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

Davies 2000.

Study characteristics
Methods Parallel randomised trial
Study conducted between February 1998 and August 1999.
Participants Setting: UK
Patients with chronic obstructive airways disease
Number recruited: hospital at home: 100, hospital: 50
Interventions Hospital at home
Type of service: admission avoidance from A&E. Care provided by outreach specialist nurses and GP and community nurses if required.
Outcomes Respiratory function, readmission, quality of life
Notes Few details on measure of quality of life
Follow up: 2 weeks and 3 months
Funding: North Mersey Community (NHS) Trust and University of Liverpool (UK)
Conflicts of interest: none declared
Ethical approval: district ethical committee
This author contributed IPD for a previous update of this review (Shepperd 2016a).
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk Ratio of 2:1 (hospital at home: hospital)
Allocation concealment (selection bias) Low risk Opaque, sealed envelopes
Baseline outcome measurements (selection bias) Low risk Baseline outcome measurements done prior to intervention for respiratory function; no relevant differences found
Baseline characteristics (selection bias) Low risk Baseline characteristics of the study and control groups are reported and are similar
Blinding of participants and personnel (performance bias)
All outcomes Low risk Blinding of participants and personnel not possible
Hospital readmission was a primary outcome, with decision to admit made by hospital staff
Blinding of outcome assessment (detection bias)
Subjective outcomes Unclear risk A small group of participants completed the St George's Respiratory Questionnaire
Blinding of outcome assessment (detection bias)
Objective outcomes Low risk Low risk for admission to hospital, changes in FEV1 score
Incomplete outcome data (attrition bias)
All outcomes Low risk Loss to follow‐up: hospital at home: 7/100; hospital: 5/50
Selective reporting (reporting bias) Low risk All outcomes reported (received trial data set)