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1.
Int J Cardiol ; 174(3): 484-91, 2014 Jul 01.
Article in English | MEDLINE | ID: mdl-24801076

ABSTRACT

Acute decompensated heart failure is a common cause of hospitalisation. This is a period of vulnerability both in altered pathophysiology and also the potential for iatrogenesis due to therapeutic interventions. Renal dysfunction is often associated with heart failure and portends adverse outcomes. Identifying heart failure patients at risk of renal dysfunction is important in preventing progression to chronic kidney disease or worsening renal function, informing adjustment to medication management and potentially preventing adverse events. However, there is no working or consensus definition in international heart failure management guidelines for worsening renal function. In addition, there appears to be no concordance or adaptation of chronic kidney disease guidelines by heart failure guideline development groups for the monitoring of chronic kidney disease in heart failure. Our aim is to encourage the debate for an agreed definition given the prognostic impact of worsening renal function in heart failure. We present the case for the uptake of the Acute Kidney Injury Network criteria for acute kidney injury with some minor alterations. This has the potential to inform study design and meta-analysis thereby building the knowledgebase for guideline development. Definition consensus supports data element, clinical registry and electronic algorithm innovation as instruments for quality improvement and clinical research for better patient outcomes. In addition, we recommend all community managed heart failure patients have their baseline renal function classified and routinely monitored in accordance with established renal guidelines to help identify those at increased risk for worsening renal function or progression to chronic kidney disease.


Subject(s)
Acute Kidney Injury/diagnosis , Acute Kidney Injury/epidemiology , Consensus , Heart Failure/diagnosis , Heart Failure/epidemiology , Kidney/physiology , Acute Kidney Injury/physiopathology , Animals , Heart Failure/physiopathology , Humans , Meta-Analysis as Topic , Retrospective Studies
2.
Med J Aust ; 190(S11): S144-9, 2009 06 01.
Article in English | MEDLINE | ID: mdl-19485865

ABSTRACT

OBJECTIVES: To develop and test a standardised clinical handover discharge strategy for improving information transfer between private mental health hospitals and community practitioners. DESIGN, SETTING AND PARTICIPANTS: A quality improvement intervention using collaborative, iterative methods to develop a standardised discharge and outcome assessment strategy. 150 patient participants were consecutively recruited from two private mental health care hospitals in New South Wales between April and September 2008. Opinions of community practitioners and patients on the discharge process and discharge documentation were solicited by written questionnaires and telephone interviews. MAIN OUTCOME MEASURES: Community practitioner satisfaction; patient satisfaction; documentation of discharge date at least 48 hours before discharge; faxing of discharge summaries to community practitioners within 48 hours of discharge; proportion of patients receiving a follow-up telephone call within 7 days or 14 days of discharge. RESULTS: Both community practitioners and patients believed the intervention was positive. Between Cycle 2 and Cycle 3, documentation of the discharge date at least 48 hours before discharge remained unchanged at 50%; the proportion of discharge summaries faxed within 48 hours of discharge went from 0 to 82% in Cycle 2 and fell to 65% in Cycle 3. Telephone follow-up of patients within 7 days and within 14 days improved by 10% and 6%, respectively, between Cycle 2 and Cycle 3. CONCLUSIONS: A standardised discharge communication strategy improved the timeliness, content, and format of information provided to community practitioners. The intervention was well accepted by patients and providers.


Subject(s)
Community Mental Health Services , Continuity of Patient Care/organization & administration , Patient Discharge , Quality Assurance, Health Care/organization & administration , Adult , Aged , Attitude of Health Personnel , Australia , Female , Hospitals, Psychiatric , Humans , Male , Middle Aged , Needs Assessment , Patient Satisfaction , Program Evaluation
3.
Med J Aust ; 184(2): 71-5, 2006 Jan 16.
Article in English | MEDLINE | ID: mdl-16411872

ABSTRACT

To provide physical activity recommendations for people with cardiovascular disease, an Expert Working Group of the National Heart Foundation of Australia in late 2004 reviewed the evidence since the US Surgeon General's Report: physical activity and health in 1996. The Expert Working Group recommends that: people with established clinically stable cardiovascular disease should aim, over time, to achieve 30 minutes or more of moderate intensity physical activity on most, if not all, days of the week; less intense and even shorter bouts of activity with more rest periods may suffice for those with advanced cardiovascular disease; and regular low-to-moderate level resistance activity, initially under the supervision of an exercise professional, is encouraged. Benefits from regular moderate physical activity for people with cardiovascular disease include augmented physiological functioning, lessening of cardiovascular symptoms, enhanced quality of life, improved coronary risk profile, superior muscle fitness and, for survivors of acute myocardial infarction, lower mortality. The greatest potential for benefit is in those people who were least active before beginning regular physical activity, and this benefit may be achieved even at relatively low levels of physical activity. Medical practitioners should routinely provide brief, appropriate advice on physical activity to people with well-compensated, clinically stable cardiovascular disease.


Subject(s)
Cardiovascular Diseases/therapy , Exercise Therapy , Cardiovascular Diseases/physiopathology , Cardiovascular Diseases/psychology , Energy Metabolism/physiology , Exercise Tolerance/physiology , Humans , Quality of Life
4.
Med J Aust ; 182(S9): S1-16, 2005 05 02.
Article in English | MEDLINE | ID: mdl-15865580

ABSTRACT

Patients with acute coronary syndromes represent a clinically diverse group and their care remains heterogeneous. These patients account for a significant burden of morbidity and mortality in Australia. Optimal patient outcomes depend on rapid diagnosis, accurate risk stratification and the effective implementation of proven therapies, as advocated by clinical guidelines. The challenge is in effectively applying evidence in clinical practice. Objectivity and standardised quantification of clinical practice are essential in understanding the evidence-practice gap. Observational registries are key to understanding the link between evidence-based medicine, clinical practice and patient outcome. Data elements for monitoring clinical management of patients with acute coronary syndromes have been adapted from internationally accepted definitions and incorporated into the National Health Data Dictionary, the national standard for health data definitions in Australia. Widespread use of these data elements will assist in the local development of "quality-of-care" initiatives and performance indicators, facilitate collaboration in cardiovascular outcomes research, and aid in the development of electronic data collection methods.


Subject(s)
Coronary Disease/therapy , Data Collection/methods , Myocardial Infarction/therapy , Quality Assurance, Health Care/statistics & numerical data , Vocabulary, Controlled , Acute Disease , Australia , Dictionaries as Topic , Evidence-Based Medicine , Humans , Practice Guidelines as Topic , Quality Indicators, Health Care , Reference Standards
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