguiar, C, Almahmeed, W, Arnar, DO, Barili, F, Bloch, KD, Bolger, AF, Botker, HE, Bozkurt, B, Bugiardini, R, Cannon, C, de Lemos, J, Eberli, FR, Escobar, E, Hlatky, M, James, S, Kern, KB, Moliterno, DJ, Mueller, C, Neskovic, AN, Pieske, BM, Schulman, SP, Storey, RF, Taubert, KA, Vranckx, P, Wagner, DR Joint ESC/ACCF/AHA/WHF Task Force for Universal Definition of Myocardial Infarction; Authors/Task Force Members Chairpersons, Biomarker Subcommittee, ECG Subcommittee, Imaging Subcommittee, Classification Subcommittee, Intervention Subcommittee, Trials & Registries Subcommittee, Trials & Registries Subcommittee, Trials & Registries Subcommittee, Trials & Registries Subcommittee, ESC Committee for Practice Guidelines (CPG); Document Reviewers, Third universal definition of myocardial infarction.. J Am Coll Cardiol. (2012). 60 1581–98 [Article] [PubMed]
Leonardi, S, Armstrong, P, Schulte, P, Ohman, E, Newby, L Implementation of standardized assessment and reporting of myocardial infarction in contemporary randomized controlled trials: A systematic review.. Eur Heart J. (2013). 34 894–902d [Article] [PubMed]
Myles, PS, Leslie, K, Silbert, B, Paech, MJ, Peyton, P A review of the risks and benefits of nitrous oxide in current anaesthetic practice.. Anaesth Intensive Care. (2004). 32 165–72 [PubMed]
Ermens, AA, Refsum, H, Rupreht, J, Spijkers, LJ, Guttormsen, AB, Lindemans, J, Ueland, PM, Abels, J Monitoring cobalamin inactivation during nitrous oxide anesthesia by determination of homocysteine and folate in plasma and urine.. Clin Pharmacol Ther. (1991). 49 385–93 [Article] [PubMed]
Badner, NH, Drader, K, Freeman, D, Spence, JD The use of intraoperative nitrous oxide leads to postoperative increases in plasma homocysteine.. Anesth Analg. (1998). 87 711–3 [PubMed]
Myles, PS, Chan, MT, Kaye, DM, McIlroy, DR, Lau, CW, Symons, JA, Chen, S Effect of nitrous oxide anesthesia on plasma homocysteine and endothelial function.. Anesthesiology. (2008). 109 657–63 [Article] [PubMed]
Chambers, JC, McGregor, A, Jean-Marie, J, Obeid, OA, Kooner, JS Demonstration of rapid onset vascular endothelial dysfunction after hyperhomocysteinemia: An effect reversible with vitamin C therapy.. Circulation. (1999). 99 1156–60 [Article] [PubMed]
Nagele, P, Zeugswetter, B, Wiener, C, Burger, H, Hüpfl, M, Mittlböck, M, Födinger, M Influence of methylenetetrahydrofolate reductase gene polymorphisms on homocysteine concentrations after nitrous oxide anesthesia.. Anesthesiology. (2008). 109 36–43 [Article] [PubMed]
Myles, PS, Chan, MT, Forbes, A, Leslie, K, Paech, M, Peyton, P Preoperative folate and homocysteine status in patients undergoing major surgery.. Clin Nutr. (2006). 25 736–45 [Article] [PubMed]
Nagele, P, Brown, F, Francis, A, Scott, MG, Gage, BF, Miller, JP VINO Study Team, Influence of nitrous oxide anesthesia, B-vitamins, and MTHFR gene polymorphisms on perioperative cardiac events: The vitamins in nitrous oxide (VINO) randomized trial.. Anesthesiology. (2013). 119 19–28 [Article] [PubMed]
Badner, NH, Beattie, WS, Freeman, D, Spence, JD Nitrous oxide-induced increased homocysteine concentrations are associated with increased postoperative myocardial ischemia in patients undergoing carotid endarterectomy.. Anesth Analg. (2000). 91 1073–9 [PubMed]
