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Journal articles on the topic 'Patient’s experience'

Author: Grafiati

Published: 4 June 2021

Last updated: 8 February 2022

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1

Duddy, Irene. "The patient’s experience." Nursing Standard 5, no. 9 (1990): 7. http://dx.doi.org/10.7748/ns.5.9.7.s70.

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Gaille, Marie. "“Patient’s lived experience”." Medicine, Health Care and Philosophy 22, no. 3 (2019): 339–42. http://dx.doi.org/10.1007/s11019-019-09896-5.

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Fink, Regina M., Mary Beth Flynn Makic, Ann Will Poteet, and Kathleen S. Oman. "The Ventilated Patient’s Experience." Dimensions of Critical Care Nursing 34, no. 5 (2015): 301–8. http://dx.doi.org/10.1097/dcc.0000000000000128.

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Banzett, Robert B. B., Andrew R. Sheridan, Kathy M. Baker, Robert W. Lansing, and Jennifer P. Stevens. "‘Scared to death’ dyspnoea from the hospitalised patient’s perspective." BMJ Open Respiratory Research 7, no. 1 (2020): e000493. http://dx.doi.org/10.1136/bmjresp-2019-000493.

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Because dyspnoea is seldom experienced by healthy people, it can be hard for clinicians and researchers to comprehend the patient’s experience. We collected patients’ descriptions of dyspnoea in their own words during a parent study in which 156 hospitalised patients completed a quantitative multidimensional dyspnoea questionnaire. These volunteered comments describe the severity and wide range of experiences associated with dyspnoea and its impacts on a patients’ life. They provide insights not conveyed by structured rating scales. We organised these comments into the most prominent themes, w

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Rush, Brenda. "A patient’s experience of orthopaedic care." Journal of Orthopaedic Nursing 12, no. 3-4 (2008): 166–70. http://dx.doi.org/10.1016/j.joon.2008.08.001.

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Benson, Philip. "Measuring the patient’s experience of treatment." Journal of Orthodontics 38, no. 1 (2011): 1–2. http://dx.doi.org/10.1179/14653121141146.

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Renik, Owen. "The Patient’s Experience of Therapeutic Benefit." Psychoanalytic Quarterly 70, no. 1 (2001): 231–41. http://dx.doi.org/10.1002/j.2167-4086.2001.tb00597.x.

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Durham, Justin, Catherine Exley, Mike T. John, and Donald R. Nixdorf. "Persistent Dentoalveolar Pain: The Patient’s Experience." Journal of Orofacial Pain 27, no. 1 (2013): 6–13. http://dx.doi.org/10.11607/jop.1022.

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Talen, Mary R., Jeffrey Rosenblatt, Christina Durchholtz, and Geraldine Malana. "Turning the tables: Using resident physicians’ experiences as patients for leveraging patient-centered care." International Journal of Psychiatry in Medicine 53, no. 5-6 (2018): 405–14. http://dx.doi.org/10.1177/0091217418802163.

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Training physicians to become person-centered is a primary goal of behavioral health curriculum. We have curriculum on doctor–patient communication skills and patient narratives to help physicians relate to the patient’s experiences. However, there is nothing more effective than actually being the patient that gives providers an “aha” experience of the patient’s perspective. In this article, we will share personal resident physician-patient stories based on their experiences within acute urgent care, chronic disease management, and routine well health care. In each narrative, the physician-pat

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Jeganathan, Sarangapany, Don Smith, and Julian Gold. "Early clinical experience with atazanavir in treatment-experienced patients." Sexual Health 3, no. 1 (2006): 33. http://dx.doi.org/10.1071/sh05022.

