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Four Models of the Physician-Patient Relationship

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Four Models of the Physician-Patient Relationship
Emanuel, Ezekiel J; Emanuel, Linda L
JAMA; Apr 22, 1992; 267, 16; Research Library
pg. 2221
Reproduced with permission of the copyright owner. Further reproduction prohibited without permission.
Reproduced with permission of the copyright owner. Further reproduction prohibited without permission.
Reproduced with permission of the copyright owner. Further reproduction prohibited without permission.
Reproduced with permission of the copyright owner. Further reproduction prohibited without permission.
Reproduced with permission of the copyright owner. Further reproduction prohibited without permission.
... Model is a hypothetical description of a complex entity or process (WordWeb Dictionary, 2006 Emanuel and Emanuel (1992) Before exploring the model adopted for the study, an examination of other models that were not initially captured in chapter one is attempted. A review by Oprea (2009:125-135) offers some insights. ...
... The deliberative model gives more room for turn-taking through its negotiating conversation than the other models in the categorisation of Emanuel and Emanuel (1992) model of DPR. This is in accordance with its deliberative tendency. ...
... models. The consensus among scholars (likeEmanuel and Emanuel, 1992, Pellegrino, 2006;Oprea, 2009) is that the adoption of the paternalistic pattern in doctor-patient interaction should be discarded. For instance, some critics of the paternalistic model assumed that it is capable of reducing respect for patients' opinion. ...
Thesis
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Neurologist-patient interaction, an important hospital situation that focuses on the care for people with language-related disorders or impairments, has attracted interest from various disciplinary standpoints. Global attention to neurologist-patient interaction is growing, with focus on communication models, patterns, applications, and various indices in the interactional contexts. Similar attention remains scanty within the Nigerian context. This study, therefore, investigated communication model in neurologist-patient interaction in selected university teaching hospitals (UTHs) in southwestern Nigeria, in order to identify the communication goals and patterns, discourse strategies, pragmatic acts, and contexts that shape the interaction. Jacob Mey's Pragmatic Acts, complemented by Emanuel and Emanuel's model of doctor-patient relationship, served as the theoretical framework. Data comprising 40 audio-recorded neurologist-patient interactions were collected from the UTHs of Olabisi Onabanjo University, Sagamu (nine); Ekiti State University, Ado-Ekiti (eight) and Ladoke Akintola University of Technology, Osogbo (six) and University College Hospital, Ibadan (17). These were supplemented with patients' case notes and interviews conducted with neurologists. The data were transcribed following modified Arminen's notations of conversation analysis and subjected to pragmatic analysis. Four models of communication, namely paternalistic, informative, interpretive, and deliberative, exhibited through varying discourse strategies were identified in the neurologist-patient interaction with the diagnostic and therapeutic communication as goals. The paternalistic model reflected slightly casual conversational conventions and registers. These were achieved through the pragmemic activities of situated speech acts, psychological and physical acts, via patients' quarrel-induced acts, controlled and managed through neurologists' shared situation knowledge. All these produced empathising, pacifying, promising and instructing practs. The patients' practs were explaining, provoking, associating and greeting in the paternalistic model. The informative model reveals the use of adjacency pairs, formal turn-taking, precise detailing, institutional talks and dialogic strategies. Through the activities of the speech, prosody and physical acts, the practs of declaring, alerting and informing were utilised by neurologists, while the patients exploited adapting, requesting and selecting practs. Monologic contribution was the norm in the interpretive model. It involves the confirmatory and routine opening-and-closing discourse strategies. The communicative activities through the speech, prosody and physical acts showed the utilisation of deducing, predicting, prioritising and interpreting practs by neurologists; while patients adopted conforming, inquiring, requesting and deciding practs. The negotiating conversational strategy of the deliberative model featured in the speech, prosody and physical acts. In this model, practs of suggesting, teaching, persuading and convincing were utilised by the neurologists. The patients deployed the practs of questioning, demanding, considering and deciding. The contextual variables revealed that the four models often coalesced in the selected UTHs within the situational and psychological contexts. However, the paternalistic model was predominantly employed by neurologists with over six years in practice, while the interpretive, informative and deliberative models were found among neurologists below six years in practice in the selected UTHs. Neurologist-patient interaction in university teaching hospitals in southwestern Nigeria is shaped by neurologists' experience, patients' peculiarities and shared knowledge. All these reinforce the paternalistic as an invaluable model for enhanced and effective communication.