Button, KS, Ioannidis, JP, Mokrysz, C, Nosek, BA, Flint, J, Robinson, ES, Munafò, MR Power failure: Why small sample size undermines the reliability of neuroscience.. Nat Rev Neurosci. (2013). 14 365–76 [Article] [PubMed]
Leslie, K, Myles, PS, Forbes, A, Chan, MT The effect of bispectral index monitoring on long-term survival in the B-aware trial.. Anesth Analg. (2010). 110 816–22 [Article] [PubMed]
Nagele, P, Brown, F, Gage, BF, Gibson, DW, Miller, JP, Jaffe, AS, Apple, FS, Scott, MG High-sensitivity cardiac troponin T in prediction and diagnosis of myocardial infarction and long-term mortality after noncardiac surgery.. Am Heart J. (2013). 166 325–332.e1 [Article] [PubMed]
Monk, TG, Saini, V, Weldon, BC, Sigl, JC Anesthetic management and one-year mortality after noncardiac surgery.. Anesth Analg. (2005). 100 4–10 [Article] [PubMed]
Bijker, JB, van Klei, WA, Vergouwe, Y, Eleveld, DJ, van Wolfswinkel, L, Moons, KG, Kalkman, CJ Intraoperative hypotension and 1-year mortality after noncardiac surgery.. Anesthesiology. (2009). 111 1217–26 [Article] [PubMed]
Desai, H, Aronow, WS, Ahn, C, Gandhi, K, Amin, H, Lai, HM, Tsai, FS, Sharma, M, Babu, S Incidence of perioperative myocardial infarction and of 2-year mortality in 577 elderly patients undergoing noncardiac vascular surgery treated with and without statins.. Arch Gerontol Geriatr. (2010). 51 149–51 [Article] [PubMed]
Fleisher, LA, Fleischmann, KE, Auerbach, AD, Barnason, SA, Beckman, JA, Bozkurt, B, Davila-Roman, VG, Gerhard-Herman, MD, Holly, TA, Kane, GC, Marine, JE, Nelson, MT, Spencer, CC, Thompson, A, Ting, HH, Uretsky, BF, Wijeysundera, DN American College of Cardiology; American Heart Association, 2014 ACC/AHA guideline on perioperative cardiovascular evaluation and management of patients undergoing noncardiac surgery: A report of the American College of Cardiology/American Heart Association Task Force on practice guidelines.. J Am Coll Cardiol. (2014). 64 e77–137 [Article] [PubMed]
POISE Study Group, Effects of extended-release metoprolol succinate in patients undergoing non-cardiac surgery (POISE trial): A randomised controlled trial.. Lancet. (2008). 371 1839–47 [Article] [PubMed]
Devereaux, PJ, Sessler, DI, Leslie, K, Kurz, A, Mrkobrada, M, Alonso-Coello, P, Villar, JC, Sigamani, A, Biccard, BM, Meyhoff, CS, Parlow, JL, Guyatt, G, Robinson, A, Garg, AX, Rodseth, RN, Botto, F, Lurati Buse, G, Xavier, D, Chan, MT, Tiboni, M, Cook, D, Kumar, PA, Forget, P, Malaga, G, Fleischmann, E, Amir, M, Eikelboom, J, Mizera, R, Torres, D, Wang, CY, Vanhelder, T, Paniagua, P, Berwanger, O, Srinathan, S, Graham, M, Pasin, L, Le Manach, Y, Gao, P, Pogue, J, Whitlock, R, Lamy, A, Kearon, C, Chow, C, Pettit, S, Chrolavicius, S, Yusuf, S POISE-2 Investigators, Clonidine in patients undergoing noncardiac surgery.. N Engl J Med. (2014). 370 1504–13 [Article] [PubMed]
