Cited by 29Nursing care and researchCancer survivorship and careFamily Support in Illness

The Psychosocial Impact of Spouse-Caregiver Chronic Health Conditions and Personal History of Cancer on Well-being in Patients With Advanced Cancer and Their Caregivers

Open access
Ketcher, Dana, Otto, Amy K., Vadaparampil, Susan T., Heyman, Richard E., Ellington, Lee, Reblin, Maija·2021·Journal of Pain and Symptom Management

Abstract

Context Caregiving during advanced cancer presents many physical and psychological challenges, especially for caregivers who are coping with their own history of cancer or their own chronic health conditions. There is growing recognition that caregiver health and patient health are interdependent. Objectives The objective of this study was to use quantitative and interview data to examine and explore the impact of a caregiver's personal cancer history and chronic health conditions on the psychosocial well-being of both the caregiver and patient. Methods This was a secondary analysis of data from 88 patients with advanced lung/gastrointestinal cancer and their spouse-caregivers. Participants self-reported subjective health, chronic health conditions (including cancer), anxiety and depression symptoms, and social support and social stress. Caregivers self-reported caregiving burden and preparedness for caregiving. Caregivers also completed semistructured interviews. Results Participants were mostly white, non-Hispanic, and in their mid-60s. Caregivers reported 1.40 (SD = 1.14) chronic conditions on average; 11 reported a personal history of cancer ("survivor-caregivers"). The number of caregiver chronic health conditions was positively associated with patient depression symptoms. Patients of survivor-caregivers also reported more depression symptoms than patients of caregivers without cancer (t(85) = -2.35, P = 0.021). Survivor-caregivers reported higher preparedness for caregiving than caregivers without cancer (t(85) = -2.48, P = 0.015). Interview data enriched quantitative findings and identified factors that may drive patient depression, including emotions such as resentment or guilt. Experiencing cancer personally may provide caregivers unique insight into the patient experience. Conclusion Providers should be aware of caregiver chronic conditions and cancer history, given the potential negative effects on patient psychosocial well-being.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.jpainsymman.2020.12.008

Cites

1 of 1 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Los síntomas de depresión en los cuidadores estuvieron asociados de forma positiva al número de condiciones crónicas de salud del cuidador (p = .041).

    “Los síntomas de depresión en los cuidadores estuvieron asociados de forma positiva a el número de condiciones crónicas de salud del cuidador (p = .041).”

    From Sobrecarga de trabajo en cuidadores de pacientes en cuidados paliativos oncológicos: Una revisión bibliográfica (2023) · cites this paper as Ketcher et al., 2021

    The Results section explicitly says the number of caregiver chronic conditions was not significantly associated with caregiver depression. The positive association at p = .041 was with patient depression symptoms, not caregiver depression symptoms. (LLM, conf=0.94)

    Checked by a reasoning model — may be wrong.

    Experimental — accuracy not yet measured
  • Los principales factores que impulsan la depresión emocional son el resentimiento y la culpa.

    “además se identificó como principales factores que impulsan la depresión emociones como el resentimiento y la culpa.”

    From Sobrecarga de trabajo en cuidadores de pacientes en cuidados paliativos oncológicos: Una revisión bibliográfica (2023) · cites this paper as Ketcher et al., 2021

    The Abstract (Results) says interviews identified emotions such as resentment and guilt as factors that may drive depression in patients with advanced cancer. The citing sentence presents them as the principal drivers of depression without the paper’s uncertainty or patient-specific scope. (LLM, conf=0.86)

    Experimental — accuracy not yet measured
  • La carga del cuidador se correlacionó con el número de condiciones tanto del cuidador como del paciente (p = 0,001).

    “La CdC se correlacionó con el número de condiciones tanto del cuidador como del pacientes (p = 0,001)”

    From Sobrecarga de trabajo en cuidadores de pacientes en cuidados paliativos oncológicos: Una revisión bibliográfica (2023) · cites this paper as Ketcher et al., 2021

    The Results section reports that caregiver stress burden was associated with the number of chronic conditions in both caregivers and patients. However, p = .001 applies only to caregiver conditions; the association with patient conditions was in the opposite direction and had p = .023. The paper found no association with objective or demand burden. (LLM, conf=0.91)

    Experimental — accuracy not yet measured
  • Los síntomas de depresión en los cuidadores están asociados al número de condiciones crónicas de salud del cuidador, y la carga del cuidador se correlaciona con el número de condiciones tanto del cuidador como del paciente.

