Coronary Artery Disease, Major Surgery
Conditions
Brief summary
In this study, we want to find out if laughing gas (nitrous oxide) leads to a higher rate of cardiac complications after surgery in patients with a specific genetic profile (mutations in the MTHFR gene) and if this risk can be prevented by giving patients vitamin B12 and folate during surgery.
Detailed description
Background and significance: Recent studies have shown that nitrous oxide (N2O) anesthesia may be associated with an increased risk of adverse cardiovascular outcomes. It is well-known that N2O inhibits vitamin B12-dependent enzymes and as a result increases plasma homocysteine concentrations. Homocysteine has been identified as risk factor for cardiovascular disease. Therefore elevations in homocysteine after N2O may be a causative factor in N2O toxicity. In a previous investigation, we found that patients who carry a homozygous mutation in the MTHFR gene develop higher homocysteine levels after N2O anesthesia than non-carriers. These patients might be at higher risk for adverse cardiac outcomes from N2O. Thus, there may be a pharmacogenetic mechanism to account for the adverse cardiac outcomes from N2O. Moreover, prevention of N2O-increased homocysteine concentrations in these high risk patients by perioperative vitamin B12 and folate supplementation might decrease the incidence of adverse cardiac outcomes. Hypothesis: Patients carrying a homozygous MTHFR 677C\>T or 1298 A\>C variant allele will have a higher incidence rate of postoperative myocardial ischemia after N2O anesthesia \[detected by serial TnI measurements\] due to elevated homocysteine levels than normal wild-type non-carriers, and that the incidence rate will be reduced if they receive perioperative vitamin B12/folate supplementation. Primary outcome: Myocardial ischemia in the first 72 hours after surgery (measured by serial troponin and ECGs). Secondary outcome: Composite endpoint of 30-day mortality and major cardiac morbidity (non-fatal MI) Design: Randomized controlled trial. 500 patients will receive N2O during surgery and will be randomized to receive B-vitamins or placebo. 125 patients will receive no N2O and no B-vitamins (control arm). Mendelian randomization of MTHFR genotype. Intervention: IV vitamin B12 (1 mg) and folate (5 mg) pre- and postoperatively Study setting: Barnes-Jewish-Hospital, St. Louis, MO Patients: Patients scheduled for major surgery with or at risk for coronary artery disease
Interventions
1 mg vitamin B12 IV 5 mg folic acid IV in 100 ml NS infusion
Sponsors
Study design
Eligibility
Inclusion criteria
* Adult patients; age \>18 yrs, ASA III-IV * Previously diagnosed coronary artery disease or at risk for coronary artery disease * Scheduled for major surgery (\>2 hrs)
Exclusion criteria
* Patients not expected to live past 24 hours (ASA 5) * Patients with significant pulmonary disease requiring supplemental oxygen * Patients taking supplemental vitamin B12 or folate * Contraindication against N2O (pneumothorax, mechanical bowel obstruction, middle ear occlusion, laparoscopic surgery, raised intracranial pressure) * Hypersensitivity to cobalamins * Leber's disease (hereditary optic nerve atrophy) \[vitamin B12 interaction\] * Seizure disorder \[folate interference\]
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Myocardial Ischemia | first 3 postoperative days | Measured by serial troponin and ECG |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Non-fatal MI | 30 day postoperative | Myocardial Infarction per Third Definition of MI |
Countries
United States
Participant flow
Recruitment details
687 patients signed consent for enrollment; only 625 were analyzed.
Participants by arm
| Arm | Count |
|---|---|
| Treatment Vitamin B12 and folic acid
Vitamin B12 and folic acid: 1 mg vitamin B12 IV 5 mg folic acid IV in 100 ml NS infusion | 250 |
| Comparator Nitrous oxide and placebo
Nitrous oxide and placebo | 250 |
| Standard of Care standard of care
standard of care | 125 |
| Total | 625 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 | FG002 |
|---|---|---|---|---|
| Overall Study | surgery canceled; or subject or anesthes | 26 | 31 | 5 |
Baseline characteristics
| Characteristic | Total | Treatment | Comparator | Standard of Care |
|---|---|---|---|---|
| ACE-Inhibitor | 225 Participants | 94 Participants | 88 Participants | 43 Participants |
| Age, Continuous | 65.5 years STANDARD_DEVIATION 10.7 | 64.7 years STANDARD_DEVIATION 10.6 | 65.2 years STANDARD_DEVIATION 10.7 | 67.6 years STANDARD_DEVIATION 10.9 |
| ASA staging ASA 1-A normal healthy patient | 1 Participants | 1 Participants | 0 Participants | 0 Participants |
| ASA staging ASA 2 A patient with mild systemic disease | 98 Participants | 45 Participants | 42 Participants | 11 Participants |
| ASA staging ASA 3 - A patient with severe systemic disease | 501 Participants | 199 Participants | 196 Participants | 106 Participants |
| ASA staging ASA 4 -A patient with severe systemic disease tha | 23 Participants | 5 Participants | 10 Participants | 8 Participants |
| Chronic renal failute | 67 Participants | 16 Participants | 35 Participants | 16 Participants |
| Congestive heart failure | 73 Participants | 27 Participants | 31 Participants | 15 Participants |
| Coronary artery disease | 372 Participants | 140 Participants | 148 Participants | 84 Participants |
| Diabetes | 223 Participants | 96 Participants | 88 Participants | 39 Participants |
| Diuretic | 194 Participants | 79 Participants | 87 Participants | 28 Participants |
| Hypertension | 504 Participants | 200 Participants | 204 Participants | 100 Participants |
| Lee's revised cardiac risk index (Mean | 2.0 units on a scale STANDARD_DEVIATION 0.8 | 1.9 units on a scale STANDARD_DEVIATION 0.8 | 2.0 units on a scale STANDARD_DEVIATION 0.9 | 2.1 units on a scale STANDARD_DEVIATION 0.8 |
| Medications Aspirin | 332 Participants | 126 Participants | 137 Participants | 69 Participants |
| Medications Beta-Blocker | 330 Participants | 119 Participants | 141 Participants | 70 Participants |
| Medications Clopidogrel | 111 Participants | 42 Participants | 45 Participants | 24 Participants |
| Medications Warfarin | 62 Participants | 28 Participants | 21 Participants | 13 Participants |
| MTHFR A1298C plymorphism 1298AA | 303 Participants | 133 Participants | 120 Participants | 50 Participants |
| MTHFR A1298C plymorphism 1298AC | 236 Participants | 86 Participants | 105 Participants | 45 Participants |
| MTHFR A1298C plymorphism 1298CC | 50 Participants | 24 Participants | 19 Participants | 7 Participants |
| MTHFR C677T polymorphism 677CC | 324 Participants | 137 Participants | 130 Participants | 57 Participants |
| MTHFR C677T polymorphism 677CT | 202 Participants | 76 Participants | 89 Participants | 37 Participants |
| MTHFR C677T polymorphism 677TT | 63 Participants | 29 Participants | 26 Participants | 8 Participants |
| on hemodialysis | 5 Participants | 1 Participants | 3 Participants | 1 Participants |
| Peripheral vascular disease | 210 Participants | 81 Participants | 85 Participants | 44 Participants |
| Plasma total homocysteine mol/L | 13.1 mcmol/L STANDARD_DEVIATION 5.5 | 13.5 mcmol/L STANDARD_DEVIATION 5.7 | 13.4 mcmol/L STANDARD_DEVIATION 5.8 | 11.6 mcmol/L STANDARD_DEVIATION 4.2 |
| Region of Enrollment United States | 625 Participants | 250 Participants | 250 Participants | 125 Participants |
| Sex: Female, Male Female | 234 Participants | 92 Participants | 97 Participants | 45 Participants |
| Sex: Female, Male Male | 391 Participants | 158 Participants | 153 Participants | 80 Participants |
| Smoking history | 464 Participants | 195 Participants | 175 Participants | 94 Participants |
| Statin | 345 Participants | 130 Participants | 146 Participants | 69 Participants |
| Surgical procedure ENT | 59 Participants | 22 Participants | 20 Participants | 17 Participants |
| Surgical procedure gyn | 55 Participants | 26 Participants | 21 Participants | 8 Participants |
| Surgical procedure Orthopedic | 194 Participants | 88 Participants | 81 Participants | 25 Participants |
| Surgical procedure Urology | 50 Participants | 22 Participants | 22 Participants | 6 Participants |
| Surgical procedure Vascular | 216 Participants | 76 Participants | 87 Participants | 53 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk |
|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 250 | 3 / 250 | 1 / 125 |
| other Total, other adverse events | 39 / 250 | 61 / 250 | 27 / 125 |
| serious Total, serious adverse events | 0 / 250 | 3 / 250 | 1 / 125 |
Outcome results
Myocardial Ischemia
Measured by serial troponin and ECG
Time frame: first 3 postoperative days
| Arm | Measure | Category | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| B-Vitamin Group | Myocardial Ischemia | Cardiac troponin elevation | 33 Participants |
| B-Vitamin Group | Myocardial Ischemia | No Cardiac troponin elevation | 217 Participants |
| Comparator | Myocardial Ischemia | Cardiac troponin elevation | 34 Participants |
| Comparator | Myocardial Ischemia | No Cardiac troponin elevation | 216 Participants |
| Standard of Care | Myocardial Ischemia | Cardiac troponin elevation | 17 Participants |
| Standard of Care | Myocardial Ischemia | No Cardiac troponin elevation | 108 Participants |
Non-fatal MI
Myocardial Infarction per Third Definition of MI
Time frame: 30 day postoperative
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| B-Vitamin Group | Non-fatal MI | 7 Participants |
| Comparator | Non-fatal MI | 15 Participants |
| Standard of Care | Non-fatal MI | 8 Participants |