Relevant bibliographies by topics / Patients’ experiences

Contents

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

Academic literature on the topic 'Patients’ experiences'

Author: Grafiati
Published: 4 June 2021
Last updated: 18 February 2022

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Journal articles on the topic "Patients’ experiences"

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Cerruti, Gabriella, Maria Cotto, Margherita Rivetti, Luciana Servetti, Maddalena Baracco, and Renata Ferrero. "Patients’ Group Experiences." Peritoneal Dialysis International: Journal of the International Society for Peritoneal Dialysis 13, no. 2_suppl (1993): 199–201. http://dx.doi.org/10.1177/089686089301302s48.

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In 11 years of experience with dialysis, we have tried to supply a kind of treatment In our center that takes the patient's physical, psychological, and social needs Into account. We have been able to observe how Important It Is to share the common problems connected with a chronic illness in order to make them appear less dramatic. This led to the Idea of organizing a group holiday in which the patients and their families would be able to spend some time together. As a result of this positive experience, we decided to organize group encounters In which all the problems could be freely discuss
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Johansson, Lena, and Andrzej Werbart. "Patients' Views of Therapeutic Action in Psychoanalytic Group Psychotherapy." Group Analysis 42, no. 2 (2009): 120–42. http://dx.doi.org/10.1177/0533316409104361.

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Patients' views of curative and hindering factors in psychoanalytic group psychotherapy are explored, starting with semi-structured interviews with 28 young adult patients at therapy termination. Using grounded theory methodology, a theoretical model of therapeutic action is constructed, elucidating the interactions between positive and negative experiences in the group. The focal point appears to be the patient's experience of their own activity within the context of the group as whole, leading to increased self-knowledge and improved handling of emotions. The positively experienced change is
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Wahyuni, Sri Eka, Mahnum Lailan Nst, and Wardiyah Daulay. "The Patient Experiences Hallucinations with Schizophrenia." Open Access Macedonian Journal of Medical Sciences 9, T3 (2021): 112–15. http://dx.doi.org/10.3889/oamjms.2021.6350.

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BACKGROUND: Hallucination is the psychosis symptom which mostly experienced by patients with schizophrenia. It is also the experience of false perception undergone by patients without any stimulus from the environment. That experience of perception is real to the patients but not for others who do not have similar perception of experience with the patients.
 AIM: This research is phenomenological and aims for describing experiences of patients with schizophrenia who had hallucination.
 MATERIALS AND METHODS: This research took 15 patients. In this research, approaches and trust-build
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van der Aa, Maartje J., Jennifer R. van den Broeke, Karien Stronks, and Thomas Plochg. "Patients with Multimorbidity and Their Experiences with the Healthcare Process: A Scoping Review." Journal of Comorbidity 7, no. 1 (2017): 11–21. http://dx.doi.org/10.15256/joc.2017.7.97.

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Background The number of patients with multimorbidity (two or more conditions) is increasing. Observational research has shown that having multiple health problems is associated with poorer outcomes in terms of health, quality of care, and costs. Thus, it is imperative to understand how patients with multimorbidity experience their healthcare process. Insight into patient experiences can be used to tailor healthcare provision specifically to the needs of patients with multimorbidity. Objective To synthesize self-reported experiences with the healthcare process of patients with multimorbidity,
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Lucas, Shawn. "Assessing Transcendental Experiences vs Mental Illnesses." Journal of Pastoral Care & Counseling: Advancing theory and professional practice through scholarly and reflective publications 71, no. 4 (2017): 267–73. http://dx.doi.org/10.1177/1542305017737780.

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In our experience, being able to differentiate between mental illness and transcendent experiences has led patients to remain engaged in treatment. This is important since those who have experienced religious preoccupation are the least likely to seek out mental health care. We have developed a “Transcendent Assessment Tool” to assist clinicians and clients in discerning whether an experience is a delusion or part of a transcendent experience.
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Outlaw, Peter, Shiva Tripathi, and Jacqueline Baldwin. "Using patient experiences to develop services for chronic pain." British Journal of Pain 12, no. 2 (2018): 122–31. http://dx.doi.org/10.1177/2049463718759782.

