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. 2016 Mar 31;2016(3):CD011390. doi: 10.1002/14651858.CD011390.pub2

Summary of findings for the main comparison. Laparoscopic versus open transhiatal oesophagectomy for oesophageal cancer: primary outcomes.

Laparoscopic versus open transhiatal oesophagectomy for oesophageal cancer
Patient or population: patients with oesophageal cancer
 Settings: upper gastrointestinal surgery unit
 Intervention: laparoscopic transhiatal oesophagectomy
Control: open transhiatal oesophagectomy
Outcomes Illustrative comparative risks* (95% CI) Relative effect
 (95% CI) No of participants
 (studies) Quality of the evidence
 (GRADE)
Assumed risk Corresponding risk
Open transhiatal oesophagectomy Laparoscopic transhiatal oesophagectomy
Short‐term mortality
(in hospital or within 3 months)
11 per 1000 5 per 1000 
 (1 to 47) RR 0.44 
 (0.05 to 4.09) 326
 (5 studies) ⊕⊝⊝⊝
 very low1,2,3
Long‐term mortality 
 Follow‐up: median 2 years 355 per 1000 346 per 1000 
 (299 to 398) HR 0.97 
 (0.81 to 1.16) 193
 (2 studies) ⊕⊝⊝⊝
 very low1,3
Serious adverse events (proportion) 211 per 1000 103 per 1000 
 (51 to 208) RR 0.49 
 (0.24 to 0.99) 213
 (3 studies) ⊕⊝⊝⊝
 very low1,3
Anastomotic stenosis 81 per 1000 111 per 1000 
 (27 to 462) RR 1.37 
 (0.33 to 5.7) 73
 (1 study) ⊕⊝⊝⊝
 very low1,2,3
None of the studies reported post‐operative dysphagia or health‐related quality of life.
*The basis for the assumed risk was the mean control group proportion. 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; RR: Risk ratio; HR: Hazard 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 Risk of bias was unclear or high in the study/studies.
 2 The confidence intervals were wide (overlapped clinically significant effects and no effect).
 3 The sample size was small.