Relevant bibliographies by topics / Care of patient

Contents

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

Academic literature on the topic 'Care of patient'

Author: Grafiati
Published: 4 June 2021
Last updated: 5 February 2022

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Journal articles on the topic "Care of patient"

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SCHROCK, SUZY. "PATIENT CARE: Perioperative Patient Care." AORN Journal 58, no. 6 (December 1993): 1200–1201. http://dx.doi.org/10.1016/s0001-2092(07)64927-8.

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Mıstık, Selçuk, Ülkü Elif Demir, and Sinan Demir. "Evaluation of Diabetic Patient Care Quality in Primary Care." Turkish Nephrology Dialysis Transplantation 25, no. 1 (January 22, 2016): 46–51. http://dx.doi.org/10.5262/tndt.2016.1001.04.

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Mohiuddin, AK. "Patient-Provider Relationship: Compliance with Care." International Journal of Research and Development in Pharmacy & Life Sciences 7, no. 6 (November 2018): 3138–49. http://dx.doi.org/10.21276/ijrdpl.2278-0238.2018.7(6).3138-3149.

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Kusnanto, Hari. "Patient-Centered Care." Review of Primary Care Practice and Education (Kajian Praktik dan Pendidikan Layanan Primer) 1, no. 2 (May 31, 2018): 51. http://dx.doi.org/10.22146/rpcpe.36009.

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..........In the context of patient services constrained by cost barriers, physicians often find it unfavorable to choose an option that prioritizes patient interest. As has been the practice of physicians since Hippocrates, physicians position themselves as the one who best knows what is the most appropriate for the patient. This is in contrary to the concept of patient-centered care. Supported by the ethical principle of patient autonomy, patient-centered services / PCC (LBP/Layanan Berpusat Pasien) empower patients through the provision of more clear and accurate information, allowing patients to be partners in decision-making concerning their health........The cultural shift and the way services are delivered to the patients must be designed, managed and rewarded financially. Patients are no longer merely customers who receive services, but partners in the process of prevention and cure of the disease. The expected benefits of patient-centered services are greater patient and family satisfaction, increased reputation of the physician or the health care provider institution, increased morale and clinical productivity of supporting staffs, and cost savings and service efficiency.......
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Shindul-Rothschild, Judith. "Patient Care." American Journal of Nursing 96, no. 3 (March 1996): 22–24. http://dx.doi.org/10.1097/00000446-199603000-00013.

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&NA;. "Patient Care." Journal of Infusion Nursing 34 (2011): S15—S19. http://dx.doi.org/10.1097/nan.0b013e31820313d5.

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Oliveira, Ciane Martins de, Angela Maria Ramos Canuto Machado, Régia Cristina da Silva Pereira Alves, Zenaide Soares do Mar, Amanda Alves Fecury, Cláudio Alberto Gellis de Mattos Dias, Euzébio de Oliveira, and Carla Dendasck. "The evolution of patient care with Leprosy: the leprosaria to multidrug therapy." Revista Científica Multidisciplinar Núcleo do Conhecimento 06, no. 08 (August 20, 2016): 68–80. http://dx.doi.org/10.32749/nucleodoconhecimento.com.br/health/evolution-of-patient-care.

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Davis, R. "Patient Care in Neurosurgery, 3rd Ed. (Patient Care Series)." Neurology 41, no. 1 (January 1, 1991): 160. http://dx.doi.org/10.1212/wnl.41.1.160-b.

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Boumbulian, Paul J., MacGregor W. Day, Thomas L. Delbanco, Susan Edgman-Levitan, David R. Smith, and Ron J. Anderson. "Patient-Centered Patient-Valued Care." Journal of Health Care for the Poor and Underserved 2, no. 3 (1991): 338–46. http://dx.doi.org/10.1353/hpu.2010.0193.

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Singh, Urmil, and Abhishek Raizada. "Assessing Operational Methodology of Health Care Organizations With Reference to Patient Care." Journal of Advances and Scholarly Researches in Allied Education 15, no. 6 (August 1, 2018): 247–51. http://dx.doi.org/10.29070/15/57905.

