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1.
Health Res Policy Syst ; 18(1): 13, 2020 Jan 31.
Artículo en Inglés | MEDLINE | ID: mdl-32005254

RESUMEN

BACKGROUND: Cross-sector collaborative partnerships are a vital strategy in efforts to strengthen research-informed policy and practice and may be particularly effective at addressing the complex problems associated with chronic disease prevention. However, there is still a limited understanding of how such partnerships are implemented in practice and how their implementation contributes to outcomes. This paper explores the operationalisation and outcomes of knowledge mobilisation strategies within the Australian Prevention Partnership Centre - a research collaboration between policy-makers, practitioners and researchers. METHODS: The Centre's programme model identifies six knowledge mobilisation strategies that are hypothesised to be essential for achieving its objectives. Using a mixed methods approach combining stakeholder interviews, surveys, participant feedback forms and routine process data over a 5-year period, we describe the structures, resources and activities used to operationalise these strategies and explore if and how they have contributed to proximal outcomes. RESULTS: Results showed that Centre-produced research, resources, tools and methods were impacting policy formation and funding. Policy-makers reported using new practical methodologies that were helping them to design, implement, evaluate and obtain funding for scaled-up policies and programmes, and co-creating compelling prevention narratives. Some strategies were better implemented and more impactful than others in supporting these outcomes, with variation in who they worked for. The activities used to effect engagement, capacity-building and partnership formation were mostly generating positive results, but co-production could be enhanced by greater shared decision-making. Considerably more work is needed to successfully operationalise knowledge integration and adaptive learning. CONCLUSIONS: Describing how collaborative cross-sector research partnerships are operationalised in practice, and with what effects, can provide important insights into practical strategies for establishing and growing such partnerships and for maximising their contributions to policy. Findings suggest that the Centre has many strengths but could benefit from more inclusive and transparent governance and internal processes that facilitate dialogue about roles, expectations and co-production practices.


Asunto(s)
Enfermedad Crónica/psicología , Investigación sobre Servicios de Salud/organización & administración , Enfermedades no Transmisibles/prevención & control , Formulación de Políticas , Servicios Preventivos de Salud/organización & administración , Investigación Biomédica Traslacional/organización & administración , Comités Consultivos/organización & administración , Australia , Creación de Capacidad/organización & administración , Comunicación , Procesos de Grupo , Personal de Salud/organización & administración , Humanos , Difusión de la Información/métodos , Relaciones Interinstitucionales , Liderazgo , Investigadores/organización & administración
2.
Public Health Res Pract ; 28(3)2018 Sep 27.
Artículo en Inglés | MEDLINE | ID: mdl-30406262

RESUMEN

OBJECTIVES: To accelerate the use of evidence in policy and practice through cross-sectoral, multidisciplinary partnership research, founded on shared governance and coproduction. Type of program or service: A National Health and Medical Research Council (NHMRC) Partnership Centre for Better Health. METHODS: We present our views and experiences based on the first 5 years of operation of The Australian Prevention Partnership Centre. RESULTS: We have undertaken an ambitious and complex 5-year program of work taking a systems approach to prevention research, and have grown the size and reach of the collaboration to become a focus for prevention research in Australia. We have progressed towards reaching our objectives. However, there have been challenges including trust building between stakeholders, the complexities of incorporating coproduction into every research project, and the production of research that is implementable within different policy environments. LESSONS LEARNT: Working within the partnership model has provided the time, resources and flexibility to coproduce policy-relevant, timely research.


Asunto(s)
Relaciones Comunidad-Institución , Servicios Preventivos de Salud/organización & administración , Práctica de Salud Pública , Australia , Creación de Capacidad , Enfermedad Crónica , Conducta Cooperativa , Política de Salud , Investigación sobre Servicios de Salud/organización & administración , Humanos , Evaluación de Programas y Proyectos de Salud
3.
J Paediatr Child Health ; 47(9): 581-4, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21951436

RESUMEN

Doctors sometimes struggle with ethically challenging requests for treatment from children's parents. For instance, we have recently had two requests by parents of children, a girl and a boy, each with a severe developmental disability, for hormonal therapy to suppress growth and puberty: the girl's parents requested, in addition, hysterectomy and mastectomy. We propose a reliable approach to assessing the ethical and legal aspects of these and other requests for 'non-therapeutic' treatment of a minor who lacks the capacity to give informed consent. We argue that a doctor should first assess whether the request is one that he or she can, in conscience, accede to, and then, if it is, seek the authorisation of a court. We outline considerations relevant to the doctor's assessment of both the ethical issues and to the need for court authorisation.


