Distress experienced by lung cancer patients and their family caregivers in the first year of their cancer journey

被引:13
作者
Aubin, Michele [1 ,2 ,3 ]
Vezina, Lucie [1 ]
Verreault, Rene [3 ]
Simard, Sebastien [2 ,4 ]
Hudon, Eveline [5 ]
Desbiens, Jean-Francois [3 ,6 ]
Fillion, Lise [6 ,7 ]
Dumont, Serge [3 ,8 ]
Tourigny, Andre [3 ,9 ]
Daneault, Serge [5 ,10 ]
机构
[1] Univ Laval, Dept Family Med & Emergency Med, Quebec City, PQ, Canada
[2] Inst Cardiol & Pneumol Quebec IUCPQ, Res Ctr, Quebec City, PQ, Canada
[3] VITAM Ctr Rech Sante Durable, Quebec City, PQ, Canada
[4] UQAC, Dept Hlth Sci, Quebec City, PQ, Canada
[5] Univ Montreal, Dept Family Med & Emergency Med, Montreal, PQ, Canada
[6] Univ Laval, Fac Nursing, Quebec City, PQ, Canada
[7] CHU Quebec, Res Ctr, Quebec City, PQ, Canada
[8] Univ Laval, Fac Social Sci, Quebec City, PQ, Canada
[9] CHU Quebec, Ctr Excellence Aging, Quebec City, PQ, Canada
[10] CHU Montreal, Res Ctr, Montreal, PQ, Canada
关键词
Cancer supportive care; Cohort study; Distress; Family caregiver; Lung cancer; Patient; QUALITY-OF-LIFE; MENTAL-HEALTH; PSYCHOLOGICAL DISTRESS; SUPPORT SERVICES; HOSPITAL ANXIETY; DEPRESSION; PREVALENCE; BURDEN; SYMPTOMS; NEEDS;
D O I
10.1017/S1478951521000377
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Objectives Diagnosis of cancer is emotionally threatening not only for patients but also for their family caregivers (FC) who witness and share much of the illness experience. This study compares distress experienced by lung cancer patients and their FC during the year following the diagnosis. Methods A prospective cohort study of 206 patients recently diagnosed with inoperable lung cancer (participation rate 79.5%) and 131 FC (participation rate 63.6%) was conducted in an ambulatory oncology clinic in Quebec City (Canada). They completed validated questionnaires regarding their personal and psychological characteristics (Hospital and Anxiety Depression Scale-HADS), in the first months after the diagnosis of lung cancer and after 6 and 12 months. Univariate, bivariate, and linear mixed models were conducted to compare patient and FC distress. Results At baseline, 7.8% of patients reported distress (HADS total score >15) and their mean distress score was 7.0 +/- 4.9 (range 0-42). In contrast, 33.6% of FC presented significant distress and their mean distress score was 12.0 +/- 7.2 (P < 0.0001). Proportions of patients and FC with distress remained relatively stable at 6 and 12 months, and at every time point, FC reported higher levels of distress compared to their relative with cancer (P < 0.0001). Comparable trends were found when looking at the mean scores of distress, anxiety, and depression throughout the study. Significance of results Being diagnosed with lung cancer and going through its different phases seems to affect more FC than patients. The psychological impact of such diagnosis appears early after the diagnosis and does not significantly change over time. These findings reinforce the importance for oncology teams, to include FC in their systematic distress screening program, in order to help them cope with their own feelings and be able to play their role in patient support and care throughout the cancer journey.
引用
收藏
页码:15 / 21
页数:7
相关论文
共 50 条
  • [41] Family Peace and Affecting Factors in Family Caregivers of Patients With Cancer: A Cross-Sectional Study
    Sahin, Furkan
    Sahin, Fatma Sinem
    Ozkaraman, Ayse
    JOURNAL OF PALLIATIVE CARE, 2025, 40 (01) : 28 - 40
  • [42] Caregiving experiences of Korean family caregivers of cancer patients: An integrative literature review
    Lee, Eunice E.
    Lee, Shin-Young
    PSYCHO-ONCOLOGY, 2020, 29 (10) : 1486 - 1503
  • [43] Interdisciplinary Palliative Care for Lung Cancer Patients and Family Caregivers
    Koczywas, Marianna
    Sun, Virginia
    Hurria, Arti
    Cristea, Mihaela
    Raz, Dan J.
    Kim, Jae Y.
    Reckamp, Karen
    Zachariah, Finly
    Williams, Anna Cathy
    Borneman, Tami
    Fujinami, Rebecca
    Del Ferraro, Catherine
    Uman, Gwen
    Ferrell, Betty
    JOURNAL OF THORACIC ONCOLOGY, 2015, 10 (09) : S365 - S366
  • [44] Supporting the patients with advanced cancer and their family caregivers: what are their palliative care needs?
    Chua, Gek Phin
    Pang, Grace Su Yin
    Yee, Alethlea Chung Pheng
    Neo, Patricia Soek Hui
    Zhou, Siqin
    Lim, Cindy
    Wong, Yin Yee
    Qu, Debra Limin
    Pan, Fang Ting
    Yang, Grace Meijuan
    BMC CANCER, 2020, 20 (01)
  • [45] Psychological Distress and Social Support Availability in Different Family Caregivers of Latinas With Breast Cancer
    Segrin, Chris
    Badger, Terry
    Sikorskii, Alla
    JOURNAL OF TRANSCULTURAL NURSING, 2021, 32 (02) : 103 - 110
  • [46] Distress, Depression, Anxiety, and Resilience in Patients With Cancer and Caregivers
    Deshields, Teresa L.
    Asvat, Yasmin
    Tippey, Amaris R.
    Vanderlan, Jessica R.
    HEALTH PSYCHOLOGY, 2022, 41 (04) : 246 - 255
  • [47] Quality of Life of Family Caregivers of Patients With Cancer in Korce, Albania
    Judkins, Jonathon
    Laska, Irena
    Paice, Judith
    Kumthekar, Priya
    JOURNAL OF PALLIATIVE CARE, 2019, 34 (02) : 118 - 125
  • [48] Dyadic Psychosocial Intervention for Advanced Lung Cancer Patients and Their Family Caregivers: Results of a Randomized Pilot Trial
    Badr, Hoda
    Smith, Cardinale B.
    Goldstein, Nathan E.
    Gomez, Jorge E.
    Redd, William H.
    CANCER, 2015, 121 (01) : 150 - 158
  • [49] Delirium in Advanced Cancer Leading to Distress in Patients and Family Caregivers
    Cohen, Marlene Z.
    Pace, Ellen A.
    Kaur, Guddi
    Bruera, Eduardo
    JOURNAL OF PALLIATIVE CARE, 2009, 25 (03) : 164 - 171
  • [50] Quality of life of family caregivers of cancer patients in Singapore and globally
    Lim, Haikel A.
    Tan, Joyce Y. S.
    Chua, Joanne
    Yoong, Russell K. L.
    Lim, Siew Eng
    Kua, Ee Heok
    Mahendran, Rathi
    SINGAPORE MEDICAL JOURNAL, 2017, 58 (05) : 258 - 261