Auswahl der wissenschaftlichen Literatur zum Thema „Chronically ill“

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Zeitschriftenartikel zum Thema "Chronically ill"

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Nisevic, Sanja. "The importance of social support to chronically ill adolescents." Medical review 59, no. 7-8 (2006): 331–34. http://dx.doi.org/10.2298/mpns0608331n.

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Introduction. Improvements in medicine have significantly prolonged life of chronically ill children and adolescents in the past several decades. There is a great variability in adaptation to illness among chronically ill persons - some of them seem to be very well adapted, with almost no problems. However, research results suggest that chronically ill children are more likely to have psychological problems than their healthy peers. Material and methods. Eighty-four subjects, all elementary school pupils, participated in the study. The first group included adolescents with chronical illness (m
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Maas, Vera K., Frederik H. Dibbets, Vincent J. T. Peters, Bert R. Meijboom, and Daniëlle van Bijnen. "The never-ending patient journey of chronically ill patients: A qualitative case study on touchpoints in relation to patient-centered care." PLOS ONE 18, no. 5 (2023): e0285872. http://dx.doi.org/10.1371/journal.pone.0285872.

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Background Healthcare professionals caring for chronically ill patients increasingly want to provide patient-centered care (PCC). By understanding each individual patient journey, they can significantly improve the quality of PCC. A patient journey consists of patient interactions, so-called touchpoints, with healthcare professionals distributed over three periods: pre-service, service, and post-service period. The aim of this study was to ascertain chronically ill patients’ needs for digital alternatives for touchpoints. Specifically, we aimed to explore which digital alternatives patients wo
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Rego, Mark D. "On Being Chronically Ill." American Journal of Psychiatry 172, no. 6 (2015): 510–11. http://dx.doi.org/10.1176/appi.ajp.2015.15020165.

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Wilson, M., CJ Scott, and A. McKinlay. "FEEDING THE CHRONICALLY ILL*." Journal of the Royal College of Physicians of Edinburgh 33, no. 2 (2003): 114–18. https://doi.org/10.1177/1478271520033302015.

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JELLINEK, MICHAEL S. "The Chronically Ill Child." Pediatric News 39, no. 3 (2005): 23. http://dx.doi.org/10.1016/s0031-398x(05)70035-7.

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&NA;. "The Chronically Critically Ill." Journal of Hospice & Palliative Nursing 10, no. 2 (2008): 89–90. http://dx.doi.org/10.1097/01.njh.0000306733.24097.22.

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Koesel, Niki. "The Chronically Critically Ill." Journal of Hospice & Palliative Nursing 10, no. 2 (2008): 83–88. http://dx.doi.org/10.1097/01.njh.0000306735.31721.6e.

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Cutler, David L. "The chronically mentally ill." Community Mental Health Journal 21, no. 1 (1985): 3–13. http://dx.doi.org/10.1007/bf00754702.

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Mason, Marlys J., Debra L. Scammon, and Robert P. Huefner. "Does Health Status Matter? Examining the Experiences of the Chronically Ill in Medicaid Managed Care." Journal of Public Policy & Marketing 21, no. 1 (2002): 53–65. http://dx.doi.org/10.1509/jppm.21.1.53.17610.

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Managed care's promises of improved cost efficiency and continuity of care to the general population are being tested by the higher demands of Medicare and Medicaid populations, including many chronically ill individuals. By examining and comparing satisfaction among chronically ill and healthier enrollees and between Medicaid and non-Medicaid enrollees, the authors develop an understanding of how satisfaction among the chronically ill provides assessments that are important to all enrollees. The authors examine public policy initiatives in the context of the special needs of the chronically i
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Abraham, Jean M., Anne Beeson Royalty, and Thomas DeLeire. "Measuring the Financial Exposure from Medical Care Spending Among Families with Employer Sponsored Insurance." Forum for Health Economics and Policy 16, no. 1 (2013): 193–217. http://dx.doi.org/10.1515/fhep-2012-0012.

