Clint Parker - Academia.edu (original) (raw)

Papers by Clint Parker

Research paper thumbnail of ETHICS CASE Disclosing Information about the Risk of Inherited Disease

Mrs. Durham was diagnosed with an invasive epithelial ovarian cancer and, in conjunction with con... more Mrs. Durham was diagnosed with an invasive epithelial ovarian cancer and, in conjunction with conversations about her treatment, was offered genetic testing for the BRCA1 and BRCA2 mutations. It was revealed that she carried a harmful BRCA1 mutation that is known to increase the lifetime risk of breast and ovarian cancer significantly. Once the results came back, her oncologist brought up the option of a prophylactic mastectomy and advised her to inform her living relatives of the results of the test. Mrs. Durham's primary care physician, Dr. Bartlett, expected she would do so, too. At her first appointment after the diagnosis, Dr. Bartlett asked Mrs. Durham how she was holding up and how her sister, Mrs. Weir-her only living family member and also one of Dr. Bartlett's patients-had taken the news. "Oh. Well, I haven't told her." "Are you going to?" asked Dr. Bartlett. Mrs. Durham responded, "You know we haven't spoken in quite some time, and I can't imagine making this the topic of our first conversation." "Yes, I know…but I think this is important information that may affect her health." Mrs. Durham sighed. "We're estranged, for one thing, and for another, I want to keep my cancer private. I don't want people knowing I'm sick and pitying me." Dr. Bartlett felt pulled in two directions-his obligation to respect Mrs. Durham's wishes and protect her privacy conflicted with his obligation to promote Mrs. Weir's health. BRCA1 mutations are not "reportable" illnesses like HIV and tuberculosis, so he was not compelled by law to break Mrs. Durham's confidentiality. Dr. Bartlett considered how he might be able to encourage Mrs. Durham's sister to be tested for the BRCA mutations while preserving Mrs. Durham's confidentiality.

Research paper thumbnail of Disclosing Information about the Risk of Inherited Disease

AMA journal of ethics, Sep 1, 2015

Mrs. Durham was diagnosed with an invasive epithelial ovarian cancer and, in conjunction with con... more Mrs. Durham was diagnosed with an invasive epithelial ovarian cancer and, in conjunction with conversations about her treatment, was offered genetic testing for the BRCA1 and BRCA2 mutations. It was revealed that she carried a harmful BRCA1 mutation that is known to increase the lifetime risk of breast and ovarian cancer significantly. Once the results came back, her oncologist brought up the option of a prophylactic mastectomy and advised her to inform her living relatives of the results of the test. Mrs. Durham's primary care physician, Dr. Bartlett, expected she would do so, too. At her first appointment after the diagnosis, Dr. Bartlett asked Mrs. Durham how she was holding up and how her sister, Mrs. Weir-her only living family member and also one of Dr. Bartlett's patients-had taken the news. "Oh. Well, I haven't told her." "Are you going to?" asked Dr. Bartlett. Mrs. Durham responded, "You know we haven't spoken in quite some time, and I can't imagine making this the topic of our first conversation." "Yes, I know…but I think this is important information that may affect her health." Mrs. Durham sighed. "We're estranged, for one thing, and for another, I want to keep my cancer private. I don't want people knowing I'm sick and pitying me." Dr. Bartlett felt pulled in two directions-his obligation to respect Mrs. Durham's wishes and protect her privacy conflicted with his obligation to promote Mrs. Weir's health. BRCA1 mutations are not "reportable" illnesses like HIV and tuberculosis, so he was not compelled by law to break Mrs. Durham's confidentiality. Dr. Bartlett considered how he might be able to encourage Mrs. Durham's sister to be tested for the BRCA mutations while preserving Mrs. Durham's confidentiality.

