The experiences of patients and carers living with multimorbid, noncommunicable diseases

Stephen R. Leeder*, Tanisha Jowsey, Justin W. McNab

*Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer-review

2 Citations (Scopus)

Abstract

Background 

Non-communicable diseases (NCDs) are increasing in prevalence and straining health systems globally. This creates a so-called ‘burden of disease', which can be traced in terms of fiscal health system matters and in terms of quality of life and lived experiences of people with NCDs. The United Nations has called for a global agenda to manage NCDs and reduce their burden. 

Objectives 

The purpose of this article is to summarise key findings from the Serious and Continuing Illness Policy and Practice Study concerning patients' and carers' experiences of multimorbid NCDs in Australia. We focus on the relevance of findings for policy and general practitioners in Australia. 

Discussion 

We suggest that a complex multimorbidity policy is needed to contextualise and guide single-illness NCD policies. Our research suggests that specialist NCD nurses and allied health professionals could have important roles in improving care coordination between general practices and community health centres.

Original languageEnglish
Pages (from-to)24-27
Number of pages4
JournalAustralian Journal of General Practice
Volume47
Issue number1-2
DOIs
Publication statusPublished - Jan 2018
Externally publishedYes

Fingerprint

Dive into the research topics of 'The experiences of patients and carers living with multimorbid, noncommunicable diseases'. Together they form a unique fingerprint.

Cite this