Relevant bibliographies by topics / Patient experience

Contents

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

Academic literature on the topic 'Patient experience'

Author: Grafiati
Published: 4 June 2021
Last updated: 20 February 2023

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Patient experience.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Patient experience"

1

Pavlov, Kathren, Fernando Montalvo, Jordan A. Sasser, Luciana Jones, Daniel S. McConnell, and Janan A. Smither. "Applying User Experience Principles to Patient Experiences." Proceedings of the Human Factors and Ergonomics Society Annual Meeting 66, no. 1 (September 2022): 761–65. http://dx.doi.org/10.1177/1071181322661478.

Full text
Abstract:
Patient experiences within the healthcare system are often negative due to the predominantly system-centric nature of healthcare, as well as the physical or mental symptoms of the medical condition being experienced. Improved patient experiences are likely to improve patient visits, engagement with treatment, reduce frustration, and in some medical conditions, improve treatment outcomes. One way to improve patient experiences is to apply user experience principles to the design of patient interactions within the healthcare system. The present study utilized Arhippainen’s User Experience heuristics to identify ways in which patient experiences can be improved. Fundamental restructuring towards patient-centric experiences and general security practices would lead to improved PX and perceptions of healthcare.
APA, Harvard, Vancouver, ISO, and other styles
2

Outlaw, Peter, Shiva Tripathi, and Jacqueline Baldwin. "Using patient experiences to develop services for chronic pain." British Journal of Pain 12, no. 2 (February 28, 2018): 122–31. http://dx.doi.org/10.1177/2049463718759782.

Full text
Abstract:
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 heightened emotional response to their interaction with the service or staff. A short trigger film was compiled to illustrate these touchpoints to staff and gain their commitment to improve patients’ experiences when using the service. A patient experience event was held at which patients discussed the touchpoints and identified the most significant areas for change that would improve their experiences of using the chronic pain service. Results: A wide range of touchpoints were identified. The lack of information provided before arriving for a procedure and the need for a short debrief after clinic were prioritised for improvement. Patients valued the development of good relationships with clinic staff and feeling properly listened to for the first time. The patient experience event allowed the key points patients would like to know before a procedure, to be drawn up in a list, which could be passed onto staff. Conclusion: This study featured collaboration between patients and staff to improve patients’ experiences of using chronic pain services. Through patient participation, a comprehensive list of recommendations for service improvement was produced, and possible solutions were identified. The involvement of patients in driving change and re-designing services is shaping a more patient-centred chronic pain clinic and improving the experience for all the patients who use the service.
APA, Harvard, Vancouver, ISO, and other styles
3

Wolf, Jason A. "Patient Experience." Frontiers of Health Services Management 33, no. 3 (2017): 3–16. http://dx.doi.org/10.1097/hap.0000000000000002.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Guler, Pamela H. "Patient Experience." Frontiers of Health Services Management 33, no. 3 (2017): 17–29. http://dx.doi.org/10.1097/hap.0000000000000003.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Fox, Susan. "Patient Experience." Frontiers of Health Services Management 33, no. 3 (2017): 42–48. http://dx.doi.org/10.1097/hap.0000000000000004.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Kneeland, Patrick P. "Patient Experience." Hospital Medicine Clinics 5, no. 1 (January 2016): 137–51. http://dx.doi.org/10.1016/j.ehmc.2015.08.011.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Ambrose, Kate. "Patient experience." Emergency Nurse 17, no. 7 (November 4, 2009): 9. http://dx.doi.org/10.7748/en.17.7.9.s14.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Williams, Ruth. "Patient experience." Nursing Management 19, no. 2 (April 26, 2012): 11. http://dx.doi.org/10.7748/nm.19.2.11.s7.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Niederhauser, Victoria, and Jason Wolf. "Patient Experience." Nursing Administration Quarterly 42, no. 3 (2018): 211–16. http://dx.doi.org/10.1097/naq.0000000000000293.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Stahl, Katja, and Oliver Groene. "ASK ME!—Routine measurement of patient experience with patient safety in ambulatory care: A mixed-mode survey." PLOS ONE 16, no. 12 (December 1, 2021): e0259252. http://dx.doi.org/10.1371/journal.pone.0259252.

Full text
Abstract:
Objective Routine measurement of patient safety from the patients’ perspective receives increasing attention as an important component of safety measurement systems. The aim of this study was to examine patients’ experience with patient safety in ambulatory care and the results’ implications for routine patient safety measurement in ambulatory care. Design Cross-sectional mixed-mode survey. Setting General practitioner and specialist practices. Participants Patients aged >18 years seeking care in ambulatory care practices between February and June 2020. Methods A 22-item-questionnaire was completed in the practice or at home either on paper or online. Multivariate logistic regression was used to analyse the influence of survey mode and patient characteristics on patient experience with patient safety. Results The overall response rate was 71.1%. Most patients completed the questionnaire on site (76.6%) and on paper (96.1%). Between 30.1% to 68.5% of the respondents report the most positive option for patient experience with the main domains of patient safety. A total of 2.9% of patients reported having experienced a patient-safety event (PSE) during the last 12 months. Patients who filled in the questionnaire off site were more likely to report negative experiences for the scales communication & information (OR 1.2, 95% CI 1.0–1.5), rapport & participation (OR 1.4, 95% CI 1.1–1.7) and access (OR 1.3, 95% CI 0.9–1.4) than those who completed it on site. Those who chose a paper questionnaire were more likely to report negative experiences for all five scales compared to web responders. Conclusion Routine measurement of patient experience with factors contributing to the occurrence of PSEs can achieve high response rates by offering flexible participation options. Results gained from mixed-mode surveys need to take mode-effects into account when interpreting and using the results. Further research is needed in how to adequately assess number and type of experienced events in routine measurements.
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Patient experience"

