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Journal articles on the topic '# CONSENT IS SPECIFIC'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

McIlwain, Jeffrey C. "Procedure-Specific Consent Forms." Annals of The Royal College of Surgeons of England 91, no. 7 (2009): 629. http://dx.doi.org/10.1308/003588409x464739.

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Danhauser, Katharina, Larissa Dorothea Lina Mantoan, Jule Marie Dittmer, et al. "On-site electronic consent in pediatrics using generic Informed Consent Service (gICS): Creating a specialized setup and collecting consent data." PLOS Digital Health 3, no. 11 (2024): e0000661. http://dx.doi.org/10.1371/journal.pdig.0000661.

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Enrolling in a clinical trial or study requires informed consent. Furthermore, it is crucial to ensure proper consent when storing samples in biobanks for future research, as these samples may be used in studies beyond their initial purpose. For pediatric studies, consent must be obtained from both the child and their legal guardians, requiring the recording of multiple consents at once. Electronic consent has become more popular recently due to its ability to prevent errors and simplify the documentation of multiple consents. However, integrating consent capture into existing study software s

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Kenney-Herbert, E., M. Mylonas, J. Todd, and K. Tipples. "Consent Consensus: Time for a National Site-Specific Consent Form for Radiotherapy?" Clinical Oncology 33, no. 1 (2021): 1–4. http://dx.doi.org/10.1016/j.clon.2020.05.020.

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Clark, Scott K., Barbara L. Leighton, and Joseph L. Seltzer. "A risk-specific anesthesia consent form may hinder the informed consent process." Journal of Clinical Anesthesia 3, no. 6 (1991): 481. http://dx.doi.org/10.1016/0952-8180(91)90100-2.

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Clark, Scott K., Barbara L. Leighton, and Joseph L. Seltzer. "A risk-specific anesthesia consent form may hinder the informed consent process." Journal of Clinical Anesthesia 3, no. 1 (1991): 11–13. http://dx.doi.org/10.1016/0952-8180(91)90199-w.

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6

YU, Ho-Jong. "Doctors Duty of Informed Consent and Patient Informed Consent Form." Korean Journal of Medical Ethics 5, no. 1 (2002): 27–41. http://dx.doi.org/10.35301/ksme.2002.5.1.27.

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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

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7

Wright, David. "Redesigning Informed Consent Tools for Specific Research." Technical Communication Quarterly 21, no. 2 (2012): 145–67. http://dx.doi.org/10.1080/10572252.2012.641432.

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8

Catalona, William J. "Informed consent for prostate-specific antigen screening." Urology 61, no. 1 (2003): 17–19. http://dx.doi.org/10.1016/s0090-4295(02)02007-1.

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Carter, H. Ballentine. "Informed consent for prostate-specific antigen screening." Urology 61, no. 1 (2003): 13–14. http://dx.doi.org/10.1016/s0090-4295(02)02009-5.

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Wilkinson, Simon, and Gerald Chodak. "Informed consent for prostate-specific antigen screening." Urology 61, no. 1 (2003): 2–4. http://dx.doi.org/10.1016/s0090-4295(02)02010-1.

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Gann, Peter H. "Informed consent for prostate-specific antigen testing." Urology 61, no. 1 (2003): 5–6. http://dx.doi.org/10.1016/s0090-4295(02)02157-x.

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12

Davies, D. R., and J. C. Rigby. "The doctrine of specific consent and research." Psychiatric Bulletin 13, no. 1 (1989): 37–38. http://dx.doi.org/10.1192/pb.13.1.37-b.

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13

Arunakirinathan, Meena, Ahmed Sadiq, and Anand Rajasekaran. "A case for procedure-specific consent forms." International Journal of Surgery 9, no. 7 (2011): 561. http://dx.doi.org/10.1016/j.ijsu.2011.07.326.

