Key Takeaways for Optometrists
- Ask cosmetic-using DED patients specifically about make-up removal practices and periocular skin symptoms during routine assessment, since this remains a commonly overlooked contact point with the ocular surface.
- Consider gentle, preservative-free periocular skincare as an adjunct—not a replacement—to standard DED therapy in patients presenting with lid erythema and MGD, particularly those with a history of eye-cosmetic use.
- The 37% absolute reduction in periocular erythema and significant MGD grading improvement occurred without any worsening cases and with favorable tolerability (0% itching, 15% mild stinging/warmth), suggesting low clinical risk in trialing this approach.
- TBUT and SPEED score improvements were numerically favorable but did not reach statistical significance in this small cohort; set patient expectations accordingly and consider this regimen as one component of a broader DED management plan rather than a standalone solution.
Study design and primary clinical outcomes for adjunctive periocular skincare
The retrospective chart review evaluated 27 female DED patients (mean age 53 years) treated at a single optometric practice, assessed at baseline and 28-day follow-up.1 All patients had diagnosed DED and MGD and were existing eye-cosmetic users. Adjunctive periocular skincare consisted of a sensitive eye make-up remover (preservative-free, ionized-water-based) and a sensitive eye daily renewal cream (preservative-free, barrier-supportive; Optase Life; Scope Eyecare), added alongside each patient’s existing concomitant DED therapies, which included intense pulsed light, cyclosporine, perfluorohexyloctane, artificial tears, warm compresses, hypochlorous acid spray, and omega-3 supplementation as clinically indicated.
The primary end point, periocular erythema, showed a statistically significant reduction from 63% prevalence at baseline to 26% at day 28, a 37% absolute reduction (McNemar P = .004), with 10 of 27 patients improved and none worsened.1 MGD grading also improved significantly (P = .020), with 30% of patients (4 of 27) showing improvement and the proportion of patients with no MGD findings increasing from 0% at baseline to 4% at day 28, alongside a shift away from grade 1+ and elimination of grade 2+ findings.
Numerical improvements in tear break-up time (TBUT) and SPEED symptom scores did not reach statistical significance: TBUT improved from a mean of 4.48 seconds to 5.22 seconds (+0.74 seconds, 56% of patients improved; P = .180), and SPEED scores decreased from a mean of 14.7 to 13.7 (30% of patients achieved a 3-point or greater reduction; P = .313).1 Corneal or conjunctival staining improved in 40% of patients with evaluable baseline staining (6 of 15).
Patient-reported satisfaction and tolerability of preservative-free periocular regimen
Tolerability was favorable, with no serious adverse events reported across the cohort.1 Local tolerability assessments showed stinging in 15% of patients (4 of 27), warmth or burning in 15% (4 of 27), and no reported itching. One patient discontinued treatment due to an undesirable effect; no serious adverse events were associated with this discontinuation.
Patient-reported satisfaction was high across measured domains (n = 27): 96% reported the regimen as nonirritating, 93% indicated intent to continue use, and 70% reported preferring the regimen to their prior periocular care.1 Individual satisfaction items ranged from 81% to 96% agreement, including skin feeling less dry (96%), eyelids feeling soothed (96%), skin feeling refreshed (96%), and willingness to recommend to others (96%). Patient comments captured in the poster described the eye make-up remover as effective without stinging and the renewal cream as improving hydration and comfort.
“Cosmetic use on the periocular skin can affect ocular surface disease; it is important that we educate patients about this and recommend safe products that will not worsen their condition,” Hornick said.
The study authors noted several limitations, including its retrospective, single-center design with a small, all-female cohort limiting generalizability, the absence of a control arm, and the use of multimodal concomitant DED therapies that limit attribution of the observed improvements to the periocular skincare regimen specifically.1 Prospective, randomized, controlled studies with longer follow-up and standardized patient-reported outcome measures were identified as warranted to confirm the contribution of adjunctive periocular skincare to overall DED management.
References
Hornick L, Duffy E, Bhattacharrya S. Clinical benefits of adjunctive periocular skincare in dry eye patients: a retrospective analysis of periocular erythema, MGD, tear film stability, symptom burden & patient-reported outcomes. Poster presented at: AOA Annual Meeting; June 2026; Phoenix, AZ. Poster #40.
Craig JP, Nichols KK, Akpek EK, et al. TFOS DEWS II definition and classification report. Ocul Surf. 2017;15(3):276-283. doi:10.1016/j.jtos.2017.05.008