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使用单病例试验对晚期癌症患者口干情况进行毛果芸香碱滴眼液测试:一项可行性研究。

Testing pilocarpine drops for dry mouth in advanced cancer using n-of-1 trials: A feasibility study.

作者信息

Nikles Jane, Mitchell Geoffrey K, Hardy Janet, Agar Meera, Senior Hugh, Carmont Sue-Ann, Schluter Philip J, Good Phillip, Vora Rohan, Currow David

机构信息

The School of Medicine, The University of Queensland, Ipswich, QLD, 4035, Australia

The School of Medicine, The University of Queensland, Ipswich, QLD, 4035, Australia.

出版信息

Palliat Med. 2015 Dec;29(10):967-74. doi: 10.1177/0269216315585473. Epub 2015 May 22.

Abstract

BACKGROUND

Dry mouth is a common and troublesome symptom in palliative care. Pilocarpine is a cholinergic agent that promotes salivation.

AIM

This study aimed to test the feasibility of using n-of-1 trials to test pilocarpine drops compared to placebo, for patients of palliative care units with advanced cancer, who experienced dry mouth.

DESIGN

This was an N-of-1 study, in which each participant was offered three cycles of pilocarpine drops 4% (6 mg tds) (3 days) and placebo drops (3 days) in random order.

SETTING/PARTICIPANTS: Participants were patients of specialist palliative care services with advanced cancer assessed as having a dry mouth, defined as having a score of ⩾ 3 on an 11-point self-rated xerostomia numerical rating scale, from any cause. Patients self-completed a diary using validated symptom and quality-of-life scores. The randomisation order was unmasked at the end of each person's trial by a clinician independent of the trial to allow a treatment decisions for individual patients to be made.

RESULTS

Nine patients completed at least 1 cycle; 33 cycles of data were completed in total, comprising 438 doses of pilocarpine. Four patients completed the trial: two responded and two did not. Most withdrawals related to deteriorating condition, unacceptable toxicity, non-compliance with study procedures or withdrawal of consent. Many issues contributed to slow recruitment and high withdrawal rate.

CONCLUSION

The formulation of pilocarpine drops proved unacceptable to most participants. More work is required to determine an appropriate formulation, dose and method of delivery and then a retest of pilocarpine drops for this symptom.

摘要

背景

口干是姑息治疗中常见且令人困扰的症状。毛果芸香碱是一种促进唾液分泌的胆碱能药物。

目的

本研究旨在测试针对晚期癌症姑息治疗病房中出现口干症状的患者,采用单病例试验来比较毛果芸香碱滴剂与安慰剂的可行性。

设计

这是一项单病例研究,每位参与者按随机顺序接受三个周期的4%毛果芸香碱滴剂(6毫克,每日三次)(3天)和安慰剂滴剂(3天)。

设置/参与者:参与者为专科姑息治疗服务的晚期癌症患者,经评估存在口干症状,定义为在11分的自我评定口干数字评分量表上得分≥3分,病因不限。患者使用经过验证的症状和生活质量评分自行填写日记。在每个人的试验结束时,由独立于试验的临床医生揭开随机化顺序,以便为个体患者做出治疗决策。

结果

9名患者完成了至少1个周期;总共完成了33个周期的数据,包括438剂毛果芸香碱。4名患者完成了试验:2名有反应,2名无反应。大多数退出与病情恶化、不可接受的毒性、不遵守研究程序或撤回同意有关。许多问题导致招募缓慢和退出率高。

结论

大多数参与者认为毛果芸香碱滴剂的剂型不可接受。需要开展更多工作来确定合适的剂型、剂量和给药方法,然后针对该症状重新测试毛果芸香碱滴剂。

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