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Kenney-Herbert, E., and K. Tipples. "Consent Consensus – Site-specific Consent for Radiotherapy in Prostate Cancer, Where Are We?" Clinical Oncology 32, no. 5 (2020): e133. http://dx.doi.org/10.1016/j.clon.2020.01.018.

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15

Pohlman, Katherine, and Nadine Schwab. "Consent and Release." Journal of School Nursing 17, no. 3 (2001): 162–65. http://dx.doi.org/10.1177/10598405010170030801.

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Because school nursing practice by definition involves delivering services to minors, school nurses often find themselves with questions about consent. Because school districts, much like other health care providers, occasionally face liability for the undesired health care outcomes of their clients (i.e., students), another question that surfaces frequently deals with release from liability. Each question must be answered based on analysis of the specific facts and applicable laws. This article provides an overview of the principles that provide school nurses with general guidance on consent

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16

Brawley, Otis W. "Informed consent for prostate-specific antigen-based screening." Urology 61, no. 1 (2003): 10–12. http://dx.doi.org/10.1016/s0090-4295(02)02323-3.

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17

Lin, Charles J., Charles Luke, Daniel Sullivan, and Richard Kidwell. "Development of specific peripheral nerve block consent form." Journal of Clinical Anesthesia 54 (May 2019): 33–36. http://dx.doi.org/10.1016/j.jclinane.2018.10.030.

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18

St John, Edward, Ara Askari, Dickson Fenn, et al. "Digital procedure specific consent forms (OpInform) compared to handwritten surgical consent forms in breast surgery." European Journal of Surgical Oncology (EJSO) 43, no. 5 (2017): S5. http://dx.doi.org/10.1016/j.ejso.2017.01.033.

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19

Manson, Neil C. "The biobank consent debate: Why ‘meta-consent’ is not the solution?" Journal of Medical Ethics 45, no. 5 (2018): 291–94. http://dx.doi.org/10.1136/medethics-2018-105007.

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Over the past couple of decades, there has been an ongoing, often fierce, debate about the ethics of biobank participation. One central element of that debate has concerned the nature of informed consent, must specific reconsent be gained for each new use, or user, or is broad consent ethically adequate? Recently, Thomas Ploug and Søren Holm have developed an alternative to both specific and broad consent: what they call a meta-consent framework. On a meta-consent framework, participants can choose the type of consent framework they require, for different kinds of use, different types of user

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20

Magnusson, Roger S. "Testing for HIV without specific consent: a short review." Australian and New Zealand Journal of Public Health 20, no. 1 (1996): 57–60. http://dx.doi.org/10.1111/j.1467-842x.1996.tb01337.x.

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21

Crozier, Jack, Ann Williams, Steven T. F. Chan, and Graeme Thompson. "Randomized trial of laparoscopic cholecystectomy procedure-specific consent form." ANZ Journal of Surgery 88, no. 1-2 (2017): E55—E59. http://dx.doi.org/10.1111/ans.13888.

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22

Nguyen, Minh Thu, Jack Goldblatt, Rosario Isasi, et al. "Model consent clauses for rare disease research." BMC Medical Ethics 20, no. 1 (2019): 55. https://doi.org/10.1186/s12910-019-0390-x.

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<strong>Background: </strong>Rare Disease research has seen tremendous advancements over the last decades, with the development of new technologies, various global collaborative efforts and improved data sharing. To maximize the impact of and to further build on these developments, there is a need for model consent clauses for rare diseases research, in order to improve data interoperability, to meet the informational needs of participants, and to ensure proper ethical and legal use of data sources and participants' overall protection.<strong>Methods: </strong>A global Task Force was set up to

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23

Barritt, Andrew W., Laura Clark, Victoria Teoh, Adam MM Cohen, and Paul A. Gibb. "Assessing the adequacy of procedure-specific consent forms in orthopaedic surgery against current methods of operative consent." Annals of The Royal College of Surgeons of England 92, no. 3 (2010): 246–49. http://dx.doi.org/10.1308/003588410x12628812458257.

