单侧先天性白内障和胎儿血管持续存在患儿的手术效果。

Clinical ophthalmology (Auckland, N.Z.) Pub Date : 2024-08-24 eCollection Date: 2024-01-01 DOI:10.2147/OPTH.S472028
Sirpa Loukovaara
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引用次数: 0

摘要

目的:描述被诊断患有先天性白内障和胎儿血管持续性(PFV)的儿童的特征、手术干预和视觉结果:2009年1月1日至2019年12月31日期间,赫尔辛基大学医院开展了一项单中心回顾性观察研究。全国队列包括82名年龄从出生到15岁的儿童,他们接受了晶状体切除术、3孔玻璃体切除术或联合手术,目的是实现视力康复。在手术队列中,对国际疾病分类(ICD-10)代码为Q14.0(PFV)和Q12.0(先天性白内障)的儿科病例进行了识别和分析。通过全面审查病历收集数据,包括临床病史(出生体重)、性别分布、眼部参数(侧位、眼压[IOP]、视力[VA])、白内障和玻璃体视网膜手术干预细节、手术适应症、术后眼部并发症以及功能和解剖结果评估:该组共有11名儿童,年龄从6个月到12岁不等。在接受手术治疗的儿童中,有9只眼睛至少获得了光感视力,占81.8%。其中,两只眼睛(18.2%)获得了手部运动视力,5 只眼睛(55.6%)获得了数手指或更好的视力。此外,有两只眼睛(18.2%)达到了斯奈伦视力表上的视力。然而,有一只眼睛(9.1%)的视力完全丧失,而对侧眼睛则出现了交感神经性眼炎:结论:先天性白内障伴PHV且无眼前节病变者术后视力最佳,而伴有眼前节病变或复杂后节病变者视力预后较差。手术病例的选择非常重要,因为术后可能会发生交感神经性眼炎。我们需要更深入地了解 PFV 的发病机制。
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Surgical Outcomes of Children with Unilateral Congenital Cataract and Persistent Fetal Vasculature.

Purpose: To delineate the characteristics, surgical interventions, and visual outcomes among children diagnosed with congenital cataract and persistent fetal vasculature (PFV).

Patients and methods: Retrospective observational single-center study was conducted between January 1, 2009, and December 31, 2019, at Helsinki University Hospital. The national cohort encompassed 82 children aged from birth to 15 years who underwent lensectomy, 3-port vitrectomy, or a combined procedure, with the objective of achieving visual rehabilitation. Among the surgical cohort, paediatric cases with International Classification of Disease (ICD-10) codes Q14.0 for PFV and Q12.0 for congenital cataract were identified and analyzed. Data were collected through a comprehensive review of medical records, encompassing clinical history (birth weight), gender distribution, ocular parameters (laterality, intraocular pressure [IOP], visual acuity [VA]), details of cataract and vitreoretinal surgical interventions, indications for surgery, postoperative ophthalmic complications, as well as evaluations of functional and anatomical outcomes.

Results: The cohort consisted of 11 children, ranging in age from 6 months to 12 years. Surgical intervention resulted in the attainment of at least light perception vision in nine of the operated eyes, representing 81.8% of cases. Among these, two eyes (18.2%) achieved hand motion vision, while 5 eyes (55.6%) achieved vision of finger counting or better. Additionally, two eyes (18.2%) achieved visual acuity measurable on the Snellen chart. However, one eye (9.1%) experienced complete vision loss, while the contralateral eye developed sympathetic ophthalmia.

Conclusions: Congenital cataract with PHV without anterior segment pathology associated with best postoperative VA, while eyes with anterior segment pathology or a complex posterior segment pathology had poor visual prognosis. Case selection for surgery is considered of great importance, since sympathetic ophthalmia may occur postoperatively. Understanding more deeply pathogenesis of PFV is warranted.

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