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Статті в журналах з теми "Medical consent"

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Автор: Grafiati

Опубліковано: 10 грудня 2022

Оновлено: 29 січня 2023

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1

Eonas, Anthony, John D. McCoy, and Silviya H. M. Eaton. "Medical Informed Consent." Journal of Hospital Marketing & Public Relations 16, no. 1-2 (August 30, 2006): 69–88. http://dx.doi.org/10.1300/j375v16n01_06.

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2

Hadden, Kristie B., Latrina Y. Prince, Tina D. Moore, Laura P. James, Jennifer R. Holland, and Christopher R. Trudeau. "Improving readability of informed consents for research at an academic medical institution." Journal of Clinical and Translational Science 1, no. 6 (December 2017): 361–65. http://dx.doi.org/10.1017/cts.2017.312.

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IntroductionThe final rule for the protection of human subjects requires that informed consent be “in language understandable to the subject” and mandates that “the informed consent must be organized in such a way that facilitates comprehension.” This study assessed the readability of Institutional Review Board-approved informed consent forms at our institution, implemented an intervention to improve the readability of consent forms, and measured the first year impact of the intervention.MethodsReadability assessment was conducted on a sample of 217 Institutional Review Board-approved informed consents from 2013 to 2015. A plain language informed consent template was developed and implemented and readability was assessed again after 1 year.ResultsThe mean readability of the baseline sample was 10th grade. The mean readability of the post-intervention sample (n=82) was seventh grade.ConclusionsProviding investigators with a plain language informed consent template and training can promote improved readability of informed consents for research.

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3

Shreekrishna, H. K., and Aruna B. Rao. "Consent in medical practice." International Journal of Preclinical and Clinical Research 2, no. 1 (March 25, 2021): 13–17. http://dx.doi.org/10.51131/ijpccr/v2i1.4.

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Consent is an expression of autonomy and represents the right of a patient to make a decision in a medical matter concerning him. Consent is not just a procedural formality but also a legal requirement. The process of informed consent occurs when communication between a patient and physician results in the patient’s authorization or agreement to undergo a specific medical intervention. In India, the number of suits against doctors is increasing because of failure to take informed consent or inadequate consent from patients for various procedures. Any examination of a patient by the doctor without his consent amounts to assault (351IPC). Ignorance of laws is not a defense in negligence cases, so every practicing doctor should be aware of their responsibilities about consent in medical practice. Consent is not an option but a necessity in medical practice. Keywords: Consent; informed consent; autonomy

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4

Stauch, Marc. "Consent in Medical Law." British Journal of Nursing 7, no. 2 (January 22, 1998): 84. http://dx.doi.org/10.12968/bjon.1998.7.2.84.

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5

Heneghan, Christopher. "Consent to medical treatment." Lancet 337, no. 8738 (February 1991): 421. http://dx.doi.org/10.1016/0140-6736(91)91185-w.

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6

Fernando, LMB. "Consent in medical practice." Galle Medical Journal 12, no. 1 (September 25, 2009): 28. http://dx.doi.org/10.4038/gmj.v12i1.1082.

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7

Rhodes, Ann Marie. "Consent For Medical Treatment." MCN, The American Journal of Maternal/Child Nursing 12, no. 2 (March 1987): 133. http://dx.doi.org/10.1097/00005721-198703000-00012.

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8

Barnes, Stephen. "Consent to medical treatment." AustralAsian Journal of Cardiac and Thoracic Surgery 1, no. 1 (September 1991): 27–28. http://dx.doi.org/10.1016/1037-2091(91)90012-2.

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9

Yu, Bo, Duminda Wijesekera, and Paulo Costa. "Informed Consent in Electronic Medical Record Systems." International Journal of Reliable and Quality E-Healthcare 4, no. 1 (January 2015): 25–44. http://dx.doi.org/10.4018/ijrqeh.2015010103.

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Informed consents, either for treatment or use/disclosure, that protect the privacy of patient information subject to law that in certain circumstances may override patient wishes, are mandatory practice in healthcare. Although the healthcare industry has widely adopted Electronic Medical Record (EMR) systems, consents are still obtained and stored primarily on paper or scanned electronic documents. Integrating a consent management system into an EMR system involves various implementation challenges. The authors show how consents can be electronically obtained and enforced using a system that combines medical workflows and ontologically motivated rule enforcement. Finally, the authors describe an implementation that uses open-source software based addition of these components to an open-source EMR system, so that existing systems needn't be scrapped or otherwise rendered obsolete.

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10

Chuchalin, Alexandr G. "Consent. Modern interpretation: "Voluntary Informed Consent"." Terapevticheskii arkhiv 93, no. 5 (May 15, 2021): 640–44. http://dx.doi.org/10.26442/00403660.2021.05.200797.

