Literature DB >> 30075946

The Patient Information Sheet (PIS) and Informed Consent (IC) for case reports and case series: Proposal for a standard model for presentations in congresses and other scientific publications.

Juana Cruz Del Río1, Isabel Sastre Gervás2, Susana Romero Yuste3.   

Abstract

A standard model of the Patient Information Sheet (PIS) and Informed Consent (IC) would facilitate compliance with the guaranteed rights of the patient when their health data is used in any form for purposes other than medical assistance, like the release of case reports and case series. This model would be suitable for the presentation of case reports in a congress in any form (verbal communication, poster or presentation), for its publication in a journal that does not require the completion of its own model, or even for teaching practice. A standard model of the PIS and IC would facilitate the application of the current regulations and good clinical practices in clinical research: it would guarantee the compliance of the professionals' duty of protection of the patient's privacy against the use of their health data for purposes other than medical assistance.
Copyright © 2018. Publicado por Elsevier España, S.L.U.

Entities:  

Keywords:  Autonomía personal; Case Reports; Consentimiento informado; DeCS: Derechos del paciente; Informed Consent; Informes de casos; MeSH: Patient Rights; Personal Autonomy

Mesh:

Year:  2018        PMID: 30075946     DOI: 10.1016/j.reuma.2018.07.001

Source DB:  PubMed          Journal:  Reumatol Clin (Engl Ed)        ISSN: 2173-5743


  1 in total

1.  [Contributions on the editorial: "Importance of Research Ethics Committees in Family Medicine"].

Authors:  Isabel Sastre Gervás; Juana María Cruz Del Río; Natalia Cal Purriños; Rosendo Bugarín González
Journal:  Aten Primaria       Date:  2019-10-22       Impact factor: 1.137

  1 in total

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