survivorship issues

  • 文章类型: Journal Article
    背景:需要更好地了解接受免疫检查点阻断(ICB)治疗的晚期癌症幸存者的生存相关问题。这项研究的目的是确定与生存有关的问题,专注于心理困扰,认知抱怨,身体后遗症,对家庭动态的影响,和不可切除的护理需求,ICB治疗晚期癌症幸存者。
    方法:在布鲁塞尔大学医院随访的幸存者中进行了半结构化访谈和患者报告的结果测量(PROMs)。我们对半结构化访谈进行了内容分析,并对PROM进行了描述性分析。
    结果:70名癌症幸存者(71.4%)同意在2022年7月至2023年11月期间参加。癌症复发(FCR)的临床恐惧存在于54.3%的癌症幸存者中,18.6%的人认知投诉升高。我们确定了与临床上重要的心理困扰有关的触发因素,如免疫相关的不良事件,疾病的进展/复发,治疗后难以适应生活,和共存的生活压力源,除了持续的身体问题和未满足的心理和营养护理需求。
    结论:我们的结果表明存在持续的心理,物理,和认知问题,并支持FCR常规筛查的需要。确定的与严重心理困扰相关的触发因素可以帮助临床医生及时转诊患者,从而提高生存护理。
    BACKGROUND: There is a need for a better understanding of survivorship-related issues in advanced cancer survivors treated with immune checkpoint blockade (ICB). The purpose of this study was to identify survivorship-related issues, with a focus on psychological distress, cognitive complaints, physical sequelae, impact on family dynamics, and care needs in unresectable, advanced cancer survivors treated with ICB.
    METHODS: Semi-structured interviews and patient-reported outcome measures (PROMs) were conducted in survivors followed up at the University Hospital Brussels. We performed content analysis on the semi-structured interviews and analyzed the PROMs descriptively.
    RESULTS: 70 cancer survivors (71.4%) consented to participate between July 2022 and November 2023. Clinical fear of cancer recurrence (FCR) was present in 54.3% of the cancer survivors, and 18.6% had elevated cognitive complaints. We identified triggers related to clinically important psychological distress, such as immune-related adverse events, the progression/recurrence of disease, difficulties in adjusting to life after treatment, and co-existing life stressors, alongside persistent physical issues and unmet psychological and nutritional care needs.
    CONCLUSIONS: Our results indicate the existence of persistent psychological, physical, and cognitive issues, and support the need for routine screening for FCR. The identified triggers related to severe psychological distress can aid clinicians in timely referring the patient, thereby enhancing survivorship care.
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  • 文章类型: Journal Article
    目的:由于流行病学转变和人类发展指数的变化,亚洲乳腺癌的发病率显着增加。医疗技术的进步改善了预后,从而增加了生存问题。乳腺癌的诊断和治疗效果受患者的文化信仰和社会制度的影响。本范围审查旨在总结亚洲乳腺癌女性的担忧和应对机制,并了解现有文献中的差距。
    方法:我们使用人口概念背景策略进行了范围审查。对MEDLINE(PubMed,WebofScience),CINAHL,Scopus,Embase在亚洲对被诊断患有乳腺癌的女性进行了研究,确定他们的担忧和应对机制,在2011年1月至2021年1月之间发布。纳入研究的数据使用频率和百分比进行报告。
    结果:我们纳入了163项研究,其中大部分(81%)在医院环境中进行。80%的研究报告了情绪和心理问题,其次是46%的人对身体外观和身体形象的关注。社会支持(59%)基于情绪的应对(46%),灵性,以问题为基础的应对(37%)是主要的应对系统。
    结论:映射文献记录了焦虑,抑郁症,对癌症复发的恐惧主导了女性的情感担忧。妇女在社会支持的帮助下应对,积极的重新评估,对上帝和宗教的信仰。照顾者的致敏,包括医疗保健专业人员和家庭成员,针对特定环境的关注和对患者可用支持系统的调查对于加强乳腺癌妇女的康复和应对至关重要。
    OBJECTIVE: The incidence of breast cancer has increased significantly in Asia due to epidemiological transition and changes in human development indices. Advancement in medical technology has improved prognosis with a resultant increase in survivorship issues. The effects of breast cancer diagnosis and treatment are influenced by the patient\'s cultural beliefs and social systems. This scoping review aims to summarise concerns and coping mechanisms of women with breast cancer in Asia and understand gaps in the existing literature.
    METHODS: We performed a scoping review using the population-concept-context strategy. A systematic search of MEDLINE (PubMed, Web of Science), CINAHL, SCOPUS, and Embase was conducted for studies conducted in Asia on women diagnosed with breast cancer, identifying their concerns and coping mechanisms, published between January 2011 and January 2021. Data from included studies were reported using frequencies and percentages.
    RESULTS: We included 163 studies, of which most (81%) were conducted in hospital settings. Emotional and psychological concerns were reported in 80% of studies, followed by physical appearance and body-image concerns in 46%. Social support (59%), emotion-based coping (46%), spirituality, and problem-based coping (37%) were the major coping systems documented.
