unmet needs

未满足的需求
  • 文章类型: Journal Article
    排卵障碍是育龄妇女异常子宫出血的常见原因。国际妇产科联合会目前提供了排卵障碍的因果分类系统,但没有提供明确的治疗建议。治疗实践仍然存在地区差异,经常受到机构和保险法规以及文化和宗教习俗的影响。一个专家小组评估了当前排卵障碍管理指南中的差距,并讨论了解决这些未满足需求的潜在策略。主要差距包括缺乏关于雌激素和孕激素联合用药与单独使用孕激素的有效性的共识,缺乏关于不同激素分子相对有效性的证据,缺乏关于最佳治疗持续时间的数据,以及对最佳治疗顺序的指导有限。建议包括制定序贯治疗方法和制定解决所有国家共同的治疗方案的临床指南,然后可以适应当地的做法。还一致认为,目前的指南没有解决某些患者群体的独特临床挑战。小组讨论了患者群体的复杂性和多样性如何使单一疾病管理算法的发展变得不可能;然而,一个简化的,决策点层次结构可能有助于指导治疗选择。总的来说,专家小组强调,更多的倡导采用量身定制的方法治疗排卵障碍,包括更广泛地考虑非雌激素疗法,可以帮助改善因卵巢功能异常子宫出血的患者的护理。
    Ovulatory disorders are a common cause of abnormal uterine bleeding in women of reproductive age. The International Federation of Gynecology and Obstetrics currently offers a causal classification system for ovulatory disorders but does not provide clear management recommendations. There remains regional disparity in treatment practices, often influenced by institutional and insurance regulations as well as cultural and religious practices. A panel of experts evaluated current gaps in ovulatory disorder management guidelines and discussed potential strategies for addressing these unmet needs. Key gaps included a lack in consensus about the effectiveness of combined estrogen and progestogen versus progestogen alone, a paucity of evidence regarding the relative effectiveness of distinct hormonal molecules, a lack of data regarding optimal treatment duration, and limited guidance on optimal sequencing of treatment. Recommendations included development of a sequential treatment-line approach and development of a clinical guide addressing treatment scenarios common to all countries, which can then be adapted to local practices. It was also agreed that current guidelines do not address the unique clinical challenges of certain patient groups. The panel discussed how the complexity and variety of patient groups made the development of one single disease management algorithm unlikely; however, a simplified, decision-point hierarchy could potentially help direct therapeutic choices. Overall, the panel highlighted that greater advocacy for a tailored approach to the treatment of ovulatory disorders, including wider consideration of non-estrogen therapies, could help to improve care for people living with abnormal uterine bleeding due to ovarian dysfunction.
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  • 文章类型: Journal Article
    目标:为了支持结直肠癌夫妇应对癌症,我们开发了一个基于夫妇的未满足的支持性护理需求干预计划,以支持性护理需求框架为指导,并检查了可行性,可接受性,以及未满足的支持性护理需求计划的初始效果。
    方法:在中国结直肠癌夫妇中进行了干预前后研究的设计。干预措施通过面对面和电话干预相结合的方式分五次进行。通过招聘和保留率衡量计划的可行性,并通过定量和定性干预后计划评估来测试计划的可接受性。完整的数据(N=20对)用于计算效果大小以评估初始干预效果。
    结果:在招募率(66.7%)和保留率(83.3%)方面,有证据表明干预计划是可行的。参与者对该计划的满意度也证明了其可接受性。干预措施(Cohen=0.15-0.56)在改善未满足的支持性护理需求和结直肠癌夫妇的大多数癌症适应结果方面具有小-中等效应大小。验证程序的初始效果。
    结论:未满足的支持性护理需求计划是可行的,可接受,并初步有效地支持中国结直肠癌夫妇改善未满足的支持性护理需求和癌症适应性,正如这项研究所提供的。
    OBJECTIVE: To support colorectal cancer couples cope with cancer, we developed a couple-based unmet supportive care needs intervention program guided by the Supportive Care Needs Framework and examined the feasibility, acceptability, and initial effects of the unmet supportive care needs program.
