Base de datos - (CIANE)

Presentación de esta base de datos documental (Sitio web de CIANE)
Actualmente 3111 registros
➡ Canal de YouTube (tutorial)

https://ciane.net/id=474

Creado el : 13 Feb 2004
Alterado em : 01 Nov 2018

➡ Editar este registro
¡Sólo siga este enlace si tiene una contraseña de editor!

Ficha bibliográfica (sin autores) :

Editor’s choice. Abusing patients by denying them choice. The British Medical Journal, 328 (14 February)

Autores :

Smith R.

Año de publicación :

2004

URL(s) :

http://bmj.bmjjournals.com/cgi/content/full/328/74…
https://doi.org/10.1136/bmj.328.7436.0-f

Résumé (français)  :

Abstract (English)  :

A useful tip for smart are medical students. If asked: “What is the treatment for x?”Don’t answer: “y.” Instead answer: “Whatever the patient chooses together with me after being fully informed of the pluses and minuses of all options.” Giving patients choice incomplex circumstances emerges as a theme in this issue—with the sombre overtone that not to give patients choice is to abuse them.
It first hit me that denying patients choice is a form of abuse when about six years ago I read a paper on patient choice in screening for colorectal cancer. One hundred Californian patients were given full information on five options: nothing, faecal occult bloodtesting, barium enema examination, flexible sigmoidoscopy, or colonoscopy. Patients were told about the nature of the test, the preparation required, the need for sedation, the time required, how often the test would be repeated, the likely results with both positive and negative outcomes in detail, and the cost. The result was that patients chose very different options.

Steve Woolf, a family physician and North American editor of the BMJ,wrote: “Suppose these same 100 patients had not received this information and were instead cared for by a physician who routinely performs flexible sigmoidoscopy because he considers it the best test. According to these data, fully 87% of the patients would undergo a procedure other than the one they would prefer if properly informed” (J Fam Pract 1997;45: 205-8). Nine out of 10 patients have been abused.
Mark Sculpher and others describe how they used something called a discrete choice experiment to help men with non-metastatic prostate cancer to choose between different options for treatment (p 382). The main conclusions are that men are willing to engage in this complex process and will trade life expectancy in order to avoid side effects. Mandy Ryan discusses how the technique can be used in other circumstances (p 358).

Some 15-20 years ago an editorial in the BMJ suggested that every menopausal woman should have hormone replacement therapy. That now looks like bad advice not only because therapy increases the risk of breast cancer, heart disease, and thrombembolism but also because only women themselves can trade off how they value the benefits and risks. A group from Leicester present a detailed decision analysis of the harms and benefits of therapy in the light of the latest evidence and conclude that two important variables are perceived symptoms and baseline risk of breast cancer (p 371). Klim McPherson weighs up hormone replacement therapy and also draws lessons from the whole sorry story of the mass drugging of women for largely non-existent benefits (p 357).
The main arguments against fully informing patients are that “It’s too difficult, costly, and time consuming.” But they are neither evidence based nor politically sustainable.

Sumário (português)  :

Resumen (español)  :

Texto completo (public) :

Comentarios :

Editorial de 2004 dans BMJ. Concerne la santé en général, sur l’exemple du dépistage du cancer colorectal. L’auteur affirme que de ne pas permettre au patient de choisir est une forme de maltraitance (“denying patient choice is a form of abuse“). Le contre argument comme quoi l’information des patients est “trop difficile, coûteuse et prend du temps“ n’est ni fondé sur des preuves, ni recevable politiquement

Argument (français) :

Les principaux arguments contre l’information complète des patients sont les suivants: «C’est trop difficile, coûteux et prend beaucoup de temps». Mais ils ne sont ni fondés sur des preuves ni politiquement viables.

Argument (English):

The main arguments against fully informing patients are that “It’s too difficult, costly, and time consuming.” But they are neither evidence based nor politically sustainable.

Argumento (português):

Os principais argumentos contra a informação completa dos pacientes são: “É muito difícil, dispendioso e demorado“. Mas eles não são baseados em evidências nem politicamente sustentáveis.

Argumento (español):

Palabras claves :

➡ formación en partería ; medicina basada en la evidencia ; violencia ginecológica y obstétrica ; partera ; ética profesional ; consentimiento informado

Autor de este registro :

Cécile Loup — 13 Feb 2004
➡ última modificación : Bernard Bel — 01 Nov 2018