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罗替高汀透皮贴剂联合肠内左旋多巴输注治疗帕金森病 1 年的耐受性:1 种 24 小时治疗选择。

Tolerability of overnight rotigotine transdermal patch combined with intrajejunal levodopa infusion at 1 year: a 24-h treatment option in Parkinson's disease.

机构信息

Department of Basic and Clinical Neurosciences, The Maurice Wohl Clinical Neuroscience Institute, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, SE5 9RT, UK.

Parkinson's Foundation Centre of Excellence, King's College Hospital, London, UK.

出版信息

J Neural Transm (Vienna). 2022 Jul;129(7):889-894. doi: 10.1007/s00702-022-02506-4. Epub 2022 May 3.

Abstract

BACKGROUND

Twenty-four-hour treatment options could provide a continuous drug delivery strategy in advanced Parkinson's disease and can ameliorate motor and non-motor complications. Use of levodopa infusion is often limited to 12-16 h/day due to its cost. Adjunctive overnight rotigotine transdermal patch is a continuous drug delivery option successfully used in clinical practice coupled with apomorphine infusion. However, real-life data addressing the tolerability of transdermal dopamine agonist therapy with concomitant use of intrajejunal levodopa infusion in advanced Parkinson's disease are not available.

OBJECTIVE

To evaluate the tolerability and beneficial effects of combined therapy with overnight rotigotine transdermal patch and intrajejunal levodopa infusion over a follow-up period of 12 months in advanced Parkinson's disease.

METHOD

In this retrospective data analysis, data before and after the initiation of the continuous drug delivery combined therapy using overnight rotigotine transdermal patch and intrajejunal levodopa infusion were collected from the ongoing non-motor-international-longitudinal study (NILS) and local clinical practice at King's College Hospital (London, United Kingdom). 12 advanced Parkinson's disease patients on intrajejunal levodopa therapy who were additionally treated with overnight rotigotine transdermal patch (mean dose 5.67 ± 4.19 mg) are included. Tolerability over a 12-month period was assessed. In addition, changes in motor symptoms (SCales for Outcomes in Parkinson's disease, SCOPA-Motor), non-motor symptoms (Non-Motor Symptoms Scale, NMSS) and quality of life (Parkinson's disease Questionnaire-8, PDQ-8) before and 12-month after continuous drug delivery combined therapy initiation are evaluated.

RESULTS

Tolerability was 100% irrespective of age, disease duration, stages of disease. (Treatment with overnight rotigotine transdermal patch that was maintained for a minimum of 6 months was considered "tolerated", primary tolerability). In addition, we noted a significant reduction of the NMSS total score (p = 0.009) and the NMSS domain 3 score (mood and apathy domain) (p = 0.028), although the latter did not remain statistically significant after correction for multiple testing (p2 = 0.252) at 12 months.

CONCLUSION

Combination of intrajejunal levodopa infusion with overnight rotigotine transdermal patch is well tolerated and extend the beneficial effects of infusion with excellent tolerability; and also improved aspects of mood and apathy sustained at 12 months in advanced Parkinson's disease.

摘要

背景

24 小时治疗方案可在晚期帕金森病中提供持续的药物输送策略,并可改善运动和非运动并发症。由于成本原因,左旋多巴输注通常限制在 12-16 小时/天。佐剂夜间罗替高汀透皮贴剂是一种连续药物输送选择,已成功应用于临床实践,并与阿扑吗啡输注联合使用。然而,在晚期帕金森病中,关于同时使用肠内左旋多巴输注的透皮多巴胺激动剂治疗的耐受性的真实数据尚不可用。

目的

评估在晚期帕金森病中使用夜间罗替高汀透皮贴剂和肠内左旋多巴输注联合治疗 12 个月的耐受性和有益效果。

方法

在这项回顾性数据分析中,从正在进行的非运动性国际纵向研究(NILS)和英国伦敦国王学院医院的当地临床实践中收集了在开始使用夜间罗替高汀透皮贴剂和肠内左旋多巴输注进行连续药物输送联合治疗前后的数据。纳入了 12 名正在接受肠内左旋多巴治疗的晚期帕金森病患者,他们还接受了夜间罗替高汀透皮贴剂治疗(平均剂量为 5.67±4.19mg)。在 12 个月的时间内评估了耐受性。此外,评估了在开始连续药物输送联合治疗之前和之后 12 个月,运动症状(帕金森病结果量表,SCOPA-Motor)、非运动症状(非运动症状量表,NMSS)和生活质量(帕金森病问卷-8,PDQ-8)的变化。

结果

无论年龄、疾病持续时间、疾病阶段如何,耐受性均为 100%。(维持至少 6 个月的夜间罗替高汀透皮贴剂治疗被认为是“可耐受的”,这是主要的耐受性)。此外,我们注意到 NMSS 总分(p=0.009)和 NMSS 第 3 域评分(情绪和淡漠域)(p=0.028)显著降低,尽管在经过多次测试校正后(p2=0.252),这一结果在 12 个月时不再具有统计学意义。

结论

肠内左旋多巴输注与夜间罗替高汀透皮贴剂联合使用具有良好的耐受性,并延长了输注的有益效果,且具有极好的耐受性;并且在晚期帕金森病中,还改善了情绪和淡漠等方面的情况,并且在 12 个月时仍保持稳定。

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