    METHODS: The design of a pre-and post-intervention study was conducted among Chinese colorectal cancer couples. The intervention was delivered in five sessions through in-person and telephone interventions combined. To measure program feasibility through recruitment and retention rates, and to test program acceptability through quantitative and qualitative post-intervention program assessments. The complete data (N = 20 pairs) were used to calculate effect sizes to assess the initial intervention effect.
    RESULTS: There was evidence of the feasibility of the intervention program in terms of recruitment (66.7%) and retention (83.3%) rates. Participants\' satisfaction with the program also attested to its acceptability. The intervention (Cohen\'s = 0.15-0.56) had a small-moderate effect size in improving unmet supportive care needs and most cancer-adapted outcomes for colorectal cancer couples, validating the initial effect of the program.
    CONCLUSIONS: The unmet supportive care needs program is feasible, acceptable, and preliminarily effective in supporting Chinese colorectal cancer couples to improve unmet supportive care needs and cancer adaptability, as provided by this study.
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  • 文章类型: Journal Article
    目的:治疗完成后,结直肠癌(CRC)幸存者经历各种未满足的需求。这篇综述旨在综合CRC幸存者治疗后未满足的需求,并确定人口统计学,疾病或治疗相关,医疗保健相关,和与未满足的需求相关的社会心理因素。
    方法:从五个电子数据库中系统地检索了关注CRC幸存者治疗后未满足需求的英文或中文文章,其中包括CINAHL,PubMed,Embase,PsycINFO,和中国学术期刊全文数据库,从数据库的推出到2023年7月。进一步筛选了后续文章的参考文献列表。
    结果:根据支持性护理框架,从50份手稿中提取的136个个人需求被分为9个领域。CRC幸存者确定的前四个未满足的需求是对癌症复发的恐惧。关于在家管理疾病和副作用的信息,情感或心理上的支持和安慰,帮助解决性问题。手术后,CRC幸存者在身体上表现出强烈的需求,心理,和信息领域。在1年内完成治疗的幸存者比完成1-3年的幸存者有更多样化的需求。在年轻的儿童权利公约幸存者中,未满足的需求可能更大,女性,受过更多的教育,未婚。此外,更大的未满足的需求与痛苦有关,焦虑,抑郁症,更糟糕的生活质量。
    结论:尽管治疗后CRC幸存者经历了不同的需求,主要关注癌症复发的恐惧,信息,心理支持,注意到性需求。未来的研究应进一步探讨特定治疗后和不同治疗时期CRC幸存者的需求。
    OBJECTIVE: Following treatment completion, colorectal cancer (CRC) survivors experience various unmet needs. This review aims to synthesize the unmet needs of CRC survivors after treatment and to identify demographic, disease or treatment-related, healthcare-related, and psychosocial factors correlated with unmet needs.
    METHODS: English or Chinese articles that focused on CRC survivors\' post-treatment unmet needs were systematically searched from the five electronic databases, which included CINAHL, PubMed, Embase, PsycINFO, and the China Academic Journal Full-text Database, from the launch of databases to July 2023. The reference lists of the subsequent articles were further screened.
    RESULTS: 136 individual needs extracted from 50 manuscripts were classified into nine domains based on the Supportive Care Framework. The top four unmet needs identified by CRC survivors were assistance with fears of cancer recurrence, information about managing illness and side effects at home, emotional or psychological support and reassurance, and help with sexuality problems. Following surgery, CRC survivors showed strong demand in the physical, psychological, and information domains. Survivors completed treatment within 1-year had more diverse needs than those who completed 1-3 years. Unmet needs may be greater among CRC survivors who were young, female, more educated, and unmarried. Furthermore, greater unmet needs were associated with distress, anxiety, depression, and worse quality of life.
