Готові списки джерел за темами / Cancer caregiving

Добірка наукової літератури з теми "Cancer caregiving"

Автор: Grafiati

Опубліковано: 10 грудня 2022

Оновлено: 29 січня 2023

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Статті в журналах з теми "Cancer caregiving"

Sitaraman, Kartick. "Caregiving." Cancer Research, Statistics, and Treatment 5, no. 2 (2022): 265. http://dx.doi.org/10.4103/crst.crst_56_22.

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Nassar, Nadia Al, and Kristin Litzelman. "Partner Effects on Depressed Mood in Caregiving Dyads Are Most Pronounced in Cancer Caregiving, Partner Caregiving." Innovation in Aging 4, Supplement_1 (December 1, 2020): 352. http://dx.doi.org/10.1093/geroni/igaa057.1132.

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Abstract Theory and empirical evidence indicate that the well-being of caregivers and their care recipients is interrelated, although conflicting evidence has emerged across different caregiving populations. To establish a more nuanced understanding of this phenomenon, we used data from the National Health and Aging Trends Survey and the National Survey on Caregivers (2015 and 2017, n=759 dyads with complete longitudinal data) to construct actor-partner interdependence models assessing how spillover of depression varies by care recipient health condition (cancer, dementia, stroke, diabetes, or other conditions) and relationship type (spouse/partner, child, or other). Across condition types, the largest magnitude partner effects were observed in dyads with cancer, in which a one-point increase in caregiver depressed mood was associated with a 0.23-point increase in subsequent care recipient depressed mood (p=0.02) and a one-point increase in care recipient depressed mood was associated with a 0.33-point increase in subsequent caregiver depressed mood (p<0.01). Moderation by cancer status was statistically significant (pinteraction=0.03). Among spouse/partner caregivers, caregivers’ depressed mood was associated with subsequent depressed mood in the care recipient (p<0.05) but there was no evidence of spillover from the care recipient to the caregiver. Conversely, in both adult child caregivers and other caregivers, there was evidence for spillover from the care recipient to the caregiver (p<0.05) but not the reverse. The findings show that the interrelationship in the well-being of caregivers and care recipients varies by key caregiving characteristics, with implications for the development, dissemination, and implementation of interventions targeting caregiver, care recipient, and dyadic well-being.

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Opsomer, Sophie, Jan De Lepeleire, Emelien Lauwerier, and Peter Pype. "Resilience in advanced cancer caregiving." British Journal of General Practice 70, suppl 1 (June 2020): bjgp20X711041. http://dx.doi.org/10.3399/bjgp20x711041.

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BackgroundFamily caregivers of advanced cancer patients are at risk for developing mental disorders. Despite this risk, the majority seem to adapt well, and throughout the caregiving period, their trajectory is characterised by healthy functioning. However, GPs struggle with making timely assessments of caregivers at risk for mental dysfunction, since they often fail to seek medical help for themselves and the appropriate research about resilience in cancer caregivers is scarce. Moreover, research is hampered by the lack of a universal definition or theoretical framework.AimTo propose a comprehensive definition and framework for further research in family caregiving for advanced cancer patients.MethodInspired by the hermeneutic methodology, reviews and concept analyses on resilience following a potentially traumatic event were searched and analysed. Conforming to the hermeneutic methodology, article collection from PubMed, EMBASE, CINAHL, and PsycInfo was followed by analysis and was stopped when saturation was reached. Elements consistently arising from the definitions of resilience were listed and the theoretical frameworks were compared.ResultsThe APA definition: ‘resilience is the process of adapting well in the face of adversity, trauma or threats’ and Bonanno’s framework ‘temporal elements of resilience’ are proposed.ConclusionThere is a need for studies on resilience in caregivers of advanced cancer patients. Resilience is context-dependent, hence, study results cannot be transferred as such from one clinical situation to another. Furthermore, conceptual ambiguities hinder the interpretation and comparison of study results. For further research on resilience in caregivers of advanced cancer patients, we suggest the APA definition of resilience and Bonanno’s framework.

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Stetz, Kathleen M. "Caregiving demands during advanced cancer." Cancer Nursing 10, no. 5 (October 1987): 260???268. http://dx.doi.org/10.1097/00002820-198710000-00004.

