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1.
BMC Pregnancy Childbirth ; 21(1): 205, 2021 Mar 12.
Artigo em Inglês | MEDLINE | ID: mdl-33711957

RESUMO

BACKGROUND: Recent UK maternity policy changes recommend that a named midwife supports women throughout their pregnancy, birth and postnatal care. Whilst many studies report high levels of satisfaction amongst women receiving, and midwives providing, this level of continuity of carer, there are concerns some midwives may experience burnout and stress. In this study, we present a qualitative evaluation of the implementation of a midwife-led continuity of carer model that excluded continuity of carer at the birth. METHODS: Underpinned by the Conceptual Model for Implementation Fidelity, our evaluation explored the implementation, fidelity, reach and satisfaction of the continuity of carer model. Semi-structured interviews were undertaken with midwives (n = 7) and women (n = 15) from continuity of carer team. To enable comparisons between care approaches, midwives (n = 7) and women (n = 10) from standard approach teams were also interviewed. Interviews were recorded, transcribed and analysed using thematic analysis. RESULTS: For continuity of carer team midwives, manageable caseloads, extended appointment times, increased team stability, and flexible working patterns facilitated both care provided and midwives' job satisfaction. Both continuity of carer and standard approach midwives reported challenges in providing postnatal continuity given the unpredictable timing of labour and birth. Time constraints, inadequate staffing and lack of administrative support were reported as additional barriers to implementing continuity of carer within standard approach teams. Women reported continuity was integral to building trust with midwives, encouraged them to disclose mental health issues and increased their confidence in making birth choices. CONCLUSIONS: Our evaluation highlighted the successful implementation of a continuity of carer model for ante and postnatal care. Despite exclusion of the birth element in the model, both women and midwives expressed high levels of satisfaction in comparison to women and midwives within the standard approach. Implementation successes were largely due to structural and resource factors, particularly the combination of additional time and smaller caseloads of women. However, these resources are not widely available within the resources of maternity unit budgets. Future research should further explore whether a continuity of carer model focusing on antenatal and postnatal care delivery is a feasible and sustainable model of care for all women.


Assuntos
Continuidade da Assistência ao Paciente , Serviços de Saúde Materna , Tocologia , Enfermeiros Obstétricos/psicologia , Preferência do Paciente , Assistência Perinatal , Adulto , Atitude do Pessoal de Saúde , Continuidade da Assistência ao Paciente/organização & administração , Continuidade da Assistência ao Paciente/tendências , Feminino , Humanos , Serviços de Saúde Materna/organização & administração , Serviços de Saúde Materna/normas , Tocologia/métodos , Tocologia/organização & administração , Modelos Organizacionais , Inovação Organizacional , Parto/psicologia , Preferência do Paciente/psicologia , Preferência do Paciente/estatística & dados numéricos , Assistência Perinatal/métodos , Assistência Perinatal/tendências , Gravidez , Pesquisa Qualitativa , Apoio Social , Reino Unido
2.
Public Health ; 178: 151-158, 2020 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-31698137

RESUMO

OBJECTIVES: Expansion of newborn bloodspot screening (NBS) within England, which practices an informed consent model, justified examining acceptability and effectiveness of alternative consent models. STUDY DESIGN: Qualitative focus groups. METHODS: Forty-five parents and 37 screening professionals (SPs) participated. Data were analysed using thematic analysis. RESULTS: Parents and SPs initially appeared to have differing views about appropriate consent models. Most parents accepted assumed consent, if adequately informed; however, once aware of bloodspot storage, informed consent was wanted. SPs valued informed consent, but acknowledged it was difficult to obtain. Both samples wanted parents to be informed but were unclear how this could be achieved. Most parents felt NBS was not presented as optional. CONCLUSION: The simultaneous exploration of parents and SPs views, in real time is original. This rigour avoided the reliance on retrospective accounts which make it difficult to establish how decisions were made at the time. It is also unique in providing pre-interview consent models to drive the depth of data. It was rigorous in member checking. Findings suggested a preference for full disclosure of all information with some parents valuing this more than choice. Both samples queried whether current consent was sufficiently informed and voluntary. Results suggest differing tolerances of consent type if screening is solely for diagnostic purposes vs bloodspot storage. Results highlight the need for caution when examining consent model preferences without also checking knowledge, as opinions may be based on incomplete knowledge. Future research is needed to examine efficacy of proposed changes. FUNDING: National Institute for Health Research Health Technology Assessment HTAProgramme (11/62/02). TRIAL REGISTRATION: ISRCTN70227207.