    CONCLUSIONS: Despite diverse needs experienced by post-treatment CRC survivors, a predominant focus on fears of cancer recurrence, information, psychological support, and sexuality needs is noted. Future studies should further explore the needs of CRC survivors after specific treatment and in different post-treatment periods.
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  • 文章类型: Journal Article
    目的:未满足的支持治疗需求与抑郁和焦虑等心理症状相关。然而,到目前为止,很少有研究探讨未满足需求的保护性心理因素。因此,本研究旨在探讨自我同情对中国癌症患者未满足需求的保护作用,并探讨自我同情在治疗期间对这些需求的预测作用.
    方法:在西安陕西省肿瘤医院进行了一项纵向研究,中国。共有153名异质性癌症患者在首次诊断(T1)后进行了评估,在医疗开始(T2)和结束(T3)。使用分层线性回归分析来检查研究问题。
    结果:横断面回归分析显示,T1时的自我同情与T1时的心理需求显著相关。T1时的消极自我同情与总的未满足需求显着相关,心理需求,卫生系统,信息和性需求。纵向回归分析表明,T1时的自我同情显著预测了总的未满足的需求;T2时的卫生系统和信息(HSI)需求,T3时的心理需求和T1时的消极自我同情显著预测了总的未满足的需求,HSI需要,身体需要,当控制T1未满足的需求时,患者在T2的护理需求。积极的自我同情并不能预测未满足的需求。
    结论:自我同情可能是癌症患者未满足需求的保护因素。未来的干预研究应侧重于提高癌症患者的整体自我同情水平和降低患者的消极自我同情水平,以减少患者的未满足需求。
    OBJECTIVE: Unmet supportive care needs are associated with psychological symptoms such as depression and anxiety. However, so far, few studies have explored the protective psychological factors of unmet needs. Therefore, this study intends to explore the protective effect of self-compassion on unmet needs of Chinese cancer patients and to examine the predictive role of self-compassion on these needs during treatment.
    METHODS: A longitudinal study was performed at Shaanxi Provincial Cancer Hospital in Xi\'an, China. A total of 153 heterogeneous cancer patients were assessed after the first diagnosis (T1), at the beginning (T2) and end (T3) of medical treatment. Hierarchical linear regression analyses were used to examine the research questions.
    RESULTS: Cross-sectional regression analyses showed that self-compassion at T1 was significantly related to psychological needs at T1. Negative self-compassion at T1 was significantly related to total unmet needs, psychological needs, health system, and information and sexual needs. Longitudinal regression analyses showed that self-compassion at T1 significantly predicted total unmet needs; health system and information (HSI) needs at T2, psychological needs at T3, and negative self-compassion at T1 significantly predicted total unmet needs, HSI needs, physical needs, and patient care needs at T2 when controlling for unmet needs at T1. Positive self-compassion was not a predictor of unmet needs.
    CONCLUSIONS: Self-compassion can be a protective factor of unmet needs in cancer patients. Future intervention studies should focus on improving the overall level of self-compassion and reducing the level of negative self-compassion in cancer patients to reduce patients\' unmet needs.
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  • 文章类型: Journal Article
    背景:了解癌症患者对化疗相关症状管理的未满足需求将有助于临床医生制定量身定制的干预计划。对于肺癌和结直肠癌患者的感知沟通效能与未满足的症状管理护理需求之间的关联知之甚少。
    目的:研究肺癌和结直肠癌患者在症状管理方面未满足的护理需求及其与感知沟通效能的关系。
    方法:于2020年7月至11月在中国一家三级医院进行了横断面调查。方便样本的203例肺癌和结直肠癌化疗患者完成调查问卷,包括MD安德森症状量表和患者-医师互动量表中的感知功效。
    结果:大约43%的参与者至少有一种症状的需求未得到满足。据报道,疲劳是发生率最高的症状(66%)。对支持性护理的需求最高(36%),以及未满足需求的患病率最高(19%)。低水平的感知沟通效能独立预测了参与者对症状管理的未满足需求(β=-0.13,p=0.011)。
    结论:本研究强调了引入临床评估工具和指南以解决肺癌和结直肠癌患者的疲劳和其他化疗引起的症状的必要性。旨在积极吸引癌症患者表达其需求并加强其沟通功效的临床计划也是必要的。
    BACKGROUND: Understanding cancer patients\' unmet needs for chemotherapy-related symptom management will assist clinicians in developing tailored intervention programs. Little is known about the association between perceived communication efficacy and unmet care needs for symptom management in patients with lung and colorectal cancer.
