Relevant bibliographies by topics / Patient's experience

Contents

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

Academic literature on the topic 'Patient's experience'

Author: Grafiati
Published: 4 June 2021
Last updated: 31 January 2023

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Journal articles on the topic "Patient's experience"

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Prior, Denise, and James Heathcote. "Patient's experience." BMJ 329, no. 7464 (August 26, 2004): 500.2–501. http://dx.doi.org/10.1136/bmj.329.7464.500-a.

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Rees, Colin John. "Patient's experience." BMJ 332, no. 7536 (February 2, 2006): 277.1. http://dx.doi.org/10.1136/bmj.332.7536.277.

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Patel and Roxy Senior. "Patient's experience." BMJ 332, no. 7542 (March 16, 2006): 644.1. http://dx.doi.org/10.1136/bmj.332.7542.644.

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Verma, Anant Kumar. "Patient's Experience and Expectations of Breaking Bad News." Asian Journal of Medical Research 8, no. 1 (March 2019): PY05—PY09. http://dx.doi.org/10.21276/ajmr.2019.8.1.py2.

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Murray, T. Jock. "Personal Time: The Patient's Experience." Annals of Internal Medicine 132, no. 1 (January 4, 2000): 58. http://dx.doi.org/10.7326/0003-4819-132-1-200001040-00010.

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Dodendorf, Diane M., Gurvinder K. Deogun, Amy Risch Rodie, and Louis G. Pol. "Assessing the Patient's Mammogram Experience." Health Care Management Review 29, no. 1 (January 2004): 77–87. http://dx.doi.org/10.1097/00004010-200401000-00009.

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Menkes, David B., Mary P. Davison, Shaun A. Costello, and Chrystal Jaye. "Stereotactic radiosurgery: the patient's experience." Social Science & Medicine 60, no. 11 (June 2005): 2561–73. http://dx.doi.org/10.1016/j.socscimed.2004.11.021.

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McDonald, Marguerite B. "The Patient's Experience of Blepharitis." Ocular Surface 7, no. 2 (April 2009): S17—S18. http://dx.doi.org/10.1016/s1542-0124(12)70622-5.

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Taniar, David. "Retroperitoneal Liposarcoma: A Patient's Experience." Journal of Patient Experience 9 (January 2022): 237437352211439. http://dx.doi.org/10.1177/23743735221143951.

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Anh, Nguyen Thi Thuy, Nguyen Thi Hoai Thu, Le Thi Thao Ly, and Nguyen Thi Thu Ha. "The experience of inpatient pediatric patients’ relatives at Ninh Binh Obstetrics and Gynecology Hospital in 2021." Journal of Health and Development Studies 06, no. 05 (October 30, 2022): 75–82. http://dx.doi.org/10.38148/jhds.0605skpt22-036.

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Objective: Describe the experience of inpatient pediatric patients’ relatives at Ninh Binh Obstetrics and Gynecology Hospital in 2021. Methods: A cross-sectional descriptive study carried out on 245 inpatient pediatric patients’ relatives at Ninh Binh Obstetrics and Gynecology Hospital from July 2021 to April 2022. In this study, we used a set of questionnaires to assess service users' experience of medical facilities and health care systems (Consumer Assessment of Healthcare Providers and Systems – CAHPS) developed by the US Agency for Healthcare Research and Quality (AHRQ). Results: Overall assessment of the hospital, the rate of positive experiences of the patients’ relatives at the hospital reached 54.7%. In which, positive experience on hospital discharge accounted for the highest rate (over 64%). The aspect of doctor and nursing care accounted for over 40% of positive experiences. The subsection on experience in this treatment of the patients’ relatives had the highest positive experience rate with 43.8%. Besides, the hospital environment were positively experienced by relatives of pediatric patients, from 30 to 35%. The understanding of care after leaving the hospital had the lowest positive rate <30%. Conclusion: The overall positive experience rate of patients’ relatives were above 50%. Further studies are needed to understand the causes and processes by which the patient's family members have negative experiences at the hospital. Keywords: Experience, CAHPS, Family members of pediatric patient, Inpatient treatment, Ninh Binh Obstetrics and Gynecology Hospital.
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Dissertations / Theses on the topic "Patient's experience"

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Jones, Jane. "The patient's experience of day surgery." Thesis, University of Southampton, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.285645.

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Hamill, Michelle C. "Letters in cognitive analytic therapy : the patient's experience." Thesis, University of East Anglia, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.430597.