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Purpose: The aim of this study was to improve the overall experience for patients using chronic pain services at a large teaching hospital in England. Experience-based co-design methodology was used to gain a greater understanding of patients’ experiences and to produce a list of priorities for change when improving the patient experience. Method: A total of seven video-recorded patient interviews were conducted to capture a range of patient experiences of using the chronic pain service. The interviews were analysed to identify ‘touchpoints’ which are areas in which patients experienced a heig
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Örmon, Karin, and Ulrica Hörberg. "The unnecessary suffering and abuse caused by healthcare professionals needs to stop: A study regarding experiences of abuse among female patients in a general psychiatric setting." Clinical Nursing Studies 5, no. 4 (2017): 59. http://dx.doi.org/10.5430/cns.v5n4p59.

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Objective: Healthcare, from a caring science perspective, aims to support the patients’ health processes. All healthcare is, however, not experienced as being caring by the patients. Consequences of abuse in healthcare (AHC) services have effects on the patients’ health and well-being. The aim of this study was to explore experiences of abuse from healthcare professionals among female patients in a general psychiatric clinic.Methods: In the cross-sectional study design, data from female patients receiving outpatient or inpatient care at a general psychiatric clinic about their experiences of a
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MACARIE, George, Ruxandra FILIPESCU, and Ana Voichita TEBEANU. "Framing the Cancer Patients Life Experiences and Attitudes: a Psychosomatic Approach." Postmodern Openings 4, no. 1 (2013): 103–16. http://dx.doi.org/10.18662/po/2013.0401.08.

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Johansson, Anders, Monica Larsson, and Bodil Ivarsson. "Patients’ Experiences With a Digital Primary Health Care Concept Using Written Dialogues: A Pilot Study." Journal of Primary Care & Community Health 11 (January 2020): 215013272091056. http://dx.doi.org/10.1177/2150132720910564.

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Background: The changing health care environment promotes the adoption of new information technologies to connect patients and health care providers. However, individuals greatly vary in their ability to use new digital systems, and in their feelings regarding integrity and validation. Caregivers in southern Sweden plan to implement a new digital primary health care (DPHC) service, and patients’ experiences must be studied to guide the best possible implementation of this service. Purpose: To examine the patients’ experiences with DPHC using written dialogues. Method: Patients were consecutive
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Maguire, N. "Personal experiences of home haemodialysis: patients' and carers' experiences." Clinical Kidney Journal 4, suppl 3 (2011): iii25—iii26. http://dx.doi.org/10.1093/ndtplus/sfr125.

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Dissertations / Theses on the topic "Patients’ experiences"

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Bainbridge, Samantha. "Experiences of hospitalized patients with dementia." Honors in the Major Thesis, University of Central Florida, 2012. http://digital.library.ucf.edu/cdm/ref/collection/ETH/id/657.

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People with dementia are hospitalized for a variety of reasons. The combination of dementia with additional health conditions creates a unique challenge to caregivers in acute care settings. There is a dearth of information available to provide guidance to the nursing staff caring for these patients. This integrated review of the literature examined the experiences of hospitalization from the perspective of the older adult with dementia, the family caregiver, and the patient care staff. Results showed a limited body of literature that addressed hospital experiences of people with dementia and
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Day, Jennifer Carol. "Schizophrenic patients' experiences of neuroleptic medication." Thesis, University of Liverpool, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.262388.

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Nordin, Catharina. "Patients’ experiences of patient participation prior to and within multimodal pain rehabilitation." Licentiate thesis, Luleå tekniska universitet, Hälsa och rehabilitering, 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-25852.