    “los síntomas de depresión en los cuidadores estuvieron asociados a el número de condiciones crónicas de salud del cuidador y la CdC se correlacionó con el número de condiciones tanto del cuidador como del pacientes (Ketcher et al., 2021).”

    From Sobrecarga de trabajo en cuidadores de pacientes en cuidados paliativos oncológicos: Una revisión bibliográfica (2023) · cites this paper as Ketcher et al., 2021

    The quantitative Results report that caregiver stress burden was associated with the number of chronic conditions in both patients and caregivers, although the association with patient conditions was negative. They explicitly report no significant association between caregivers’ chronic conditions and caregivers’ depression symptoms; the depression association was with patients’ symptoms instead. The burden finding is limited to stress burden, not the other burden measures examined. (LLM, conf=0.91)

    Experimental — accuracy not yet measured
  • Gender differences have been linked to differences in caregiver stress, burden, anxiety, depression, and coping styles, as well as how caregiver's gender impacts patient outcomes in the context of advanced cancer patients.

    “Further, gender differences have been linked to differences in caregiver stress, burden, anxiety, depression, and coping styles, as well as how caregiver’s gender impacts patient outcomes in the context of advanced cancer patients [10, 14].”

    From Preparedness, resilience and unmet needs of informal caregivers of advanced cancer patients in a Regional Mission Hospital in Kenya: Qualitative Study (2023) · cites this paper as [14]

    The Results (Sample Characteristics; page unavailable) report caregivers’ genders, but do not compare outcomes by gender. The Methods (Data Analysis; page unavailable) and Results instead examine chronic conditions and caregivers’ cancer history. Searches for gender differences and caregiver gender found no passage linking gender to caregiver stress, burden, anxiety, depression, coping styles, or patient outcomes. (LLM, conf=0.76)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 46

  1. [1]Marengoni A, Angleman S, Melis R, Aging with multimorbidity: a systematic review of the literature. Ageing research reviews 2011; 10: 430– 439. 21402176
  2. [2]King DE, Xiang J, Pilkerton CS. Multimorbidity trends in United States adults, 1988–2014. The Journal of the American Board of Family Medicine 2018; 31: 503– 513. 29986975 PMC6368177
  3. [3]Shapiro CL. Cancer Survivorship. New England Journal of Medicine 2018; 379: 2438– 2450. 30575480
  4. [4]Guy GP Jr., Yabroff KR, Ekwueme DU, Economic Burden of Chronic Conditions Among Survivors of Cancer in the United States. Journal of clinical oncology: official journal of the American Society of Clinical Oncology 2017; 35: 2053– 2061. 28471724 PMC6059377
  5. [5]Salive ME. Multimorbidity in older adults. Epidemiol Rev 2013; 35: 75– 83. 23372025
  6. [6]Bevans M, Sternberg EM. Caregiving burden, stress, and health effects among family caregivers of adult cancer patients. Jama 2012; 307: 398– 403. 22274687 PMC3304539
  7. [7]Northouse LL, Katapodi MC, Schafenacker AM, Weiss D. The Impact of Caregiving on the Psychological Well-Being of Family Caregivers and Cancer Patients. Seminars in Oncology Nursing 2012; 28: 236– 245. 23107181
  8. [8]Tolbert E, Bowie J, Snyder C, Bantug E, Smith K. A qualitative exploration of the experiences, needs, and roles of caregivers during and after cancer treatment: “That’s what I say. I’m a relative survivor”. Journal of Cancer Survivorship 2018; 12: 134– 144. 29101710
  9. [9]Wang T, Molassiotis A, Chung BPM, Tan J-Y. Unmet care needs of advanced cancer patients and their informal caregivers: a systematic review. BMC Palliative Care 2018; 17: 96. 30037346 PMC6057056
  10. [10]Giovannetti ER, Wolff JL, Xue QL, Difficulty assisting with health care tasks among caregivers of multimorbid older adults. J Gen Intern Med 2012; 27: 37– 44. 21874385 PMC3250537
  11. [11]Huang I-C, Hudson MM, Robison LL, Krull KR. Differential impact of symptom prevalence and chronic conditions on quality of life in cancer survivors and non-cancer individuals: a population study. Cancer epidemiology and prevention biomarkers 2017; 26: 1124– 1132. PMC5500424 28336581
  12. [12]Streck BP, Wardell DW, LoBiondo-Wood G, Beauchamp JES. Interdependence of physical and psychological morbidity among patients with cancer and family caregivers: Review of the literature. Psycho-Oncology 2020; 29: 974– 989. 32227401
  13. [13]Lyons KS, Lee CS. The Theory of Dyadic Illness Management. Journal of Family Nursing 2018; 24: 8– 28. 29353528
  14. [14]Jacobs JM, Shaffer KM, Nipp RD, Distress is Interdependent in Patients and Caregivers with Newly Diagnosed Incurable Cancers. Ann Behav Med 2017; 51: 519– 531. 28097515 PMC5513787
  15. [15]Streck BP, Wardell DW, LoBiondo-Wood G, Beauchamp JE. Interdependence of physical and psychological morbidity among patients with cancer and family caregivers: Review of the literature. Psycho-Oncology 2020. 32227401
  16. [16]Cook WL, Kenny DA. The Actor–Partner Interdependence Model: A model of bidirectional effects in developmental studies. International Journal of Behavioral Development 2005; 29: 101– 109.
  17. [17]Rusbult CE, Van Lange PA. Why we need interdependence theory. Social and Personality Psychology Compass 2008; 2: 2049– 2070.
  18. [18]Hendriksen E, Rivera A, Williams E, Manifestations of anxiety and coping strategies in patients with metastatic lung cancer and their family caregivers: a qualitative study. Psychology & health 2019; 34: 886– 899. 31155947
  19. [19]Mishra SI, Brakey HR, Kano M, Nedjat-Haiem FR, Sussman AL. Health related quality of life during cancer treatment: Perspectives of young adult (23–39 years) cancer survivors and primary informal caregivers. European Journal of Oncology Nursing 2018; 32: 48– 54. 29353632
  20. [20]Badr H, Herbert K, Reckson B, Unmet needs and relationship challenges of head and neck cancer patients and their spouses. Journal of psychosocial oncology 2016; 34: 336– 346. 27269579 PMC4951153
  21. [21]Sterba KR, Zapka J, Armeson KE, Physical and emotional well-being and support in newly diagnosed head and neck cancer patient–caregiver dyads. Journal of psychosocial oncology 2017; 35: 646– 665. 28459393 PMC5976502
  22. [22]Reblin M, Sutton SK, Vadaparampil ST, Heyman RE, Ellington L. Behind closed doors: How advanced cancer couples communicate at home. Journal of Psychosocial Oncology 2018; 37: 228– 241. 30372376 PMC7771241
  23. [23]Reblin M, Heyman RE, Ellington L, Everyday couples’ communication research: Overcoming methodological barriers with technology. Patient education and counseling 2018; 101: 551– 556. 29111310
  24. [24]Ware JE Jr, Sherbourne CD. The MOS 36-item short-form health survey (SF-36): I. Conceptual framework and item selection. Medical care 1992: 473– 483. 1593914
  25. [25]Zigmond AS, Snaith RP. The hospital anxiety and depression scale. Acta psychiatrica scandinavica 1983; 67: 361– 370. 6880820
  26. [26]Parkerson GR Jr., Broadhead WE, Tse CK. Validation of the Duke Social Support and Stress Scale. Fam Med 1991; 23: 357– 60. 1884930
  27. [27]Montgomery RJ, Borgatta EF, Borgatta ML. Societal and family change in the burden of care. In: Liu WT, Kendig H, eds. Who should care for the elderly? An East–West value divide, New Jersey: World Scientific, 2000: 27– 54.
  28. [28]Archbold PG, Stewart BJ, Greenlick MR, Harvath TA. The clinical assessment of mutuality and preparedness in family caregiver to frail older people. In: Funk SG, Tornquist EM, Champagne MT, Copp LA, eds. Key aspects of elder care, New York: Springer Publishing Compnay, 1992: 328– 339.
  29. [29]Kenny DA. Models of non-independence in dyadic research. Journal of Social and Personal Relationships 1996; 13: 279– 294.
  30. [33]Lee CS, Sethares KA, Thompson JH, Patterns of Heart Failure Dyadic Illness Management: The Important Role of Gender. Journal of Cardiovascular Nursing 2020; 35: 416– 422. 32496366
  31. [34]Lee CS, Lyons KS. Patterns, relevance, and predictors of dyadic mental health over time in lung cancer. Psychooncology 2019; 28: 1721– 1727. 31216606
  32. [35]Kelley DE, Kent EE, Litzelman K, Mollica MA, Rowland JH. Dyadic associations between perceived social support and cancer patient and caregiver health: An actor-partner interdependence modeling approach. Psycho-oncology 2019; 28: 1453– 1460. 30993811 PMC6749989
  33. [36]Ivziku D, Clari M, Piredda M, De Marinis MG, Matarese M. Anxiety, depression and quality of life in chronic obstructive pulmonary disease patients and caregivers: an actor–partner interdependence model analysis. Quality of Life Research 2019; 28: 461– 472. 30341578
  34. [37]Ybema JF, Kuijer RG, Buunk BP, DeJong GM, Sanderman R. Depression and perceptions of inequity among couples facing cancer. Personality and Social Psychology Bulletin 2001; 27: 3– 13.
  35. [38]Williamson GM, Martin-Cook K, Weiner MF, Caregiver resentment: Explaining why care recipients exhibit problem behavior. Rehabilitation Psychology 2005; 50: 215.
  36. [39]Ellis KR, Janevic MR, Kershaw T, Meaning-based coping, chronic conditions and quality of life in advanced cancer & caregiving. Psychooncology 2017; 26: 1316– 1323. 27147405 PMC5097695
  37. [41]Park CL. Positive psychology perspectives across the cancer continuum: Meaning, spirituality, and growth. In: Carr B, Steel J, eds. Psychological aspects of cancer, Boston, MA: Springer, 2013.
  38. [42]Molina Y, Yi JC, Martinez-Gutierrez J, Resilience among patients across the cancer continuum: diverse perspectives. Clinical journal of oncology nursing 2014; 18: 93– 101. 24476731 PMC4002224
  39. [43]Manne SL, Kashy DA, Virtue S, Acceptance, social support, benefit-finding, and depression in women with gynecological cancer. Quality of Life Research 2018; 27: 2991– 3002. 30128785 PMC6196117
  40. [44]Park HY, Kim MJ, Kim JY, Could Peer Support Programs Be a Good Resource for Managing the Unmet Needs of Cancer Patients? Journal of Cancer Education 2019; 34: 950– 957. 30091013 PMC6785582
  41. [45]Loprinzi Brauer CE, Clark MM, Solberg Nes L, Miller LK. Peer Mentorship Programs for Breast Cancer Patients. Journal of Pain and Symptom Management 2016; 51: e5– e7. 27033161
  42. [46]Robinson JD, Tian Y. Cancer Patients and the Provision of Informational Social Support. Health Communication 2009; 24: 381– 390. 19657821
  43. [47]Bradley N, Lloyd-Williams M, Dowrick C. Effectiveness of palliative care interventions offering social support to people with life-limiting illness—A systematic review. European Journal of Cancer Care 2018; 27: e12837. 29573500 PMC6001732
  44. [49]Hu Y, Liu T, Li F. Association between dyadic interventions and outcomes in cancer patients: a meta-analysis. Supportive Care in Cancer 2019; 27: 745– 761. 30604008
  45. [50]Pefoyo AJ, Bronskill SE, Gruneir A, The increasing burden and complexity of multimorbidity. BMC Public Health 2015; 15: 415. 25903064 PMC4415224
  46. [51]Ritchie CS, Kvale E, Fisch MJ. Multimorbidity: an issue of growing importance for oncologists. Journal of oncology practice 2011; 7: 371– 374. 22379419 PMC3219463

