Neparidze Natalia, Godara Amandeep, Lin Dee, Le Hoa H, Fixler Karen, Shea Lisa, Everson Stephanie, Brittle Christine, Brunisholz Kimberly D
Yale School of Medicine, Yale University, New Haven, CT 06510, USA.
Huntsman Cancer Institute, Salt Lake City, UT 84112, USA.
Healthcare (Basel). 2024 Aug 20;12(16):1660. doi: 10.3390/healthcare12161660.
Multiple myeloma (MM) is a common hematologic malignancy, but due to its incurable nature, patients experience many relapses in their lifetime and hence face unique challenges. This mixed-methods study consisting of an online survey and subsequent focus groups aimed to understand how social and identity experiences affected the diagnostic, treatment, and care journey for patients with MM. Twenty-three adult patients with MM participated in this study. The survey participants identified common determinants negatively impacting their health, including mental health concerns (experienced by 90.5% of respondents), worries about food shortage (42.9%), and transportation concerns (28.6%). Focus group participants described high physical and mental health burdens associated with MM. Frequent monitoring, fear of a relapse, and unpredictable side effects contributed to high anxiety. Participants indicated that MM differed from other types of cancer and chronic health conditions in many ways, particularly how and where the diagnosis was made, disease progression and relapse, treatments and side effects, and financial concerns. Most participants (65.0%) reported ≥1 social need that negatively impacted health outcomes including lack of knowledge about MM, financial instability, and lack of insurance, transportation, and social support. The findings reveal that patients with MM continually experience patient-specific mental and physical health burdens indicating high unmet needs throughout the disease journey.
多发性骨髓瘤(MM)是一种常见的血液系统恶性肿瘤,但由于其无法治愈的特性,患者在一生中会经历多次复发,因此面临着独特的挑战。这项混合方法研究包括一项在线调查和随后的焦点小组讨论,旨在了解社会和身份经历如何影响MM患者的诊断、治疗和护理过程。23名成年MM患者参与了这项研究。调查参与者确定了对他们的健康有负面影响的常见决定因素,包括心理健康问题(90.5%的受访者有此经历)、对食物短缺的担忧(42.9%)和交通问题(28.6%)。焦点小组参与者描述了与MM相关的巨大身心负担。频繁的监测、对复发的恐惧和不可预测的副作用导致了高度焦虑。参与者表示,MM在许多方面与其他类型的癌症和慢性健康状况不同,特别是在诊断的方式和地点、疾病进展和复发、治疗和副作用以及经济问题方面。大多数参与者(65.0%)报告了≥1种对健康结果有负面影响的社会需求,包括对MM缺乏了解、经济不稳定以及缺乏保险、交通和社会支持。研究结果表明,MM患者在整个疾病过程中持续经历特定于患者的身心负担,表明存在大量未满足的需求。