    OBJECTIVE: To examine the unmet care needs for symptom management of patients with lung and colorectal cancer and their association with perceived communication efficacy.
    METHODS: A cross-sectional survey was conducted in a tertiary hospital in China from July to November 2020. A convenience sample of 203 patients with lung and colorectal cancer undergoing chemotherapy completed survey questionnaires, including the MD Anderson Symptom Inventory Scale and the Perceived Efficacy in Patient‒Physician Interactions Scale.
    RESULTS: Approximately 43% of participants had at least one symptom with unmet needs. Fatigue was reported as the symptom with the highest occurrence (66%), the highest demand for supportive care (36%), and the highest prevalence of unmet needs (19%). Low levels of perceived communication efficacy independently predicted participants\' unmet needs for symptom management (β=-0.13, p = 0.011).
    CONCLUSIONS: This study highlights the necessity of introducing clinical assessment tools and guidelines to address fatigue and other chemotherapy-induced symptoms in patients with lung and colorectal cancer. Clinical programs designed to actively engage cancer patients to voice their needs and strengthen their communication efficacy are also warranted.
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  • 文章类型: Journal Article
    目的:建立一个支持性护理框架,以解决乳腺癌幸存者未满足的需求,为医疗保健提供者评估和管理这些需求提供实用指导,最终提高乳腺癌幸存者的健康结果和生活质量。
    方法:我们进行了两轮Delphi调查,以收集有关乳腺癌幸存者未满足需求的支持性护理框架的专家意见。
    方法:通过文献检索和专家小组讨论,初步框架确定和调查问卷创建。其中包括来自护理实践的15名专家,临床医学,采用德尔菲调查法进行护理管理和护理教育。建立共识,进行了两轮德尔福民意调查,使用基于平均值(≥4.0)的标准,变异系数(CV<0.25)和总分百分比(≥20%)。
    结果:专家达成共识,导致六个护理模块,和28个护理条目:肿瘤检测支持(三个护理条目),抗肿瘤治疗并发症的管理(七个护理条目),健康生活方式管理(五个护理条目),性和生育支持(四个护理条目),社会心理支持(四个护理条目)和资源和联系支持(五个护理条目)。
    结论:为了解决乳腺癌幸存者未满足的需求,制定了一个支持框架,以积极改善他们的健康结果。然而,需要使用移动设备或人工智能进行进一步的改进和可行性测试。
    这个开创性的框架优先解决未满足的需求,并使医疗保健提供者能够有效地评估和管理这些需求,促进旨在改善乳腺癌幸存者福祉的计划的实施。
    本研究以德尔菲研究(CREDES)(姑息医学,31(8)、684,2017)。
    没有患者或公共捐款。
    Delphi研究方法不需要注册。
    OBJECTIVE: To establish a supportive care framework for addressing unmet needs among breast cancer survivors, providing practical guidance for healthcare providers to assess and manage these needs, ultimately enhancing the health outcomes and quality of life of breast cancer survivors.
    METHODS: We conducted a two-round Delphi survey to gather expert opinions regarding the unmet needs supportive care framework for breast cancer survivors.
    METHODS: Initial framework identification and inquiry questionnaire creation was achieved via literature search and expert group discussions, which included 15 experts from nursing practice, clinical medicine, nursing management and nursing education was conducted using a Delphi survey. To establish consensus, a two-round Delphi poll was done, using criteria based on the mean (≥4.0), coefficient of variation (CV < 0.25) and percentage for entire score (≥20%).
    RESULTS: Experts reached a consensus, leading to six care modules, and 28 care entries: Tumour Detection Support (three care entries), Management of Complications of Antitumor Therapy (seven care entries), Healthy Lifestyle Management (five care entries), Sexual and Fertility Support (four care entries), Psychosocial Support (four care entries) and Resource and Linkage Support (five care entries).
    CONCLUSIONS: To address breast cancer survivors\' unmet needs, a supportive framework was developed to actively enhance their health outcomes. However, further refinement and feasibility testing using mobile devices or artificial intelligence are required.
    UNASSIGNED: This pioneering framework prioritises addressing unmet needs and equips healthcare providers to assess and manage these needs effectively, facilitating the implementation of programs aimed at improving the well-being of breast cancer survivors.
    UNASSIGNED: This study was guided by a modified guideline for the Conducting and Reporting of Delphi Studies (CREDES) (Palliative Medicine, 31(8), 684, 2017).
    UNASSIGNED: No Patient or Public Contribution.
    UNASSIGNED: The Delphi study methodology does not require registration.
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  • 文章类型: Journal Article
    尿路上皮癌(UC)是全球第10大最常见的癌症,男性患病率几乎高4倍。高龄是尿路上皮癌发生的主要危险因素,吸烟,砷污染,接触致癌物。转移性尿路上皮癌(mUC)的总体预后较差,5年总体生存率仅<5%。护理标准包括铂类化疗,但反应往往无法持续。成立了一个工作组,目的是讨论有关感兴趣的泌尿生殖系统肿瘤的最新临床数据,该工作组由拉丁美洲的专家组成。新兴亚洲(中国除外,Japan,和韩国),非洲,和中东(被称为新兴市场或新兴市场)。各地区在死亡率和发病率分布不均方面存在明显差异。流行病学数据缺乏和/或不足,治疗,以及EM中的结果。缺乏登记处会影响医疗保健决策,该地区较低的发病率可能无法反映真正的疾病负担。通过了解mUC的当前疾病负担和治疗方法,并确定与管理相关的差距和挑战,可以改善mUC的治疗结果。因此,本文进行了文献综述,总结了mUC跨EM的当前疾病负担和治疗方法.该综述还强调了EM中mUC管理未满足的需求,并提出了改善现状的方法,以更好地为患者服务。
    Urothelial carcinoma (UC) is the 10th most common cancer globally with an almost 4 times higher prevalence in men. The main risk factors for development of urothelial carcinoma are advanced age, smoking, arsenic contamination, exposure to carcinogens. Metastatic urothelial carcinoma (mUC) has overall poor prognosis with a 5-year overall survival rate of only < 5%. The standard of care comprises of platinum-based chemotherapy, but the responses are often not sustained. A working group was established with an objective to discuss the most recent clinical data on the genitourinary tumors of interest and comprised of experts across Latin America, Emerging Asia (except China, Japan, and South Korea), Africa, and the Middle East (known as Emerging Markets or EM). There is an evident disparity in terms of uneven mortality and incidence rate distribution among various regions. There is a lack and/or insufficient data on epidemiology, treatment, and outcomes in the EM. The lack of registries impacts the healthcare decisions and the lower incidence from the region might not be reflective of the true disease burden. The treatment outcomes of mUC can be improved by understanding the current disease burden and treatment approach of mUC and identifying the gaps and challenges associated with management. Hence, a literature review was developed to summarize the current disease burden and treatment approach of mUC across EM. The review also highlights the unmet needs for mUC management in EM and suggests a way forward to improve the current situation in order to better serve the patients.