Research paper thumbnail of OUP accepted manuscript

Journal of Medicine and Philosophy, 2018

Research paper thumbnail of Bioethical Boundaries, Critiques of Current Paradigms, and the Importance of Transparency

The Journal of Medicine and Philosophy: A Forum for Bioethics and Philosophy of Medicine, 2021

This issue of The Journal of Medicine and Philosophy is dedicated to topics in clinical ethics wi... more This issue of The Journal of Medicine and Philosophy is dedicated to topics in clinical ethics with essays addressing clinician participation in state sponsored execution, duties to decrease ecological footprints in medicine, the concept of caring and its relationship to conscientious refusal, the dilemmas involved in dual use research, a philosophical and practical critique of principlism, conundrums that arise when applying surrogate decision-making models to patients with moderate intellectual disabilities, the phenomenology of chronic disease, and ethical concerns surrounding the use of artificial intelligence in medicine. Throughout the issue, the themes of conceptual and moral boundaries in bioethics, critiques of current clinical ethics paradigms, and the importance of transparency are prominent.

Research paper thumbnail of Below the Surface of Clinical Ethics

The Journal of Medicine and Philosophy: A Forum for Bioethics and Philosophy of Medicine

Often lurking below the surface of many clinical ethical issues are questions regarding backgroun... more Often lurking below the surface of many clinical ethical issues are questions regarding background metaphysical, epistemological, meta-ethical, and political beliefs. In this issue, authors critically examine the effects of background beliefs on conscientious objection, explore ethical issues through the lenses of particular theoretical approaches like pragmatism and intersectional theory, rigorously explore the basic concepts at play within the patient safety movement, offer new theoretical approaches to old problems involving decision making for patients with dementia, explicate and explore the problems and promises of machine learning in medicine, and offer us a non-rights-based argument for the just distribution of healthcare resources.

Research paper thumbnail of Against Multiplying Clinical Ethics Standards without Necessity: The Case for Parsimony in Evaluating Decision-making Capacity

The American Journal of Bioethics

Research paper thumbnail of ETHICS CASE Disclosing Information about the Risk of Inherited Disease

Research paper thumbnail of Author's response to reviews Title: Pain as a Global Public Health Priority Authors

We are pleased to resubmit a revised version of our manuscript entitled "Pain as a Global Public ... more We are pleased to resubmit a revised version of our manuscript entitled "Pain as a Global Public Health Priority." We found the Reviewers' suggestions inordinately helpful, and have endeavored to incorporate them into the revised manuscript. Pursuant to the author instructions for revision and resubmission, we have included in this cover letter a point-by-point response to the Reviewers' concerns. Please do not hesitate to contact us if we may be of any assistance during this stage of the review process.

Research paper thumbnail of Head Transplantation and Immortality: When Is Life Worth Living Forever?

The Journal of Medicine and Philosophy: A Forum for Bioethics and Philosophy of Medicine, 2021

Head transplantation fits within the broader conceptual space occupied by transhumanists and othe... more Head transplantation fits within the broader conceptual space occupied by transhumanists and others who seek to extend the lives of human beings indefinitely. It is reasonable to reflect on whether, under what circumstances, and in what ways human immortality would be good. In this paper, I disambiguate the ways in which immortality might be considered a human good and then argue that immortality is neither necessary nor sufficient condition for objective meaning in life. I also argue that mortality is not a necessary condition for objective meaning in life.

Research paper thumbnail of Disclosing Information about the Risk of Inherited Disease

The AMA Journal of Ethic, 2015

Mrs. Durham was diagnosed with an invasive epithelial ovarian cancer and, in conjunction with con... more Mrs. Durham was diagnosed with an invasive epithelial ovarian cancer and, in conjunction with conversations about her treatment, was offered genetic testing for the BRCA1 and BRCA2 mutations. It was revealed that she carried a harmful BRCA1 mutation that is known to increase the lifetime risk of breast and ovarian cancer significantly. Once the results came back, her oncologist brought up the option of a prophylactic mastectomy and advised her to inform her living relatives of the results of the test. Mrs. Durham's primary care physician, Dr. Bartlett, expected she would do so, too. At her first appointment after the diagnosis, Dr. Bartlett asked Mrs. Durham how she was holding up and how her sister, Mrs. Weir-her only living family member and also one of Dr. Bartlett's patients-had taken the news. "Oh. Well, I haven't told her." "Are you going to?" asked Dr. Bartlett. Mrs. Durham responded, "You know we haven't spoken in quite some time, and I can't imagine making this the topic of our first conversation." "Yes, I know…but I think this is important information that may affect her health." Mrs. Durham sighed. "We're estranged, for one thing, and for another, I want to keep my cancer private. I don't want people knowing I'm sick and pitying me." Dr. Bartlett felt pulled in two directions-his obligation to respect Mrs. Durham's wishes and protect her privacy conflicted with his obligation to promote Mrs. Weir's health. BRCA1 mutations are not "reportable" illnesses like HIV and tuberculosis, so he was not compelled by law to break Mrs. Durham's confidentiality. Dr. Bartlett considered how he might be able to encourage Mrs. Durham's sister to be tested for the BRCA mutations while preserving Mrs. Durham's confidentiality.

