Inagaki Natsuko, Tsuchiya Mio, Otani Kazuki, Nakayama Takeo
Department of Cardiology, Tokyo Medical University, Tokyo, Japan.
Department of Clinical Genetics Center, Tokyo Medical University, Tokyo, Japan.
Mol Genet Metab Rep. 2022 Aug 10;32:100899. doi: 10.1016/j.ymgmr.2022.100899. eCollection 2022 Sep.
Fabry disease is a rare, progressive genetic lysosomal disorder that can cause multisystem organ dysfunction. With increasing treatment options for Fabry disease, it is imperative that patients discuss and select treatment plans in conjunction with their physicians. Although shared decision making (SDM) should be recommended for clinical decision making in disease management, evidence is limited as to how patients in Japan are involved in the choice of their Fabry disease treatment and if other gaps exist with physicians in the perception of Fabry disease management.
The main objective of the study was to assess the degree of agreement between patients and treating physicians in the SDM process as assessed by the SDM-Q-9 and SDM-Q-Doc questionnaires. In parallel, this study also investigated other factors that might impact the SDM process.
This was a cross-sectional web-based questionnaire survey of Japanese patients with Fabry disease and their treating physicians conducted from February 2021 to June 2021. Online surveys were developed for patients and physicians, consisting of seven items, including the Japanese version of the 9-item SDM Questionnaire for patients (SDM-Q-9) and physicians (SDM-Q-Doc). Physicians were divided into two cohorts: non-paired and paired with patients. Only the paired cohort physicians answered the SDM questionnaire.
A total of 99 physicians and 30 patients answered the respective questionnaires. Among these, 13 physicians were included in a paired SDM analysis with patients. Mean (standard deviation [SD]) patient age at diagnosis of Fabry disease was 47.5 (15.8) years, and 14 (46.7%) were male. Both physicians in the paired cohort and patients considered patient-reported outcomes (both 76.7%) and the findings from laboratory testing as important (90.0% and 60.0% respectively). However, regarding symptoms that affect quality of life of patients, perception gaps were identified in that physicians in the paired cohort placed less importance on patient-reported outcome-related symptoms such as sweating abnormalities and gastrointestinal symptoms than their patients (0% [0/17] and 44.4% [8/18], 11.8% [2/17] and 38.9% [7/18], respectively). In the paired analysis, there was no significant difference in total SDM score between patients and physicians ( = 0.82). However, the largest discordance in perception between patients and physicians was identified for the explanation of the advantages and disadvantages of the treatment options (weighted Kappa coefficient = 0.14).
This survey revealed a gap in the perception of disease burden affecting patients' quality of life, and a recognition gap between physicians and patients when they discussed the advantages and disadvantages of treatment options. To improve the SDM process in Fabry disease management and treatment, practical solutions for bridging these gaps should be considered.
法布里病是一种罕见的、进行性遗传性溶酶体疾病,可导致多系统器官功能障碍。随着法布里病治疗选择的增加,患者与医生共同讨论并选择治疗方案至关重要。尽管在疾病管理的临床决策中应推荐共同决策(SDM),但关于日本患者如何参与法布里病治疗选择以及医生在法布里病管理认知方面是否存在其他差距的证据有限。
本研究的主要目的是通过SDM-Q-9和SDM-Q-Doc问卷评估患者与治疗医生在共同决策过程中的一致程度。同时,本研究还调查了可能影响共同决策过程的其他因素。
这是一项于2021年2月至2021年6月对日本法布里病患者及其治疗医生进行的基于网络的横断面问卷调查。为患者和医生开发了在线调查问卷,包括七个项目,其中包括患者版9项共同决策问卷(SDM-Q-9)和医生版(SDM-Q-Doc)的日语版本。医生分为两组:非配对组和与患者配对组。只有配对组的医生回答共同决策问卷。
共有99名医生和30名患者回答了各自的问卷。其中,13名医生被纳入与患者的配对共同决策分析。法布里病诊断时患者的平均(标准差[SD])年龄为47.5(15.8)岁,14名(46.7%)为男性。配对组的医生和患者都认为患者报告的结果(均为76.7%)和实验室检测结果很重要(分别为90.0%和60.0%)。然而,关于影响患者生活质量的症状,发现存在认知差距,即配对组的医生对患者报告的与结果相关的症状(如出汗异常和胃肠道症状)的重视程度低于患者(分别为0%[0/17]和44.4%[8/18],11.8%[2/17]和38.9%[7/18])。在配对分析中,患者和医生的共同决策总分无显著差异( = 0.82)。然而,患者和医生在治疗方案优缺点解释方面的认知差异最大(加权Kappa系数 = 0.14)。
本次调查揭示了在影响患者生活质量的疾病负担认知方面存在差距,以及医生和患者在讨论治疗方案优缺点时存在认知差距。为改善法布里病管理和治疗中的共同决策过程,应考虑弥合这些差距的实际解决方案。