... Notwithstanding the inclusion of value clarification modules in previous decision aids for other medical contexts [15], it remains unclear from the available literature what value clarification exactly should be like, what it aims for and how it should be scripted into (an online) design [16]. The value clarification paradigm has been discussed in length within the context of moral education (Raths et al. in 10) [17,18]. Drawing heavily on value theory and theories on moral education, we came up with four questions that are relevant in the development of the OnVaCT intervention: ...
... With the assumptions being transparent, we believe that patients gain the freedom to choose the values they consider important and discard those which seem irrelevant. However, in order to not only confirm personal preferences but also support critical reflection at home and during consultations, users are actively invited to participate in a dialogue or critical deliberation [9,[17][18][19] through open questions that are incorporated into the OnVaCT. In our view, exploring options for participation in early phase clinical trials needs to go hand in hand with thinking more broadly about palliative care and quality of (the last phase of) life [38]. ...
... Health information-seeking behavior (HISB) refers to an individual's intentional action to find health information [1]. HISB can have advantageous cognitive (e.g., informed decision-making), behavioral (e.g., better communication better poised to challenge the longstanding paternalistic physician-patient relationship [7,8]. Thus, the deliberative model [7]--whereby health professionals support patient autonomy and help determine the quality of health information retrieved from other sources--is encouraged [6]. ...
... HISB can have advantageous cognitive (e.g., informed decision-making), behavioral (e.g., better communication better poised to challenge the longstanding paternalistic physician-patient relationship [7,8]. Thus, the deliberative model [7]--whereby health professionals support patient autonomy and help determine the quality of health information retrieved from other sources--is encouraged [6]. ...
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The subpopulation of adults depends on non-online health information sources including their social networks and health professionals, to the exclusion of online sources. In view of the digital divide and health information disparities, the roles of race/ethnicity and digital skills are yet to be explored. A nationally representative sample of 6,830 adults from the Program for the International Assessment of Adult Competencies (PIAAC) was analyzed, using binary logistic regression. Black adults and adults with higher digital skills were less likely to be reliant on non-online health information sources, compared to White adults and those with lower digital skills, respectively. Differences in non-online health information source reliance by race/ethnicity and digital skills might be further nuanced by the relevant demographic and socioeconomic characteristics. Increasing digital skills may expand one’s health information sources to include reliable online sources and empower adults to promote their health.
... Additionally, researchers would have a conflict of interest, and such a process could make adolescents vulnerable to exploitation by exposing them to risks that they would not consent to otherwise. 35 Second, our findings illustrate contrasting preferences towards decision-making by the study respondents, suggesting that further research is needed to develop agreement on a framework (or perhaps on contextspecific frameworks) to guide HCWs and research teams about working with ALHs and their caregivers. Rather than simply entrusting researchers or HCWs to make these decisions, an SDM approach for research participation might be more appropriate. ...
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Introduction: Efforts to improve health outcomes among adolescents and young adults living with HIV (ALHs) are hampered by limited adolescent engagement in HIV-related research. We sought to understand the views of adolescents, caregivers and healthcare workers (HCWs) about who should make decisions regarding ALHs’ research participation. Methods: We conducted focus group discussions (FGDs) and in-depth interviews (IDIs) with ALHs (aged 14–24 years), caregivers of ALHs and HCWs from six HIV care clinics in Western Kenya. We used semi-structured guides to explore ALHs’ involvement in research decisions. Transcripts were analysed using thematic analysis; perspectives were triangulated between groups. Results: We conducted 24 FGDs and 44 IDIs: 12 FGDs with ALHs, 12 with caregivers, and 44 IDIs with HCWs, involving 216 participants. HCWs often suggested that HIV research decision-making should involve caregivers and ALHs deciding together. In contrast, ALHs and parents generally thought decisions should be made individually, whether by HCWs/research teams (although this is likely ethically problematic), adolescents or caregivers. Caregiver and ALH preferences depended on ALHs’ age, with younger ALHs requiring more support. A few caregivers felt that ALHs should consult with the research team/HCWs due to their greater knowledge of clinical care. ALHs emphasised that they should independently decide because they thought they had the right to do so and the capacity to consent. Poor communication and parental non-disclosure of HIV status influenced ALHs’ views to exclude caregivers from decision-making. Regarding influences on research decision-making, ALHs were more willing to participate based on perceived contribution to science and less interested in participating in studies with potential risks, including loss of confidentiality. Discussion: While research teams and HCWs felt that adolescents and caregivers should jointly make research decisions, ALHs and caregivers generally felt individuals should make decisions. As ALHs sometimes find caregiver support lacking, improving family dynamics might enhance research engagement.
