PICOS | Inclusion criteria | Exclusion criteria |
---|---|---|
Population | Patients from any country undergoing elective surgery | Patients undergoing emergency surgery or non-surgical treatments (e.g. chemotherapy) |
Intervention | A preoperative prehabilitation programme (any setting), defined as a (set of) intervention(s) aimed at optimising functioning and reducing disability in individuals awaiting surgery. The intervention(s) had to include at least one component of physio- or occupational therapy and at least one in-person meeting between the patient(s) and health care professional(s). The ‘dose’, i.e. the programme’s duration (overall and per session) and frequency, had to be sufficiently longa to have an effect if the patients fully adhered to it | Purely medical/nutritional interventions, an intervention combined with additional postoperative rehabilitation, cognitive behaviour therapy or health counselling/education alone, purely web/app-based prehabilitation programmes |
Control | Usual preoperative care as defined by the study authors, i.e. the routine care that patients with a given condition receive in the respective hospital (extended only by the baseline measurements performed as part of the trial) | Another prehabilitation intervention; no comparator |
Outcome | Clinical effectiveness and costs, any timeframe for follow-up | Clinical effectiveness only |
Study type | Full (i.e. cost–benefit, cost-effectiveness and cost–utility analyses) or partial economic evaluations (i.e. cost-minimization analysis), trial-basedb or model-based economic evaluations regardless of their statusc, cost perspective, publication year, language and type (i.e. full article, conference abstract) | Systematic reviews, simple, non-comparative cost analyses (i.e. studies that only calculated the costs of the intervention), commentaries/letters, animal studies |