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Abstract We develop an empirical method to assess the degree of financial exposure associated with medical care spending among non-elderly US families with employer-sponsored insurance. A key feature of this method is its simplicity – it only requires data on out-of-pocket (OOP) health care spending and total health care spending and does not require detailed knowledge of health insurance benefit design. We apply our method to assess whether families with a chronically ill member face more financial exposure given their level of total spending relative to families with no chronically ill membe
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Dissertationen zum Thema "Chronically ill"

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Coppa, Kay. "Self-help groups in the Hunter region : a qualitative study of their role in chronic illness management /." [St. Lucia, Qld. : s.n.], 2002. http://www.library.uq.edu.au/pdfserve.php?image=thesisabs/absthe16644.pdf.

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Stanberry-Beall, Jenny Kay. "Building a case for lifespan respite the effects of formal respite care on caregivers of family members with chronic dependencies /." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 242 p, 2007. http://proquest.umi.com/pqdweb?did=1251902551&sid=1&Fmt=2&clientId=8331&RQT=309&VName=PQD.

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Fiala, Samuel E. "Camp counselors working with chronically ill children." Texas A&M University, 2005. http://hdl.handle.net/1969.1/3210.

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A growing body of empirical evidence suggests that attending specialized summer camps is beneficial for chronically ill youth (Briery & Rabian, 1999). However, there is some inconsistency across studies regarding these benefits (Hazzard & Angert, 1986). One potential explanation for these differences across camps is that they may differ in how well they recruit and train effective volunteer camp counselors. This possibility cannot be explored until more research is conducted identifying what type of person volunteers to work with chronically ill children and how they differ from others. In res
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Lindström, Caisa. "Burnout in parents of chronically ill children." Doctoral thesis, Örebro universitet, Institutionen för hälsovetenskaper, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-47391.

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Parents of children with a chronic disease are usually highly involved in their child’s treatment and may be affected by the heavy demands and constant stress. This can increase the risk of developing burnout, which is an individual reaction to long-term stress consisting of symptoms associated with emotional exhaustion, as well as physical and cognitive fatigue. The overall aim was to estimate the prevalence of burnout in parents of children with Type 1 Diabetes Mellitus (T1DM) and inflammatory bowel disease (IBD) (paper I), identify the risk factors associated with parenting a child with T1D
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Elzen, Henrike Anje. "Self-management for chronically ill older people." [S.l. : [Groningen : s.n.] ; University Library Groningen] [Host], 2006. http://irs.ub.rug.nl/ppn/297661620.

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Lees, Nancy Berman. "The self-esteem of chronically ill adolescents." CSUSB ScholarWorks, 1991. https://scholarworks.lib.csusb.edu/etd-project/852.

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Fung, Shuk-man Amy. "Psychosocial risk and protective factors in chronic childhood illnesses : the case of thalassaemia major /." Hong Kong : University of Hong Kong, 1996. http://sunzi.lib.hku.hk/hkuto/record.jsp?B17390084.

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Steuten, Lotte Maria Gertruda. "Evaluation of disease management programmes for chronically ill." Maastricht : Maastricht : UPM, Universitaire Pers Maastricht ; University Library, Maastricht University [Host], 2006. http://arno.unimaas.nl/show.cgi?fid=7668.

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Turner, Roxanne. "Depression in older persons who are chronically ill." DigitalCommons@Robert W. Woodruff Library, Atlanta University Center, 1990. http://digitalcommons.auctr.edu/dissertations/1471.

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This study explores the severity of depression in older persons who are chronically ill. The study was an attempt to determine if there is a significant relationship between four independent variables—family support, social support, marital status, and gender. The study was conducted while respondents were hospitalized at Clayton General Hospital. The research concluded that most older chronically ill persons were not depressed or were only mildly depressed. Significant factors were gender. Females reported more incidence of depression than males and single respondents reported higher incidenc
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Driskill, Gail. "Chronically Ill Children: Maternal Stress and Psychological Symptomatology." Thesis, University of North Texas, 1995. https://digital.library.unt.edu/ark:/67531/metadc279114/.

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This study used a parenting stress and coping model to identify predictors of symptomatology for 13 8 mothers of medically compromised children. This model proposed that: child characteristics (severity of the chronic illness and child related parenting stressors); parent characteristics (self-esteem, sense of competence, and parents' perceived stress/distress); and environmental characteristics (social support, general life stressor events, and demographic variables) contribute to psychological symptomatology for these mothers. Multiple regression analysis found a relationship between general
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Bücher zum Thema "Chronically ill"

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Gray, Garwood S., ed. Chronically ill children. Pro-Ed, 1986.

