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. 2013 Jul 29;2013(7):CD007083. doi: 10.1002/14651858.CD007083.pub3

Summary of findings for the main comparison. Neuraxial versus general anaesthesia for lower‐limb revascularization.

Neuraxial versus general anaesthesia for lower‐limb revascularization
Patient or population: participants with lower‐limb revascularization
 Settings:Intervention: Neuraxial versus general anaesthesia
Outcomes Illustrative comparative risks* (95% CI) Relative effect
 (95% CI) No of participants
 (studies) Quality of the evidence
 (GRADE) Comments
Assumed risk Corresponding risk
Control Neuraxial versus general anaesthesia
MortalityAt any time Study population OR 0.89 
 (0.38 to 2.07) 696
 (4 studies) ⊕⊕⊝⊝
 low1  
43 per 1000 38 per 1000 
 (17 to 85)
Medium‐risk population
55 per 1000 49 per 1000 
 (22 to 108)
Myocardial infarctionSpinal anaesthesia Study population OR 1.89 
 (0.5 to 7.21) 306
 (2 studies) ⊕⊕⊝⊝
 low1,2  
25 per 1000 46 per 1000 
 (13 to 156)
Medium‐risk population
24 per 1000 44 per 1000 
 (12 to 151)
Myocardial infarctionEpidural anaesthesia Study population OR 0.98 
 (0.37 to 2.58) 390
 (3 studies) ⊕⊕⊝⊝
 low1,2  
50 per 1000 49 per 1000 
 (19 to 120)
Medium‐risk population
44 per 1000 43 per 1000 
 (17 to 106)
Amputation rateSpinal anaesthesia Study population OR 1.04 
 (0.35 to 3.06) 235
 (2 studies) ⊕⊕⊝⊝
 low1,2  
71 per 1000 74 per 1000 
 (26 to 190)
Medium‐risk population
69 per 1000 72 per 1000 
 (25 to 185)
Amputation rateEpidural anaesthesia Study population OR 0.66 
 (0.21 to 2.07) 230
 (2 studies) ⊕⊕⊝⊝
 low1,2  
81 per 1000 55 per 1000 
 (18 to 154)
Medium‐risk population
79 per 1000 54 per 1000 
 (18 to 151)
Pneumonia Study population OR 0.37 
 (0.15 to 0.89) 201
 (2 studies) ⊕⊝⊝⊝
 very low2,3,4  
196 per 1000 83 per 1000 
 (35 to 178)
Medium‐risk population
196 per 1000 83 per 1000 
 (35 to 178)
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
 CI: Confidence interval; OR: Odds ratio.
GRADE Working Group grades of evidence
 High quality: Further research is very unlikely to change our confidence in the estimate of effect
 Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate
 Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate
 Very low quality: We are very uncertain about the estimate

1 All trials recruited participants from elective surgery and did not define criteria for participants with high risk, moderate risk or low risk. Authors did not describe blinding. In Christopherson 1993, the cardiologists assessing cardiac outcomes were blinded to the group to which participants were allocated. Christopherson 1993, Cook 1986 and Dodds 2007 included few participants.
 2 In Christopherson 1993, the rate of missing data was described as 3.1% in the intervention group and 1.9% in the control group. Cook 1986 reported that 11/50 intervention participants and 4/51 control participants were lost to follow‐up. Dodds 2007 did not report mortality during one‐year follow up. Bode 1996 reported complete data collection for non‐surgical outcomes during hospitalization in 423 participants. However, surgical outcomes over 30 postoperative days were reported for only 264 participants (159 missing).
 3Cook 1986 described that more elderly participants and smokers were allocated to the general anaesthesia group and that this can influenced results
 4 In Cook 1986, participants were analysed during hospital stay