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The article is devoted to voluntary informed consent. It considers the historical issues of the formation of this concept in modern health care and medical science. The article highlights a historical role of the Nuremberg Code which was taken as the basis for the Universal Declaration of Human Rights, the World Medical Association (WMA) Code of Ethics, the Declaration on Bioethics and Human Rights, i.e. documents that defined the world order after the end of World War II.

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11

Srivastava, CP. "Consent." Journal of Universal College of Medical Sciences 1, no. 4 (January 12, 2014): 69–70. http://dx.doi.org/10.3126/jucms.v1i4.9581.

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12

Gillon, R. "Medical treatment, medical research and informed consent." Journal of Medical Ethics 15, no. 1 (March 1, 1989): 3–11. http://dx.doi.org/10.1136/jme.15.1.3.

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13

Dickens, Bernard M. "Reproduction Law and Medical Consent." University of Toronto Law Journal 35, no. 3 (1985): 255. http://dx.doi.org/10.2307/825675.

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14

Koo, Young Mo. "Informed Consent and Medical Confidentiality." Journal of the Korean Medical Association 44, no. 10 (2001): 1052. http://dx.doi.org/10.5124/jkma.2001.44.10.1052.

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15

DeRenzo, E. G. "Informed consent in medical research." British Journal of Cancer 85, no. 11 (November 27, 2001): 1811–12. http://dx.doi.org/10.1054/bjoc.2001.2135.

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16

Evans, John Grimley, and Peter Beck. "Informed consent in medical research." Clinical Medicine 2, no. 3 (May 1, 2002): 267–72. http://dx.doi.org/10.7861/clinmedicine.2-3-267.

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17

Almassi, Ben. "Medical Ghostwriting and Informed Consent." Bioethics 28, no. 9 (February 28, 2013): 491–99. http://dx.doi.org/10.1111/bioe.12017.

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18

Schmidt, K. "Informed Consent in Medical Research." Focus on Alternative and Complementary Therapies 6, no. 4 (June 14, 2010): 301. http://dx.doi.org/10.1111/j.2042-7166.2001.tb03168.x.

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19

Manthous, Constantine A., Angela DeGirolamo, Christopher Haddad, and Yaw Amoateng-Adjepong. "Informed Consent for Medical Procedures *." Chest 124, no. 5 (November 2003): 1978–84. http://dx.doi.org/10.1378/chest.124.5.1978.

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20

Darr, Kurt. "Nexus: Medical Education and Consent." Hospital Topics 66, no. 6 (November 1988): 8–9. http://dx.doi.org/10.1080/00185868.1988.10543629.

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21

Vansweevelt, T. "Medical Experimentation and Informed Consent." Acta Clinica Belgica 50, no. 1 (January 1995): 1–3. http://dx.doi.org/10.1080/17843286.1995.11718412.

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22

Ajlouni, KamelM. "History of informed medical consent." Lancet 346, no. 8980 (October 1995): 980. http://dx.doi.org/10.1016/s0140-6736(95)91608-3.

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23

Rothman, DavidJ. "History of informed medical consent." Lancet 346, no. 8990 (December 1995): 1633. http://dx.doi.org/10.1016/s0140-6736(95)91970-8.

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24

Martinez, Jorge A., John M. Lyons, and J. Patrick O'Leary. "Medical Malpractice Matters: Informed Consent." Journal of Surgical Education 66, no. 3 (May 2009): 174–75. http://dx.doi.org/10.1016/j.jsurg.2008.12.006.

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25

Vollmann, Jochen, Rolf Winau, and J. H. Baron. "History of informed medical consent." Lancet 347, no. 8998 (February 1996): 410. http://dx.doi.org/10.1016/s0140-6736(96)90597-8.

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26

Wu, William C., and Robert A. Pearlman. "Consent in medical decision making." Journal of General Internal Medicine 3, no. 1 (January 1988): 9–14. http://dx.doi.org/10.1007/bf02595749.

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27

Ilfeld, Brian M. "Informed Consent for Medical Research." Regional Anesthesia and Pain Medicine 31, no. 4 (July 2006): 353–57. http://dx.doi.org/10.1097/00115550-200607000-00010.

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28

DICKENS, BERNARD M. "MEDICAL CONSENT LEGISLATION IN ONTARIO." Medical Law Review 2, no. 3 (1994): 283–301. http://dx.doi.org/10.1093/medlaw/2.3.283.

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29

Bratt, D. E., P. Soutter, M. Bland, P. Little, I. Williamson, D. O. Chanter, S. Stewart-Brown, et al. "Informed consent in medical research." BMJ 314, no. 7092 (May 17, 1997): 1477. http://dx.doi.org/10.1136/bmj.314.7092.1477.

