Sarapa Nenad
Expert Opin Drug Saf. 2007 Sep;6(5):595-607. doi: 10.1517/14740338.6.5.595.
The FDA mandates that digital electrocardiograms (ECGs) from 'thorough' QTc trials be submitted into the ECG Warehouse in Health Level 7 extended markup language format with annotated onset and offset points of waveforms. The FDA did not disclose the exact Warehouse metrics and minimal acceptable quality standards. The author describes the Warehouse scoring algorithms and metrics used by FDA, points out ways to improve FDA review and suggests Warehouse benefits for pharmaceutical sponsors. The Warehouse ranks individual ECGs according to their score for each quality metric and produces histogram distributions with Warehouse-specific thresholds that identify ECGs of questionable quality. Automatic Warehouse algorithms assess the quality of QT annotation and duration of manual QT measurement by the central ECG laboratory.
美国食品药品监督管理局(FDA)规定,来自“全面的”QTc试验的数字心电图(ECG)应以健康级别7扩展标记语言格式提交至心电图仓库,并标注波形的起始点和结束点。FDA未披露确切的仓库指标和最低可接受质量标准。作者描述了FDA使用的仓库评分算法和指标,指出了改进FDA审查的方法,并提出了仓库对制药赞助商的益处。仓库根据每个质量指标的得分对个体心电图进行排名,并生成带有特定仓库阈值的直方图分布,以识别质量存疑的心电图。仓库自动算法评估QT标注的质量以及中央心电图实验室手动测量QT的时长。