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. 2015 Nov 25;2015(11):CD010576. doi: 10.1002/14651858.CD010576.pub2

Summary of findings 2. Total thyroidectomy compared to bilateral subtotal thyroidectomy for Graves disease and Graves' opthalmopathy.

Total thyroidectomy compared to bilateral subtotal thyroidectomy for Graves disease/Graves' opthalmopathy
Patient: patients with Graves' disease/Graves' opthalmopathy
 Settings: university hospitals in Germany and Poland
 Intervention: total thyroidectomy
 Comparison: bilateral subtotal thyroidectomy
Outcomes Illustrative comparative risks* (95% CI) Relative effect
 (95% CI) No of participants
 (studies) Quality of the evidence
 (GRADE) Comments
Assumed riska Corresponding risk
Bilateral subtotal thyroidectomy Total thyroidectomy
R ate of recurrent hyperthyroidism 
 [measured by thyroid function tests]
 Follow‐up: 6 months and 6 years 67 per 1000 9 per 1000 
 (3 to 30) OR 0.13 
 (0.04 to 0.44) 300
 (2) ⊕⊕⊕⊝
 moderateb
Regression of Graves' ophthalmopathy 
 [ophthalmology assessment]
 Follow‐up: 6 months and 6 years 791 per 1000 818 per 1000 
 (707 to 893) OR 1.19 
 (0.64 to 2.21) 260
 (2) ⊕⊕⊝⊝
lowc
Permanent recurrent laryngeal nerve palsy 
 [patient reported, confirmation by laryngoscopy]
 Follow‐up: 6 months and 6 years 13 per 1000 13 per 1000 
 (2 to 88) OR 1.00 
 (0.14 to 7.15) 300
 (2) ⊕⊕⊝⊝
 lowd
Permanent hypocalcaemia/hypoparathyroidism 
 [measured by serum calcium levels]
 Follow‐up: 6 months and 6 years 20 per 1000 40 per 1000 
 (11 to 138) OR 2.04 
 (0.53 to 7.85) 300
 (2) ⊕⊕⊝⊝
 lowd
All‐cause mortality
Follow‐up: 6 months and 6 years
See comment See comment Not estimable 300
 (2) See comment Only one death reported in total thyroidectomy group
Health‐related quality of life See comment See comment Not estimable See comment See comment Not investigated
Socioeconomic effects See comment See comment Not estimable See comment See comment Not investigated
*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; RR: Risk 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.

aAssumed risk was derived from the event rates in the intervention comparator groups.
 bDowngraded by one level because of high risk of performance bias in both trials.
 cDowngraded by two levels because of high risk of performance bias in both trials and imprecision.
 dDowngraded by two levels because of high risk of performance bias in both trials, imprecision and low event rates.