Saw S M, Gazzard G, Au Eong K-G, Tan D T H
Department of Community, Occupational and Family Medicine, National University of Singapore, 16 Medical Drive, Singapore 117597, Republic of Singapore.
Br J Ophthalmol. 2002 Nov;86(11):1306-11. doi: 10.1136/bjo.86.11.1306.
Previous studies have evaluated the efficacy of several interventions to decrease the progression of myopia. These include devices that alter the perception of the visual environment and pharmacological treatments. There is no conclusive evidence thus far that alteration of the pattern of spectacle wear, bifocals, ocular hypotensives, or contact lenses retards the progression of myopia. Several randomised clinical trials have demonstrated that the rate of progression of myopia is lower in children given atropine eye drops than those given placebo. However, atropine is associated with short term side effects such as photophobia and possible long term adverse events including light induced retinal damage and cataract formation. Other more selective antimuscarinic agents such as pirenzipine are presently being evaluated. Further well conducted randomised clinical trials with large sample sizes and adequate follow up designed to evaluate treatments to retard the progression of myopia should be conducted, since the identification of an effective intervention may have a greater public health impact on the burden and morbidity from myopia than the few treatments currently available.
先前的研究已经评估了几种干预措施在减缓近视进展方面的疗效。这些措施包括改变视觉环境感知的设备以及药物治疗。迄今为止,尚无确凿证据表明改变眼镜佩戴方式、使用双焦点眼镜、降眼压药物或隐形眼镜能延缓近视进展。多项随机临床试验表明,使用阿托品滴眼液的儿童近视进展速度低于使用安慰剂的儿童。然而,阿托品会带来畏光等短期副作用,以及包括光诱导视网膜损伤和白内障形成在内的可能的长期不良事件。目前正在评估其他更具选择性的抗毒蕈碱药物,如哌仑西平。鉴于确定一种有效的干预措施对近视负担和发病率可能产生的公共卫生影响,可能会超过目前现有的少数治疗方法,因此应该开展更多设计良好、样本量大且随访充分的随机临床试验,以评估延缓近视进展的治疗方法。