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Romito, Francesca, Gil Goldzweig, Claudia Cormio, Mariët Hagedoorn, and Barbara L. Andersen. "Informal caregiving for cancer patients." Cancer 119 (May 20, 2013): 2160–69. http://dx.doi.org/10.1002/cncr.28057.

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Teo, Irene, Drishti Baid, Semra Ozdemir, Chetna Malhotra, Ratna Singh, Richard Harding, Rahul Malhotra, et al. "Family caregivers of advanced cancer patients: self-perceived competency and meaning-making." BMJ Supportive & Palliative Care 10, no. 4 (December 5, 2019): 435–42. http://dx.doi.org/10.1136/bmjspcare-2019-001979.

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BackgroundFamily caregivers of patients with advanced cancer have been reported to provide long hours of care and be at risk for poor psychological outcomes. Although research has focused on the nature of caregiving burden, little attention has been paid to identifying protective factors that improve caregiver psychological outcomes.AimWe examined the relationship between caregivers’ time spent caregiving and the following psychological outcomes: anxiety, depression and caregiving esteem. Subsequently, we explored the main and moderating effects of caregiver-perceived self-competency and sense of meaning on caregiver psychological outcomes.Design/participantsCross-sectional analysis was conducted using the baseline data from an ongoing cohort study. Family caregivers of advanced cancer patients (n=287) were recruited from two tertiary hospitals in Singapore.ResultsTime spent caregiving was not significantly associated with caregiver anxiety, depression or caregiving esteem. However, significant main effects of self-competency on anxiety and caregiving esteem; and sense of meaning on anxiety, depression and caregiving esteem were observed. Moderator analyses further indicated that self-competency attenuated the positive relationship between time spent caregiving and anxiety, while sense of meaning attenuated the negative relationship between time spent caregiving and caregiving esteem.ConclusionGreater perceived self-competency and sense of meaning are related to better caregiver psychological outcomes, and protect caregivers from worsening outcomes as caregiving hours increase. Our findings suggest that screening caregivers for distress is an important part of care, and that supportive interventions for caregivers should aim to enhance their perceived caregiving competencies and the ability to make meaning of their caregiving role.

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W N, Sachintha Dilhani, Sivayogan S, Jayamal De Silva, Thushari Hapuarachchi, Kandapolaarachchi P, and Suraj Perera. "Primary caregivers of children with cancer, Sri Lanka; A journey through their Psychological distress, Psychosocial needs, and Knowledge on caregiving." Asian Journal of Interdisciplinary Research 5, no. 4 (December 30, 2022): 1–13. http://dx.doi.org/10.54392/ajir2241.

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Identifying and addressing the psychosocial needs and psychological distress of primary caregivers of children and adolescents with cancers is emerging globally as a component that should be incorporated into quality cancer care. The objective of this study was to describe the psychosocial needs, psychological distress, knowledge of caregiving, and associated factors among the primary caregivers of children and adolescents with cancers attending the leading cancer treatment center in Sri Lanka. A descriptive cross-sectional study was conducted among childhood cancer caregivers in the early post-diagnosis stage using a needs and knowledge assessment questionnaire and General Health Questionnaire-30. Associations were sought between variables by bivariate analysis and further multivariate analysis. Consecutively, emotional needs, financial needs, informational needs, practical needs, and need for family and social support were at the top of the unmet needs list. All study participants had at least one item of unmet psychosocial needs. A lower education level was significantly associated with higher unmet psychosocial needs (OR=4.990; CI=1.96-12.72). Almost all the primary caregivers were psychologically distressed (97.6 %; CI = 95.3% - 99.9%) during the early post-diagnosis period. Only 18% of caregivers had a good overall knowledge of childhood cancer caregiving. Good overall knowledge of childhood cancer caregiving was associated with low distress levels (OR =2.46; 95% CI= 1.04 – 5.83). Almost all primary caregivers of children and adolescents with cancers at the early stages of diagnosis were highly distressed and had multiple unmet psychosocial needs with poor awareness of caregiving.