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  • 文章类型: Journal Article
    中国人口老龄化导致残疾老年人数量大幅增加。这些人在获得适当的日常生活活动(ADL)援助方面面临巨大挑战。该人群中未满足的ADL需求可能会导致严重的健康后果,并使本已负担沉重的护理系统紧张。这项研究旨在使用六种机器学习方法来确定影响年龄最大的老年人(80岁及以上)未满足的ADL需求的因素。
    来自中国纵向健康长寿调查(CLHLS)2017-2018年数据,我们采用了6种机器学习方法来预测年龄最大的老年残疾患者中未满足的ADL需求.使用Shapley加法扩张(SHAP)探索了各种因素对未满足的ADL需求的预测影响。
    随机森林模型在测试的六种机器学习方法中显示出最高的预测精度。基于随机森林模型的SHAP分析显示,户籍等因素,残疾班级,经济排名,自我评估的健康,照顾者的意愿,感知控制,经济满意度,养老金,教育程度,对儿童的经济支持,生活安排,儿童数量,主要看护者在年龄最大的老年人残疾患者未满足的ADL需求中发挥了重要作用.
    我们的研究强调了社会经济因素的重要性(例如,户籍和经济排名),健康状况(例如,残疾类别和自测健康),和护理关系因素(例如,照顾者意愿和感知控制)减少中国年龄最大的残疾老人未满足的ADL需求。旨在弥合城乡鸿沟的政府干预措施,针对健康状况恶化的群体,和提高照顾者的技能对于确保这一弱势群体的福祉至关重要。这些发现可以为政策决策和干预措施提供信息,以更好地解决年龄最大的残疾老人未满足的ADL需求。
    UNASSIGNED: The ageing population in China has led to a significant increase in the number of older persons with disabilities. These individuals face substantial challenges in accessing adequate activities of daily living (ADL) assistance. Unmet ADL needs among this population can result in severe health consequences and strain an already burdened care system. This study aims to identify the factors influencing unmet ADL needs of the oldest old (those aged 80 and above) with disabilities using six machine learning methods.
    UNASSIGNED: Drawing from the Chinese Longitudinal Healthy Longevity Survey (CLHLS) 2017-2018 data, we employed six machine learning methods to predict unmet ADL needs among the oldest old with disabilities. The predictive effects of various factors on unmet ADL needs were explored using Shapley Additive exPlanations (SHAP).
    UNASSIGNED: The Random Forest model showed the highest prediction accuracy among the six machine learning methods tested. SHAP analysis based on the Random Forest model revealed that factors such as household registration, disability class, economic rank, self-rated health, caregiver willingness, perceived control, economic satisfaction, pension, educational attainment, financial support given to children, living arrangement, number of children, and primary caregiver played significant roles in the unmet ADL needs of the oldest old with disabilities.
    UNASSIGNED: Our study highlights the importance of socioeconomic factors (e.g., household registration and economic rank), health status (e.g., disability class and self-rated health), and caregiving relationship factors (e.g., caregiver willingness and perceived control) in reducing unmet ADL needs among the oldest old with disabilities in China. Government interventions aimed at bridging the urban-rural divide, targeting groups with deteriorating health status, and enhancing caregiver skills are essential for ensuring the well-being of this vulnerable population. These findings can inform policy decisions and interventions to better address the unmet ADL needs among the oldest old with disabilities.