1

Avlijas, Tanja. "A Concept Analysis of the Patient Experience in Acute Care." Thesis, Université d'Ottawa / University of Ottawa, 2019. http://hdl.handle.net/10393/39715.

Full text
Abstract:
Background: Patient experience has become an essential quality indicator in healthcare. Purpose: The purpose of this thesis was to conduct a concept analysis of the patient experience. Methods: Walker and Avant’s methodology served as the framework for this concept analysis. Data were retrieved from seven databases and one search engine. The literature search used keywords related to "patient experience" and included articles published at any time up until March 2018. A total of 257 articles and organizational websites were included in the analysis after meeting the inclusion criteria. Results: Twenty attributes were found to define the patient experience: communication, respect for patients, information/education, patient-centered care, comfort/pain, discharge from hospital, hospital environment, professionalism/trust, clinical care/staff competency, access to care, global ratings, medication, transitions/continuity, emotional dimension, outcomes, hospital processes, safety/security, interdisciplinary team, social dimension, and patient dependent features. Conclusion: The results of this study will guide and clarify the critical concepts towards an explicit definition of the patient experience.
APA, Harvard, Vancouver, ISO, and other styles
2

Oi, Katsuya. "Understanding the Role of Patient Activation in the Association between Patient Socio-Economic Demographics and Patient Experience." PDXScholar, 2012. https://pdxscholar.library.pdx.edu/open_access_etds/467.

Full text
Abstract:
This study focuses on the association between patient characteristics, which include both demographic and contextual factors, and patients' experiences with health care. The pre-existing literature provides rich information about patients' various demographics related to patient experience. Despite the abundance of empirical evidence showing that patients' demographics do affect how they perceive their health care. However, there is little to no empirical knowledge explaining the significance of such factors. As the existing literature points out the need for taking into contextual factors such as patient's beliefs, attitudes, skills that are pertinent to dealing with health care, my study proposes patient activation as such a contextual factor that explains the association between patient demographics and patient experience. Findings suggest that patient activation is a strong predictor of two patient experience measures: patients' rating of doctor-patient communication and their self-reported difficulties in getting needed care. However, it is also observed that the mediating effects of patient activation vary by the two dimensions of patient experiences. Though this study demonstrates that promoting patient activation may be able to normalize how patients report the quality of doctor-patient interaction, further research is needed to address access to care issues.
APA, Harvard, Vancouver, ISO, and other styles
3

Ghazali, R. J. "Patient satisfaction : the Malaysian experience." Thesis, Swansea University, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.637051.

Full text
Abstract:
The problem of scarce resources and escalating cost of health care has made the Malaysian governments to think about the corporatization of public hospitals. It is vital to understand the current situation before embarking on such a big project. The fundamental aim of the research was to assess the level of patient satisfaction in seven hospitals. In referral hospitals, only medical, surgical, orthopaedic, obstetric and gynaecology wards were selected. In non-referral hospitals, the wards selected were limited to male and female wards. Inpatients were given self-administered questionnaires after selection based on a set of inclusion and exclusion criteria. As for the staff, the same questionnaires were given to doctors, nurses and attendants who were working during that time. SERVQUAL, which was developed by Parasuraman, Zeithami and Berry, was used as a tool for measuring satisfaction. Apart from SERVQUAL, the questionnaires also include a session on respondent requests. Respondents were asked to list and prioritise five important things that they want from the hospital services. In this study the rate of patient satisfaction was low in all the seven hospitals. None of the hospitals had a patient satisfaction score greater than 45%. However in all the hospitals, the levels of dissatisfaction were only mild. In terms of SERVQUAL, patients and staff were least dissatisfied in the dimension of Empathy. Meanwhile, the greatest level of patient dissatisfaction was in the dimension of Responsiveness. For staff, the greatest level of dissatisfaction was Tangibles. Staff perceived that hospital equipment was not up-to-date. Patients understand that being a public hospital, it could only provide facilities to a certain extent. However they expect the staff to respond promptly to their needs. This study also has proven the hypothesis: The patient satisfaction will deteriorate if staff knowledge about patient requests/expectations decreases.
APA, Harvard, Vancouver, ISO, and other styles
4

Salmon, Pauline Adora. "Improving the Patient Experience with Communication." ScholarWorks, 2020. https://scholarworks.waldenu.edu/dissertations/7839.