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Patient participation is a concept used to describe the patients’ involvement in their healthcare. The aim of this licentiate thesis was to explore primary healthcare patients’ experiences of patient participation prior to and within multimodal pain rehabilitation. Qualitative interviews were conducted with seventeen patients, 14 women and 3 men, who had completed multimodal pain rehabilitation for persistent pain. Data was analyzed using qualitative content analysis.The findings show that patient participation can be understood as a complex and individualized interaction between the patient a
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Bashir, Kifah, and Yvonne Bengtsson. "Palliative care for pancreatic cancer - patients´ experiences." Thesis, Kristianstad University College, Department of Teacher Education, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:hkr:diva-4609.

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<p>To receive a diagnosis of pancreatic cancer can lead to a tremendous change in a person’s life. Thoughts regarding death may cause a personal crisis which can have negative influences on the patient’s social, mental and spiritual state. Most people with pancreatic cancer are diagnosed in a late stage of the disease. Therefore, palliative care is often one of the options that are offered to patients. Moreover, to be able to provide patients with nursing care and tend to their needs, it is very important to see them as unique individuals. The purpose with the literature review was to illustra
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Malmgren, Helena. "Patients’ experiences of Preimplantation Genetic Diagnosis (PGD)." Thesis, Uppsala universitet, Institutionen för folkhälso- och vårdvetenskap, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-230901.

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The aim of the present study was to investigate the experiences and attitudes concerningpreimplantation genetic diagnosis (PGD) among the couples that have undergone PGD in Sweden.PGD is an alternative to conventional prenatal diagnosis for couples with a high risk of having a childwith genetic disease. Couples opting for PGD have to perform in vitro fertilisation, generatedembryos are subjected to biopsy and diagnosis, and healthy embryos can be transferred to the femaleuterus. Hopefully a pregnancy will be established. However, PGD is a strategy that implies bothphysical and psychological st
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Persson, Elene, and Söderqvist Linda. "Patienters upplevelser av delaktighet inom slutenvård : - En litteraturstudie." Thesis, Högskolan i Gävle, Avdelningen för hälso- och vårdvetenskap, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-16531.

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Kommunikation, lärande och sociala relationer är tre grundstenar som ingår i begreppet delaktighet. Möjligheten att få ta del i sin omvårdnad kan påverka vården på ett sätt som är mer gynnsamt för patienten. I omvårdnaden är begreppet KASAM kärnan. Syftet med studien var att genom en litteraturstudie beskriva patienters upplevelser av delaktighet inom slutenvård utifrån KASAM:s komponenter efter att ha varit inskriven på en vårdavdelning. Syftet var även att granska urvalsmetod samt dataanalys i de vetenskapliga artiklar som studerades. En beskrivande användes för att svara på syftet. Artiklar
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Hörnsten, Åsa. "Experiences of diabetes care - patients' and nurses' perspectives." Doctoral thesis, Umeå universitet, Institutionen för omvårdnad, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-258.

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Background: In order to provide good diabetes care it is important for the health care professionals to share patients’ personal understanding of living with diabetes, which differs from a professional understanding of the illness. Patients’ beliefs about health, illness, control and cure are predictive of the outcome of lifestyle changes and pharmacological treatment. Narratives about illness could be used to elucidate what people believe to be central to their experience of an illness and its management. The overall aim of this thesis was to investigate experiences of diabetes and diabetes c
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Hörnsten, Åsa. "Experiences of diabetes care - patients' and nurses' perspectives /." Umeå : Univ, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-258.

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Kooken, Wendy Carter. "Vigilance Experiences: Cancer Patients, Family Members, and Nurses." Thesis, Connect to resource online, 2008. http://hdl.handle.net/1805/1849.

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Thesis (Ph.D.)--Indiana University, 2008.<br>Title from screen (viewed on August 27, 2009). School of Nursing, Indiana University-Purdue University Indianapolis (IUPUI). Advisor(s): Joan Haase, Janet Carpenter, Patricia Ebright, Rangaraj Ramanujam. Includes vita. Includes bibliographical references (leaves 303-316).
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Khatun, Mahbuba. "Self-disgust : experiences of patients post-bariatric surgery." Thesis, University of East London, 2016. http://roar.uel.ac.uk/5420/.