Research paper thumbnail of The Importance of Clear and Careful Thinking in Clinical Ethics

The Journal of Medicine and Philosophy: A Forum for Bioethics and Philosophy of Medicine, 2021

Clear and careful thinking is an indispensable aid in the pursuit of answers to the difficult eth... more Clear and careful thinking is an indispensable aid in the pursuit of answers to the difficult ethical question faced by clinicians, patients, and families. In this issue of The Journal of Medicine and Philosophy devoted to issues in clinical ethics, the authors engage in this enterprise by reflecting on morally good medical decision making, conscientious objection, presumed consent in organ donation, the permissibility of surrogate decision making, and the failure of legislative limits on the scope of euthanasia in Belgium.

Research paper thumbnail of Religion, Authenticity, and Clinical Ethics Consultation

HEC Forum, 2019

A clinical ethics consultant (CEC) may, at times, be called upon to make independent substantive ... more A clinical ethics consultant (CEC) may, at times, be called upon to make independent substantive moral judgments and then offer justifications for those judgments. A CEC does not act unprofessionally by utilizing background beliefs that are religious in nature to justify those judgments. It is important, however, for a CEC to make such judgments authentically and, when asked, to offer up one’s reasons for why one believes the judgment is true in a transparent fashion.

Research paper thumbnail of The Clinical Ethics Consultant: What Role is There for Religious Beliefs?

Research paper thumbnail of Clinical Ethics Consultation After God: Implications for Advocacy and Neutrality

HEC Forum, 2017

In After God: Morality and Bioethics in a Secular Age, H. Tristram Engelhardt, Jr. explores the b... more In After God: Morality and Bioethics in a Secular Age, H. Tristram Engelhardt, Jr. explores the broad implications for moral reasoning once a culture has lost a God’s-eye perspective. In this paper, I focus on the implications of Engelhardt’s views for clinical ethics consultation. I begin by examining the question of whether clinical ethics consultants (CECs) should advocate a particular viewpoint and/or process during consultations or adopt a neutral stance. I then examine the implications of Engelhardt’s views for this question. Finally, I discuss some of Engelhardt’s foundational ontological, metaphysical, meta-ethical, and epistemological commitments and how these commitments connect to his views on clinical ethics consultation.

Research paper thumbnail of Implications of Christian Truth Claims for Bioethics

Christian Bioethics, 2016

Research paper thumbnail of The Virtue of Integrity in Baruch Brody’s Moral Framework

Philosophy and Medicine

... Brody emphasizes a different sense of integrity—fidelity to values. In particular, Brody is i... more ... Brody emphasizes a different sense of integrity—fidelity to values. In particular, Brody is interested in fidelity to personal values. ... In this section, I will analyze two important objections to Brody's account of integrity. Brody argues that fidelity to core personal values is virtuous. ...

Research paper thumbnail of A Legal and Ethical Analysis of the Effects of Triggering Conditions on Surrogate Decision-Making in End-of-Life Care in the US

HEC forum : an interdisciplinary journal on hospitals' ethical and legal issues, Jan 18, 2015

The central claim of this paper is that American states' use of so-called "triggering co... more The central claim of this paper is that American states' use of so-called "triggering conditions" to regulate surrogate decision-making authority in end-of-life care leaves unresolved a number of important ethical and legal considerations regarding the scope of that authority. The paper frames the issue with a case set in a jurisdiction in which surrogate authority to withdraw life-sustaining treatment is triggered by two specific clinical conditions. The case presents a quandary insofar as the clinical facts do not satisfy the triggering conditions, and yet both the appropriate surrogates and the care team agree that withdrawal of life-sustaining treatment is in the best interest of the patient. The paper surveys applicable law across the 50 states and weighs the arguments for and against the inclusion of such triggering conditions in relevant legal regimes. The paper concludes by assessing the various legal and policy options states have for regulating surrogate deci...

Research paper thumbnail of Conscience and Collective Duties: Do Medical Professionals Have a Collective Duty to Ensure That Their Profession Provides Non-discriminatory Access to All Medical Services?

Journal of Medicine and Philosophy, 2011

Recent debates have led some to question the legitimacy of physicians refusing to provide legally... more Recent debates have led some to question the legitimacy of physicians refusing to provide legally permissible services for reasons of conscience. In this paper, I will explore the question of whether medical professionals have a collective duty to ensure that their profession provides nondiscriminatory access to all medical services. I will argue that they do not. I will also argue for an approach to dealing with intractable moral disagreements between patients and physicians that gives both parties veto power with regards to participation. Finally, I will respond to three objections to allowing physicians broad freedom to act on their consciences: such allowances would violate the conscience of the patient, would lead to unfairness, and would thwart important societal goals.

Research paper thumbnail of Cherry Picking in ESRD: An Ethical Challenge in the Era of Pay for Performance

Seminars in Dialysis, 2011

Research paper thumbnail of When a Mother Changes Her Mind About a DNR

Pediatrics, 2018

Generally, wide latitude is granted to parents when making decisions for their child on the basis... more Generally, wide latitude is granted to parents when making decisions for their child on the basis of the wide acceptance of the special relationship between parent and child and the important role played by parents in the lives of children. However, when high-risk decisions are made, health care teams serve as an important societal safeguard that questions whether a parent is an appropriate decision-maker for their child. Child advocacy is an essential function of the pediatric health care team. In this ethics rounds, we examine a case of an infant with a complex medical condition requiring prolonged hospitalization that results in a clash of understanding between a mother and medical team when the mother abruptly requests removal of life-sustaining treatment. We present an ethical decision-making framework for such cases and examine the impact of barriers and unconscious bias that can exclude parents from their rightful role in directing care for their child.

Research paper thumbnail of ETHICS CASE Disclosing Information about the Risk of Inherited Disease

Mrs. Durham was diagnosed with an invasive epithelial ovarian cancer and, in conjunction with con... more Mrs. Durham was diagnosed with an invasive epithelial ovarian cancer and, in conjunction with conversations about her treatment, was offered genetic testing for the BRCA1 and BRCA2 mutations. It was revealed that she carried a harmful BRCA1 mutation that is known to increase the lifetime risk of breast and ovarian cancer significantly. Once the results came back, her oncologist brought up the option of a prophylactic mastectomy and advised her to inform her living relatives of the results of the test. Mrs. Durham's primary care physician, Dr. Bartlett, expected she would do so, too. At her first appointment after the diagnosis, Dr. Bartlett asked Mrs. Durham how she was holding up and how her sister, Mrs. Weir-her only living family member and also one of Dr. Bartlett's patients-had taken the news. "Oh. Well, I haven't told her." "Are you going to?" asked Dr. Bartlett. Mrs. Durham responded, "You know we haven't spoken in quite some time, and I can't imagine making this the topic of our first conversation." "Yes, I know…but I think this is important information that may affect her health." Mrs. Durham sighed. "We're estranged, for one thing, and for another, I want to keep my cancer private. I don't want people knowing I'm sick and pitying me." Dr. Bartlett felt pulled in two directions-his obligation to respect Mrs. Durham's wishes and protect her privacy conflicted with his obligation to promote Mrs. Weir's health. BRCA1 mutations are not "reportable" illnesses like HIV and tuberculosis, so he was not compelled by law to break Mrs. Durham's confidentiality. Dr. Bartlett considered how he might be able to encourage Mrs. Durham's sister to be tested for the BRCA mutations while preserving Mrs. Durham's confidentiality.

