Relevant bibliographies by topics / Caregivers Care of the sick

Contents

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

Academic literature on the topic 'Caregivers Care of the sick'

Author: Grafiati
Published: 4 June 2021
Last updated: 11 February 2022

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Journal articles on the topic "Caregivers Care of the sick"

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Delalibera, Mayra, Alexandra Coelho, Pedro Frade, António Barbosa, and Isabel Leal. "Caregiving and bereavement in palliative care: A cross-cultural study between Brazil and Portugal." Transcultural Psychiatry 57, no. 3 (2020): 445–54. http://dx.doi.org/10.1177/1363461520909596.

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Caregiving and bereavement outcomes are strongly influenced by socio-cultural context. Past research has found higher levels of caregiver burden and psychological morbidity in Portuguese compared to Brazilian caregivers. This study compared Brazilian and Portuguese family caregivers in palliative care to identify differences in psychological morbidity and caregiver burden and their relationship with psychosocial factors such as sociodemographic variables, circumstances of end-of-life care and dying, social support, family functioning, and perception of quality of care. Prospective data were co
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Wambui, Winfred Muringi, Samuel Kimani, and Eunice Odhiambo. "Determinants of Health Seeking Behavior among Caregivers of Infants Admitted with Acute Childhood Illnesses at Kenyatta National Hospital, Nairobi, Kenya." International Journal of Pediatrics 2018 (December 16, 2018): 1–11. http://dx.doi.org/10.1155/2018/5190287.

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Background. Poor, delayed, or inappropriate health seeking for a sick infant with acute childhood illness is associated with high morbidity/mortality. Delay in health seeking is implicated with fatal complications and prolonged hospital stay. Thus, caregivers ought to identify danger signs and promptly seek professional help for a sick infant. Objective. Establish determinants of health seeking behavior among caregivers of infants admitted with acute childhood illnesses in Kenyatta National Hospital. Methods. A mixed method cross-sectional study involving caregivers (n=130) of sick infants. Se
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Medrano, Martin, Rebeca López Rosario, Anyolina Núñez Payano, and Natacha Reynoso Capellán. "Burden, anxiety and depression in caregivers of Alzheimer patients in the Dominican Republic." Dementia & Neuropsychologia 8, no. 4 (2014): 384–88. http://dx.doi.org/10.1590/s1980-57642014dn84000013.

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Alzheimer's disease (AD) has a major impact by limiting the ability to live independently. This condition of dependency involves all members of the family, particularly those who take direct care of patients. The changes that take place in caregivers' lives may alter their health and have an effect on the care of the sick. OBJECTIVE: To determine the presence of burden, anxiety and depression in caregivers of Alzheimer's patients. METHOD: A descriptive cross-sectional study was performed in 67 family caregivers from the Alzheimer's Clinic Research Unit, Memory and Alzheimer, in the city of San
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Wang, Fei, and Yangdi Han. "FUTURE PLANNING AMONG OLDER CAREGIVERS OF FAMILY MEMBERS WITH INTELLECTUAL DISABILITY OR MENTAL ILLNESS." Innovation in Aging 3, Supplement_1 (2019): S287. http://dx.doi.org/10.1093/geroni/igz038.1060.

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Abstract Objectives: This study aims to examine future planning among older caregivers for family members with intellectual disability or mental illness, focusing on preferences, predictors and barriers. Method: Data were drawn from 260 caregivers (aged 50 or older) to a family member with intellectual disability or mental illness in Shanghai, China. Caregivers rated six types of future care arrangement under three circumstances: (1) the ideal situation, (2) unable to provide care due to age-related illnesses, and (3) caregivers are deceased. Socio-demographic factors associated with future pl
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Eseigbe, Edwin E., Jane O. Anyiam, Gboye O. Ogunrinde, Robinson D. Wammanda, and Hassan A. Zoaka. "Health Care Seeking Behavior among Caregivers of Sick Children Who Had Cerebral Malaria in Northwestern Nigeria." Malaria Research and Treatment 2012 (January 26, 2012): 1–4. http://dx.doi.org/10.1155/2012/954975.

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Cerebral malaria is a significant cause of childhood morbidity in our region. The challenges of effective management include time and quality of treatment. The study appraised the health care seeking behavior of caregivers of sick children who developed cerebral malaria, in Zaria, northwestern Nigeria. Caregivers indentified were parents 29 (87.9%) and grandparents 4 (12.1%). Most of them were in the upper social classes. Health care options utilized before presentation at our facility were formal health facility 24 (72.7%), patent medicine seller 12 (36.4%), home treatment 10 (30.3%), and her
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Cruz-Oliver, Dulce M., Manas Parikh, Cara L. Wallace, Theodore K. Malmstrom, and Sandra Sanchez-Reilly. "What Did Latino Family Caregivers Expect and Learn From Education Intervention “Caregivers Like Me”?" American Journal of Hospice and Palliative Medicine® 35, no. 3 (2017): 404–10. http://dx.doi.org/10.1177/1049909117709550.

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Objective: US Latinos historically have underutilized end-of-life (EOL) resources. This study reports the views of family caregivers before and after education intervention Caregivers Like Me geared to improve knowledge and attitudes regarding EOL resources among Latino caregivers. Methods: This is a qualitative substudy within a multicentered cross-sectional study design. Educational intervention was offered to family caregivers of Latino elders from 3 different communities, using an audiovisual presentation, including a case-based video telenovela and pre–posttest questionnaires with open-en
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Hansen, Lissi, Shirin Hiatt, and Karen Lyons. "Palliative Care Research: Successful Recruitment and Retention Strategies of Patient-Caregiver Dyads." Innovation in Aging 4, Supplement_1 (2020): 245. http://dx.doi.org/10.1093/geroni/igaa057.791.

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Abstract Research shows that the well-being of patients with serious illness and their family caregivers is significantly associated. Thus, to build the scientific knowledge upon which to establish high quality palliative and end-of-life care practices for these patients and their caregivers, research studies should include successful recruitment and retention strategies that focus on the patient-caregiver dyad. Aims: To review the literature focusing on successful dyadic recruitment and retention strategies and to describe successful recruitment and retention strategies, and attrition in a lo
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Verma, Rahul, Yasna Mehdian, Neel Sheth, et al. "101 Screening for Psychosocial Risk in Families of Children with Medical Complexity (CMC)." Paediatrics & Child Health 25, Supplement_2 (2020): e42-e42. http://dx.doi.org/10.1093/pch/pxaa068.100.

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Abstract Background Children with medical complexity (CMC) are defined by their medical fragility, dependence on assistive technology and substantial care needs. Family caregivers of CMC have unique challenges, such as prolonged hospitalizations and poor care coordination, which result in extensive caregiver stress. There is a great need to quantify the level of psychosocial stress and resilience in these caregivers to allow for appropriate allocation of health care resources. The Psychosocial Assessment Tool (PAT) is a brief parent-reported screening tool for measuring psychosocial risk in ca
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Tilinger, Ana, and Ana Štambuk. "Problemi neformalnih (obiteljskih) njegovatelja u skrbi za osobe s demencijom – kvalitativni pristup." Hrvatska revija za rehabilitacijska istraživanja 54, no. 2 (2019): 59–70. http://dx.doi.org/10.31299/hrri.54.2.6.

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Alzheimer’s disease, as the most common form of dementia, is a progressive, incurable condition that can lead to total dependence on others. The whole family, especially the family member who serves as caregiver of a patient, faces many problems and is in a very difficult situation. By taking over the demanding role of care for the family member, the carer often becomes a “victim of the disease” who needs to find ways to shoulder everything that the disease brings. Studies outside Croatia show that some interventions assist caregivers in their role, such as knowledge of the disease process, kn
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Raymond, Martha. "Cancer burden: Exploring the parallels between cancer hardship and the well-being of cancer caregivers." Journal of Clinical Oncology 36, no. 30_suppl (2018): 162. http://dx.doi.org/10.1200/jco.2018.36.30_suppl.162.

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162 Background: The latest 2016 data from the National Cancer Institute’s Surveillance, Epidemiology & End Results (SEER) Program estimates there are 15.5 million cancer survivors in the U.S. Millions of cancer survivors rely on cancer caregivers every day. Cancer caregivers play a vital role throughout the care continuum, and greatly impact a patient’s quality of life. Caring for a cancer patient affects all aspects of a caregiver’s life, including: changes to daily routine, work and family life; financial hardship; and emotional and psychological distress. Our study explores the cancer b
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Dissertations / Theses on the topic "Caregivers Care of the sick"

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Graf, Theresa M. "Sense of coherence, relational functioning and concepts of health in adult daughter caregivers as compared with an age cohort of women /." Access Digital Full Text version, 1994. http://pocketknowledge.tc.columbia.edu/home.php/bybib/11625235.

