Gotowe bibliografie tematyczne / Informed consent

Gotowa bibliografia na temat „Informed consent”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 1 sierpnia 2024

Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych

Wybierz rodzaj źródła:

Spis treści

Zobacz listy aktualnych artykułów, książek, rozpraw, streszczeń i innych źródeł naukowych na temat „Informed consent”.

Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.

Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.

Artykuły w czasopismach na temat "Informed consent"

1

Lie, Rico, i Loes Witteveen. "Visual informed consent: informed consent without forms". International Journal of Social Research Methodology 20, nr 1 (11.12.2015): 63–75. http://dx.doi.org/10.1080/13645579.2015.1116835.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
2

YU, Ho-Jong. "Doctors Duty of Informed Consent and Patient Informed Consent Form". Korean Journal of Medical Ethics 5, nr 1 (czerwiec 2002): 27–41. http://dx.doi.org/10.35301/ksme.2002.5.1.27.

Pełny tekst źródła
Streszczenie:
1. When a patient goes to a hospital, he is expected to give consent to the treatment his/her doctor may provide. The initial consent, however, does not include all the consents to the following treatment a patient is going to receive. For further treatments, especially for concrete treatments, the doctor must seek for additional consents. 2. A doctor must offer sufficient informations to his patient when getting a consent. While doing this a pre-written patient informed consent form can be convenient as well as effective. The doctor can explain systematically without leaving out any important point, and the patient can understand much better what the doctor is explaining by reading the paper repeatedly. Furthermore this same form can be useful later on when any legitimate question arise. 3. I reviewed many patient informed consent forms previously made by many academies of medical science in specific medical fields. I find the papers lacking in sufficient informations especially on alternative treatment measures. Even if there are, they are described negatively, which make the forms suspicious of giving biased informations. Above all the terms used are too difficult for the patients to understand. I, therefore, propose a patient informed consent form, which I believe might be ideal.
Style APA, Harvard, Vancouver, ISO itp.
3

Moody, Harry R. "From Informed Consent to Negotiated Consent1". Gerontologist 28, Suppl (1.06.1988): 64–70. http://dx.doi.org/10.1093/geront/28.suppl.64.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
4

Liew, J., i M. Winston. "Informed consent". British Dental Journal 230, nr 2 (styczeń 2021): 59. http://dx.doi.org/10.1038/s41415-021-2614-y.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
5

Myers, William R. "Informed Consent". Oral and Maxillofacial Surgery Clinics of North America 5, nr 1 (luty 1993): 179–84. http://dx.doi.org/10.1016/s1042-3699(20)30678-6.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

Tait, Ann. "Informed consent". Nursing Standard 3, nr 36 (3.06.1989): 51. http://dx.doi.org/10.7748/ns.3.36.51.s74.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
7

&NA;. "Informed consent". Inpharma Weekly &NA;, nr 1201 (sierpień 1999): 20. http://dx.doi.org/10.2165/00128413-199912010-00043.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

Wilson, Peter, i P. Gerber. "Informed consent". Medical Journal of Australia 142, nr 13 (czerwiec 1985): 704–5. http://dx.doi.org/10.5694/j.1326-5377.1985.tb113604.x.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

Drew, J. H. "Informed consent". Medical Journal of Australia 143, nr 3 (sierpień 1985): 129. http://dx.doi.org/10.5694/j.1326-5377.1985.tb122855.x.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Cotton, Peter B. "Informed consent". Gastrointestinal Endoscopy 96, nr 1 (lipiec 2022): 163. http://dx.doi.org/10.1016/j.gie.2022.03.018.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
Więcej źródeł

Rozprawy doktorskie na temat "Informed consent"

1

Baker, Eileen F. "Autonomy and Informed Consent". Bowling Green State University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1491391673593916.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
2

Gibb, Winna. "Informed consent : a liberal perspective". Thesis, Queensland University of Technology, 1998.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

