Evaluation of the Ocular Surface Disease Index Questionnaire as a Discriminative Test for Clinical Findings in Dry Eye Disease Patients

To investigate to what extent the OSDI can be utilized as a discriminative test for clinical findings. One thousand and ninety patients with dry eye disease (DED) were consecutively included and examined for osmolarity, tear film break-up time (TFBUT), ocular protection index (OPI), ocular surface s...

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Published inCurrent eye research Vol. 44; no. 9; pp. 941 - 947
Main Authors Yazdani, Mazyar, Chen, Xiangjun, Tashbayev, Behzod, Utheim, Øygunn A., Ræder, Sten, Hua, Yanjun, Eidet, Jon R., Stojanovic, Aleksandar, Dartt, Darlene A., Utheim, Tor P.
Format Journal Article
LanguageEnglish
Published England Taylor & Francis 02.09.2019
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Summary:To investigate to what extent the OSDI can be utilized as a discriminative test for clinical findings. One thousand and ninety patients with dry eye disease (DED) were consecutively included and examined for osmolarity, tear film break-up time (TFBUT), ocular protection index (OPI), ocular surface staining (OSS), Schirmer I test (ST), meibum expressibility (ME), meibum quality (MQ), and diagnosis of meibomian gland dysfunction (MGD). Receiver-operating characteristic curve (ROC) analysis considering optimum balanced sensitivity and specificity (close to 50%) was used for assessment. The present study on more than 1,000 patients indicates that the OSDI in the ROC curve analysis is a poor discriminator of pathological scores for TFBUT ≤ 5 (AUC = 0.553; p = .012) and ≤10 s (AUC = 0.608; p = .002), OSS ≥ 3 (AUC = 0.54; p = .043), ST ≤ 5 (AUC = 0.550; p = .032) and ≤10 mm/5 min (AUC = 0.544; p = .016), and ME ≥ 1 (AUC = 0.594; p = <0.001). Pathological scores for osmolarity >308 and >316 mOsm/L, OPI, OSS > 1, MQ, and MGD could not be discriminated by OSDI (p > .05). Cut-off values for the OSDI can be defined to discriminate pathological TFBUT (≤5 and ≤10), OSS (≥3), ST (≤5 and ≤10) and ME, however, the discriminability was low. Our comprehensive study emphasises the importance of taking both symptoms and signs into account in DED management.
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ISSN:0271-3683
1460-2202
DOI:10.1080/02713683.2019.1604972