Full text
Abstract:
A quality patient experience is one of the highest priorities for hospitals as patients and families are looking to healthcare providers to meet their demands for quality service. The Hospital Consumer Assessment of Healthcare Providers and Systems (HCAHPS) survey measures the extent to which providers effectively communicate pertinent information such as communication about medications. On a 20-bed intermediate care unit, the HCAHPS item scores relating to nurse communication and communication about medicine were inconsistent and, on most occasions, were below the comparison benchmark of the 50th percentile when compared to other like hospitals. The purpose of this quality improvement project guided by the patient-centered care model, needs based theory, and adult learning theory, was to test the impact of an educational module for nurses on best practices for teaching patients about medications. Thirty nurses consented to participate in the teach-back sessions. Results of the pre- and posttest, evaluating the nurses' knowledge and attitude about teach-back, were analyzed using the Wilcoxon Signed Ranks test and findings showed an improvement in knowledge scores (z = -2.833, p = .005). However, no statistically significant changes occurred in nurse attitudes toward teach-back. A comparison of descriptive HCAHPS scores on communication about medications and nurse communication showed that scores improved from a low of 58% top box to 74% after the teach-back education. These findings indicated that using teach-back could enhance communication about medications. Effectively communicating pertinent health information using teach-back may have significant consequences for nurse-patient-family engagement contributing to positive social change.
APA, Harvard, Vancouver, ISO, and other styles
5

Marshall, L. "Healthcare environment design and patient experience." Thesis, Canterbury Christ Church University, 2018. http://create.canterbury.ac.uk/17671/.

Full text
Abstract:
The design of healthcare environments has been shown to produce positive effects for patient outcomes, particularly in mental healthcare. However, relatively little is known about patient experience of design within physical healthcare environments. In this study, fourteen cancer patients were interviewed about their experiences of using a newly built cancer centre that incorporates art and design. Grounded theory methodology provided a framework for the analysis of results and the construction of a theoretical model which represents a first attempt at explaining the relationship between healthcare environments and patients with respect to emotional wellbeing. Results show that central aspects of this particular healthcare environment – orientation, physical aspects of design, and atmosphere – were not like a hospital and these led to diverse patient experiences depending on the individual context, in other words the personal histories and preferences that patients brought. Implications for research and clinical practice, including the benefits of drawing upon helpful aspects of environments as part of a holistic approach to treatment, are discussed.
APA, Harvard, Vancouver, ISO, and other styles
6

Fuller, Valerie J., and Valerie J. Fuller. "The Patient Experience of Postoperative Delirium." Diss., The University of Arizona, 2017. http://hdl.handle.net/10150/625719.

Full text
Abstract:
Background: Postoperative delirium (POD) is a common neurocognitive disorder in patients undergoing surgical procedures. Delirium is a disorder that is poorly understood, frequently unrecognized and associated with numerous adverse outcomes including longer hospital stays, significantly higher costs and increased morbidity and mortality. While there has been a great deal of research on proposed etiologies, risk factors and outcomes of delirium, few studies have explored the patient’s subjective experience of the phenomenon. Purpose: The purpose of this qualitative descriptive research was to investigate the patient experience of postoperative delirium and measure the distress associated with the experience. The Delirium Symptoms Experience Model (DSEM) provided the theoretical framework in which to understand the postoperative delirium experience. The three specific aims used to guide the investigation were: 1) Identify patient age, gender, race, type and length of surgery, past medical and surgical history, length of admission, delirium subtype (if known), and medications (including anesthetic agents) used in the perioperative period to better characterize the sample and provide context for the qualitative findings; 2) Describe the postoperative patients’ experience of being and feeling delirious; and, 3) Measure the distress associated with the recall of delirium using the Delirium Experience Questionnaire (DEQ) Methods: Ten participants ranging in age from 33-75 years (mean = 66.2 years of age) who experienced postoperative delirium were interviewed. Patients were screened for persistent delirium or cognitive impairment as assessed with the Confusion Assessment Method and the Mini-Cog™ Instruments. Results: Three organizing themes emerged from the content analysis: 1) Altered Perceptions of Reality; 2) Stuck in the Confusion; and, 3) Seeking Reality. The analysis of the quantitative measures and descriptive data demonstrated a high rate of psychological distress associated with delirium recall with 80% participants reporting it caused severe to very severe distress. The anesthetic drug propofol was the common medication prescribed in the perioperative period and given to all ten participants. Conclusion: Understanding this phenomenon from the patients’ perspective may provide a better understanding of the delirium experience and aid in the development of interventions and treatments to improve care and reduce suffering.
APA, Harvard, Vancouver, ISO, and other styles
7

Karlsson, Terese. "Improvements within patient experience during MRI." Thesis, KTH, Människa och Kommunikation, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-209939.

