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2.
PLoS One ; 16(5): e0251192, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-33979383

RESUMEN

CONTEXT: The use of ethnic identifiers in health systems is recommended in several European countries as a means to identify and address heath inequities. There are barriers to implementation that have not been researched. OBJECTIVE: This study examines whether and how ethnicity data can be collected in Irish general practices in a meaningful and acceptable way. METHODS: Qualitative case study data generation was informed by Normalization Process Theory (NPT) constructs about 'sense' making and 'engagement'. It consisted of individual interviews and focus group discussions based on visual participatory techniques. There were 70 informants, including 62 general practitioner (GP) users of diverse ethnic backgrounds recruited through community organisations and eight GPs identified through an inter-agency steering group. Data were analysed according to principles of thematic analysis using NPT. RESULTS: The link between ethnicity and health was often considered relevant because GP users grasped connections with genetic (skin colour, lactose intolerance), geographic (prevalence of disease, early years exposure), behavioural (culture/food) and social determinant (housing) factors. The link was less clear with religion. There was some scepticism and questions about how the collection of data would benefit GP consultations and concerns regarding confidentiality and the actual uses of these data (e.g. risk of discrimination, social control). For GPs, the main theme discussed was relevance: what added value would it bring to their consultations and was it was their role to collect these data? Their biggest concern was about data protection issues in light of the European Union (EU) General Data Protection Regulation (GDPR). The difficulty in explaining a complex concept such as 'ethnicity' in the limited time available in consultations was also worrying. CONCLUSIONS: Implementation of an ethnicity identifier in Irish general practices will require a strong rationale that makes sense to GP users, and specific measures to ensure that its benefits outweigh any potential harm. This is in line with both our participants' views and the EU GDPR.


Asunto(s)
Recolección de Datos/tendencias , Etnicidad/estadística & datos numéricos , Actitud del Personal de Salud/etnología , Competencia Clínica , Recolección de Datos/ética , Recolección de Datos/métodos , Etnicidad/clasificación , Medicina Familiar y Comunitaria/ética , Grupos Focales/métodos , Medicina General/ética , Médicos Generales/educación , Médicos Generales/psicología , Humanos , Irlanda , Percepción/ética , Investigación Cualitativa , Derivación y Consulta
4.
Rev. Hosp. Ital. B. Aires (2004) ; 40(4): 208-218, dic. 2020. ilus
Artículo en Español | LILACS | ID: biblio-1145506

RESUMEN

La práctica de la medicina se encuentra atravesando una crisis, en la cual muchas de las prácticas médicas que se realizan son de poco valor y con frecuencia generan daño a las personas. Se presenta una revisión bibliográfica no sistematizada en la que se analizan en conjunto los diversos factores que contribuyen al desarrollo de excesos médicos y a los daños que estos generan. Consideramos que su conocimiento puede contribuir a mejorar la calidad de los cuidados que se ofrecen a nuestros pacientes. (AU)


The practice of medicine is going through a crisis, in which many of the medical practices that are carried out are of little value and often cause harm to people. An unsystematic bibliographic review is presented in which various factors that contribute to the development of medical excesses are analyzed. Their knowledge can contribute to improving the quality of medical care offered to our patients. (AU)


Asunto(s)
Humanos , Medicalización/organización & administración , Daño del Paciente , Calidad de la Atención de Salud , Medicina Basada en la Evidencia/ética , Medicina General/ética , Medicalización/tendencias , Medicalización/ética , Uso Excesivo de los Servicios de Salud , Práctica Integral de Atención/ética , Prevención Cuaternaria/tendencias , Mala Praxis
8.
Med Sci (Paris) ; 35(8-9): 674-681, 2019.
Artículo en Francés | MEDLINE | ID: mdl-31532380

RESUMEN

A placebo drug is defined as a treatment without any specific pharmacological efficacy, that works when the patient thinks to receive an active treatment, through a psychological and physiological mechanism. This study aimed to evaluate the use of placebo in French hospitals, in Polyvalent Medicine units. A questionnaire comprising 15 items was sent to 372 units. The analysis of 153 responses was conducted from dynamic crosstabs in Excel and using the R software available online. The survey confirmed that the use of placebos in hospital is frequent, with nearly 2/3 of professionals answering the questionnaire declared to use it. The oral capsule is the most commonly used form. Placebo is mainly administered at night, in case of pain, insomnia or anxiety, to so-called "difficult" patients. Placebo is not always given after medical prescription. In most cases, patients are not informed that they receive a placebo. The majority of professionals believed in the placebo effect but considered to be insufficiently informed and trained in the use of placebo in current practice. Although the placebo effect is now demonstrated, ethical and legal considerations recommend placebo treatment only on medical prescription, with the prior information of the patient. The placebo could be used as complementary therapy to conventional treatment in the cases of this therapeutic effectiveness has been demonstrated. Professionals should be trained in the use of placebo in order to avoid nocebo effect and potentiate beneficial effects of placebo.


