Littérature scientifique sur le sujet « Patient centeredne »

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Articles de revues sur le sujet "Patient centeredne"

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Alshahrani, Shadia Hamoud, Talal H. Alshahrani, Premalatha Paulsamy et Eva Lobelle Ederango. « Patient Centered Care and Centeredness Perspective ». Universal Journal of Public Health 10, no 4 (août 2022) : 339–45. http://dx.doi.org/10.13189/ujph.2022.100407.

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Kamimura, Akiko, Shannon Weaver, Bianca Armenta, Bethany Gull et Jeanie Ashby. « Patient centeredness : The perspectives of uninsured primary care patients in the United States ». International Journal of Care Coordination 22, no 1 (mars 2019) : 19–26. http://dx.doi.org/10.1177/2053434519836424.

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Introduction Patient-centered care has become increasingly important within the United States (US) healthcare system. Given that patient-centered care predicts patient satisfaction, health outcomes, and cost-effectiveness, it is of the utmost importance to study patient-centered care from the perspectives of marginalized populations including minorities, immigrants, and other underserved populations. The purpose of this study is to examine factors that affect underserved primary care patients’ perceptions of patient centeredness. Methods The data were cross-sectional and collected in Fall 2016. Free clinic patients (N = 723) completed a self-administered survey, which measures patient centeredness, patient involvement in care, and clinical empathy. Validated measures were part of the survey, and the internal consistency of scales was tested. The general linear model was performed to predict factors associated with patients’ perceptions of patient centeredness. Results Higher levels of perceived patient involvement in care and higher levels of perceived empathy in consultation are related to higher levels of patient centeredness. While better physical health is associated with higher levels of perceived empathy in consultation, high levels of emotional health and depression are not. Conclusions Patients’ perceptions of involvement and empathy are important factors for patient-centered care, although this study did not show causal directions among variables. Based on the findings of this study, it is recommended that future studies should focus on the following three points: (1) to develop and evaluate trainings for providers, (2) develop education classes for patients who utilize free clinics, (3) analyze how these programs affect patient-centered care and health outcomes.
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Jeon, Jaehee, et Seunghye Choi. « Factors Influencing Patient-Centeredness among Korean Nursing Students : Empathy and Communication Self-Efficacy ». Healthcare 9, no 6 (12 juin 2021) : 727. http://dx.doi.org/10.3390/healthcare9060727.

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In recent years, there is a growing tendency in the extent to which patients wish to be actively involved in processes related to their healthcare and relevant decision-making. This was a cross sectional study. We examined undergraduate nursing students’ patient-centeredness and investigated its associated factors including empathy and communication self-efficacy using a structured questionnaire. A total of 201 undergraduate nursing students who provided written consent to participate in the study completed measures on patient-centeredness (sharing and caring), empathy (fantasy, perspective taking, personal distress, and empathic concern), and communication self-efficacy. The factors affecting patient-centeredness were analyzed using multiple regression. Communication self-efficacy affected patient-centered sharing, while age, empathy (fantasy, personal distress, empathic concern), and communication self-efficacy affected patient-centered caring. Empathy and communication self-efficacy positively affected patient-centeredness. Therefore, strategies that promote empathy and communication self-efficacy are needed to increase patient-centered care competency.
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Mapes, Marianna V., Peter A. DePergola et William T. McGee. « Patient-Centered Care and Autonomy : Shared Decision-Making in Practice and a Suggestion for Practical Application in the Critically Ill ». Journal of Intensive Care Medicine 35, no 11 (26 août 2019) : 1352–55. http://dx.doi.org/10.1177/0885066619870458.

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Decision-making for the hospitalized dying and critically ill is often characterized by an understanding of autonomy that leads to clinical care and outcomes that are antithetical to patients’ preferences around suffering and quality of life. A better understanding of autonomy will facilitate the ultimate goal of a patient-centered approach and ensure compassionate, high-quality care that respects our patients’ values. We reviewed the medical literature and our experiences through the ethics service, palliative care service, and critical care service of a large community teaching hospital. The cumulative experience of a senior intensivist was filtered through the lens of a medical ethicist and the palliative care team. The practical application of patient-centered care was discerned from these interactions. We determined that a clearer understanding of patient-centeredness would improve the experience and outcomes of care for our patients as well as our adherence to ethical practice. The practical applications of autonomy and patient-centered care were evaluated by the authors through clinical interactions on the wards to ascertain problems in understanding their meaning. Clarification of autonomy and patient-centeredness is provided using specific examples to enhance understanding and application of these principles in patient-centered care.
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Hansen, Martha Monrad, et Karen Korning Zethsen. « Is Electronic Access to Medical Records an Empowering and Patient-centered Initiative ? – a Qualitative Contextual and Linguistic Analysis of Danish Electronic Records ». HERMES - Journal of Language and Communication in Business, no 58 (22 décembre 2018) : 157–73. http://dx.doi.org/10.7146/hjlcb.v0i58.111683.

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Political correctness demands a patient empowering and patient-centered approach to health care and today patients are increasingly involved in, and responsible for, their own health. Patients are potentially subjected to large amounts of health information and, in a Danish context, patients have recently gained easy electronic access to their hospital records. Access, which used to be by application, is now only a few clicks away. This initiative is praised as patient empowering and patient-centered even though the e-records are not written for patients, but are the working tool of health professionals. Thus, an expert language text, as it stands, has to function as patient information. In this article, we examine the language of the e-records with a view to determining potential lay-friendliness and thus patient-centeredness. We also discuss whether access, by definition, is a progressive initiative and whether patient empowerment is always the same as patient-centeredness.
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Sharma, Meenakshi. « Need to Adopt a Patient Centered Approach for Obtaining Favourable Results of NonPharmacological Interventions among Knee Osteoarthritis Patients in Out Patient Department Settings ». International Journal of Healthcare Education & ; Medical Informatics 05, no 02 (24 août 2018) : 21–26. http://dx.doi.org/10.24321/2455.9199.201809.

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Khodyakov, Dmitry, Sean Grant, Brian Denger, Kathi Kinnett, Ann Martin, Marika Booth, Courtney Armstrong et al. « Using an Online, Modified Delphi Approach to Engage Patients and Caregivers in Determining the Patient-Centeredness of Duchenne Muscular Dystrophy Care Considerations ». Medical Decision Making 39, no 8 (novembre 2019) : 1019–31. http://dx.doi.org/10.1177/0272989x19883631.

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Purpose. To determine the patient-centeredness of endocrine and bone health Duchenne muscular dystrophy (DMD) care considerations using the RAND/PPMD Patient-Centeredness Method (RPM), which is a novel, online, modified-Delphi approach to engaging patients and caregivers in clinical guideline development. Methods. We solicited input on the patient-centeredness of care considerations from 28 individuals with DMD and 94 caregivers, randomly assigned to 1 of 2 mixed panels. During a 3-round online modified-Delphi process, participants rated the importance and acceptability of 19 DMD care considerations (round 1), reviewed and discussed the initial results (round 2), and revised their original ratings (round 3). Patient-centeredness was operationalized as importance and acceptability of recommendations. We considered a care consideration to be patient-centered if both panels deemed it important and acceptable. Results. Ninety-five panelists (78%) participated in this study. Of these, 88 (93%) participated in round 1, 74 (78%) in round 2, and 56 (59%) in round 3. Panelists deemed 12 care considerations to be patient-centered: 3 weight management, 3 bone health, 4 vertical growth, and 2 puberty recommendations. Seven care considerations did not meet patient-centeredness criteria. Common reasons were lack of evidence specific to DMD and concerns about insurance coverage, access to treatment, and patient safety. Conclusions. Using the RPM, Duchenne families considered most care considerations to be patient-centered. Besides being clinically appropriate, these considerations are likely to be consistent with the preferences, needs, and values of Duchenne families. While all relevant care considerations should be discussed during patient-provider encounters, those that did not meet patient-centeredness criteria in particular should be carefully considered as part of joint decision making between Duchenne families and their providers. Study Registration: HSRProj 20163126.
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Perfetto, Eleanor, Elisabeth Oehrlein, Marc Boutin, Sarah Reid et Eric Gascho. « OP38 Improving The Patient Centricity Of Value Assessments : A Rubric ». International Journal of Technology Assessment in Health Care 33, S1 (2017) : 17–18. http://dx.doi.org/10.1017/s0266462317001337.

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INTRODUCTION:Value frameworks, analogous to Health Technology Assessment (HTA) internationally, have emerged in the United States to aid stakeholders in assessing the value of new treatments. Since patient perspectives on value may differ significantly from other stakeholders, formalized procedures to involve patients in their work have been created. Despite these efforts, concerns persist that patient involvement is insufficient or “rhetoric.” To assist in this effort, the National Health Council (NHC) created a rubric to aid decision makers in improving the patient centricity of their value assessments.METHODS:A convenience sample of twenty-eight organizations was invited to participate in a roundtable discussion. Participants discussed experiences with value frameworks; debated and thematically grouped hallmark patient-centeredness characteristics; and developed illustrative examples of the characteristics. These materials were organized into the rubric, and subsequently vetted via multi-stakeholder peer review.RESULTS:Participants agreed upon six key domains of patient centeredness: partnership (patients are involved in every step of development/dissemination processes), transparency (assumptions/inputs are disclosed in an understandable, timely way), inclusiveness (perspectives drawn from broad range of stakeholders), diversity (differences in subpopulations, trajectory of disease, and stage of a life should be accounted for), outcomes (includes those that patients have identified as important), and data (variety of credible data sources are used allowing for timely incorporation of new information and account for the diversity of patient populations and patient-centered outcomes). The Rubric describes each domain and includes illustrative examples of how patient engagement/centeredness can be operationalized through direct and indirect pathways.CONCLUSIONS:The NHC Rubric is a first step toward creating patient-centered value assessments that patients and their families can rely on. It is intended to assist all stakeholders, especially the patient community, in assessing the level of patient centeredness and engagement in a given framework or model. It can be a guide to support developers in conceptualizing plans for meaningfully engaging patients.
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Siouta, Eleni, et Ulf Olsson. « Patient Centeredness from a Perspective of History of the Present : A Genealogical Analysis ». Global Qualitative Nursing Research 7 (janvier 2020) : 233339362095024. http://dx.doi.org/10.1177/2333393620950241.

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The overall aim of this study, performed in Sweden, was to problematize the contemporary national and transnational discourse on patient centeredness, which during recent decades has become a given, having become established as a dogma in conversations, writing, and thinking about patients and health care. We did that by showing that ideas such as patient centeredness can be seen differently from the way they are depicted in contemporary discourses about health care. In the presented analysis, we drew on Foucault’s concepts of governmentality, ‘history of the present’ and genealogy. This means that we reflected on contemporary conceptions of how phenomena, such as the care seeker, have been constructed within other discourses about health care. Empirically, we used different health policy documents—government reports from three different historical periods. The analysis showed that contemporary narratives about centeredness are neither more, nor less, care seeker-centered than the narratives of yesteryear. Rather, the phenomenon of the care seeker is given different frames and meanings within the framework of different economic and historical discourses about health care. Our analysis raised questions about the contemporary construction of patient centeredness. In a world with such huge economic differences between nations, as well as between citizens within most nations, the contemporary discourse may be limited as it does not problematize structural issues in the same way as previous discourses had done. Perhaps what is needed today are national and international patient-centered or person-centered discourses which also discuss policies and practices that are population- and social group-centered. In the final discussion of the analysis, we identified a new patient-centered discourse, which views the patient as a resource among other resources. The most important limitation of this type of study is that it is only about discourses and policy issues and not about daily practical activities.
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Mann, Keith J., Amber Hoffman, DeeJo Miller, Sheryl Chadwick et Denise Bratcher. « The Effect of a Patient- and Family-Centered Care Curriculum on Pediatrics Residents' Patient-Centeredness ». Journal of Graduate Medical Education 5, no 1 (1 mars 2013) : 36–40. http://dx.doi.org/10.4300/jgme-d-11-00254.1.

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Abstract Background Patient- and family-centered care (PFCC) approaches to care are important in enhancing the patient-centeredness of the health care experience, yet little is known about the effectiveness of formal approaches for teaching patient-centeredness in residency. Intervention We developed and implemented a PFCC curriculum and assessed its impact on residents' self-perceptions of patient-centered behavior and practices. Methods We used a quasi-experimental, nonrandomized approach with a pretest-posttest design. An experimental group of 24 interns filled out the Patient Practitioner Orientation Scale (PPOS) before residency, and a control group of 18 graduating residents who had not been exposed to a PFCC curriculum also completed the PPOS. After 2 years of residency and exposure to a PFCC curriculum, interns in the experimental group repeated the PPOS. We compared mean total and subscale PPOS scores. Results There was no difference in baseline total or subscale PPOS scores between the experimental and control group. The mean total PPOS score for the experimental group after exposure to the curriculum was 4.55 (P = .45), reflecting no change in patient-centeredness. The 17 female interns in the intervention group were more patient centered (4.8 ± 0.36) than the 6 male interns (4.2 ± 0.38) (P = .005), scoring significantly higher (4.6 ± 0.39 versus 4.0 ± 0.38) in the sharing domain (P = .001). Conclusion Interns' exposure to a PFCC curriculum did not result in a change in their perceived patient-centeredness. Most pediatrics residents at our children's hospital perceive themselves as patient and family centered at the start of residency and remain so throughout.
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Thèses sur le sujet "Patient centeredne"

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Rees, Brian Christopher Kern Carolyn W. « Adult client outcomes differences between counselors with education in child-centered play therapy versus counselors without education in child-centered play therapy / ». [Denton, Tex.] : University of North Texas, 2007. http://digital.library.unt.edu/permalink/meta-dc-3923.

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Blackwelder, Reid B. « Patient Centered Medicine ». Digital Commons @ East Tennessee State University, 2003. https://dc.etsu.edu/etsu-works/6937.

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Blackwelder, Reid B. « Patient-Centered Care ». Digital Commons @ East Tennessee State University, 2010. https://dc.etsu.edu/etsu-works/6982.

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Berglund, Malin, et Maria Kostecka. « Patientcentrerad vård och helhetssyn i vården - skiljer sig begreppen ? : En litteraturstudie ». Thesis, Uppsala universitet, Institutionen för folkhälso- och vårdvetenskap, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-142806.

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SAMMANFATTNING Begrepp som patientcentrerad vård och helhetssyn i vården verkar användas av olika yrkeskategorier, inom hälso- och sjukvård, vilket kan ur kvalitetssynpunkt kan resultera i oklarheter inom den kliniska verksamheten. Syfte: Syftet med studien var att ta reda på vilka likheter och skillnader begreppen patientcentrerad vård och helhetssyn i vården har i den vetenskapliga litteraturen. Begreppen söktes i databaserna CINAHL och PubMed. Metod: Den metod som används för att jämföra begreppen byggde på Segestens begreppsanalysmodell. Resultat: Det som främst skiljer begreppet helhetssyn i vården från patientcentrerad vård är den andliga dimensionens centrala roll. Resultatet visar även att ett patientcentrerat arbetssätt förbättrar ekonomiska resultat. Det är främst sjuksköterskor som använder sig av helhetssyn i vården. Patientcentrerad vård verkar användas främst av läkare men begreppet förekommer även bland sjuksköterskor. Det gemensamma för begreppen då det gäller karaktäristika, förutsättningar och konsekvenser, är det som definieras i kraven på god vård enligt hälso- och sjukvårdslagen. Slutsats: sjukvårdspersonalens arbetssätt och syn på patienten utifrån patientcentrerad vård och helhetssyn i vården värnar om patientens bästa. Det som skiljer begreppen kan bero på vilken yrkesgrupp som undersökts i respektive studie. Studier av begreppet patientcentrerad vård uppfattas vara mer genomförda på läkargruppen samtidigt som helhetssyn i vården tycks vara mer förekommande då det gäller sjuksköterskegruppen. Fler studier behövs för att identifiera användningen av dessa begrepp och om deras betydelse i den kliniska verksamheten.
SUMMARY Concepts such as patient-centered care and holistic care seem to be used by different professions in healthcare. Looking upon these concepts from the aspect of quality, ambiguities can arise in clinical practice. Objective: The purpose of this study was to compare the similarities and differences between the concepts of patientcentered care and holistic care as they are presented in scientific literature. The terms were searched for in the databases CINAHL and PubMed. Method: The method used to compare the concepts was based on Segesten concept analysis model. Results: what differentiates the concept of holistic care of the patient-centered care is the central role of spiritual dimension. The results also show that a patient-centered care improves economic results. The term holistic health care seems to be used primarily by nurses, while patient-centered care seems to be used primarly by physicians, even though the term does occur among nurses. Conclusion: both patient-centered care and holistic care seem to have the same goal, that of preserving the patient`s best interests. What distinguishes the concepts may depend on the profession which was examined in each study. Research studies on patient-centered care have been carried out primarily on physicians, while studies on the holistic approach in health care have focused on nurses. More studies are needed to identify the use of these concepts and their importance in clinical practice. Nyckelord: Patient-centeredness, patient-centered care, holistic care, holistic nursing.
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Carrillo, Victor A. « Community and Patient-Centered Medical Home in the Care of Chronically Ill Patients ». ScholarWorks, 2016. https://scholarworks.waldenu.edu/dissertations/3143.

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Large portions of the US population live in poor inner-city communities. Health needs assessment data have shown that these communities have disproportionately high rates of chronic illnesses. The patient-centered medical home (PCMH) model was developed to address the gaps that exist in the primary care system, and emphasizes a redesign of primary care that is patient centered, utilizes multiple levels of healthcare professionals, information technology, and care coordination. However, little evidence exists on the value of this model which may explain why it has not gained wide acceptance by primary care providers. Therefore, this study was designed to examine the efficacy of the PCMH model through emergency department and inpatient utilization reductions, and with a specific focus on the role of social connectedness. This research used existing data on 706 participants from Columbia University and a local New York inner-city hospital. An in-depth analysis of hospital utilization data, using an unpaired two-sample t-test and linear regression, found that the PCMH framework strengthens continuity of care and care coordination, and helps reduce avoidable hospitalization utilization. Additionally, these reductions were greater for study participants with strong social support networks. This research highlights the relationships between primary care, social support networks, and good health outcomes. Over time, further enhancement of the PCMH and systemic changes to the delivery of care may contribute to the development of a stronger primary care system that place patients at the center of care, focuses on the importance of social connectedness, and contributes to a lasting impact on society through the development of overall healthier communities.
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Blackwelder, Reid B. « Practical Approach to Patient-Centeredness ». Digital Commons @ East Tennessee State University, 2018. https://dc.etsu.edu/etsu-works/6947.

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Presentation Goals: Remember Why You Went into Medicine! Describe Patient-Centered Care Challenge you to become and remain Patient-Centered Review Patient-Centered EBM Implement (or Prevent) Attitude Shifts Give you hope!
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Smith, Cheryl. « Patients’ Perceptions of Patient-Centered Care and the Hospital Experience Pre- and Post-Discharge ». Digital Commons @ East Tennessee State University, 2018. https://dc.etsu.edu/etd/3388.

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Florence Nightingale used the principles of patient-centered care as the foundation for nursing practice. Today, patient-centered care delivery is part of the healthcare reform process that extends interprofessionally throughout all settings of healthcare in the United States (U.S.). Patient satisfaction measurement is one primary determinant of effective patient-centered care. The standardized Hospital Consumer Assessment of Healthcare Providers and Systems (HCAHPS) survey and methods is a nation-wide tool used to measure patient satisfaction. However, this method of patient satisfaction assessment relies on recollections of patients’ hospital experiences and requires accurate memory and recall. This study sought to examine the effect of the memory-experience gap on patients’ perceptions of their hospital experiences and address this research question: Are there any statistical differences between in-hospital and two-week post-discharge perceptions of patient-centered care as measured with HCAHPS patient satisfaction ratings on (a) the composite scores for communication with nurses, communication with physicians, communication about medicines, pain management, staff responsiveness, (b) the individual scores for the hospital environment’s cleanliness and quietness, and the inclusion of patient and family preferences in the plan of care, and (c) the overall global rating score? The design was a non-experimental, prospective, descriptive correlational study. The setting was a 255-bed regional hospital that serves individuals from eight surrounding rural counties in southern middle Tennessee. The case-mix contained diverse individuals with multiple economic, environmental, physical, social and spiritual dynamics. A convenience sample of 82 adult patients ages 26 - 93 represented mainly Caucasian females with mostly cardiovascular and respiratory illnesses who had a minimum one-day stay.
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Østerlund, Carsten Svarrer 1965. « Documenting dreams : patient-centered records versus practice-centered records ». Thesis, Massachusetts Institute of Technology, 2002. http://hdl.handle.net/1721.1/8005.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Sloan School of Management, February 2003.
Includes bibliographical references (leaves 261-268).
This thesis explores how doctors and nurses use documents to share their knowledge within and across healthcare settings. In addressing this question I draw on a 15-month, multi-sited ethnographic study in several pediatric health care settings, following patients from primary care clinics, to emergency rooms, and in-patient units. The analysis focuses on the practices that go into documenting patients' histories and care, which include recordings on various on-line systems, preprinted forms, and whiteboards. By combining the previously distinct lenses of 1) knowing in practice, 2) time-space analysis of social interaction, and 3) communicative genre and genre systems, I suggest that doctors and nurses employ various types of document genres to manage, not only their distributed knowing about patients' care, but also their own movements across time-space. I outline a perspective on documents and knowing which attempts to highlight the role of human practice in how people use documents to coordinate their activities, share their capabilities, and get things done in complex distributed organizational work. The data suggest that doctors and nurses use medical documents as maps and itineraries to organize their distributed work practices. Doctors and nurses record patients' histories many times in different documents, with each document serving as a map and itinerary for a different constituency of people. Each of these documents is rarely used in isolation from other documents. Doctors and nurses constantly recombine the documents they use, which allows them to both appropriate documents from other settings into their local organization of work and build unique local combinations of documents.
(cont.) I introduce the concept of "re-localizing" to describe how doctors and nurses use documents to share their knowing within and across healthcare settings. Re-localization involves many healthcare professionals' parallel rewriting of a patient's history based on a recombination of each other's maps and itineraries and the patient's own accounts. By integrating the concrete case and the maps and itineraries based on those cases the notion of relocalization overcomes the dichotomy between the abstract and the situated, the local and global. Documents are not seen as mere vessels for abstract representations, but integral parts of distributed knowing within and across settings.
by Carsten Svarrer Østerlund.
Ph.D.
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Rose, Douglas, Leonard Brian Cross et Ivy A. Click. « The Patient-Centered Care Committee (PC3) ». Digital Commons @ East Tennessee State University, 2013. https://dc.etsu.edu/etsu-works/6396.

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Blackwelder, Reid B. « Practical Approach to Patient-Centered Medicine ». Digital Commons @ East Tennessee State University, 2014. https://dc.etsu.edu/etsu-works/6955.

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Livres sur le sujet "Patient centeredne"

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B, Frampton Susan, Gilpin Laura 1950- et Charmel Patrick A, dir. Putting patients first : Designing and practicing patient-centered care. San Francisco : Jossey-Bass, 2003.

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B, Frampton Susan, et Charmel Patrick A, dir. Putting patients first : Best practices in patient-centered care. 2e éd. San Francisco : Jossey-Bass, 2009.

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Frezza, Eldo E. Patient-Centered Healthcare. Boca Raton : Routledge/Taylor & Francis, 2020. : Productivity Press, 2019. http://dx.doi.org/10.4324/9780429032226.

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Margaret, Gerteis, et Picker/Commonwealth Program for Patient-Centered Care., dir. Through the patient's eyes : Understanding and promoting patient-centered care. San Francisco : Jossey-Bass, 1993.

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Margaret, Gerteis, et Picker/Commonwealth Program for Patient-Centered Care., dir. Through the patient's eyes : Understanding and promoting patient-centered care. San Francisco : Jossey-Bass, 2002.

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Blount, Alexander. Patient-Centered Primary Care. Cham : Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-17645-7.

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Vance, Wilson E., dir. Patient-centered e-health. Hershey, PA : Medical Information Science Reference, 2009.

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L, Shortridge Dennis, et Watson Phyllis M. 1947-, dir. Patients first : Experiences of a patient-focused pioneer. Chicago, Ill : Health Administration Press, 1996.

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DiGioia, Anthony M., et Shapiro Eve. The Patient Centered Value System. Boca Raton : Taylor & Francis, 2018. | “A CRC title, part of the Taylor & Francis imprint, a member of the Taylor & Francis Group, the academic division of T&F Informa plc.“ : Productivity Press, 2017. http://dx.doi.org/10.1201/9781315165615.

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Patlak, Margie, Erin Balogh et Sharyl Nass, dir. Patient-Centered Cancer Treatment Planning. Washington, D.C. : National Academies Press, 2011. http://dx.doi.org/10.17226/13155.

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Chapitres de livres sur le sujet "Patient centeredne"

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Frezza, Eldo E. « Patient-Centered Care ». Dans Patient-Centered Healthcare, 3–9. Boca Raton : Routledge/Taylor & Francis, 2020. : Productivity Press, 2019. http://dx.doi.org/10.4324/9780429032226-1.

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Frezza, Eldo E. « Confusion over Care ». Dans Patient-Centered Healthcare, 71–78. Boca Raton : Routledge/Taylor & Francis, 2020. : Productivity Press, 2019. http://dx.doi.org/10.4324/9780429032226-10.

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Frezza, Eldo E. « Coordinating Patients’ Participation ». Dans Patient-Centered Healthcare, 79–85. Boca Raton : Routledge/Taylor & Francis, 2020. : Productivity Press, 2019. http://dx.doi.org/10.4324/9780429032226-11.

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Frezza, Eldo E. « Scheduling ». Dans Patient-Centered Healthcare, 87–92. Boca Raton : Routledge/Taylor & Francis, 2020. : Productivity Press, 2019. http://dx.doi.org/10.4324/9780429032226-12.

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Frezza, Eldo E. « Do Patients Want to Participate ? » Dans Patient-Centered Healthcare, 93–98. Boca Raton : Routledge/Taylor & Francis, 2020. : Productivity Press, 2019. http://dx.doi.org/10.4324/9780429032226-13.

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Frezza, Eldo E. « Transparency and Honesty ». Dans Patient-Centered Healthcare, 101–7. Boca Raton : Routledge/Taylor & Francis, 2020. : Productivity Press, 2019. http://dx.doi.org/10.4324/9780429032226-14.

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Frezza, Eldo E. « The True North Alignment ». Dans Patient-Centered Healthcare, 109–14. Boca Raton : Routledge/Taylor & Francis, 2020. : Productivity Press, 2019. http://dx.doi.org/10.4324/9780429032226-15.

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Frezza, Eldo E. « Quality Values ». Dans Patient-Centered Healthcare, 115–21. Boca Raton : Routledge/Taylor & Francis, 2020. : Productivity Press, 2019. http://dx.doi.org/10.4324/9780429032226-16.

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Frezza, Eldo E. « Optimized Healthcare Services ». Dans Patient-Centered Healthcare, 123–29. Boca Raton : Routledge/Taylor & Francis, 2020. : Productivity Press, 2019. http://dx.doi.org/10.4324/9780429032226-17.

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Frezza, Eldo E. « Healing Relationships ». Dans Patient-Centered Healthcare, 131–36. Boca Raton : Routledge/Taylor & Francis, 2020. : Productivity Press, 2019. http://dx.doi.org/10.4324/9780429032226-18.

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Actes de conférences sur le sujet "Patient centeredne"

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Elkefi, Safa, Onur Asan et Tina W F Yen. « Using Human factors approach to evaluate patient-centered cancer care ». Dans 13th International Conference on Applied Human Factors and Ergonomics (AHFE 2022). AHFE International, 2022. http://dx.doi.org/10.54941/ahfe1002186.

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Patient-centered care (PCC) approaches are critical for the delivery of high-quality care in cancer care where the therapeutic alliance between patients and the oncologists is frequent over extended periods of time. The concept of patient-centered care has received increased attention since the publication of the 2001 Institute of Medicine (IOM) report Crossing the Quality Chasm. In this study, we create and evaluate a new framework for patient-centered care in cancer using human factors approaches. Many initiatives focused on developing technologies that help foster PCC by increasing patients’ access to information and facilitating self-monitoring and patient convenience. This paper makes an important contribution to the literature by historically examining the evolution of the definitions of care approaches from disease-centered care focusing on curing the diseases to patient-centered care satisfying patients’ needs to person-centered care. Instead of treating people like victims of diseases, this model recognizes their need for more than one professional to support them emphasizing their capabilities and potential to improve their own health by themselves. It also provides a different and complementary way to the visit-oriented approach furnishing more accessible and continuous care over time, Our contribution also covers summarizing the existing measures adopted to measure its components and finally suggests a socio-technical framework based on the human factors approach to measuring PCC effectiveness. Our approach to measuring PCC is grounded in the conceptual framework we are suggesting that evaluates the effectiveness of patient-centered care based on a socio-technical perspective. We link the cognitive perception of patients towards PCC (Cognitive Sensory Input) to their exposure to external factors (Exposure) that may affect their (Cognition) behavior. A holistic approach recognizing health care as a dynamic socio-technical system in which sub-elements interact with each other remains necessary to better understand the system and its constraints in cancer care. We use a case study to emphasize the importance and need of such a human factors-based framework in providing a better quality of care and improving health outcomes. Achieving high-quality care is a complex pursuit in any setting especially for cancer care and improving the patient journey requires an integrated system of care and productive interactions among many system levels. By understanding the work system components, the design and integration of tasks, technology, and clinical processes can be reviewed to better support the respective needs of individuals while optimizing system performance. A supportive work environment and a highly engaged workforce are highly correlated with improved quality of patient-centered care and hospital performance. At the population level, case managers, navigators, quality officers, and administrators may track outcomes across patients.This framework can help organize clinical interventions that aim to control cancer patients’ behavior from a patient-centered perspective. It can also help technology designers by giving them insight into how patient-centeredness in the design of health informatics can impact cancer patients’ behavior. In addition, patient-centered designs can enhance technology acceptance among cancer patients making it easier to adopt technology for follow-up reasons by involving human factors and ergonomics principles in order to ensure successful results.
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Mo, Zhiwei. « On the Product Service System Design of Diabetes Management for Patients ». Dans Human Interaction and Emerging Technologies (IHIET-AI 2022) Artificial Intelligence and Future Applications. AHFE International, 2022. http://dx.doi.org/10.54941/ahfe100922.

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The increasing number of chronic patients is still a problem for the Italian medical system. In the age of digitalization, digital technology offers many opportunities for helping these patients solve problems, through advanced technologies such as the Internet of Things, big data, and cloud computing, smart devices can be used to collect and analyze the health information of diabetic patients, and transmit it to medical institutions in a form of visual models for obtaining reasonable treatment recommendations timely. This smart product can analyze the patient's health data in real time, meet the needs of the patient, and facilitate the connection between the patient and various medical institutions. This paper studies the product service system centered on diabetic patients, designs a smart device with blood sugar testing, and provides an Italian localized solution.
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Arunachalam, Priya, et Brendan D’Souza. « Patient-Centered Hospital Gowns : A Novel Redesign of Inpatient Attire to Improve Both the Patient and Provider Experience ». Dans 2022 Design of Medical Devices Conference. American Society of Mechanical Engineers, 2022. http://dx.doi.org/10.1115/dmd2022-1058.

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Abstract During their inpatient stays, patients are often required – or highly encouraged – to wear hospital gowns. While these gowns are intended to be convenient for patients and their providers, their design has remained largely unchanged over time. As healthcare moves towards greater emphasis on patient-centered care, the hospital gown is an opportunity to improve patient care. Patients have expressed frustration with the traditional hospital gown, especially with how revealing the gown can be. Here, we introduce a redesigned hospital gown that addresses many common concerns related to patients’ comfort and privacy. Our design introduces novel midline, rear, and shoulder panels, which provide healthcare workers with convenient access to the patient while maintaining coverage over areas of the patient that are not being examined. These panels also make it less likely for patients to be inappropriately exposed during routine activities. A prototyped gown was developed to test design features, and evaluation of this prototype demonstrated that this novel design has the potential to address many concerns while protecting the usability of traditional gowns. Further improvements to the gown’s design are also discussed.
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Wati, Dian Kusuma, Eti Poncorini Pamungkasari et Ari Natalia Probandari. « Patient-Centered Care : How do Patients Perceive Its Implementation ? » Dans The 5th Intenational Conference on Public Health 2019. Masters Program in Public Health, Universitas Sebelas Maret, 2019. http://dx.doi.org/10.26911/theicph.2019.05.10.

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Müller, Lorenz, Niels Hinricher, Janina Gersie et Claus Backhaus. « Prototype of a piece of clothing for patients for quick and easy patient mobilizations in healthcare facilities ». Dans 13th International Conference on Applied Human Factors and Ergonomics (AHFE 2022). AHFE International, 2022. http://dx.doi.org/10.54941/ahfe1002122.

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Caregivers are exposed to musculoskeletal strains during patient mobilizations. Especially for patient transfers, hoists were developed, but hoists have a low acceptance and when used incorrectly strains are still high. This paper develops a user-centered prototype to increase the use of hoists. The developed prototype is based on a market comparison, workflow analyses (n = 88), semi-structured interviews (n = 10) and a usability test with caregivers (n = 12). Instead of slings, the prototype lifts patients directly by their clothing. This reduces the transfer time and the steps required to lift a patient. The usability and the caregiver acceptance is high. Improvements address patients' comfort.
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Wilcox, Lauren, Steven Feiner, Noemie Elhadad, David Vawdrey et Tran Tran. « Remedy : Supporting Consumer-Centered Medication Information Search ». Dans ICTs for improving Patients Rehabilitation Research Techniques. IEEE, 2013. http://dx.doi.org/10.4108/icst.pervasivehealth.2013.252102.

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Kalra, Jay, Zoher Rafid-Hamed, Lily Wiebe et Patrick Seitzinger. « Medical Error Disclosure : A Quality Perspective and Ethical Dilemma in Healthcare Delivery ». Dans 13th International Conference on Applied Human Factors and Ergonomics (AHFE 2022). AHFE International, 2022. http://dx.doi.org/10.54941/ahfe1002107.

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Medical errors are a significant public health concern that affects patient care and safety. Highlighted as a substantial problem in the 1999 Institute of Medicine report, medical errors have become the third leading cause of death in the United States of America. Failure to inform the patient of adverse events caused by a medical error compromises patient autonomy. Disclosure of adverse events to patients and families is critical in managing the consequences of a medical error and essential for maintaining patient trust. When errors occur, healthcare practitioners are faced with the ethical and moral dilemmas of if and to whom to disclose the error. Healthcare providers face these disclosure dilemmas across all disciplines, locations, and generations and have far-reaching implications on healthcare quality and the progress of medicine. We have previously reported the Canadian provincial initiatives encouraging open disclosure of adverse events and have suggested its integration into a 'no-fault' model. Though similar in content, the Canadian provincial initiatives remain isolated because of their non-mandatory nature and absence of federal or provincial laws on disclosure. The purpose of this study was to review and compare the disclosure policies implemented by individual health care regions/authorities in various parts of Canada to identify quality issues related to medical error disclosure based on several ethical and professional principles. The complexities of medical error disclosure to patients present ideal opportunities for medical educators to probe how learners balance the moral complexities involved in error disclosure. Effective communication between health care providers, patients, and their families throughout the disclosure process is integral in sustaining and developing the physician-patient relationship. We believe that the disclosure policies can provide a framework and guidelines for appropriate disclosure, leading to more transparent practices. We suggest that disclosure practice can be improved by creating a uniform policy centered on addressing errors in a non-punitive manner and respecting the patient's right to an honest disclosure and be implemented as part of the standard of care.
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Gonzales, Michael, et Laurel Riek. « Co-designing Patient-centered Health Communication Tools for Cancer Care ». Dans ICTs for improving Patients Rehabilitation Research Techniques. IEEE, 2013. http://dx.doi.org/10.4108/icst.pervasivehealth.2013.252109.

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Carvajal, Diana. « Patient-centered care… ? provider perspectives on contraceptive counseling for latina/x patients ». Dans NAPCRG 49th Annual Meeting — Abstracts of Completed Research 2021. American Academy of Family Physicians, 2022. http://dx.doi.org/10.1370/afm.20.s1.2674.

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Shimmick, John, et Charles Munnerlyn. « Corneal Analysis with a Rectilinear Photokeratoscope ». Dans Ophthalmic and Visual Optics. Washington, D.C. : Optica Publishing Group, 1992. http://dx.doi.org/10.1364/ovo.1992.tuf1.

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Photorefractive keratectomy (PRK) involves precisely sculpting a lens on the anterior cornea by excimer laser photoablation (1). Consequently, patient positioning relative to the laser must be within certain predefined tolerance levels (2), and the procedure should be centered on the patient's line of sight (3).
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Rapports d'organisations sur le sujet "Patient centeredne"

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Starkey, Sandra, et Jean L. Parsons. Exploring Patient Centered Care Through the Design of Personal Storage for Patients. Ames : Iowa State University, Digital Repository, 2014. http://dx.doi.org/10.31274/itaa_proceedings-180814-914.

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Hynes, Denise, Jose Arruda, Michael Berbaum, Ifeanyi Chukwudozie, Michael Fischer, Marian Fitzgibbon, Anna Porter et Linda Schiffer. Evaluating a Patient-Centered Medical Home for Patients Receiving Dialysis for Kidney Disease. Patient-Centered Outcomes Research Institute® (PCORI), août 2019. http://dx.doi.org/10.25302/5.2019.ih.12115420.

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Haut, Elliott, Brandyn Lau, Deborah Hobson, Dauryne Shaffer, Peggy Kraus, Jonathan Aboagye, Norma Farrow et al. Preventing Venous Thromboembolism : Empowering Patients and Enabling Patient-Centered Care via Health Information Technology. Patient-Centered Outcomes Research Institute (PCORI), novembre 2018. http://dx.doi.org/10.25302/11.2018.ce.12114489.

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Ell, Kathleen, Maria Aranda, Shinyi Wu, Hyunsung Oh et Pey-Jiuan Lee. A Helping Hand to Activate Patient-Centered Depression Care among Low-Income Patients (AHH). Patient-Centered Outcomes Research Institute (PCORI), mars 2018. http://dx.doi.org/10.25302/3.2018.ad.13047364.

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DiBenedetti, Dana B., T. Michelle Brown, Carla Romano, Claire Ervin, Sandy Lewis et Sheri Fehnel. Conducting Patient Interviews Within a Clinical Trial Setting. RTI Press, août 2018. http://dx.doi.org/10.3768/rtipress.2018.op.0054.1808.

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Qualitative data centered on patients’ experiences and perspectives typically go uncollected in clinical trial settings. Yet patients’ treatment experiences offer complementary insights and context on topics such as disease management, treatment gaps, and previous treatments outside of those gathered in traditional patient-reported outcome questionnaires. Qualitative interviews can capture patients’ perceptions of treatment needs, more fully explore meaningful changes experienced as a result of treatment, and reveal outcomes that are most important to patients. Asking patients detailed questions can provide insight into the “why” of a patient’s expressed thought or feeling. The inclusion of patient interviews within clinical trials is a relatively new and evolving field of research. This article delineates the types of data that may be collected during interviews with clinical trial participants and outlines two approaches to conducting qualitative research in the clinical trial setting, with a focus on maximizing the value of the resulting data.
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Damiano, Peter C., Julie C. Reynolds, Jill Boylston Herndon, Susan C. McKernan et Raymond A. Kuthy. Patient-Centered Dental Home development project. Iowa City, Iowa : University of Iowa Public Policy Center, mars 2016. http://dx.doi.org/10.17077/fwo6-ezo4.

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Wilkins, Consuelo, Sarah Stallings, Sarah Stallings, Victoria Villalta-Gil, Mckenzie Houston, Yolanda Vaughn, Alan Richmond et al. Comparing Methods to Make Research More Patient Centered. Patient-Centered Outcomes Research Institute® (PCORI), décembre 2019. http://dx.doi.org/10.25302/12.2019.me.130603342.

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Perry, Rebecca, Nancy McCall, Suzanne Wensky et Susan Haber. Care Continuity in a Patient-Centered Medical Home Setting. RTI Press, février 2016. http://dx.doi.org/10.3768/rtipress.2016.rr.0026.1602.

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Velentgas, Priscilla, Donna Messner et Evan Myers. Comparing Patient-Centered Outcomes after Treatment for Uterine Fibroids. Patient-Centered Outcomes Research Institute (PCORI), mai 2018. http://dx.doi.org/10.25302/5.2018.ce.12114430.

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David, Guy, Philip Saynisch et Aaron Smith-McLallen. The Inner Workings of the Patient Centered Medical Home Model. Cambridge, MA : National Bureau of Economic Research, juillet 2016. http://dx.doi.org/10.3386/w22429.

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