Limberi 2003.
Methods | RCT Approved by the ethics committee and written informed consent obtained Setting: Greece Funding: unspecified |
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Participants | 50 patients with coronary artery disease scheduled for elective upper abdominal surgery for non‐vascular disease Exclusion criteria were preoperative electrocardiogram that interfered with accurate diagnosis of myocardial ischaemia (bundle branch block, left ventricular hypertrophy with strain pattern, ventricular ectasia), valvular heart disease, prior digoxin therapy, contraindication to insertion of an epidural catheter, localized infection, septicaemia, preoperative coagulopathy, neurological disease) and partial oxygen pressure < 60 mm Hg |
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Interventions |
Treatment group: thoracic or lumbar (T12‐L1 or L1‐L2) epidural analgesia tested with 2 mL of 2% lidocaine with epinephrine 5 mcg/mL, followed by 7 to 15 mL of 0.5% bupivacaine for a sensory level from T4 to L5 at 20 minutes before surgical incision and morphine 2 mg at skin closure (n = 25) Control group: IV morphine (n = 25) General anaesthesia for all participants |
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Outcomes | Pain: Epidural group had better pain control | |
Notes | No outcome of interest available at our selected time points. VAS scores provided are computed scores for 24‐hour periods. Study authors contacted on 23 February 2016. Data are no longer available | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | "table of random numbers" |
Allocation concealment (selection bias) | Unclear risk | Not mentioned |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Not mentioned |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Not mentioned |
Incomplete outcome data (attrition bias) All outcomes | Low risk | No loss to follow‐up |
Selective reporting (reporting bias) | Low risk | All results reported |
Other bias | Low risk | Groups well balanced |