Research paper thumbnail of Disclosing Information about the Risk of Inherited Disease

AMA journal of ethics, Sep 1, 2015

Mrs. Durham was diagnosed with an invasive epithelial ovarian cancer and, in conjunction with con... more Mrs. Durham was diagnosed with an invasive epithelial ovarian cancer and, in conjunction with conversations about her treatment, was offered genetic testing for the BRCA1 and BRCA2 mutations. It was revealed that she carried a harmful BRCA1 mutation that is known to increase the lifetime risk of breast and ovarian cancer significantly. Once the results came back, her oncologist brought up the option of a prophylactic mastectomy and advised her to inform her living relatives of the results of the test. Mrs. Durham's primary care physician, Dr. Bartlett, expected she would do so, too. At her first appointment after the diagnosis, Dr. Bartlett asked Mrs. Durham how she was holding up and how her sister, Mrs. Weir-her only living family member and also one of Dr. Bartlett's patients-had taken the news. "Oh. Well, I haven't told her." "Are you going to?" asked Dr. Bartlett. Mrs. Durham responded, "You know we haven't spoken in quite some time, and I can't imagine making this the topic of our first conversation." "Yes, I know…but I think this is important information that may affect her health." Mrs. Durham sighed. "We're estranged, for one thing, and for another, I want to keep my cancer private. I don't want people knowing I'm sick and pitying me." Dr. Bartlett felt pulled in two directions-his obligation to respect Mrs. Durham's wishes and protect her privacy conflicted with his obligation to promote Mrs. Weir's health. BRCA1 mutations are not "reportable" illnesses like HIV and tuberculosis, so he was not compelled by law to break Mrs. Durham's confidentiality. Dr. Bartlett considered how he might be able to encourage Mrs. Durham's sister to be tested for the BRCA mutations while preserving Mrs. Durham's confidentiality.

Research paper thumbnail of OUP accepted manuscript

Journal of Medicine and Philosophy, 2018

Research paper thumbnail of Bioethical Boundaries, Critiques of Current Paradigms, and the Importance of Transparency

The Journal of Medicine and Philosophy: A Forum for Bioethics and Philosophy of Medicine, 2021

This issue of The Journal of Medicine and Philosophy is dedicated to topics in clinical ethics wi... more This issue of The Journal of Medicine and Philosophy is dedicated to topics in clinical ethics with essays addressing clinician participation in state sponsored execution, duties to decrease ecological footprints in medicine, the concept of caring and its relationship to conscientious refusal, the dilemmas involved in dual use research, a philosophical and practical critique of principlism, conundrums that arise when applying surrogate decision-making models to patients with moderate intellectual disabilities, the phenomenology of chronic disease, and ethical concerns surrounding the use of artificial intelligence in medicine. Throughout the issue, the themes of conceptual and moral boundaries in bioethics, critiques of current clinical ethics paradigms, and the importance of transparency are prominent.

Research paper thumbnail of Below the Surface of Clinical Ethics

The Journal of Medicine and Philosophy: A Forum for Bioethics and Philosophy of Medicine

Often lurking below the surface of many clinical ethical issues are questions regarding backgroun... more Often lurking below the surface of many clinical ethical issues are questions regarding background metaphysical, epistemological, meta-ethical, and political beliefs. In this issue, authors critically examine the effects of background beliefs on conscientious objection, explore ethical issues through the lenses of particular theoretical approaches like pragmatism and intersectional theory, rigorously explore the basic concepts at play within the patient safety movement, offer new theoretical approaches to old problems involving decision making for patients with dementia, explicate and explore the problems and promises of machine learning in medicine, and offer us a non-rights-based argument for the just distribution of healthcare resources.

Research paper thumbnail of Against Multiplying Clinical Ethics Standards without Necessity: The Case for Parsimony in Evaluating Decision-making Capacity

The American Journal of Bioethics

Research paper thumbnail of ETHICS CASE Disclosing Information about the Risk of Inherited Disease

Research paper thumbnail of Author's response to reviews Title: Pain as a Global Public Health Priority Authors

We are pleased to resubmit a revised version of our manuscript entitled "Pain as a Global Public ... more We are pleased to resubmit a revised version of our manuscript entitled "Pain as a Global Public Health Priority." We found the Reviewers' suggestions inordinately helpful, and have endeavored to incorporate them into the revised manuscript. Pursuant to the author instructions for revision and resubmission, we have included in this cover letter a point-by-point response to the Reviewers' concerns. Please do not hesitate to contact us if we may be of any assistance during this stage of the review process.

