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Subject = Informed consent;
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Displaying Results 1 - 12 of 12 on page 1 of 1
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'It's your body, but...Mixed messages in childbirth education: findings from a hospital ethnography
(2017)
NEWNHAM, ELIZABETH; MCKELLAR, LOIS; PINCOMBE, JAN
'It's your body, but...Mixed messages in childbirth education: findings from a hospital ethnography
(2017)
NEWNHAM, ELIZABETH; MCKELLAR, LOIS; PINCOMBE, JAN
Abstract:
Objective: to investigate the personal, social, cultural and institutional influences on women making decisions about using epidural analgesia in labour. In this article we discuss the findings that describe practices around the gaining of consent for an epidural in labour, which we juxtapose with similar processes relating to use of water for labour and/or birth. Design: ethnography. Setting: tertiary hospital in Australian city. Participants: sequential interviews were conducted with 16 women; hospital staff (primarily midwives and doctors) participated during six months of participatory observation fieldwork. Findings: women were not given full disclosure of either practice and midwives tailored the information they gave according to the institutional policies rather than evidence. Key conclusions: informed consent is an oft-cited human right in health care, yet in maternity care the micropolitics of how informed consent is gained is difficult to ascertain, leading to a situation...
http://hdl.handle.net/2262/81927
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Communicating BRCA research results to patients enrolled in international clinical trials: lessons learnt from the AGO-OVAR 16 study
(2016)
Pulford, David J; Harter, Philipp; Floquet, Anne; Barrett, Catherine; Suh, Dong H; Frie...
Communicating BRCA research results to patients enrolled in international clinical trials: lessons learnt from the AGO-OVAR 16 study
(2016)
Pulford, David J; Harter, Philipp; Floquet, Anne; Barrett, Catherine; Suh, Dong H; Friedlander, Michael; Arranz, José A; Hasegawa, Kosei; Tada, Hiroomi; Vuylsteke, Peter; Mirza, Mansoor R; Donadello, Nicoletta; Scambia, Giovanni; Johnson, Toby; Cox, Charles; Chan, John K; Imhof, Martin; Herzog, Thomas J; Calvert, Paula; Wimberger, Pauline
Abstract:
Abstract Background The focus on translational research in clinical trials has the potential to generate clinically relevant genetic data that could have importance to patients. This raises challenging questions about communicating relevant genetic research results to individual patients. Methods An exploratory pharmacogenetic analysis was conducted in the international ovarian cancer phase III trial, AGO-OVAR 16, which found that patients with clinically important germ-line BRCA1/2 mutations had improved progression-free survival prognosis. Mechanisms to communicate BRCA results were evaluated, because these findings may be beneficial to patients and their families. Results Communicating individual BRCA results was not anticipated during clinical trial design. Consequently, options were not available for patients ...
http://dx.doi.org/10.1186/s12910-016-0144-y
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Consent for routine neonatal procedures: A study of practices in Irish neonatal units. How do we compare with the gold standard BAPM guidelines?
(2017)
Ryan, M A; Ryan, C A; Dempsey, E; O’Connell, R
Consent for routine neonatal procedures: A study of practices in Irish neonatal units. How do we compare with the gold standard BAPM guidelines?
(2017)
Ryan, M A; Ryan, C A; Dempsey, E; O’Connell, R
Abstract:
The Irish National Consent Policy (NCP)¹ proposes that the legal requirement for consent extends to all forms of interventions, investigations and treatment, carried out on or behalf of the Health Service Executive (HSE). This study employs a quantitative descriptive approach to investigate the practices for obtaining consent for an identified group of routine neonatal procedures in neonatal facilities throughout Ireland. The BAPM (British Association of Perinatal Medicine)² guidelines were identified as ‘gold standard’ for the purposes of this study. The results indicated a lack of consistency between participating units pertaining to the modes of consent utilised and notable variances from ‘gold standard’ guidelines. Unanimity was evident for 3 procedures only (administering BCG, 6-in-1, and donor breast milk to infant). Significant findings related to EEG with video recordings, MRI/CT and gastro intestinal imaging, screening of an infant with suspected substance abuse or retinopa...
http://hdl.handle.net/10147/622501
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Ethical Issues in Internet Research: International Good Practice and Irish Research Ethics Documents
(2013)
Felzmann, Heike
Ethical Issues in Internet Research: International Good Practice and Irish Research Ethics Documents
(2013)
Felzmann, Heike
Abstract:
This chapter discusses the main research ethical concerns that arise in internet research and reviews existing research ethical guidance in the Irish context in relation to its application to internet research. The chapter begins with a brief outline of high profile cases in the early history of the internet that highlighted specific emerging ethical concerns regarding the new medium and the first development of ethical guidance in this context. Important research ethical concerns in internet research are then presented. These include: (i) understanding the specific relationship between researchers, participants and the online materials, and the ethical significance of contributors' potential lack of awareness of research conducted on their online interactions, (ii) clarifying privacy expectations and ethical requirements regarding the access to and use of online materials, (iii) implementing ethically appropriate consent processes in the online medium, (iv) doing justice to c...
http://hdl.handle.net/10379/3844
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Good medical practice in seeking informed consent to treatment
(2009)
Medical Council
Good medical practice in seeking informed consent to treatment
(2009)
Medical Council
http://hdl.handle.net/10147/234061
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Guidelines in relation to obtaining clinical consent in an acute setting
(2006)
Health Service Executive (HSE)
Guidelines in relation to obtaining clinical consent in an acute setting
(2006)
Health Service Executive (HSE)
http://hdl.handle.net/10147/75681
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P026 The role of fibrocytes in mesenteric Crohn's disease.
