Patient Perceptions of Physical Rehabilitation and Its Method of Delivery for a Variety of Adverse Physical Effects following Breast Cancer Surgery: An Observational Mixed Methods Study

IF 1.8 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES European Journal of Cancer Care Pub Date : 2024-06-20 DOI:10.1155/2024/6612611
Deirdre E. McGhee, Anne T. McMahon, Julie R. Steele
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Abstract

Purpose. To investigate patient perceptions of physical rehabilitation received for various adverse physical effects following breast cancer surgery and the content and delivery methods of the physical rehabilitation received. Methods. Cross-sectional study of 509 Australian women living with breast cancer (n = 178 (35%) (Breast Conserving Surgery (BCS)), n = 168 (33%) (Mastectomy (MAST)), and n = 163 (32%) (Breast Reconstruction Surgery (BRS)). Retrospective, online survey investigated the physical rehabilitation received after surgery/treatment. The survey explored the respondents′ perceptions (open response) and satisfaction levels with the physical rehabilitation received and its content and delivery method (closed responses). Perceptions were analyzed using a thematic analysis; satisfaction levels and delivery methods for each adverse physical effect were tabulated. Results. Major perceptions: (i) unaware of and unprepared for adverse physical effects, (ii) unsuitable information delivery, and (iii) insufficient follow-up from health professionals. Physical rehabilitation content focused on shoulder issues and lymphedema; less than half of respondents received any information about scars, torso, and donor site issues or physical discomfort disturbing sleep. The proportion that received each delivery method varied for each adverse physical effect. Pamphlets and verbal instruction were the most common delivery methods and sessions with health professionals where issues were physically assessed, checked, or progressed the least common. Satisfaction levels varied for each adverse physical effect; all were less than 50%. Conclusion. Women perceived their physical rehabilitation did not prepare them for the adverse physical effects they experienced, the method and timing of delivery did not meet their needs at various stages of recovery, and the follow-up was insufficient. Quantitative data on the content and delivery method support these perceptions. Explanations of why these perceptions occurred and recommendations to improve physical rehabilitation through greater use of patient-related outcome measures and spreading limited physical rehabilitation resources using a three-level model of care are recommended. Although many women recover from breast cancer, improved physical rehabilitation could enable women to manage any immediate or long-term side effects of their breast cancer surgery and treatment.

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患者对乳腺癌手术后各种不良身体影响的物理康复及其实施方法的看法:观察性混合方法研究
目的调查患者对乳腺癌手术后各种不良身体反应所接受的物理康复治疗的看法,以及所接受的物理康复治疗的内容和方法。方法:横断面研究对 509 名患有乳腺癌的澳大利亚妇女进行横断面研究(n = 178(35%)(保乳手术 (BCS))、n = 168(33%)(乳房切除术 (MAST))和 n = 163(32%)(乳房重建手术 (BRS))。回顾性在线调查调查了受访者在手术/治疗后接受物理康复的情况。调查探讨了受访者对所接受的身体康复治疗的看法(开放式回答)和满意度,以及康复治疗的内容和实施方法(封闭式回答)。采用主题分析法对受访者的看法进行了分析,并将受访者对每种不良身体影响的满意度和实施方法制成表格。结果主要看法是:(i) 没有意识到身体的不良反应,也没有做好准备;(ii) 信息提供不合适;(iii) 医务人员的后续服务不足。身体康复的内容主要集中在肩部问题和淋巴水肿;不到一半的受访者收到了有关疤痕、躯干和供体部位问题或影响睡眠的身体不适的信息。对于每种不良身体影响,接受每种传递方法的比例都不尽相同。小册子和口头指导是最常见的传递方法,而与医疗专业人员进行身体评估、检查或进展情况的会议则最不常见。对每种不良身体影响的满意度各不相同,但都低于 50%。结论妇女认为她们的身体康复并没有为她们所经历的不良身体影响做好准备,提供的方法和时间也不能满足她们在不同康复阶段的需求,而且后续跟踪也不够充分。有关康复内容和方法的定量数据支持了这些看法。建议解释出现这些看法的原因,并建议通过更多地使用与患者相关的结果测量来改善身体康复,并使用三级护理模式来分散有限的身体康复资源。尽管许多妇女都能从乳腺癌中康复,但改善身体康复可使妇女能够控制乳腺癌手术和治疗的任何直接或长期副作用。
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来源期刊
European Journal of Cancer Care
European Journal of Cancer Care 医学-康复医学
CiteScore
4.00
自引率
4.80%
发文量
213
审稿时长
3 months
期刊介绍: The European Journal of Cancer Care aims to encourage comprehensive, multiprofessional cancer care across Europe and internationally. It publishes original research reports, literature reviews, guest editorials, letters to the Editor and special features on current issues affecting the care of cancer patients. The Editor welcomes contributions which result from team working or collaboration between different health and social care providers, service users, patient groups and the voluntary sector in the areas of: - Primary, secondary and tertiary care for cancer patients - Multidisciplinary and service-user involvement in cancer care - Rehabilitation, supportive, palliative and end of life care for cancer patients - Policy, service development and healthcare evaluation in cancer care - Psychosocial interventions for patients and family members - International perspectives on cancer care
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