Study characteristic | Inclusion criteria | Exclusion criteria |
---|---|---|
Patient population | Adults undergoing spinal surgical procedures. Pediatric population undergoing spinal surgical procedures. | Patients undergoing non-surgical management of spinal conditions Traumatic patients without surgery |
Intervention-treatment | 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 | Standard of care, no treatment, or placebo | Â |
Outcomes | 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 outcomes (e.g., costs of patient stay) | Â |
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 |
Timing | Perioperative process-preadmission, preoperative, intraoperative, and postoperative setting | Studies incorporating long-term (greater than three months) postoperative rehabilitation |