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氯氮平的降尿酸作用:药物依从性的潜在指标?

Hypouricemic effect of zuclopenthixol: a potential marker of drug compliance?

作者信息

Bloch M, Gur E, Shalev A Y

机构信息

Department of Psychiatry, Hadassah University Hospital, Jerusalem, Israel.

出版信息

Psychopharmacology (Berl). 1992;109(3):377-8. doi: 10.1007/BF02245887.

DOI:10.1007/BF02245887
PMID:1365639
Abstract

Twelve newly-admitted psychotic patients were treated with clinical doses of zuclopenthixol (ZPT). Plasma uric acid (PUA) was measured before and during treatment. ZPT reduced PUA in all the patients by an average of 29.6% (P < 0.0001). PUA levels during treatment correlated with those obtained before treatment (R = 0.871, P < 0.0002). PUA returned to initial levels on discontinuation of treatment. Uric acid excretion increased during treatment. It is concluded that ZPT is a potent uricosuric agent, capable of producing persistent hypouricemia while administered. Such hypouricemia might be a useful indicator of drug compliance.

摘要

12名新入院的精神病患者接受了临床剂量的珠氯噻醇(ZPT)治疗。在治疗前和治疗期间测量血浆尿酸(PUA)。ZPT使所有患者的PUA平均降低了29.6%(P < 0.0001)。治疗期间的PUA水平与治疗前测得的水平相关(R = 0.871,P < 0.0002)。停药后PUA恢复到初始水平。治疗期间尿酸排泄增加。结论是ZPT是一种有效的促尿酸排泄剂,在给药时能够产生持续性低尿酸血症。这种低尿酸血症可能是药物依从性的一个有用指标。

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本文引用的文献

1
Drug and sociotherapy in the aftercare of schizophrenic patients. One-year relapse rates.精神分裂症患者后续护理中的药物治疗与社会心理治疗。一年复发率。
Arch Gen Psychiatry. 1973 Jan;28(1):54-64. doi: 10.1001/archpsyc.1973.01750310038007.
2
Long-term depot maintenance of chronic schizophrenic out-patients: the seven year follow-up of the Medical Research Council fluphenazine/placebo trial. II. The incidence of compliance problems, side-effects, neurotic symptoms and depression.
Br J Psychiatry. 1985 May;146:469-74. doi: 10.1192/bjp.146.5.469.
3
Acute oliguria associated with chlorprothixene overdosage.与氯丙硫蒽过量相关的急性少尿
依从性的建模与模拟:治疗学中的方法与应用
AAPS J. 2005 Oct 5;7(2):E390-407. doi: 10.1208/aapsj070240.
Nephron. 1988;48(1):71-3. doi: 10.1159/000184873.
4
The hypouricemic effect of chlorprothixene.氯丙硫蒽的降尿酸作用。
Clin Pharmacol Ther. 1987 Nov;42(5):562-6. doi: 10.1038/clpt.1987.197.
5
Serum concentrations and clinical effect of zuclopenthixol in acutely disturbed, psychotic patients treated with zuclopenthixol acetate in Viscoleo.
Psychopharmacology (Berl). 1986;90(3):412-6. doi: 10.1007/BF00179201.
6
Plasma level monitoring of antipsychotic drugs. Clinical utility.抗精神病药物的血药浓度监测。临床应用。
Clin Pharmacokinet. 1986 Jan-Feb;11(1):36-61. doi: 10.2165/00003088-198611010-00003.
7
Chlorprothixene-induced hypouricemia: a biologic indicator of drug compliance.
J Clin Psychiatry. 1989 Nov;50(11):424-7.
8
Clinical pharmacology of adinazolam and N-desmethyladinazolam mesylate after single oral doses of each compound in healthy volunteers.单次口服阿地唑仑和甲磺酸N-去甲基阿地唑仑后在健康志愿者体内的临床药理学。
Clin Pharmacol Ther. 1990 Dec;48(6):652-64. doi: 10.1038/clpt.1990.209.
9
Perphenazine decanoate and cis(z)-flupentixol decanoate in maintenance treatment of schizophrenic outpatients. Serum levels at the minimum effective dose.癸酸奋乃静和顺式(z)-癸酸氟哌噻吨用于精神分裂症门诊患者的维持治疗。最低有效剂量时的血清水平。
Psychopharmacology (Berl). 1991;105(1):42-8. doi: 10.1007/BF02316862.
10
Further observations on the duration of depot neuroleptic maintenance therapy in schizophrenia.关于精神分裂症长效抗精神病药物维持治疗疗程的进一步观察
Br J Psychiatry. 1979 Dec;135:524-30. doi: 10.1192/bjp.135.6.524.