Research paper thumbnail of Head Transplantation and Immortality: When Is Life Worth Living Forever?

The Journal of Medicine and Philosophy: A Forum for Bioethics and Philosophy of Medicine, 2021

Head transplantation fits within the broader conceptual space occupied by transhumanists and othe... more Head transplantation fits within the broader conceptual space occupied by transhumanists and others who seek to extend the lives of human beings indefinitely. It is reasonable to reflect on whether, under what circumstances, and in what ways human immortality would be good. In this paper, I disambiguate the ways in which immortality might be considered a human good and then argue that immortality is neither necessary nor sufficient condition for objective meaning in life. I also argue that mortality is not a necessary condition for objective meaning in life.

Research paper thumbnail of Disclosing Information about the Risk of Inherited Disease

The AMA Journal of Ethic, 2015

Mrs. Durham was diagnosed with an invasive epithelial ovarian cancer and, in conjunction with con... more Mrs. Durham was diagnosed with an invasive epithelial ovarian cancer and, in conjunction with conversations about her treatment, was offered genetic testing for the BRCA1 and BRCA2 mutations. It was revealed that she carried a harmful BRCA1 mutation that is known to increase the lifetime risk of breast and ovarian cancer significantly. Once the results came back, her oncologist brought up the option of a prophylactic mastectomy and advised her to inform her living relatives of the results of the test. Mrs. Durham's primary care physician, Dr. Bartlett, expected she would do so, too. At her first appointment after the diagnosis, Dr. Bartlett asked Mrs. Durham how she was holding up and how her sister, Mrs. Weir-her only living family member and also one of Dr. Bartlett's patients-had taken the news. "Oh. Well, I haven't told her." "Are you going to?" asked Dr. Bartlett. Mrs. Durham responded, "You know we haven't spoken in quite some time, and I can't imagine making this the topic of our first conversation." "Yes, I know…but I think this is important information that may affect her health." Mrs. Durham sighed. "We're estranged, for one thing, and for another, I want to keep my cancer private. I don't want people knowing I'm sick and pitying me." Dr. Bartlett felt pulled in two directions-his obligation to respect Mrs. Durham's wishes and protect her privacy conflicted with his obligation to promote Mrs. Weir's health. BRCA1 mutations are not "reportable" illnesses like HIV and tuberculosis, so he was not compelled by law to break Mrs. Durham's confidentiality. Dr. Bartlett considered how he might be able to encourage Mrs. Durham's sister to be tested for the BRCA mutations while preserving Mrs. Durham's confidentiality.

Research paper thumbnail of The Importance of Clear and Careful Thinking in Clinical Ethics

The Journal of Medicine and Philosophy: A Forum for Bioethics and Philosophy of Medicine, 2021

Clear and careful thinking is an indispensable aid in the pursuit of answers to the difficult eth... more Clear and careful thinking is an indispensable aid in the pursuit of answers to the difficult ethical question faced by clinicians, patients, and families. In this issue of The Journal of Medicine and Philosophy devoted to issues in clinical ethics, the authors engage in this enterprise by reflecting on morally good medical decision making, conscientious objection, presumed consent in organ donation, the permissibility of surrogate decision making, and the failure of legislative limits on the scope of euthanasia in Belgium.

Research paper thumbnail of Religion, Authenticity, and Clinical Ethics Consultation

HEC Forum, 2019

A clinical ethics consultant (CEC) may, at times, be called upon to make independent substantive ... more A clinical ethics consultant (CEC) may, at times, be called upon to make independent substantive moral judgments and then offer justifications for those judgments. A CEC does not act unprofessionally by utilizing background beliefs that are religious in nature to justify those judgments. It is important, however, for a CEC to make such judgments authentically and, when asked, to offer up one’s reasons for why one believes the judgment is true in a transparent fashion.

Research paper thumbnail of The Clinical Ethics Consultant: What Role is There for Religious Beliefs?

