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用于验证严重不良事件报告准确性的内部标准:以一项对190,924名患者的针灸研究为例。

An internal standard for verifying the accuracy of serious adverse event reporting: the example of an acupuncture study of 190,924 patients.

作者信息

Endres H G, Molsberger A, Lungenhausen M, Trampisch H J

机构信息

Department of Medical Informatics, Statistics and Epidemiology, Ruhr University Bochum, D-44801 Bochum, Germany.

出版信息

Eur J Med Res. 2004 Dec 22;9(12):545-51.

Abstract

BACKGROUND

Reporting of all serious adverse events (SAEs) is a requirement for regulatory approval of a drug. Can equally rigorous reporting standards be expected in studies of non-drug treatments and how can underreporting, if any, be detected and proven? Using data from our large-scale prospective cohort study of acupuncture on outpatients, we examine the use of an internal standard, a principle taken from laboratory medicine, to quantify real event rates.

METHODS

A total of 190,924 patients (68.6% women) seeking treatment for chronic pain (headache, low back pain, coxarthrosis or gonarthrosis) from 12,000 physicians in private practice in Germany were observed during a six-month period ending in May 2002. Most received ten sessions of body acupuncture. Mean treatment time was six weeks. All practitioners were certified in acupuncture and received written instructions on completing forms for basic patient data and SAE monitoring. They were also informed that payment by insurers would be made only upon return of the completed form. All SAEs occurring between start of the first acupuncture session and end of the last one were to be reported, whether causally related to the treatment or not. Multiple minor adverse events (AEs) per single patient were to be reported only once. As the internal standard we chose the expected number of deaths, based on the death rate for the German population, adjusted for age, sex distribution and mean observation time of our study patients.

RESULTS

45 SAEs and 14,404 AEs were reported (i.e. 2.4 SAEs and 754 AEs per 10,000 patients). The number of reported deaths (9) was only 5% of the statistically expected number (180). Applying the resulting correction factor of 20 to all reported SAEs, resulted in 900 expected SAEs (versus 45 reported) or 47 per 10,000 patients.

CONCLUSIONS

Without verifying the accuracy of a measurement, results remain speculative. Our internal standard for the first time provides a means of verifying the accuracy of the reported SAE rate and correcting it to the statistically expected SAE rate.

摘要

背景

报告所有严重不良事件(SAE)是药物获得监管批准的一项要求。在非药物治疗研究中是否能期待同样严格的报告标准,以及如何检测和证明(若存在的话)报告不足的情况?利用我们对门诊患者进行的针灸大规模前瞻性队列研究的数据,我们探讨采用一种源自检验医学的内部标准来量化实际事件发生率。

方法

在截至2002年5月的6个月期间,观察了德国12000名私人执业医生接诊的共190924例寻求慢性疼痛(头痛、腰痛、髋关节炎或膝关节炎)治疗的患者(女性占68.6%)。大多数患者接受了10次体针治疗。平均治疗时间为6周。所有从业者均具备针灸资质,并收到了关于填写基本患者数据表格和SAE监测表格的书面说明。他们还被告知,保险公司仅在返还填写完整的表格后才会付款。要报告首次针灸治疗开始至最后一次治疗结束期间发生的所有SAE,无论其与治疗是否存在因果关系。每位患者发生的多个轻微不良事件(AE)仅报告一次。作为内部标准,我们根据德国人口死亡率,针对我们研究患者的年龄、性别分布和平均观察时间进行调整后,选择了预期死亡人数。

结果

报告了45例SAE和14404例AE(即每10000例患者中有2.4例SAE和754例AE)。报告的死亡人数(9例)仅为统计学预期人数(180例)的5%。将得出的20的校正因子应用于所有报告的SAE,得出预期SAE为900例(而报告的为45例),即每10000例患者中有47例。

结论

在未验证测量准确性的情况下,结果仍具有推测性。我们的内部标准首次提供了一种验证报告的SAE发生率准确性并将其校正为统计学预期SAE发生率的方法。

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