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Petricone-Westwood, Danielle, Jacqueline Galica, Sarah Hales, Elisa Stragapede, and Sophie Lebel. "An Investigation of the Effect of Attachment on Distress among Partners of Patients with Ovarian Cancer and Their Relationship with the Cancer Care Providers." Current Oncology 28, no. 4 (August 4, 2021): 2950–60. http://dx.doi.org/10.3390/curroncol28040258.

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Caregivers of patients with ovarian cancer experience distress related to caregiving difficulties within cancer care. Attachment insecurity is a well-known protector of distress, particularly as it relates to support from others. Using multivariate analyses, this study sought to determine the contribution of attachment insecurity and experiences with cancer care on symptoms of depression and anxiety, and investigated whether attachment insecurity moderated the relationship between caregiving experiences and distress. Multiple hierarchical regression analyses were conducted as part of a larger cross-sectional questionnaire study of distress among partners of patients with ovarian cancer. Participants (n = 82) were predominantly male, white, had household incomes over $100,000 and postsecondary education. Caregiving experiences explained 56% of the variance in depression, and 28% of the variance in anxiety. Specifically, lack of time for social relations as a result of caregiving significantly predicted depression and anxiety. Attachment anxiety correlated with both depression and anxiety, but attachment avoidance did not. Neither attachment anxiety nor attachment avoidance significantly contributed to distress variance, and neither moderated any of the relationships between caregiving experiences and distress outcomes. This study highlights the importance for cancer care to recognize the effect of caregiving responsibilities upon caregivers’ mental health, regardless of vulnerability to distress.

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Braun, Michal, Mario Mikulincer, Anne Rydall, Andrew Walsh, and Gary Rodin. "Hidden Morbidity in Cancer: Spouse Caregivers." Journal of Clinical Oncology 25, no. 30 (October 20, 2007): 4829–34. http://dx.doi.org/10.1200/jco.2006.10.0909.

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Purpose This study assesses psychological distress among advanced cancer patients and their spouse caregivers, while examining the relative contribution of caregiving burden and relational variables (attachment orientation and marital satisfaction) to depressive symptoms in the spouse caregivers. Methods A total of 101 patients with advanced GI or lung cancer and their spouse caregivers were recruited for the study. Measures included Beck Depression Inventory–II (BDI-II), Caregiving Burden scale, Experiences in Close Relationships scale, and ENRICH Marital Satisfaction scale. Results A total of 38.9% of the caregivers reported significant symptoms of depression (BDI-II ≥ 15) compared with 23.0% of their ill spouses (P < .0001). In a hierarchical regression predicting caregiver's depression, spouse caregiver's age and patient's cancer site were entered in the first step, objective caregiving burden was entered in the second step, subjective caregiving burden was entered in the third step, caregiver's attachment scores were entered in the fourth step, and caregiver's marital satisfaction score was entered in the fifth step. The final model accounted for 37% of the variance of caregiver depression, with subjective caregiving burden (β = .38; P < .01), caregiver's anxious attachment (β = .21; P < .05), caregiver's avoidant attachment (β = .20; P < .05), and caregiver's marital satisfaction (β = −.18; P < .05) making significant contributions to the model. Conclusion Spouse caregivers of patients with advanced cancer are a high-risk population for depression. Subjective caregiving burden and relational variables, such as caregivers' attachment orientations and marital dissatisfaction, are important predictors of caregiver depression.

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Liu, Zhu. "Caregiving Burden among Family Caregivers of People with Advanced Cancer: A Literature Review." Nursing & Healthcare International Journal 5, no. 3 (2021): 1–8. http://dx.doi.org/10.23880/nhij-16000240.

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This literature review focus on the research methods, levels, influencing factors and types of family caregiver burden caring patients with advanced cancer, aiming to improve medical worker’s understanding of caregiver burden, provide a basis for building their support system, and produce new insights for nursing practice and research in the future.

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Дисертації з теми "Cancer caregiving"

Nijboer, Christine. "Caregiving to patients with colorectal cancer a longitudinal study on caregiving by partners /." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2000. http://dare.uva.nl/document/81019.

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Mazanec, Polly M. "Distance Caregiving of a Parent with Advanced Cancer." Case Western Reserve University School of Graduate Studies / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=case1247250761.

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Steinwedel, Cynthia M. "The impact of cancer caregiving on cancer caregivers| Stories of lives in transition." Thesis, The University of Wisconsin - Milwaukee, 2014. http://pqdtopen.proquest.com/#viewpdf?dispub=3602366.