Aveyard, H. "Does informed consent theory inform nursing practice? : an exploration of the application of informed consent prior to nursing care procedures". Thesis, King's College London (University of London), 2000. https://kclpure.kcl.ac.uk/portal/en/theses/does-informed-consent-theory-inform-nursing-practice--an-exploration-of-the-application-of-informed-consent-prior-to-nursing-care-procedures(39554aa7-cfb4-41e6-81bd-a522ccf1d851).html.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
4

Alderson, Dorothea Priscilla. "Informed consent : problems of parental consent to paediatric cardiac surgery". Thesis, Goldsmiths College (University of London), 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.702485.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
5

Scott, John. "Informed consent and respect for autonomy". Thesis, University of Sunderland, 2007. http://sure.sunderland.ac.uk/3561/.

Pełny tekst źródła
Streszczenie:
In this thesis I examine the medical concept of informed consent and the philosophical concept of autonomy in conjunction with the relationship between them. This examination is complicated because autonomy can refer to decisions or persons. Further autonomy may have instrumental or intrinsic value. These differences mean autonomy may be respected in different ways. This examination is further complicated because whilst a vast wealth of medical literature exists on informed consent and mentions autonomy, very little of this literature does more than mention autonomy. As a result of my examination I argue for the following. Firstly I argue the form of autonomy underlying informed consent should be personal autonomy and to respect autonomy means accepting autonomous decisions. Secondly I show in certain contexts a surrogate decision maker cannot make a decision on behalf of an incompetent patient that would be generally agreed to be in his best interests. I will argue in such contexts a patient’s decision should always be accepted as the concept of competence becomes detached from the concept of informed consent. Thirdly I show a patient may make an autonomous decision based only on understanding the purpose of the procedure he is consenting to. I will argue it follows a patient should not be required to understand details of the nature of the procedure he is consenting to for his consent to be accepted. Fourthly I argue an autonomous decision must be one an agent identifies with and has some persistence. I will show these conditions are satisfied by an autonomous agent’s absence of restlessness to change his decision Lastly I argue informed consent decisions should be linked to a patient’s ability to understand the risk involved in his decision and not directly linked to the degree of risk involved in his decision.
Style APA, Harvard, Vancouver, ISO itp.
6

Bullock, Emma Cecelia. "Informed consent and justified hard paternalism". Thesis, University of Birmingham, 2012. http://etheses.bham.ac.uk//id/eprint/3400/.

Pełny tekst źródła
Streszczenie:
According to the doctrine of informed consent medical procedures are morally permissible when a patient has consented to the treatment. Problematically it is possible for a patient to consent to or refuse treatment which consequently leads to a decline in her best interests. Standardly, such conflicts are resolved by prioritising the doctrine of informed consent above the requirement that the medical practitioner acts in accordance with the duty of care. This means that patient free choice is respected regardless as to whether her choice leads to a decline in her best interests, since to disrespect patient choice would be an instance of ‘unwarranted’ paternalism. This thesis defends the claim that in cases where patient consent comes into conflict with her best interests, paternalistic interference is in fact justified. The ambition of the thesis is thus twofold: in the first place I argue that the doctrine of informed consent cannot be used as an ethical guarantor for medical decision making. Secondly I will conclude that hard paternalism is justified in medical practice, thereby calling for a reversal of the prioritisation of informed consent procedures over the medical practitioner’s duty of care.
Style APA, Harvard, Vancouver, ISO itp.
7

Walker, Nancy L. Hamilton. "The relationship between patient perceptions of informed consent and recall of information received during the informed consent process". Virtual Press, 1993. http://liblink.bsu.edu/uhtbin/catkey/865959.

