Stewart Kent W, Pretty Christopher G, Shaw Geoffrey M, Chase J Geoffrey
1 Department of Mechanical Engineering, Centre for Bio-Engineering, University of Canterbury, Christchurch, New Zealand.
2 Department of Intensive Care, Christchurch Hospital, Christchurch, New Zealand.
J Diabetes Sci Technol. 2018 Sep;12(5):967-975. doi: 10.1177/1932296818786518. Epub 2018 Jul 12.
This study investigates blood glucose (BG) measurement interpolation techniques to represent intermediate BG dynamics, and the effect resampling of retrospective BG data has on key glycemic control (GC) performance results. GC protocols in the ICU have varying BG measurement intervals ranging from 0.5 to 4 hours. Sparse data pose problems, particularly in comparing GC performance or model fitting, and thus interpolation is required.
Retrospective data from SPRINT in Christchurch Hospital Intensive Care Unit (ICU) (2005-2007) were used to analyze several interpolation techniques. Piecewise linear, spline, and cubic interpolation functions, which force interpolation through measured data, as well as 1st and 2nd Order B-spline basis functions, are used to identify the interpolated trace. Dense data were thinned to increase sparsity and obtain measurements (Hidden Measurements) for comparison after interpolation. Performance is assessed based on error in capturing hidden measurements. Finally, the effect of minutely versus hourly sampling of the interpolated trace on key GC performance statistics was investigated using retrospective data received from STAR GC in Christchurch Hospital ICU, New Zealand (2011-2015).
All of the piecewise functions performed considerably better than the fitted interpolation functions. Linear piecewise interpolation performed the best having a mean RMSE 0.39 mmol/L, within 2 standard deviations of the BG sensor error. Minutely sampled BG resulted in significantly different key GC performance values when compared to raw sparse BG measurements.
Linear piecewise interpolation provides the best estimate of intermediate BG dynamics and all analyses comparing GC protocol performance should use minutely linearly interpolated BG data.
本研究调查血糖(BG)测量插值技术以呈现中间血糖动态,以及回顾性BG数据重采样对关键血糖控制(GC)性能结果的影响。重症监护病房(ICU)中的GC方案具有从0.5到4小时不等的BG测量间隔。稀疏数据会带来问题,尤其是在比较GC性能或模型拟合时,因此需要进行插值。
使用克赖斯特彻奇医院重症监护病房(ICU)(2005 - 2007年)SPRINT研究的回顾性数据来分析几种插值技术。使用强制通过测量数据进行插值的分段线性、样条和三次插值函数,以及一阶和二阶B样条基函数来确定插值轨迹。对密集数据进行稀疏化处理以增加稀疏性,并在插值后获取测量值(隐藏测量值)用于比较。基于捕获隐藏测量值时的误差来评估性能。最后,使用从新西兰克赖斯特彻奇医院ICU的STAR GC获得的回顾性数据,研究插值轨迹每分钟采样与每小时采样对关键GC性能统计数据的影响。
所有分段函数的表现均明显优于拟合的插值函数。线性分段插值表现最佳,平均均方根误差(RMSE)为0.39 mmol/L,在BG传感器误差的2个标准差范围内。与原始稀疏BG测量值相比,每分钟采样的BG导致关键GC性能值有显著差异。
线性分段插值能最好地估计中间血糖动态,所有比较GC方案性能的分析都应使用每分钟线性插值的BG数据。