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The purpose of the study was to examine the impact of cancer caregiving on primary caregivers, exploring their personal narratives looking back on the entire experience from diagnosis, through treatment, and beyond. Caregiving is associated with exacerbation of stress-related disorders such as hypertension and heart disease and may also be associated with increased mortality rates. Transitions theory served as the conceptual framework for the study. Eleven adult caregivers, pre-retirement age, each participated in two semi-structured interviews. Caregivers were recruited from a community cancer resource center and were purposively selected to achieve maximum variation in terms of outcome of cancer treatment. The sample included 8 females and 3 males; there were 3 husbands, 6 wives, and 2 daughters. Caregivers provided care for patients with a variety of cancer types and a variety of treatment outcomes, from cancer free with sequelae to deceased. Each caregiver interview recording was transcribed, and preliminary examination of each transcript helped guide subsequent interviews. NVivo9 software was used to assist with data management. Data saturation was achieved. Narrative within-case analyses as well as thematic analysis were used to address research questions. Thematic analysis resulted in seven themes: Burden: The Load that Never Ends; Disconnectedness and Isolation: The Invisible Person; Helplessness and Loss of Control: Tied to This Ride; Dealing with the Healthcare System; Role Disruption: Spinning the Plates; Loss, Change, and Grief: Reaction to the Whole; and Carrying Forward with Scars: New Priorities and Permanent Change. All of the caregivers changed their employment or social responsibilities due to the demands of caregiving. Themes were present in different parts of the cancer trajectory and in differing intensities in all interviews. Findings included disconnectedness and isolation as a central feature of cancer caregiving, plus significant grief present through the cancer trajectory, especially in the post-treatment phase. Furthermore, the experience of cancer caregiving remained one of significant impact years after treatment had ended. Successful transitioning requires connectedness and mastery, but participants in this study identified that their caregiving trajectories were full of isolation, grief, burden, and helplessness. Many suggested the need for support, even though they tended to deny their own physical and emotional needs while caregiving. Healthcare professionals can help by providing information, support, listening, and grief counselling. Research is needed on interventions that may reduce isolation, helplessness, and burden for caregivers.

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Stamataki, Zoe. "The Cancer Caregiving Experience : Testing a Model and Exploring Perceptions." Thesis, University of Kent, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.523641.

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Al, Awar Zeina. "Using HIT to Support Informal Caregivers of Cancer Patients at Home: a Needs Assessment." Thesis, Université d'Ottawa / University of Ottawa, 2016. http://hdl.handle.net/10393/34112.

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Introduction: This research investigated the requirements of an HIT solution that is usable and useful to informal caregivers of cancer patients on home palliative care. Methodology: A needs assessment method was used with an exploratory and a confirmatory stage. Eight semi-structured interviews and two focus groups were used for data collection. Qualitative content analysis was used to analyse caregiver experiences with both inductive and deductive coding. Results/Discussion: Expressed and unexpressed caregiver needs were extracted into four categories, Implementation, Presentation, Information, and Practical Caregiving, and used to create the application requirements. Five user personas were created based on caregiving intensity and the functional level of the patients, a method of tailoring the application content to the different personas was created, and a low-fidelity prototype of the application was designed. Conclusion: The findings of this research can improve the preparedness and coping of informal caregivers of cancer patients on home palliative care.

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Bernard, Lori Lynn. "Husband's and Daughter's Role Strain During Breast Cancer Hospice Patient Caregiving and Bereavement Adjustment." Thesis, University of North Texas, 2000. https://digital.library.unt.edu/ark:/67531/metadc2542/.

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Current literature regarding caregiver bereavement adjustment has advanced two competing models explaining adjustment in relation to caregiver interrole conflict: the Relief Model and Complicated Grief Model. This research has primarily focused on the experience of those providing care to dementia patients. This study tests these competing models of bereavement adjustment for husband and daughter caregivers of breast cancer hospice patients. For husbands, greater psychological strain and health strain were predictive of greater difficulty with bereavement adjustment, supporting the Complicated Grief Model of bereavement adjustment. For daughters, strain was not a significant predictor of bereavement adjustment, and thus did not support either bereavement adjustment model. While daughter caregivers experienced more role strain than husband caregivers during patient care, the degree of role strain was predictive of bereavement adjustment for husbands but not for daughters, suggesting that relationship type (husbands versus daughters) between caregiver and patient impacts which factors influence bereavement adjustment.

