scholarly journals Work Ability Among Long-term Breast Cancer Survivors – Exploring the Role of Social Support in a Nation-wide Study

Author(s):  
kathrine vandraas ◽  
Ragnhild Sørum Falk ◽  
Synne Bøhn ◽  
Cecilie Kiserud ◽  
Hanne Lie ◽  
...  

Abstract work ability (WA) is scarce. We aimed to identify factors, including social support, associated with excellent WA in a nation-wide population of long-term BCS. MethodsAll long-term BCSs (20-65 years) diagnosed with early-stage BC in 2011 or 2012 were identified by the Norwegian Cancer Registry in 2019 and invited to participate in a survey (n=2803). WA was assessed using the Work Ability Index. Factors associated with excellent WA were identified using univariate and multivariate logistic regression analyses, adjusted for sociodemographic-, health- and cancer related variables. ResultsThe final sample consisted of 926 BCSs with a mean age of 56 years at survey. WA was reduced from 8.9 (SD 2.3) at diagnosis to 6.3 (SD 3.1) eight years later. One in three BCSs reported poor WA, and seven out of ten reported that their physical WA was reduced due to cancer. Survivors with excellent WA reported high social support from supervisors and colleagues compared to BCSs with low WA. Additionally, cognitive impairment and fatigue were negatively associated with WA. ConclusionWA remains a significant challenge in long-term BC survivorship, with a substantial proportion of BCSs reporting poor WA eight years after diagnosis. Collegial support appears to be a protective factor for sustained WA, whilst survivors struggling with fatigue and cognitive impairments may represent a particularly vulnerable group for discontinued employment. Increased attention to WA in follow-up care is warranted.

2013 ◽  
Vol 52 (2) ◽  
pp. 423-429 ◽  
Author(s):  
Kathrine Carlsen ◽  
Anette Jung Jensen ◽  
Reiner Rugulies ◽  
Jane Christensen ◽  
Pernille Envold Bidstrup ◽  
...  

2021 ◽  
Author(s):  
Jane Hwang ◽  
Hillary Nicole Peregrina ◽  
Dale Dagar Maglalang ◽  
Grace J. Yoo

Abstract Breast cancer rates among Asian American women are increasing. Despite this, there are limited studies on help-seeking and social support in this population. This paper examines qualitatively the trajectory of help-seeking among Asian American breast cancer survivors. A subsample of Asian American women (n = 52) from a larger study of spirituality, quality of life, mood, and social support was examined. To be eligible for the study, participants needed to: 1) have had a diagnosis of breast cancer (Stage 0, I & II) within the past four years, 2) have completed primary treatment, and 3) speak and/or write English, Cantonese, or Spanish. In-depth interviews and surveys were conducted. Key findings illustrate a trajectory of help-seeking among Asian American women diagnosed with early stage breast cancer. Stages in this trajectory move from keeping their diagnosis personal and not asking for help (Phase 0), maintaining their diagnosis personal but asking for help (Phase 1), and sharing their diagnosis to others and are asking for help (Phase 2). Findings illustrate that seeking support is a process for Asian American with breast cancer, with implications for health and service providers who offer social support to this population.


2006 ◽  
Vol 24 (18_suppl) ◽  
pp. 5024-5024 ◽  
Author(s):  
U. A. Matulonis ◽  
A. Kornblith ◽  
H. Lee ◽  
J. Bryan ◽  
C. Gibson ◽  
...  

