Common patient-reported sources of cancer-related distress in adults with cancer: A systematic review

被引:4
|
作者
Stevens, Jennifer M. [1 ]
Montgomery, Kathleen [1 ]
Miller, Megan [1 ]
Saeidzadeh, Seyedehtanaz [2 ]
Kwekkeboom, Kristine L. [1 ]
机构
[1] Univ Wisconsin Madison, Sch Nursing, 701 Highland Ave,Suite 3134, Madison, WI 53705 USA
[2] Edmonton Clin Hlth Acad, Edmonton, AB, Canada
来源
CANCER MEDICINE | 2024年 / 13卷 / 13期
关键词
cancer-related distress; concerns; problem list; sources contributing to cancer-related distress; THERMOMETER PROBLEM LIST; QUALITY-OF-LIFE; PSYCHOLOGICAL DISTRESS; PREVALENCE; WOMEN; ASSOCIATION; PREDICTORS; MANAGEMENT; ANXIETY; LEVEL;
D O I
10.1002/cam4.7450
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundCancer-related distress (CRD) is widely experienced by people with cancer and is associated with poor outcomes. CRD screening is a recommended practice; however, CRD remains under-treated due to limited resources targeting unique sources (problems) contributing to CRD. Understanding which sources of CRD are most commonly reported will allow allocation of resources including equipping healthcare providers for intervention.MethodsWe conducted a systematic review to describe the frequency of patient-reported sources of CRD and to identify relationships with CRD severity, demographics, and clinical characteristics. We included empirical studies that screened adults with cancer using the NCCN or similar problem list. Most and least common sources of CRD were identified using weighted proportions computed across studies. Relationships between sources of CRD and CRD severity, demographics, and clinical characteristics were summarized narratively.ResultsForty-eight studies were included. The most frequent sources of CRD were worry (55%), fatigue (54%), fears (45%), sadness (44%), pain (41%), and sleep disturbance (40%). Having enough food (0%), substance abuse (3%), childbearing ability (5%), fevers (5%), and spiritual concerns (5%) were infrequently reported. Sources of CRD were related to CRD severity, sex, age, race, marital status, income, education, rurality, treatment type, cancer grade, performance status, and timing of screening.ConclusionsSources of CRD were most frequently emotional and physical, and resources should be targeted to these sources. Relationships between sources of CRD and demographic and clinical variables may suggest profiles of patient subgroups that share similar sources of CRD. Further investigation is necessary to direct intervention development and testing. imageWe identified the most and least common causes of distress reported by people living with cancer. People reported worry, fatigue, sleep disturbance, fears, and sadness were the most common sources of their distress. Having enough food, substance abuse, ability to have children, fevers, and spiritual concerns were rarely reported as causing distress. Cancer care teams can use this information to ensure they ask patients about common sources of distress and to develop better ways to support people with cancer if distress becomes a problem.
引用
收藏
页数:30
相关论文
共 50 条
  • [41] Patient-Reported Upper Extremity Outcome Measures Used in Breast Cancer Survivors: A Systematic Review
    Harrington, Shana
    Michener, Lori A.
    Kendig, Tiffany
    Miale, Susan
    George, Steven Z.
    ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION, 2014, 95 (01): : 153 - 162
  • [42] Patient-reported depression measures in cancer: a meta-review
    Wakefield, Claire E.
    Butow, Phyllis N.
    Aaronson, Neil A.
    Hack, Thomas F.
    Hulbert-Williams, Nicholas J.
    Jacobsen, Paul B.
    LANCET PSYCHIATRY, 2015, 2 (07): : 635 - 647
  • [43] Use of patient-reported controls for secular trends to study disparities in cancer-related job loss
    Blinder, Victoria S.
    Eberle, Carolyn E.
    Tran, Christina
    Bao, Ting
    Malik, Manmeet
    Jung, Gabriel
    Hwang, Caroline
    Kampel, Lewis
    Patil, Sujata
    Gany, Francesca M.
    JOURNAL OF CANCER SURVIVORSHIP, 2021, 15 (05) : 685 - 695
  • [44] Patient-reported outcome measures (PROMs) in the management of lung cancer: A systematic review
    Ben Bouazza, Youssef
    Chiairi, Ibrahim
    El Kharbouchi, Ouiam
    De Backer, Lesley
    Vanhoutte, Greetje
    Janssens, Annelies
    Van Meerbeeck, Jan P.
    LUNG CANCER, 2017, 113 : 140 - 151
  • [45] A systematic review of patient-reported outcome measures in head and neck cancer surgery
    Pusic, Andrea
    Liu, Jeffrey C.
    Chen, Constance M.
    Cano, Stefan
    Davidge, Kristen
    Klassen, Anne
    Branski, Ryan
    Patel, Snehal
    Kraus, Dennis
    Cordeiro, Peter G.
    OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2007, 136 (04) : 525 - 535
  • [46] Patient-reported outcomes as predictors of survival in patients with bowel cancer: a systematic review
    Claudia Rutherford
    Rachel Campbell
    Kate White
    Madeleine King
    Quality of Life Research, 2019, 28 : 2871 - 2887
  • [47] A systematic review of patient-reported outcome measures for advanced skin cancer patients
    Reinhardt, Myrna Eliann
    Sun, Tiffany
    Pan, Catherina X.
    Schmults, Chrysalyne D.
    Lee, Erica H.
    Waldman, Abigail B.
    ARCHIVES OF DERMATOLOGICAL RESEARCH, 2023, 315 (06) : 1473 - 1480
  • [48] Predicting general and cancer-related distress in women with newly diagnosed breast cancer
    Gibbons, Andrea
    Groarke, AnnMarie
    Sweeney, Karl
    BMC CANCER, 2016, 16
  • [49] Patient-reported outcomes for keloids: a systematic review
    Tan, Andrea
    Glass, Donald A., II
    GIORNALE ITALIANO DI DERMATOLOGIA E VENEREOLOGIA, 2019, 154 (02): : 148 - 165
  • [50] Assessing Patient-reported Quality of Life Outcomes in Vulva Cancer Patients: A Systematic Literature Review
    Froeding, Ligita Paskeviciute
    Greimel, Elfriede
    Lanceley, Anne
    Oberguggenberger, Anne
    Schmalz, Claudia
    Radisic, Vesna Bjelic
    Nordin, Andy
    Galalaei, Razvan
    Kuljanic, Karin
    Vistad, Ingvild
    Schnack, Tine Henrichsen
    Jensen, Pernille Tine
    INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2018, 28 (04) : 808 - 817