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硫酸舌下阿托品对氯氮平引起的唾液分泌过多的影响:一项多中心、随机、安慰剂对照试验。

The effect of sublingual atropine sulfate on clozapine-induced hypersalivation: a multicentre, randomised placebo-controlled trial.

机构信息

Missenden Mental Health Services, Royal Prince Alfred Hospital, Sydney, Australia.

Department of Pharmacy, Royal Prince Alfred Hospital, Missenden Rd, Camperdown, NSW, 2050, Australia.

出版信息

Psychopharmacology (Berl). 2020 Oct;237(10):2905-2915. doi: 10.1007/s00213-020-05627-4. Epub 2020 Sep 2.

DOI:10.1007/s00213-020-05627-4
PMID:32876732
Abstract

BACKGROUND

Hypersalivation and drooling are commonly reported in clozapine-treated patients. Current management strategies have been evaluated using subjective measures. Many case reports describe the successful use of atropine in the treatment of the condition.

AIMS

To measure the effect and safety of sublingual atropine on nocturnal unstimulated saliva secretion. Secondary aims were to evaluate the patient's satisfaction with the atropine effect on hypersalivation (or sialorrhea), drooling, and sleep.

METHOD

Twenty-one clozapine-treated patients with hypersalivation, or drooling, were randomised to take a single 600-μg dose of sublingual atropine drops or a matching placebo. The saliva secretion was measured over 5 min at baseline and 2 h after the administration of the study medication.

RESULTS

Sublingual atropine reduced the saliva secretion significantly more than the placebo (mean difference = - 57.21%, 95% CI: - 104.30, - 10.11, P = 0.02). A significant decrease in standing pulse rate was recorded in the participants in the atropine group (- 5.8 (- 9.54, - 2.15), P = 0.002). Subjectively, more patients in the atropine group found their pillow to have less saliva the following morning and found their sleep to be better.

CONCLUSIONS

Sublingual atropine drops significantly reduces nocturnal unstimulated clozapine-induced saliva secretion. More research is required to compare the effect of sublingual atropine with other anticholinergic medications and different dosage forms.

TRIAL REGISTRATION

ACTRN12618000051246.

摘要

背景

氯氮平治疗的患者常报告唾液分泌过多和流涎。目前的管理策略已经使用主观措施进行了评估。许多病例报告描述了阿托品在治疗这种情况中的成功应用。

目的

测量舌下给予阿托品对夜间非刺激性唾液分泌的作用和安全性。次要目的是评估患者对阿托品治疗唾液分泌过多(或流涎)、流口水和睡眠的满意度。

方法

21 名氯氮平治疗的唾液分泌过多或流涎患者随机分为舌下给予 600μg 剂量的阿托品滴剂或匹配的安慰剂。在基线和研究药物给药后 2 小时测量 5 分钟的唾液分泌量。

结果

与安慰剂相比,舌下给予阿托品可显著减少唾液分泌(平均差异=-57.21%,95%CI:-104.30,-10.11,P=0.02)。在阿托品组中,记录到参与者的站立脉搏率显著下降(-5.8(-9.54,-2.15),P=0.002)。主观上,阿托品组的更多患者发现他们的枕头第二天早上的唾液较少,并且发现他们的睡眠更好。

结论

舌下给予阿托品滴剂可显著减少氯氮平引起的夜间非刺激性唾液分泌。需要进一步研究比较舌下给予阿托品与其他抗胆碱能药物和不同剂型的效果。

试验注册

ACTRN12618000051246。

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