TY - JOUR
T1 - Patients' perspectives on the medical primary-secondary care interface
T2 - systematic review and synthesis of qualitative research
AU - Sampson, Rod
AU - Cooper, Jamie
AU - Barbour, Rosaline
AU - Polson, Rob
AU - Wilson, Philip
N1 - Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.
PY - 2015/10/15
Y1 - 2015/10/15
N2 - Objectives: To synthesise the published literature on the patient experience of the medical primary- secondary care interface and to determine priorities for future work in this field aimed at improving clinical outcomes. Design: Systematic review and metaethnographic synthesis of primary studies that used qualitative methods to explore patients' perspectives of the medical primary-secondary care interface. Setting: International primary-secondary care interface. Data sources: EMBASE, MEDLINE, CINAHL Plus with Full text, PsycINFO, Psychology and Behavioural Sciences Collection, Health Business Elite, Biomedica Reference Collection: Comprehensive Library, Information Science and Technology Abstracts, eBook Collection, Web of Science Core Collection: Citation Indexes and Social Sciences Citation Index, and grey literature. Eligibility criteria for selecting studies: Studies were eligible for inclusion if they were full research papers employing qualitative methodology to explore patients' perspectives of the medical primary- secondary care interface. Review methods: The 7-step metaethnographic approach described by Noblit and Hare, which involves cross-interpretation between studies while preserving the context of the primary data. Results: The search identified 690 articles, of which 39 were selected for full-text review. 20 articles were included in the systematic review that encompassed a total of 689 patients from 10 countries. 4 important areas specific to the primary-secondary care interface from the patients' perspective emerged: barriers to care, communication, coordination, and 'relationships and personal value'. Conclusions and implications of key findings: Patients should be the focus of any transfer of care between primary and secondary systems. From their perspective, areas for improvement may be classified into four domains that should usefully guide future work aimed at improving quality at this important interface.
AB - Objectives: To synthesise the published literature on the patient experience of the medical primary- secondary care interface and to determine priorities for future work in this field aimed at improving clinical outcomes. Design: Systematic review and metaethnographic synthesis of primary studies that used qualitative methods to explore patients' perspectives of the medical primary-secondary care interface. Setting: International primary-secondary care interface. Data sources: EMBASE, MEDLINE, CINAHL Plus with Full text, PsycINFO, Psychology and Behavioural Sciences Collection, Health Business Elite, Biomedica Reference Collection: Comprehensive Library, Information Science and Technology Abstracts, eBook Collection, Web of Science Core Collection: Citation Indexes and Social Sciences Citation Index, and grey literature. Eligibility criteria for selecting studies: Studies were eligible for inclusion if they were full research papers employing qualitative methodology to explore patients' perspectives of the medical primary- secondary care interface. Review methods: The 7-step metaethnographic approach described by Noblit and Hare, which involves cross-interpretation between studies while preserving the context of the primary data. Results: The search identified 690 articles, of which 39 were selected for full-text review. 20 articles were included in the systematic review that encompassed a total of 689 patients from 10 countries. 4 important areas specific to the primary-secondary care interface from the patients' perspective emerged: barriers to care, communication, coordination, and 'relationships and personal value'. Conclusions and implications of key findings: Patients should be the focus of any transfer of care between primary and secondary systems. From their perspective, areas for improvement may be classified into four domains that should usefully guide future work aimed at improving quality at this important interface.
KW - Communication
KW - Humans
KW - Patient Preference
KW - Physician-Patient Relations
KW - Primary Health Care/standards
KW - Qualitative Research
KW - Secondary Care/standards
U2 - 10.1136/bmjopen-2015-008708
DO - 10.1136/bmjopen-2015-008708
M3 - Review
C2 - 26474939
SN - 2044-6055
VL - 5
SP - e008708
JO - BMJ Open
JF - BMJ Open
IS - 10
ER -