干眼病的泪液渗透压和眼间变异性诊断分析

M. Wang, S. Ormonde, A. Muntz, J. Craig
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引用次数: 3

摘要

泪液高渗是干眼病的中心标志,并使眼表炎症和泪液膜不稳定的恶性循环长期存在。泪液渗透压和眼间变异性的测量构成了泪液膜和眼表学会干眼研讨会II (TFOS DEWS II)推荐的全球共识干眼诊断标准的一部分。本研究旨在评估泪液渗透压和眼间变异性在检测其他干眼体征和症状时的鉴别能力和最佳阈值。这项研究得到了机构伦理委员会的批准,并符合《赫尔辛基宣言》的原则。参与者必须年满16岁,在参加研究前3个月内没有接受过眼科手术。866名参与者提供了书面同意,满足诊断准确性功率计算(样本量≥814,估计患病率= 40%,预期灵敏度= 70%,置信水平= 95%,绝对精度= 5%,功率= 80%)。进行5项干眼调查问卷和眼表疾病指数干眼调查问卷,评估右眼眼表参数(Oculus Keratograph 5M)。一位独立的观察者测量了双眼的泪液渗透压(TearLab Osmometer),并记录了较高的读数和眼间差异。根据TFOS DEWS II诊断标准确定非渗透性干眼体征和症状的存在(表1)。渗透压测量检测其他干眼体征和症状的判别能力由受试者工作特征曲线下面积(c -统计量)确定,并使用配对DeLong检验进行比较。然后计算约登最佳诊断截止灵敏度和特异性值。泪液渗透压判别能力(C-statistic = 0.82;95%可信区间[CI], 0.79-0.85)大于眼间变异性(C-statistic = 0.68;95% ci, 0.65-0.72;P < 0.0001),但两者均显著大于概率(P < 0.0001)。泪液渗透压的最佳诊断临界值为≥308 mOsm/L;
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Diagnostic profile of tear osmolarity and inter‐ocular variability for dry eye disease
Tear hyperosmolarity is a central hallmark of dry eye disease, and perpetuates a vicious cycle of ocular surface inflammation and tear film instability. The measurement of tear osmolarity and inter-ocular variability forms part of the global consensus dry eye diagnostic criteria recommended by the Tear Film and Ocular Surface Society Dry Eye Workshop II (TFOS DEWS II). This investigator-masked diagnostic accuracy study sought to evaluate the discriminative ability and optimal thresholds for tear osmolarity and interocular variability in detecting other dry eye signs and symptoms. The study received institutional ethics committee approval and conformed to the tenets of the Declaration of Helsinki. Participants were required to be 16 years or older, with no ophthalmic surgical procedures in the 3 months preceding study participation. Written consent was provided by 866 participants, satisfying diagnostic accuracy power calculations (sample size ≥ 814, estimated prevalence = 40%, anticipated sensitivity = 70%, confidence level = 95%, absolute precision = 5%, power = 80%). The 5-Item Dry Eye Questionnaire and Ocular Surface Disease Index dry eye questionnaires were administered, and right eye ocular surface parameters (Oculus Keratograph 5M) assessed. An independent observer measured tear osmolarity from both eyes (TearLab Osmometer), and the higher reading and inter-ocular difference was recorded. The presence of nonosmolar dry eye signs and symptoms was determined according to the TFOS DEWS II diagnostic criteria (Table 1). The discriminative ability of osmolarity measurements in detecting other dry eye signs and symptoms was determined by the area under the receiver operating characteristic curve (C-statistic) and compared using the paired DeLong test. Youden-optimal diagnostic cut-off sensitivity and specificity values were then calculated. The discriminative ability of tear osmolarity (C-statistic = 0.82; 95% confidence interval [CI], 0.79-0.85) was greater than inter-ocular variability (C-statistic = 0.68; 95% CI, 0.65-0.72; P < 0.0001), although both were significantly greater than chance (both P < 0.0001). The optimal diagnostic cut-off for tear osmolarity was ≥308 mOsm/L,
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