(2017)
Kiernan, Miranda G; Sahebally, Shaheel M; Kiely, Patrick A; Waldron, David; Moloney, M;...
P026 The role of fibrocytes in mesenteric Crohn's disease.
(2017)
Kiernan, Miranda G; Sahebally, Shaheel M; Kiely, Patrick A; Waldron, David; Moloney, M; Skelly, M; Faul, P.N; O'Leary, D.P; Lowery, Aoife J; Walsh, L.G; Dunne, Colum; Coffey, John C
Abstract:
The full text of this article will not be available on ULIR until the embargo expires on the 26/1/2018
The mesentery in Crohn’s disease frequently displays disease manifestations, such as mesenteric thickening and fat wrapping. Fibrocytes are a precursor cell type that can differentiate into fibroblasts or adipocytes [1]. They have previously been identified in the mesentery in inflammatory conditions such as mesenteric panniculitis [2]. This study aimed to investigate the role of fibrocytes in Crohn’s mesenteric disease manifestations.
ACCEPTED
peer-reviewed
http://hdl.handle.net/10344/5800
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Parental and Clinical Perception of Informed Consent in Neonatal Research
(2015)
O Shea, Niamh
Parental and Clinical Perception of Informed Consent in Neonatal Research
(2015)
O Shea, Niamh
Abstract:
<p>D. Abstract Objectives: To systematically explore the perceptions parents and clinicians have of the informed consent process in neonatal research. Methods: A comprehensive literature review of peer reviewed studies, all of which are related to the topic of this dissertation. Additionally, an original questionnaire based study was conducted. The study recruited parents of newborn infants who had been an inpatient of the Neonatal Intensive Care Unit of the Cork University Maternity Hospital and clinicians currently employed in either a paediatric or neonatal setting. Results: Parent perception of informed consent in neonatal research is a relatively well studied area. Parents have a lack of understating of certain study procedures including the element of randomisation. 72% of clinicians believe approaching parents antenatally with information about a neonatal study leads to a greater uptake in consent and 57% of parents stated a preference to being approached with informati...
http://epubs.rcsi.ie/mscttheses/83
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Privacy by Design: Informed consent and Internet of Things for smart health
(2017)
O'Connor, Yvonne; Rowan, Wendy; Lynch, Laura; Heavin, Ciara
Privacy by Design: Informed consent and Internet of Things for smart health
(2017)
O'Connor, Yvonne; Rowan, Wendy; Lynch, Laura; Heavin, Ciara
Abstract:
Check: I accept the terms and conditions and privacy policy statements associated with this technological artefact! The informed consent process is becoming more of a challenge with the emergence of Internet of Things (IoT) as data may be collected without the digital health citizen being aware. It is argued in this paper that the first phase for universal usability of IoT within the smart health domain is to ensure that digital health citizens (i.e. user of technology) are fully aware of what they are consenting to when they register an account with such technological artefacts. This point is further reinforced by the proposed ‘Privacy by Design’ requirements associated with the forthcoming General Data Protection Regulation (GDPR). This paper proposes some practical approaches which should be considered when designing and developing IoT for data collection and data sharing within the health domain.
http://hdl.handle.net/10468/4850
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Specific informed consent for blood transfusion: the ethical considerations
(2017)
National Advisory Committee on Bioethics; Green, Andrew; Bradley, Colin; Gordijn, Bert;...
Specific informed consent for blood transfusion: the ethical considerations
(2017)
National Advisory Committee on Bioethics; Green, Andrew; Bradley, Colin; Gordijn, Bert; Hull, Richard; Kennedy, Harry; Madden, Deirdre; McAuley, Adam; McCarthy, Joan; McQuillan, Regina; Sheikh, Asim A.; Smith, David
Abstract:
The Minister for Health, Dr. James Reilly T.D., established the National Advisory Committee on Bioethics in March 2012. The task of this Committee is to advise the Minister on the ethical and social implications of scientific developments in human medicine and healthcare.
http://hdl.handle.net/10379/6377
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Who abandons embryos after IVF?
(2010)
Walsh, Anthony PH; Tsar, Olga M; Walsh, David J; Baldwin, P M; Shkrobot, Lyuda V; Sills...
Who abandons embryos after IVF?
(2010)
Walsh, Anthony PH; Tsar, Olga M; Walsh, David J; Baldwin, P M; Shkrobot, Lyuda V; Sills, Eric Scott
Abstract:
<p>This article is also available at <a href="http://www.imj.ie">www.imj.ie</a></p>
<p>This investigation describes features of in vitro fertilisation (IVF) patients who never returned to claim their embryos following cryopreservation. Frozen embryo data were reviewed to establish communication patterns between patient and clinic; embryos were considered abandoned when 1) an IVF patient with frozen embryo/s stored at our facility failed to make contact with our clinic for > 2 yrs and 2) the patient could not be located after a multi-modal outreach effort was undertaken. For these patients, telephone numbers had been disconnected and no forwarding address was available. Patient, spouse and emergency family contact/s all escaped detection efforts despite an exhaustive public database search including death records and Internet directory portals. From 3244 IVF cycles completed from 2000 to 2008, > or = 1 embryo was frozen in 1159 cases ...
http://epubs.rcsi.ie/obsgynart/14
Displaying Results 1 - 12 of 12 on page 1 of 1
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