1 | Population | Studies conducted in clinical environments which may include:
Acute care (inpatient and outpatient); Subacute care (rehabilitation centre); Community (general practice and aged care).
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2 | Intervention | Registry as an intervention with the following inclusion and exclusion criteria Inclusion criteria Studies will be included from the systematic review if they:
Describe either a clinical registry or a CQR which collects data on a procedure, disease or healthcare resource; Collect data systematically and on an ongoing basis from the population being investigated; Provide feedback on the performance of a health system on an ongoing basis; Collect data from more than one hospital. Exclusion criteria Studies will be excluded from the systematic review if they:
Collect and report on data from only one hospital; Do not provide feedback on an ongoing basis (such as an audit or point prevalence study); Are written in a language other than English; Were published prior to the start date on 1 January 1980 or after the end date of 31 December 2014 or were review articles.
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3 | Comparison | Comparators:
Data collecting tools other than registry (population-based data, administrative data and medical record) to monitor health outcomes; Studies without a comparator will be included.
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4 | Outcome | The primary outcome measure is impact on survival/mortality. Secondary outcome measures reflect a process or outcome of healthcare, healthcare utilisation and costs. |