Assuntos
Atitude do Pessoal de Saúde , Atitude Frente a Saúde , Pessoal de Saúde/psicologia , Consentimento Livre e Esclarecido/psicologia , Triagem Neonatal , Pais/psicologia , Adolescente , Adulto , Inglaterra , Feminino , Grupos Focais , Humanos , Recém-Nascido , Masculino , Modelos Teóricos , Pesquisa Qualitativa , Adulto Jovem
3.
BMC Public Health ; 19(1): 835, 2019 Jun 27.
Artigo em Inglês | MEDLINE | ID: mdl-31248396

RESUMO

BACKGROUND: Commissioning and monitoring of community-based interventions is a challenge due to the complex nature of the environment and the lack of any explicit cut-offs to guide decision making. At what point, for example, is participant enrolment to interventions, course completion or satisfaction deemed to be acceptable or sufficient for continued funding? We aimed to identify and quantify key progression criteria for fourteen early years interventions by (1) agreeing the top three criteria for monitoring of successful implementation and progress; and (2) agreeing boundaries to categorise interventions as 'meeting anticipated target' (green); 'falling short of targets' (amber) and 'targets not being met' (red). METHODS: We ran three workshops in partnership with the UK's Big Lottery Fund commissioned programme 'Better Start Bradford' (implementing more than 20 interventions to improve the health, wellbeing and development of children aged 0-3) to support decision making by agreeing progression criteria for the interventions being delivered. Workshops included 72 participants, representing a range of professional groups including intervention delivery teams, commissioners, intervention-monitoring teams, academics and community representatives. After discussion and activities, final decisions were submitted using electronic voting devices. All participants were invited to reconsider their responses via a post-workshop questionnaire. RESULTS: Three key progression criteria were assigned to each of the 14 interventions. Overall, criteria that participants most commonly voted for were recruitment, implementation and reach, but these differed according to each intervention. Cut-off values used to indicate when an intervention moved to 'red' varied by criteria; the lowest being for recruitment, where participants agreed that meeting less than 65% of the targeted recruitment would be deemed as 'red' (falling short of target). CONCLUSIONS: Our methodology for monitoring the progression of interventions has resulted in a clear pathway which will support commissioners and intervention teams in local decision making within the Better Start Bradford programme and beyond. This work can support others wishing to implement a formal system for monitoring the progression of public health interventions.


Assuntos
Saúde da Criança , Tomada de Decisões Gerenciais , Promoção da Saúde/organização & administração , Administração em Saúde Pública , Pré-Escolar , Feminino , Humanos , Lactente , Recém-Nascido , Gravidez , Inquéritos e Questionários , Reino Unido
4.
Fam Cancer ; 6(2): 197-203, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17520351

RESUMO

A primary care cancer genetics project, funded by Macmillan Cancer Support and the Department of Health, has been running in North Kirklees since 2004. North Kirklees has a high ethnic minority population (mainly South Asian) and 50% of its wards lie in the most deprived quintiles in England. Previous audits in the department of genetics have shown lower than expected referral rates for patients from lower socio-economic classes and no referrals from ethnic minority patients. The aims of the project included improving access to cancer genetics services for disadvantaged patients from lower socio-economic groups and the ethnic minority population. A practice nurse and a General Practitioner with a Special Interest in genetics, both with appropriate language skills, and a 0.5 FTE genetic counsellor have set up local clinics in several primary care sites in North Kirklees where they provide full genetic counselling services in the community. Demographic details, ethnic origin and education information are collected from each patient seen. Comparing information prior to and during the project demonstrates an increase in numbers of referrals for patients from lower socio-economic classes, those with educational achievements at GCSE level or below, and those from South Asian backgrounds. Local clinics and increasing awareness of cancer genetics services for professionals and the public can improve access to such services.


Assuntos
Serviços em Genética/estatística & dados numéricos , Acessibilidade aos Serviços de Saúde , Área Carente de Assistência Médica , Neoplasias/genética , Encaminhamento e Consulta/estatística & dados numéricos , Atenção à Saúde , Serviços em Genética/organização & administração , Humanos , Grupos Minoritários , Programas Nacionais de Saúde , Atenção Primária à Saúde , Fatores Socioeconômicos , Reino Unido
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