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Background: Research suggests that individuals who are obese are rated less favourably across all social groups (Wing & Jeffrey, 1999), with disgust being the strongest predictor of negative attitudes (Vartanian, 2010). Whilst some studies have explored the role of disgust in obesity, there is a distinct gap in the evidence base in relation to self-disgust and visual perspective taking, and how individual’s respond once they have transitioned out of weight-stigmatising environments. The proposed study aims to address this gap by using visual imagery to explore how individuals that have had bar
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Books on the topic "Patients’ experiences"

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Towards the emancipation of patients: Patients' experiences and the patient movement. Policy Press, 2010.

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L, Shortridge Dennis, and Watson Phyllis M. 1947-, eds. Patients first: Experiences of a patient-focused pioneer. Health Administration Press, 1996.

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Lawton, Julia. The dying process: Patients' experiences of palliative care. Routledge, 2000.

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Makoae, M. G. Life histories of pulmonary TB patients: Patients' experiences and perceptions about the disease. Institute of Southern African Studies, National University of Lesotho, 1999.

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Mrs, Austin, and DCLD, eds. Arthur: Educational experiences of Arthur Austin, Dyslexic. D.C.L.D., 1985.

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Copp, Gina. Facing impending death: Experiences of patients and their nurses. Nursing Times Books, 1999.

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Young-Mason, Jeanine. The patient's voice: Experiences of illness. 2nd ed. F.A. Davis Company, 2016.

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Burton, S. Acute in-patient mental health care: A qualitative study of the experiences of patients' carers. Oxford Brookes University, 2002.

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Killigrew, Steve. Holism in complementary therapies: Patients' experiences of traditional Chinese medicine. University of Derby], 2002.

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Broom, Alex. Therapeutic pluralism: Exploring the experiences of cancer patients and professionals. Routledge, 2008.

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Book chapters on the topic "Patients’ experiences"

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Haljamäe, H., I. Bergbom-Engberg, and B. Hallenberg. "Patients’ Experiences of Mechanical Ventilation." In Update 1990. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-84125-5_22.

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Belkin, Sheila. "Personal Experiences of Six Patients." In Cicatricial Alopecia. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-8399-2_10.

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Troisi, Alfonso. "Patients’ Motivations, Expectations, and Experiences." In Bariatric Psychology and Psychiatry. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-44834-9_2.

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Beitat, Katja. "Experiences of Patients and Medical Practitioners." In Trust and Incidents. Springer Fachmedien Wiesbaden, 2015. http://dx.doi.org/10.1007/978-3-658-09670-0_3.

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Huang, Lan-Ling, Hsi-Hsun Yang, Chang-Franw Lee, and Mei-Hsiang Chen. "Improvement Design of the Clinical Upper Extremity Rehabilitation Product for Stroke Patients." In Design, User Experience, and Usability: Novel User Experiences. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-40355-7_57.

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Küfner, Heinrich, and Wilhelm Feuerlein. "Patients’ Attitudes to and Experiences of Treatment." In In-Patient Treatment for Alcoholism. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74388-7_11.

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Kristensen, Dorthe Brogård. "Being Mapuche in Modern Chile: Illness Experiences, Medical Choices and Social Positions." In Patients, Doctors and Healers. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-97031-8_5.

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Weel, Angelique, Marc Kok, and Deirisa Lopes Barreto. "Better Experiences for Inflammatory Arthritis Patients Through Value-Based Patient Journey." In Personalized Specialty Care. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-63746-0_13.

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Laffer, U., M. Dürig, H. R. Bloch, and J. Landmann. "Surgical Experiences with 191 Implanted Venous Port-a-Cath Systems." In Supportive Care in Cancer Patients II. Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-84138-5_21.

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Flatley, Mary. "Hospitalisation and discharge of stroke patients: the relatives’ experiences." In Research in health promotion and nursing. Macmillan Education UK, 1993. http://dx.doi.org/10.1007/978-1-349-23067-9_13.