Full text
Abstract:
MRI is one of the biggest and most growing imaging techniques. Even though itis one of the most harmless technologies a big portion of the patients experienceanxiety during the exam. By improving the patient experience unnecessary psychologicalstress for the patient can be prevented, the patient movement wouldthen decrease and therefore the imaging can be improved without changing thetechnique. Participant observations at four dierent MRI departments werecompleted with six interviews with radiographers and technical MRI personnelin order to get insight in the work around an MRI exam and the problemsthat patients experience. The data collection resulted in three improvementareas: the atmosphere of the waiting room, the atmosphere of the MRI roomand the headset used by the patient during the MRI exam. These improvementareas were paired up with solution suggestions which were then controlled andcommented by one MRI specialist, one MRI developer and one radiographer tovalidate the suggestions. The conclusion was that there is already much doneto improve the environment in the MRI room, even though more can be done.The waiting room, on the other hand ,has not been an object for studies orfor improvements before. Therefore more calculation about how big of a protit could be, to improving the atmosphere in the waiting room, should be doneso one knows how much resources one can be put into that improvement area.Lastly there are potential solutions for how to create a much better headset butbecause the generated solutions in this area are so technically challenging moreresearch has to be done before it can be realised.
MR är en av de största och mest växande medicinsk bildgivande teknikerna som finns. Även om tekniken är helt ofarlig är det många patienter som lider av ångest kopplad till undersökningen. Genom att förbättra patientens upplevelse kan man förbygga den ångesten, då kommer också patienten kunna ligga mera still under undersökningen och därför kommer bilderna kunna förbättras utan att ändra tekniken.Datainsamlingen bestod av deltagande observationer på fyra olika röntgenavdelningar tillsammans med sex stycken intervjuer med både röntgensköterskor och personal som jobbar med MR-tekniken. Detta för att få en inblick i jobbet runt en MR undersökning och problemtiken som patienterna upplever. Datainsamlingen resulterade i tre olika förbättringsområden: väntrummet, undersökningsrummet och headsetet som patienten använder under MR-undersökningen. Dessa förbättringsområden parades ihop med förbättringsförs-lag och validerades sedan med en MR speciallist, en utvecklare och en röntgensköterska.Slutsatsen var att det idag görs mycket för att förbättre miljön i undersökningsrummet, även om mycket mer kan göras. Väntrummet, och andra sidan, har inte varit föremål för varken studier eller förbättringar och därför behöver uträkningar göras på hur stor vinst det skulle vara med en förbättrad miljö där för att veta hur mycket resurser som kan läggas på det. Till sist kan det konstateras att det finns potentiella lösningar för hur ett bättre headset skulle kunna skapas, men eftersom de förslagen som genererats i den här studien är så tekniskt avancerade behövs mer forskning för att kunna realisera lösningarna.
APA, Harvard, Vancouver, ISO, and other styles
8

DeAdder, Dawna Nadine. "The illness experience of patients following a myocardial infarction : implications for patient education." Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/29706.

Full text
Abstract:
This study used the research method of phenomenology to elicit the patient's perspective of the illness experience following a myocardial infarction (MI). The purpose of studying this experience was to gain an understanding of what it meant to men and women to have a MI, what the learning needs were following a MI, and how these learning needs were met. It was proposed that patients would view the illness experience differently from health professionals, thus the patients would identify different learning needs. Anderson's (1985) adaptation of Kleinman's health care system framework was used to conceptualize this problem. Three males and two females, ranging in age from 42 to 77 years, participated in the study. Data were collected through 11 in-depth interviews. From analysis of this data significant statements were extracted to provide a description of the phenomenon under study. The findings of this study suggest that health professionals and patients do view the MI experience from different perspectives. The emphasis of the patients on understanding the MI experience from the reality of their world is reflected in their attempts to rationalize the occurrence of the MI and their desires to know more about their own MI, prognosis, and treatment. In order to plan patient education that will assist post-MI patients in their recovery health professionals must assess patients individually for their: (1) beliefs regarding risk factors and causes of MI; (2) desire for Information; (3) preference for method of instruction; and, (4) preference for timing of education.
Applied Science, Faculty of
Nursing, School of
Graduate
APA, Harvard, Vancouver, ISO, and other styles
9

Johansson, Sofia, and Emelie Mörk. "Patientens upplevelse av omvårdnad vid ortopediska skador." Thesis, Uppsala universitet, Institutionen för folkhälso- och vårdvetenskap, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-294953.

Full text
Abstract:
SAMMANFATTNING                                                                                                       Bakgrund Den ortopediska skadan kan för patienten vara en mycket smärtsam process och orsaka långvarigt lidande. Detta ställer höga krav på sjuksköterskans kompetens som utifrån patientens individuella behov måste tillämpa en god personcentrerad omvårdnad. Syfte Syftet med denna litteraturstudie är att undersöka patientens upplevelse av omvårdnadsåtgärder vid ortopediska skador, samt få en ökad förståelse för betydelsen av personcentrerad omvårdnad vid dessa åtgärder. Metod Då författarna valde att använda redan publicerad forskning användes litteraturstudie som metod. Artiklarna söktes fram i databaserna Cinahl och Pubmed med sökorden orthopaedic, patient, experience, interview. Efter noggrann granskning och värdering av artiklarna inkluderades totalt elva artiklar. Resultat I resultatet redovisas fyra kategorier; information, stöd från vårdpersonal, främja delaktighet och smärtlindring, som för patienten fick en stor betydelse för upplevelsen av omvårdnadsåtgärder vid ortopediska skador. Slutsats Denna studies resultat visar att det utifrån patienternas upplevelser finns ett behov av förbättring. Följaktligen kan vårdpersonalen förbättra sitt utförande av ortopediska omvårdnadsåtgärder, och därmed tillämpa en personcentrerad omvårdnad.     Nyckelord: orthopedic, patient, experience, nursing.
ABSTRACT Background The orthopaedic injury can be a painful experience and cause long-time suffering. This put up for high requirements for the nurse who needs to apply a person-centered care. The aim The aim of the study was to investigate the patient´s experience of provided care when having an orthopedic injury. The second purpose was to obtain knowledge about the meaning of person-centered care. Method A Literature review was used as method though the writers wanted to use already published material. The search of the articles was made in the databases Cinahl and PubMed with the words orthopedic, patient, experience interview. After examining the articles a total of 11 articles were included. Result The results revealed four categories; information, support from the medical staff, participation and alleviation of pain. These categories had a big impact of the patient´s experience of the provided care they were given. Conclusion In this study the result showed that the patients’ experiences found a need of improvement in the work of the nursing-staff. Therefore the nursing-staff can improve their orthopedic care and apply a person-centered care. Keywords: orthopedic, patient, experience, nursing.
APA, Harvard, Vancouver, ISO, and other styles
10