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Dissertations / Theses on the topic "Care of patient"

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Kshetri, Kanak Bikram. "Modelling patient states in intensive care patients." Thesis, Massachusetts Institute of Technology, 2011. http://hdl.handle.net/1721.1/76985.

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Thesis (M. Eng.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2011.
Cataloged from PDF version of thesis.
Includes bibliographical references (p. 71-74).
Extensive bedside monitoring in hospital Intensive Care Units (ICU) has resulted in a deluge of information on patient physiology. Consequently, clinical decision makers have to reason with data that is simultaneously large and high-dimensional. Mechanisms to compress these datasets while retaining their salient features are in great need. Previous work in this area has focused exclusively on supervised models to predict specific hazardous outcomes like mortality. These models, while effective, are highly specific and do not generalize easily to other outcomes. This research describes the use of non-parametric unsupervised learning to discover abstract patient states that summarize a patient's physiology. The resulting model focuses on grouping physiologically similar patients instead of predicting particular outcomes. This type of cluster analysis has traditionally been done in small, low-dimensional, error-free datasets. Since our real-world clinical dataset affords none of these luxuries, we describe the engineering required to perform the analysis on a large, high-dimensional, sparse, noisy and mixed dataset. The discovered groups showed cohesiveness, isolation and correspondence to natural groupings. These groups were also tested for enrichment towards survival, Glasgow Coma Scale values and critical heart rate events. In each case, we found groups which were enriched and depleted towards those outcomes.
by Kanak Bikram Kshetri.
M.Eng.
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Blackwelder, Reid B. "Patient-Centered Care." Digital Commons @ East Tennessee State University, 2010. https://dc.etsu.edu/etsu-works/6982.

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Söderholm, Werkö Sophie. "Patient patients? : achieving patient empowerment through active participation, increased knowledge and organisation /." Stockholm : School of Business, Stockholm University, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-7261.

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Almemani, Basima Abdalla Husein. "Pharmacogenetics in patient care." Thesis, Queen's University Belfast, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.546000.

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McHenry, Kristen L. "Safety and Patient Care." Digital Commons @ East Tennessee State University, 2018. https://dc.etsu.edu/etsu-works/2537.

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McHenry, Kristen L. "Safety & Patient Care." Digital Commons @ East Tennessee State University, 2019. https://dc.etsu.edu/etsu-works/5443.

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Petit, Amanda. "Patient-Provider Communication in Patients with Inflammatory Bowel Disease." Ohio University Honors Tutorial College / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=ouhonors1528924843222824.

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Baker, Diane. "Does team patient care mean better patient outcomes?" Thesis, California State University, Long Beach, 2016. http://pqdtopen.proquest.com/#viewpdf?dispub=10161771.

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Traditional patient care in the U.S. has been fragmented and redundant, resulting in high healthcare costs and poor patient outcomes. New team patient care models are being attempted to improve outcomes and lower the cost of care. Models of integrated and coordinated care, including the Patient-Centered Medical Home model, have demonstrated some improvements, especially for chronically ill patients. Membership in a Health Maintenance Organization (HMO) and presence of a diabetes diagnosis is tested and results for the chronically ill are discussed.

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Marepula, Lindiwe Oscarine. "Patient satisfaction with the care provided in a psychiatric hospital in Cape Town." Thesis, University of the Western Cape, 2012. http://hdl.handle.net/11394/3698.