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Thesis (Ed.D.)--Teachers College, Columbia University, 1994.<br>Includes tables and appendices. Typescript; issued also on microfilm. Sponsor: Marilyn Rawnsley. Dissertation Committee: Jane A. Monroe. Includes bibliographical references (leaves 117-131).
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Babbage, Roberta Louise. "Relieving strain in informal caregivers of the elderly." CSUSB ScholarWorks, 1989. https://scholarworks.lib.csusb.edu/etd-project/459.

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De, Boever Dave. "Being a caregiver to people living with AIDS stages on the journey /." Theological Research Exchange Network (TREN), 1991. http://www.tren.com.

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Downes, Edith A. "Spiritual companions for Alzheimers patients and those persons with other forms of dementia." Online full text .pdf document, available to Fuller patrons only, 2002. http://www.tren.com.

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Burt, John. "How to minister to individuals with family members in personal care homes." Online full text .pdf document, available to Fuller patrons only, 2002. http://www.tren.com.

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Mentzakis, Emmanouil. "Economic issues of informal care values and determinants /." Thesis, Available from the University of Aberdeen Library and Historic Collections Digital Resources, 2008. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=25213.

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Amonette, J. Fulton. "The establishment of a care team of trained volunteers from Northwest Baptist Church of Miami, Oklahoma, to serve homebound senior adults and their caregivers." Online full text .pdf document, available to Fuller patrons only, 2004. http://www.tren.com.

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Ministry research project (D. Min.)--Midwestern Baptist Theological Seminary, 2004.<br>Submitted in partial fulfillment of the requirements for the Doctor of Ministry Degree. Includes bibliographical references (leaves 220-225).
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Scannell, Alice Updike. "The Longterm Psychosocial Impacts of Caregiving on the Caregivers of Persons with Stroke." PDXScholar, 1989. https://pdxscholar.library.pdx.edu/open_access_etds/1312.

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This study is a Time 4 (T4) follow-up interview of ninety-three caregivers of persons who experienced a first stroke between 2 to 4 years (mean = 36 months) prior to the T4 interview. The first wave of data collection occurred within two months after the stroke. The second and third waves occurred six and twelve months, respectively, after the first interview. The caregivers were identified by the person with stroke as being the person closest to him/her who would be responsible for care after the stroke. Data were gathered at all four interviews using reliable and valid measures for depressiv
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Munro, Ian. "The lived experience of gay men caring for others with HIV/AIDS living, loving, and dying in the era of HIV/AIDS /." Connect to this title online, 2002. http://tux.lib.deakin.edu.au/adt-VDU/public/adt-VDU20020913.150027/.

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Risco, Vilarasau Ester. "La transició de l’atenció sociosanitària de les persones amb demència i dels seus cuidadors." Doctoral thesis, Universitat de Barcelona, 2015. http://hdl.handle.net/10803/399679.

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INTRODUCCIÓ: Per tal de dissenyar noves estratègies per estabilitzar la situació de les persones que tenen un diagnòstic de demència i que viuen en el domicili, s'ha desenvolupat un estudi que descriu l’entorn de la transició des del domicili fins a una institució de llarga en persones grans amb demència i dels seus cuidadors. METODOLOGIA: Aquesta investigació s'ha realitzat en dues etapes. En la primera etapa es compara, a nivell europeu, la reacció dels cuidadors informals en la demència, els nivells d’associació de la dependència i els símptomes neuropsiquiàtrics amb la institucion
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Books on the topic "Caregivers Care of the sick"

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Schonhoff, Shelly. Family caregivers guide. Simon & Kolz Pub., 1998.

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1949-, Elizabeth Patricia, ed. Caregiver revolution: 5 steps to enlightened caregiving. Gateways Books and Tapes, 2011.

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Eliason, Marguerite M. Caregiving: An errand of the heart. Covenant Communications, 1995.

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Drattell, Alan. The other victim: How caregivers survive a loved one's chronic illness. Seven Locks Press, 1996.

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Harvey, Verna Foster. Partnering with caregivers: Learn how to help those who help others. WinePress Publishing, 2010.

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Shimo, Masamune. Ōru karā irasuto de yoku wakaru hajimete no kaigo. Seibidō Shuppan, 2006.

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1952-, Weisman Roanne, ed. In sickness as in health: Helping couples cope with the complexities of illness. Roundtree Press, 2013.

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Elizabeth, Putman, ed. Ways you can help: Creative, practical suggestions for family and friends of patients and caregivers. Warner Books, 1996.

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Revenson, Tracey A. Caregiving in the illness context. Palgrave Macmillan, 2015.

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Foyder, Joan Ellen. Family caregiver's guide. Futuro Co., 1986.

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Book chapters on the topic "Caregivers Care of the sick"

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Grande, Gunn, and Gail Ewing. "Informal/Family Caregivers." In Textbook of Palliative Care. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-77740-5_52.

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Grande, Gunn, and Gail Ewing. "Informal/Family Caregivers." In Textbook of Palliative Care. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-31738-0_52-1.

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Gately, Megan, and Keren Ladin. "Family and Other Caregivers." In Chronic Illness Care. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-71812-5_9.

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Perkins, Henry S. "Care for Family Caregivers." In A Guide to Psychosocial and Spiritual Care at the End of Life. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-6804-6_9.

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Beck, Richard. "Care for the Caregivers." In The Wiley-Blackwell Handbook of Group Psychotherapy. John Wiley & Sons, Ltd, 2011. http://dx.doi.org/10.1002/9781119950882.ch28.

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Wallsten, Sharon M. "Elderly Caregivers and Care Receivers." In Handbook of Neuropsychology and Aging. Springer US, 1997. http://dx.doi.org/10.1007/978-1-4899-1857-4_31.

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Basu, Ipsita, and Susmita Mukhopadhyay. "Psychological Health of Dementia Caregivers: An Overview." In Dementia Care. Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-3864-0_12.

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Trounce, J. Q., T. J. Stephenson, and A. D. Milner. "Monitoring the Sick Infant." In Care of the Critically Ill Patient. Springer London, 1992. http://dx.doi.org/10.1007/978-1-4471-3400-8_77.

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Milićević-Kalašić, Aleksandra. "Caregivers Care with Alzheimer’s Disease, Prevention of Caregivers Burn-Out." In Self Management of Chronic Disease. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-00326-4_5.

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O'Dwyer, Louise M., and Christopher L. Norkus. "Caring for the Caregivers." In Veterinary Technician's Manual for Small Animal Emergency and Critical Care. John Wiley & Sons, Inc., 2018. http://dx.doi.org/10.1002/9781119536598.ch27.

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Conference papers on the topic "Caregivers Care of the sick"

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Lim, Ee Jane, Seng Beng Tan, Andrew Yeoh, et al. "4 Wellbeing of informal caregivers." In The APM’s Annual Supportive and Palliative Care Conference, In association with the Palliative Care Congress, “Towards evidence based compassionate care”, Bournemouth International Centre, 15–16 March 2018. British Medical Journal Publishing Group, 2018. http://dx.doi.org/10.1136/bmjspcare-2018-aspabstracts.31.

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Kim, Gyungha, Hwawoo Jeon, Sungkee Park, Yong Suk Choi, and Yoonseob Lim. "Care Guide System for Caregivers of People with Dementia*." In 2020 42nd Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) in conjunction with the 43rd Annual Conference of the Canadian Medical and Biological Engineering Society. IEEE, 2020. http://dx.doi.org/10.1109/embc44109.2020.9176513.

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Terskikh, Marina. "Communication Policy Of Charity Foundations Supporting Sick Children: Persuasion Tools." In ECCE 2018 VII International Conference Early Childhood Care and Education. Cognitive-Crcs, 2018. http://dx.doi.org/10.15405/epsbs.2018.07.76.

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Mikatavage, M., H. Dillon, K. Oestenstad, and V. Rose. "87. Assessing the Prevalence of Sick Building Syndrome in Offices with Different Ventilation Systems." In AIHce 1996 - Health Care Industries Papers. AIHA, 1999. http://dx.doi.org/10.3320/1.2765200.

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MIZUNO, FUMIO, TOMOAKI HAYASAKA, TOSHIHIKO YOSHIDA, KEN-ICHI TSUBOTA, SHIGEO WADA, and TAKAMI YAMAGUCHI. "HOME-HEALTH CARE SUPPORT SYSTEM FOR CAREGIVERS USING WEARABLE SYSTEM." In Proceedings of the Final Symposium of the Tohoku University 21st Century Center of Excellence Program. IMPERIAL COLLEGE PRESS, 2006. http://dx.doi.org/10.1142/9781860948800_0106.