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30

Harbour, Anthony, Sue Bailey, and William Bingley. "Children's consent to medical treatment." Psychiatric Bulletin 24, no. 5 (May 2000): 196–97. http://dx.doi.org/10.1192/pb.24.5.196-a.

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31

Borchgrevink, Christian F. "Informed Consent and Medical Research." Family Practice 4, no. 1 (1987): 78–80. http://dx.doi.org/10.1093/fampra/4.1.78.

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32

Finkelstein, Daniel. "Informed Consent and Medical Ethics." Archives of Ophthalmology 111, no. 3 (March 1, 1993): 324. http://dx.doi.org/10.1001/archopht.1993.01090030042034.

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33

Bolsin, Stephen, and Kym Saunders. "Informed consent in medical practice." Trends in Urology & Men's Health 3, no. 5 (September 2012): 34–36. http://dx.doi.org/10.1002/tre.288.

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34

Katvan, Eyal, and Boaz Shnoor. "Informed consent to legal treatment – lessons from medical informed consent." International Journal of the Legal Profession 24, no. 2 (February 8, 2017): 125–44. http://dx.doi.org/10.1080/09695958.2017.1280041.

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35

Memon, Khalida Naz, Champa Sushel, Shazia Shaikh, and Fahad Ahmed Memon. "INFORMED CONSENT." Professional Medical Journal 22, no. 10 (October 10, 2015): 1262–67. http://dx.doi.org/10.29309/tpmj/2015.22.10.975.

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Introduction: Informed consent is the back bone of patients’ autonomy. Theadvancement in medical technology has further increased its importance. In the developingcountries including Pakistan, general physicians play a vital role in providing health careto the patients but unfortunately majority of them are unaware about the ethical aspects oftheir medical practice. Methodology: Objectives: 1. To determine the level of awarenessabout informed consent among general practitioners. 2. To assess the association betweenvarious socio-demographic factors to the awareness about informed consent. Study Design:Community based cross sectional study. Settings: General medical practitioners of districtHyderabad were the study population. Period Of Study: Two months. Material & Methods:One hundred & forty subjects were selected for the study through purposive non-probabilitysampling. A pretested self-administered questionnaire was the tool for the data collection. Thedata was analyzed by using SPSS version 16.The variables of interest were gender of generalpractitioners, their age, level of qualifications, residence & occasions when informed consentwas taken. The association between various socio-demographic variables was determined byapplying Chi-square test at ≤0.05 level of significance. Results: One hundred & forty generalmedical practitioners of varying ages from 32-60 years participated in the study. The meanage of the general physician was 39 ± 1.8 years. The awareness about informed consent wasfound among 128(91.4%) subjects but unfortunately only 45.7%of them actually practiced it.The results regarding awareness as well as practice of informed consent among males andfemales were however not significant (p=0.520). The young general practitioners i.e age 31-40years were less practicing informed consent as compared to older general practitioners i.e.age 51-60 years and onwards (p= 0.04).The physicians practicing in urban areas were morecognizant about informed consent (p=0.05).Informed consent from patients was obtainedbefore giving local anesthesia (80%), blood transfusion (24.3%)&before examination of femalepatients (46.4%). Conclusions: Informed consent taking is not a routine process adopted bygeneral medical practitioners so there is a strong need for general practitioners to change theirattitude and acknowledge the patient’s autonomy by taking informed consent, which is thebasis of modern medical ethics.

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36

Manion, F., K. Hsieh, M. Harris, and S. H. Fenton. "Informed Consent." Applied Clinical Informatics 06, no. 03 (2015): 466–77. http://dx.doi.org/10.4338/aci-2014-09-soa-0081.

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Summary Background: Despite efforts to provide standard definitions of terms such as “medical record”, “computer-based patient record”, “electronic medical record” and “electronic health record”, the terms are still used interchangeably. Initiatives like data and information governance, research biorepositories, and learning health systems require availability and reuse of data, as well as common understandings of the scope for specific purposes. Lacking widely shared definitions, utilization of the afore-mentioned terms in research informed consent documents calls to question whether all participants in the research process — patients, information technology and regulatory staff, and the investigative team — fully understand what data and information they are asking to obtain and agreeing to share. Objectives: This descriptive study explored the terminology used in research informed consent documents when describing patient data and information, asking the question “Does the use of the term “medical record” in the context of a research informed consent document accurately represent the scope of the data involved?” Methods: Informed consent document templates found on 17 Institutional Review Board (IRB) websites with Clinical and Translational Science Awards (CTSA) were searched for terms that appeared to be describing the data resources to be accessed. The National Library of Medicine’s (NLM) Terminology Services was searched for definitions provided by key standards groups that deposit terminologies with the NLM. Discussion: The results suggest research consent documents are using outdated terms to describe patient information, health care terminology systems need to consider the context of research for use cases, and that there is significant work to be done to assure the HIPAA Omnibus Rule is applied to contemporary activities such as biorepositories and learning health systems. Conclusions: “Medical record”, a term used extensively in research informed consent documents, is ambiguous and does not serve us well in the context of contemporary information management and governance. Citation: Fenton SH, Manion F, Hsieh K, Harris M. Informed Consent: Does Anyone Really Understand What Is Contained In The Medical Record? Appl Clin Inform 2015; 6: 466–477http://dx.doi.org/10.4338/ACI-2014-09-SOA-0081