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Background: Atazanavir (ATV) is a newly approved protease inhibitor following successful clinical trials in naive and treatment-experienced patients. We describe early experience with ATV in treatment-experienced patients attending a single ambulatory care clinic in Sydney. Methods: Patients commencing ATV between February 2003 and May 2004 in an expanded access program were identified from the clinic pharmacy’s database. Data were retrospectively collected from patients’ medical records. Results: Data from 30 patients were analysed. Reasons for commencing ATV were: virological failure in six

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Vo, Phuoc Thao Nguyen, Anh Tuan Tran, Hoat Van Nguyen, and Minh Van Hoang. "Evaluation of Inpatient Experience at Some Clinical Departments of Kien Giang General Hospital, Kien Giang Province, Vietnam, 2020: An Analytical Cross-Sectional Study." Health Services Insights 14 (January 2021): 117863292110208. http://dx.doi.org/10.1177/11786329211020843.

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Patient experience is being widely considered in evaluating the quality of health care services. This is a cross-sectional study with 860 inpatients hospitalized in 4 clinical departments (General Internal Medicine; Cardiology; General Surgery; Surgery, and Orthopedic Trauma) of the Kien Giang General Hospital, from April to June 2020. Data was collected through a two-part questionnaire used to evaluate the inpatient experience during hospital treatment, using the Likert scale 5 points. The patient’s experience is classified into 3 aspects (environment—facilities, healthcare staff's care, trea

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Susleck, Dacia, Amy Willocks, Janet Secrest, et al. "The Perianesthesia Experience From the Patient’s Perspective." Journal of PeriAnesthesia Nursing 22, no. 1 (2007): 10–20. http://dx.doi.org/10.1016/j.jopan.2006.11.004.

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Tillman, Laura. "A Patient’s Experience as a Research Participant." Creative Nursing 15, no. 3 (2009): 127–28. http://dx.doi.org/10.1891/1078-4535.15.3.127.

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Williams, Marion. "The patient’s experience in a plaster cast." International Journal of Orthopaedic and Trauma Nursing 14, no. 3 (2010): 132–41. http://dx.doi.org/10.1016/j.ijotn.2010.03.007.

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Nandra, Kulvir, Jessica Bishop-Royse, and Dennis Tsilimingras. "A Patient’s Experience with an Adverse Event." Medical Science Educator 23, no. 4 (2013): 656–57. http://dx.doi.org/10.1007/bf03341693.

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Pawelczyk, Joanna, and Małgorzata Talarczyk. "‘What should a woman do and imagine to have bulimia?’: Co-constructing patient expertise in psychotherapy with bulimia patients." Communication and Medicine 14, no. 2 (2018): 135–49. http://dx.doi.org/10.1558/cam.30380.

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One of the goals of psychotherapy with bulimia patients is identification of the functions of the eating disorder in their lives. Thus, as in any psychotherapeutic approach, the therapist should facilitate the patient’s disclosure of his or her experience of living with bulimia. Talking about one’s dysphoric experiences and, particularly in the case of bulimia, symptoms and experiences that commonly deprive people with bulimia of dignity, constitutes an emotional challenge for the patient and an equally challenging interactional task for the therapist. Using the example of one therapy session

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Nuño-Solínis, Roberto, Sara Ponce, Maider Urtaran-Laresgoiti, Esther Lázaro, and María Errea Rodríguez. "Factors Influencing Healthcare Experience of Patients with Self-Declared Diabetes: A Cross-Sectional Population-Based Study in the Basque Country." Healthcare 9, no. 5 (2021): 509. http://dx.doi.org/10.3390/healthcare9050509.

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Background: Diabetes affects more than 400 million people around the world. Few published studies incorporate questionnaires that comprehensively cover every aspect of a patient’s experience of healthcare. This study analyzes potential differences in the healthcare experience for patients with diabetes based on their sociodemographic, economic, and health-related characteristics from a comprehensive viewpoint in an integrated delivery system. Methods: We used data from the 2018 Basque Health Survey, which includes a questionnaire for the measurement of the experiences of patients with chronic

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Hafiz, Azrul, Noor Ellyyu Hafizah, and Nur Nisrin Nabihah. "Patient’s Perception of Pain and Discomfort Towards Orthodontic Treatments." European Journal of Dental and Oral Health 2, no. 2 (2021): 15–17. http://dx.doi.org/10.24018/ejdent.2021.2.2.47.