Pełny tekst źródła
Streszczenie:
Informed consent is a requirement by law. Informed consent is a two part process: giving the patient sufficient information so that an educated choice can be made and obtaining assent in writing (Coy, 1989; Fiesta 1991; Sweeney, 1991;). The purpose of this study is to determine the ability to recall information and the perception of patients about the process of receiving information after signing a consent to participate in a large research trial. Patients signing consents for participation in the Breast Cancer Prevention Trial were asked to complete the surveys. Thirty three patients were asked to complete the questionnaires. Twenty - four (72%) of the respondents returned the completed questionnaires. Confidentiality will be maintained since no names or identifying markers will be used.A modified Patient Recall Survey (Casselith, Zupkis, Sutton - Smith, & March, 1980) and a modified Consent Form Survey (Casselith et al, 1980) were used. The significance of the study is that the results will assist in improving the type of information given to patients and how that information is provided. By increasing patients awareness about the need for and rights of giving informed consent patients will be more knowledgeable health care consumers. Imogene King(1981) provides the theoretical framework for this study using the concept of perceptions as the basis.The first research question illustrated that the majority of the respondents were able to recall at least three risks or complications of participation in the Breast Cancer Prevention Trial. The second research question revealed eighty - seven percent of the patients agreed that informed consents are necessary. However, 27.8 % of the respondents perceived the informed consent as a legal document to protect the physician rights, while only 19.6 % felt that the consent represented a legal document to protect patient rights. Eighty three percent of the respondents understood that a consent did not have to be signed. However, responses to a second question revealed only 21.3 % understood that the informed consent was a chance to refuse or change treatment. Results to research question 3 illustrated that patients felt that informed consents are necessary. Finally, 79.2 % of patients reported that nurses provided the majority of informed consent information. When patients are able to understand and participate in health care decisions, patients will feel more control in determining outcomes.
School of Nursing
Style APA, Harvard, Vancouver, ISO itp.
8

Ahmed, Abdul-Kareem H. "SIGN HERE : informed consent in personalized medicine". Thesis, Massachusetts Institute of Technology, 2013. http://hdl.handle.net/1721.1/83832.

Pełny tekst źródła
Streszczenie:
Thesis (S.M. in Science Writing)--Massachusetts Institute of Technology, Dept. of Comparative Media Studies, 2013.
Vita. Cataloged from PDF version of thesis.
Includes bibliographical references (pages 27-30).
The next era of medicine will be one of personalization, scientists and physicians promise. Personalized medicine is a refined clinical approach in which clinicians will utilize your genomic information to help you prevent disease, and tailor targeted therapies for you when you fall ill. This is the future science has slowly been approaching. However, the human genome is not enough, not unless we can decipher its language. One ambitious study to this effect is the Personal Genome Project, led by Dr. George Church at Harvard Medical School. This project will eventually recruit 100,000 volunteers to donate their genomes and a full body of information concerning their biological health. With this data, Church hopes others can cross-analyze these profiles and better determine the role in disease of each gene of the human genome. However, the Personal Genome Project is as much a study in the ethical, legal and social aspects of genomic studies as it is an effort toward personalized medicine. Church envisions a future where privacy cannot be guaranteed. Society is becoming more open and technology is more invasive than ever. Considering this, Church has informed his participants that their information will likely not remain anonymous. With their fully informed consent, he has in turn made all this data public, to promote open science. This ethical approach raises several important questions about expansive genomic studies. The scientific community will have to decide on an approach that will eventually deliver personalized medicine. On one end of the spectrum, there is Church's open approach, and the other, more security, more firewalls and more legislation. In order for personalized medicine to become a reality, society will have to prepare itself for our ever-changing ethical, technological and scientific landscape.
by Abdul-Kareem H. Ahmed.
S.M.in Science Writing
Style APA, Harvard, Vancouver, ISO itp.
9

Carr, Kelly Marie. "The Impact of Verbal Explanation and Modified Consent Materials on Orthodontic Informed Consent". The Ohio State University, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=osu1298904481.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Moloi, Gaotswake Patience. "Informed consent : communication and miscommunication in clinical trials". Thesis, Stellenbosch : Stellenbosch University, 2012. http://hdl.handle.net/10019.1/20157.

