The Role of Informed Consent in Clinical and Research Settings.
| Autor: | Hariri E; Department of Internal Medicine, Cleveland Clinic Foundation, 9500 Euclid Ave, G10 Clinic, Cleveland OH 44195, USA., Al Hammoud M; Gilbert and Rose-Marie Chagoury School of Medicine, Lebanese American University, P.O. Box 36, Byblos, Lebanon., Donovan E; Department of Communication Studies, The University of Texas at Austin, 2504A Whitis Ave, Austin, TX 78712, USA., Shah K; Department of Medicine, Division of Cardiology, University of Utah Hospital, 30 North 1900 East, Rm 4A100, Salt Lake City, UT 84132, USA., Kittleson MM; Department of Cardiology, Smidt Heart Institute, Cedars-Sinai, Medical Center, 8670 Wilshire Blvd, 2nd floor, Beverly Hills, CA 90211, USA. Electronic address: mitchelle.kittleson@cshs.org. |
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| Jazyk: | angličtina |
| Zdroj: | The Medical clinics of North America [Med Clin North Am] 2022 Jul; Vol. 106 (4), pp. 663-674. |
| DOI: | 10.1016/j.mcna.2022.01.008 |
| Abstrakt: | Informed consent plays an integral role in governing the patient-physician relationship with origins traced back to ancient Greek philosophy. The main pillars of informed consent are autonomy, integrity, respect, and care. In the last century, these notions have been codified into legislation to promote healthy patient-physician relationships. Understanding the process of informed consent is critical for patients, researchers, and medical practitioners. In this article, the authors provide a brief historical narrative of informed consent, elaborate on the process of obtaining an ethically and legally valid informed consent, and present some of the future challenges in the field. (Copyright © 2022 Elsevier Inc. All rights reserved.) |
| Databáze: | MEDLINE |
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