Title
Uncovering Treatment Burden as a Key Concept for Stroke Care: A Systematic Review of Qualitative Research
Date Issued
01 June 2013
Access level
open access
Resource Type
review
Author(s)
Gallacher K.
Morrison D.
Jani B.
Macdonald S.
May C.R.
Erwin P.J.
Batty G.D.
Eton D.T.
Langhorne P.
Mair F.S.
Mayo Clinic
Abstract
Background:Patients with chronic disease may experience complicated management plans requiring significant personal investment. This has been termed 'treatment burden' and has been associated with unfavourable outcomes. The aim of this systematic review is to examine the qualitative literature on treatment burden in stroke from the patient perspective.Methods and Findings:The search strategy centred on: stroke, treatment burden, patient experience, and qualitative methods. We searched: Scopus, CINAHL, Embase, Medline, and PsycINFO. We tracked references, footnotes, and citations. Restrictions included: English language, date of publication January 2000 until February 2013. Two reviewers independently carried out the following: paper screening, data extraction, and data analysis. Data were analysed using framework synthesis, as informed by Normalization Process Theory. Sixty-nine papers were included. Treatment burden includes: (1) making sense of stroke management and planning care, (2) interacting with others, (3) enacting management strategies, and (4) reflecting on management. Health care is fragmented, with poor communication between patient and health care providers. Patients report inadequate information provision. Inpatient care is unsatisfactory, with a perceived lack of empathy from professionals and a shortage of stimulating activities on the ward. Discharge services are poorly coordinated, and accessing health and social care in the community is difficult. The study has potential limitations because it was restricted to studies published in English only and data from low-income countries were scarce.Conclusions:Stroke management is extremely demanding for patients, and treatment burden is influenced by micro and macro organisation of health services. Knowledge deficits mean patients are ill equipped to organise their care and develop coping strategies, making adherence less likely. There is a need to transform the approach to care provision so that services are configured to prioritise patient needs rather than those of health care systems.Systematic Review Registration:International Prospective Register of Systematic Reviews CRD42011001123 Please see later in the article for the Editors' Summary. © 2013 Gallacher et al.
Volume
10
Issue
6
Language
English
OCDE Knowledge area
Enfermería Neurología clínica
Scopus EID
2-s2.0-84879357091
PubMed ID
Source
PLoS Medicine
ISSN of the container
15491277
Sponsor(s)
DTE is currently receiving federal funding from the U.S. National Institutes of Health (National Institute of Nursing Research) to conduct research on the burden of treatment concept. Grant number: 1R21NR012984-01A1. FSM and CRM have also received funding from the ESRC previously to help develop a NPT web enabled toolkit. All other authors have declared that no competing interests exist.
Sources of information: Directorio de Producción Científica Scopus