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"Written words don't fade, they endure through space and time, bearing witness to the work of therapy and immortalising it" (Epston, 1994: p31) Aim: This study explored how the therapeutic letters, which are used as a standard procedure in Cognitive Analytic Therapy (CAT), contribute to the therapy from the perspective of patients. Background: CAT is a structured, time-limited psychotherapy (Ryle & Kerr, 2002). Letters form an important part of the reformulation and ending stages in CAT. However, little is known about the impact these letters have on the therapeutic process and how they are used from the perspective of the patient. Exploring the meaning and use of letters may further our understanding of this process, as well as giving value to patients' opinions. Method: Semi-structured interviews were used to elicit eight participants' perspectives of how the letters in CAT contributed to their therapy. A thematic analysis based on certain grounded theory principles was used to analyse the interview transcripts. Results: The analysis of participants' accounts suggested that the letters in CAT contributed to therapy through a process of `connecting' patients in varying degrees in the following four ways to: `understanding and awareness of self', `relationship with therapist', `perception of the structure and process of therapy', and `communicating self with others'. CAT theory has addressed many of these findings. However, the dilemmas and risk associated with the letters, such as re-invoking painful emotions by re-reading them and whether to share them with others, pervaded patients' accounts, offering a more complex understanding of the part the letters played, beyond those currently proposed by CAT theory. Discussion: It is proposed that it is the letters' ability to tap into patients' experience of connecting and relating, internally and externally, and the difficulties entailed in this that makes them such potentially powerful therapeutic tools. Clinical and theoretical implications and suggestions for future research are also discussed
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Paul, Ninu. "The orthognathic surgery patient's experience : a Grounded Theory study." Thesis, University of Sheffield, 2017. http://etheses.whiterose.ac.uk/20395/.

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Objective: Facial visible difference has a range of impacts not only functional and aesthetic but also in terms of the emotional and social wellbeing of patients. The aim of the study is to develop a theory that explains a person’s experience of the orthognathic treatment. Methods: The study was a qualitative cross-sectional grounded theory study. Semi-structured interviews were used to explore the experience of orthognathic patients undergoing treatment in a NHS hospital in the UK. Face to face interviews with 22 orthognathic patients (4 male and 18 female; age range 18-66 years) were conducted. Of these, 12 participants had had surgery six-eight weeks prior to the interview, six were in the decision making phase for orthognathic treatment and four participants had had the surgery one-two years prior to the interview. Further theoretical sampling and data collection was carried out from online blogs and forums on orthognathic treatment. Grounded theory methodology was used for the analysis of the data collected. Results: Analysis of the interviews indicated that during the process of orthognathic surgery, patients go through a status passage of ‘normal facing’. Orthognathic patients were inducted into this passage through their dentists, peer influence in the form of teasing and bullying about facial appearance, knowledge of orthodontic treatment gained from peers and their own perceptions of self-image. Decision making for orthognathic treatment influenced this status passage of ‘normal facing’, which, in turn, was influenced both positively and negatively by external factors. Temporality played a key role in normal facing. The factors that influenced the shape of this passage were the patient’s social support system, post-surgery recovery, quality of care, age of the patient, patient’s own life priorities, the preparedness of the patients in the form of information about the treatment, and the role of professionals involved in care provision. ‘Normal facing’ appeared to positively influence the patient’s coping behaviour and self-perception. Conclusions: Orthognathic patients undergo a scheduled status passage of ‘normal facing’, which appears to be influenced by various clinical, demographic and psychosocial factors. This status passage consequently influenced the person’s self-perception.
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Ricci, Tamra Marie. "The patient's hospital experience, a grounded theory analysis of personal accounts." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/nq22926.pdf.

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Schlodder, Michelle Ingrid. "Termination of psychotherapy : a phenomenological exploration of the therapist's and the patient's experience." Thesis, Rhodes University, 1997. http://hdl.handle.net/10962/d1002558.

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Therkleson, Tessa C. "A phenomenological inquiry into the patient's experience of the external application of ginger." Thesis, Edith Cowan University, Research Online, Perth, Western Australia, 2003. https://ro.ecu.edu.au/theses/1336.

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This Research Study explores the quality of the experience for the patient of the external application of ginger using a Husserllan phenomenological methodology, In this Study the phenomenon Is the patient's experience of the external application of ginger. A group of Anthroposophical Nurses in the Hawkes Bay of New Zealand personally selected seven appropriate consenting adults to receive one external application of ginger. Following their experience, the patients were asked a series of open-ended questions by the researcher, These Interviews were audio taped. The interview data have been transcribed and reduced to themes that have been explored and reflected on alongside relevant literature in the field. Four Interpretative themes capturing the patients experience were identified. These are patient experience: •warmth in the body as increasing In intensity and radiating outwards; •Increasing stimulation of internal activity within their body; •changes In thought-life, sensory perception and bodily tension; •centredness within themselves and a greater sense of personal boundary In relation to the world. The warmth response was slow and subtle initially and experienced externally on the skin beneath the ginger compress. Gradually the heat Intensified and developed into deep inner warmth. Patients were astonished at the strength and depth the heat generated. The warmth penetrated deep within the body spreading as far as the limbs. There was a definite awareness that this internal heat response was caused by the ginger compress, remaining long after the treatment and stimulating internal body activity. Patients experienced an enlivening of internal activity within the digestive, excretory and circulatory organs of the body. The increasing activity within the circulation moved and energised the metabolism. There was an awareness of increased blood flow throughout the body accompanied by a sense of an opening up within. Digestive disturbances and increased energy ware experienced; It was as If the body received something extra that enabled a movement internally. Patients experienced a stimulated thought life, including a transition from a dreamy to a wakeful state, changing sensations within the skin, activation of the senses and a relief of aches and tensions in the body. Following the ginger compress thinking was alert and active along with a general Increase In vitality and a sense of being present. There was a sense of being more centred, more connected to oneself and more aware of one's physical body. Patients experienced the opportunity to revisit their inner self, the inner core of their being. For all the patients the experience of the ginger compress was positive. Some of the patients expressed the wish to have repeated treatments. Future research on the experience of a series of ginger compresses for patients with specific conditions would be significant.
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Dyer, Annabella. "ICU psychosis : the patient's experience : an investigation of patients' understanding of hallucinations and delusions whilst in intensive care and post-discharge." Thesis, University of East London, 2005. http://roar.uel.ac.uk/3761/.

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This study explores how patients understand their hallucinatory and delusional type experiences whilst in intensive care and how they feel about these experiences after they have been discharged from hospital. The aims were to elicit their subjective accounts in order to gain further insights into the phenomena and to improve clinical practice. The study employed a qualitative methodology and eight participants took part in the research. Participants were interviewed using a semi-structured interview design and the interviews were tape-recorded. The transcripts were analysed using an interpretative phenomenological approach. The analysis revealed four super-ordinate categories: awareness of self and surroundings, dream-like experiences, understanding of dreamlike experiences and adjustment after hospital discharge. These contained several subordinate categories. Participants labelled their hallucinatory and delusional experiences as 'dream-like experiences'. These consisted of various sequences that evoked torturous, threatening and persecutory themes or less frightening themes such as escape and adventure. All participants reported their experiences during intensive care as highly distressing. The participants thought that their dream-like experiences were related to parts of themselves that had been incorporated into their dream sequences. They also acknowledged the role of medication and the intensive care unit context. These experiences had a profound effect on some participants in that they felt it had altered their sense of self whereas others felt they were not disturbed by these experiences. The implications of these findings for future research and clinical practice are discussed.
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Thorpe, Mark Richard. "A phenomenological investigation into the psychotherapist's experience of identifying, containing and processing the patient's projective identifications." Thesis, Rhodes University, 1989. http://hdl.handle.net/10962/d1002580.

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The aim of the study was to describe the therapist's lived experience of identifying, containing and processing the feelings, thoughts or fantasies evoked in him by the patient's projective identifications. A question which would elicit the experience of this phenomenon was formulated by examining case histories, and modified through the use of individual pilot studies. Fifteen experienced, psychoanalytically oriented psychotherapists were interviewed. The eight psychologically richest accounts were chosen for the study. Using the empirical phenomenological method, the four protocols that most clearly reflected the phenomenon were analysed in detail, while the remaining four were used to clarify areas of uncertainty. Projective identification is conceptualised as the process whereby the patient coerces the therapist to embody an un-appropriated aspect of his (patient's) world. The context of processing a patient's projective identification was discovered to be such that the therapist finds himself coerced to embody an incongruent, unfamiliar, confusing and inauthentic state of being which is consonant with the patient's perception of him. The discomfort of the experience leads the therapist to bring to awareness and thematise his feeling-state. He alternates between avoiding this state of being, which results in conf1ict with the patient and the therapist's own values, and appropriating it, which feels inauthentic. The therapist moves from a position of trying to understand the experience in relation to his own world, to the realisation that it is co-determined by the patient. From a position of reflective distance he re-appropriates aspects of his world that were closed to him while under the influence of the patient, in addition to appropriating previously unowned aspects. The therapist dialogues these appropriations with the invoked feelings, allowing him to differentiate those aspects of his feeling-state which are authentically his from those which are unowned aspects of the patient's aspects of his world that were closed to him while under the influence of the patient, in addition to appropriating previously unowned aspects. The therapist dialogues these appropriations with the invoked feelings, allowing him to differentiate those aspects of his feeling-state which are authentically his from those which are unowned aspects of the patient's world that he has been forced to embody. Through this process the therapist clarifies and gives meaning to his feelings. The therapist fee1s re1ieved and lighter, when in the service of the therapy, he temporarily gives himself over to the patient's experience of him, without feeling drawn to either disowning or appropriating it, while simultaneously remaining open to his own authentic reality. These findings were dialogued with the literature on projective identification.
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Qaid, Rafa T. A. "Patients' and nurses' perspectives on patients' experience for coronary care unit stressors using a mixed method approach." Thesis, Brunel University, 2011. http://bura.brunel.ac.uk/handle/2438/6359.

