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2004 年至 2006 年德国透皮芬太尼的使用情况。

Utilisation of transdermal fentanyl in Germany from 2004 to 2006.

机构信息

Bremen Institute for Prevention Research and Social Medicine (BIPS), Bremen, Germany.

出版信息

Pharmacoepidemiol Drug Saf. 2012 Feb;21(2):191-8. doi: 10.1002/pds.2164. Epub 2011 Jun 17.

DOI:10.1002/pds.2164
PMID:21681850
Abstract

PURPOSE

Oral morphine is the first-choice opioid for moderate to severe cancer pain. Transdermal fentanyl is an alternative in patients with stable requirements of high-potency opioids (HPO) or if drugs cannot be taken orally. Drug regulatory authorities have issued several alerts to use transdermal fentanyl only for chronic pain and in HPO-tolerant patients to minimise the risk of severe opioid side effects. The aim of this study was to characterise utilisation of transdermal fentanyl in Germany.

METHODS

The analysis was based on data from four German statutory health insurances from the years 2004-2006. Descriptive analyses were performed in new users of transdermal fentanyl to assess HPO-naïvety, potential difficulties with the oral route in HPO-naïve patients and the number of transdermal fentanyl dispensations. The initial dose in new users was assessed in 2005-2006 after marketing of transdermal fentanyl 12.5 µg/hour.

RESULTS

Of 35 262 patients with new use of transdermal fentanyl, 29 793 (84.5%) were assessed as HPO-naïve. Of those, 21 596 (72.5%) did not have diagnoses indicating difficulties with the oral route. For 71.2% of the HPO-naïve new users of transdermal fentanyl, the first dose exceeded the recommended dose of 12.5 µg/hour, and 49.3% of them received only one prescription of the drug.

CONCLUSIONS

Transdermal fentanyl was used as a first-choice opioid, which may increase the risk of serious opioid side effects, in a substantial number of HPO-naïve patients. Inappropriate prescribing included also high initial doses in HPO-naïve patients and possible prescription for acute pain in a considerable proportion of patients.

摘要

目的

口服吗啡是治疗中重度癌痛的首选阿片类药物。对于稳定需要使用高剂量阿片类药物(HPO)的患者或不能口服药物的患者,可选择经皮芬太尼。为了将严重阿片类药物副作用的风险降到最低,药品监管部门已发布了几项关于仅将经皮芬太尼用于慢性疼痛和 HPO 耐受患者的警报。本研究旨在描述德国经皮芬太尼的使用情况。

方法

本分析基于 2004-2006 年德国四家法定健康保险公司的数据。对新使用经皮芬太尼的患者进行描述性分析,以评估 HPO 初治情况、HPO 初治患者经口给药的潜在困难以及经皮芬太尼的发放数量。在经皮芬太尼上市后(2005-2006 年),评估了新使用经皮芬太尼患者的初始剂量。

结果

在 35262 例新使用经皮芬太尼的患者中,有 29793 例(84.5%)被评估为 HPO 初治。其中,有 21596 例(72.5%)没有表明经口给药困难的诊断。在 HPO 初治的经皮芬太尼新使用者中,有 71.2%的患者首次剂量超过推荐剂量 12.5µg/h,有 49.3%的患者仅获得一剂该药物。

结论

在相当数量的 HPO 初治患者中,经皮芬太尼被用作一线阿片类药物,这可能会增加严重阿片类药物副作用的风险。不适当的处方包括 HPO 初治患者的初始剂量过高以及相当一部分患者可能开具了急性疼痛的处方。

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