Africa Health Research Institute, KwaZulu-Natal, South Africa.
Nelson R Mandela School of Medicine, College of Health Sciences, University of KwaZulu-Natal, South Africa.
Int J Epidemiol. 2018 Feb 1;47(1):236-245. doi: 10.1093/ije/dyx134.
It is common to use the mid-point between the latest-negative and earliest-positive test dates as the date of the infection event. However, the accuracy of the mid-point method has yet to be systematically quantified for incidence studies once participants start to miss their scheduled test dates.
We used a simulation-based approach to generate an infectious disease epidemic for an incidence cohort with a high (80-100%), moderate (60-79.9%), low (40-59.9%) and poor (30-39.9%) testing rate. Next, we imputed a mid-point and random-point value between the participant's latest-negative and earliest-positive test dates. We then compared the incidence rate derived from these imputed values with the true incidence rate generated from the simulation model.
The mid-point incidence rate estimates erroneously declined towards the end of the observation period once the testing rate dropped below 80%. This decline was in error of approximately 9%, 27% and 41% for a moderate, low and poor testing rate, respectively. The random-point method did not introduce any systematic bias in the incidence rate estimate, even for testing rates as low as 30%.
The mid-point assumption of the infection date is unjustified and should not be used to calculate the incidence rate once participants start to miss the scheduled test dates. Under these conditions, we show an artefactual decline in the incidence rate towards the end of the observation period. Alternatively, the single random-point method is straightforward to implement and produces estimates very close to the true incidence rate.
通常将最近一次阴性结果和最早一次阳性结果之间的时间中点作为感染事件的日期。然而,一旦参与者开始错过预定的检测日期,对于发病率研究来说,中点法的准确性尚未得到系统地量化。
我们使用基于模拟的方法生成了一个发病率队列的传染病流行情况,该队列的检测率较高(80-100%)、中度(60-79.9%)、较低(40-59.9%)和较差(30-39.9%)。接下来,我们在参与者最近一次阴性结果和最早一次阳性结果之间的日期内插一个中点和随机点值。然后,我们将这些插补值得出的发病率与模拟模型生成的真实发病率进行比较。
一旦检测率降至 80%以下,中点发病率估计值就会错误地朝着观察期末端下降。对于中度、低度和较差的检测率,这种下降分别约为 9%、27%和 41%。随机点方法即使在检测率低至 30%的情况下,也不会对发病率估计值引入任何系统偏差。
一旦参与者开始错过预定的检测日期,感染日期的中点假设就不合理,不应用于计算发病率。在这些条件下,我们观察到发病率在观察期末端的人为下降。或者,单点随机方法实施起来非常简单,并且产生的估计值非常接近真实的发病率。