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In order to comply with California’s End of Life Option Act, healthcare organizations must post their medical aid in dying (AID) policy on their publicly accessible website. We analyzed available policies for whether organizations choose to participate in AID and whether organizations add restrictions to or conditions of participation for healthcare providers or patients that are not contained in the text of the law. Our research demonstrates that healthcare organizations, most of them private, mediate medical decision-making rights granted by the state. This chapter focuses on a few organizations’ AID policies to illustrate this process, and demonstrates how employment contracts with healthcare professionals and medical staff bylaws and staff privileges for physicians constrain involvement in AID and affect the physician–patient relationship. This chapter argues that the spread of AID across the United States is mostly a symbolic victory for patient rights advocates because in practice, this option is not available to many patients due to healthcare organizations’ policies. This chapter concludes by suggesting changes to informed consent practices so that seriously ill patients are informed about whether their current care providers participate in AID before the patients would need to make the request, so they can find new doctors if this is an end-of-life option they wish to pursue.
Although linked fate has been recognized as a driving force in the politics of various identity groups, should this theoretical framework be applied to queer politics? I ask, what are the outcomes and dynamics of linked fate among members of the queer community? How does linked fate shape queer political participation? Is the concept an adequate indicator of politicized queer identity? Drawing on data from the Collaborative Multiracial Post-Election Survey, I uncover widespread linked fate among queer Americans, with significant variation along the lines of intersectional identity. Linked fate can motivate participation, but more powerfully shapes participation beyond the ballot box. I close by calling for a queer-specific metric of linked fate that accounts for several dimensions of queer political identity. As the queer community grows increasingly salient in US party politics, this study identifies avenues for future research into this diverse population.
Chapter 5 takes stock and considers the bigger picture in normative ethics. I first make explicit the analogy to the three strategies outlined in Chapter 1 and what we can learn from this about the analogous strategies in ethics. I discuss the charge of gimmickyness against conseqentializing and deontologizing, arguing that these algorithms in ethics are more plausible than similar ones in science. Still, I acknowledge the need for case studies, arguing that, even though much has been missing so far, we have a very strong case study in Parfit and that, due to the completeness of moral theories, this might already establish more than one might think at first sight. Next, I draw a map of underdetermination in ethics, assessing each version of the thesis that has been identified for the scientific realm in Chapter 1 in terms of its status in ethics. To finish, I outlinethe three most important impacts of moral underdetermination for the future of normative moral theorizing, having to do with falsification, the role of theoretical virtues, and the justification of moral theorizing itself.
The ability of private law to shape health care and public health is evident in the effects that tort law had on improving patient safety in anesthesiology and curtailing the marketing of tobacco products. One would think of health care costs as a fertile area for litigation, for many reasons: widespread provider of opportunism that invites legal challenges under a number of theories; the considerable resources that payers and health policy philanthropies have available to invest in litigation strategies; and the high stakes involved in a large industry that is unusually aggressive in the chase for consumer and health insurance dollars. One can find numerous examples of parties pursuing legal action to lower costs, often successfully. But what is striking about these cases is how isolated they are – largely individual, uncoordinated efforts – and how they have failed to meaningfully curtail provider excesses. Most tellingly, the problem of balance billing by out-of-network physicians never gave rise to significant litigation and was resolved by Congressional action that, ironically, incorporated existing common law doctrines.
This paper reviews instances of provider opportunism to obtain higher prices, including contriving to bill “charges” rather than accepting market prices for services; “upcoding” for services by overstating the amount of work involved; and consolidation to achieve market concentration and power vis-a-vis payers. It then discusses available legal theories to remedy such conduct and inventories efforts to invoke them. Finally, it applies political science theories to analyze potential explanations for the dearth of litigation in this area.
Chapter 7 discussesa novel position in metaethics that the skeptical argument might give rise to: constructive deonticism. This position is structurally analogous to one of the most discussed anti-realist positions in science, Bas van Fraassen’s constructive empiricism. I start with an overview of van Fraassen’s view, discussing both its most important features and how it relates to its main rivals, scientific realism and logical positivism. Next, I flesh out the new position in ethics, focussing on the pragmatic understanding of moral explanation that it entails. Following this, I discuss how constructive deonticism should be classified as a metaethical position. I show that it is clearly not part of the expressivist family and at most half error theory (or fictionalism). However, the position is arguably not what realists are looking for either, instead prompting us to rethink how the metaethical realism debate has been framed. Finally, I point out what I consider to be the two most important challenges, i.e., whether we can draw such a sharp distinction bewteen deontic and explanatory claims and whether the position is a stable one.