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INTRODUCTION This is an audit of patient understanding following their consent for orthopaedic procedures and uses information on new Orthoconsent forms endorsed by the British Orthopaedic Association as the set standard. The objectives were to: (i) assess whether patients& understanding of knee arthroscopy (KA) and total knee replacement (TKR) at the point of confirming their consent reaches the set standard; and (ii) to ascertain whether issuing procedure-specific Orthoconsent forms to patients can improve this understanding. SUBJECTS AND METHODS This was a prospective audit using questi

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Arnander, M., V. Teoh, A. Barabas, S. Umarji, and A. Fleming. "IMPROVED PATIENT AWARENESS AND SATISFACTION USING PROCEDURE SPECIFIC CONSENT FORMS IN CARPAL TUNNEL DECOMPRESSION SURGERY." Hand Surgery 18, no. 01 (2013): 53–57. http://dx.doi.org/10.1142/s021881041350010x.

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Carpal tunnel decompression (CTD) is a common procedure amenable to procedure specific consent forms (PSCFs). These may help better inform patients and so increase patient satisfaction with the consent process. We assessed the use of a PSCF for CTD. The PSCF mentions eight complications of carpal tunnel surgery and alternative non-operative treatments. Two groups of 40 patients each were compared prospectively. Patients in one group were issued with a PSCF prior to admission whereas those in the other group were not. After standard pre-operative consent, patients were interviewed prior to surg

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Sibold, Hannah Claire, Gavin Paul Campbell, John Bourgeois, Margie D. Dixon, R. Donald Harvey, and Rebecca D. Pentz. "Improving consent forms for first-in-human trials through participant feedback." Journal of Clinical Oncology 39, no. 15_suppl (2021): e13563-e13563. http://dx.doi.org/10.1200/jco.2021.39.15_suppl.e13563.

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e13563 Background: Risks and benefits of investigational agents that have not been tested in humans are, at best, incompletely characterized in nonclinical investigations. Despite the growing emphasis to include patient voices in clinical trial design, no published research has explored patient preferences on how best to convey the information that the agent has not been tested in humans. This study established that First in Human (FIH) consent forms present this information in different locations and queried participants for their input on the preferable FIH consent form structure. Methods: C

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Rasmusen, Sven Carsten, Manuel Penz, Stephanie Widauer, et al. "Raising Consent Awareness With Gamification and Knowledge Graphs: An Automotive Use Case." International Journal on Semantic Web and Information Systems 18, no. 1 (2022): 21. https://doi.org/10.4018/IJSWIS.300820.

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Consent is one of GDPR’s lawful bases for data processing and specific requirements for it apply. Consent should be specific, unambiguous and most of all informed. However, an informed consent request does not guarantee having individuals who are aware of what it means to consent and the implications that follow. Consent is often given blindly now, in particular because of information overload from long privacy policies written in legal language and complex interface designs that cause consent fatigue on the users' side. This paper presents a knowledge graph-based user interface for

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Finch, William JG, Mark A. Rochester, and Robert D. Mills. "A Randomised Trial of Conventional versus BAUS Procedure-Specific Consent Forms for Transurethral Resection of Prostate." Annals of The Royal College of Surgeons of England 91, no. 3 (2009): 232–38. http://dx.doi.org/10.1308/003588409x359277.

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INTRODUCTION Conventional consent forms often contain incomplete information regarding risks associated with invasive procedures. BAUS has introduced procedure-specific consent forms (PSCF) documenting the risks associated with urological procedures. We compared patients' understanding of the risks and benefits of TURP after the consenting process with either conventional documentation or PSCF. PATIENTS AND METHODS One hundred patients were randomised to be consented with either a conventional or PSCF. After 3 h, their understanding was assessed with a questionnaire asking patients to document

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28

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 part

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Shreekrishna, H. K., and Aruna B. Rao. "Consent in medical practice." International Journal of Preclinical and Clinical Research 2, no. 1 (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 with

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Alblas, Maaike, Maartje Schermer, Yvonne Vergouwe, and Ineke Bolt. "Autonomy Challenges in Epigenetic Risk-Stratified Cancer Screening: How Can Patient Decision Aids Support Informed Consent?" Journal of Personalized Medicine 9, no. 1 (2019): 14. http://dx.doi.org/10.3390/jpm9010014.

