Pena-Verdeal Hugo, García-Resúa Carlos, Miñones Mercedes, Giraldez Maria J, Yebra-Pimentel Eva
*OD, MSc †OD, PhD ‡OD, MSc, PhD Departamento de Física Aplicada, Área de Optometría (Grupo de Optometría), Universidade de Santiago de Compostela, Santiago de Compostela, España (all authors).
Optom Vis Sci. 2015 Sep;92(9):e273-83. doi: 10.1097/OPX.0000000000000669.
The purpose of this study was to examine the precision and accuracy of the Fiske 110 Osmolarity System under different protocols to determine the possible applications of this device in tear film research and clinical practice.
Three separate studies were performed. In the first, Fiske 110 measurements were made on undiluted and diluted (1:1, 1:4, and 1:9 dilutions) standard samples of different osmolarity values: 50, 290, and 850 mOsm/kg and 297 and 338 mOsm/L. In the second study, measurements were made on different types of contact lens care solutions. Finally, in an agreement study, measurements were made in two sets of 60 subjects to compare TearLab versus Fiske 110 (using both 2- and 4-μL tear sample).
Although osmolarity measurements for undiluted solutions differed statistically from reference standard values, all biases were in the tolerance range proposed by the manufacturer except for the 850-mOsm/kg solution. No significant differences from reference osmolarity values were observed for the 1:1 and 1:4 diluted 297- and 338-mOsm/L H2O solutions, respectively, although all diluted solutions showed a possible bias out of the range provided. Osmolarities for the soft contact lens solutions fell within the range 293 to 309 mOsm/kg with the exception of Opti-Free Express (225 mOsm/kg). In the agreement study, significant differences were observed between measurements obtained using the TearLab and both Fiske 110 procedures, although the Fiske 110 (4 μL) procedure was closer to the TearLab than the Fiske (2 μL) procedure.
For undiluted solutions, the Fiske 110 shows good performance, making it a useful device for osmolarity measurements in lens care solutions or eye drops. A worse performance was observed for more diluted standard solution samples. When testing diluted samples, performance was acceptable for osmolarity values close to tear values.
本研究旨在检测Fiske 110渗透压系统在不同方案下的精密度和准确性,以确定该设备在泪膜研究和临床实践中的可能应用。
进行了三项独立研究。第一项研究中,对不同渗透压值(50、290和850 mOsm/kg以及297和338 mOsm/L)的未稀释和稀释(1:1、1:4和1:9稀释)标准样品进行Fiske 110测量。第二项研究中,对不同类型的隐形眼镜护理液进行测量。最后,在一致性研究中,对两组60名受试者进行测量,以比较TearLab和Fiske 110(使用2 μL和4 μL泪液样本)。
尽管未稀释溶液的渗透压测量值与参考标准值在统计学上存在差异,但除850 mOsm/kg溶液外,所有偏差均在制造商提出的公差范围内。对于1:1和1:4稀释的297和338 mOsm/L H2O溶液,分别未观察到与参考渗透压值的显著差异,尽管所有稀释溶液均显示出超出规定范围的可能偏差。软性隐形眼镜护理液的渗透压在293至309 mOsm/kg范围内,但Opti-Free Express除外(225 mOsm/kg)。在一致性研究中,使用TearLab和两种Fiske 110方法获得的测量值之间观察到显著差异,尽管Fiske 110(4 μL)方法比Fiske(2 μL)方法更接近TearLab。
对于未稀释溶液,Fiske 110表现出良好的性能,使其成为测量隐形眼镜护理液或滴眼液渗透压的有用设备。对于稀释度更高的标准溶液样品,观察到性能较差。在测试稀释样品时,对于接近泪液值的渗透压值,性能是可以接受的。