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McClelland, Nelson. Aged, disabled & chronically ill: Report. Dept. of Health, 1987.

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L, Bachrach Leona, and Nadelson Carol C, eds. Treating chronically mentally ill women. American Psychiatric Press, 1988.

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Maryland Health Resources Planning Commission., ed. The Chronically mentally ill in Maryland. MHRPC, Division of Health Systems Planning, 1987.

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Gagne, Tammy. Ways to help chronically ill children. Mitchell Lane Publishers, 2011.

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M, Perrin James, and Ireys Henry T, eds. Chronically ill children and their families. Jossey-Bass, 1985.

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Dempsey, Sharon. Extreme parenting: Parenting your chronically ill child. Jessica Kingsley Publishers, 2008.

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E, Gerber Kenneth, and Nehemkis Alexis M, eds. Compliance: The dilemma of the chronically ill. Springer Pub. Co., 1986.

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Dempsey, Sharon. Extreme parenting: Parenting your chronically ill child. Jessica Kingsley Publishers, 2008.

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W, Shayne May, and Bloom Sheila R, eds. Home and community care for chronically ill children. Oxford University Press, 1993.

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Buchteile zum Thema "Chronically ill"

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Glynn, Shirley M. "The Chronically Mentally Ill." In Research in Psychiatry. Springer US, 1992. http://dx.doi.org/10.1007/978-1-4899-0688-5_18.

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Carson, Shannon S., and Kathleen Dalton. "The Chronically Critically Ill." In The Organization of Critical Care. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-0811-0_13.

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Melamed, Barbara G. "Parenting the Chronically Ill Infant." In Parenthood and Mental Health. John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470660683.ch25.

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Flemming, Carol. "Hope for the Chronically Ill." In The Other Side of Medical Care. Macmillan Education UK, 1986. http://dx.doi.org/10.1007/978-1-349-18179-7_9.

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Mitler, Merrill M., Steven Poceta, Stuart J. Menn, and Milton K. Erman. "Insomnia in the Chronically Ill." In Case Studies in Insomnia. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4757-9586-8_14.

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Paul, Thomas, and Andreas Thiel. "Treatment of Chronically Ill Patients." In Handbook of Eating Disorders and Obesity. Springer Berlin Heidelberg, 2024. http://dx.doi.org/10.1007/978-3-662-67662-2_52.

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Shore, Miles F., and Martin D. Cohen. "Homelessness and the Chronically Mentally Ill." In Homelessness. Springer US, 1992. http://dx.doi.org/10.1007/978-1-4899-0679-3_6.

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Rinnenburger, Dagmar. "The Strain of Being Chronically Ill." In Chronicity. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-66873-0_4.

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Miller-Smith, Laura, Ásdís Finnsdóttir Wagner, and John D. Lantos. "Chronically Critically Ill with Technological Dependence." In Bioethics in the Pediatric ICU: Ethical Dilemmas Encountered in the Care of Critically Ill Children. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-00943-4_7.

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Colaluca, Beth, and Jonelle Ensign. "Assessing and Intervening with Chronically Ill Children." In Best Practices in School Neuropsychology. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118269855.ch27.

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Konferenzberichte zum Thema "Chronically ill"

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Mack, Kelly, Emma J. McDonnell, Leah Findlater, and Heather D. Evans. "Chronically Under-Addressed: Considerations for HCI Accessibility Practice with Chronically Ill People." In ASSETS '22: The 24th International ACM SIGACCESS Conference on Computers and Accessibility. ACM, 2022. http://dx.doi.org/10.1145/3517428.3544803.

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Batista, Susana, and Rosa Martins. "Personality and Suffering in the Hospitalized Chronically Ill." In 2nd icH&Hpsy International Conference on Health and Health Psychology. Cognitive-crcs, 2016. http://dx.doi.org/10.15405/epsbs.2016.07.02.41.

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Jurenikova, Petra. "COMPLIANCE OF CHRONICALLY ILL PATIENTS BEFORE STARTING AN EDUCATIONAL PROCESS." In 6th SWS International Scientific Conference on Social Sciences ISCSS 2019. STEF92 Technology, 2019. http://dx.doi.org/10.5593/sws.iscss.2019.3/s12.056.

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Desai, A., L. Rho, and J. Nelson. "Helping the Chronically Critically Ill To Communicate: Speaking Valve Pilot Trial." In American Thoracic Society 2009 International Conference, May 15-20, 2009 • San Diego, California. American Thoracic Society, 2009. http://dx.doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a3083.

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Maier, Edith, Pascale Baer-Baldauf, Peter Jaeschke, Ulrich Reimer, and Tom Ulmer. "Continuous real-time remote monitoring of severely or chronically ill children." In The 18th international symposium on health information management research. Linnaeus University Press, 2022. http://dx.doi.org/10.15626/ishimr.2020.12.

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Compared to parents of healthy children, parents of severely or chronically ill children have significantly worse physical and mental health and a lower quality of life, e.g. because of lack of sleep. The proposed solution aims at assisting caregivers by means of a remote monitoring service run by professional nursing staff which should allow parents to get a good night’s sleep. A smart algorithm has been developed to detect if a particular parameter (heart rate, respiration rate or oxygen saturation) has exceeded a pre-defined threshold and thus may imply an emergency. Parents are only alerte
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Ciudad Gutierrez, P., A. Rodríguez Pérez, L. Rodríguez De Francisco, et al. "4CPS-032 Pharmaceutical interventions for medication reconciliation in complex chronically ill patients." In 28th EAHP Congress, Bordeaux, France, 20-21-22 March 2024. British Medical Journal Publishing Group, 2024. http://dx.doi.org/10.1136/ejhpharm-2024-eahp.136.

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Laverman, M., J. H. M. Schonk, P. J. M. van der Boog, and M. A. Neerincx. "Personalized and contextualized information in self-management systems for chronically ill patients (PERISCOPE)." In the 28th Annual European Conference. ACM Press, 2010. http://dx.doi.org/10.1145/1962300.1962370.

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Mihovska, Albena, Sofoklis A. Kyriazakos, and Ramjee Prasad. "eWall for active long living: Assistive ICT services for chronically ill and elderly citizens." In 2014 IEEE International Conference on Systems, Man and Cybernetics - SMC. IEEE, 2014. http://dx.doi.org/10.1109/smc.2014.6974251.

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Jian, Yuan, Tan Kok Kiong, and Lee Tong Heng. "Development of an e-Guardian for the Single Elderly or the Chronically-Ill Patients." In 2010 International Conference on Communications and Mobile Computing (CMC). IEEE, 2010. http://dx.doi.org/10.1109/cmc.2010.167.

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Wijngaarde, Ricardo O., Faisal Ahmed, Reema Mujey, Shelna Aisath, and Dirk T. Ubbink. "296 Baseline measurement of shared decision-making with chronically ill children in the Maldives." In 12th International Shared Decision Making Conference. BMJ Publishing Group Ltd, 2024. http://dx.doi.org/10.1136/bmjebm-2024-sdc.295.

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Berichte der Organisationen zum Thema "Chronically ill"

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Albers, Karen. A Study of Multnomah County community support services for the chronically mentally ill. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.5294.

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Stanek, Richard. Residential Options for the Institutionalized Chronically Mentally Ill: The Impact of Psychosis on Choice. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.6515.

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Brubaker, Tom. A descriptive study of demography & transportation issues of chronically mentally ill in the eastern Oregon comprehensive community mental health catchment area. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.2812.

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Homan, Rick, and Catherine Searle. Programmatic implications of a cost study of home-based care programs in South Africa. Population Council, 2005. http://dx.doi.org/10.31899/hiv14.1001.

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The HIV/AIDS epidemic has meant that an increasing number of chronically ill people need ongoing assistance with care and support. Programs providing home-based care (HBC) services are a key component of the response to HIV/AIDS. However, few programs are using operations research, including cost studies, to decide what services to provide and how to structure their services. In 2004, the Horizons Program undertook a study of six HBC programs from different South African provinces to provide key information to NGOs, government ministries, donors, and the programs themselves to inform decisions
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