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. 2017 Aug 14;2017(8):CD012763. doi: 10.1002/14651858.CD012763

Kvolik 2012b.

Methods Study design: prospective, randomized study
Sample size calculation: no information available
Participants Number of randomized participants: 24
Inclusion criteria: euthyroid, undergoing general anaesthesia for thyroidectomy
Exclusion criteria: no information available
Interventions Anaesthesia: propofol and fentanyl
NMBA: single intubating dose: rocuronium 0.6 mg/kg; maintenance dose: rocuronium 0.1 mg/kg
Comparison: neostigmine 50 µg/kg vs sugammadex 2 mg/kg
Administration time of sugammadex or neostigmine: end of surgery
Outcomes Thyroid hormones (FT3, FT4, and TSH) measured before surgery, 1 hour after reversal, and 24 hours after surgery
Notes Publication type: meeting abstract
Country: Croatia
Conversions: none
Authors’ conclusions: Sugammadex treatment did not change levels of thyroid hormones and may be safely used in patients undergoing total thyroidectomy
Contact: first trial author Slavica Kvolik contacted by e‐mail: slavica.kvolik@os.t‐com.hr on 24.05.2016; no reply received
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk "Randomized study"; no further information available
Allocation concealment (selection bias) Unclear risk Unable to assess owing to insufficient information
Blinding of participants (performance bias) Unclear risk Unable to assess owing to insufficient information
Blinding of personnel (performance bias) Unclear risk Unable to assess owing to insufficient information
Blinding of primary outcome assessment (detection bias) Unclear risk Unable to assess owing to insufficient information
Blinding of safety assessment (detection bias) Unclear risk Unable to assess owing to insufficient information
Incomplete outcome data (attrition bias) 
 All outcomes Unclear risk Unable to assess owing to insufficient information
Selective reporting (reporting bias) Low risk Study protocol not available, but published meeting abstract clearly includes all expected outcomes
Funding bias Unclear risk Unable to assess owing to insufficient information
Other bias Unclear risk No information on sample size calculation. No differences regarding participant characteristics and drug consumption between groups