Pełny tekst źródła
Streszczenie:
Thesis (MCur)--Stellenbosch University, 2012.
ENGLISH ABSTRACT: Background Informed Consent (IC) has been proposed as the optimal method for ensuring the ethical entry of patients into clinical trials. IC is a vital part of the research process and as such entails more than obtaining a signature on a form. The IC must be given freely, without coercion, and must be based on a clear understanding of what participation involves. Aim The overall aim of this study was to attain an understanding of participants' knowledge regarding informed consent when participating in a research project. Methods The study was conducted at two public hospitals in a city in the Eastern Cape Province of South Africa. The quantitative study used descriptive survey design. A self administered questionnaire was used as a tool for data collection. Results The sample size consisted of 170 women with an average of 25.9 years. The majority had completed secondary level education. More than half of the participants did not have knowledge of the purpose of the original study. The majority of participants did not have knowledge of their responsibilities. Forty-two percent gave uninformative responses and 26% indicated they did not know their responsibilities. None of the participants understood the concept of randomization. The majority (85.9%) of participants indicated that information provided on the IC forms was sufficient for them to decide to participate. Conclusion Despite extensive efforts to ensure that participants understood their participation in the original studies, this study found poor recall of vital information for IC. A signed informed consent does not guarantee that participants understand information given. Recommendations The existing methods of communicating and obtaining of an informed consent seem to be insufficient for participants to make an informed decision. A new approach with more interactive features such as combination of audio-visual techniques might increase the possibilities of the understanding.
AFRIKAANSE OPSOMMING: Agtergrond Ingeligte toestemming (IT) is voorgestel as die optimale metode om die etiese toelating van die pasiënte vir kliniese toetse te verseker. IT is 'n belangrike deel van die navorsingsproses en as sodanig behels dit meer as die verkryging van 'n handtekening op 'n vorm. Die IT moet vrylik gegee word, sonder dwang en moet gebaseer wees op 'n duidelike begrip van wat die deelname behels. Doel Die algemene doel van hierdie studie is om 'n begrip van die deelnemers se kennis met betrekking tot ingeligte toestemming te bepaal, wanneer hulle deelneem aan 'n navorsingsprojek. Metodes Die studie is uitgevoer by twee openbare hospitale in ’n stad in die Oos-Kaap in Suid-Afrika. Die navorsingsontwerp is beskrywend van aard en ’n kwantitatiewe benadering is toegepas. ‘n Self-geadministreerde vraelys is as 'n instrument gebruik om data in te samel. Resultate Die steekproefgrootte het bestaan uit 170 vroue met 'n gemiddelde ouderdom van 25.9 jaar. Die meerderheid van die vroue het opleiding tot op sekondêre vlak. Meer as die helfte van die deelnemers het geen kennis van die doel van die oorspronklike studie gehad nie. Die meerderheid van die deelnemers het ook nie kennis van hul verantwoordelikhede gehad nie. Twee-en-veertig persent het nie toepaslike antwoorde gegee nie en 26% het aangedui dat hulle nie weet wat hul verantwoordelikhede in die studie is nie. Nie een van die deelnemers het die konsep van verewekansiging verstaan nie. Die meerderheid (85.9%) van die deelnemers het aangedui dat die inligting wat deur die IT verskaf word voldoende was om te besluit of hulle aan die studie wou deelneem. Gevolgtrekking Ten spyte van uitgebreide pogings om te verseker dat deelnemers hulle deelname verstaan het in die oorspronklike toetsing, het hierdie studie die swak herroeping van belangrike inligting aangaande IT bewys. ‘n Ondertekende ingeligte toestemming gee geen waarborg dat die deelnemers die inligting waarvoor toestemming geteken is, verstaan nie. Aanbevelings Die bestaande metodes van die kommunikasie en verkryging van ingeligte toestemming blyk onvoldoende te wees om deelnemers ingeligte besluite te laat neem. ‘n Nuwe benadering met meer interaktiewe eienskappe soos ’n kombinasie van oudio-visuele tegnieke mag die moontlikhede om te verstaan, meer duidelik maak.
Style APA, Harvard, Vancouver, ISO itp.
Więcej źródeł