Cited by

Sorted by citations

Authors
Ketcher, D., Otto, A. K., Vadaparampil, S. T., Heyman, R. E., Ellington, L., & Reblin, M.
Affiliations
  • Moffitt Cancer Center (US)
  • University of Miami (US)
  • New York University (US)
  • University of Utah (US)
Corresponding author
Reblin, Maija
Venue
Journal of Pain and Symptom Management
Publisher
Elsevier BV
Published
2021-08
Volume
62
Issue
2
Pages
303-311
ISSN
0885-3924 (ISSN-L)
OpenAlex
W3113092761
Cited by
29
References
1
Citations by year
2026: 4 · 2025: 3 · 2024: 6 · 2023: 9 · 2022: 7
FWCI
6.18
Type
journal article
Language
en
Open access
Locations
  • Journal of Pain and Symptom Management (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Cancer Institute (T32CA090314)
  • National Institutes of Health
  • American Cancer Society (MRSG 13\u2013234\u201301-PCSM, MRSG 13?, 01-PCSM)
Topics
  • Health Sciences › Health Professions › Pharmacy › Nursing care and research
  • Health Sciences › Medicine › Oncology › Cancer survivorship and care
  • Social Sciences › Sociology and Political Science › Family Support in Illness
Keywords
spousal caregivers, advanced cancer, patient depression, caregiver depression, caregiver burden, social support, social stress, lung cancer, gastrointestinal cancer, psychosocial well-being
MeSH terms
Adaptation, Psychological, Depression, Humans, Neoplasms, Stress, Psychological, Caregivers, Spouses

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review