Devereaux, PJ, Mrkobrada, M, Sessler, DI, Leslie, K, Alonso-Coello, P, Kurz, A, Villar, JC, Sigamani, A, Biccard, BM, Meyhoff, CS, Parlow, JL, Guyatt, G, Robinson, A, Garg, AX, Rodseth, RN, Botto, F, Lurati Buse, G, Xavier, D, Chan, MT, Tiboni, M, Cook, D, Kumar, PA, Forget, P, Malaga, G, Fleischmann, E, Amir, M, Eikelboom, J, Mizera, R, Torres, D, Wang, CY, VanHelder, T, Paniagua, P, Berwanger, O, Srinathan, S, Graham, M, Pasin, L, Le Manach, Y, Gao, P, Pogue, J, Whitlock, R, Lamy, A, Kearon, C, Baigent, C, Chow, C, Pettit, S, Chrolavicius, S, Yusuf, S POISE-2 Investigators, Aspirin in patients undergoing noncardiac surgery.. N Engl J Med. (2014). 370 1494–503 [Article] [PubMed]
McFalls, EO, Ward, HB, Moritz, TE, Goldman, S, Krupski, WC, Littooy, F, Pierpont, G, Santilli, S, Rapp, J, Hattler, B, Shunk, K, Jaenicke, C, Thottapurathu, L, Ellis, N, Reda, DJ, Henderson, WG Coronary-artery revascularization before elective major vascular surgery.. N Engl J Med. (2004). 351 2795–804 [Article] [PubMed]
World Health Organization, International Classification of Functioning, Disability and Health. (2008). Geneva, Switzerland World Health Organization 1–299
Shulman, M, Myles, P, Chan, M, McIlroy, D, Wallace, S, Ponsford, J Measurement of disability-free survival after surgery.. Anesthesiology. (2015). 122 524–36 [Article] [PubMed]
Lindholm, ML, Träff, S, Granath, F, Greenwald, SD, Ekbom, A, Lennmarken, C, Sandin, RH Mortality within 2 years after surgery in relation to low intraoperative bispectral index values and preexisting malignant disease.. Anesth Analg. (2009). 108 508–12 [Article] [PubMed]
Kertai, M, Palance, B, Pal, N, Burnside, B, Zhang, L, Sadiq, F, Finkel, KJ, Avidan, MS B-Unaware Study Group, Bispectral index monitoring, duration of bispectral index below 45, patient risk factors, and intermediate-term mortality after noncardiac surgery in the B-Unaware Trial.. Anesthesiology. (2011). 114 545–56 [Article] [PubMed]
Story, DA, Leslie, K, Myles, PS, Fink, M, Poustie, SJ, Forbes, A, Yap, S, Beavis, V, Kerridge, R REASON Investigators, Australian and New Zealand College of Anaesthetists Trials Group, Complications and mortality in older surgical patients in Australia and New Zealand (the REASON study): A multicentre, prospective, observational study.. Anaesthesia. (2010). 65 1022–30 [Article] [PubMed]
Valentijn, TM, Galal, W, Hoeks, SE, van Gestel, YR, Verhagen, HJ, Stolker, RJ Impact of obesity on postoperative and long-term outcomes in a general surgery population: A retrospective cohort study.. World J Surg. (2013). 37 2561–8 [Article] [PubMed]
Reilly, DF, McNeely, MJ, Doerner, D, Greenberg, DL, Staiger, TO, Geist, MJ, Vedovatti, PA, Coffey, JE, Mora, MW, Johnson, TR, Guray, ED, Van Norman, GA, Fihn, SD Self-reported exercise tolerance and the risk of serious perioperative complications.. Arch Intern Med. (1999). 159 2185–92 [Article] [PubMed]
Leslie, K, Myles, P, Devereaux, P, Williamson, E, Rao-Melancini, P, Forbes, A, Xu, S, Foex, P, Pogue, J, Arrieta, M, Bryson, G, Paul, J, Paech, M, Merchant, R, Choi, P, Badner, N, Peyton, P, Sear, J, Yang, H Neuraxial block, death and serious cardiovascular morbidity in the POISE trial.. Br J Anaesth. (2013). 111 382–90 [Article] [PubMed]
Appendix: Evaluation of Nitrous Oxide in the Gas Mixture for Anaesthesia (ENIGMA)-II Investigators Participating in the 1-yr Follow-up Study
Australia (ANZCA Clinical Trials Network Members)
Alfred Hospital
Investigators: P. Myles, S. Wallace, W. Galagher, C. Farrington, and A. Ditoro.