... This is a critical area of research when it comes to the relationship between patients and physicians. Public health research points to positive outcomes when patients feel empowered and autonomous about their healthcare decisions (Emanuel & Emanuel, 1992). ...
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This study’s purpose was to examine the role of power distance in physicians’ desired impression by patients, as well as doctors’ attitudes toward utilizing new media technologies. Qualitative interviews were conducted in the United States and the Philippines - which have divergent power distance scores. Results revealed three major themes. First, power distance was manifested in how each country’s doctors wanted to be perceived by patients. The second theme was that doctors perceived today’s patients to be more informed than in the past; however, Philippine doctors viewed this as a challenge while U.S. doctors viewed it as an opportunity to initiate conversation. The third theme identified differences in litigation concerns, which influenced attitudes toward using new media technologies in their practice.
... A small number of empirical studies, mostly conducted in the US and the UK, did investigate this topic [31,34]. In reviewing these latter studies, we found a temporal shift in parents' understanding and experiences of ASD throughout their trajectory in ASD care; and found that parents might expect several implications of an ASD diagnosis that pertain to the psychological and relational domain [35][36][37][38]. These findings inspired the research question and design of this study. ...
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This study suggests important issues for clinicians to bear in mind during a consultation with parents who request an ASD assessment of their young child. We argue that attending to and communicating about parents' expectations prior to their child's ASD assessment may help clinicians to better understand parents' requests for help, and to address their needs more effectively.
... Since the middle of the twentieth century, the way of understanding the physicianpatient relationship has been changing due to the socialization of medicine, its specialization, and the continuous technological advances. Since then, the bioethical discourse has tried to describe the physician-patient relationship with different models or metaphors: the paternalistic or autonomy model, the contract, alliance, or negotiation model, and the mutual participation model, among others [For example, see [24][25][26][27][28][29][30][31][32]]. ...
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The central idea of this paper is that in bioethics there are two types of discourses or approaches, one procedural and the other one substantive or content approach. The first one seems to be predominant because it responds better to the demand in contemporary times by offering procedures, rules, and guidelines to help healthcare professionals to find solutions to ethical issues, rather than the second one, which is focused on the trait of characters, attitudes, and the moral content. Since the digital era started, data as moral content and systems have become the most valuable resource. This has been manifested in multiple areas such as social network, business, and politics, among others. In medicine, the potential impact of novel technologies based on data like artificial intelligence and machine learning, among others, may bring preventive, diagnostic, and therapeutic benefits for patients as well as result in potential issues, and the majority are still unknown. In order to guarantee respect to the new moral content, and compliance with bioethics principles within procedures and systems in the digital era a third approach is required: bioethics by-design.
... Understanding how and why a particular decision was made is critical for all stakeholders in the medical ecosystem. First and foremost, patients are entitled to an explanation for a particular diagnosis or proposed treatment plan (109,110). These decisions will ultimately be made by doctors who utilise AI models as tools, and thus, they need to understand the outputs and workings of those models themselves. ...
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Recent years have seen a rapid increase in digital medicine research in an attempt to transform traditional healthcare systems to their modern, intelligent, and versatile equivalents that are adequately equipped to tackle contemporary challenges. This has led to a wave of applications that utilise AI technologies; first and foremost in the fields of medical imaging, but also in the use of wearables and other intelligent sensors. In comparison, computer audition can be seen to be lagging behind, at least in terms of commercial interest. Yet, audition has long been a staple assistant for medical practitioners, with the stethoscope being the quintessential sign of doctors around the world. Transforming this traditional technology with the use of AI entails a set of unique challenges. We categorise the advances needed in four key pillars: Hear, corresponding to the cornerstone technologies needed to analyse auditory signals in real-life conditions; Earlier, for the advances needed in computational and data efficiency; Attentively, for accounting to individual differences and handling the longitudinal nature of medical data; and, finally, Responsibly, for ensuring compliance to the ethical standards accorded to the field of medicine. Thus, we provide an overview and perspective of HEAR4Health: the sketch of a modern, ubiquitous sensing system that can bring computer audition on par with other AI technologies in the strive for improved healthcare systems.
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