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Magister Curationis - MCur
Background: Patient satisfaction is a well-researched area in general medicine worldwide, yet a full exploration of patient satisfaction amongst psychiatric patients appears to be lacking in South Africa. Patient satisfaction has become important because of the awareness of the patient’s human rights. There is an increasing practice of applying a consumer viewpoint to health care, while safeguarding patients’ rights and taking their views into account. This has been brought about by the inception of the Mental Health Care Act no. 17 of 2002.Purpose: The purpose of this study was to describe psychiatric inpatients’ satisfaction with the care provided in a psychiatric hospital in Cape Town.Objectives : (1) To describe the psychiatric inpatients’ satisfaction with the care provided in a psychiatric teaching hospital in terms of their views on the: care provided by nurses (interpersonal/nurse-patient- interaction and technical skills); care provided by doctors (interpersonal/doctor-patient interaction and technical skills; and the nature of the environment of care, and (2) to describe the psychiatric inpatients’ overall satisfaction with the care received in a psychiatric teaching hospital in terms of the: quality of care received from nurses and doctors; nature of the environment of care; and the likelihood of future utilization of the hospital serviceMethod/Design: The study made use of the quantitative descriptive design using the Primary Provider Theory of patient satisfaction and the Batho Pele Principles served as the conceptual framework. Data were collected from discharged patients using a self-administered questionnaire which was mailed to individual participants. A five and a four point Likert scales were used for different sections in the questionnaire.The study made use of 120 participants between the ages of 18 and 60.Findings: Generally respondents were satisfied with the care provided in thispsychiatric hospital. Greater satisfaction was noted on aspects of staff-patient interactions. Low satisfaction scores were observed on nurses’ technical aspects of care. The Batho Pele principles of information, openness and transparency,consultation, access and redress seem not to have been adhered to.Conclusions: General inpatient satisfaction in psychiatric hospital care was good.However, more innovative methods for improvement in the areas of dissatisfaction need to be developed. Special attention should be given to the implementation of the Batho Pele Principles and the protection of the patients’ rights.
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Abrahamsen, Grøndahl Vigdis. "Patients’ perceptions of actual care conditions and patient satisfaction with care quality in hospital." Doctoral thesis, Karlstads universitet, Avdelningen för omvårdnad, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:kau:diva-9023.

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There are theoretical and methodological difficulties in measuring the concepts of quality of care and patient satisfaction, and the conditions associated with these concepts. A theoretical framework of patient satisfaction and a theoretical model of quality of care have been used as the theoretical basis in this thesis. Aim. The overall aim was to describe and explore relationships between person-related conditions, external objective care conditions, patients’ perceptions of quality of care, and patient satisfaction with care in hospital. Methods. Quantitative and qualitative methods were used. In the quantitative study (I-III), 528 patients (83.7%) from eight medical, three surgical and one mixed medical/surgical ward in five hospitals in Norway agreed to participate (10% of total discharges). Data collection was conducted using a questionnaire comprising four instruments: Quality from Patients’ Perspective (QPP); Sense of Coherence scale (SOC); Big Five personality traits – the Single-Item Measures of Personality (SIMP); and Emotional Stress Reaction Questionnaire (ESRQ). In addition, questions regarding socio-demographic data and health conditions were asked, and data from ward statistics were included. Multivariate statistical analysis was carried out (I-III). In the qualitative study 22 informants were interviewed (IV). The interviews were analysed by conventional content analysis. Main findings. Patients’ perceptions of quality of care and patient satisfaction ranged from lower to higher depending on whether all patients or groups of patients were studied. The combination of person-related and external objective care conditions explained 55% of patients’ perceptions of quality of care (I). 54.7% of the variance in patient satisfaction was explained, and the person-related conditions had the strongest impact, explaining 51.7% (II). Three clusters of patients were identified regarding their scores on patient satisfaction and patients’ perceptions of quality of care (III). One group consisted of patients who were most satisfied and had the best perceptions of quality of care, a second group of patients who were less satisfied and had better perceptions, and a third group of patients who were less satisfied and had the worst perceptions. The qualitative study revealed four categories of importance for patients’ satisfaction: desire to regain health, need to be met in a professional way as a unique person, perspective on life, and need to have balance between privacy and companionship (IV). Conclusions. Patients’ perceptions of quality of care and patient satisfaction are two different concepts. The person-related conditions seem to be the strongest predictors of patients’ perceptions of quality of care and patient satisfaction. Registered nurses need to be aware of this when planning and conducting nursing care. There is a need of guidelines for handling over‑occupancy, and of procedures for emergency admissions on the wards. The number of registered nurses on the wards needs to be considered. Healthcare personnel must do their utmost to provide the patients with person‑centred care.
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Books on the topic "Care of patient"

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Williams, Erica Koch. Patient care. New York: McGraw-Hill, Health Professions Division, 1999.

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Chitwood, Linda B. Ambulatory patient care. La Mesa, CA: Western Schools Press, 1994.

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1928-, Dodge Gwen H., ed. Perioperative patient care. 2nd ed. Boston: Jones and Bartlett Publishers, 1991.

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Grol, Richard, Michel Wensing, Martin Eccles, and David Davis, eds. Improving Patient Care. Oxford, UK: John Wiley & Sons, Ltd, 2013. http://dx.doi.org/10.1002/9781118525975.

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Sanchez, Juan A., Paul Barach, Julie K. Johnson, and Jeffrey P. Jacobs, eds. Surgical Patient Care. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-44010-1.

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Batehup, Lynn, and Jenifer Wilson-Barnett, eds. Planning Patient Care. London: Macmillan Education UK, 1988. http://dx.doi.org/10.1007/978-1-349-10102-3.

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Duesterhaus, Minor Scott, ed. Patient care skills. 3rd ed. Norwalk, Conn: Appleton & Lange, 1995.

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Duesterhaus, Minor Scott, ed. Patient care skills. 6th ed. Upper Saddle River, N.J: Pearson Education, 2010.

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Carey, Timothy A. Patient-Perspective Care. Milton Park, Abingdon, Oxon ; New York, NY : Routledge, 2018.: Routledge, 2017. http://dx.doi.org/10.4324/9781351227988.

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Minor, Mary Alice D. Patient care skills. 4th ed. Stamford, Conn: Appleton & Lange, 1999.

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Book chapters on the topic "Care of patient"

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Ramer, Karen, and Abass Alavi. "Patient Care." In Nuclear Medicine Technology, 139–44. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-09010-7_15.

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Ringel, Marc. "Patient Care." In Digital Healing, 111–36. Boca Raton : Taylor & Francis, 2018. | “A Routledge title, part of the Taylor & Francis imprint, a member of the Taylor & Francis Group, the academic division of T&F Informa plc.”: Productivity Press, 2018. http://dx.doi.org/10.4324/9781315115757-9.

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Makanjee, Chandra, Deon Xu, and Drishti Sarswat. "Patient Care." In General Radiography, 137–56. First edition. | Boca Raton : CRC Press, 2020. |: CRC Press, 2020. http://dx.doi.org/10.1201/9781003047278-8.

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Santos, Eugene, Joseph M. Rosen, Keum Joo Kim, Fei Yu, Deqing Li, Elizabeth A. Jacob, and Lindsay B. Katona. "Patient Care." In Modeling and Simulation in the Medical and Health Sciences, 147–74. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118003206.ch9.

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Lindsay, Mark. "Mayo Post Acute Care Program and Care Continuum." In Patient Flow, 447–72. Boston, MA: Springer US, 2013. http://dx.doi.org/10.1007/978-1-4614-9512-3_19.

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Øvretveit, John, and Eskil Degsell. "Implementing Patient and Carer Participation in Self-Care and Co-Care in Sweden: Policy, Practice and the Future of Person-Centred Care." In Patient Engagement, 63–89. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-14101-1_4.

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Ong, Mei-Sing, and Enrico Coiera. "Handoff and Care Transitions." In Patient Safety, 35–51. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-7419-7_3.

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Frezza, Eldo E. "Patient-Centered Care." In Patient-Centered Healthcare, 3–9. Boca Raton : Routledge/Taylor & Francis, 2020.: Productivity Press, 2019. http://dx.doi.org/10.4324/9780429032226-1.

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Frezza, Eldo E. "Confusion over Care." In Patient-Centered Healthcare, 71–78. Boca Raton : Routledge/Taylor & Francis, 2020.: Productivity Press, 2019. http://dx.doi.org/10.4324/9780429032226-10.

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Frezza, Eldo E. "Access to Care." In Patient-Centered Healthcare, 11–17. Boca Raton : Routledge/Taylor & Francis, 2020.: Productivity Press, 2019. http://dx.doi.org/10.4324/9780429032226-2.

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Conference papers on the topic "Care of patient"

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Barinov, Evgeny, Nadezhda Dobrovolskaya, Anastasia Ivanova, Ruslan Kalinin, Alexander Manin, Natalya Mikheeva, and Pavel Romodanovsky. "Patient dissatisfaction with medical dental care." In Issues of determining the severity of harm caused to human health as a result of the impact of a biological factor. ru: Publishing Center RIOR, 2020. http://dx.doi.org/10.29039/conferencearticle_5fdcb03a353ad3.76128786.

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The article provides information on the results of studying the materials of 150 commission of forensic medical examinations on the facts of patient dissatisfaction with the provision of medical care. The relevance of the problem of the legal relationship between a doctor and a patient is revealed and shown. The lack of information on these issues leads to a high probability of disputed situations in the providing dental care, so there is an urgent need for an integrated approach to the implementation of legally defined rights of patients. Media coverage of the above-mentioned problems plays an important role in improving the level of legal competence of patients. At the same time, the direct relationship between the doctor and the patient is the most important mechanism for implementing the patient's rights at the dental appointment and preventing conflicts. Behavior of doctors in such cases should be strictly regulated by normative legal acts. The process of information sharing with patients and transfer of information to the patient's relatives should receive in medical preventive institution specific legal basis under sections 30, 31, 48, 61 “Principles of legislation of the Russian Federation about health protection of citizens”, to be fixed in job descriptions with the designation of responsibility.
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Cohen, Tal, Angela Y. Birkes, Chien H. Hsiung, and Robert E. Fulton. "Modeling Patient Care for Multimedia Database." In ASME 1995 15th International Computers in Engineering Conference and the ASME 1995 9th Annual Engineering Database Symposium collocated with the ASME 1995 Design Engineering Technical Conferences. American Society of Mechanical Engineers, 1995. http://dx.doi.org/10.1115/edm1995-0843.

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Abstract In the medical arena, the number of uses for new technology is increasing rapidly. In the last few decades, physicians have been using more computerized tools and are basing their diagnoses on high-tech lab results. While the tools used for diagnoses — such as catscans, MRI’s and the myriad of other high-tech equipment — have improved greatly over the years, the method of storing these results into a medical record has not changed much. In fact, the medical system is using antiquated methods of paper-based record, and this results in inefficiency. The record-keeping system simply does not allow for the hightech equipment to be used to their greatest potential. Medical professionals are confronted with a basic issue: How should they manage the huge amount of different types of information so that they can improve medical treatment and upgrade patient care? The case study presented in this paper deals with the Emory Clinic, located in Atlanta, Georgia, which treats a very high volume of patients. This paper provides a study of the patient care process, development of an initial product data model, characterizes and identifies multimedia datasets and finally presents a screen mockup that reflect some of the datasets.
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Nejat, Goldie, Brian Allison, Nadia Gomez, and Andrew Rosenfeld. "The Design of an Interactive Socially Assistive Robot for Patient Care." In ASME 2007 International Mechanical Engineering Congress and Exposition. ASMEDC, 2007. http://dx.doi.org/10.1115/imece2007-41811.

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It is anticipated that the use of assistive robots will be one of the most important service applications of robotic systems of the future. In this paper, a unique non-contact socially assistive robot consisting of a human-like demeanor is presented for utilization in hospital wards and veteran homes to study its role and impact on the well-being of patients, addressing patient’s needs and its overall effect on the quality of patient care. The robot will be an embodied entity that will participate in hands-off non-contact social interaction with a patient during the convalescence, rehabilitation or end-of-life care stage. The robot has been designed as a platform to incorporate the three design parameters of embodiment, emotion and non-verbal dialog to encourage natural interactions between the patient and itself. For perception, we describe the first application of utilizing varying intensity depth imaginary, via a 3D camera, for non-contact and non-restricting 3D gesture recognition and characterization.
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Ciliberti, Rosella, Alessandro Bonsignore, Liliana Lorettu, Maurizio Secchi, Michele Minuto, Pierluigi Santi, and Ilaria Baldelli. "Physician/patient relationship following hospital discharge – new methods of therapeutic and care continuity." In the 8th International Workshop on Innovative Simulation for Healthcare. CAL-TEK srl, 2019. http://dx.doi.org/10.46354/i3m.2019.iwish.013.