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Background: Getting admitted to CCU is viewed as a stressful event by patients. However, numerous studies have indicated that nurses do not always accurately perceive the stressors of their clients. Therefore, it is important for nurses to know what seems most stressful from the patients‘ perspective so that appropriate nursing measures can be directed towards minimizing such stressors. Objectives: The purpose of this study was to explore the perception of CCU stressors experienced by patients from both patients and nurses perspective and to compare between them, identify the effect of socio-demographic characteristics of participant's on the level of stress perception and to what extent clinical guidelines fulfil CCU needs. Methodology: A mixed method approach (qualitative and quantitative) was applied. Purposive random sampling was used to recruit data. Ethical approval was obtained prior to data collection. Data was collected from three CCUs within the West and Northwest NHS Trusts. Participants who met the inclusion criteria were interviewed and asked to rank the Environmental Stressor Questionnaire (ESQ). Qualitative data was analyzed using Gorgi's method of analysis. A quantitative data was analyzed using the SPSS software version 15. Results: There was some consistency in the data where patients and nurses provided same ranking for CCU stressors. Consistently nurses ranked physiological stressors higher than psychological stressors. Patients showed consistency in the findings between what they ranked in the ESQ and their narratives more than their counterparts. Perception of stress was affected by participant's socio-demographic characteristics. A key finding is that the current guidelines do not serve patients and nurses needs. Conclusions: Nurses should be well equipped with knowledge and experience to overcome stressful situations. Educational programs should be made available for nurses to improve stress management. Nurses should assess patient's needs by applying effectively communication skills.
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Eriksson, Christopher, and Evaldsson Esther Kim. "Livskvalitet hos personer med svårläkta bensår : Upplevelsen av att leva med svårläkta bensår." Thesis, Röda Korsets Högskola, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:rkh:diva-546.

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Bakgrund: Vid omvårdnad av personer med bensår är det lätt att lägga fokus på bensåret med risk för att den subjektiva upplevelsen kan komma i skymundan. Därför kan det vara viktigt att belysa patienters upplevelser ur ett holistiskt perspektiv. I tidigare forskning har det framkommit att livskvaliteten påverkas negativt där smärta visat sig vara en betydelsefull faktor. Syfte: Att ur ett livskvalitetsperspektiv belysa personers upplevelse av att leva med svårläkt bensår. Metod: En litteraturöversikt baserad på 10 vetenskapliga artiklar med kvalitativ ansats. En deduktiv analys av materialet gjordes utifrån World Health Organisations definition av livskvalitet och dess sex domäner. Dessa domäner är: Fysisk domän, Psykologisk domän, Grad av oberoende, Sociala relationer, Omgivning och miljö samt Andlighet, religion och personlig tro. Resultat: Svårläkta bensår påverkade personers livskvalitet inom samtliga domänerna utom Andlighet, religion och personlig tro. Slutsats: Personer hade liknande upplevelser av att leva med svårläkta bensår. De upplevde en försämrad livskvalitet där smärtan var en framträdande upplevelse som påverkade de flesta domänerna. Klinisk betydelse: Resultatet i denna studie visade på vikten av att använda ett holistiskt perspektiv vid omvårdnadssituationer.
Background: When caring for people with chronic leg ulcer there is a risk that the attention of the caregiver is laid towards the leg ulcer and the subjective feelings of this person are in the background. Therefore it is of importance to illuminate peoples experience with a holistic perspective. Previous research in the field has shown that the quality of life is affected in a negative way and the pain has proven to be a significant factor. Purpose: To illuminate person‟s experience of living with a chronic leg ulcer from a quality of life perspective. Method: A review based on 10 articles with qualitative approach. The material was analyzed with a deductive method from the World Health Organization. These domains are: physical domain, psychological domain, level of independence, social relationships, environment and spirituality/religion/personal beliefs. Results: Study findings showed that chronic leg ulcers affected quality of life in all domains except within the domain Spirituality, religion and personal beliefs Conclusion: People had similar experience when living with a chronic leg ulcer. They experience a loss in quality of life due to the chronic leg ulcer and pain was a notable finding that affected almost every domain. Clinical importance: The finding in this study shows the importance of using a holistic perspective in caring-situation.
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Books on the topic "Patient's experience"

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Macarthur, Juliet. The patient's experience of surgery. (Edinburgh): Scottish Office, 1993.

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Lean healthcare: Improving the patient's experience. Chichester, West Sussex: Kingsham Press, 2008.

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Brown, Caroline. Leaving the coronary care unit a phenomenological exploration of the patient's experience. (s.l: The Author), 2004.

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Dyer, Annabella. ICU psychosis: The patient's experience: an investigation of patients'understanding of hallucinations and delusions whilst in intensive care and post-discharge. London: UEL, 2005.

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Rogers, M. J. A phenomenological investigation of the patient's experience in the first month following palliative radiotherapy for non-small cell lung cancer. Oxford: Oxford Brookes University, 2000.

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

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

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Appleton, Jane M. Patient's narrative experiences of palliative care. Oxford: Oxford Brookes University, 2002.

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

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Crespin, Peter. Patient experience survey 2002. Kenley, Surrey: Sodexho Ltd, 2002.

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Book chapters on the topic "Patient's experience"

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Hemphill, Philip. "Patient Experience." In Integrated Care in Addiction Treatment, 94–98. New York: Routledge, 2021. http://dx.doi.org/10.4324/9781003128571-10.

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Toni, Martina, and Giovanni Mattia. "Patient Experience." In The Digital Healthcare Revolution, 63–78. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-16340-1_7.

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Crane, Jody, and Chuck Noon. "Patient Experience." In The Definitive Guide to Emergency Department Operational Improvement, 299–315. Second edition. | New York : Routledge, 2020.: Productivity Press, 2019. http://dx.doi.org/10.4324/9781315151915-14.

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Benson, Tim. "Patient Experience." In Patient-Reported Outcomes and Experience, 111–23. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-97071-0_10.

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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, 597–605. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-40355-7_57.

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Thompson, James. "Communicating with patients." In The Experience of Illness, 87–108. London: Routledge, 2022. http://dx.doi.org/10.4324/9781003283966-5.

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Kolvekar, Shyam K., Natalie L. Simon, and Trupti Kolvekar. "Patient Experience Before and After Treatment: Psychological Effects and Patients’ Personal Experience." In Chest Wall Deformities and Corrective Procedures, 161–67. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-23968-2_18.

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Beleffi, Elena, Paola Mosconi, and Susan Sheridan. "The Patient Journey." In Textbook of Patient Safety and Clinical Risk Management, 117–27. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-59403-9_10.

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AbstractThe wide implementation of patient safety improvement efforts continues to face many barriers including insufficient involvement of all stakeholders in healthcare, lack of individual and organizational learning when medical errors occur and scarce investments in patient safety. The promotion of systems-based approaches offers methods and tools to improve the safety of care. A multidisciplinary perspective must include the involvement of patients and citizens as fundamental contributors to the design, implementation, and delivery of health services.The patient journey is a challenging example of using a systems approach. The inclusion of the patient’s viewpoint and experience about their health journey throughout the time of care and across all the care settings represents a key factor in improving patient safety. Patient engagement ensures that the design of healthcare services are aligned with the values, the preferences, and needs of the patient community and integrates the real-life experience and the skills of the people to enhance patient safety in the patient journey.The utmost priority to implement patient engagement is the training of patients. Therefore, training for both patients/families/advocates and health professionals is the foundation on which to build active engagement of patients and consequently an effective and efficient patient journey.The chapter offers examples of successful training courses designed to foster strategic alliances among healthcare professionals and researchers with patients and their organizations. Training of patients constitutes the first step to develop shared knowledge, co-produced projects, and the achievement of active multilevel participation of patients for the implementation of patient safety in the patient journey.
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Choctaw, William T. "The Patient Experience." In Transforming the Patient Experience, 9–15. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-16928-6_4.

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Edwards, Brian E., and Christopher Jason. "The Patient Experience." In Hospital Medicine, 117–23. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-49092-2_12.

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Conference papers on the topic "Patient's experience"

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Sung, C., S. L. Feder, K. A. Crothers, and K. M. Akgun. "The Intubated Patient's Experience: Are We Paying Attention?" In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a6484.

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Camacho, Lea, Eliana Penedos-Santiago, and Elga Ferreira. "Health and Design at Service of a Refugee Camp in Iraq." In 13th International Conference on Applied Human Factors and Ergonomics (AHFE 2022). AHFE International, 2022. http://dx.doi.org/10.54941/ahfe1001412.