Książki na temat "Informed consent"

1

Wear, Stephen. Informed Consent. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-015-8122-6.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
2

Victoria, Law Reform Commission of. Informed consent. [Melbourne: The Commission], 1987.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

Fix, R. M. Informed consent. Orange Park, FL: Frontline Pub. Co., 2007.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
4

Byrne, John A. Informed consent. New York: McGraw-Hill, 1996.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
5

Carmi, Amnon. Informed consent. Redaktor UNESCO Chair in Bioethics at the University of Haifa. Haifa, Israel: Israel National Commission for UNESCO, 2003.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

Copyright Paperback Collection (Library of Congress), red. Informed consent. New York: New American Library, 1986.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
7

Corsino, Bruce V. Informed consent: Policy & practice. White River Junction, VT (VAMC & ROC, White River Junction 05009): National Center for Clinical Ethics, 1996.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

Fan, Ruiping, red. Family-Oriented Informed Consent. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-12120-8.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

Corsino, Bruce V. Informed consent: Policy & practice. White River Junction, VT (VAMC & ROC, White River Junction 05009): National Center for Clinical Ethics, 1996.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Corsino, Bruce V. Informed consent: Policy & practice. White River Junction, VT (VAMC & ROC, White River Junction 05009): National Center for Clinical Ethics, 1996.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
Więcej źródeł

Części książek na temat "Informed consent"

1

ten Have, Henk, i Maria do Céu Patrão Neves. "Consent, Informed Consent". W Dictionary of Global Bioethics, 351–52. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-54161-3_171.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
2

Rieske, Robert D., Stephanie C. Babbitt, Joe H. Neal i Julie A. Spencer. "Informed Consent". W Handbook of Treatments for Autism Spectrum Disorder, 67–84. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-61738-1_5.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

Fox, Anthony W. "Informed Consent". W Principles and Practice of Pharmaceutical Medicine, 79–83. Oxford, UK: Wiley-Blackwell, 2010. http://dx.doi.org/10.1002/9781444325263.ch8.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
4

Annas, George J. "Informed Consent". W The Rights of Patients, 83–103. Totowa, NJ: Humana Press, 1992. http://dx.doi.org/10.1007/978-1-4612-0397-1_6.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
5

Stanton-Jean, Michèle, Hubert Doucet i Thérèse Leroux. "Informed Consent". W Handbook of Global Bioethics, 737–53. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-2512-6_117.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

Carey, Eileen, i Ruth Ryan. "Informed Consent". W Handbook of Intellectual Disabilities, 221–45. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-20843-1_14.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
7

Kraushar, Marvin F. "Informed Consent". W Risk Prevention in Ophthalmology, 65–75. New York, NY: Springer New York, 2008. http://dx.doi.org/10.1007/978-0-387-73341-8_7.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

DeFabrique, Nathalie. "Informed Consent". W Encyclopedia of Clinical Neuropsychology, 1807–8. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-57111-9_994.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

Dunn, Laura B., i Laura Weiss Roberts. "Informed Consent". W Encyclopedia of Women’s Health, 649–51. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-0-306-48113-0_217.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Mallia, Pierre. "Consent: Informed". W Encyclopedia of Global Bioethics, 1–9. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-05544-2_120-1.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.

Streszczenia konferencji na temat "Informed consent"

1

Utz, Christine, Martin Degeling, Sascha Fahl, Florian Schaub i Thorsten Holz. "(Un)informed Consent". W CCS '19: 2019 ACM SIGSAC Conference on Computer and Communications Security. New York, NY, USA: ACM, 2019. http://dx.doi.org/10.1145/3319535.3354212.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
2

Kulhawy, Darlene, i Alberta Edmonton. "Informed consent? Or is it?" W 1st Annual Worldwide Nursing Conference (WNC 2013). Global Science and Technology Forum Pte Ltd, 2013. http://dx.doi.org/10.5176/2315-4330_wnc13.18.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