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"Healthcare organization aims to shorten hospitalization times, both to facilitate patient turnover and to avoid the risks of the nosocomial environment. Between March and September 2018, patients that were discharged after hospitalization for scheduled reconstructive breast surgery were given a portable device with the Dr. Link app installed, created to allow real-time communication with physicians. Patients and physicians completed a satisfaction survey on their experience with the use of the device. Analysis shows overall patient satisfaction in terms of improvement in relationships and quality of life. Physicians reported more responsible patient behaviour, better compliance, and earlier treatment of complications. Continuous interactive assistance can improve the discharged patient’s quality of life and therapeutic path. However, the device risks becoming a negative tool if the health care professional has not made the proper initial emotional investment in the relationship, delegating the totality of the therapeutic relationship to the tablet."
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"MYCOLOGY 2020 Cutting edge research, optimal patient care." In MYCOLOGY 2020 Cutting edge research, optimal patient care. Frontiers Media SA, 2021. http://dx.doi.org/10.3389/978-2-88963-592-4.

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

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V, Ramya. "Embedded Intensive Patient Care Unit." In First International Conference on Artificial Intelligence, Soft Computing and Applications. Academy & Industry Research Collaboration Center (AIRCC), 2011. http://dx.doi.org/10.5121/csit.2011.1315.

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Lee, Soyoung, Charlotte Tang, Sun Young Park, and Yunan Chen. "Loosely formed patient care teams." In the ACM 2012 conference. New York, New York, USA: ACM Press, 2012. http://dx.doi.org/10.1145/2145204.2145334.

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Cakici, Ozden Engin, Rajiv Dewan, and Marshall Freimer. "Patient Choice in Acute Care." In Hawaii International Conference on System Sciences. Hawaii International Conference on System Sciences, 2017. http://dx.doi.org/10.24251/hicss.2017.678.

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McGlothlin, James P., Sriveni Vedire, Evan Crawford, James Pappas, Brenda Bruneau, and Lorenzo Obregon. "Improving patient care through analytics." In 2016 4th International Symposium on Computational and Business Intelligence (ISCBI). IEEE, 2016. http://dx.doi.org/10.1109/iscbi.2016.7743265.

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Reports on the topic "Care of patient"

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Eliason, Paul, Paul L. Grieco, Ryan McDevitt, and James Roberts. Strategic Patient Discharge: The Case of Long-Term Care Hospitals. Cambridge, MA: National Bureau of Economic Research, September 2016. http://dx.doi.org/10.3386/w22598.

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Starkey, Sandra, and Jean L. Parsons. Exploring Patient Centered Care Through the Design of Personal Storage for Patients. Ames: Iowa State University, Digital Repository, 2014. http://dx.doi.org/10.31274/itaa_proceedings-180814-914.

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Dy, Sydney M., Julie M. Waldfogel, Danetta H. Sloan, Valerie Cotter, Susan Hannum, JaAlah-Ai Heughan, Linda Chyr, et al. Integrating Palliative Care in Ambulatory Care of Noncancer Serious Chronic Illness: A Systematic Review. Agency for Healthcare Research and Quality (AHRQ), February 2020. http://dx.doi.org/10.23970/ahrqepccer237.