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This project emerges from the need to counteract a scenario of risk and unpredictability in the care provided to patients in illness situations, which stems from a poor or non-existent health record system (HRS). The direct contact in the year of 2017 with an emergency medical Non-Governmental Organization (NGO), working in context of humanitarian crises, demonstrated the precarious and yet scarce presence of such a system. The lack of practicality, easy understanding and access to other health partners proved to compromise the quality of care.Since a functional HRS (via paper or electronic means) is a core component for the management, delivery, and safety of quality in healthcare, the identification of a simple and yet effective system, capable of maintaining a history of care provided, is imperative. This need increases exponentially when the focus is on a humanitarian crisis context, in which populations have been forced into displacement and the health system is disrupted, of which the Internal Displaced Persons in Iraq are an example (commonly referred as refugees). The constraint of resources and the clash of different cultures and experiences between professionals, can hinder or even compromise the provision and quality of care, as well as the experience and perception of patients themselves regarding the services provided.With this study I propose the mapping of a HRS within an emergency medical field hospital, in a refugee camp in Iraq, to ensure the quality of emergency management and delivery of care, in a scenario of instability and political uncertainty. This system, which functions as a systematically collected database, presents specific health characteristics of a given patient when receiving differentiated care essential to guarantee high standards of care.A service design methodology to test the hypothesis will be used through a service blueprint development, capable of mapping the activities, processes and systems involved in a patient's health experience. Design research methods such as service safari and user shadowing with informal ethnographic interviews will be implemented, as well as workshops with national and international health professionals involved with NGO work.Thus, it is expected to re-design a robust monitoring and patient track, with faster access of the patient’s history to health professionals, a better prevention of medication errors and duplication, and a greater transparency in the management and delivery of care. The easy implementation of the system will also allow an easier communication of patient’s needs and care, between different health stakeholders.
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Batista Gomes Ferreira, Cristiane, Larissa Thuanny da Cruz Farria, Vitória Nunes Mattos, Eduardo Viana Ricardo, and Carolina Magalhães dos Santos. "Ostomy and sexuality." In 7th International Congress on Scientific Knowledge. Biológicas & Saúde, 2021. http://dx.doi.org/10.25242/8868113820212417.

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Colorectal cancer, diverticulitis and Crohn's disease are morbidities that in some cases require the need for a colostomy as part of the treatment, which has beneficial purposes for recovery and increases patient survival. When performing the colostomy, individuals are faced with a new reality to be experienced. Areality that generates impactful changes in both bodily and psychic aspects. Starting from the moment of surgery until its completion. Which reverberate in the depression of their self-image, and especially in their sexual experience The present work consists of a survey on the sexuality of a patient with an intestinal ostomy, aiming at the relationship of self-image. For this, the ostomy patient's perception of sexuality will be analyzed, identifying factors correlated with self-image and the impact on sexuality, in addition to raising negative consequences experienced by these patients, analyzing the strategies for daily coping with the use of colostomy. Does the colostomy bag affect the sexuality of colostomy patients? This is a field research with a qualitative approach. The sample will be composed of colostomized individuals, members of the Ostomized People Program, in the city of Campos dos Goytacazes. The data collection instrument will consist of a semi-structured questionnaire, with open and closed questions, and a recorded interview, in order to analyze the patients' perception of sexuality. The results of the sociodemographic profile will be analyzed using descriptive statistics while the interview data will be analyzed using content analysis, according to Bardin's conception. The study intends to suggest the implementation of actions and conducts related to the proposed theme, in order to encourage further research in this area. It is also expected to contribute to the research subjects, academic community, health professionals and society in general.
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Vaz, Marisa Monteiro. "Dreams and Prophecy: The Mantic Interpretation on Psychotherapy." In 7th International Conference on Spirituality and Psychology. Tomorrow People Organization, 2022. http://dx.doi.org/10.52987/icsp.2022.002.

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Abstract The mantic and prophetic dream interpretation is an ancient practice that has been applied in different contexts and at different historical times. With Freud's psychoanalytic proposal to interpret patients' dreams, the meaning of dream content and experience becomes a central element of the psychotherapeutic process. Freud obviously had an enormous cultural knowledge of ancient texts and ancient practices. The incubation technique in Freud's psychotherapeutic proposal was considered an innovative psychological strategy for understanding the patient's thoughts and feelings, but little attention was paid to the mantic quality that had distinguished the incubation process and dream interpretation for many centuries and across several civilizations. In recent decades, the mantic meaning of dreams has been considered useful within the ethnopsychiatric approach to restore the patient's ability to develop a new perspective in relation to a traumatic situation. In this article I will try to explain the use of mantic dream interpretation during the psychotherapeutic process. KEYWORDS: mantic dreams; prophecy; psychotherapy; ethnopsychiatry; dream- interpretation; trauma
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Brotons, A., JJ Mira, J. Lacueva, B. Germán, MF García-Sepulcre, and J. Sola-Vera. "DEVELOPMENT AND VALIDATION OF A COLONOSCOPY SATISFACTION AND SAFETY QUESTIONNAIRE BASED ON PATIENT'S EXPERIENCE (CSSQP)." In ESGE Days 2018 accepted abstracts. Georg Thieme Verlag KG, 2018. http://dx.doi.org/10.1055/s-0038-1637670.

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Anzeneder, T., U. Ohlms, D. Schmitt, and C. Waldner. "5 Years Experience in Collecting Tumor Specimen at Patient's Tumor Bank of Hope (PATH) – A Decentralized, Independent Biobank in Germany Controlled by Patients." In Abstracts: Thirty-Second Annual CTRC‐AACR San Antonio Breast Cancer Symposium‐‐ Dec 10‐13, 2009; San Antonio, TX. American Association for Cancer Research, 2009. http://dx.doi.org/10.1158/0008-5472.sabcs-09-3074.

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Carrion, B., P. Portillo-Palma, and EA Mendez. "ROLE-PLAY SIMULATION OF TELEMEDICINE FOR UNDERGRADUATE HEALTH STUDENTS." In The 7th International Conference on Education 2021. The International Institute of Knowledge Management, 2021. http://dx.doi.org/10.17501/24246700.2021.7145.

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Telemedicine has reemerged as the way to provide patient care amid the COVID-19 pandemic. It poses a safe and cost-efficient alternative to presence-based health appointments. Integrating remote patient care into healthcare training during their pre-clerkship curriculum is crucial for them to acquire professional skills to succeed in their postgraduate practices. One technique to achieve this is role-playing. It provides a learning environment for students to experience their future professional context in a safe, controlled setting. An educational innovation was implemented in the Preclinical Skills course to train students to carry out a teleconsult using peer role-play simulation. The study considered a mixed approach with a cross-sectional and descriptive design. The sample consisted of 75 students in the third semester on a health undergraduate program at Tecnologico de Monterrey organized in teams; each member represented a different role: health professional, patient, and observer-evaluator. Three clinical cases (abdominal pain, bad breath, and insomnia) randomly assigned. Each one with a script containing the patient's background, present illness with medical history. Students had to simulate a teleconsult according to their role, and the observer had to score a classmate's performance. To describe their experience, students completed an anonymous questionnaire. Our results showed that students identified key points that allow a teleconsult to successfully develop, even when not having the same role in the dynamic. They also recognized their opportunity areas and highlighted these tools as useful for obtaining skills that will help them excel in their professional practice even after the COVID-19 pandemic. Keywords: emergency adaptation, remote teaching, educational innovation, role-play, simulation, telemedicine, health education, skills, role-play
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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 appointment. Lowering the number of inappropriately prescribed drugs reduces the risk of adverse drug events that frequently contribute to prolonged and expensive hospital admissions. In the near future, a new approach is needed for long term results. Pharmacists will have to reshape the old concept of patient care, moving out of the negative feelings area derived from sickness and start to protect health instead of managing disease. It will result a shift from sick care to proactive healthcare experiences. Pharmacists will anticipate and solve patient’s problems before they can produce a displeasure. For maintaining a well-being state of patients is now necessarily to adopt or implement a patient centred strategy based on customer experience pillars. In Romania integrity matters most in customer experience, closely followed by personalization. In the new Era of pharmaceutical care, pharmacists will have to focus on patient experience and patient journey.
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Sarmento, Carlos Eduardo, Daniel Guerra, Deborah Dantas, Emanuel Arnaud, Hallysson Santos, João Pedro Dias, Matheus Andrade, and Alyson Souza. "POSTER: Dagda - A Virtual Reality Experience for Pediatric Patients with Cancer in Chemotherapy." In XXI Symposium on Virtual and Augmented Reality. Sociedade Brasileira de Computação - SBC, 2019. http://dx.doi.org/10.5753/svr_estendido.2019.8467.

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During the process of chemotherapy of pediatric patients with cancer, the discomfort proves to be one of the many challenges for the patient, intensified by the ease at which the child becomes upset or annoyed. As a form of distraction during part of the treatment, this poster proposes an application of virtual reality to mask the process, and additionally, allows for association within the cancer patient’s situation
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Mitchell-Thain, Robert, Andrew Yeoman, and Vinod Hegade. "O70 Patient reported experiences through PBC foundation app: what impacts upon a PBC patient’s experience?" In Abstracts of the BSG Campus, 21–29 January 2021. BMJ Publishing Group Ltd and British Society of Gastroenterology, 2021. http://dx.doi.org/10.1136/gutjnl-2020-bsgcampus.70.

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Reports on the topic "Patient's experience"

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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, August 2018. http://dx.doi.org/10.3768/rtipress.2018.op.0054.1808.

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Qualitative data centered on patients’ experiences and perspectives typically go uncollected in clinical trial settings. Yet patients’ treatment experiences offer complementary insights and context on topics such as disease management, treatment gaps, and previous treatments outside of those gathered in traditional patient-reported outcome questionnaires. Qualitative interviews can capture patients’ perceptions of treatment needs, more fully explore meaningful changes experienced as a result of treatment, and reveal outcomes that are most important to patients. Asking patients detailed questions can provide insight into the “why” of a patient’s expressed thought or feeling. The inclusion of patient interviews within clinical trials is a relatively new and evolving field of research. This article delineates the types of data that may be collected during interviews with clinical trial participants and outlines two approaches to conducting qualitative research in the clinical trial setting, with a focus on maximizing the value of the resulting data.
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Rogers, Katherine, Karina Lovell, Peter Bower, and Christopher Armitage. “What are Deaf sign language users’ experiences as patients in healthcare services?”: A scoping review protocol. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, January 2022. http://dx.doi.org/10.37766/inplasy2022.1.0102.

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Review question / Objective: A scoping review with specific reference to the context of Deaf populations, in relation to Deaf people’s experience of health and mental health services, including the use of a questionnaire regarding their experience as a patient, is needed in order to assess and synthesise the current knowledge. As this is an exploratory type of review drawing on qualitative as well as quantitative work, the PICo approach Population, (Phenomena of) Interest and Context, will guide the question formulation. Following the identification of the gap in the existing systematic reviews and scoping searches concerning patient experience and Deaf people’s experience of using healthcare services, the research question is as follows: “What are Deaf sign language users’ experiences as patients in healthcare services?”. Information sources: The bibliographic databases that will be searched for this review will includes PsycINFO, PubMed, Web of Science, CINAHL, and Medline. Grey literature sources (e.g., policy, practice, and guideline documents), including contacting the relevant investigators working in the field of Deaf populations, will be searched for this review study. Forward citation sources, from the relevant reference lists, will also be searched to ensure the process is thorough.
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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, June 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, June 2020. http://dx.doi.org/10.35565/cqi.2020.2012.

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Squiers, Linda, Mariam Siddiqui, Ishu Kataria, Preet K. Dhillon, Aastha Aggarwal, Carla Bann, Molly Lynch, and Laura Nyblade. Perceived, Experienced, and Internalized Cancer Stigma: Perspectives of Cancer Patients and Caregivers in India. RTI Press, April 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 caregiver dyads was drawn from an ongoing population-based cohort study. Overall, 85 percent of patients and 75 percent of caregivers reported experiencing some level (i.e., yes response to at least one of the items) of perceived, experienced, or internalized stigma. Both patients (85 percent) and caregivers (65 percent) perceived that community members hold at least one stigmatizing belief or attitude toward people with cancer. About 60 percent of patients reported experiencing stigma, and over one-third of patients and caregivers had internalized stigma. The findings indicate that fatalistic beliefs about cancer are prevalent, and basic education about cancer for the general public, patients, and caregivers is required. Cancer-related stigma in India should continue to be studied to determine and address its prevalence, root causes, and influence on achieving physical and mental health-related outcomes.
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Layman, Diane L. The Perioperative Experience of the Ambulatory Surgery Patient. Fort Belvoir, VA: Defense Technical Information Center, September 2000. http://dx.doi.org/10.21236/ad1012321.

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

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YARIKOV, A. V., and I. I. SMIRNOV. EXPERIENCE OF DENERVATION OF INTERVERTEBRAL JOINTS OF THE LUMBAR SPINE. Science and Innovation Center Publishing House, April 2022. http://dx.doi.org/10.12731/978-0-615-67340-0-1.

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In this work, the immediate and long-term results of denervation of intervertebral joints in 30 patients with pain syndrome in the lumbar spine were studied. The catamnesis was collected from 18 patients in terms from 1.7 months to 18 months after surgery. Pain syndrome on a visually analog scale after surgery decreased by an average of 20-30 mm. Subclinically expressed anxiety/depression persists in all patients with a “good” result of treatment, the assessment was carried out using the hospital Anxiety and Depression Scale (HADS). According to the Nurick scale, treatment results were assessed at level 2 (improvement) in 93.3% of cases (n=28), level 3 (unchanged condition) - 6.7% of cases (n=2). According to the results of the study, denervation of the intervertebral joints is an effective minimally invasive method of treating facet syndrome. It allows in the early and long-term postoperative periods to significantly reduce the pain syndrome and improve the quality of life of patients. The authors also admit that the pain syndrome in the back is polyethological, which requires careful selection of patients for this type of procedure.
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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, January 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. New York, NY United States: Commonwealth Fund, January 2016. http://dx.doi.org/10.15868/socialsector.25060.

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