Study characteristic | Inclusion criteria | Exclusion criteria |
---|---|---|
Patient population (P) | Adults undergoing spinal surgical procedures; Paediatric population undergoing spinal surgical procedures; | Patients undergoing non-surgical management of spinal conditions; Spinal trauma patients; |
Intervention-treatment(I) | Twenty-two pre-defined components of an ERSS pathway (as outlined in Table 1) alone or in combination with another component; Other proposed ERSS pathways incorporating one or more pre-defined interventions will be included; | Â |
Comparator(C) | Standard of care, no treatment or placebo; | Â |
Outcomes(O) | •Mortality from all causes; •Morbidity including: pulmonary, cardiac and renal complication rates, surgical complication rates (including readmissions); •Patient reported experiences and outcomes (PROMs/PREMS): pain-related outcomes (e.g. pain score rating, pain management satisfaction), quality of care (readiness for surgery, quality of care patient scores, quality of recovery after surgery); •Health service-related outcomes: length of stay (in hospital, in ICU)and economic/financial outcome; |  |
Timing | Perioperative process-preadmission, preoperative, intraoperative and postoperative setting; | Studies incorporating long-term (greater than 3 months) postoperative rehabilitation; |
Study design | Systematic reviews, meta-analysis Randomized controlled trials Non-randomized studies Observational studies (cohort studies, case-control studies, cross-sectional studies, case series); | Case reports; |
Study setting | Inpatient care (including patients whose condition requires admission to a hospital same day discharge surgical); | Outpatient clinics, medical and non-surgical management of spinal conditions; |