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Conference papers on the topic "Patients’ experiences"

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Souza, Carlos Henrique Rorato, Daniel Machado de Oliveira, Luciana De Oliveira Berreta, and Sérgio Teixeira de Carvalho. "A Distributed Exergame for Telerehabilitation: An Engaging Alternative to Improve Patients’ Quality of Life." In Life Improvement in Quality by Ubiquitous Experiences Workshop. Brazilian Computing Society, 2021. http://dx.doi.org/10.5753/lique.2021.15714.

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There are many factors that have a direct impact on the effectiveness of rehabilitation sessions. Among the main ones are: the availability of treatment, the active participation of the physiotherapist and the patient’s motivation and engagement in performing the exercises. In this sense, this project presents the construction of a distributed exergame that, using equipment and sensors coupled to the cycle ergometer (device used in the activity), aims to allow telerehabilitation sessions, where the patient and physiotherapist are in their respective houses, and perform these activities in a le
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Blejan, Emilian Ionuţ, Gabriela Ciupitu, and Andreea Arsene. "Connecting the Customer Experience Concept with Pharmaceutical Care for Improving the Healthcare Status of Patients." In International Conference Innovative Business Management & Global Entrepreneurship. LUMEN Publishing, 2020. http://dx.doi.org/10.18662/lumproc/ibmage2020/19.

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Healthcare costs are rising worldwide, due to a series of factors related to increased spending on medication, aging, medication errors, adverse drug events and hospital admissions. Aging phenomenon is closely followed by an increasing burden of chronic diseases. New therapies used to treat chronic diseases have intensified the economic pressure on healthcare organizations. Pharmacists play an important role in lowering costs by reviewing the pharmacotherapy of patients. Pharmacists are also the link between the physician and the patient, providing free medical advice without the need for an a
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Pike, Katharine, Paula Kelly, Stephanie Brotherston, Mollie Riley, and Martin Samuels. "115 Family experiences of flying and testing: ‘fitness to fly’." In GOSH Conference 2020 – Our People, Our Patients, Our Hospital. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2020. http://dx.doi.org/10.1136/archdischild-2020-gosh.115.

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Gardener, Carole, Gail Ewing, and Morag Farquhar. "23 Implementing the support needs approach for patients (SNAP): patient experiences." In Marie Curie Palliative Care Research Conference. British Medical Journal Publishing Group, 2019. http://dx.doi.org/10.1136/spcare-2019-mariecuriepalliativecare.23.

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Pratt, Michael A., and Henry Chu. "Predicting healthcare associated infections using patients' experiences." In SPIE Commercial + Scientific Sensing and Imaging, edited by Liyi Dai, Yufeng Zheng, Henry Chu, and Anke D. Meyer-Bäse. SPIE, 2016. http://dx.doi.org/10.1117/12.2228618.

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Carter, Louise. "48 Children’s experiences of personal protective equipment (PPE) during the COVID-19 pandemic." In GOSH Conference 2020 – Our People, Our Patients, Our Hospital. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2020. http://dx.doi.org/10.1136/archdischild-2020-gosh.48.

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Wibbeler, Eva, Angela Schulz, Miriam Nickel, and Christoph Schwering. "Experiences with Cannabidiol in Patients with NCL Disease." In Abstracts of the 45th Annual Meeting of the Society for Neuropediatrics. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1698230.

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Li, Hongyan. "CLINICAL EXPERIENCES OF NURSING CARE IN LEUKEMIA PATIENTS." In 2016 International Conference on Biotechnology and Medical Science. WORLD SCIENTIFIC, 2016. http://dx.doi.org/10.1142/9789813145870_0037.

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Nielsen, Kirsten Hald, Anne Dichmann Sorknaes, and Bettina Nissen Pedersen. "Patients initial experiences of sleep apnea CPAP treatment." In ERS International Congress 2018 abstracts. European Respiratory Society, 2018. http://dx.doi.org/10.1183/13993003.congress-2018.pa1512.