    CONCLUSIONS: The mapped literature documented that anxiety, depression, and fear of cancer recurrence dominated women\'s emotional concerns. Women coped with the help of social support, positive reappraisal, and faith in God and religion. Sensitization of caregivers, including healthcare professionals and family members, to context-specific concerns and inquiry into the patients\' available support systems is essential in strengthening breast cancer women\'s recovery and coping.
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  • 文章类型: Journal Article
    OBJECTIVE: Quality of life (QOL) in breast cancer survivors is affected by various long term sequelae of breast cancer treatment. The present study was conducted with the objectives to estimate prevalence of various survivorship issues, and to identify those which are most predictive of limitations in QOL after completion of primary therapy.
    UNASSIGNED: This study was conducted in 230 breast cancer survivors (BCs) and 112 controls at an academic centre in Northern India. Assessment of QOL was done by SF-36 and FACT-B questionnaires. Survivorship issues were noted from a checklist of 14 commonly reported symptoms. Main outcome measures were (1) frequencies of survivorship issues and QOL scores among three groups of survivors divided on the basis of time elapsed since treatment (<2, 2-5, and >5 year follow up) (2) Issues most predictive of limitations in QOL, identified by stepwise logistic regression analysis.
    RESULTS: Longer term BCs showed higher QOL scores as compared to those in early follow up. However their QOL scores remained poorer compared to healthy women. The most prevalent survivorship issues were fatigue (60%), restriction of shoulder movement (59.6%), body and joint pain (63.5%), chemotherapy induced cessation of menstruation (73.3%) and loss of sexual desire (60%). Issues which had maximum impact on QOL scores were emotional distress (r = -11.375), fatigue (r = -9.27) and premature menopause (r = -2.085) and its related symptoms.
    CONCLUSIONS: Management of these issues should be priority areas for supportive care, especially in settings with limited resource.
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  • 文章类型: Journal Article
    BACKGROUND: Sexual health is an important quality-of-life issue for many cancer survivors; however, this issue remains inadequately discussed by healthcare providers (HCPs) and patients.
    OBJECTIVE: The purpose of this study is to explore whether clinical oncology HCPs have adequate knowledge and are comfortable addressing sexual health issues, and to explore and describe patients\' attitudes, beliefs, and informational needs regarding sexual health.
    METHODS: A survey was completed by HCPs and three patient focus groups were conducted to learn more about sexual health. Survey data were analyzed using descriptive statistics, and qualitative responses were analyzed using content analysis.
    RESULTS: The majority of survey respondents reported on the importance of discussing sexual concerns with patients, lacked sexual health training, and were uncomfortable discussing sexual health with patients. Focus group participants wanted access to timely information during treatment, online educational resources, and brochures and handouts; involvement of significant others; support from providers, peers, and survivors; and expert consultation.
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  • 文章类型: Journal Article
    BACKGROUND: Sarcopenic obesity, the dual condition of decreased muscle mass with increased fat mass, can affect morbidity, mortality, and quality of life in adult cancer survivors.
    OBJECTIVE: The purpose of this project was to determine the effects of the use of an educational toolbox on advanced practice nurses\' (APNs\') confidence in identifying and managing adult cancer survivors at risk for sarcopenic obesity.
    METHODS: APNs in an outpatient practice who care for adult cancer survivors received an educational toolbox with strategies to identify and manage adult cancer survivors at risk for sarcopenic obesity.
    RESULTS: APNs reported being more confident in their ability to identify adult patients with cancer at risk for sarcopenic obesity and in their ability to manage these patients compared to prior to the intervention. Educational resources provided an effective tool for identifying and managing patients at risk for sarcopenic obesity.
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  • 文章类型: Journal Article
    BACKGROUND: Little is known about fertility outcomes after fertility sparing surgery (FSS) for localized ovarian cancers.
    METHODS: A random sample of 783 women treated for ovarian cancer were identified from the California Cancer Registry for survey (age 18-40 years at diagnosis; diagnosed from 1993-2007). We evaluated outcomes including post-treatment amenorrhea, infertility, early menopause (age <45), and disease recurrence. Logistic regression was used to determine the probability of amenorrhea, infertility, and recurrence. Censored data methods were used to determine the probability of early menopause.
    RESULTS: A total of 382 women replied. One hundred and sixteen and 266 completed our survey. Two hundred and forty-five reported treatment with potential to impact fertility (i.e., systemic chemotherapy ± radiation/surgery to the abdomen/pelvis). A total of 125 had disease/stage eligible for FSS and 82 (66%) underwent FSS. While many who attempted conception did conceive, 32% did not. Younger age at diagnosis was associated with higher rates of early menopause (P < 0.001) after FSS. Recurrence rates for those undergoing FSS were 8-10%, while none of the women who underwent non-FSS surgery had a recurrence.
    CONCLUSIONS: FSS maintains an ability to conceive for most patients. However, after FSS, there may be risks of infertility, early menopause with earlier age of treatment, and increased probability of disease recurrence.
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