Literature DB >> 23194419

'No one wants to be the face of Herpes London': a qualitative study of the challenges of engaging patients and the public in sexual and reproductive health and HIV/AIDS services.

Nicola Robinson1, Ava Lorenc.   

Abstract

OBJECTIVES: To explore barriers, challenges and best practice within patient and public engagement (PPE) in sexual and reproductive health and HIV (SRHH) services in London.
METHODS: Consultation exercise using qualitative interviews with 27 stakeholders including commissioners, managers, voluntary/community organizations (VCOs) clinicians and patients, analysed using Framework Analysis and Atlas.ti software.
RESULTS: Participants recognized PPE's importance, echoing recent political and NHS drives, and highlighted the need for meaningful, empowering PPE, including user-designed methods, peer research and participatory approaches. Although challenging in SRHH and requiring training and support, PPE may help tackle stigma, and promote self-management and patient-centred-care, including peer education and role modelling. Expertise may come from experienced VCOs. Themes in priority order were: organizational commitment (including lack of dedicated staff, time and money); motivating patients; changing NHS philosophy; informing patients/public; using public awareness/education campaigns; overcoming stigma; working with VCOs. 'Reaching out' to engage underrepresented groups in this sensitive area was emphasized through community outreach, incentivization and linking with existing organizations. Making engagement easy and addressing issues of public value were also important. Stigma was less hindering than anticipated, except for ethnic minorities. PPE was seen to improve patient satisfaction, increase service uptake and reduce inequalities, key priorities in SRHH, and identify innovative service delivery ideas.
CONCLUSIONS: PPE is crucial in creating a patient-led NHS and responsible society. If organizations, including the NHS, commit to implementing meaningful PPE which actively targets those at risk of poor SRHH, services can be truly patient-led and patients and communities empowered to tackle the stigma of SRHH.
© 2012 John Wiley & Sons Ltd.

Entities:  

Keywords:  HIV; patient and public engagement; public involvement; reproductive health; sexual health

Mesh:

Year:  2012        PMID: 23194419      PMCID: PMC5060775          DOI: 10.1111/hex.12024

Source DB:  PubMed          Journal:  Health Expect        ISSN: 1369-6513            Impact factor:   3.377


  14 in total

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10.  Using focus groups to develop health surveys: an example from research on social relationships and AIDS-preventive behavior.

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Journal:  Health Educ Q       Date:  1993
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  1 in total

1.  The state of health services partnering with consumers: evidence from an online survey of Australian health services.

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  1 in total

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