Ethics Committee: Alfred Hospital Ethics Committee, Research and Ethics Unit, Alfred Health, P. O. Box 315, Prahran, Victoria 3181, Australia.
Austin Hospital
Investigators: P. Peyton, S. Baulch, and S. Sidiropoulos.
Ethics Committee: Austin Health Human Research Ethics Committee, Research Ethics Unit, Austin Hospital, P. O. Box 5555, Heidelberg, Victoria 3084, Australia.
Dandenong Hospital
Investigators: R. Bulach and D. Bryant.
Ethics Committee: Southern Health Research Directorate, Monash Medical Centre, 246 Clayton Road, Clayton, Victoria 3168, Australia.
Fremantle Hospital
Investigators: E. O’Loughlin and V. Mitteregger.
Ethics Committee: South Metropolitan Area Health Service Human Research Ethics Committee, Fremantle Hospital and Health Service, Alma Street, Fremantle, Western Australia 6160, Australia.
Geelong Hospital
Investigators: S. Bolsin and C. Osborne.
Ethics Committee: The Barwon Health Research and Ethics Advisory Committee, The Geelong Hospital, P. O. Box 281, Geelong, Victoria 3220, Australia.
Monash Medical Centre
Investigators: R. McRae and M. Backstrom.
Ethics Committee: Human Research Ethics Committee-B, Southern Health 246 Clayton Road, Clayton, Victoria 3168, Australia.
Royal Melbourne Hospital
Investigators: K. Leslie and R. Cotter.
Ethics Committee: Melbourne Health Human Research Ethics Committee, Royal Melbourne Hospital, Grattan Street, Parkville, Victoria 3050, Australia.
Royal Perth Hospital
Investigators: M. Paech and S. March.
Ethics Committee: Royal Perth Hospital Ethics Committee, Royal Perth Hospital Wellington Street, G. P. O. Box X2213, Perth, Western Australia 6847, Australia.
St. Vincent’s Hospital
Investigators: B. Silbert and S. Said.
Ethics Committee: Human Research Ethics Committee-D, St. Vincent’s Hospital, Grattan Street, Fitzroy, Victoria 3065, Australia.
Westmead Hospital
Investigators: R. Halliwell and J. Cope.
Ethics Committee: Sydney West Area Health Service Human Research Ethics Committee, Westmead Hospital, Hawkesbury Road, Westmead, New South Wales 2145, Australia.
Calvary Wakefield Hospital
Investigators: D. Fahlbusch and D. Crump.
Ethics Committee: Calvary Health Care Adelaide Human Research and Ethics Committee, Calvary Health Care Adelaide, 89 Strangways Terrace, North Adelaide, South Australia 5006, Australia.
Peter MacCallum Cancer Centre
Investigator: G. Thompson.
Ethics Committee: Peter MacCallum Cancer Centre Ethics Committee, Peter MacCallum Cancer Centre, St. Andrews Place, East Melbourne, Victoria 3002, Australia.
Western Hospital
Investigator: A. Jefferies.
Ethics Committee: Melbourne Health Human Research Ethics Committee, Royal Melbourne Hospital, Grattan Street, Parkville, Victoria 3050, Australia.
North West Regional Hospital
Investigator: M. Reeves.
Ethics Committee: Tasmanian Human Research Ethics Committee, Health and Medical Office of Research Services, University of Tasmania, Hobart, Tasmania 7001, Australia.
Canada
McMaster University
Investigators: N. Buckley and T. Tidy.
Ethics Committee: The Hamilton Health Sciences/McMaster Health Sciences Research Ethics Board, 293 Wellington Street, Hamilton, Ontario, L8L 8E7, Canada.
Royal Victoria Hospital
Investigators: T. Schricker, R. Lattermann, and D. Iannuzzi.