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  • 文章类型: Journal Article
    这项研究调查了中国老年人对家庭和社区服务(HCBS)的未满足需求的轨迹是否与生活满意度相关,以及这种联系是否受到心理弹性的调节。数据来自中国纵向健康长寿调查(CLHLS)的五次浪潮(2005-2018年)。潜在类别增长分析揭示了感知到的未满足的HCBS需求的三个不同轨迹:“增加”(n=977,36.24%),“持久”(n=570,21.14%),和“递减”(n=1149,42.62%)。多元回归估计显示,增加组的生活满意度较低,这种联系是由心理弹性调节的,尤其是对于男性的老年人,生活在农村,和最古老的老。结果表明,累积暴露于未满足的HCBS需求的不平等可能进一步导致生活满意度的不平等加剧。应考虑采取旨在最大程度地减少HCBS的供应-需求差距和增强个人韧性的干预措施,以改善老年人的生活满意度。
    This study examined whether trajectories of perceived unmet needs for Home and Community-Based Services (HCBS) were associated with life satisfaction among Chinese older adults and whether the association was moderated by psychological resilience. Data came from five waves (2005-2018) of the Chinese Longitudinal Healthy Longevity Survey (CLHLS). Latent class growth analysis revealed three distinct trajectories of perceived unmet HCBS needs: \"increasing\" (n = 977, 36.24%), \"persistent\" (n = 570, 21.14%), and \"decreasing\" (n = 1149, 42.62%). Multiple regression estimates showed that the increasing group was associated with lower life satisfaction, and the association was moderated by psychological resilience, especially for older adults who were male, living in rural, and oldest-old. Results indicate that inequalities in cumulative exposure to perceived unmet HCBS needs may further lead to increasing inequalities in life satisfaction. Interventions focused on minimizing the provision-need gap of HCBS and enhancing personal resilience should be considered to improve the life satisfaction of older adults.
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  • 文章类型: Journal Article
    目的:本研究旨在描述接受免疫检查点抑制剂治疗的癌症患者的综合需求水平,探索综合需求与人口因素之间的关系,并考察综合需求与治疗变量之间的关系。
    方法:采用横断面描述性研究设计。2021年9月至2022年7月,在浙江省三级教学医院采用便利抽样方法,招募了194例接受免疫检查点抑制剂治疗的癌症患者,中国。癌症患者综合需求评估工具(CNAT)和评估人口统计学和临床特征的问卷用于收集数据。
    结果:接受免疫检查点抑制剂治疗的癌症患者的平均综合需求评分为39.2±17.2。患者报告了高水平的医疗护理需求,知识信息需求,医院设施需求和护理需求,但宗教精神支持需求水平较低,心理情感需求,实际支持需求,和身体症状需要。多元逐步线性回归显示,年龄,主要照顾者,癌症类型,免疫治疗疗程数和免疫相关不良事件(irAEs)的发生是影响ICIs治疗癌症患者综合需求的主要因素(p<0.05)。
    结论:年龄,主要照顾者,癌症类型,免疫治疗疗程数和irAE的发生是影响接受免疫检查点抑制剂治疗的癌症患者的综合未满足需求的重要因素。护士应根据患者的不同情况进行有针对性的干预,以提高护理质量。
    OBJECTIVE: This study aimed to describe the level of comprehensive needs among cancer patients treated with immune checkpoint inhibitors, to explore the relationship between comprehensive needs and demographic factors, and to examine the relationship between comprehensive needs and treatment variables.
    METHODS: A cross-sectional descriptive study design was adopted. From September 2021 to July 2022, 194 cancer patients treated with immune checkpoint inhibitors were recruited using a convenience sampling method in tertiary teaching hospitals in Zhejiang Province, China. The Comprehensive Needs Assessment Tool for Cancer Patients (CNAT) and questionnaires to assess demographic and clinical characteristics were used to collect data.
    RESULTS: The average comprehensive needs score for cancer patients treated with immune checkpoint inhibitors was 39.2 ± 17.2. Patients reported high levels of medical care needs, knowledge information needs, hospital facilities needs and nursing needs but low levels of religious spiritual support needs, psychoemotional needs, actual support needs, and physical symptom needs. Multiple stepwise linear regression showed that age, primary caregivers, cancer type, number of immunotherapy courses and the occurrence of immune-related adverse events (irAEs) were the main factors affecting the comprehensive needs of cancer patients treated with ICIs (p < 0.05).
    CONCLUSIONS: Age, primary caregivers, cancer type, number of immunotherapy treatment courses and the occurrence of irAEs are important factors affecting the comprehensive unmet needs of cancer patients treated with immune checkpoint inhibitors. Nurses should perform targeted interventions according to the different situations of patients to improve the quality of care.
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