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1.
J Crohns Colitis ; 14(8): 1037-1048, 2020 Sep 07.
Artículo en Inglés | MEDLINE | ID: mdl-32032423

RESUMEN

The management of inflammatory bowel disease [IBD] is complex, and requires tight control of disease activity, close monitoring to avoid treatment side effects, health care professionals with expertise in IBD, and an interdisciplinary, holistic approach. Despite various efforts to standardise structures, processes, and outcomes,1-8 and due to the high variability at the local, national, and international levels, there are still no clear definitions or outcome measures available to establish quality of care standards for IBD patients which are applicable in all contexts and all countries. For this reason, the European Crohn's and Colitis Organisation [ECCO] supported the construction of a list of criteria summarising current standards of care in IBD. The list comprises 111 quality standard points grouped into three main domains [structure n = 31, process n = 42, outcomes n = 38] and is based on scientific evidence, interdisciplinary expert consensus, and patient-oriented perspectives. The list of proposed criteria is intended to represent the position of ECCO regarding the optimum quality of care that should be available to patients. Since health care systems and regulations vary considerably between countries, this list may require adaptation at local and national levels. It is recognised that not all these criteria that have been identified as optimal will be available in every unit. However, ECCO will continue its efforts to develop and coordinate projects and initiatives that will help to guarantee optimal quality of care for all IBD patients.


Asunto(s)
Colitis Ulcerosa , Enfermedad de Crohn , Manejo de Atención al Paciente , Pautas de la Práctica en Medicina , Mejoramiento de la Calidad/organización & administración , Nivel de Atención/organización & administración , Colitis Ulcerosa/epidemiología , Colitis Ulcerosa/terapia , Enfermedad de Crohn/epidemiología , Enfermedad de Crohn/terapia , Europa (Continente)/epidemiología , Salud Holística/normas , Humanos , Comunicación Interdisciplinaria , Evaluación de Resultado en la Atención de Salud/métodos , Evaluación de Resultado en la Atención de Salud/normas , Gravedad del Paciente , Manejo de Atención al Paciente/métodos , Manejo de Atención al Paciente/normas , Pautas de la Práctica en Medicina/organización & administración , Pautas de la Práctica en Medicina/normas , Estándares de Referencia
3.
J Natl Compr Canc Netw ; 10 Suppl 1: S1-9, 2012 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-23042831

RESUMEN

The quality of patient care varies based on numerous factors, such as health care setting, geographic location, access to medications, insurance coverage, and treatment protocols. Recently, the issue of whether use of clinical pathways can reduce costs and inappropriate variability in care has been the subject of much debate. As clinical treatment guidelines and pathways are increasingly deployed in oncology practice, they have a growing impact on the quality of treatment and how it is delivered. To fulfill the current need to discuss the use of pathways and clinical treatment guidelines in oncology and to address how patient care is impacted by their use, the National Comprehensive Cancer Network convened the NCCN Oncology Policy Summit: Equity in Cancer Care-Pathways, Protocols, and Guidelines. The summit was a forum to discuss the use and implementation of pathways, including how much flexibility pathways should allow in care, pathways' impact on public and private health insurance benefit design, what data is used to select pathway regimens and protocols, and ultimately what impact pathways may have on variation in care. The use and implementation of clinical treatment guidelines in practice was also explored from a variety of perspectives.


Asunto(s)
Protocolos Clínicos , Vías Clínicas , Accesibilidad a los Servicios de Salud , Neoplasias/terapia , Guías de Práctica Clínica como Asunto , Protocolos Clínicos/normas , Vías Clínicas/legislación & jurisprudencia , Vías Clínicas/organización & administración , Industria Farmacéutica/economía , Industria Farmacéutica/legislación & jurisprudencia , Industria Farmacéutica/organización & administración , Accesibilidad a los Servicios de Salud/legislación & jurisprudencia , Accesibilidad a los Servicios de Salud/organización & administración , Humanos , Oncología Médica/legislación & jurisprudencia , Oncología Médica/métodos , Oncología Médica/organización & administración , Oncología Médica/tendencias , Neoplasias/economía , Calidad de la Atención de Salud/legislación & jurisprudencia , Calidad de la Atención de Salud/organización & administración , Sociedades Médicas/legislación & jurisprudencia , Sociedades Médicas/organización & administración , Nivel de Atención/economía , Nivel de Atención/legislación & jurisprudencia , Nivel de Atención/organización & administración , Nivel de Atención/tendencias , Estados Unidos
4.
Pediatr Diabetes ; 13 Suppl 16: 49-61, 2012 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-22931224

RESUMEN

INTRODUCTION: ISPAD guidelines recommend age appropriate diabetes education concepts for young patients and their families as well as tools for nutritional management, psychosocial assessment, and psychological advice but their implementation in Europe is presently unknown. METHODS: On the basis of a structured survey among the European SWEET members information on established tools and programs in national languages were analyzed using an extensive literature and desk search. These were differentiated according to five age-groups and five target groups (young people with diabetes, parents, and other close relations, carers in school and nursery, and healthcare professionals). RESULTS: Responses and original tools were received from 11 SWEET countries reflecting the European status in 2011. More or less structured information for parents, close relations, and carers in school or nursery are available in all 11 participating countries. However, only two countries followed the recommendations of having published a structured, curriculum lead, and evaluated program for different age-groups and carers. One of these was evaluated nationwide and funded by the respective National Health Care System after accreditation. In addition a huge variety of creative tools, e.g., booklets, leaflets, games, videos, and material for educating children of different age-groups and their parents are available - but most of them are not linked to a structured education program. CONCLUSIONS: Harmonizing and integrating these materials into quality assured structured holistic national education programs will be an important future task for the ongoing SWEET project. A comprehensive European diabetes educational toolbox is aimed to be published and continuously updated on the SWEET website.


Asunto(s)
Diabetes Mellitus/terapia , Endocrinología/normas , Educación del Paciente como Asunto , Pediatría/métodos , Pediatría/organización & administración , Acreditación/legislación & jurisprudencia , Acreditación/métodos , Adolescente , Niño , Preescolar , Diabetes Mellitus/epidemiología , Endocrinología/educación , Endocrinología/legislación & jurisprudencia , Endocrinología/organización & administración , Europa (Continente)/epidemiología , Humanos , Cooperación Internacional , Grupo de Atención al Paciente/legislación & jurisprudencia , Grupo de Atención al Paciente/organización & administración , Grupo de Atención al Paciente/normas , Educación del Paciente como Asunto/legislación & jurisprudencia , Educación del Paciente como Asunto/métodos , Educación del Paciente como Asunto/organización & administración , Pediatría/legislación & jurisprudencia , Pediatría/normas , Estándares de Referencia , Nivel de Atención/organización & administración
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