| Literature DB >> 26597867 |
Megan E Passey1, Jo M Longman1, Jennifer J Johnston1, Louisa Jorm2, Dan Ewald3, Geoff G Morgan1, Margaret Rolfe1, Bronwyn Chalker4.
Abstract
INTRODUCTION: Rates of potentially preventable hospitalisations (PPH) are used as a proxy measure of effectiveness of, or access to community-based health services. The validity of PPH as an indicator in Australia has not been confirmed. Available evidence suggests that patient-related, clinician-related and systems-related factors are associated with PPH, with differences between rural and metropolitan settings. Furthermore, the proportion of PPHs which are actually preventable is unknown. The Diagnosing Potentially Preventable Hospitalisations study will determine the proportion of PPHs for chronic conditions that are deemed preventable and identify potentially modifiable factors driving these, in order to develop effective interventions to reduce admissions and improve measures of health system performance. METHODS AND ANALYSIS: This mixed methods data linkage study of approximately 1000 eligible patients with chronic PPH admissions to one metropolitan and two regional hospitals over 12 months will combine data from multiple sources to assess the: extent of preventability of chronic PPH admissions; validity of the Preventability Assessment Tool (PAT) in identifying preventable admissions; factors contributing to chronic PPH admissions. Data collected from patients (quantitative and qualitative methods), their general practitioners, hospital clinicians and hospital records, will be linked with routinely collected New South Wales (NSW) Admitted Patient Data Collection, the NSW Registry of Births, Death and Marriages death registration and Australian Bureau of Statistics mortality data. The validity of the PAT will be assessed by determining concordance between clinician assessment and that of a 'gold standard' panel. Multivariable logistic regression will identify the main predictor variables of admissions deemed preventable, using study-specific and linked data. ETHICS AND DISSEMINATION: The NSW Population and Health Services Research Ethics Committee granted ethical approval. Dissemination mechanisms include engagement of policy stakeholders through a project Steering Committee, and the production of summary reports for policy and clinical audiences in addition to peer-review papers. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/Entities:
Keywords: PRIMARY CARE; ambulatory care sensitive conditions; avoidable hospital admission; potentially preventable hospitalisations
Mesh:
Year: 2015 PMID: 26597867 PMCID: PMC4663419 DOI: 10.1136/bmjopen-2015-009879
Source DB: PubMed Journal: BMJ Open ISSN: 2044-6055 Impact factor: 2.692
Relationship between project objectives and substudies
| Substudy 1: comprehensive data collection for each admission | Substudy 2: validation of the PAT | Substudy 3: qualitative study | Substudy 4: data linkage | |
|---|---|---|---|---|
| Objective 1: validate PAT | X | X | ||
| Objective 2: assess proportion of PPH admissions deemed preventable | X | X | ||
| Objective 3: identify factors contributing to preventable hospitalisations | X | X | X | |
| Objective 4: recommend refinements to PPH measures | X | X | ||
| Objective 5: identify interventions to reduce chronic PPH admissions | X | X | X |
PAT,Preventability Assessment Tool; PPH, potentially preventable hospitalizations.
Diagnoses for inclusion
| Any of the following as principal diagnosis only | |
| I 50 | Heart failure |
| I 50.0 | Congestive heart failure |
| I 50.1 | Left ventricular failure |
| I 50.9 | Heart failure, unspecified |
| I 11.0 | Hypertensive heart disease with (congestive) heart failure |
| J 81 | Pulmonary oedema |
| Any of the following as principal diagnosis only | |
| I 20 | Angina pectoris |
| I 20.0 | Unstable angina |
| I 20.1 | Angina pectoris with documented spasm |
| I 20.8 | Other forms of angina pectoris |
| I 20.9 | Angina pectoris, unspecified |
| I 24.0 | Coronary thrombosis not resulting in myocardial infarction |
| I 24.8 | Other forms of acute ischaemic heart disease |
| I 24.9 | Acute ischaemic heart disease, unspecified |
| Any of the following as principal diagnosis only | |
| J 41 | Simple and mucopurulent chronic bronchitis |
| J 42 | Unspecified chronic bronchitis |
| J 43 | Emphysema |
| J 44 | Other chronic obstructive pulmonary disease |
| J 47 | Bronchiectasis |
| J20 as principal diagnosis ONLY if additional diagnoses of J41, J42, J43, J44, J47 | |
| J 20 | Acute bronchitis |
| Any of the following as principal diagnosis only | |
| E 10 | Type 1 diabetes mellitus with or without complications |
| E 11 | Type 2 diabetes mellitus with or without complications |
| E 12 | Malnutrition-related diabetes mellitus |
| E 13 | Other specified diabetes mellitus |
| E 14 | Unspecified diabetes mellitus |
| E 10–E 14 as additional diagnoses where the principal diagnosis is one of | |
| E 87.0 | Hyperosmolarity |
| E 87.2 | Acidosis |
| G 45 | Transient ischaemic attack |
| G 50—G 64 | Nerve disorders and neuropathies |
| H 25—H 28 | Cataracts and lens disorders |
| H 30—H 36 | Retinal disorders |
| H 40 & H 42 | Glaucoma (all) |
| I 20 | Angina pectoris |
| I 21—I 22 | Myocardial infarction |
| I 23—I 25 | Other acute and chronic ischaemic heart diseases |
| I 25 | Chronic ischaemic heart disease |
| I 50 | Heart failure |
| I 60—I 64, I 69 | Stroke and sequelae |
| I 70—I 74 | Peripheral vascular disease |
| K 05 | Gingivitis and periodontal diseases |
| N 00—N 29 | Kidney diseases including end-stage renal disease |
| Z 49 | Renal dialysis |
Difference detectable for various rates of the factor of interest and proportions of admissions classified as preventable
| Proportion classified as preventable | |||
|---|---|---|---|
| 15% | 25% | 35% | |
| Rate of factor of interest in non-preventable groups | Difference detectable | ||
| 10% | 11.7% | 9.5% | 8.6% |
| 20% | 14.4% | 11.7% | 10.6% |