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Background: Patient undergoes orthodontic treatment with removable and fixed appliances will usually complaint of pain and discomfort. The level of pain and discomfort experience by patient will determined the cooperation and compliance towards the treatment. This study explores the perception of pain and type of discomfort experience by patients when undergoes orthodontic treatment. Material and method: This cross-sectional study involve a set of questionnaires regarding patient social demographic and factors contributing to pain and discomfort among patients with removable and fixed ap

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Leung, Kelvin, Foluke Odeyale, and Itoro Udo. "Travelling at a hundred miles an hour and not being able to get off: Examining a patient’s journey from medically unexplained symptoms." European Journal for Person Centered Healthcare 6, no. 3 (2018): 400. http://dx.doi.org/10.5750/ejpch.v6i3.1514.

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Objectives: To understand a patient’s experience of treatment and recovery from medically unexplained tremors affecting hand and neck. The patient attended a Liaison Psychiatry Outpatient Clinic.Method: A case study using interview method focusing on the nature and severity of illness; effects of symptoms; expectations of treatment; changes observed and the patient’s expectation of services.Results: The patient was “extremely” stressed about his symptoms and “apprehensive” about attending mental health services. He experienced resolution of physical symptoms and improvements in mental wellbein

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Yu, Tsung-Hsien, Kuo-Piao Chung, Yu-Chi Tung, and Hsin-Yun Tsai. "Insight into Patients’ Experiences of Cancer Care in Taiwan: An Instrument Translation and Cross-Cultural Adaptation Study." International Journal of Environmental Research and Public Health 15, no. 8 (2018): 1772. http://dx.doi.org/10.3390/ijerph15081772.

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Background: Since Taiwan launched the Cancer Prevention Act in 2003, several prevention strategies and early detection programs have been implemented to reduce the incidence, morbidity and mortality rates of cancer. However, most of the programs have concentrated on healthcare providers. Evaluations from the patient’s perspective have been lacking. Thus, in this study a cancer patient experience questionnaire was developed in the Taiwanese context and a preliminary nationwide investigation was conducted on the status of cancer care from the patient’s perspective. Methods: An extensive literatu

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Rambod, Masoume, Farkhondeh Sharif, Zahra Molazem, and Kate Khair. "Pain: the voiceless scream in every haemophilia patient’s life." Journal of Haemophilia Practice 3, no. 1 (2016): 8–13. http://dx.doi.org/10.17225/jhp00061.

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Abstract Pain is a major problem in haemophilia patients’ lives. The perspective of pain in such patients is unique and may be different from other chronic illnesses. This qualitative hermeneutic phenomenological study aims to describe and interpret pain experience of haemophilia patients. Participants were selected from a haemophilia clinic affiliated with Shiraz University of Medical Sciences, Shiraz, Iran. Taking the main theme, “pain: the voiceless scream in every moment of haemophilia life”, with two subthemes, “a life full of pain” and “describing complex pain quality”, data was collecte

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Woodall, RD. "Living with leg ulcers: a patient’s personal experience." Nursing Standard 10, no. 45 (1996): 52. http://dx.doi.org/10.7748/ns.10.45.52.s51.

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Kuzbit, Paula. "Improving the patient’s experience of cancer-related fatigue." Cancer Nursing Practice 1, no. 9 (2002): 31–37. http://dx.doi.org/10.7748/cnp2002.11.1.9.31.c8101.

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Press, Irwin. "Concern for the patient’s experience comes of age." Patient Experience Journal 1, no. 1 (2014): 4–6. http://dx.doi.org/10.35680/2372-0247.1001.

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Besendorfer, Andrea. "The Patient’s Experience in the Intensive Care Unit." Pflege 15, no. 6 (2002): 301–8. http://dx.doi.org/10.1024/1012-5302.15.6.301.