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Redjem, R., S. Kharraja, X. Xie, and E. Marcon. "Coordinated multi-criteria scheduling of caregivers in home health Care Services." In 2011 IEEE International Conference on Automation Science and Engineering (CASE 2011). IEEE, 2011. http://dx.doi.org/10.1109/case.2011.6042527.

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Wongpun, Sukontip, and Sumanta Guha. "Elderly care recommendation system for informal caregivers using case-based reasoning." In 2017 IEEE 2nd Advanced Information Technology, Electronic and Automation Control Conference (IAEAC). IEEE, 2017. http://dx.doi.org/10.1109/iaeac.2017.8054075.

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van Heek, Julia, Martina Ziefle, and Simon Himmel. "Caregivers’ Perspectives on Ambient Assisted Living Technologies in Professional Care Contexts." In 4th International Conference on Information and Communication Technologies for Ageing Well and e-Health. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0006691400370048.

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Argyriou, K., A. Kapsoritakis, E. Tsakiridou, and S. Potamianos. "PWE-063 Caregivers’ need for self care in inflammatory bowel disease." In British Society of Gastroenterology, Annual General Meeting, 19–22 June 2017, Abstracts. BMJ Publishing Group Ltd and British Society of Gastroenterology, 2017. http://dx.doi.org/10.1136/gutjnl-2017-314472.309.

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Parks, Michellai K., and Lisa W. Zetley. "Housing Instability Among Families and Caregivers of Children in Foster Care." In AAP National Conference & Exhibition Meeting Abstracts. American Academy of Pediatrics, 2021. http://dx.doi.org/10.1542/peds.147.3_meetingabstract.90.

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Reports on the topic "Caregivers Care of the sick"

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Skufca, Laura. Primary Care Providers' Experiences with Family Caregivers. AARP Research, 2019. http://dx.doi.org/10.26419/res.00273.001.

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Smith, Kristin, and Andrew Schaefer. Who cares for the sick kids? parents’ access to paid time to care for a sick child. University of New Hampshire Libraries, 2012. http://dx.doi.org/10.34051/p/2020.171.

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Duncan, Marie. Alzheimer's Disease Caregivers: The Transition from Home Care to Formal Care. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.3220.

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Skufca, Laura. Primary Care Providers' Experiences with Family Caregivers: Infographic. AARP Research, 2019. http://dx.doi.org/10.26419/res.00273.002.

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Butler, Mary, Joseph E. Gaugler, Kristine M. C. Talley, et al. Care Interventions for People Living With Dementia and Their Caregivers. Agency for Healthcare Research and Quality (AHRQ), 2020. http://dx.doi.org/10.23970/ahrqepccer231.

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Guengerich, Terri. 2018 AARP Utah Caregiving Survey: Overwhelming Support for Respite Care for Family Caregivers. AARP Research, 2018. http://dx.doi.org/10.26419/res.00259.004.

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Reynolds, Margaret. Adult daughters as caregivers to elderly parents : an exploration of the care relationship. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.5676.

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Murray, Kate, Merle Edwards-Orr, Highsmith Rich, Molly Morris, and Kathleen Ujvari. LTSS Choices: Paying Family Caregivers to Provide Care during the Pandemic--and Beyond. AARP Public Policy Institute, 2021. http://dx.doi.org/10.26419/ppi.00127.001.

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Reuben, David, Neil Wenger, Lee Jennings, and Ronald Hays. Testing a Way to Help Patients with Dementia and Their Caregivers Set Goals for Care. Patient-Centered Outcomes Research Institute® (PCORI), 2019. http://dx.doi.org/10.25302/10.2019.me.13035845.

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Hall, Sarah, Mark Vincent Aranas, and Amber Parkes. Making Care Count: An Overview of the Women’s Economic Empowerment and Care Initiative. Oxfam, 2020. http://dx.doi.org/10.21201/2020.6881.

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Across the globe, unpaid care and domestic work (UCDW) sustains communities and economies, provides essential care for children, sick and elderly people and those living with disabilities, and keeps households clean and families fed. Without unpaid care, the global economy as we know it would grind to a halt. Yet this work falls disproportionately on women and girls, limiting their opportunities to participate in decent paid employment, education, leisure and political life. Heavy and unequal UCDW traps women and girls in cycles of poverty and stops them from being part of solutions. To help a
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