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37

Chuchalin, A. G. "Voluntary informed consent." PULMONOLOGIYA 31, no. 1 (February 19, 2021): 116–20. http://dx.doi.org/10.18093/0869-0189-2021-31-1-116-120.

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Анотація:

This article discusses voluntary informed consent (VIC), a prerequisite for any medical intervention. The article touches upon the history of this issue in modern health care and medical science. The role of the Nuremberg Code is emphasized, which is the basis for the Universal Declaration of Human Rights, the Code of Medical Ethics of the World Medical Association, and the Declaration on Bioethics and Human Rights. These documents helped define the world order after the end of World War II. The first part of the article reflects the history of the concept of VIC, while the second outlines the modern ethical views on this issue.

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38

Iacono, Maureen. "Informed consent." Journal of PeriAnesthesia Nursing 15, no. 3 (June 2000): 180–81. http://dx.doi.org/10.1053/jpan.2000.7510.

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39

Sappington, G. Mark. "Substitute consent: Reconciling negative treatment and consent to routine medical treatment." Journal of Legal Medicine 7, no. 3 (September 1986): 341–55. http://dx.doi.org/10.1080/01947648609513475.

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40

Segal, Jonathan P., and Richard Hansen. "Medical images, social media and consent." Nature Reviews Gastroenterology & Hepatology 18, no. 8 (April 23, 2021): 517–18. http://dx.doi.org/10.1038/s41575-021-00453-1.

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41

Khanagwal, Vijay Pal, Kunal Khanna, Tarun Dagar, and Sandeep Kumar Giri. "Rules of consent in medical practice." Journal of Indian Academy of Forensic Medicine 44, suppl (2022): 30–34. http://dx.doi.org/10.5958/0974-0848.2022.00008.2.

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42

Mullick, Parul, Ajay Kumar, Smita Prakash, and Aseem Bharadwaj. "Consent and the Indian medical practitioner." Indian Journal of Anaesthesia 59, no. 11 (2015): 695. http://dx.doi.org/10.4103/0019-5049.169989.

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43

Miller, Tim. "Informed Consent: A Medical Board Analysis." Journal of Medical Regulation 96, no. 3 (September 1, 2010): 16–22. http://dx.doi.org/10.30770/2572-1852-96.3.16.

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44

Leung, Wai-Ching, and Liam J. Donaldson. "Consent to Medical Treatment and Children." AVMA Medical & Legal Journal 3, no. 4 (July 1997): 114–18. http://dx.doi.org/10.1177/135626229700300403.

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45

Arora, Vijay. "ROLE OF CONSENT IN MEDICAL PRACTICE." Journal of Evolution of medical and Dental Sciences 2, no. 9 (March 4, 2013): 1225–29. http://dx.doi.org/10.14260/jemds/386.

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46

Korgaonkar, Gill, and Diana Tribe. "Children and consent to medical treatment." British Journal of Nursing 2, no. 7 (April 8, 1993): 383–84. http://dx.doi.org/10.12968/bjon.1993.2.7.383.

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47

Williams, Kevin. "Pre-Operative Consent and Medical Negligence." Anglo-American Law Review 14, no. 2 (April 1985): 169–83. http://dx.doi.org/10.1177/147377958501400205.

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48

Riley, Geoffrey J., and Ralph L. Simmonds. "Informed consent in modern medical practice." Medical Journal of Australia 157, no. 5 (September 1992): 336–38. http://dx.doi.org/10.5694/j.1326-5377.1992.tb137195.x.

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49

Robinson, Jean. "Consent, medical students and anaesthetized women." British Journal of Midwifery 13, no. 5 (May 2005): 273. http://dx.doi.org/10.12968/bjom.2005.13.5.18086.

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50

Harder, Sirko. "Medical Non-Disclosure and Hypothetical Consent." King's Law Journal 20, no. 3 (October 2009): 435–55. http://dx.doi.org/10.1080/09615768.2009.11423683.

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