5024 Background: Quality of life (QOL) assessments in early stage (stage I and II) ovarian cancer survivors (CS) are limited and have to date not focused on CS who have received adjuvant platinum- and taxane-based chemotherapy (CT). Methods: 55 early stage ovarian patients (pts) were identified from patient logs from the Dana-Farber Cancer Institute and Massachusetts General Hospital. 54 pts. received CT. QOL and long-term medical sequelae were measured in pts who were > 3 years from diagnosis and had no evidence of recurrent cancer. Pts were interviewed by phone, and the following surveys were administered: EORTC QLQ-C30 (EORTC) and QLQ-OV28 (OV-28), MHI-17, CALGB sexual functioning, GOG Neuropathy, FACT Fatigue, Beck’s Hopelessness, Fear of Recurrence (FOR), Dyadic Adjustment Scale (DAS), PCL-C post-traumatic stress disorder (PTSD), Unmet Needs, FACT-Spirituality (FACT-Sp), complementary therapy use, and MOS Social Support (MOS). Results: 55 pts were interviewed (mean age 58 yrs, range 34 to 77 yrs). Mean time between diagnosis and interview was 5.6 yrs. CS reported significantly higher MHI-17 scores than the population norm, and higher MHI-17 scores were associated with better overall QOL (EORTC, r = 0.57, p < 0.0001), increased social support (MOS, r = 0.54, p < 0.0001), and better marital relationships (DAS, r = 0.42, p < 0.001). Sexual problems (1.57 out of 6) and unmet needs (1.5 out of 14) were minimal. FOR was correlated with lowered overall QOL (EORTC, r = −0.63, p < 0.0001), increased abdominal symptoms (OV-28 abdominal scale, r = 0.48, p < 0.0002), increased hopelessness (Beck’s, r = 0.46, p < 0.0005), and increased spirituality (FACT-Sp, r = −0.57, p < 0.0001). CS were using 5.4 complementary therapies for QOL purposes and 5.8 for cancer treatment. Minimal negative socioeconomic impact was observed in CS (0.16 out of 4). However, 12.5% of pts had scores indicative of a diagnosis of PTSD. Conclusions: Long-term QOL follow-up of early stage ovarian cancer survivors demonstrated minimal long-term symptoms, excellent mental health, minimal unmet needs, and minimal socioeconomic impact. No significant financial relationships to disclose.


2017 ◽  
Vol 26 (11) ◽  
pp. 1914-1921 ◽  
Author(s):  
Estrella Durá-Ferrandis ◽  
Jeanne S. Mandelblatt ◽  
Jonathan Clapp ◽  
George Luta ◽  
LeighAnne Faul ◽  
...  

2011 ◽  
Vol 17 (5) ◽  
pp. 627-639 ◽  
Author(s):  
Sophie Lelorain ◽  
Philippe Tessier ◽  
Agnès Florin ◽  
Angélique Bonnaud-Antignac

Cancers ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 1896 ◽  
Author(s):  
Florence Joly ◽  
Marie Lange ◽  
Melanie Dos Santos ◽  
Ines Vaz-Luis ◽  
Antonio Di Meglio

Survivors of early-stage breast cancer may report treatment-related side effects that persist for several years after the end of primary treatment. Among these, fatigue and cognitive disorders are frequent complaints and can negatively impact quality of life. Cancer-related fatigue is a very prevalent and distressing long-term side effect among breast cancer survivors that typically improves after completion of treatment, although many patients report severe fatigue several years post-treatment. Cognitive disorders are also common among survivors of breast cancer, especially if treated with chemotherapy. These symptoms are usually mild-to-moderate and often transient. Cognitive recovery is frequently observed within months or a few years after completion of chemotherapy or endocrine therapy. However, some breast cancer survivors may have persistent cognitive difficulties. Several types of interventions have proved to be beneficial in reducing cancer-related fatigue and cognitive difficulties. Most of these interventions for cancer-related fatigue are thought to be effective by reducing inflammation or disrupting pro-inflammatory circuits. Further studies are needed on cognitive management that has showed promising results. This narrative review summarizes the state of the art regarding long-term fatigue and cognitive disorders in patients with early breast cancer, describing prevalence, impact, pathophysiology, and risk factors, and focusing on available interventions.


2021 ◽  
Vol 53 (01) ◽  
pp. 22-26

Doege D, Thong MS, Koch-Gallenkamp L et al.Age-specific prevalence and determinants of depression in long-term breast cancer survivors compared to female population controls. Cancer Med 2020; 9: 8713–8721. doi:10.1002/cam4.3476


The Breast ◽  
2021 ◽  
Vol 56 ◽  
pp. S80-S81
Author(s):  
P. Santiá ◽  
A. Jansana ◽  
T. Sanz ◽  
I. de la Cura ◽  
M. Padilla-Ruiz ◽  
...  

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