In the State of Ohio, the electric regulatory landscape permits local governments to become energy suppliers to residents and small businesses through community choice aggregation (CCA). Some CCAs provide enrollees 100% renewable electricity. Concurrently, the federal government offers an income tax credit (ITC) for the purchase of a solar array. With policy incentives, it is important to ensure they encourage behavior beyond the baseline scenario without the ITC. This is known as “additionality.” Renewable aggregation programs may crowd out the benefits of the ITC, violating additionality. This paper assesses additionality of the ITC in the context of Ohio’s CCA programs. The actual additionality can depend on whether renewable energy is already being supplied to the site of a solar array. Hence, we study the relationship between CCA and solar adoption probability to determine whether tax incentives are additional. Using panel data methods and post-estimation simulations, we discern if additionality is violated where these programs overlap. We find aggregation programs increase the probability of solar adoption and that $0.79 of every dollar spent on the income tax credit in Ohio is non-additional. This will help policymakers determine the efficacy of funds allocated to their programs.
Helminth infection is highly prevalent in indigenous chickens reared in semi-scavenging/ scavenging systems in Bangladesh. Here, we estimated the prevalence of gizzard worm infection in indigenous chickens, the detection of the worm-induced pathologies, the development of ex vivo cultural protocol, and anthelmintic efficacy. We randomly collected and examined 390 chickens and isolated worms from the gizzard and proventriculus. The isolated worms were identified as Cheilospirura hamulosa Diesing, 1861. The overall prevalence of C. hamulosa was 33.1% (129 out of 390). Prevalence of the worm was almost similar in both sexes but significantly (p <0.05) higher in adult chickens (44.3%) and in the summer season (47.1%). In heavy infections, C. hamulosa destroyed the muscular layer of the gizzard. The presence of brown necrotic tissues and curd-like caseous materials was detected in the affected gizzards. In severe cases, the horny lining of the gizzard was inflamed, necrotized and marked by multiple holes and brick-red colored spots. Liquefied, fetid materials oozed out from the muscular layer in extensive cases. Histopathological examination showed marked infiltrations of eosinophils. In serum-supplemented M199 and DMEM, adult C. hamulosa survived well and reproduced. Levamisole (LEV) and ivermectin (IVM) efficiently killed the worm. However, albendazole (ABZ), mebendazole (MBZ) and piperazine (PPZ) did not kill the worms. Our results suggest that C. hamulosa is highly prevalent in semi-scavenging chickens in Bangladesh. LEV and IVM can be used to treat and control the infection in chickens.
This study focused on the effect of the cognitive behavioural therapy (CBT) combined with aripiprazole on cognitive functions and psychological state of schizophrenia patients. Seventy-eight schizophrenia patients were divided into two groups. One group received aripiprazole with conventional nursing treatment for 3 months (control group, n = 39), and the other received aripiprazole with CBT for 3 months (observation group, n = 39) (1 session per week, each session lasting 60 min. In the two groups before and after treatment, the severity of symptoms was evaluated using the Psychiatric Symptom Rating Scale (BPRS). Cognitive function was assessed with the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS). The Positive and Negative Symptom Scale (PANSS) was utilised to evaluate mental status, while the Generalised Self-Efficacy Scale (GSES) measured psychological state. Additionally, the quality of life was assessed using the General Quality of Life Inventory-74 (GQOLI-74). In the final analysis, post-treatment efficacy and complications for the two groups were counted. Both groups showed significant improvements: BPRS and PANSS scores decreased, while RBANS, GSES, and GQOLI-74 scores increased. The observation group showed greater improvements than the control group. The total improvement rate was 89.74% (35/39) in the observation group, higher than the 71.79% (28/39) in the control group. The complication rate was 33.33% (13/39) in the observation group and 38.46% (15/39) in the control group. The treatment of CBT combined with aripiprazole for schizophrenia has a significantly positive effect on the cognitive functions and psychological state of patients.
