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根据路易体痴呆(DLB)诊断后的时间,对DLB患者及其照料者的特征和治疗需求以及医生对这些治疗需求的认知进行事后分析。

Post hoc analysis of the characteristics and treatment needs of patients with dementia with Lewy bodies (DLB) and their caregivers and their physicians' awareness of those treatment needs according to the duration after diagnosis of DLB.

作者信息

Ikeda Manabu, Toya Shunji, Manabe Yuta, Yamakage Hajime, Hashimoto Mamoru

机构信息

Department of Psychiatry, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Medical Science, Sumitomo Pharma Co., Ltd., Chuo-ku, Tokyo, Japan.

出版信息

Int J Geriatr Psychiatry. 2024 Aug;39(8):e6122. doi: 10.1002/gps.6122.

DOI:10.1002/gps.6122
PMID:39085743
Abstract

OBJECTIVES

To investigate the differences in patient/caregiver characteristics, their treatment needs, and the attending physician's understanding of those treatment needs according to the duration after diagnosis of dementia with Lewy bodies (DLB).

METHODS

This was a post hoc analysis of a multicenter, cross-sectional, questionnaire survey study. A total of 263 patient-caregiver pairs were reclassified into two groups according to the median duration after diagnosis of DLB as follows: short (<24 months; S-group) and long (≥24 months; L-group) post-DLB diagnosis duration. Treatment need was defined as the symptom domain that caused the patient or caregiver the most distress. Concordance rates between patient-physician and caregiver-physician were calculated for physicians' understanding of treatment needs.

RESULTS

In this analysis, 126 pairs (32 physicians) and 137 pairs (34 physicians) were classified as the S- and L-groups, respectively. Patient and caregiver characteristics were broadly similar between groups (mean age for patients 78.7 ± 6.6 vs. 79.8 ± 6.7, for caregivers 64.7 ± 12.9 vs. 64.9 ± 12.8; number of male/female for patients 61/65 vs. 67/70, for caregivers 34/92 vs. 38/99), but the prevalence of parkinsonism (82.5% vs. 66.7%) and autonomic dysfunction (49.6% vs. 33.3%), severity of parkinsonism (MDS-UPDRS Part III total scores, 29.2 ± 22.6 vs. 18.0 ± 16.4; Part II total score, 14.6 ± 12.0 vs. 7.6 ± 7.9), and caregiver burden (J-ZBI_8 score, 9.1 ± 6.7 vs. 7.5 ± 5.8) were higher in the L-group than the S-group. Regarding treatment needs, the invalid answer rates for patients were 34.9% and 46.8%, and those for caregivers were 28.6% and 34.9% in the S- and L groups, respectively. Patients' treatment needs did not significantly differ (p = 0.056), but S-group patients were more likely to select cognitive impairment (p = 0.045) as their treatment need, whereas L-group patients were more likely to select parkinsonism (p = 0.003). Caregivers' treatment needs significantly differed (p = 0.032) between groups. S-group caregivers were more likely to select cognitive impairment (p = 0.001), whereas L-group caregivers were more likely to select other symptom domains such as parkinsonism (S-group vs. L-group: 10.3% vs. 16.7%), psychiatric symptoms (20.6% vs. 24.6%), sleep-related disorder (4.0% vs. 7.1%), and autonomic dysfunction (4.8% vs. 9.5%). Concordance rates between patient-physician and caregiver-physician were low in both groups.

CONCLUSIONS

There were some differences in characteristics according to the duration after diagnosis of DLB. Cognitive dysfunction may be a particular concern for patients and caregivers soon after diagnosis of DLB. Treatment needs of patients and caregivers for parkinsonism, psychiatric symptoms, sleep-related disorder, or autonomic dysfunction were different according to the duration after diagnosis of DLB. Physicians' perception of patients'/caregivers' treatment needs was poor regardless of the duration after diagnosis of DLB.

CLINICAL TRIAL REGISTRATION

UMIN Clinical Trials Registry (UMIN000041844).

摘要

目的

根据路易体痴呆(DLB)诊断后的病程,调查患者/照料者特征、他们的治疗需求以及主治医生对这些治疗需求的理解之间的差异。

方法

这是一项对多中心横断面问卷调查研究的事后分析。根据DLB诊断后的病程中位数,将总共263对患者-照料者重新分为两组:DLB诊断后病程短(<24个月;S组)和病程长(≥24个月;L组)。治疗需求定义为给患者或照料者造成最大困扰的症状领域。计算医生对治疗需求理解的患者-医生和照料者-医生之间的一致率。

结果

在本次分析中,分别有126对(32名医生)和137对(34名医生)被归类为S组和L组。两组之间患者和照料者的特征大致相似(患者平均年龄78.7±6.6岁对79.8±6.7岁,照料者平均年龄64.7±12.9岁对64.9±12.8岁;患者男女数量61/65对67/70,照料者男女数量34/92对38/99),但L组帕金森综合征(82.5%对66.7%)和自主神经功能障碍(49.6%对33.3%)的患病率、帕金森综合征的严重程度(MDS-UPDRS第三部分总分,29.2±22.6对18.0±16.4;第二部分总分,14.6±12.0对7.6±7.9)以及照料者负担(J-ZBI_8评分,9.1±6.7对7.5±5.8)均高于S组。关于治疗需求,S组和L组患者的无效回答率分别为34.9%和46.8%,照料者的无效回答率分别为28.6%和34.9%。患者的治疗需求无显著差异(p=0.056),但S组患者更倾向于选择认知障碍(p=0.045)作为他们的治疗需求,而L组患者更倾向于选择帕金森综合征(p=0.003)。两组照料者的治疗需求有显著差异(p=0.032)。S组照料者更倾向于选择认知障碍(p=0.001),而L组照料者更倾向于选择其他症状领域,如帕金森综合征(S组对L组:10.3%对16.7%)、精神症状(20.6%对24.6%)、睡眠相关障碍(4.0%对7.1%)和自主神经功能障碍(4.8%对9.5%)。两组患者-医生和照料者-医生之间的一致率均较低。

结论

根据DLB诊断后的病程,存在一些特征差异。DLB诊断后不久,认知功能障碍可能是患者和照料者特别关注的问题。根据DLB诊断后的病程,患者和照料者对帕金森综合征、精神症状、睡眠相关障碍或自主神经功能障碍的治疗需求不同。无论DLB诊断后的病程如何,医生对患者/照料者治疗需求的认知都较差。

临床试验注册

UMIN临床试验注册中心(UMIN000041844)。

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