Khong Jwu Jin, Anderson Peter, Gray Timothy L, Hammerton Michael, Selva Dinesh, David David
Oculoplastic and Orbital Division, Department of Ophthalmology and Visual Sciences, Royal Adelaide Hospital, University of Adelaide, Adelaide, Australia.
Ophthalmology. 2006 Feb;113(2):347-52. doi: 10.1016/j.ophtha.2005.10.011.
To survey the spectrum of ophthalmic morbidity in Apert's syndrome after craniofacial surgery.
A retrospective study of patients with Apert's syndrome managed at the Australian Craniofacial Unit from 1975 to 2004.
Sixty-one patients (31 females and 30 males) had final ophthalmic reviews at a mean age of 9.3 years (standard deviation, 9.2; range, 0.2-48.3; median, 8.2 years).
Patients were identified from the unit database, and case notes were reviewed. Cases that had < or =2 recorded variables were excluded. Demographic details, age at last ophthalmic review, and total craniofacial operations performed were documented.
Best-corrected visual acuity, cycloplegic refractions, strabismus, amblyopia, corneal abnormality, fundoscopic findings, and visually evoked potentials.
The average number of craniofacial operations performed was 2 (range, 1-4; median, 2). Visual impairment was found in 54% of patients in at least one eye and in 19% of patients in their better eye. The most common cause was amblyopia, with a prevalence of 35%. Optic atrophy caused visual impairment in 5% of patients and corneal scarring in 8%. Sixty-three percent of patients had strabismus with more esotropia than exotropia. Ametropia was found in 69% of patients (42% were hypermetropic and 27% were myopic). Anisometropia of > or =0.75 diopters was present in 16 cases (50%).
Visual impairment is a common finding in Apert's syndrome and amblyopia is the major cause. Ametropia, astigmatism, anisometropia, and strabismus frequently occur in patients with Apert's syndrome at final ophthalmic review. Although optic atrophy was the major cause of visual loss in the era prior to craniofacial surgery, the prevalence of optic atrophy is low since the adoption of current surgical protocols. Corneal damage also contributed toward visual impairment. Early detection and adequate management of amblyopia, timely decompressive surgery before the presence of optic atrophy, and protection of the cornea should be the management goals of ophthalmologists in craniofacial units managing these patients.
调查颅面外科手术后Apert综合征患者的眼科疾病谱。
对1975年至2004年在澳大利亚颅面外科中心接受治疗的Apert综合征患者进行回顾性研究。
61例患者(31例女性和30例男性)在平均年龄9.3岁时(标准差9.2;范围0.2 - 48.3;中位数8.2岁)接受了最终眼科检查。
从该中心数据库中识别出患者,并查阅病历。排除记录变量≤2的病例。记录人口统计学细节、最后一次眼科检查时的年龄以及进行的颅面手术总数。
最佳矫正视力、睫状肌麻痹验光、斜视、弱视、角膜异常、眼底检查结果和视觉诱发电位。
平均进行的颅面手术次数为2次(范围1 - 4;中位数2)。54%的患者至少一只眼睛存在视力损害,19%的患者较好眼睛存在视力损害。最常见的原因是弱视,患病率为35%。视神经萎缩导致5%的患者视力损害,角膜瘢痕导致8%的患者视力损害。63%的患者存在斜视,内斜视多于外斜视。69%的患者存在屈光不正(42%为远视,27%为近视)。16例(50%)患者存在≥0.75屈光度的屈光参差。
视力损害在Apert综合征中很常见,弱视是主要原因。在最终眼科检查时,屈光不正、散光、屈光参差和斜视在Apert综合征患者中经常出现。虽然在颅面外科手术时代之前,视神经萎缩是视力丧失的主要原因,但自从采用当前手术方案以来,视神经萎缩的患病率较低。角膜损伤也导致了视力损害。早期发现和适当治疗弱视、在视神经萎缩出现之前及时进行减压手术以及保护角膜应该是颅面外科中心管理这些患者的眼科医生的治疗目标。