Townsend, Daphne. "Informed Consent in Biomedical Research". W Conference Proceedings. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2006. http://dx.doi.org/10.1109/iembs.2006.260448.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
4

Townsend, Daphne. "Informed Consent in Biomedical Research". W Conference Proceedings. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2006. http://dx.doi.org/10.1109/iembs.2006.4398348.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
5

Sterling, S. Revi, i Nimmi Rangaswamy. "Constructing informed consent in ICT4D research". W the 4th ACM/IEEE International Conference. New York, New York, USA: ACM Press, 2010. http://dx.doi.org/10.1145/2369220.2369264.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

Henley, Jessica, i Simon Kirby. "Robotic Surgery – Implications for Informed Consent". W The Hamlyn Symposium on Medical Robotics: "MedTech Reimagined". The Hamlyn Centre, Imperial College London London, UK, 2022. http://dx.doi.org/10.31256/hsmr2022.17.

Pełny tekst źródła
Streszczenie:
Informed consent can be a complicated medico-legal process to ensure that a patient understands the risks involved with medical treatment or procedure. Surgeons in particular continue to face legal liability on the claim that informed consent was not properly achieved before surgery, which is likely to be further complicated by evolving technological advances in medicine [1],[2]. Robotic surgery introduces ambiguity for physicians to achieve informed consent. In addition to explaining the procedure according to the plan, the physician must describe the risk inherent to the technology that could create risk during the procedure. In the relatively new and ever-progressing world of surgical robotics, the surgeon may not have a complete understanding of what can go wrong based on their knowledge of the technology. This ambiguity leaves room for legal vulnerability for both the physician and the patient in achieving informed consent, as well as ambiguity in who can be held responsible. With the development and implementation of surgical robotics, no standardized protocol or training has been developed for how to approach informed consent discussions with patients. This poster considers the implications of surgical robotics on informed consent.
Style APA, Harvard, Vancouver, ISO itp.
7

Grobler, Jan Harm Fouche. "Practical Application of Free Prior Informed Consent". W SPE International Conference and Exhibition on Health, Safety, Security, Environment, and Social Responsibility. Society of Petroleum Engineers, 2018. http://dx.doi.org/10.2118/190574-ms.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

Alshevsky, Vladimir. "Problems of informed consent in domestic medicine". W Issues of determining the severity of harm caused to human health as a result of the impact of a biological factor. ru: Publishing Center RIOR, 2020. http://dx.doi.org/10.29039/conferencearticle_5fdcb03a27a5f7.62532593.

Pełny tekst źródła
Streszczenie:
Since 1993, the requirement to obtain informed consent from a patient before a medical intervention has not been properly implemented to date. This is partly due to the wording of a number of articles of the current Federal Law of November 21, 2011 № 323-FZ and orders of the Ministry of Health of the Russian Federation, which set the trend for profanity in informing the patient. Evasion of the doctor from proper informing the patient creates the prerequisites for the doctor to commit acts falling under the Criminal Code, as well as in civil proceedings.
Style APA, Harvard, Vancouver, ISO itp.
9

Luger, Ewa, i Tom Rodden. "An informed view on consent for UbiComp". W UbiComp '13: The 2013 ACM International Joint Conference on Pervasive and Ubiquitous Computing. New York, NY, USA: ACM, 2013. http://dx.doi.org/10.1145/2493432.2493446.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Vallance, Shirley, Julie Potter, Anne O'Connor, Bridget O'Bree, Dorrilyn Rajbhandari, Ellen McDonald, Andrea Tkaczyk i in. "Informed Consent For An International Thromboprophylaxis Trial". W American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a6046.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.

Raporty organizacyjne na temat "Informed consent"

1

Santos, Elsa, Silvia Llaguno i Ricardo Vernon. Mexico: Protecting informed consent. Population Council, 1999. http://dx.doi.org/10.31899/rh4.1190.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
2

Hamilton, Leslie. Defining and obtaining informed consent. BJUI Knowledge, sierpień 2019. http://dx.doi.org/10.18591/bjuik.0359.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

Deborah Schrag, Deborah Schrag, Andrea Andrea Enzinger, Christine Cronin i Jennifer Wind. Improving Informed Consent for Palliative Chemotherapy. Patient-Centered Outcomes Research Institute® (PCORI), sierpień 2019. http://dx.doi.org/10.25302/7.2019.ce.13046517.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
4

Bertalan, Margit. What is Free, Prior and Informed Consent (FPIC)? Wildlife Conservation Society, 2021. http://dx.doi.org/10.19121/2021.report.45032.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
5

McGrory, Elizabeth, Barbara Friedland, Cynthia Woodsong i Kathleen MacQueen. Informed Consent in HIV Prevention Trials: Report of an International Workshop. Population Council, 2006. http://dx.doi.org/10.31899/hiv1.1021.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

Dickert, Neal, Andrea Mitchell, Candace Speight, Michael Frankel, Sara Goldkind, Yi-An Ko, Raul Nogueira i in. Understanding and Improving Informed Consent for Clinical Trials during Health Emergencies. Patient-Centered Outcomes Research Institute (PCORI), wrzesień 2020. http://dx.doi.org/10.25302/09.2020.me.140210638.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
7

Biesecker, Barbara, Melissa Raspa, Douglas Rupert, Rebecca Moultrie, Robert Furberg i Lauren A. McCormack. Making Clinical Trials More Patient-Centered Using Digital Interactive E-Consent Tools. RTI Press, październik 2019. http://dx.doi.org/10.3768/rtipress.2019.op.0063.1910.

Pełny tekst źródła
Streszczenie:
Research participants are required to give their consent to participate in clinical trials and nonexempt government-funded studies. The goal is to facilitate participant understanding of the intent of the research, its voluntary nature, and the potential benefits and harms. Ideally, participants make an informed choice whether to participate; one that is based on having sufficient relevant knowledge and that is consistent with their values and preferences. Achieving this objective can be challenging, and as such, many scholars have declared the consent process flawed or “broken.” Moreover, clinical trials are complex studies, and compelling evidence suggests that current consent processes are inadequate in achieving informed choice. E-consent offers a dynamic, engaging consent delivery mode that can effectively support making informed decisions about whether to participate in a trial.
Style APA, Harvard, Vancouver, ISO itp.
8

Friedland, Barbara, Louis Apicella, Katie Schenk, Meredith Sheehy i Paul Hewett. Evaluation of the informed consent process for male circumcision scale-up in Swaziland. Population Council, 2011. http://dx.doi.org/10.31899/hiv1.1012.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

Wood, Susan, Barbara Friedland i Elizabeth McGrory. Informed consent: From good intentions to sound practices—A report of a seminar. Population Council, 2002. http://dx.doi.org/10.31899/rh5.1004.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Judith, Meyer, i David Keller. H - Requirement No. 1. OceanNETs, wrzesień 2020. http://dx.doi.org/10.3289/oceannets_d10.1.

Pełny tekst źródła
Streszczenie:
The purpose of this deliverable is to provide detailed information on the informed consent procedures that will be implemented for the participation of humans, including the information about the management of informed consent forms. This pertains to work conducted in WP 2 Governance, policy, and international law, WP 3 Public perception, WP 6 Ocean alkalinization case studies, and WP 7 Stakeholder Dialogue and the Provision of Knowledge, which involves the collection of information from laypersons and stakeholders.
Style APA, Harvard, Vancouver, ISO itp.
Możesz być także zainteresowany rozszerzonymi bibliografiami na temat „Informed consent” dla poszczególnych typów źródeł:
Artykuły w czasopismach Rozprawy doktorskie Książki
Oferujemy zniżki na wszystkie plany premium dla autorów, których prace zostały uwzględnione w tematycznych zestawieniach literatury. Skontaktuj się z nami, aby uzyskać unikalny kod promocyjny!

Do bibliografii