Research paper thumbnail of Clinical Ethics Consultation After God: Implications for Advocacy and Neutrality

HEC Forum, 2017

In After God: Morality and Bioethics in a Secular Age, H. Tristram Engelhardt, Jr. explores the b... more In After God: Morality and Bioethics in a Secular Age, H. Tristram Engelhardt, Jr. explores the broad implications for moral reasoning once a culture has lost a God’s-eye perspective. In this paper, I focus on the implications of Engelhardt’s views for clinical ethics consultation. I begin by examining the question of whether clinical ethics consultants (CECs) should advocate a particular viewpoint and/or process during consultations or adopt a neutral stance. I then examine the implications of Engelhardt’s views for this question. Finally, I discuss some of Engelhardt’s foundational ontological, metaphysical, meta-ethical, and epistemological commitments and how these commitments connect to his views on clinical ethics consultation.

Research paper thumbnail of Implications of Christian Truth Claims for Bioethics

Christian Bioethics, 2016

Research paper thumbnail of The Virtue of Integrity in Baruch Brody’s Moral Framework

Philosophy and Medicine

... Brody emphasizes a different sense of integrity—fidelity to values. In particular, Brody is i... more ... Brody emphasizes a different sense of integrity—fidelity to values. In particular, Brody is interested in fidelity to personal values. ... In this section, I will analyze two important objections to Brody's account of integrity. Brody argues that fidelity to core personal values is virtuous. ...

Research paper thumbnail of A Legal and Ethical Analysis of the Effects of Triggering Conditions on Surrogate Decision-Making in End-of-Life Care in the US

HEC forum : an interdisciplinary journal on hospitals' ethical and legal issues, Jan 18, 2015

The central claim of this paper is that American states' use of so-called "triggering co... more The central claim of this paper is that American states' use of so-called "triggering conditions" to regulate surrogate decision-making authority in end-of-life care leaves unresolved a number of important ethical and legal considerations regarding the scope of that authority. The paper frames the issue with a case set in a jurisdiction in which surrogate authority to withdraw life-sustaining treatment is triggered by two specific clinical conditions. The case presents a quandary insofar as the clinical facts do not satisfy the triggering conditions, and yet both the appropriate surrogates and the care team agree that withdrawal of life-sustaining treatment is in the best interest of the patient. The paper surveys applicable law across the 50 states and weighs the arguments for and against the inclusion of such triggering conditions in relevant legal regimes. The paper concludes by assessing the various legal and policy options states have for regulating surrogate deci...

Research paper thumbnail of Conscience and Collective Duties: Do Medical Professionals Have a Collective Duty to Ensure That Their Profession Provides Non-discriminatory Access to All Medical Services?

Journal of Medicine and Philosophy, 2011

Recent debates have led some to question the legitimacy of physicians refusing to provide legally... more Recent debates have led some to question the legitimacy of physicians refusing to provide legally permissible services for reasons of conscience. In this paper, I will explore the question of whether medical professionals have a collective duty to ensure that their profession provides nondiscriminatory access to all medical services. I will argue that they do not. I will also argue for an approach to dealing with intractable moral disagreements between patients and physicians that gives both parties veto power with regards to participation. Finally, I will respond to three objections to allowing physicians broad freedom to act on their consciences: such allowances would violate the conscience of the patient, would lead to unfairness, and would thwart important societal goals.

Research paper thumbnail of Cherry Picking in ESRD: An Ethical Challenge in the Era of Pay for Performance

Seminars in Dialysis, 2011

Research paper thumbnail of When a Mother Changes Her Mind About a DNR

Pediatrics, 2018

Generally, wide latitude is granted to parents when making decisions for their child on the basis... more Generally, wide latitude is granted to parents when making decisions for their child on the basis of the wide acceptance of the special relationship between parent and child and the important role played by parents in the lives of children. However, when high-risk decisions are made, health care teams serve as an important societal safeguard that questions whether a parent is an appropriate decision-maker for their child. Child advocacy is an essential function of the pediatric health care team. In this ethics rounds, we examine a case of an infant with a complex medical condition requiring prolonged hospitalization that results in a clash of understanding between a mother and medical team when the mother abruptly requests removal of life-sustaining treatment. We present an ethical decision-making framework for such cases and examine the impact of barriers and unconscious bias that can exclude parents from their rightful role in directing care for their child.