Boston University School of Medicine, Boston, USA.
Brigham and Women's Hospital, Boston, USA.
Neurocrit Care. 2019 Apr;30(2):316-321. doi: 10.1007/s12028-018-0607-8.
Automated devices collecting quantitative measurements of pupil size and reactivity are increasingly used for critically ill patients with neurological disease. However, there are limited data on the effect of ambient light conditions on pupil metrics in these patients. To address this issue, we tested the range of pupil reactivity in healthy volunteers and critically ill patients in both bright and dark conditions.
We measured quantitative pupil size and reactivity in seven healthy volunteers and seven critically ill patients with the Neuroptics-200 pupillometer in both bright and dark ambient lighting conditions. Bright conditions were created by overhead LED lighting in a room with ample natural light. Dark conditions consisted of a windowless room with no overhead light source. The primary outcome was the Neurological Pupil Index (NPi), a composite metric ranging from 0 to 5 in which > 3 is considered normal. Secondary outcomes included resting and constricted pupil size, change in pupil size, constriction velocity, dilation velocity, and latency. Results were analyzed with multi-level linear regression to account for both inter- and intra-subject variability.
Fourteen subjects underwent ten pupil readings each in bright and dark conditions, yielding 280 total measurements. In healthy subjects, median NPi in bright and dark conditions was 4.2 and 4.3, respectively. In critically ill subjects, median NPi was 2.85 and 3.3, respectively. Multi-level linear regression demonstrated significant differences in pupil size, pupil size change, constriction velocity, and dilation velocity in various light levels in healthy patients, but not NPi. In the critically ill, NPi and pupil size change were significantly affected.
Ambient light levels impact pupil parameters in both healthy and critically ill subjects. Changes in NPi under different light conditions are small and more consistent in healthy subjects, but significantly differ in the critically ill. Practitioners should standardize lighting conditions to maximize measurement reliability.
用于患有神经疾病的危重病患者的自动设备越来越多地用于收集瞳孔大小和反应性的定量测量。然而,关于这些患者的环境光照条件对瞳孔指标的影响的数据有限。为了解决这个问题,我们在明亮和黑暗条件下测试了健康志愿者和危重病患者的瞳孔反应范围。
我们使用 Neuroptics-200 瞳孔计在明亮和黑暗的环境光照条件下对 7 名健康志愿者和 7 名患有神经疾病的危重病患者进行了瞳孔大小和反应性的定量测量。明亮条件是在一个自然光充足的房间里用头顶 LED 照明创造的。黑暗条件由没有头顶光源的无窗房间组成。主要结果是神经瞳孔指数(NPi),这是一个复合指标,范围从 0 到 5,其中>3 被认为是正常的。次要结果包括静止和收缩的瞳孔大小、瞳孔大小变化、收缩速度、扩张速度和潜伏期。结果采用多级线性回归进行分析,以考虑到个体间和个体内的变异性。
14 名受试者在明亮和黑暗条件下各进行了 10 次瞳孔读数,共产生 280 次测量。在健康受试者中,明亮和黑暗条件下的 NPi 中位数分别为 4.2 和 4.3。在患有危重病的患者中,NPi 的中位数分别为 2.85 和 3.3。多级线性回归显示,在健康患者中,瞳孔大小、瞳孔大小变化、收缩速度和扩张速度在不同的光照水平下存在显著差异,但 NPi 没有差异。在危重病患者中,NPi 和瞳孔大小变化受到显著影响。
环境光照水平会影响健康和危重病患者的瞳孔参数。在不同光照条件下,NPi 的变化较小,在健康受试者中更一致,但在危重病患者中差异显著。从业者应标准化照明条件,以最大限度地提高测量的可靠性。