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Information of an individual's epigenome can be useful in cancer screening to enable personalised decision making on participation, treatment options and further screening strategies. However, adding this information might result in complex risk predictions on multiple diseases, unsolicited findings and information on (past) environmental exposure and behaviour. This complicates informed consent procedures and may impede autonomous decision-making. In this article we investigate and identify the specific features of epigenetic risk-stratified cancer screening that challenge the current informe

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Chadha, Neil K., Rohit Pratap, and Antony A. Narula. "Consent processes in common nose and throat procedures." Journal of Laryngology & Otology 117, no. 7 (2003): 536–39. http://dx.doi.org/10.1258/002221503322112950.

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The NHS Plan identified the need for changes in consent practice, and led to the issuing of a model consent policy and standard consent forms for use in the NHS. The aim of this study was to determine current consent practices for common rhinology and laryngology procedures.A telephone survey was conducted of 40 otolaryngology Senior House Officers (SHOs) across England and Wales, asking about local consent procedure, and the specific complications discussed before common operations.The responsibility for routine consenting belonged to SHOs in 95 per cent of departments. Model NHS consent form

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McGinn, Thomas G. "Informed consent decreased patient interest in prostate-specific antigen screening." ACP Journal Club 125, no. 3 (1996): 75. http://dx.doi.org/10.7326/acpjc-1996-125-3-075.

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Ito, Kazuto, and Fritz H. Schrder. "Informed consent for prostate-specific antigen-based screening—European view." Urology 61, no. 1 (2003): 20–22. http://dx.doi.org/10.1016/s0090-4295(02)02258-6.

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Schrems, Berta M. "Informed consent, vulnerability and the risks of group-specific attribution." Nursing Ethics 21, no. 7 (2014): 829–43. http://dx.doi.org/10.1177/0969733013518448.

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People in extraordinary situations are vulnerable. As research participants, they are additionally threatened by abuse or exploitation and the possibility of harm through research. To protect people against these threats, informed consent as an instrument of self-determination has been introduced. Self-determination requires autonomous persons, who voluntarily make decisions based on their values and morals. However, in nursing research, this requirement cannot always be met. Advanced age, chronic illness, co-morbidity and frailty are reasons for dependencies. These in turn lead to limited abi

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Cooper, Lilli, Ash Mosahebi, Mark Henley, et al. "Developing procedure-specific consent forms in plastic surgery: Lessons learnt." Journal of Plastic, Reconstructive & Aesthetic Surgery 70, no. 3 (2017): 428–30. http://dx.doi.org/10.1016/j.bjps.2016.11.015.

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36

Manning, Donal. "Proxy Consent in Neonatal Care?Goal-Directed or Procedure-Specific?" Health Care Analysis 13, no. 1 (2005): 1–9. http://dx.doi.org/10.1007/s10728-005-2566-4.

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Courtney, MJ, and TJ Royle. "Current use of procedure specific consent forms for laparoscopic cholecystectomy." Annals of The Royal College of Surgeons of England 100, no. 6 (2018): 446–49. http://dx.doi.org/10.1308/rcsann.2018.0099.

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Introduction Procedure specific consent forms (PSCFs) have been shown to improve consenting practice for a standardised list of complications. The aim of this study was to assess the current usage and quality of PSCFs in the National Health Service (NHS) for cholecystectomy, specifically comparing the listed complications with those mentioned on the NHS website. Methods A freedom of information request was sent to all NHS trusts asking whether they perform laparoscopic cholecystectomy and whether they have a PSCF for this. A copy of the PSCF was also requested. Complications stated on these fo

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Conboy-Hill, Suzanne. "Vulnerable adults: Assessing capacity to consent." Clinical Psychology Forum 1, no. 158 (2006): 19–23. http://dx.doi.org/10.53841/bpscpf.2006.1.158.19.