Ethics Committee: SDR Committee, McGill University Health Centre, 687 Avenue des Pins, Montreal, Quebec, H3A 1A1, Canada.
Toronto General Hospital
Investigators: S. Beattie and J. Carroll.
Ethics Committee: University Health Network Research Ethics Board, 700 University Avenue, Toronto, Ontario, M5G 1Z5, Canada.
University of Alberta Hospital
Investigators: M. Jacka and C. Bryden.
Ethics Committee: Health Research Ethics Board (Biomedical Panel), Heritage Medical Research Centre, University of Alberta, Edmonton, Alberta, T6G 2S2, Canada.
London Health Sciences
Investigator: N. Badner.
Ethics Committee: The University of Western Ontario Research Ethics Board for Health Sciences Research Involving Human Subjects, The University of Western Ontario, London, Ontario, N6A 5C1, Canada.
Hong Kong
Prince of Wales
Investigators: M. T. V. Chan (ANZCA Clinical Trials Network member) and M. W. Y. Tsang.
Ethics Committee: The Joint Chinese University of Hong Kong, New Territories East Cluster Clinical Research Ethics Committee, Prince of Wales Hospital, Shatin, Hong Kong.
Tuen Mun Hospital
Investigators: B. C. P. Cheng and A. C. M. Fong.
Ethics Committee: New Territories West Cluster Clinical and Research Ethics Committee, Tuen Mun Hospital, Tuen Mun, New Territories, Hong Kong.
Pamela Youde Nethersole Eastern Hospital
Investigators: L. C. Y. Chu and E. G. Y. Koo.
Ethics Committee: New Territories West Cluster Clinical and Research Ethics Committee, Tuen Mun Hospital, Tuen Mun, New Territories, Hong Kong.
Malaysia
Hospital Kuala Lumpur
Investigators: N. Mohd and L. E. Ming.
Ethics Committee: Jawatankuasa Etika Perubatan Pusta Perubatan Universiti Malaya, Lembah Pantai, Kuala Lumpur 59100, Malaysia.
New Zealand (ANZCA Clinical Trials Network Members)
Auckland Hospital
Investigators: D. Campbell and D McAllister
Ethics Committee: New Zealand-Health and disability Ethics Committees, Multi-Region Ethics Committee, Ministry of Health, Wellington, New Zealand.
Middlemore Hospital
Investigators: S. Walker and S. Olliff.
Ethics Committee: New Zealand-Health and Disability Ethics Committees, Multi-Region Ethics Committee, Ministry of Health, Wellington, New Zealand.
Christchurch Hospital
Investigators: R. Kennedy.
Ethics Committee: New Zealand-Health and Disability Ethics Committees, Multi-Region Ethics Committee, Ministry of Health, Wellington, New Zealand.
Saudi Arabia
King Saud University Hospital
Investigators: A. Eldawlatly and T. Alzahrani.
Ethics Committee: College of Medicine Research Centre, King Saud University, P. O. Box 2925, Riyadh 1146, Saudi Arabia.
Singapore
Tan Tock Seng Hospital
Investigators: N. Chua.
Ethics Committee: National Health Group Domain Specific Review Board, 6 Commonwealth Lane, Singapore 149547, Singapore.
United Kingdom
Plymouth NHS Trust
Investigators: R. Sneyd and H. McMillan.
Ethics Committee: NRES Committee, South West-Central Bristol Bristol Research Ethics Committee Centre, Whitefriars Level 3, Block B Lewin’s Mead, Bristol, BS1 2NT, United Kingdom.
Royal Lancaster Infirmary
Investigators: I. Parkinson.
Ethics Committee: NRES Committee, South West-Central Bristol Bristol Research Ethics Committee Centre, Whitefriars Level 3, Block B Lewin’s Mead, Bristol, BS1 2NT, United Kingdom.
Bradford Teaching Hospital
Investigators: A. Brennan.
Ethics Committee: NRES Committee, South West-Central Bristol Bristol Research Ethics Committee Centre, Whitefriars Level 3, Block B Lewin’s Mead, Bristol, BS1 2NT, United Kingdom.