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Oroojeni Mohammad Javad, Mahsa, Stephen Agboola, Kamal Jethwani, Ibrahim Zeid, and Sagar Kamarthi. "Reinforcement Learning Algorithm for Blood Glucose Control in Diabetic Patients." In ASME 2015 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/imece2015-53420.

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In this paper a reinforcement learning algorithm is applied to regulating the blood glucose level of Type I diabetic patients using insulin pump. In this approach the agent learns from its exploration and experiences to selects its actions. In the current reinforcement learning algorithm, body weight, A1C level, and physical activity define the state of a diabetic patient. For the agent, insulin dose levels constitute the actions. There are five alternative actions for the agent: (1) raising the insulin infusion rate during 24 hours, (2) keeping it the same, (3) decreasing insulin infusion rat
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Reports on the topic "Patients’ experiences"

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Stocking, Corrine. Transgender Patients' Experiences of Discrimination at Mental Health Clinics. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.2994.

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DiBenedetti, Dana B., T. Michelle Brown, Carla Romano, Claire Ervin, Sandy Lewis, and Sheri Fehnel. Conducting Patient Interviews Within a Clinical Trial Setting. RTI Press, 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 questio
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Wright, Bill, Lauren Broffman, Natalie Kenton, et al. Effect of Integrating Mental and Physical Health on Patients’ Experiences of Care. Patient-Centered Outcomes Research Institute® (PCORI), 2020. http://dx.doi.org/10.25302/03.2020.ihs.131008388.

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Squiers, Linda, Mariam Siddiqui, Ishu Kataria, et al. Perceived, Experienced, and Internalized Cancer Stigma: Perspectives of Cancer Patients and Caregivers in India. RTI Press, 2021. http://dx.doi.org/10.3768/rtipress.2021.rr.0044.2104.

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Cancer stigma may lead to delayed diagnosis and treatment, especially in low- and middle-income countries. This exploratory, pilot study was conducted in India to explore the degree to which cancer stigma is perceived, experienced, and internalized among adults living with cancer and their primary caregivers. We conducted a survey of cancer patients and their caregivers in two Indian cities. The survey assessed perceived, experienced, and internalized stigma; demographic characteristics; patient cancer history; mental health; and social support. A purposive sample of 20 cancer survivor and car
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Dy, Sydney M., Julie M. Waldfogel, Danetta H. Sloan, et al. Integrating Palliative Care in Ambulatory Care of Noncancer Serious Chronic Illness: A Systematic Review. Agency for Healthcare Research and Quality (AHRQ), 2020. http://dx.doi.org/10.23970/ahrqepccer237.

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Objectives. To evaluate availability, effectiveness, and implementation of interventions for integrating palliative care into ambulatory care for U.S.-based adults with serious life-threatening chronic illness or conditions other than cancer and their caregivers We evaluated interventions addressing identification of patients, patient and caregiver education, shared decision-making tools, clinician education, and models of care. Data sources. We searched key U.S. national websites (March 2020) and PubMed®, CINAHL®, and the Cochrane Central Register of Controlled Trials (through May 2020). We a
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Tranby, Eric, Rebekah Fiehn, Mattt Jacob, and Julie Frantsve-Hawley. Patients Give High Marks to Their Teledentistry Experience. DentaQuest Partnership for Oral Health Advancement, 2020. http://dx.doi.org/10.35565/dqp.2020.2012.

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Tranby, Eric, Rebekah Fiehn, Matt Jacob, and Julie Frantsve-Hawley. Patients Give High Marks to Their Teledentistry Experience. CareQuest Institute for Oral Health, 2020. http://dx.doi.org/10.35565/cqi.2020.2012.

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Layman, Diane L. The Perioperative Experience of the Ambulatory Surgery Patient. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ad1012321.

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Oi, Katsuya. Understanding the Role of Patient Activation in the Association between Patient Socio-Economic Demographics and Patient Experience. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.467.

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Ryan, Jamie Ryan, and Dana O. Sarnak Sarnak. How High-Need Patients Experience the Health Care System in Nine Countries. Commonwealth Fund, 2016. http://dx.doi.org/10.15868/socialsector.25060.

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