Asunto(s)
Protección a la Infancia/ética , Protección a la Infancia/legislación & jurisprudencia , Niños con Discapacidad/legislación & jurisprudencia , Crecimiento , Hormonas/administración & dosificación , Discapacidad Intelectual , Pubertad , Australia , Niño , Femenino , Humanos , Masculino , Consentimiento Paterno/ética , Consentimiento Paterno/legislación & jurisprudencia , Pediatría/ética , Pediatría/legislación & jurisprudencia
5.
Aust N Z J Obstet Gynaecol ; 44(5): 452-7; discussion 377, 2004 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-15387869

RESUMEN

AIMS: Maternal mortality has declined dramatically over the past 30 years in developed countries. This retrospective study aims to provide an epidemiological overview of maternal deaths in Australia between 1973 and 1996. METHODS: Data were abstracted from national maternal mortality data collection and triennial reports for the period 1973-1996 for women who died from pregnancy-related causes while pregnant or within 42 days of a pregnancy being delivered or terminated. Deaths were restricted to those classified as direct or indirect maternal deaths. Maternal mortality age-specific mortality ratios were calculated. The leading causes of death were examined. RESULTS: Of the 584 deaths, 363 were direct and 221 indirect. The leading causes of direct death were pulmonary embolism (18.4%) and hypertensive disorders (16.3%). Cardiovascular disease accounted for 41% of indirect deaths. The maternal mortality ratio declined from 12.7 deaths per 100,000 confinements in 1973-1975 to 6.2 in 1991-1993, and was 10.0 for the entire 24-year period. For women aged 40-44 years the ratio declined from 165.1 to 14.2 between 1973 and 1996. The ratio for Indigenous mothers was three times higher than for non-Indigenous mothers, being 34.8 in the most recent triennium 1994-1996. CONCLUSIONS: Although maternal deaths are rare in Australia, apparent health inequality persists with Indigenous mothers continuing to have a higher risk of maternal death. While mortality in traditionally higher risk women aged > 40 years has declined, women with morbid cardiovascular disease continue to be over-represented in the deaths. The comparatively high rate of deaths from pulmonary embolism needs to be addressed.


Asunto(s)
Causas de Muerte/tendencias , Mortalidad Materna/tendencias , Factores de Edad , Australia/epidemiología , Embolia de Líquido Amniótico/mortalidad , Femenino , Humanos , Hipertensión/complicaciones , Hipertensión/mortalidad , Hemorragia Posparto/mortalidad , Embarazo , Complicaciones del Embarazo/epidemiología , Embarazo Ectópico/mortalidad , Embolia Pulmonar/mortalidad , Estudios Retrospectivos , Factores de Riesgo
6.
Aust N Z J Obstet Gynaecol ; 43(2): 148-51, 2003 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-14712972

RESUMEN

OBJECTIVE: To determine the prevalence and incidence of lower limb lymphoedema (LLL) in a cohort of women who had treatment for gynaecological cancer between May 1995 and April 2000. DESIGN: A retrospective survey. SETTING: The study took place at an urban referral centre in an Australian tertiary referral women's hospital. SAMPLE: The data collection was based on 66% of 743 women on the database of the Gynaecological Cancer Centre. METHODS: Interviews and assessments were conducted to determine the status of lower limbs; medical records were reviewed for age, weight, site and type of cancer and treatment. MAIN OUTCOME MEASURES: Leg swelling, diagnosed lower limb lymphoedema, no swelling of the legs and type of surgery were determined as the main outcome measures. RESULTS AND CONCLUSIONS: The diagnosis of lower limb lymphoedema was made in 18% of the total sample: 53% of these were diagnosed within 3 months of treatment, a further 18% within 6 months, 13% within 12 months and the remaining 16% up to 5 years following treatment. Women most at risk for developing LLL were those who had treatment for vulvar cancer with removal of lymph nodes and follow up radiotherapy. For this subsample, the prevalence was 47%. The finding that LLL occurs within the first year is earlier than hitherto generally believed. It is therefore imperative for all health professionals to include care and assessment of the legs particularly during the immediate pre- and postoperative period.


Asunto(s)
Neoplasias de los Genitales Femeninos/etiología , Linfedema/etiología , Complicaciones Posoperatorias/epidemiología , Femenino , Procedimientos Quirúrgicos Ginecológicos , Humanos , Pierna , Linfedema/epidemiología , Prevalencia , Estudios Retrospectivos
7.
Med Educ ; 36(7): 614-21, 2002 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-12109980

RESUMEN

OBJECTIVES: Overseas-trained doctors (OTDs) have limited access and formal interaction with the Australian health care system prior to joining the Australian medical workforce. A pre-employment programme was designed to familiarize OTDs with the Australian health care system. METHOD: All OTDs who had passed their Australian Medical Council (AMC) exams and were applying for a pre-registration year in New South Wales were invited to participate in the voluntary, free programme. A 4-week full-time programme was developed consisting of core group teaching and a hospital attachment. The curriculum included communication, health and workplace skills; and sessions on culture shock and the role of junior doctors. A pilot programme was run in 1997. The programme was repeated in 1998 and 1999. The OTDs' confidence regarding the general duties of internship, and attitudes towards hospital workplace skills were examined. RESULTS: The 66 OTDs reported greater understanding of staff and communication issues and familiarization with the hospital environment. They reported a more realistic understanding of the role of a junior doctor, the need for separation of workplace and personal responsibilities and knowledge of pathways for future professional development. The course structure, with a focus on hospital attachments, establishment of a peer network, and workplace familiarization facilitated entry into the hospital workforce. CONCLUSION: The pre-employment programme enabled the OTDs to have a more equitable entry into the public hospital system, resulting in a more integrated, confident and functional workforce.


Asunto(s)
Educación Médica/métodos , Médicos Graduados Extranjeros/normas , Australia , Comunicación , Cultura , Curriculum , Humanos , Cooperación Internacional , Médicos/organización & administración
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