Literature DB >> 27534587

Did I Tell You That? Ethical Issues Related to Using Computational Methods to Discover Non-Disclosed Patient Characteristics.

Kenrick D Cato1, Walter Bockting2, Elaine Larson3.   

Abstract

Widespread availability of electronic health records coupled with sophisticated statistical methods offer great potential for a variety of applications for health and disease surveillance, developing predictive models and advancing decision support for clinicians. However, use of "big data" mining and discovery techniques has also raised ethical issues such as how to balance privacy and autonomy with the wider public benefits of data sharing. Furthermore, electronic data are being increasingly used to identify individual characteristics, which can be useful for clinical prediction and management, but were not previously disclosed to a clinician. This process in computer parlance is called electronic phenotyping, and has a number of ethical implications. Using the Belmont Report's principles of respect for persons, beneficence, and justice as a framework, we examined the ethical issues posed by electronic phenotyping. Ethical issues identified include the ability of the patient to consent for the use of their information, the ability to suppress pediatric information, ensuring that the potential benefits justify the risks of harm to patients, and acknowledging that the clinician's biases or stereotypes, conscious or unintended, may become a factor in the therapeutic interaction. We illustrate these issues with two vignettes, using the person characteristic of gender minority status (i.e., transgender identity) and health history characteristic of substance abuse. Data mining has the potential to uncover patient characteristics previously obscured, which can provide clinicians with beneficial clinical information. Hence, ethical guidelines must be updated to ensure that electronic phenotyping supports the principles of respect for persons, beneficence, and justice.
© The Author(s) 2016.

Entities:  

Keywords:  LGBT; informed consent; LGBTQ; and burdens of research/beneficence and non-maleficence; benefits; clinical settings; data mining; data sharing; electronic health record; other clinical; risks

Mesh:

Year:  2016        PMID: 27534587      PMCID: PMC4991620          DOI: 10.1177/1556264616661611

Source DB:  PubMed          Journal:  J Empir Res Hum Res Ethics        ISSN: 1556-2646            Impact factor:   1.742


  34 in total

1.  Misunderstandings about the effects of race and sex on physicians' referrals for cardiac catheterization.

Authors:  L M Schwartz; S Woloshin; H G Welch
Journal:  N Engl J Med       Date:  1999-07-22       Impact factor: 91.245

2.  The principles of the Belmont report revisited. How have respect for persons, beneficence, and justice been applied to clinical medicine?

Authors:  E J Cassell
Journal:  Hastings Cent Rep       Date:  2000 Jul-Aug       Impact factor: 2.683

Review 3.  Improving the informed consent process for research subjects with low literacy: a systematic review.

Authors:  Leonardo Tamariz; Ana Palacio; Mauricio Robert; Erin N Marcus
Journal:  J Gen Intern Med       Date:  2012-07-11       Impact factor: 5.128

4.  Concern about security and privacy, and perceived control over collection and use of health information are related to withholding of health information from healthcare providers.

Authors:  Israel T Agaku; Akinyele O Adisa; Olalekan A Ayo-Yusuf; Gregory N Connolly
Journal:  J Am Med Inform Assoc       Date:  2013-08-23       Impact factor: 4.497

5.  Subjects agree to participate in environmental health studies without fully comprehending the associated risk.

Authors:  Robin Lee; Samantha Lampert; Lynn Wilder; Anne L Sowell
Journal:  Int J Environ Res Public Health       Date:  2011-03-11       Impact factor: 3.390

6.  Transgender patient perceptions of stigma in health care contexts.

Authors:  Kami Kosenko; Lance Rintamaki; Stephanie Raney; Kathleen Maness
Journal:  Med Care       Date:  2013-09       Impact factor: 2.983

7.  Challenges in creating an opt-in biobank with a registrar-based consent process and a commercial EHR.

Authors:  Keith Marsolo; Jeremy Corsmo; Michael G Barnes; Carrie Pollick; Jamie Chalfin; Jeremy Nix; Christopher Smith; Rajesh Ganta
Journal:  J Am Med Inform Assoc       Date:  2012-08-09       Impact factor: 4.497

8.  Developing a simplified consent form for biobanking.

Authors:  Laura M Beskow; Joëlle Y Friedman; N Chantelle Hardy; Li Lin; Kevin P Weinfurt
Journal:  PLoS One       Date:  2010-10-08       Impact factor: 3.240

9.  Electronic medical records and the transgender patient: recommendations from the World Professional Association for Transgender Health EMR Working Group.

