Forty-three eyes of 27 patients with blepharoptosis underwent blepharoptosis surgery, and 29 eyes of 18 patients with dermatochalasis underwent blepharoplasty at the Department of Ophthalmology, Kyoto Prefectural University of Medicine between February 2012 and November 2013 and were included in the study. In the blepharoptosis group, 12 males and 15 females with a mean (±SD) age of 63.8 ± 10.0 years (range, 45–80 years) were recruited. None of these patients were in our previous study. Sixteen patients had bilateral blepharoptosis, and 11 were unilateral. In the dermatochalasis group, 7 males and 11 females with a mean age of 68.4 ± 7.68 years (range, 51–84 years) were recruited. Blepharoptosis surgery consisted of a transcutaneous levator advancement, and blepharoplasty consisted of an en-bloc resection of skin, subcutaneous tissue, and orbicularis oculi muscle. The upper eyelid height before and after surgery was assessed from standardized photographs, using margin reflex distance-1 (MRD-1), which is defined as the distance from the central pupil reflex to the upper eyelid margin, with the eyes in primary position.
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Patients with preoperative dry eye symptoms, lacrimal drainage obstruction on syringing, ectropion, entropion, periocular trauma causing eyelid malpositions, lagophthalmos, previous eyelid surgery, and punctual plugs were excluded. Further exclusion criteria were evidence of ocular surface disease which might result in epiphora such as conjunctivitis, keratitis, trichiasis, blepharitis, and thyroid eye disease. Patients using any drops such as artificial tears, antiglaucoma drops, antibiotic drops, and topical steroids were also excluded. Patients who underwent blepharoptosis repair and blepharoplasty at the same time were excluded. We also excluded patients with congenital, myogenic, neurogenic, mechanical, and traumatic ptosis and poor levator function (<10 mm), and those <18 years of age. Thus, pure involutional or contact lens-related blepharoptosis and involutional dermatochalasis were included in this study.
Tear volume was analyzed by measuring the tear meniscus radius (
R) with video meniscometry.
13,14 This method is a noninvasive method for measuring tear meniscus curvature based on the concave mirror formula, using the image obtained from the central lower tear meniscus, which is correlated with tear volume.
15 All measurements were taken of the menisci of both eyes, in the region of the center of the lower eyelid. In order to minimize any effect of gaze position on tear meniscus shape, subjects were asked to look straight ahead in the horizontal plane and were encouraged to blink spontaneously. If the patients used contact lens on the examination day, measurements were taken 2 hours after contact lens removal. Temperature and humidity of the examination room during all tests were maintained at 25°C and 30%, respectively.
MRD-1 and R were measured preoperatively and at 1.5, 3, and 6 months postoperatively. Fluorescein break-up time (FBUT) was also measured pre- and postoperatively. FBUT was measured three times, and an averaged value was used for evaluation. Patients were questioned regarding dry eye symptoms and foreign body sensation pre- and postoperatively.
Changes in MRD-1 or R were analyzed by the paired Student t-test. The reduction rate of R (ΔR) after surgery was calculated using the equation ΔR (%) = [(preoperative R – postoperative R)/(preoperative R)] × 100. The correlations between preoperative R and ΔR and postoperative MRD-1 and ΔR and the increased degree of MRD-1 (ΔMRD-1) and ΔR at each postoperative point were analyzed by Spearman rank correlation coefficient as well.
Informed consent was obtained from each patient prior to the start of the study. The Institutional Review Board of the Kyoto Prefectural University of Medicine approved this study, and it followed the tenets of the Declaration of Helsinki.