Wahl, Grendi Heidi. "Measuring Patient Experience in Hospital Maternity Care." Thesis, KTH, Skolan för elektroteknik och datavetenskap (EECS), 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-281290.

Full text
Abstract:
This thesis concerns Patient Experience (PX), in hospital maternity care in Sweden. The focus lies in the development of a measure to describe the current state of PX. The thesis uses a semi-sequential mixed-methods study design; exploration of the patient journey, through qualitative methods, informs the adaptation of an existing maternity care experience survey instrument. The resulting survey instrument is tried in a pilot study and renders a composite measure of PX. Part of the analysis is dedicated to understanding the e!ect of information and communication in PX; Exploratory Factor Analysis is used to test the model and attempt an answer. The results show that it is possible to describe PX using the proposed survey instrument. The composite measure preserves di!erences in perceptions better than an arithmetic average of two discrete VAS-1 type measurements, and is more appropriate when measuring attitudes, and opinions using Likert-type measures. A three component solution describes 65.44% of the total sample variance. Determining to what degree PX is influenced by information and communication remains di"cult to quantify, but these initial results indicate that the manner of the attending sta! during aftercare and the respondent’s mastery of information during discharge are important dimensions of patients’ total PX (ANOVA R .695, R Square .483). The model’s three components are almost entirely built from items that address interpersonal skills and information assimilation. These correspond to two of the three Service Quality Dimensions, namely Interaction Quality and Outcome Quality. Most important of the three is the component “Chemistry in aftercare”. The predictive strength of the model shows merit under the context of the study and could advise further e!orts to develop measurements for PX in maternity care in a Swedish hospital setting. Lastly, this study contextualises Service Design in hospital maternity healthcare; the study therefore o!ers ample opportunity for innovation.
Arbetet handlar om Patientupplevelse (PU), i förlossningsvården i Sverige. Fokus ligger på utvecklingen av ett mätvärde att beskriva den nuvarande patientupplevelsen. Arbetet använder kvalitativa och kvantitativa metoder (mixed-methods), i en semi-sekventiell design; utforskning av patientresan ligger till grund för anpassningen av ett existerande mätinstrument. Det nya mätinstrumentet testas i en pilotstudie och ger ett kompositmätvärde av PU. En del av analysen ägnas åt att förstå vilken e!ekt information och kommunikation har på PU; Explorativ faktoranalys används för ändamålet. Resultaten visar att det är möjligt att beskriva PU genom det föreslagna mätinstrumentet. Det resulterande kompositvärdet är bättre på att beskriva skillnader i uppfattning än ett medelvärde av två diskreta variabler av VAS-1 typen, och är också lämpligare när attityder och åsikter mäts med hjälp av Likert-skalor. En trekomponentslösning beskriver 65.44% av den totala stickprovsvariansen. Att avgöra hur mycket PU påverkas av information och kommunikation förblir svårt att kvantifiera, men dessa inledande resultat visar att patientbemötande under eftervårdstiden och patientens förmåga att bemästra information under utskrivningen är viktiga dimensioner av patienters totala PU (ANOVA R .695, R Square .483). Modellens tre komponenter är nästan uteslutande uppbyggda av variabler som fångar upp personliga relationer och assimilering av information. Dessa motsvarar två av de tre dimensionerna i Servicekvalitetsmodellen, nämligen Interaktionskvalitet och Utfallskvalitet. Viktigaste komponenten är Personlig kemi under eftervården. Modellens förutsägningsstyrka visar förtjänst under studiens kontext och kunde informera framtida ansträngningar att utveckla mätvärden för förlossningsvården inom svensk sjukhusmiljö. Till sist kan nämnas att studien kontextualiserar Service Design inom förlossningsvården; studien erbjuder därför omfattande möjligheter för innovation.
APA, Harvard, Vancouver, ISO, and other styles
More sources

Books on the topic "Patient experience"

1

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

Find full text
APA, Harvard, Vancouver, ISO, and other styles
2

Choctaw, William T. Transforming the Patient Experience. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-16928-6.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

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

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Patient encounters: The experience of disease. Charlottesville: University Press of Virginia, 1989.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
5

Buchanan, James H. Patient encounters: The experience of disease. New York: H. Holt, 1991.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
6

Warne, Tony, and Sue McAndrew, eds. Using Patient Experience in Nurse Education. London: Macmillan Education UK, 2005. http://dx.doi.org/10.1007/978-1-137-20436-3.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Sinnott, Patricia A. Pharmacists' illness experience and the pharmacist-patient relationship. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1999.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
8