Authors:  Madeline B Deutsch; Jamison Green; JoAnne Keatley; Gal Mayer; Jennifer Hastings; Alexandra M Hall
Journal:  J Am Med Inform Assoc       Date:  2013-04-30       Impact factor: 4.497

10.  Risk stratification using data from electronic medical records better predicts suicide risks than clinician assessments.

Authors:  Truyen Tran; Wei Luo; Dinh Phung; Richard Harvey; Michael Berk; Richard Lee Kennedy; Svetha Venkatesh
Journal:  BMC Psychiatry       Date:  2014-03-14       Impact factor: 3.630

View more
  9 in total

1.  Precision health: Advancing symptom and self-management science.

Authors:  Kathleen T Hickey; Suzanne Bakken; Mary W Byrne; Donald Chip E Bailey; George Demiris; Sharron L Docherty; Susan G Dorsey; Barbara J Guthrie; Margaret M Heitkemper; Cynthia S Jacelon; Teresa J Kelechi; Shirley M Moore; Nancy S Redeker; Cynthia L Renn; Barbara Resnick; Angela Starkweather; Hilaire Thompson; Teresa M Ward; Donna Jo McCloskey; Joan K Austin; Patricia A Grady
Journal:  Nurs Outlook       Date:  2019-01-18       Impact factor: 3.250

2.  Developing machine learning-based models to help identify child abuse and neglect: key ethical challenges and recommended solutions.

Authors:  Aviv Y Landau; Susi Ferrarello; Ashley Blanchard; Kenrick Cato; Nia Atkins; Stephanie Salazar; Desmond U Patton; Maxim Topaz
Journal:  J Am Med Inform Assoc       Date:  2022-01-29       Impact factor: 4.497

3.  Utilizing Big Data and Twitter to Discover Emergent Online Communities of Cannabis Users.

Authors:  Peter Baumgartner; Nicholas Peiper
Journal:  Subst Abuse       Date:  2017-06-06

Review 4.  Precision public health to inhibit the contagion of disease and move toward a future in which microbes spread health.

Authors:  David S Thaler; Michael G Head; Andrew Horsley
Journal:  BMC Infect Dis       Date:  2019-02-06       Impact factor: 3.090

5.  The anatomy of electronic patient record ethics: a framework to guide design, development, implementation, and use.

Authors:  Tim Jacquemard; Colin P Doherty; Mary B Fitzsimons
Journal:  BMC Med Ethics       Date:  2021-02-04       Impact factor: 2.652

6.  Considerations for an integrated population health databank in Africa: lessons from global best practices.

Authors:  Jude O Igumbor; Edna N Bosire; Marta Vicente-Crespo; Ehimario U Igumbor; Uthman A Olalekan; Tobias F Chirwa; Sam M Kinyanjui; Catherine Kyobutungi; Sharon Fonn
Journal:  Wellcome Open Res       Date:  2021-08-23

7.  Will Big Data and personalized medicine do the gender dimension justice?

Authors:  Antonio Carnevale; Emanuela A Tangari; Andrea Iannone; Elena Sartini
Journal:  AI Soc       Date:  2021-06-01

8.  Examination and diagnosis of electronic patient records and their associated ethics: a scoping literature review.

Authors:  Tim Jacquemard; Colin P Doherty; Mary B Fitzsimons
Journal:  BMC Med Ethics       Date:  2020-08-24       Impact factor: 2.652

9.  Algorithmic prediction of HIV status using nation-wide electronic registry data.

Authors:  Magnus G Ahlström; Andreas Ronit; Lars Haukali Omland; Søren Vedel; Niels Obel
Journal:  EClinicalMedicine       Date:  2019-11-05
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.