首页> 外文期刊>Postgraduate Medical Journal >Republished paper: Where errors occur in the preparation and administration of intravenous medicines: a systematic review and Bayesian analysis.
【24h】

Republished paper: Where errors occur in the preparation and administration of intravenous medicines: a systematic review and Bayesian analysis.

机译:重新发表的论文:静脉内药物的制备和管理中发生错误的地方:系统评价和贝叶斯分析。

获取原文
获取原文并翻译 | 示例
       

摘要

OBJECTIVE: To investigate the overall probability of error in preparing and administering intravenous medicines; to identify at which stage of the process an error is most likely to occur; and to determine the impact of error correction on the error probability. Design Systematic review and random-effects Bayesian conditional independence modelling. METHODS: Medline and EMBASE were searched for studies on intravenous medicines. The error rates of each stage were extracted. These, expert estimates, and error rates from generic tasks, were used in a Bayesian conditional independence model to find error 'hot-spots.' The main outcome measure was the probability of at least one error occurring during intravenous therapy. RESULTS: Nine published studies were identified for inclusion in the systematic review and meta-analysis. The overall probability of making at least one error in intravenous therapy was 0.73 (95% credible interval (CrI) 0.54 to 0.90). If error-checking was introduced at each stage of the process, the overall rate fell to 0.22 (95% CrI 0.14 to 0.31). Errors were most likely in the reconstitution step. Removing the reconstitution step by providing preprepared injections would reduce the overall error rate to 0.17 (95% CrI 0.09 to 0.27). CONCLUSIONS: Intravenous therapy is complex and error-prone. Error-checking at each stage could reduce the error probability. The use of preprepared injections may help by eliminating errors in the reconstitution of drug and diluent. However, it will be important to ensure that benefits are not outweighed by practical disadvantages such as an increase in selection errors.
机译:目的:调查静脉注射药物的制备和使用中出现错误的总体可能性;确定在过程的哪个阶段最有可能发生错误;并确定纠错对错误概率的影响。设计系统评价和随机效应贝叶斯条件独立模型。方法:对Medline和EMBASE进行静脉药物研究。提取每个阶段的错误率。这些,专家估计和通用任务的错误率被用于贝叶斯条件独立模型中,以查找错误的“热点”。主要结果指标是静脉治疗期间发生至少一项错误的可能性。结果:确定了九项已发表的研究,以纳入系统评价和荟萃分析。静脉治疗中发生至少一个错误的总概率为0.73(95%可信区间(CrI)为0.54至0.90)。如果在该过程的每个阶段都引入了错误检查,则总错误率将降至0.22(95%CrI为0.14至0.31)。重建步骤中最有可能发生错误。通过提供预先准备的进样来取消重建步骤,会将总错误率降低到0.17(95%CrI 0.09至0.27)。结论:静脉治疗是复杂的并且容易出错。在每个阶段进行错误检查都可以降低错误概率。预先准备的注射剂的使用可以消除药物和稀释剂重构中的错误,从而有所帮助。但是,重要的是要确保收益不会被选择缺点增加之类的实际缺点所抵消。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号