The cancer experience: The doctor, the patient, the journey. Lanham: Rowman & Littlefield Publishers, 2012.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
9

World Health Organization. Regional Office for Europe, ed. Patient mobility in the European union: Learning from experience. Copenhagen: World Health Organization, Regional Office for Europe, 2006.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
10

Patient satisfaction: Understanding and managing the experience of care. 2nd ed. Chicago, IL: Health Administration Press, 2005.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Book chapters on the topic "Patient experience"

1

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

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

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Le Cam, Yann, and Matthew Bolz-Johnson. "Expert by Experience: Valuing Patient Engagement in Healthcare." In Patient Engagement, 233–67. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-14101-1_9.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Choctaw, William T. "Change Is Inevitable." In Transforming the Patient Experience, 1–2. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-16928-6_1.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Choctaw, William T. "The Power of Common Ground." In Transforming the Patient Experience, 3–5. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-16928-6_2.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Choctaw, William T. "Relentless Pursuit of “0” Harm." In Transforming the Patient Experience, 7–8. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-16928-6_3.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Patient experience"

1

"Patient experience." In Proceedings of UK Imaging and Oncology Congress Online 2021. The British Institute of Radiology, 2021. http://dx.doi.org/10.1259/conf-pukrc.2021-i-patex.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Andersen, Tariq O., Pernille R. D. Andersen, Anders C. Kornum, and Trine M. Larsen. "Understanding patient experience." In PervasiveHealth '17: 11th EAI International Conference on Pervasive Computing Technologies for Healthcare. New York, NY, USA: ACM, 2017. http://dx.doi.org/10.1145/3154862.3154868.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Miles, Jon, and Karl Ballance. "Omalizumab: The Patient Experience." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a1340.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

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.

Full text
Abstract:
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.
APA, Harvard, Vancouver, ISO, and other styles
5

Arunachalam, Priya, and Brendan D’Souza. "Patient-Centered Hospital Gowns: A Novel Redesign of Inpatient Attire to Improve Both the Patient and Provider Experience." In 2022 Design of Medical Devices Conference. American Society of Mechanical Engineers, 2022. http://dx.doi.org/10.1115/dmd2022-1058.

Full text
Abstract:
Abstract During their inpatient stays, patients are often required – or highly encouraged – to wear hospital gowns. While these gowns are intended to be convenient for patients and their providers, their design has remained largely unchanged over time. As healthcare moves towards greater emphasis on patient-centered care, the hospital gown is an opportunity to improve patient care. Patients have expressed frustration with the traditional hospital gown, especially with how revealing the gown can be. Here, we introduce a redesigned hospital gown that addresses many common concerns related to patients’ comfort and privacy. Our design introduces novel midline, rear, and shoulder panels, which provide healthcare workers with convenient access to the patient while maintaining coverage over areas of the patient that are not being examined. These panels also make it less likely for patients to be inappropriately exposed during routine activities. A prototyped gown was developed to test design features, and evaluation of this prototype demonstrated that this novel design has the potential to address many concerns while protecting the usability of traditional gowns. Further improvements to the gown’s design are also discussed.
APA, Harvard, Vancouver, ISO, and other styles
6

Hatley, Ross, Louise Rowe, Ian Rabbetts, and Filippo Quadrelli. "Optimizing patient experience of nebulizer treatments." In ERS International Congress 2016 abstracts. European Respiratory Society, 2016. http://dx.doi.org/10.1183/13993003.congress-2016.pa4082.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Peres, Nick. "0012 Patientvr – a virtual reality experience from the patient perspective." In Conference Proceedings of the Association for Simulation Practice in Healthcare (ASPiH) Annual Conference. 3rd to 5th November 2015, Brighton, UK. The Association for Simulated Practice in Healthcare, 2015. http://dx.doi.org/10.1136/bmjstel-2015-000075.1.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
10

Rathnayake, S. D., and W. O. Gamage. "mpact of vernacular architecture elements on patient waiting experience in rural government hospitals in Sri Lanka." In Independence and interdependence of sustainable spaces. Faculty of Architecture Research Unit, 2022. http://dx.doi.org/10.31705/faru.2022.10.

Full text
Abstract:
The role of architecture in hospitals is a sensitive topic; the prominence given to the programmatic requirements has led to disregard of the in-between function of waiting identified as the user experience in the recovery process. Healing, in other words cure means a state of physical & mental wellbeing that a patient experiences in a hospital. It’s a waiting process between the time of treatment & recovery. The waiting experience in Sri Lankan public hospitals is critical because spaces are designed only prioritizing standards while little consideration is given to the impact of local contextual parameters that generate familiar user experiences. This research investigates the impact of design options derived through principles abstracted by vernacular architecture elements on the waiting experience of patients in healthcare facilities. Vernacular elements of identification of centre and openness, articulation of transition space & domestic scaled spaces was used to interpret design options that can be adapted to reorganize the waiting scenarios of hallway, outpatient, and inpatient waiting spaces. The research further investigate how they will help alleviate the user experience of waiting and increase wellbeing.
APA, Harvard, Vancouver, ISO, and other styles

Reports on the topic "Patient experience"

1

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

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.

