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1 dry eye who would benefit from a lipid-based artificial tear.
2 acy and tolerability versus cyclosporine and artificial tears.
3 eal thickness obtained after instillation of artificial tears.
4 eal thickness obtained after instillation of artificial tears.
5 % diclofenac sodium; and group IV, control + artificial tears.
6 D below the mean value for eyes administered artificial tears.
7 cal NSAIDs, while the control group received artificial tears.
8 lity in older adult patients and those using artificial tears.
9 eparated by 28(+/- 3) days of treatment with artificial tears.
10 d with a nationwide outbreak of contaminated artificial tears.
11 ditional therapies such as preservative free artificial tears.
12 ndomised 1:1 to receive laughter exercise or artificial tears (0.1% sodium hyaluronic acid eyedrop, c
14 The results demonstrated that compared with artificial tears, 2% RBM significantly increased the TBU
15 Following a 14-day run-in period with an artificial tear administered 2 times per day, eligible p
19 patients with presbyopia who were started on artificial tears and had no history of topical pilocarpi
20 mental modifications, dietary modifications, artificial tears and lubricants, punctal occlusion, inte
22 ces in therapy include improved nonpreserved artificial tears and therapies targeted at decreasing oc
23 gical ointment, 0.1% cyclosporine eye drops, artificial tears, and 0.5% loteprednol for keratoplasty
24 DED by a clinician, (2) the prescription of artificial tears, and/or (3) symptoms of dry eyes for at
26 allergic reaction followed by application of artificial tears (ATs), 5 minutes of cold compress (CC),
35 treatment groups: group I, 0.5% cidofovir + artificial tears; group II, 0.5% cidofovir + 0.5% ketoro
36 in the adverse events between the 2% RBM and artificial tears groups were nonsignificant (SMD = 1.23,
37 ed that four of the six animals administered artificial tears had damage involving 100% of the neural
41 red to both eyes twice daily for 7 days, and artificial tears, ketorolac, and diclofenac four times d
42 riamcinolone acetonide (TA), and lipid-based artificial tears (LBAT)-were tested in cadaveric porcine
43 with DED were randomized to receive topical artificial tears, loteprednol etabonate 0.5%, or lotepre
45 therapies such as preserved and nonpreserved artificial tears, nutritional supplements, topical cyclo
50 Eight trials compared interventions with artificial tears or saline (n = 4) or with steroids (n =
52 ng inadequate sleep (p-value < 0.001), using artificial tears (p-value < 0.001), and number of hours
53 he peptide in one of four delivery vehicles: artificial tears, PBS, methylcellulose, and aquaphor cre
55 oing SLT were randomized to receive placebo (artificial tears), prednisolone acetate 1%, or ketorolac
56 ender, preoperative and postoperative use of artificial tears, preoperative and postoperative margina
57 overall DED-related symptom scores than did artificial tears (SMD = - 1.61, 95% CI = - 2.61 to - 0.6
59 each of the first 4 extinction sessions, an artificial tear solution or tetracaine hydrochloride was
60 contact lens care disinfecting solutions or artificial tear solutions containing polyquaternium-1.
62 ting of the cornea, by applying and removing artificial tears, temperature changes (35 degrees C-15 d
64 zed 1:1 to receive a bimatoprost insert plus artificial tears twice daily or a placebo insert plus ti
68 ement in ocular-surface health, reduction in artificial tear use, and improved contact lens comfort i
69 in dry eye symptoms, ocular-surface status, artificial tear use, contact lens comfort, and tear brea
72 ase-patients had increased odds of receiving artificial tears versus controls (crude matched OR, 5.0;
75 t C-25 (10 mug/mL), cyclosporine (0.05%), or artificial tears were topically administered to eyes of
76 n, it was dry eye (42.26%, with major use of artificial tears), with many self-stopping (e.g., gentam