This study was performed to test viscoelastic artificial tears (VAT) based
on both subjective and clinical parameters in patients with keratoconjuncti
vitis sicca (KCS). Twenty-eight patients were evaluated in a randomized dou
ble-blind study. Sodium hyaluronate was used in two different concentration
s (0.4%, 0.25%) and in combination with chondroitin sulfate. Each preparati
on was used for one week preceded by another weekly cycle using a sodium ch
loride solution. Before and after each cycle, clinical examinations were pe
rformed: tear film break-up time, Schirmer's test, lipid-layer thickness an
d fluorescein staining. Patients kept a record of the drop-frequency, subje
ctive response and side effects. After the study, they were asked to give a
rating of the various preparations. The severity of KCS was expressed base
d on a sicca score and correlated with response to viscoelastic treatment.
Both the subjective and the clinical parameters revealed no statistically s
ignificant differences between the various viscoelastic agents or between t
he viscoelastics and the sodium chloride solutions. Severe side effects did
not occur. There was a positive correlation of response to viscoelastic tr
eatment with severe KCS (+0.36) but not with mild KCS (-0.07). The VAT seem
s to be indicated in severe cases of dry-eye syndrome. Sodium chloride solu
tions may be a useful short-term alternative to other tear formulations. (C
) 2001 Elsevier Science Ltd. All rights reserved.