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Chen, AM, DR Leff, J. Simpson, SJD Chadwick, and PJ McDonald. "Variations in Consenting Practice for Laparoscopic Cholecystectomy." Annals of The Royal College of Surgeons of England 88, no. 5 (2006): 482–85. http://dx.doi.org/10.1308/003588406x114857.

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INTRODUCTION To compare the variations in consenting practice amongst trainees and consultant surgeons for laparoscopic cholecystectomy with specific reference to the documentation of significant risks of surgery. PATIENTS AND METHODS A proforma was devised which included significant and/or commonly recognised complications of laparoscopic cholecystectomy. This was then cross-referenced with the consent forms for the 80 patients included in the study and the documented risks explained in each case were noted. RESULTS The results showed that there is considerable variation between the three gra

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Indrakusuma, R., S. Kalkman, M. J. W. Koelemay, R. Balm, and D. L. Willems. "Context-Relative Norms Determine the Appropriate Type of Consent in Clinical Biobanks: Towards a Potential Solution for the Discrepancy between the General Data Protection Regulation and the European Data Protection Board on Requirements for Consent." Science and Engineering Ethics 26, no. 6 (2020): 3271–84. http://dx.doi.org/10.1007/s11948-020-00271-9.

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AbstractClinical biobanks processing data of participants in the European Union (EU) fall under the scope of the General Data Protection Regulation (GDPR), which among others includes requirements for consent. These requirements are further specified by the Article 29 Working Party (WP29)—an EU advisory body currently known as the European Data Protection Board (EDPB). Unfortunately, their guidance is cause for some confusion. While the GDPR allows participants to give broad consent for research when specific research purposes are still unknown, the WP29 guidelines suggest that additional cons

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Pai, Satvik N. "Informed Consent in Orthopaedic cases." International Journal of Research in Orthopaedics 7, no. 4 (2021): 868. http://dx.doi.org/10.18203/issn.2455-4510.intjresorthop20212439.

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<p>Informed consent is an exercise to provide patients with adequate information before undergoing a medical procedure. Orthopaedic surgeons need to be aware of all aspects of informed consent and also certain modifications it requires as per the diagnosis/procedure planned. Extensive literature was reviewed regarding informed consent in orthopaedic cases. Medico-legal verdicts relating to orthopaedic cases where the informed consent played a vital part were analysed in detail. Specific orthopaedic cases and the common complications occurring after them were also analysed.</p><p

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Hall, Helen. "Exorcism, Religious Freedom and Consent." Journal of Criminal Law 80, no. 4 (2016): 241–53. http://dx.doi.org/10.1177/0022018316657950.

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The ruling in R v Brown that consent could not be a defence to actual bodily harm or more serious injury unless a recognised exemption applied has been much criticised. When considered exclusively in light of adult sexual activity, such criticisms may appear extremely persuasive. However, the issue of assault within exorcism reveals that there are other contexts in which the arguments appear more complex. This article examines the criminal law relating to consent and exorcism and asks how we should deal with the interplay between the general and the specific when it comes to formulating legal

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Klosko, George. "Reformist Consent and Political Obligation." Political Studies 39, no. 4 (1991): 676–90. http://dx.doi.org/10.1111/j.1467-9248.1991.tb01395.x.

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It is commonly held that theories of political obligation based on consent, whether express or tacit, cannot account for most people's obligations; that political obligations generally stem from being born into specific societies rather than from voluntary choice. In recent years, consent theorists have turned to ‘reformist’ consent, arguing that consent theory could be rescued if political institutions were reformed to allow the possibility of widespread consent. Various possible reforms are examined and shown to be inadequate. The most obvious mechanism, ‘consent-or-leave’, is disqualified b

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Wilbanks, John. "Design Issues in E-Consent." Journal of Law, Medicine & Ethics 46, no. 1 (2018): 110–18. http://dx.doi.org/10.1177/1073110518766025.