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Edmonds, Maura Fulham. "Managing Change| The Process of Caregiving for Informal Caregivers of Head and Neck Cancer Patients." Thesis, University of Maryland, Baltimore, 2013. http://pqdtopen.proquest.com/#viewpdf?dispub=3563316.

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Purpose: The goal of this study was to gain a better understanding of the process undertaken by the informal caregivers of head and neck cancer (HNC), with an eye toward theory development. Although the development of a theory was beyond the scope of this project, it was meant to be a first step toward understanding the important categories and concepts that are part of this process.

Methods: This study used grounded theory methods and was conducted at a large urban National Cancer Institute (NCI)-designated cancer center in the Mid-Atlantic region of the US. Constant comparative analysis and theoretical sampling were used to gather and analyze data from six caregivers of HNC patients. Audio-recorded and transcribed, de-identified raw data were analyzed using Atlas ti Software™.

Results: The caregiving process was described in terms that yielded a core category and two other categories. Subcategories were identified as well as dimensions of some of the subcategories. The core category was entitled Managing Change and the two other categories were entitled Types of Change and Strategies for Managing Change. Types of Change encompassed the subcategories of Changes in Life Patterns, Witnessing Physical Changes, Relationship Changes, and Increased Uncertainty. Strategies for Managing Change included the subcategories of Controlling Life Pattern Changes, Utilizing the Quality of the Relationship, and Managing Stress. Key findings included the identification of many different types of change, variation in types and amounts of change over time, utilization of quality of the relationship between patient and caregiver as an important strategy for caregivers, and caregivers’ use of a variety of strategies to manage change.

Conclusions: This study has attempted to broaden the understanding of the role of a caregiver of a patient with HNC using grounded theory methods. This work is the first step in developing a theory of caregiving related to this population which may also be applied to a broader population of caregivers.

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Mori, Hiroko. "Characteristics of caregiver perceptions of end-of-life caregiving experiences in cancer survivorship: in-depth interview study." 京都大学 (Kyoto University), 2012. http://hdl.handle.net/2433/157856.

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Lamanna, Jennifer. "A brief problem-solving intervention for caregivers of children with cancer." VCU Scholars Compass, 2012. http://scholarscompass.vcu.edu/etd/2709.

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OBJECTIVE: Pediatric cancer treatment is stressful for caregivers. Research has indicated that problem-solving coping reduces stress related to caregiving. The current study examines the effects of a problem-solving intervention (Parent Empowerment Program), based on Problem-Solving Therapy, for caregivers of children on active cancer treatment. It was hypothesized that participants who received the intervention would show decreases in caregiving stress and posttraumatic stress symptoms, and increases in problem-solving ability between baseline and post-test assessments compared to those who received an attention control. METHOD: Thirty-nine caregivers (all parents; 48% participation rate) participated. The majority were mothers (90%), married or partnered (59%) and Caucasian (56%). Participants were randomly assigned to condition (intervention vs. attention control) after completing baseline questionnaires. Participants who received the intervention received one session of problem solving intervention and a follow-up session. Those in the attention control condition received two general support sessions. Participants were assessed at baseline, one month after the second session, and three months after the second session. RESULTS: There were no effects of the intervention on any of the outcome variables when data for all participants was examined. However, there was a significant effect of the intervention on problem-solving ability among participants of children between 4-16 weeks post-diagnosis. CONCLUSIONS: There were many factors that contributed to the lack of effect, including small sample size, variations in time since diagnosis, low participation rates, and limited number of sessions. Future studies should target parents who are under the highest levels of stress and increase the intensity of sessions. However, the finding that the intervention has an effect on problem-solving ability early in the treatment trajectory replicates previous research and has potential clinical utility.

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Thomas, Sarah Nichole. "Decisions to Seek and Share: A Mixed Methods Approach to Understanding Caregivers Surrogate Information Acquisition Behaviors." The Ohio State University, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1595545894518707.