Hull Royal Infirmary
Investigator: P. Balaji.
Ethics Committee: NRES Committee, South West-Central Bristol Bristol Research Ethics Committee Centre, Whitefriars Level 3, Block B Lewin’s Mead, Bristol, BS1 2NT, United Kingdom.
Portsmouth Hospital
Investigators: J. Nightingale.
Ethics Committee: NRES Committee, South West-Central Bristol Bristol Research Ethics Committee Centre, Whitefriars Level 3, Block B Lewin’s Mead, Bristol, BS1 2NT, United Kingdom.
King’s College Hospital
Investigators: G. Kunst.
Ethics Committee: NRES Committee, South West-Central Bristol Bristol Research Ethics Committee Centre, Whitefriars Level 3, Block B Lewin’s Mead, Bristol, BS1 2NT, United Kingdom.
Royal Surrey County Hospital
Investigators: M. Dickinson.
Ethics Committee: NRES Committee, South West-Central Bristol Bristol Research Ethics Committee Centre, Whitefriars Level 3, Block B Lewin’s Mead, Bristol, BS1 2NT, United Kingdom.
United States of America
Beth Israel Deaconess Medical Center
Investigators: B. Subramaniam and V. Banner-Godspeed.
Ethics Committee: Committee on Clinical Investigation, Beth Israel Deaconess Medical Center, 330 Brookline Avenue, Boston, Massachusetts 02215.
Cleveland Clinic
Investigators: D. I. Sessler, J. Liu, A. Kurz, B. Hesler, A. Y. Fu, C. Egan, A. N. Fiffick, M. T. Hutcherson, A. Turan, and A. Naylor.
Ethics Committee: Institutional Review Board, Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, Ohio 44195.
Louisville Medical Centre
Investigators: D. Obal and E. Cooke.
Ethics Committee: Institutional Review Board, Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, Ohio 44195.
Fig. 1.
Flow diagram.
Flow diagram.
Fig. 1.
Flow diagram.
×
Fig. 2.
Kaplan–Meier survival curve for death for randomized treatment groups (P = 0.18).
Kaplan–Meier survival curve for death for randomized treatment groups (P = 0.18).
Fig. 2.
Kaplan–Meier survival curve for death for randomized treatment groups (P = 0.18).
×
Table 1.
ORs for the Composite Primary Outcome of Death or Major Cardiovascular Events (Nonfatal Myocardial Infarction, Cardiac Arrest, Pulmonary Embolism, and Stroke)*
ORs for the Composite Primary Outcome of Death or Major Cardiovascular Events (Nonfatal Myocardial Infarction, Cardiac Arrest, Pulmonary Embolism, and Stroke)*×
ORs for the Composite Primary Outcome of Death or Major Cardiovascular Events (Nonfatal Myocardial Infarction, Cardiac Arrest, Pulmonary Embolism, and Stroke)*
Table 1.
ORs for the Composite Primary Outcome of Death or Major Cardiovascular Events (Nonfatal Myocardial Infarction, Cardiac Arrest, Pulmonary Embolism, and Stroke)*
ORs for the Composite Primary Outcome of Death or Major Cardiovascular Events (Nonfatal Myocardial Infarction, Cardiac Arrest, Pulmonary Embolism, and Stroke)*×
×
Table 2.
ORs for Disability or Death*
ORs for Disability or Death*×
ORs for Disability or Death*
Table 2.
ORs for Disability or Death*
ORs for Disability or Death*×
×
Table 3.
HRs for Death*
HRs for Death*×
HRs for Death*
Table 3.
HRs for Death*
HRs for Death*×
×
Table 4.
ORs for Myocardial Infarction*
ORs for Myocardial Infarction*×
ORs for Myocardial Infarction*
Table 4.
ORs for Myocardial Infarction*
ORs for Myocardial Infarction*×
×
Table 5.
ORs for Stroke*
ORs for Stroke*×
ORs for Stroke*
Table 5.
ORs for Stroke*
ORs for Stroke*×
×