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Electronic informed consent represents an opportunity to redesign the way that participants understand and elect to enroll in clinical research studies. However, electronic consent faces certain barriers common to all informed consent processes and other barriers specific to the technical environment. At Sage Bionetworks, we designed an electronic consent process as a software product and released it as an open source tool. We believe that using contemporary design processes to intentionally create cognitive friction, where potential study participants are confronted with interfaces that requi

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GOLDWORTH, AMNON. "Informed Consent in the Genetic Age." Cambridge Quarterly of Healthcare Ethics 8, no. 3 (1999): 393–400. http://dx.doi.org/10.1017/s0963180199803181.

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As our knowledge of the genetic constitution of human beings expands, testing to determine an individual's disposition toward a given disease will also increase. Since genes are a family affair, to know that an individual is genetically disposed toward a specific disease is an indicator that members of this individual's family may also be so disposed.

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Tonge, Xenia N., Henry Crouch-Smith, Vijay Bhalaik, and William D. Harrison. "Do we achieve the Montgomery standard for consent in orthopaedic surgery?" British Journal of Hospital Medicine 82, no. 4 (2021): 1–7. http://dx.doi.org/10.12968/hmed.2020.0504.

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Aims/Background The Montgomery v Lanarkshire Health Board (2015) case set a precedent that has driven the modernisation of consenting practice. Failure to demonstrate informed consent is a common source of litigation. This quality improvement project aimed to provide pragmatic guidance for surgeons on consent and to improve the patient experience during decision making. Methods Elective orthopaedic patients were assessed and the quality of documented consent was recorded. Data were collected over two discrete cycles, with cycle 1 used as a baseline in practice. The following criteria were revi

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Swales, Lee. "The Protection of Personal Information Act 4 of 2013 in the Context of Health Research: Enabler of Privacy Rights or Roadblock?" Potchefstroom Electronic Law Journal 25 (March 9, 2022): 1–32. http://dx.doi.org/10.17159/1727-3781/2022/v25ia11180.

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Data is an exceptionally valuable asset – it is a fundamental part of the information age and is widely regarded as the world's most valuable resource. A key issue that has caused some debate in South Africa in recent times relates to the Protection of Personal Information Act 4 of 2013 (POPIA), and whether the Act requires broad or specific consent in the context of health research. The primary purpose of this article will be to answer the following question: does POPIA require broad or specific consent from persons who take part in health research? In a health research context, POPIA must be

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48

Oosthuizen, J. C., P. Burns, and C. Timon. "The changing face of informed surgical consent." Journal of Laryngology & Otology 126, no. 3 (2011): 236–39. http://dx.doi.org/10.1017/s0022215111003021.

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AbstractObjectives:To determine whether procedure-specific brochures improve patients' pre-operative knowledge, to determine the amount of information expected by patients during the consenting process, and to determine whether the recently proposed ‘Request for Treatment’ consenting process is viable on a large scale.Method:A prospective, questionnaire-based study of 100 patients admitted for selected, elective surgical procedures.Results:In total, 99 per cent of patients were satisfied with the information received in the out-patient department, regarding the proposed procedure. However, 38

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Bunnik, Eline M., A. Cecile J. W. Janssens, and Maartje H. N. Schermer. "Informed Consent in Direct-to-Consumer Personal Genome Testing: The Outline of A Model between Specific and Generic Consent." Bioethics 28, no. 7 (2012): 343–51. http://dx.doi.org/10.1111/bioe.12004.

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Gibson, Ailbhe White, Adam Cahill, Robert Piggott, James Cashman, and David O’Briain. "Patient Recall Of Informed Consent At 4 Weeks Following Arthroscopic Shoulder Surgery With Standardised Versus The Surgery-Specific Consent." Journal of Shoulder and Elbow Surgery 32, no. 5 (2023): e277. http://dx.doi.org/10.1016/j.jse.2023.02.114.

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