Full text
Abstract:
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.
APA, Harvard, Vancouver, ISO, and other styles
4

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.

Full text
Abstract:
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.
APA, Harvard, Vancouver, ISO, and other styles
5

Bland, Cynthia, Sara Zuckerbraun, Lisa M. Lines, Anne Kenyon, Marjorie Hinsdale-Shouse, Amy Hendershott, Rebekah Sanchez, et al. Challenges Facing CAHPS Surveys and Opportunities for Modernization. RTI Press, November 2022. http://dx.doi.org/10.3768/rtipress.2022.op.0080.2211.

Full text
Abstract:
Consumer Assessment of Healthcare Providers and Systems (CAHPS) surveys are a standard survey tool for obtaining patient assessments of health plans, hospitals, and health care providers. These surveys measure patient experiences of care, which is considered a component of health care quality. Providers use their survey results to improve patient experience, which is associated with better health care outcomes and reduced costs. CAHPS data also empower consumers and payers to make more informed choices about providers or facilities. Some people argue that CAHPS surveys are outdated and distract providers from clinical health care quality. In this paper, we review the benefits of CAHPS, the current challenges of these surveys, and ideas for modernization and innovation to ensure these surveys remain relevant. We encourage the Centers for Medicare & Medicaid Services (CMS) and its contractors to review and implement these innovations to the CAHPS surveys and the dissemination of their results.
APA, Harvard, Vancouver, ISO, and other styles
6

Seedu, Tegwende, Eden Manly, Taylor Moore, Laura Anderson, Beth Murray-Davis, Diane Ménage, Rebecca Seymour, and Rohan D'Souza. Understanding maternal morbidity from the perspectives of women & people with pregnancy experience: a concept analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, December 2022. http://dx.doi.org/10.37766/inplasy2022.12.0097.

Full text
Abstract:
Review question / Objective: This study will investigate the question: what is maternal morbidity from the perspective of women and people with pregnancy experience? The objectives of this study are to: 1. describe the conditions and events that WPPE conceptualize as maternal morbidities, 2. identify the themes that arise across WPPE’s experiences, such as regional and cultural differences and similarities, and 3. produce a schematic representation of how WPPE conceptualize maternal morbidity. Background: Maternal morbidity is primarily concerned with adverse pregnancy-related outcomes, excluding mortality, among the pregnant and postpartum population. Although presently a global concern, maternal morbidity was not always prioritized in healthcare and research. The increased attention towards maternal morbidity in recent decades was preceded by the initial prioritization of maternal mortality as the dominant indicator of maternal health, leading to its decreasing trend over the decades.(1) Standards of maternal care are no longer solely defined by preventing mortality; they now include preventing and better treatment of maternal morbidity to improve patient outcomes. However, there are no universally accepted criteria for describing maternal morbidity. Less evidence is available on the views of Women and People with Pregnancy Experience (WPPE), and a knowledge gap exists in conceptualizing maternal morbidity from their perspective.
APA, Harvard, Vancouver, ISO, and other styles
7

Chang, Min Cheol, Yoo Jin Choo, and Sohyun Kim. Effect of Prehabilitation in Colorectal Cancer Surgery: A Systematic Review and Meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, October 2022. http://dx.doi.org/10.37766/inplasy2022.10.0015.

Full text
Abstract:
Review question / Objective: Colorectal cancer increases with age, and elderly patients are associated with a poorer prognosis after colorectal surgery. Since comorbidity and frailty are associated with clinical outcomes, several strategies are introduced to improve clinical outcomes according to correct those.Despite efforts to improve the clinical outcome after surgery, patients with colorectal surgery still frequently experience complications. While Enhanced Recovery After Surgery has standardized principals, prehabilitation program varied among studies. The prehabilitation program according to the study showed differences in patient selection criteria, exercise, nutritional support, and methods of the outcome measurement. Therefore, various results have been reported regarding the effect of prehabilitation. The effectiveness of prehabilitation is still controversial. The aim of this study was to confirm the updated overall spectrum and measure the effect of prehabilitation in patients with colorectal cancer surgery.
APA, Harvard, Vancouver, ISO, and other styles
8

Treadwell, Jonathan R., James T. Reston, Benjamin Rouse, Joann Fontanarosa, Neha Patel, and Nikhil K. Mull. Automated-Entry Patient-Generated Health Data for Chronic Conditions: The Evidence on Health Outcomes. Agency for Healthcare Research and Quality (AHRQ), March 2021. http://dx.doi.org/10.23970/ahrqepctb38.