TITLE: Le placebo à l'hôpital - Regard sur son utilisation dans les services de médecine polyvalente. ABSTRACT: Un placebo est défini comme un traitement sans efficacité pharmacologique propre qui agit, lorsque le patient pense recevoir un traitement actif, par des mécanismes psychologiques et physiologiques. Notre étude avait pour but d'évaluer l'utilisation du placebo dans les unités de médecine polyvalente des hôpitaux français. Pour cela, un questionnaire comprenant 15 items a été transmis à plusieurs unités. L'analyse des réponses reçues confirme que l'utilisation de placebos à l'hôpital est fréquente, près des deux tiers des professionnels ayant répondu déclarent en faire usage. L'administration du placebo en gélule par voie orale est la forme la plus couramment utilisée. À l'hôpital, il est administré principalement la nuit, le plus souvent sans prescription médicale, en cas de douleur, d'insomnie ou d'anxiété, à des patients dits « difficiles ¼ (solliciteurs d'attention et de soin). Dans la plupart des cas, les patients ne sont pas informés qu'il s'agit d'un placebo. La majorité des professionnels « croit ¼ en l'effet placebo, mais se considèrent cependant insuffisamment informés et formés à son utilisation. Fréquemment utilisé à l'hôpital, son efficacité thérapeutique étant largement admise, des considérations éthiques et juridiques imposent de recommander que sa nature soit précisée au patient lors de sa prescription (au même titre que les autres préparations hospitalières). On parlera alors de « placebo ouvert ¼, c'est-à-dire que des explications sur les effets et les mécanismes d'action du placebo seront données au patient. Des études récentes montrent que dire au patient qu'il reçoit un placebo ouvert n'affecte en rien son effet.


Asunto(s)
Hospitales , Placebos/uso terapéutico , Adulto , Revelación/ética , Revelación/estadística & datos numéricos , Femenino , Francia/epidemiología , Medicina General/ética , Medicina General/métodos , Medicina General/estadística & datos numéricos , Unidades Hospitalarias/ética , Unidades Hospitalarias/normas , Unidades Hospitalarias/estadística & datos numéricos , Hospitales/ética , Hospitales/estadística & datos numéricos , Humanos , Masculino , Principios Morales , Relaciones Médico-Paciente , Efecto Placebo
18.
Anthropol Med ; 26(2): 228-243, 2019 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-29210286

RESUMEN

This paper explores the moral implications of treatment of young people with functional somatic symptoms. Based on an ethnographic field study at a Danish pain clinic for youngsters (age 8 to 18), the paper seeks to unearth the cultural, moral values that clinical practice steers by and upholds, and the implications this has for the assessment and management of ill body-selves. Through an exposition of the general practice of the clinic and an investigation of two specific cases of youngsters, it is found that the assessment of symptoms and selves and the goals of treatment are informed by cultural ideals of 'the good self' and 'the good life' in which agency and work ethic - both pertaining to the notion of individual responsibility - figure as prevalent virtues. The study underpins the findings of other researchers who have found that ideals of individual autonomy and responsibility for own life and health permeate the Western health care system and the discourses of ill individuals. The contribution of this article is to portray in ethnographic detail how such a cultural ethics manifests in practice and what implications this have for the treatment of young people with functional symptoms at a specific location and in specific cases. The two cases illustrate that the underlying norms and values can give rise to very different moral assessments of symptoms and selves within the same diagnostic category.


Asunto(s)
Medicina General , Síntomas sin Explicación Médica , Principios Morales , Clínicas de Dolor , Adolescente , Antropología Médica , Dinamarca , Femenino , Medicina General/ética , Medicina General/normas , Humanos , Clínicas de Dolor/ética , Clínicas de Dolor/normas
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