Mendonca 2001.
Methods | Randomization and treatment allocation method: yes Blinding of outcome assessment: unclear Blinding of participants: no Study period: not stated |
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Participants | Number: 60 enrolled Inclusion criteria: ASA physical status II to III patients scheduled to undergo general anaesthesia, 50 years of age and older with a history of smoking 10 cigarettes a day for 20 years Exclusion criteria: severe cardiovascular disease, morbid obesity, allergy to inhalational anaesthetics, requiring rapid sequence induction |
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Interventions | No pre‐medication and a Mapleson D breathing system Group 1: 8% vital capacity breathing in 66% N2O Group 2: 8% tidal breathing in 66% N2O Group 3: incremental tidal breathing sevoflurane in 66% N2O |
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Outcomes | Time to dropping the weighted syringe Induction event (single cough, laryngospasm, breath holding, movement of a limb, excessive salivation, hypotension and hypoxia were recorded) Smell of the anaesthetic |
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Notes | Location: UK Setting: operating room Source of funding: not stated |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: "...patients were randomly allocated using sealed envelopes to one of the three breathing techniques" |
Allocation concealment (selection bias) | Low risk | Quote: "...patients were randomly allocated using sealed envelopes to one of the three breathing techniques" |
Blinding (performance bias and detection bias) All outcomes | Unclear risk | Not stated |
Incomplete outcome data (attrition bias) All outcomes | Low risk | No missing data |
Selective reporting (reporting bias) | Low risk | Study authors reported all planned outcomes |