Mothers living in low-income families are more likely to experience depressive symptoms and parenting stress which in turn can undermine mother–child interactions adversely influencing child outcomes. Previous studies demonstrate that social support is beneficial for low-income mothers to fulfill caregiving responsibilities and promote positive child outcomes. However, the longitudinal application of the Family Stress Model with protective factors remains unexplored in the literature. Thus, we examined the association between parenting stress and depressive symptoms at year 1 with harsh and responsive parenting at year 3. Then, we examined whether parenting practices at year 3 predicted child outcomes at year 5 and the main and moderating effects of social support at year 1 and year 3 on parenting and child outcomes. The sample included 1,968 mothers from the Future of Families and Child Wellbeing Study. Results showed that parenting stress significantly predicted harsh parenting. Harsh parenting was associated with more internalizing behavior problems and decreased adaptive social behavior. Responsive parenting was associated only with fewer internalizing behavior problems. The main effects of social support on responsive and harsh parenting and child outcomes were significant. Specific intervention programs targeted at reducing parenting stress, enhancing parenting skills, and improving the social support network should be designed to support mothers in the context of economic adversity.
Air pollution exposure and its health effects are a central concern of environmental epigenetic research with birth cohorts. This article explores why researchers have turned to the placenta as a research object to study the dynamic interactions between in utero exposure to air pollution and future child health. Drawing on Science and Technology Studies, particularly the bio-object concept, this article analyses the transformation of the placenta into a technologically manipulated postgenomic bio-object through scientific discourse and practice. Building on ethnographic fieldwork conducted at an institute of epidemiology and public health in Spain, we analyse how researchers deal with the tension between the placenta’s promises for epigenetic research and the practical research realities in postgenomic sciences. First, researchers discursively call upon the placenta as a suitable research object that embodies air pollution exposure and becomes entangled with and responds to this exposure via epigenetic changes. Studying the placenta promises to elucidate the temporally dynamic and environmentally embedded process of disease development as one of postgenomics’ core epistemic concerns. Second, in practice, however, accessing and preparing the postpartum placenta for epigenetic analysis defies its promise as a postgenomic bio-object. The constraints of research with birth cohorts, such as only having access to the postpartum placenta at birth, limit what researchers can know about the dynamic process of disease development. Third, we show how researchers deal with these limitations by assembling additional data in and around this organ to recontextualise the epigenetic analysis performed in the postpartum placenta and revive its postgenomic character. We conclude by discussing how ethnographies of epistemic practices provide entry points to collaboratively reflect upon the theoretical and methodological opportunities and challenges in birth cohort research to study biosocial dynamics. We suggest avenues for using qualitative social science perspectives for future biosocial research and collaboration between the social and life sciences.
Chapter 4 looks at two recent projects that aim to establish far more radical conclusions than Parfit, so-called consequentializing and deontologizing. Proponents of these projects try to come up with a simple mechanism to produce deontically equivalent counterparts to any consequentialist or non-consequentialist theory. I first explain how the two projects work on a technical level, that is, what steps are required to achieve deontic equivalence. I then reject several interpretations of the results of these projects, from the idea that we are all consequentialists (or deontologists) to the idea that consequentialism (or deontology) turn out to be empty traditions. Finally, I introduce the underdetermination interpretation of these projects and argue why it is to be preferred to yet another interpretation, the notational variants interpretation. If consequentializing and deontologizing can be interpreted in this way, we are presented with a much more far-reaching version of moral underdetermination.
This essay considers the “great” status of Shah ‘Abbās I, the most consequential Safavid ruler, by comparing European descriptions to his portrayal in the Persian-language sources. While both depict him as energetic, resolute, and unadorned in attire and demeanor, European sources present him primarily as an empire builder while Persian-language works focus on his role as a warrior on horseback, fighting external enemies and putting down domestic revolts. Neither accounts ignore the violence that came with absolute power, but while Europeans viewed such violence as an unfortunate byproduct of power, Persian chronicles celebrate ‘Abbās as a ghāzi warrior, merciless in his efforts to root out heretics and unbelievers. The surviving image of the shah as a “great” ruler was first reported by European visitors and is primarily a composite of the way they depicted him – as a Renaissance prince and determined empire builder who remained close to his subjects and their concerns.
Decentralized research has many advantages; however, little is known about the representativeness of a source population in decentralized studies. We recruited participants aged 18-64 years from four states from June to December 2022 for a prospective cohort study to assess viral epidemiology. Our aim was to determine the association between age, gender, race/ethnicity, rurality, and socioeconomic status (SES) on study participation in a decentralized prospective cohort study.