Full text
Abstract:
Background. Automated-entry consumer devices that collect and transmit patient-generated health data (PGHD) are being evaluated as potential tools to aid in the management of chronic diseases. The need exists to evaluate the evidence regarding consumer PGHD technologies, particularly for devices that have not gone through Food and Drug Administration evaluation. Purpose. To summarize the research related to automated-entry consumer health technologies that provide PGHD for the prevention or management of 11 chronic diseases. Methods. The project scope was determined through discussions with Key Informants. We searched MEDLINE and EMBASE (via EMBASE.com), In-Process MEDLINE and PubMed unique content (via PubMed.gov), and the Cochrane Database of Systematic Reviews for systematic reviews or controlled trials. We also searched ClinicalTrials.gov for ongoing studies. We assessed risk of bias and extracted data on health outcomes, surrogate outcomes, usability, sustainability, cost-effectiveness outcomes (quantifying the tradeoffs between health effects and cost), process outcomes, and other characteristics related to PGHD technologies. For isolated effects on health outcomes, we classified the results in one of four categories: (1) likely no effect, (2) unclear, (3) possible positive effect, or (4) likely positive effect. When we categorized the data as “unclear” based solely on health outcomes, we then examined and classified surrogate outcomes for that particular clinical condition. Findings. We identified 114 unique studies that met inclusion criteria. The largest number of studies addressed patients with hypertension (51 studies) and obesity (43 studies). Eighty-four trials used a single PGHD device, 23 used 2 PGHD devices, and the other 7 used 3 or more PGHD devices. Pedometers, blood pressure (BP) monitors, and scales were commonly used in the same studies. Overall, we found a “possible positive effect” of PGHD interventions on health outcomes for coronary artery disease, heart failure, and asthma. For obesity, we rated the health outcomes as unclear, and the surrogate outcomes (body mass index/weight) as likely no effect. For hypertension, we rated the health outcomes as unclear, and the surrogate outcomes (systolic BP/diastolic BP) as possible positive effect. For cardiac arrhythmias or conduction abnormalities we rated the health outcomes as unclear and the surrogate outcome (time to arrhythmia detection) as likely positive effect. The findings were “unclear” regarding PGHD interventions for diabetes prevention, sleep apnea, stroke, Parkinson’s disease, and chronic obstructive pulmonary disease. Most studies did not report harms related to PGHD interventions; the relatively few harms reported were minor and transient, with event rates usually comparable to harms in the control groups. Few studies reported cost-effectiveness analyses, and only for PGHD interventions for hypertension, coronary artery disease, and chronic obstructive pulmonary disease; the findings were variable across different chronic conditions and devices. Patient adherence to PGHD interventions was highly variable across studies, but patient acceptance/satisfaction and usability was generally fair to good. However, device engineers independently evaluated consumer wearable and handheld BP monitors and considered the user experience to be poor, while their assessment of smartphone-based electrocardiogram monitors found the user experience to be good. Student volunteers involved in device usability testing of the Weight Watchers Online app found it well-designed and relatively easy to use. Implications. Multiple randomized controlled trials (RCTs) have evaluated some PGHD technologies (e.g., pedometers, scales, BP monitors), particularly for obesity and hypertension, but health outcomes were generally underreported. We found evidence suggesting a possible positive effect of PGHD interventions on health outcomes for four chronic conditions. Lack of reporting of health outcomes and insufficient statistical power to assess these outcomes were the main reasons for “unclear” ratings. The majority of studies on PGHD technologies still focus on non-health-related outcomes. Future RCTs should focus on measurement of health outcomes. Furthermore, future RCTs should be designed to isolate the effect of the PGHD intervention from other components in a multicomponent intervention.
APA, Harvard, Vancouver, ISO, and other styles
9

Zerbib, Olivier, Yaniv Hadi, Daniel Kovarsky, Gal Sahaf Levin, Tamar Gottesman, Mor Darkhovsky, and Shaul Lev. Multiple Recurrent Pneumothoraces and Thoracic Drain Insertion in a Mechanically Ventilated Patient Suffering from Methadone Induced Cardiomyopathy. Science Repository, January 2023. http://dx.doi.org/10.31487/j.jcmcr.2022.01.02.

Full text
Abstract:
Objective: To describe the experience of a multimodal therapeutic approach in a patient with methadone-induced dilated cardiomyopathy who developed recurrent bilateral tension pneumothorax. Setting: Department of Intensive Care. Patient: A patient with methadone-induced cardiomyopathy and severe left ventricular dysfunction who after mechanical ventilation underwent bilateral tension pneumothorax and prolonged cardiovascular resuscitation (CPR). Interventions: Cardiac Angiography, Multiple counter–shock (defibrillator dose), Multiple Thoracic Drains. Case Report: A 56-year-old man with past IV drug abuse and severe left ventricular dysfunction was transferred from the intensive cardiac care unit (ICCU) to our intensive care unit (ICU) ward due to suspected aspiration pneumonia. Multiple attempts of weaning off mechanical ventilation were unsuccessful, followed by development of septic shock. Following cardiothoracic consultation, two thoracic drains were placed. Due to repeated events of bilateral tension pneumothorax and CPR attempts, a total of seven thoracic drains were placed, permitting rapid control and improvement in the patient status. The possibility of Extracorporeal Membrane Oxygenation (ECMO) was not considered as supportive care due to methadone use and severe secondary cardiomyopathy. In the following days, control and stabilization of the patient status was obtained. Vasopressor treatment withdrawal, cessation of drainage and removal of five thoracic access points were successfully performed prior to percutaneous tracheostomy. The two remaining drains were removed later on during hospitalization. After 29 days in the ICU, the patient was discharged to a step down ward.
APA, Harvard, Vancouver, ISO, and other styles
10

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.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Patient experience' for particular source types:
Journal articles Dissertations / Theses Books
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography