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. 2024 Mar 5;2024(3):CD007491. doi: 10.1002/14651858.CD007491.pub3

Corwin 2005.

Study characteristics
Methods Parallel randomised trial
Study conducted between July 2002 and June 2003.
Participants Setting: New Zealand
Patients with cellulitis
Number recruited: treatment: 98, control: 96
Ages, mean (SD): T: 54.6 (20.6), C: 48.4 (19)
European: T: 77/98 (79%), C: 78/96 (81%)
Maori: T: 10/98 (10%), C: 5/96 (5%)
Pacific: T: 2/98 (2%), C: 1/96 (1%)
Other: T: 9/98 (9%), C: 13/96 (12%)
Interventions Hospital at home admission avoidance from the emergency department. Run by Pegasus Health, an independent practitioner's association for 230 GPs in Christchurch, New Zealand.
Care provided by GP and community care nursing staff.
Patients required IV antibiotics for cellulitis.
Outcomes Advancement of cellulitis, readmission, days on IV antibiotics, functional outcomes (SF‐36), patient satisfaction
Notes Follow up: 3 and 6 days
Funding: Pegasus Health
Conflicts of interest: none declared
Ethical approval: local ethical committee
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk Randomisation list produced by SAS code
Allocation concealment (selection bias) Low risk Telephone randomisation service
Baseline outcome measurements (selection bias) Low risk Baseline outcome measurements done prior to intervention for functional outcomes; no relevant differences found
Baseline characteristics (selection bias) Low risk Baseline characteristics of treatment and control groups are reported and similar for main characteristics
Blinding of participants and personnel (performance bias)
All outcomes Unclear risk Blinding of participants and personnel not possible
Blinding of outcome assessment (detection bias)
Subjective outcomes Unclear risk Unclear risk for pain, functional and physical health (SF‐36), and satisfaction
Blinding of outcome assessment (detection bias)
Objective outcomes Low risk Low risk for advancement of cellulitis
Incomplete outcome data (attrition bias)
All outcomes Low risk 3 from each group excluded at follow‐up
Selective reporting (reporting bias) Unclear risk Insufficient information to allocate low or high risk