Methods:
We consented 9,286 participants from 231,099 (4.0%) adults with the mean age of 45.6 years (±12.0). We used an electronic decentralized approach for recruitment. Consented participants were more likely to be non-Hispanic White, female, older, urban residents, have more health conditions, and possessed higher socioeconomic status (SES) compared to those non-consented.
Results:
We observed an interaction between SES and race-ethnicity on the odds of consent (P = 0.006). Specifically, SES did not affect non-Hispanic white participation rates(OR 1.24 95% CI 1.16 – 1.32] for the highest SES quartile compared to those with the lowest SES quartile) as much as it did participants combined across the other races (OR 1.73; 95% CI 1.45 – 2.98])
Conclusion:
The relationship between SES and consent rates might be disproportionately greater in historically disadvantaged groups, compared to non-Hispanic White. It suggests that instead of focusing on enrollment of specific minority groups in research, there is value in future research exploring and addressing the diversity of barriers to trials within minority groups. Our study highlights that decentralized studies need to address social determinants of health, especially in under-resourced populations.
States are in a difficult position. Health care costs are spiraling up and becoming increasingly unaffordable for consumers and businesses. Yet political and practical barriers constrain the government’s ability to contain health care costs through traditional regulatory channels. This Essay explores how some states have tried to maneuver around these constraints and contain costs through their contracts with health insurers and providers. We focus on three examples of state influence: health-insurance marketplaces, market-based public health insurance options, and state employee health plans. The Essay examines the impacts and limitations of state purchasing activities vis-a-vis regulatory alternatives, and discusses the opportunities and challenges that states face containing costs as purchasers. It ultimately finds that contracting solutions offer only modest political benefits over traditional regulatory approaches, and are significantly limited by consolidation in the health care provider market. Further, state officials may be hesitant to wield their market power to extract cost savings if it might result in fewer choices for consumers. However, these measures can achieve incremental savings in the right circumstances and, in the face of strong political opposition to broader health care reforms, states will need to use all levers available to hold the line on health care costs until more legislative breakthroughs can be made.
In the aftermath of the Supreme Court’s decision in Dobbs v. Jackson Women’s Health Organization, several corporations signaled their support for reproductive rights by announcing expanded abortion care coverage and/or travel stipends for employees who are forced to travel out of state to receive care, including abortion care. While such moves may be celebrated and recognized as a commitment to pro-choice politics, these decisions require scrutiny and suspicion. This article details why.
Part I of this paper will discuss the corporate response to Dobbs. It will discuss the type of benefits that corporations offered, and the class of employees these benefits were offered to (for instance, “independent contractors” were mostly excluded from availing of these benefits). Part II will discuss the movement for reproductive rights, some of the harms it reinforced, and the criticisms it received from the Reproductive Justice movement. Against this backdrop, Part III will discuss the possible intentions behind corporations conferring these benefits, including those related to staff retention, microeconomic logics, and DEI efforts. It will review them against large corporations’ histories of (not) providing reproductive supports, including a living wage, paid leave, sick leave, and childcare. It will also analyze some of the evidence in the public sphere that shows the roles some of these large corporations have played in supporting antiabortion agendas and politicians. Part IV will discuss the long-term harms that this new crop of workplace policies and benefits might create. Mainly, it will discuss how the provision of abortion care without other reproductive supports reemphasizes a reproductive rights approach despite its criticisms, which were highlighted by the Reproductive Justice movement. For instance, this section will discuss the expanding role corporations are assuming in providing healthcare, and how that may lead to the exclusion of certain historically marginalized classes of workers and people. It will also discuss the impact of these policies on the deprioritization of certain types of care, which have been overlooked for decades, including gender-affirming care and fertility treatments. Part V will suggest a few steps corporations can take to mitigate the harm created by Dobbs.
Generative artificial intelligence (AI) systems, notably ChatGPT, have emerged in legal practice, facilitating the completion of tasks, ranging from electronic communications to the drafting of documents. The generative capabilities of these systems underscore the duty of lawyers to competently represent their clients by keeping abreast of technological developments that can enhance the efficiency and effectiveness of their work. At the same time, the processing of clients’ information through generative AI systems threatens to compromise their confidentiality if disclosed to third parties, including the systems’ providers. The present paper aims to determine the impact of the use of generative AI systems by lawyers on the duties of competence and confidentiality. The findings derive from the application of doctrinal and empirical research on the legal practice and its digitalisation in Luxembourg. The paper finally reflects on the integration of generative AI systems in legal practice to raise the quality of legal services for clients.