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Книги з теми "Cancer caregiving"

Talley, Ronda C., Ruth McCorkle, and Walter F. Baile, eds. Cancer Caregiving in the United States. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-3154-1.

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Pebbling the walk: Surviving cancer caregiving. Portland, Or: Blue Heron Publishing, 2000.

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Houts, Peter S., Julia A. Bucher, and Terri B. Ades. American Cancer Society complete guide to family caregiving: The essential guide to cancer caregiving at home. 2nd ed. Atlanta, Ga: American Cancer Society/Health Promotions, 2011.

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Bucher, Julia A. American Cancer Society's Complete Guide To Family Caregiving, Second Edition: The Essential Guide T. S.l: American Cancer Society, 2008.

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Woznick, Leigh A. Living with childhood cancer. Washington, DC: American Psychological Association, 2002.

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Esther, Sales, Schulz Richard 1947-, and Mandel School of Applied Social Sciences (Case Western Reserve University), eds. Family caregiving in chronic illness: Alzheimer's disease, cancer, heart disease, mental illness, and stroke. Newbury Park, Calif: Sage Publications, 1991.

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Poirier, Suzanne. Stories of family caregiving: Reconsiderations of theory, literature, and life. Indianapolis, IN: Center Nursing Pub., 2002.

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Help me live: 20 things people with cancer want you to know. Berkeley: Celestial Arts, 2011.

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American Cancer Society. Cancer Caregiving A-Z. American Cancer Society, 2008.

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Houts, Peter S. Caregiving. 2nd ed. American Cancer Society, 2003.

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Частини книг з теми "Cancer caregiving"

Frank-Stromborg, Marilyn, and Kenneth R. Burns. "Legal Issues in Cancer Caregiving." In Cancer Caregiving in the United States, 249–63. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-3154-1_13.

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Kaufman, Dale L., Ann O’Mara, and Christine M. Schrauf. "Cancer Caregiving: Policy and Advocacy." In Cancer Caregiving in the United States, 265–86. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-3154-1_14.

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Talley, Ronda C., Ruth McCorkle, and Walter F. Baile. "Cancer and Caregiving: Changed Lives and the Future of Cancer Care." In Cancer Caregiving in the United States, 315–21. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-3154-1_16.

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Raveis, Victoria H. "Advances in Cancer Care Impacting Familial Caregiving." In Cancer Caregiving in the United States, 179–97. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-3154-1_10.

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Smith, Martin L., and Mary Elizabeth Paulk. "Caregivers of Patients with Cancer: Ethical Issues." In Cancer Caregiving in the United States, 287–311. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-3154-1_15.

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Goodheart, Carol D. "The Impact of Health Disparities on Cancer Caregivers." In Cancer Caregiving in the United States, 63–77. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-3154-1_4.

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McCorkle, Ruth, Ronda C. Talley, Walter Baile, and Anna-leila Williams. "Caring for a Loved One with Cancer: Professional and Family Issues." In Cancer Caregiving in the United States, 1–17. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-3154-1_1.

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Puchalski, Christina M. "Caregiver Stress: The Role of Spirituality in the Lives of Family/Friends and Professional Caregivers of Cancer Patients." In Cancer Caregiving in the United States, 201–28. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-3154-1_11.

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Baldwin, Dee. "The Economics of Cancer Care: Implications for Family Caregivers." In Cancer Caregiving in the United States, 229–47. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-3154-1_12.

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McCorkle, Ruth, Ronda C. Talley, Walter Baile, and Anna-leila Williams. "ERRATUM." In Cancer Caregiving in the United States, E1. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-3154-1_17.

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Тези доповідей конференцій з теми "Cancer caregiving"

Gray, Tamryn F., Nancy Borstelmann, Shoshana Rosenberg, Shari Gelber, Meghan E. Meyer, Kathryn J. Ruddy, Lidia Schapira, et al. "Abstract PS9-08: The psychosocial impact of caregiving on partners of young women with breast cancer in treatment." In Abstracts: 2020 San Antonio Breast Cancer Virtual Symposium; December 8-11, 2020; San Antonio, Texas. American Association for Cancer Research, 2021. http://dx.doi.org/10.1158/1538-7445.sabcs20-ps9-08.

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