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Objectives. To evaluate availability, effectiveness, and implementation of interventions for integrating palliative care into ambulatory care for U.S.-based adults with serious life-threatening chronic illness or conditions other than cancer and their caregivers We evaluated interventions addressing identification of patients, patient and caregiver education, shared decision-making tools, clinician education, and models of care. Data sources. We searched key U.S. national websites (March 2020) and PubMed®, CINAHL®, and the Cochrane Central Register of Controlled Trials (through May 2020). We also engaged Key Informants. Review methods. We completed a mixed-methods review; we sought, synthesized, and integrated Web resources; quantitative, qualitative and mixed-methods studies; and input from patient/caregiver and clinician/stakeholder Key Informants. Two reviewers screened websites and search results, abstracted data, assessed risk of bias or study quality, and graded strength of evidence (SOE) for key outcomes: health-related quality of life, patient overall symptom burden, patient depressive symptom scores, patient and caregiver satisfaction, and advance directive documentation. We performed meta-analyses when appropriate. Results. We included 46 Web resources, 20 quantitative effectiveness studies, and 16 qualitative implementation studies across primary care and specialty populations. Various prediction models, tools, and triggers to identify patients are available, but none were evaluated for effectiveness or implementation. Numerous patient and caregiver education tools are available, but none were evaluated for effectiveness or implementation. All of the shared decision-making tools addressed advance care planning; these tools may increase patient satisfaction and advance directive documentation compared with usual care (SOE: low). Patients and caregivers prefer advance care planning discussions grounded in patient and caregiver experiences with individualized timing. Although numerous education and training resources for nonpalliative care clinicians are available, we were unable to draw conclusions about implementation, and none have been evaluated for effectiveness. The models evaluated for integrating palliative care were not more effective than usual care for improving health-related quality of life or patient depressive symptom scores (SOE: moderate) and may have little to no effect on increasing patient satisfaction or decreasing overall symptom burden (SOE: low), but models for integrating palliative care were effective for increasing advance directive documentation (SOE: moderate). Multimodal interventions may have little to no effect on increasing advance directive documentation (SOE: low) and other graded outcomes were not assessed. For utilization, models for integrating palliative care were not found to be more effective than usual care for decreasing hospitalizations; we were unable to draw conclusions about most other aspects of utilization or cost and resource use. We were unable to draw conclusions about caregiver satisfaction or specific characteristics of models for integrating palliative care. Patient preferences for appropriate timing of palliative care varied; costs, additional visits, and travel were seen as barriers to implementation. Conclusions. For integrating palliative care into ambulatory care for serious illness and conditions other than cancer, advance care planning shared decision-making tools and palliative care models were the most widely evaluated interventions and may be effective for improving only a few outcomes. More research is needed, particularly on identification of patients for these interventions; education for patients, caregivers, and clinicians; shared decision-making tools beyond advance care planning and advance directive completion; and specific components, characteristics, and implementation factors in models for integrating palliative care into ambulatory care.
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David, Guy, Evan Rawley, and Daniel Polsky. Integration and Task Allocation: Evidence from Patient Care. Cambridge, MA: National Bureau of Economic Research, September 2011. http://dx.doi.org/10.3386/w17419.

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Hackmann, Martin, and R. Vincent Pohl. Patient vs. Provider Incentives in Long Term Care. Cambridge, MA: National Bureau of Economic Research, October 2018. http://dx.doi.org/10.3386/w25178.

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Glasz, Kevin W. Leadership Implications of the Annual Patient Care Survey. Fort Belvoir, VA: Defense Technical Information Center, April 1999. http://dx.doi.org/10.21236/ada389167.

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Foeller, Marguerite. Satisfaction and quality : patient perspectives in medical care. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.3286.

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Labib, Merna. Compassion Fatigue, the Wellness of Care Providers, and the Quality of Patient Care. Portland State University Library, January 2015. http://dx.doi.org/10.15760/honors.206.

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Haut, Elliott, Brandyn Lau, Deborah Hobson, Dauryne Shaffer, Peggy Kraus, Jonathan Aboagye, Norma Farrow, et al. Preventing Venous Thromboembolism: Empowering Patients and Enabling Patient-Centered Care via Health Information Technology. Patient-Centered Outcomes Research Institute (PCORI), November 2018. http://dx.doi.org/10.25302/11.2018.ce.12114489.

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Scholle, Sarah, Suzanne Morton, Daren Anderson, David Kendrick, Juell Homco, Kristin Rodriguez, Rachelle Jean-Paul, et al. Using Patient-Reported Outcome Measures during Routine Care of Patients with Type 2 Diabetes. Patient-Centered Outcomes Research Institute® (PCORI), January 2020. http://dx.doi.org/10.25302/12.2019.me.140210788.

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