Relevant bibliographies by topics / Patient and Person Centered Care

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Patient and Person Centered Care'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Patient and Person Centered Care"

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Lines, Lisa M., Michael Lepore, and Joshua M. Wiener. "Patient-centered, Person-centered, and Person-directed Care." Medical Care 53, no. 7 (July 2015): 561–63. http://dx.doi.org/10.1097/mlr.0000000000000387.

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Marcum, James, Jackson Griggs, and Lauren Barron. "Operationalizing person-centered medicine." European Journal for Person Centered Healthcare 2, no. 1 (February 10, 2014): 98. http://dx.doi.org/10.5750/ejpch.v2i1.712.

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To recapture medicine’s “soul” for the “care” of patients, Miles and Mezzich propose a version of person-centered medicine in which they “coalesce” both evidence-based medicine and patient-centered care. To that end, they identify 5 key principles from which they formulate a 4-part working definition of person-centered medicine. In this paper, we first analyze philosophically -ontologically, epistemologically and ethically - both their principles and definition and we then present a clinical case to operationalize their notion of person-centered medicine. We conclude with a brief comment on its feasibility for modern clinical practice.
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Morton, Rachael L., and Marcus Sellars. "From Patient-Centered to Person-Centered Care for Kidney Diseases." Clinical Journal of the American Society of Nephrology 14, no. 4 (February 27, 2019): 623–25. http://dx.doi.org/10.2215/cjn.10380818.

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Utarini, Adi. "Person-Patient-Family-Community Centered Care Semakin Penting." Journal of Hospital Accreditation 2, no. 02 (August 17, 2020): 30–31. http://dx.doi.org/10.35727/jha.v2i02.72.

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Situasi pandemi memberikan ancaman serius dalam pemberian pelayanan individual, terutama bagi pasien dengan infeksi virus Corona yang dirawat inap di rumah sakit. Aspek medis (diagnosis dan pengobatan) yang merupakan subtansi utama pelayanan masih menimbulkan tantangan dalam penatalaksanaan pasien dengan infeksi virus Corona. Namun pada situasi yang kompleks ini, pemberian pelayanan kesehatan yang berorientasi pada kebutuhan individual setiap manusia-pasien justru menjadi semakin penting. Setiap orang (termasuk pasien) membutuhkan dukungan yang lebih besar dan berarti dari keluarga dan masyarakat, serta tenaga kesehatan. Beberapa istilah sering digunakan dan memiliki makna, prinsip dan aktivitas yang berbeda, namun tumpang tindih atau merupakan suatu kontinum: person-centered care, patient-centered care dan family-centered care.
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Glick, Michael. "Precision-, patient-, and person-centered care, oh my." Journal of the American Dental Association 150, no. 3 (March 2019): 161–62. http://dx.doi.org/10.1016/j.adaj.2019.01.008.

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Zhao, Junqiang, Shangqian Gao, Jinfang Wang, Xinjuan Liu, and Yufang Hao. "Differentiation between two healthcare concepts: Person-centered and patient-centered care." International Journal of Nursing Sciences 3, no. 4 (December 2016): 398–402. http://dx.doi.org/10.1016/j.ijnss.2016.08.009.

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Ekman, Inger, Karl Swedberg, Charles Taft, Anders Lindseth, Astrid Norberg, Eva Brink, Jane Carlsson, et al. "Person-Centered Care — Ready for Prime Time." European Journal of Cardiovascular Nursing 10, no. 4 (December 2011): 248–51. http://dx.doi.org/10.1016/j.ejcnurse.2011.06.008.

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Long-term diseases are today the leading cause of mortality worldwide and are estimated to be the leading cause of disability by 2020. Person-centered care (PCC) has been shown to advance concordance between care provider and patient on treatment plans, improve health outcomes and increase patient satisfaction. Yet, despite these and other documented benefits, there are a variety of significant challenges to putting PCC into clinical practice. Although care providers today broadly acknowledge PCC to be an important part of care, in our experience we must establish routines that initiate, integrate, and safeguard PCC in daily clinical practice to ensure that PCC is systematically and consistently practiced, i.e. not just when we feel we have time for it. In this paper, we propose a few simple routines to facilitate and safeguard the transition to PCC. We believe that if conscientiously and systematically applied, they will help to make PCC the focus and mainstay of care in long-term illness.
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Garneau, Kevin, Thomas Hutchinson, Qinyi Zhao, and Patricia Dobkin. "Cultivating person-centered medicine in future physicians." European Journal for Person Centered Healthcare 1, no. 2 (November 18, 2013): 468. http://dx.doi.org/10.5750/ejpch.v1i2.688.

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Person-centered medicine, while valued implicitly, is not always taught explicitly in medical schools or during residency programs. Threats to educating and practicing person-centered medicine include perceived lack of time, stress, burnout and a paucity of mentors with a systematic approach to modeling and teaching students how to relate to patients in a way that addresses them as whole persons. Herein we review how trainee stress and burnout negatively impact patient care and outline a program designed to teach mindful medical practice that may be an antidote to these problems. Moreover, we present quantitative data and a student’s narrative to highlight how to cultivate person-centered medicine in trainees.Fifty-eight 4th year medical students completed questionnaires pertaining to: depression, burnout, stress, wellbeing, self-compassion and mindfulness before and after taking a 4-week elective entitled, Mindful Medical Practice. Statistically significant improvements were found on emotional exhaustion, depression, self-compassion and mindfulness. One student’s experiences highlighted how what he learned in the elective guided him during his family medicine residency. We conclude with a discussion of how the culture of medicine and the training of future physicians in particular, need to take the whole persons of both the physician and patient into account in order for all to be satisfied with and benefit from medical care.
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Mandal, Debashish, Robert J. McQueen, Owen Doody, and Ita Richardson. "Role of social media to support person-centered care in small healthcare practices." European Journal for Person Centered Healthcare 5, no. 2 (July 6, 2017): 170. http://dx.doi.org/10.5750/ejpch.v5i2.1258.

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Rationale, aims and objectives: Healthcare practitioners use social media to receive feedback from patients to deliver better person-centered care. The aim of this research was to investigate the ability of social media to support person-centered healthcare in small practices. The objectives of this study were to: (a) diagnose their existing patient care processes; (b) introduce social media to them as an additional channel for communication and feedback with their patients & (c) examine the effectiveness of social media to support delivery of person-centered healthcare.Method: The study used an action research method to train 20 healthcare practitioners in small practices in the use of social media. Data were collected through unstructured interviews and analysis of social media scripts. Thematic analysis of the source data was undertaken, supported by Nvivo software.Results: Practitioners reported that social media assisted and supported delivery of person-centered healthcare if suitable training and implementation processes were used. The introduction of social media increased healthcare practitioners’ socialising and personalising capabilities, which enhanced their capability to empathise with patients. Socialising increased because of improved 2-way communication and trust between practitioner and patient and improved a practitioner’s capability to personalise care for patients. Through building trust and additional communication, practitioners were better able to motivate patients to undertake behavioural changes.Conclusions: Social media use can enhance person-centered care by bridging social, economic and demographic differences between practitioner and patient. Small healthcare practitioners need suitable training in social media to support person-centered healthcare.
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Qidwai, Waris, Kashmira Nanji, Tawfik Khoja, Salman Rawaf, Nabil Yasin Al Kurashi, Faisal Alnasir, Mohammed Ali Al Shafaee, et al. "Are we ready for a person-centered care model for patient-physician consultation? A survey from family physicians of East Mediterranean Region." European Journal for Person Centered Healthcare 1, no. 2 (November 18, 2013): 394. http://dx.doi.org/10.5750/ejpch.v1i2.679.

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Background: Person-centered care has long been identified as a key component of health systems and one of the six domains of quality. This study aimed to identify the perceptions of patients and physicians regarding person-centered care in the Eastern Mediterranean Region (EMR).Methods: A multicountry, cross-sectional study was conducted in 6 countries of EMR during July 2012 to September 2012. From each country, an expert Family Physician (FP) was identified and invited for the study. During the first phase, 190 FPs practicing for at least 6 months were recruited. In the second phase, the recruited FPs approached 300 patients aged > 18 years with 1 or more recurring problems. Data analysis was conducted using SPSS version 19.Results: Of a total of 360 patients, 53% were between 25-40 years of age and the majority 55.7% were females. Among physicians, 66.8% were females and 72.1% had undergone specialization in Family Medicine from EMR. About 36% of the patients, while 62.6% of the physicians, preferred a person-centered care model of care. Among physicians, field of specialization (AOR= 0.7; 95% C.I: 0.3-0.9) and regularity in continuing medical education sessions (AOR= 0.3; 95% C.I: 0.1-0.5) were significant factors for preferring a person-centered care model. Educational status (AOR= 3.0; 95% C.I: 1.1-7.9) was associated with a preference for person-centered care among patients.Conclusion: The results of the study highlight that a majority of physicians prefer person-centered care, while patients prefer a mix of both patient- and physician-centered care. Strategies should be developed that will help physicians and patients to embrace person-centered care practices.
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Dissertations / Theses on the topic "Patient and Person Centered Care"

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Hughes, LaTonya Dickerson. "The Nurse and Certified Nursing Assistant Perception of Person-Centered Care." ScholarWorks, 2019. https://scholarworks.waldenu.edu/dissertations/6585.

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Over the last decade, long-term care facilities have transitioned from institutional care models that focus on person-centered care, in which the resident is the center of the care. The purpose of this study is to explore the nurse and certified nursing assistant perception of the person-centered care services they deliver. Jean Watson's theory of human caring is the theoretical framework that guided this study. The theory focusing on the human caring experiences and person-centered care is being characterized as a caring feeling. The carative factors of Watson's theory, the fundamental concept of caring, has been associated with improved outcomes for the resident and the caregiver. Using a phenomenology research design, 3 focus groups of 15 nurses and 10 certified nursing assistants (CNA), working in a long-term care facility, were asked questions to describe their perception of person-centered care. The responses from the 25 participants were stored and organized using Nvivo. The thematic analysis revealed that the nurses and CNAs perceived person-centered care to include the caring and compassionate approach taken when care is being delivered. The participants also shared that person-centered care included involving the resident in decision making through communicating openly and developing relationships. The discussions revealed that 8 carative factors influenced their understanding, with the main factor being the creative problem-solving method for decision making. The �ndings from this study have the potential to impact positive social change at the organizational level, influencing the delivery of care within long-term care settings.
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Gustafsson, Christopher, and Tobias Hansson. "Livet efter en genomgången hjärtinfarkt : Den förändrade vardagen." Thesis, Högskolan Väst, Avdelningen för omvårdnad - grundnivå, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:hv:diva-15443.

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Background: The number of people suffering from myocardial infarction in Sweden is decreasing, despite this the prevalence is high. Being diagnosed with myocardial infarction results in medical interventions, lifestyle changes and eventual pharmacological treatment to prevent relapse. Aim: The aim of this study was to describe patients' experience of life after amyocardial infarction. Method: A literature-based study was used, based on ten qualitative articles. The articles were analyzed in a five step-model, which resulted in three main-themes and sixsub-themes. Results: The results present life after myocardial infarction as difficult to understandand manage. This could be related to their physical and mental changes, which resulted in fear and anxiety that affected their everyday lives through experienced limitations. Fatigue where also a contributing factor in the limitations of everyday life due to energyloss. This was hard to handle without support from both relatives and health care professionals. It was essential to be meet as a unique human and not reduced to a diagnosis. Life became more valuable through the survival and gave the individuals a second chance with different priorities. Some adjusted to the lifestyle changes, while others were reluctant. Returning to work where seen as an indicator for being healthy and a return to life as before. Conclusion: To establish well-being and security through nursing, a holistic approach that is the basis of person-centered care helps nurses to see the individual situation.
I Sverige minskar antalet personer som drabbas av hjärtinfarkt trots detta är förekomsten fortfarande hög och ca 5800 avlider varje år. Hjärtinfarkten medför både fysiska och psykiska förändringar hos den drabbade. Syftet med denna litteraturstudie är att belysa patienters upplevelse av livet efter en genomgången hjärtinfarkt. I studiens resultat framkom det att både män och kvinnor såg situationen och livet efter en hjärtinfarkt som svår att hantera, då både kroppen och hjärtat inte längre upplevdes pålitligt. Detta resulterade i rädsla och oro som begränsade det vardagliga livet. Personerna upplevde att det var svårt att tolka kroppsliga signaler, vilket gav en osäkerhet som resulterade i ångest och katastrof tankar om döden. Detta medförde även att de inte vågade anstränga sig fysiskt. Känslor som ilska, frustration och nedstämdhet upplevdes på grund av den mentala och fysiska utmattningen som var svår att förstå. Personerna kunde inte utföra vardagsaktiviteter i samma utsträckning som innan hjärtinfarkten, vilket resulterade i en känsla av passivitet. Det utrycktes även ett behovav stöd från anhöriga och vårdpersonal för att klara av sin situation och det vardagligalivet. Vårdpersonalens bemötande och agerande var avgörande för hur patienterna förstod informationen som gavs, deltog i rehabilitering och klarade att genomföra nödvändiga förändringar när det gäller ohälsosamma levnadsvanor. Vårdpersonalens förmåga att skapa en trygg atmosfär tillsammans med att se patienten som människa var viktigt för att uppnå välbefinnande. Anhöriga sågs som en resurs för personerna då de kunde avlasta vardagssysslorna samtidigt som de lyssnade, vilket gav trygghet och välbefinnande hemma. Patienter upplevde att familjen satt för höga krav och fick då stödet från vänner. Partnerrelationen kunde påverkas genom den minskade sexuella relationen som grundade sig i rädsla för de fysiska förändringarna och upplevdes svårt att prata om med partnern. Livet efter en hjärtinfarkt beskrevs som en ny chans till livet där nya värderingar uppstod. Personerna upplevde att arbetsgivarens attityd och förståelse för situationen var avgörande för fortsatt sjukskrivning. För att kunna möta patientens unika behov och skapa välbefinnande genom omvårdnad, är personcentrerat förhållningssätt lämpligt för att vidhålla en helhetssyn på patienten och inte bara det fysiologiska tillståndet.
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Löfgren, Karolina, Susanna Sjöberg, and Linnea Neugebauer. "Vietnamese nursing students` perception of person-centered care. : A Minor Field Study in Vietnam." Thesis, Hälsohögskolan, Jönköping University, HHJ, Avd. för omvårdnad, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-48700.

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Summary Background: Person-centred care is a concept which aims to achieve quality in health care. Person-centred care is about taking the patient's own story into account and creating a partnership between all involved parties. Aim: Exploring nursing students` perception of person-centred care in Vietnam. Method: This study is a qualitative study with a semistructured interview guide. It has a deductive approach with a directed content analysis. Twelve nursing students were interviewed in this study. Result: The result showed that communication, nurses' knowledge, mutual respect, cooperation and family’s experienced knowledge about the patient were identified as important parts of the participants perceptions about person-centred care in Vietnam. Challenges such as time constraints and misunderstandings were shown to be a repeating problem. Conclusion: The nursing students' perception about implementing person-centred care in Vietnam is positive, but there are challenges in applying this in practice. The number of patients related to the number of nurses is uneven, which may lead to problems in Vietnam regarding person-centered care.
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Zeleskov, Lilia, and Hong Mei. "Patientnära rond : Patientens och sjukvårdspersonalens perspektiv." Thesis, Uppsala universitet, Institutionen för folkhälso- och vårdvetenskap, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-309043.

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Bakgrund: Patientnära rond är ett teamarbete mellan framförallt patient, sjuksköterska och läkare. Ett bra samarbete förbättrar relationen dem emellan. Dessutom har en framgångsrik rond mellan patient och sjukvårdspersonal stor betydelse för att patienten ska kunna få en säker och personcentrerad vård. Därför är det viktigt att få en djupare förståelse för hur patienter och sjukvårdpersonal upplever patientnära rond samt för betydelsen av teamarbetet vid patientnära rond. Syfte: Att belysa vilka effekter patientnära rond har på vårdteam samt att undersöka upplevelsen av patientnära rond utifrån perspektiven från både patienter och sjukvårdspersonal (sjuksköterskor, läkare och medicinstudenter). Metod: En litteraturstudie baserad på 14 vetenskapliga originalartiklar. Databaser som användes i studien var PubMed, Cochrane Library, Cinahl, SBU och SveMed. Resultat: Resultatet av denna studie indikerar att både patienter och sjukvårdspersonal upplever en ökad tillfredsställelse vid patientnära rond. Vidare visar resultatet att patientnära rond bidrar till att sjukvårdpersonal kan ge patienter en proaktiv omvårdnad, att samarbetet sjukvårdpersonal emellan blir mer effektivt och att patientnära rond gynnar medicinstudenters utveckling samt ökar studenters tillfredsställelse med sin utbildning. En utmaning som sjuksköterskor upplever i samband med patientnära rond är tidsbegränsning – framför allt upplever de att det tar tid för sjuksköterskor och läkare att synkronisera och koordinera mötet mellan patient och vårdpersonal samt att tid för dokumentation är bristande. Läkare upplever dessutom att deras autonomi minskas i samband med patientnära rond. Slutsats: Överlag kan patientnära rond vara ett effektivt sätt att främja personcentrerad vård. Patientnära rond har en positiv inverkan på teamarbete sjukvårdpersonal emellan samt bidrar till ökad tillfredsställelse hos både patienter och sjukvårdspersonal. Det finns dock behov av ytterligare forskning om patienters upplevelse av patientnära rond och vilka specifika åtgärder som kan vidtas för att sjukvårdpersonalen ska kunna samarbeta på ett mer effektivt sätt.
Background: The ward round is a team collaboration mainly between patient, nurse and physician. A good collaboration enhances the relationship between them. In addition, a successful round between the patient and the medical personnel is of great significance for the patient to have a safe and person-centered care. Therefore it is important to gain a deeper understanding of how patients and medical staff experience ward rounds, as well as of the importance of team work during the ward rounds. Aim: To shed light upon the effects of ward rounding on healthcare teams and to explore the experience of ward rounds from the perspectives of both patients and medical staff (nurses, physicians and medical students). Method: A literature study based on 14 scientific articles. Databases used in the study were PubMed, Cochrane Library, CINAHL, SBU and SveMed. Results: The results of this study indicate that both patients and medical personnel experience an increased satisfaction during ward rounds. Furthermore, the results show that ward rounds contribute in making medical personnel provide a proactive care to their patients, that cooperation between medical staff becomes more efficient, and that ward rounding benefits medical students’ development and increases students’ satisfaction with their education. A challenge that nurses experience during ward rounds is time limitation – mainly they experience that it takes time for nurses and physicians to synchronize and coordinate the meeting between patient and medical personnel, and also that the time for documentation is inadequate. Physicians also experience that their autonomy is reduced in relation to ward rounds. Conclusion: Overall, ward rounding can be an effective way to promote person-centered care. Ward rounds have a positive impact on teamwork between medical personnel and contribute to increased satisfaction among both patients and medical staff. However, there is need for further research on patients' perception of ward rounding and which specific measures that can be taken for the medical staff to be able to collaborate more efficiently.
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Latif, Mustafa Kanyau, and Linda Edvardsson. "Upplevelser av bemötande i vården hos patienter med fibromyalgi- en litteraturöversikt." Thesis, Högskolan Dalarna, Omvårdnad, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:du-20938.

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Bakgrund: Fibromyalgi är ett långvarigt kroniskt smärttillstånd som grundar sig på individens subjektiva smärtupplevelse. Syfte: Syftet var att beskriva hur patienter med fibromyalgi upplevt bemötande i vården. Metod: Denna litteraturöversikt baseras på tretton vetenskapliga artiklar. Resultat: Resultatet resulterade i två huvudkategorier "Patienters upplevelser av bemötande" och "Kunskap och stöd från vårdpersonalen". Patienterna med fibromyalgi upplever dåligt bemötande och att vårdpersonal saknar kunskap om både diagnos och behandling av fibromyalgi. I vården upplever dessa patienter misstro och att de blir dåligt bemötta när de söker för sina smärtsymtom. Patienter med fibromyalgidiagnos önskar ett personcentrerat bemötande och mer tid av sina läkare. Slutsatser: Litteraturöversikten visar att patienter med fibromyalgi i stor utsträckning uppger att de upplever dåligt bemötande, okunskap och brist på engagemang i vården. Framtida forskningen bör fokusera på hur vården kan arbeta mer personcentrerat i denna patientgrupp till exempel genom interventionsstudier.
Objectives: Fibromyalgia has long been a chronic pain condition that bases itself on the individual's subjective experience of pain. Aim: The aim was to describe how patients with fibromyalgia experience the treatment, support and attitudes by the health care personal. Methods: This study is a literature review based on thirteen articles’. Results: The result resulted in two main categories "Patients experiences of treatment" and "Knowledge and support from the medical staff". The patients experience that the health care personal has a lack of knowledge of both diagnosis and treatment. The patients also experience distrust in their doctors and experience a lack of adequate help when seeking for their painful symptoms. Patients with fibromyalgia diagnosis experience poor treatment in health care, and want a person-centered approach and more time by their doctors. Conclusions: This literature review shows that patients with fibromyalgia report that they experience poor treatment, ignorance and lack of commitment from health care. Research should focus on how services can work more person-centered for this group of patients, for example by intervention studies.
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Josephson, Samuel, and Matilda Freijd. "Bedsiderapportering : - En litteraturöversikt." Thesis, Hälsohögskolan, Högskolan i Jönköping, HHJ, Avd. för omvårdnad, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-29215.

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Bakgrund: Patientrapportering är det informationsutbyte mellan vårdpersonal som handlar om den vårdsökande personens hälsotillstånd. Tidigare forskning visar att kommunikationsbrister kan få allvarliga konsekvenser för den vårdsökande. Vid bedsiderapportering förflyttas rapporteringen till sängkanten. Därmed kan den vårdsökande själv vara delaktig i rapporteringen. Syfte: Att beskriva vårdsökandes och sjuksköterskors upplevelse och uppfattning av bedsiderapportering. Metod: En litteraturöversikt genomfördes utifrån 11 studier som svarade mot syftet. Dessa kvalitetsgranskades och analyserades med hjälp av Fribergs trestegsmodell. Resultat: Från artiklarna med fokus på vårdsökande personer framkom tre teman: 1) Ger ökad trygghet. 2) Integriteten kan påverkas 3) Kommunikation anpassad efter vårdsökande. Från artiklarna med fokus på sjuksköterskor framkom tre teman: 1) Att komma vårdsökande närmare. 2) Vikten av att hantera sekretess och känslig information rätt. 3) Förbättrad kommunikation. Slutsats: Huvudfynden som framkom var ökad säkerhet samt ökad delaktighet. Dessa huvudfynd är begrepp som en personcentrerad omvårdnad bygger på och för den vårdpersonal som ämnar bedriva en personcentrerad omvårdnad skulle bedsiderapportering med fördel kunna implementeras som rapporteringsmodell.
Background: Nurse-to-nurse shift report means the exchange of information about the patient’s state of health between health care professionals. Previous research shows that errors within the communication are common and that it can lead to serious consequences for the patient. Bedside handover means that the shift report is conducted to the patient’s bedside, therefore the patient can also be actively involved in it.  Aim: To describe patients' and nurses’ experience and views of bedside report. Method: A literature review was conducted based on 11 studies that corresponded to the purpose. These were quality checked and analyzed with Friberg's three-stage model. Results: Articles focusing on patients was revealed into three themes: 1) Provides increased safety. 2) The integrity could be affected. 3) Communication adapted to patient. Articles focusing on nurses was revealed into three themes: 1) To get closer to the patient. 2) The importance of dealing with privacy and sensitive information in a correct way. 3) Improved communication. Conclusion: The main findings in this literature review were increased patient safety and increased sense of patient participation. These findings are notions which the person-centered care is based on. Health care professionals who intend to pursue a person-centered care should consider implementing bedside handover as their report model.
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Rosengren, Magdalena, and Louisa Skärvstrand. "Personcentrerad vård av patienter med demenssjukdom - Sjuksköterskans erfarenheter." Thesis, Malmö universitet, Fakulteten för hälsa och samhälle (HS), 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:mau:diva-26859.

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Bakgrund: Idag finns cirka 150 000 individer i Sverige med demenssjukdom och gruppen växer i takt med att befolkningen blir äldre. Personcentrerad vård har sitt ursprung inom humanistisk psykologi och begreppet beskrevs redan på 1960-talet. Personcentrerad vård är en av sjuksköterskans sex kärnkompetenser och är en god grund för att tillgodose de varierande behov som finns hos den komplexa patientgruppen. Syfte: Syftet med litteraturstudien är att belysa vad sjuksköterskans erfarenheter är av att ge personcentrerad vård till patienter med demenssjukdom. Metod: En litteraturstudie vars resultat baseras på studier med kvalitativ ansats. Vid sökning användes databaserna; CINAHL, PsycINFO och PubMed. Resultatets femton artiklar analyserades enligt Forsberg och Wengströms (2016) femstegsmetod. Resultat: Resultatet presenterades med hjälp av fyra huvudteman; organisationen, patientrelationen, kommunikation, vårdmiljö samt sju underteman; stöd på arbetsplatsen, kompetensutveckling, tids- och personalbrist, livsberättelsen - patientens historia, personliga attribut, samverkan i team och dokumentationsrutiner. Konklusion: Hälso- och sjukvården är en komplex organisation och sjuksköterskan står inför många utmaningar. Otillräckligt stöd från både ledning och kollegor samt vårdmiljöns utformning var alla faktorer som påverkade sjuksköterskans möjlighet att tillgodose personcentrerad vård. Vidareutbildning i kommunikation och demenssjukdomar upplevde sjuksköterskorna gynnsamt för deras arbete. Även vikten av att ha en god relation till patienten och att lära sig deras livshistoria framhölls som viktiga komponenter i den personcentrerade vården.
Background: Today there is approximately 150 000 individuals with dementia in Sweden and the group is expanding at the same time the population is ageing. Person centred care has its roots in humanistic psychology and the concept was described already in the 1960’s. Person centred care is one of the nurses’ six core competencies and is a good foundation for the various needs amongst the complex patientgroup. Aim: The aim for the literature review is to illustrate nurses’ experiences of giving person centred care to patients with dementia. Method: A literature review with a result based on studies with a qualitative approach. Databases used was CINAHL, PsycINFO and PubMed. The fifteen articles of the result were analyzed according to Forsberg and Wengströms (2016) model of five steps. Results: The result was presented using four main themes; the organisation, patient-relations, communication, care environment and seven subthemes; workplace support, quality of competens, lack of time and personel, lifestory - a patient’s history, personal attributes, team cooperation and documentation routines. Conclusion: The health-care system is a complex organisation and the nurse faces many challenges. Insufficient support from both management and colleagues and the formation of the care environment was all factors that affected the nurses’ ability to provide person centred care. More education in communication and different types of dementia illnesses were seen by nurses as positive contribution in their work. Even the importance of having a good relationship with the patient and learn about their lifestory was brought to daylight as important components in person centred care.
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Brantberg, Anna Lena. "När det inte blev som planerat : Patienters delaktighet i det infektionsförebyggande arbetet och i upptäckten av tidig postoperativ infektion vid höft- eller knäprotesoperation." Thesis, Röda Korsets Högskola, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:rkh:diva-887.

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Höft- och knäprotesoperationer är idag en vanlig operation vid artros i höft- och knäled. Trotsminutiösa infektionsförebyggande förberedelser inför operationen drabbas ändå en delpatienter av postoperativa infektioner. Vid ortopedisk proteskirurgi är postoperativainfektioner ett direkt hot mot den nya inopererade leden och kan leda till långabehandlingstider som påverkar patientens livskvalitet under lång tid. Syftet med studien var att utforska patienters möjlighet till delaktighet i tidig upptäckt avpostoperativ infektion utifrån given information vid operation för höft- eller knäprotes. Semi-strukturerade intervjuer genomfördes med tio patienter med diagnostiserad postoperativinfektion efter höft- eller knäprotesoperation. Transkriberade intervjuer analyserades medinnehållsanalys. Journaler granskades för att beskriva patientens tidigare sjukdomar. Resultatet visade att första tecknen på infektion kan beskrivas med temat: Vad är normalt ochvad är inte normalt. Två kategorier beskriver patienternas Möjlighet till delaktighet ochHinder till delaktighet i det infektionsförebyggande arbete före, under och efter operation. Det handlade om hur patienten hade förstått eller inte förstått given information, vilketkategoriserades som subkategorier. Personcentrerad vård kan vara ett redskap för att stärka patienternas förutsättningar tilldelaktighet och ökar möjligheterna för att förhindra att vårdskador så som postoperativainfektioner uppstår.
Surgery with prosthetic joint replacement of the hip and knee in patients with osteoarthritis is a common procedure. Despite meticulous preparation prior to surgery, surgical site infections develop in some patients. A surgical site infection is a direct threat to the new implanted joint and can lead to long treatments that affect quality of life over time. The aim of this study was to explore patients´ participation in early detection of a surgical site infection based on the information given in conjunction to surgery for hip and knee replacement. Semi structured interviews were conducted with ten patients diagnosed with surgical site infection after hip or knee replacement surgery. Transcribed interviews were analyzed using content analysis. Medical records were reviewed to describe the patients´ comorbidity. The result showed that the first signs of infection can be described with the theme; What is normal and what is not normal? Two categories describe patients´ Possibility of participation and Barriers to participation in infection prevention before and after surgery. It was all about How the patient had understood or not understood the given information which was categorized as subcategories. Person-centered care can be a tool that enables patients´ possibilities to participate in their care and increases the possibilities to prevent adverse events such as surgical site infections.
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Berglund, Riikola Caroline, and Linda Fors. "Att vara patient på svensk akutmottagning – En litteraturöversikt." Thesis, Högskolan i Skövde, Institutionen för hälsovetenskaper, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-18361.

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Bakgrund: Patientbesöken på svenska akutmottagningar har minskat men väntetider har ökat. Systemet triage används av sjuksköterskor för att prioritera patienter med utifrån deras anamnes och symtom. En god vårdmiljö, regelbunden kommunikation, information, ökad delaktighet och personcentrerad vård kan minska uppkomsten av vårdlidande för patienter som sökt vård på svenska akutmottagningar. Syftet: Syftet var att belysa hur det är att vara patient under väntetiden på svensk akutmottagning. Metod: Studien är en litteraturöversikt som är baserad på tio vetenskapliga artiklar med kvalitativ metod. Resultat: Tre huvudkategorier mötet med sjuksköterskan, faktorer som påverkar upplevelsen, konsekvenser av bristande vård. Sex underkategorier positiva erfarenheter, negativaerfarenheter, vårdmiljöns inverkan, grundläggande behov, utsatthet och sårbarhet samt situationen accepteras. Diskussion: I diskussionen redogör författarna patientersupplevelser från akutmottagningen. Det diskuterades kring tre begrepp personcentrerad vård, vårdlidande och delaktighet. Konklusion: Det framkom att när grundläggande behov blev tillgodosedda, information gavs och när sjuksköterskan gav bekräftelse kunde delaktigheten öka och vårdlidande förhindras.
Background: Patient visits at Swedish emergency departments have decreased, but waitingtimes has increased. The triage system is used by nurses to prioritize patients based on their health background and symptoms. A good care environment, regular communication, information, increased participation and person-centered care can reduce the incidence of caregiving for patients who have sought care at Swedish emergency departments. Aim: The aim of this study was to illustrate what it is like to be a patient under waiting time at a Swedish emergency department. Method: This study is a literature review based on ten scientific articles with a qualitative method. Results: Three main categories of meeting with the nurse, factors affecting the experience, consequences of inadequate care. Six subcategories of positive experiences, negative experiences, the impact of the care environment, basic needs, exposure and vulnerability and situation is accepted. Discussion: In the discussion, the authors emphasize patients’ experiences from the emergency department. It was discussed around three concepts person-centered care, caregiving and participation. Conclusion: It emerged that when basic needs were met, information was provided and when the nurse gave confirmation, participation increased, and care sufferers could be prevented.
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Amir, Catrine, and Carolina Ringvall. "Patient upplevelsen av att leva med tarmstomi : En litteraturöversikt." Thesis, Röda Korsets Högskola, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:rkh:diva-2316.

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Bakgrund: En tarmstomi kan innebära stora fysiska och psykiska förändringar samt begränsningar i en patients liv. Kolorektalcancer och inflammatoriska tarmsjukdomar är de vanligaste orsakerna till tarmstomi. Stomiterapeuter är specialutbildade sjuksköterskor, när denna personalgrupp inte finns att tillgå, är det grundutbildade sjuksköterskors som tillgodoser omvårdnaden för patienten. Syfte: Att belysa patientens upplevelse av att leva med tarmstomi. Metod: En allmän litteraturöversikt baserad på elva kvalitativa artiklar. Resultat: Analysen resulterade i fyra teman. Påverkan i det dagliga livet, förändrade vanor som påverkade patientens liv. Kroppsuppfattningen, tarmstomin förändrade patientens syn på sin kropp. Stöd, om vikten av sjuksköterskans roll i omvårdnaden. Information, från sjuksköterskan utgjorde en viktig del i omvårdnaden av egenvård. Slutsats: Det är viktigt att sjuksköterskan i sin roll anpassar omvårdnaden individuellt samt beaktar patienten utifrån patientens individuella behov. Sjuksköterskans kan i sin roll motivera patienten till delaktighet i sin egenvård samt ge stöd för patienten till anpassningen av tarmstomin. Genom att förhålla sig till den personcentrerade vården kan sjuksköterskan beakta hela patientens upplevelse samt få en djupare kunskap av att förstå patientens upplevelse av att leva med tarmstomi. Fortsatt forskning: Som sjuksköterska är det viktigt att hela tiden ta del av aktuell forskning i syfte att förbättra omvårdnaden av patienter med tarmstomi. Vidare forskning behövs, då specifikt forskning saknades inom område personcentrerad- och tarmstomivård.
Background: An intestinal stoma could mean great physical and mental changes and restrictions in a patient's life. Colorectal cancer and inflammatory bowel diseases are the most common causes of intestinal stoma. Stoma therapists are specially trained nurses, when they are not available, it is ordinary nurses that cater to the care of the patient. Aim: To illuminate the patient's experience of living with intestinal stoma. Method: A general literature review based on eleven qualitative articles. Results: The analysis resulted in four themes. Impact on daily life, change of habits that affect the patient's life. Body image, intestinal stoma changed the patient’s view of their body. Support, the importance of the nurse's role in nursing. Information, provided by the nurse was an important element in the self-care. Conclusion: It is of importance that the nurses in their role adapts the care individually and take into account the patient based on the patient’s individual needs. The nurse can also motivate the patient to participate in self-care and provide support for the patient to the adjustment of the intestinal stoma. By relating to the person-centered care the nurse can take the patient’s whole experience into account and gain a deeper knowledge of understanding the patient’s experience of living with an intestinal stoma. Continued research: As a nurse, it is important to always take note of current research in order to improve the care of patients with intestinal stoma. Further research is needed, since specific research was lacking in the area person-centrered and intestinal stoma care
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Books on the topic "Patient and Person Centered Care"

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author, Disch Joanne Marilyn, Walton Mary K. author, and Sigma Theta Tau International, eds. Person- and family-centered care. Indianapolis, IN: Sigma Theta Tau International, Honor Society of Nursing, 2014.

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Serious mental illness: Person-centered approaches. London: Radcliffe Pub., 2011.

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Models and pathways for person-centered elder care. Baltimore, Maryland: Health Professions Press, 2014.

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Bower, Anne R. Redefining person-centered care: A roadmap for culture change. [New York City]: Alzheimer's Association, New York City Chapter, 2008.

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Goodrich, Joanna. Seeing the person in the patient: The point of care review paper. London: King's Fund, 2008.

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N, Edwards Paul R., ed. Enriched care planning: A good practice guide for delivering person-centred care. London: Jessica Kingsley Publishers, 2009.

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Rantz, Marilyn J. Person centered care: A model for nursing homes. Washington, D.C: American Nurses Association, 2003.

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Sarah, Povey, ed. The creative arts in dementia care: Practical person-centred approaches and ideas. Philadelphia: Jessica Kingsley Publishers, 2010.

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Adams, Neal. Treatment planning for person-centered care: The road to mental health and addiction recovery : mapping the journey for individuals, families, and providers. Amsterdam: Elsevier Academic Press, 2005.

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A psychodynamic understanding of modern medicine : placing the person at the center of care. London: Radcliffe Publishing, 2012.

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Book chapters on the topic "Patient and Person Centered Care"

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Weigel, Kathryn A. "Patient-/Person-Centered Care." In Dementia in Nursing Homes, 21–27. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-49832-4_3.

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Perzynski, Adam, Carol Blixen, and Martha Sajatovic. "Where Is the Patient? Finding the Person in Patient-Centered Health Care." In Health Disparities, 29–31. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-12771-8_6.

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Martinchek, Michelle, and Katherine Thompson. "Patient-Centered Care for Persons with Multiple Conditions." In Geriatric Practice, 117–27. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-19625-7_9.

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Corrigan, Patrick W., Karina J. Powell, and Patrick J. Michaels. "Beyond the rational patient: Implications for health decisions and behaviors." In Person-centered care for mental illness: The evolution of adherence and self-determination., 29–51. Washington: American Psychological Association, 2015. http://dx.doi.org/10.1037/14644-003.

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Davidson, Larry, Janis Tondora, Rebecca Miller, and Maria J. O'Connell. "Person-centered care." In Person-centered care for mental illness: The evolution of adherence and self-determination., 81–102. Washington: American Psychological Association, 2015. http://dx.doi.org/10.1037/14644-005.

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Garcia, Danilo, Kevin M. Cloninger, Kristian Molander-Söderholm, Lil Carleheden Ottosson, Inger Jönsson, Max Rapp Riccciardi, Andrzej Zielinski, et al. "Person-Centered Care." In Encyclopedia of Personality and Individual Differences, 3872–78. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-319-24612-3_2304.

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Garcia, Danilo, Kevin M. Cloninger, Kristian Molander-Söderholm, Lil Carleheden Ottosson, Inger Jönsson, Max Rapp Riccciardi, Andrzej Zielinski, et al. "Person-Centered Care." In Encyclopedia of Personality and Individual Differences, 1–7. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-28099-8_2304-1.

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Groves, Joanna. "Person-Centered Patient Perspectives." In Person Centered Psychiatry, 113–25. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-39724-5_9.

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Braunstein, Mark L., and Mark L. Braunstein. "Patient-Centered Care." In Health Informatics in the Cloud, 55–65. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-5629-2_5.

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Frezza, Eldo E. "Patient-Centered Care." In 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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Conference papers on the topic "Patient and Person Centered Care"

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Nagy, Diána. "Possibilities of Digitalization and Service Design in the Development of Patient Adherence." In New Horizons in Business and Management Studies. Conference Proceedings. Corvinus University of Budapest, 2021. http://dx.doi.org/10.14267/978-963-503-867-1_05.

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In parallel with the development of modern health systems and the growth of the welfare state, diseases have shifted towards chronic diseases. Today, instead of rapid-onset infections, most resources are focused on the long-term treatment of mostly lifelong chronic conditions. The condition for the effective use of therapies is to take the specified dose with the prescribed frequency and for the required period of time. If these parameters are met, we can talk about patient collaboration or adherence. For certain diseases and treatments, adherence is critically low. In the case of complex preparations to be taken several times a day, or diseases that do not cause serious, noticeable complaints, the initial number of patients treated is reduced to a fraction within a short time. As a result, economic harm is perceived not only by the patient but also by all those involved in the health care system, including pharmaceutical companies. However, the factors influencing patient collaboration vary widely. In order to achieve high adherence, the goal is to develop health services that coordinate the actors involved, the infrastructure, the communication, the material components to improve the user experience. As a user-centered methodology, service design can play a prominent role in the design of therapeutic services, contributing to the reduction of uncertainties in innovation processes. In my study, I assess the digital toolkit of patient education in Hungarian society. The aim is to explore digital tools and technologies that can contribute to the development of health awareness and education so that both science and the pharmaceutical and technology companies that exploit it can apply the results of research.
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Nejat, Goldie, and Maurizio Ficocelli. "Social Intelligence for a Task-Driven Assistive Robot." In ASME 2010 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. ASMEDC, 2010. http://dx.doi.org/10.1115/detc2010-28674.

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The objective of a socially assistive robot is to create a close and effective interaction with a human user for the purpose of giving assistance. In particular, the social interaction, guidance and support that a socially assistive robot can provide a person can be very beneficial to patient-centered care. However, there are a number of conundrums that must be addressed in designing such a robot. This work addresses one of the main limitations in the development of intelligent task-driven socially assistive robots: Robotic control architecture design and implementation with explicit social and assistive task functionalities. In particular, in this paper, a unique emotional behavior module is presented and implemented in a learning-based control architecture for human-robot interactions (HRI). The module is utilized to determine the appropriate emotions of the robot, as motivated by the well-being of the person, during assistive task-driven interactions. A novel online updating technique is used in order to allow the emotional model to adapt to new people and scenarios. Preliminary experiments presented show the effectiveness of utilizing robotic emotional assistive behavior during HRI in assistive scenarios.
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Thomassen, Hanne E., and Babak A. Farshchian. "A technology-enhanced service for person-centered dementia care." In PETRA '16: 9th ACM International Conference on PErvasive Technologies Related to Assistive Environments. New York, NY, USA: ACM, 2016. http://dx.doi.org/10.1145/2910674.2910722.

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Jacobs, Maia. "Designing personalized technology to augment patient-centered care." In the 2015 ACM International Joint Conference. New York, New York, USA: ACM Press, 2015. http://dx.doi.org/10.1145/2800835.2801653.

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Ruan, Ji, Wendy MacCaull, and Heather Jewers. "Enhancing Patient-Centered Palliative Care with Collaborative Agents." In 2010 IEEE/ACM International Conference on Web Intelligence-Intelligent Agent Technology (WI-IAT). IEEE, 2010. http://dx.doi.org/10.1109/wi-iat.2010.259.

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Wati, Dian Kusuma, Eti Poncorini Pamungkasari, and Ari Natalia Probandari. "Patient-Centered Care: How do Patients Perceive Its Implementation?" In 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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Wu, Chien-Ho. "A Patient-Centered Self-Care Support System for Diabetics." In 2014 IEEE 11th International Conference on e-Business Engineering (ICEBE). IEEE, 2014. http://dx.doi.org/10.1109/icebe.2014.58.

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Sant'Anna, Anita. "Activity monitoring as a tool for person-centered care: Preliminary report." In 2014 IEEE International Conference on Bioinformatics and Biomedicine (BIBM). IEEE, 2014. http://dx.doi.org/10.1109/bibm.2014.6999289.

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Gonzales, Michael, and Laurel Riek. "Co-designing Patient-centered Health Communication Tools for Cancer Care." In ICTs for improving Patients Rehabilitation Research Techniques. IEEE, 2013. http://dx.doi.org/10.4108/icst.pervasivehealth.2013.252109.

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Wahyuni, Ni Putu Sri, and Ede Surya Darmawan. "Patient Centered Care Model to Improve the Quality and Safety of Patient Care in Hospital: A Systematic Review." In The 6th International Conference on Public Health 2019. Masters Program in Public Health, Graduate School, Universitas Sebelas Maret, 2019. http://dx.doi.org/10.26911/the6thicph.04.53.

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Reports on the topic "Patient and Person Centered Care"

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Starkey, Sandra, and 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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Leavy, Michelle B., Danielle Cooke, Sarah Hajjar, Erik Bikelman, Bailey Egan, Diana Clarke, Debbie Gibson, Barbara Casanova, and Richard Gliklich. Outcome Measure Harmonization and Data Infrastructure for Patient-Centered Outcomes Research in Depression: Report on Registry Configuration. Agency for Healthcare Research and Quality (AHRQ), November 2020. http://dx.doi.org/10.23970/ahrqepcregistryoutcome.

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Background: Major depressive disorder is a common mental disorder. Many pressing questions regarding depression treatment and outcomes exist, and new, efficient research approaches are necessary to address them. The primary objective of this project is to demonstrate the feasibility and value of capturing the harmonized depression outcome measures in the clinical workflow and submitting these data to different registries. Secondary objectives include demonstrating the feasibility of using these data for patient-centered outcomes research and developing a toolkit to support registries interested in sharing data with external researchers. Methods: The harmonized outcome measures for depression were developed through a multi-stakeholder, consensus-based process supported by AHRQ. For this implementation effort, the PRIME Registry, sponsored by the American Board of Family Medicine, and PsychPRO, sponsored by the American Psychiatric Association, each recruited 10 pilot sites from existing registry sites, added the harmonized measures to the registry platform, and submitted the project for institutional review board review Results: The process of preparing each registry to calculate the harmonized measures produced three major findings. First, some clarifications were necessary to make the harmonized definitions operational. Second, some data necessary for the measures are not routinely captured in structured form (e.g., PHQ-9 item 9, adverse events, suicide ideation and behavior, and mortality data). Finally, capture of the PHQ-9 requires operational and technical modifications. The next phase of this project will focus collection of the baseline and follow-up PHQ-9s, as well as other supporting clinical documentation. In parallel to the data collection process, the project team will examine the feasibility of using natural language processing to extract information on PHQ-9 scores, adverse events, and suicidal behaviors from unstructured data. Conclusion: This pilot project represents the first practical implementation of the harmonized outcome measures for depression. Initial results indicate that it is feasible to calculate the measures within the two patient registries, although some challenges were encountered related to the harmonized definition specifications, the availability of the necessary data, and the clinical workflow for collecting the PHQ-9. The ongoing data collection period, combined with an evaluation of the utility of natural language processing for these measures, will produce more information about the practical challenges, value, and burden of using the harmonized measures in the primary care and mental health setting. These findings will be useful to inform future implementations of the harmonized depression outcome measures.
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Perry, Rebecca, Nancy McCall, Suzanne Wensky, and Susan Haber. Care Continuity in a Patient-Centered Medical Home Setting. RTI Press, February 2016. http://dx.doi.org/10.3768/rtipress.2016.rr.0026.1602.

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Zatzick, Douglas, Joan Russo, Peter Thomas, Doyanne Darnell, Harry Teter, Lauren Whiteside, Jin Wang, and Gregory Jurkovich. A Comparative Effectiveness Trial of Optimal Patient-Centered Care for US Trauma Care Systems. Patient-Centered Outcomes Research Institute (PCORI), August 2018. http://dx.doi.org/10.25302/8.2018.ih.13046319.

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Scholle, Sarah, Suzanne Morton, Daren Anderson, David Kendrick, Juell Homco, Kristin Rodriguez, Rachelle Jean-Paul, et al. Evaluating a New Patient-Centered Approach for Cancer Care in Oncology Offices. Patient-Centered Outcomes Research Institute® (PCORI), January 2020. http://dx.doi.org/10.25302/1.2020.ih.12114383.

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Gray, Bradford H. Gray, Dana O. Sarnak Sarnak, and Marit Tanke Tanke. ParkinsonNet: An Innovative Dutch Approach to Patient-Centered Care for a Degenerative Disease. New York, NY United States: Commonwealth Fund, December 2016. http://dx.doi.org/10.15868/socialsector.26197.

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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), November 2018. http://dx.doi.org/10.25302/11.2018.ce.12114489.

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

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Basu, Anirban. Economics of Individualization in Comparative Effectiveness Research and a Basis for a Patient-Centered Health Care. Cambridge, MA: National Bureau of Economic Research, March 2011. http://dx.doi.org/10.3386/w16900.

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10

Damiano, Peter C., Julie C. Reynolds, Raymond A. Kuthy, Simi Mani, and Susan C. McKernan. The need for defining a patient-centered dental home model in the era of the Affordable Care Act. Iowa City, Iowa: University of Iowa Public Policy Center, August 2015. http://dx.doi.org/10.17077/if9o-l75a.

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