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Wie die Patienten den Aufenthalt auf einer Intensivstation erleben, ist von außen häufig nicht erkennbar. Die Patienten sind oftmals sediert und in einem lebensbedrohlichen Zustand, so dass sie in der konkreten Situation nichts zu ihrem Erleben sagen können. Würde man die Patienten während der Zeit auf der Intensivstation beobachten, könnte man das Erleben der Patienten nur bedingt verstehen. Das von außen Wahrnehmbare kann nämlich in erheblichem Maße davon abweichen, wie die Patienten die Situation selbst erleben. In dieser Arbeit wurden deshalb die Patienten einige Wochen bis Monate nach ihr

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26

Sahoo, Swapnajeet, and Devashish. "Self-explored cognitive behavior therapy: A patient’s experience." Asian Journal of Psychiatry 44 (August 2019): 63–64. http://dx.doi.org/10.1016/j.ajp.2019.07.021.

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Greenwald, Elizabeth, Anonymous Patient, David Polsky, and Tracey N. Liebman. "Acral Melanoma: A Patient’s Experience and Physician’s Commentary." Dermatology and Therapy 8, no. 4 (2018): 503–7. http://dx.doi.org/10.1007/s13555-018-0260-3.

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Vavuris, Julie. "Am I dead? A patient’s experience with delirium." Intensive Care Medicine 41, no. 6 (2014): 1125. http://dx.doi.org/10.1007/s00134-014-3569-0.

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Janisse, Tom. "Graphic Medicine as Physician Tool to Understand Their Patient’s Experience of a Medical Condition." International Journal of Whole Person Care 7, no. 1 (2020): 31. http://dx.doi.org/10.26443/ijwpc.v7i1.225.

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BackgroundEngaging patients in their healthcare, listening to their stories, and improving the quality of their experience also depends on physicians understanding their patient’s experiences of a medical condition.Physicians have little time to converse with patients about this in the visit. Graphic Medicine – Comics – pictures and words together in sequence to tell a story – is a way to gain insight into a patient’s experience of what it’s like. MethodsA small, mixed-method study to test the effect on physicians of reading a comic book, “My Degeneration: Parkinson’s Disease.” The 13 particip

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Webster, Craig S., Tanisha Jowsey, Lucy M. Lu, et al. "Capturing the experience of the hospital-stay journey from admission to discharge using diaries completed by patients in their own words: a qualitative study." BMJ Open 9, no. 3 (2019): e027258. http://dx.doi.org/10.1136/bmjopen-2018-027258.

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ObjectiveTo capture and better understand patients’ experience during their healthcare journey from hospital admission to discharge, and to identify patient suggestions for improvement.DesignProspective, exploratory, qualitative study. Patients were asked to complete an unstructured written diary expressed in their own words, recording negative and positive experiences or anything else they considered noteworthy.Participants and settingPatients undergoing vascular surgery in a metropolitan hospital.Primary outcome measuresComplete diary transcripts underwent a general inductive thematic analys

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Aguilera-Serrano, Carlos, Jose Guzman-Parra, Juan A. Garcia-Sanchez, Berta Moreno-Küstner, and Fermin Mayoral-Cleries. "Variables Associated With the Subjective Experience of Coercive Measures in Psychiatric Inpatients: A Systematic Review." Canadian Journal of Psychiatry 63, no. 2 (2017): 129–44. http://dx.doi.org/10.1177/0706743717738491.

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Objective: This systematic review presents evidence regarding factors that may influence the patient’s subjective experience of an episode of mechanical restraint, seclusion, or forced administration of medication. Method: Two authors searched CINAHL, PubMed, SCOPUS, Web of Science, and Psych-Info, considering published studies between 1 January 1992 and 1 February 2016. Based on the inclusion criteria and methodological quality, 34 studies were selected, reporting a total sample of 1,869 participants. Results: The results showed that the provision of information, contact and interaction with

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Mansilla, Raíssa, Marcus André Acioly, Tayla Taynan Romão, Alison Mangolin, Jonadab Dos Santos Silva, and José Alberto Landeiro. "Patient’s Perceptions of Carpal Tunnel Surgery." JBNC - JORNAL BRASILEIRO DE NEUROCIRURGIA 30, no. 3 (2019): 197–206. http://dx.doi.org/10.22290/jbnc.v30i3.1840.

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Introduction: Carpal tunnel syndrome is a debilitating medical condition to many patients, and in cases refractory to conservative treatment, carpal tunnel decompressive surgery is indicated. In Latin America, however, little is known about the patient’s perception of the surgical procedure and their experience. Objective: In this study, we analyzed patient’s perception and the overall experience about carpal tunnel decompression in a Brazilian public institution and compared the results with literature from other countries. Methods: We conducted a prospective qualitative study with semi-struc

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Glinert, Lewis H. "Communicative and Discursive Perspectives on the Medication Experience." Pharmacy 9, no. 1 (2021): 42. http://dx.doi.org/10.3390/pharmacy9010042.

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Taking the ‘medication experience’ in the broad sense of what individuals hear and say about their medication, as well as how they experience it, this paper explores diverse research on medication information available to patients and their modes and capacities for interaction, including personal circles, doctors and pharmacists, labeling and promotion, websites, and the patient’s own inner conversations and self-expression. The goal is to illustrate, for nonspecialists in communication, how the actors, messages, mediums, genres, and contextual factors within a standard ethnographic and social

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Cooper, Steven H. "Playing in the Darkness: Use of the Object and Use of the Subject." Journal of the American Psychoanalytic Association 66, no. 4 (2018): 743–65. http://dx.doi.org/10.1177/0003065118796497.

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Play in the context of the patient’s sense of absence, loss, and compromised capacities for symbolization can be a link between unsymbolized experience and greater capacities for representation. Winnicott’s concepts of play evolved as one of the ways that analysts translate unconscious and unrepresented experience. For many patients who have experienced absence, the analyst and the analytic setting are subjected to the patient’s unconscious efforts to destroy and negate meaning and relatedness. For the analyst to be “used” as an object to be destroyed and to survive destruction, he must become

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Redmond, Stephanie, Nicole Paterson, Sarah J. Shoemaker-Hunt, and Djenane Ramalho-de-Oliveira. "Development, Testing and Results of a Patient Medication Experience Documentation Tool for Use in Comprehensive Medication Management Services." Pharmacy 7, no. 2 (2019): 71. http://dx.doi.org/10.3390/pharmacy7020071.

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The medication experience is an individual’s subjective experience of taking a medication in daily life and can be at the root of drug therapy problems. It is recommended that the patient-centered approach to comprehensive medication management (CMM) starts with an understanding of the patient’s medication experience. This study aims to develop a medication experience documentation tool for use in CMM services, and to understand the usefulness and challenges of using the tool in practice. The tool was developed based on previous research on patients’ medication experiences. It was tested in tw

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Henry, David H., Hema N. Viswanathan, Shawn M. Wade, Mariana Servin, and David Cella. "The Patient’s Experience of Fatigue: A Cross-Sectional Study of Cancer Patients." Blood 108, no. 11 (2006): 3356. http://dx.doi.org/10.1182/blood.v108.11.3356.3356.

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Abstract INTRODUCTION: Cancer-related anemia can contribute to fatigue among cancer patients (pts). Few large scale surveys of cancer pts have been conducted to characterize fatigue from the patient’s perspective. This study was conducted to assess the prevalence of fatigue in cancer pts and examine relationships between fatigue, anxiety, depression, and somatization (physical symptoms). METHODS: A cross-sectional survey was conducted from April to May 2006 using a random sample of pts from a chronic illness panel of 550,233 pts. Inclusion criteria were being at least 18 years of age, diagnose

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Sumner, Rachael L., Emme Chacko, Rebecca McMillan, et al. "A qualitative and quantitative account of patient’s experiences of ketamine and its antidepressant properties." Journal of Psychopharmacology 35, no. 8 (2021): 946–61. http://dx.doi.org/10.1177/0269881121998321.

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Background: Ketamine is central to one of the most rapidly growing areas of neuroscientific research into novel treatments for depression. Limited research has indicated that the psychedelic properties of ketamine may play a role in its antidepressant effects. Aim: The aim of the current study was to explore the psychedelic experiences and sustained impact of ketamine in major depressive disorder. Methods: In the current study, ketamine (0.44 mg/kg) was administered to 32 volunteers with major depressive disorder in a crossover design with the active-placebo remifentanil, in a magnetic resonan

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Ford, Joseph, Alexa Hepburn, and Ruth Parry. "What do displays of empathy do in palliative care consultations?" Discourse Studies 21, no. 1 (2019): 22–37. http://dx.doi.org/10.1177/1461445618814030.

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Empathy is an important way for doctors to demonstrate their understanding of patients’ subjective experiences. This research considers the role of empathy in 37 doctor–patient palliative or end-of-life care consultations recorded in a hospice. Specifically, it focuses on four contexts in which there is a disparity between patients’ displayed experience of their illness and the doctor’s biomedical, expertise-driven perspective on their illness. These include cases in which the patient is sceptical of the medical perspective, cases in which the patient’s expectations exceed what can realistical

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Citra, Resiana, Rizma Adlia Syakurah, and Eddy Roflin. "Determinants of medical students' empathy during clinical rotation." International Journal of Public Health Science (IJPHS) 10, no. 3 (2021): 629. http://dx.doi.org/10.11591/ijphs.v10i3.20747.

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Medical students in clinical rotation level have been developed comprehension and implementation of empathy, considering that they have already dealt with patients in the first hand, whereas professionalism and ethics are two main competences as a physician. This study aims to discuss and investigates determinants of medical students’ empathy towards their patients during clinical rotation in the hospital. A qualitative study with phenomenology approach using focus group discussion (FGD) was accompanied with an open-ended questionnaire to serve as preliminary data and basis of FGD topic guidel

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Herlina, Herlina, Ifa Hafifah, and Noor Diani. "Factors Associated with Patient’s Family Anxiety in the Intensive Care Unit (ICU)." Jurnal Keperawatan 11, no. 1 (2020): 32. http://dx.doi.org/10.22219/jk.v11i1.10954.

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Introduction: Critical and life-threatening patients cause anxiety in the family, which may be caused by many factors such as age, education, experience, knowledge, attitudes, and so on. Objective: The purpose of this study was factors assosiated patient’s family anxiety in the ICU. Method: Correlation research with cross sectional approach. Samples amounted to 30 people with consecutive sampling technique. The instrument used questionnaires respondent characteristics, knowledge, health services, and HARS anxiety. Data analysis using the Spearman rank test. Result: There was a relationship of

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Broide, E., V. Richter, A. Mari, T. Khoury, H. Shirin, and T. Naftali. "P250 Does Ethnicity Influence Patient’s Preferences for Treatment Outcome? The Israeli Experience." Journal of Crohn's and Colitis 15, Supplement_1 (2021): S290. http://dx.doi.org/10.1093/ecco-jcc/jjab076.376.

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Abstract Background IBD behaves differently among different ethnic groups. Patients perceptions and priorities for treatment outcome may well be influenced by their culture and beliefs. However, data on the impact of ethnicity on IBD patient’s attitude and expectation for treatment outcomes are still scares. We aimed to compare patient’s preferences and priorities for treatment outcomes among Jewish and Muslims IBD patients in Israel. Methods A prospective survey was conducted among Muslims IBD patients and compared to historical data set of Jewish IBD patients. Data included demographics and

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Martawinarti, RTS Netisa, Putri Irwanti Sari, and Vivi Meiti Berhimpong. "Life Experience of Human Immunodeficiency Virus (HIV) Sufferers: A Qualitative Systematic Review." Jurnal Ners 14, no. 3 (2020): 418. http://dx.doi.org/10.20473/jn.v14i3.17069.

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Introduction: HIV is a chronic disease that continues to increase from year to year, with many symptoms or obstacles encountered by HIV sufferers when going about their day. The experience of HIV sufferers is important to know in order to find out what they have experienced for as long as they have had the disease. The objective of this qualitative systematic review is to describe the experiences of people living with HIV.Methods: The method used was searching for journals using the pre-determined keywords of ‘experience’, ‘living with HIV’ and ‘coping’ through the databases of Scopus, ProQues

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Garrett, Roger M. "Reflections on delirium – A patient’s perspective." Journal of the Intensive Care Society 20, no. 3 (2019): 258–62. http://dx.doi.org/10.1177/1751143719851352.

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Delirium, and its importance, is briefly discussed to contextualise the intricate story of one patient’s experience of the condition. This recounting of the main episodes of delirium shows how its nature and severity changed with time and location, from ICU to the surgical ward. Reflection on these experiences provides insights and conclusions for consideration by the medical profession. Discussion of the nature of delirium, and the sort of interventions that helped, or might be provided, for recovery from, or reduction of, the condition are considered. Thought is given to what might be done t

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Laurell, Helena, Lars-Erik Hansson, and Ulf Gunnarsson. "Impact of Clinical Experience and Diagnostic Performance in Patients with Acute Abdominal Pain." Gastroenterology Research and Practice 2015 (2015): 1–7. http://dx.doi.org/10.1155/2015/590346.

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Background.The aims were to evaluate the importance of the formal competence of the emergency department physician, the patient’s time of arrival at the emergency department, and the use of a structured schedule for investigation of patients with acute abdominal pain.Methods.Patients attending the Mora Hospital with acute abdominal pain from 1997 to 2000 were registered prospectively according to a structured schedule. Registration included history, symptoms, signs, preliminary diagnosis, surgery and final diagnosis after at least one year. Results.3073 acute abdominal pain patients were inclu

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Ratelle, John T., Michelle Herberts, Donna Miller, et al. "Relationships Between Time-at-Bedside During Hospital Ward Rounds, Clinician–Patient Agreement, and Patient Experience." Journal of Patient Experience 8 (January 1, 2021): 237437352110083. http://dx.doi.org/10.1177/23743735211008303.

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Hospital medicine ward rounds are often conducted away from patients’ bedsides, but it is unknown if more time-at-bedside is associated with improved patient outcomes. Our objective is to measure the association between “time-at-bedside,” patient experience, and patient–clinician care agreement during ward rounds. Research assistants directly observed medicine services to quantify the amount of time spent discussing each patient’s care inside versus outside the patient’s room. “Time-at-bedside” was defined as the proportion of time spent discussing a patient’s care in his or her room. Patient

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Hole, E., B. Stubbs, C. Roskell, and A. Soundy. "The Patient’s Experience of the Psychosocial Process That Influences Identity following Stroke Rehabilitation: A Metaethnography." Scientific World Journal 2014 (2014): 1–13. http://dx.doi.org/10.1155/2014/349151.

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Background and Purpose.Patient experience is increasingly being recognised as a key health outcome due to its positive correlation with quality of life and treatment compliance. The aim of this study was to create a model of how patient’s experiences of rehabilitation after stroke influence their outcome.Methods.A metaethnography of qualitative articles published since 2000 was undertaken. A systematic search of four databases using the keywords was competed. Original studies were included if at least 50% of their data from results was focused on stroke survivors experiences and if they reflec

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McCall, Bridget. "Coping with Parkinson’s disease: the patient’s and carer’s experience." British Journal of Therapy and Rehabilitation 2, no. 10 (1995): 549–57. http://dx.doi.org/10.12968/bjtr.1995.2.10.549.

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Lowe, Hannah, Nichola Brown, and Eileen Andrews. "Surgical neuro-oncology patient’s hospital discharge: improving the experience." Neuro-Oncology 20, suppl_1 (2018): i17. http://dx.doi.org/10.1093/neuonc/nox238.076.

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Akoh, JacobA, KatharinaJ Schumacher, and Sarah Stacey. "Survey of Patient’s Experience of Altruistic Nondirected Kidney Donation." Saudi Journal of Kidney Diseases and Transplantation 31, no. 4 (2020): 739. http://dx.doi.org/10.4103/1319-2442.292307.

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Meaney, S., L. O’Connor, JE Lutomski, K. O’Donoghue, and RA Greene. "PP32 Qualitative analysis of maternal morbidities: the patient’s experience." Journal of Epidemiology and Community Health 68, Suppl 1 (2014): A60.1—A60. http://dx.doi.org/10.1136/jech-2014-204726.128.

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