Nakakura Shunsuke, Yamamoto Minamai, Terao Etsuko, Nagatomi Nozomi, Matsuo Naoko, Fujisawa Yausko, Fujio Yuki, Tabuchi Hitoshi, Kiuchi Yoshiaki
Department of Ophthalmology, Saneikai Tsukazaki Hospital, Himeji, Japan.
Department of Ophthalmology and Visual Sciences, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
Clin Ophthalmol. 2014 Dec 30;9:51-6. doi: 10.2147/OPTH.S75651. eCollection 2015.
We investigated the incidence of prostaglandin-associated periorbitopathy (PAP) in subjects with glaucoma treated with latanoprost ophthalmic solution.
One eye and the forehead in 22 subjects were evaluated. All patients had used latanoprost for more than 1 year (range, 12 to 45 months; mean, 26.0 months) and were prostaglandin F2α analogue treatment-naïve. Digital photographs of the subjects obtained before latanoprost therapy and at the last examination were compared retrospectively. Four signs of PAP (deepening of the upper eyelid sulcus (DUES), upper eyelid ptosis, flattening of the lower eyelid bags, and inferior scleral show) and supplemental side effects around the eyelids (eyelash growth, poliosis, and eyelid pigmentation) were judged to be negative or positive by three independent observers. If the observers unanimously rated a sign as positive, the result was defined as positive.
Twelve subjects (54.5%) had no apparent signs. Three subjects were judged to have DUES (13.6%), and two subjects each were judged to have flattening of the lower eyelid bags and eyelid pigmentation (9.0%). The other signs were judged as positive in only one subject each, respectively (4.5%). A univariate logistic regression analysis showed no significant associations between any of the signs and age, sex, or the duration of therapy.
Latanoprost induced DUES, upper eyelid ptosis, flattening of the lower eyelid bags, inferior scleral show, and supplemental side effects around the eyelids; however, the rates of such occurrence might be relatively low.
我们调查了使用拉坦前列素滴眼液治疗的青光眼患者中前列腺素相关性眶周病变(PAP)的发生率。
对22名受试者的一只眼睛和前额进行了评估。所有患者使用拉坦前列素超过1年(范围为12至45个月;平均26.0个月),且未曾接受过前列腺素F2α类似物治疗。回顾性比较了拉坦前列素治疗前和最后一次检查时获得的受试者数码照片。由三名独立观察者判断PAP的四个体征(上睑沟加深(DUES)、上睑下垂、下睑袋变平、巩膜下显露)以及眼睑周围的补充副作用(睫毛生长、白发、眼睑色素沉着)为阴性或阳性。如果观察者一致将一个体征评为阳性,则结果定义为阳性。
12名受试者(54.5%)没有明显体征。3名受试者被判定有DUES(13.6%),2名受试者分别被判定有下睑袋变平和眼睑色素沉着(9.0%)。其他体征分别仅在1名受试者中被判定为阳性(4.5%)。单因素逻辑回归分析显示,任何体征与年龄、性别或治疗持续时间之间均无显著关联。
拉坦前列素可导致DUES、上睑下垂、下睑袋变平、巩膜下显露以及眼睑周围的补充副作用;然而,这些情况的发生率可能相对较低。