Study characteristics	Eligibility criteria (Insert eligibility criteria for each characteristic as defined in the Protocol)		Yes	No	Unclear	Location in text (pg & ¶/fig/table)
Type of study	Randomized controlled trial
Participants: adults +18 years for transabdominal robotic assisted surgery in gynaecology, urology or gastroenterology
Types of interventions: TIVA vs inhalational anaesthesia
Types of outcome measures: Primary outcomes: Postoperative pain within 24 hours (as measured by included studies) PONV within 24 hours (as measured by included studies) Secondary outcomes: Adverse effects (as measured by included studies) (e.g. cerebral oedema, stroke, ocular complications) All‐cause mortality within 90 days Respiratory complications requiring treatment within 48 hours (as measured by included studies) Circulatory complications requiring treatment within 48 hours (as measured by included studies) Cognitive dysfunction (as measured by included studies) Length of stay in the postoperative ward (as measured by included studies) Costs (as measured by included studies)
INCLUDE		EXCLUDE
Reason for exclusion
Notes: