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确保 AFRINEST 和 SATT 的质量:临床标准化和监测。

Ensuring quality in AFRINEST and SATT: clinical standardization and monitoring.

机构信息

Saving Newborn Lives, Save the Children, Washington, DC 20036, USA.

出版信息

Pediatr Infect Dis J. 2013 Sep;32 Suppl 1(Suppl 1 Innovative Treatment Regimens for Severe Infections in Young Infants):S39-45. doi: 10.1097/INF.0b013e31829ff801.

Abstract

BACKGROUND

Three randomized open-label clinical trials [Simplified Antibiotic Therapy Trial (SATT) Bangladesh, SATT Pakistan and African Neonatal Sepsis Trial (AFRINEST)] were developed to test the equivalence of simplified antibiotic regimens compared with the standard regimen of 7 days of parenteral antibiotics. These trials were originally conceived and designed separately; subsequently, significant efforts were made to develop and implement a common protocol and approach. Previous articles in this supplement briefly describe the specific quality control methods used in the individual trials; this article presents additional information about the systematic approaches used to minimize threats to validity and ensure quality across the trials.

METHODS

A critical component of quality control for AFRINEST and SATT was striving to eliminate variation in clinical assessments and decisions regarding eligibility, enrollment and treatment outcomes. Ensuring appropriate and consistent clinical judgment was accomplished through standardized approaches applied across the trials, including training, assessment of clinical skills and refresher training. Standardized monitoring procedures were also applied across the trials, including routine (day-to-day) internal monitoring of performance and adherence to protocols, systematic external monitoring by funding agencies and external monitoring by experienced, independent trial monitors. A group of independent experts (Technical Steering Committee/Technical Advisory Group) provided regular monitoring and technical oversight for the trials.

CONCLUSIONS

Harmonization of AFRINEST and SATT have helped to ensure consistency and quality of implementation, both internally and across the trials as a whole, thereby minimizing potential threats to the validity of the trials' results.

摘要

背景

三项随机、开放性标签临床试验[Simplified Antibiotic Therapy Trial (SATT) Bangladesh、SATT Pakistan 和 African Neonatal Sepsis Trial (AFRINEST)]旨在测试简化抗生素方案与 7 天肠外抗生素标准方案的等效性。这些试验最初是分别构思和设计的;随后,做出了重大努力来制定和实施共同的方案和方法。本增刊中的先前文章简要描述了各个试验中使用的特定质量控制方法;本文介绍了关于系统方法的更多信息,这些方法用于最小化对有效性的威胁,并确保整个试验的质量。

方法

AFRINEST 和 SATT 的质量控制的一个关键组成部分是努力消除临床评估和资格、入组和治疗结果方面的决策差异。通过在整个试验中应用标准化方法来确保适当和一致的临床判断,包括培训、临床技能评估和复习培训。还在整个试验中应用了标准化监测程序,包括日常性能和遵守方案的内部监测、供资机构的系统外部监测以及经验丰富的独立试验监测员的外部监测。一组独立专家(技术指导委员会/技术咨询小组)为试验提供定期监测和技术监督。

结论

AFRINEST 和 SATT 的协调有助于确保内部和整个试验的执行一致性和质量,从而最大程度地降低对试验结果有效性的潜在威胁。

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