Analysis of the outcomes of three different cross‐linking protocols for treatment of paediatric keratoconus: A multicentre randomized controlled trial

圆锥角膜 角膜曲率计 医学 眼科 角膜地形图 随机对照试验 角膜胶原交联 视力 前瞻性队列研究 外科 角膜
作者
Mohammed Iqbal,Ahmed Gad,Ahmed Kotb,Mahmoud Abdelhalim
出处
期刊:Acta Ophthalmologica [Wiley]
卷期号:102 (1) 被引量:6
标识
DOI:10.1111/aos.15686
摘要

Abstract Purpose To analyse long‐term outcomes of standard cross‐linking (SCXL), accelerated cross‐linking (ACXL) and transepithelial cross‐linking (TCXL) in the treatment of progressive paediatric keratoconus regarding stability, safety and efficacy. Methods This prospective multicentre randomized controlled trial included 97 eyes of 97 paediatric patients with stages I–III ABCD keratoconus grading system, who were randomized into three groups; SCXL group (control group, n = 32; 3 mW/cm 2 × 30 min/5.4 J/cm 2 ), ACXL ( n = 33; 18 mW/cm 2 × 5 min/5.4 J/cm 2 ) and TCXL ( n = 32; 18 mW/cm 2 × 5 min/5.4 J/cm 2 ). Subjective refraction, uncorrected and corrected visual acuity, keratometry and pachymetry measurements using corneal topography were recorded preoperatively and 1, 2 and 3 years postoperatively. Results SCXL group exhibited significant successive improvements in the mean visual, refractive and keratometric parameters throughout the entire postoperative 3 years while ACXL group exhibited significant improvements in visual and keratometric parameters in the first postoperative year that remained stable in second and third postoperative years. TCXL group exhibited significant progressive deterioration in all mean parameters compared to SCXL and ACXL ( p < 0.0001). Both SCXL and ACXL revealed final 100% success rate with good stability while TCXL revealed final 22% failure rate with keratoconus progression ( p < 0.0001). Conclusion SCXL and ACXL were comparable in halting keratoconus progression and achieved good stability and safety; however, SCXL was more efficient than ACXL as it yielded greater significant postoperative mean visual, refractive and keratometric improvements achieving smoother corneal remodelling. Both SCXL and ACXL were much superior to TCXL. SCXL is the best CXL treatment option for paediatric keratoconus while ACXL is a good and effective alternative.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Boniu_wang完成签到,获得积分10
1秒前
顺利的小懒猪完成签到,获得积分10
2秒前
牛0254发布了新的文献求助10
2秒前
3秒前
量子星尘发布了新的文献求助10
4秒前
4秒前
xye发布了新的文献求助10
5秒前
5秒前
GGGG完成签到,获得积分10
6秒前
jack应助科研通管家采纳,获得10
7秒前
搜集达人应助科研通管家采纳,获得30
7秒前
充电宝应助科研通管家采纳,获得10
7秒前
Jasper应助科研通管家采纳,获得10
7秒前
jack应助科研通管家采纳,获得10
7秒前
隐形曼青应助科研通管家采纳,获得10
7秒前
jack应助科研通管家采纳,获得10
7秒前
bkagyin应助科研通管家采纳,获得10
7秒前
OMR123完成签到,获得积分10
8秒前
热情大树发布了新的文献求助10
9秒前
飞0802发布了新的文献求助10
9秒前
吴振明完成签到,获得积分10
9秒前
健忘惜萱发布了新的文献求助10
11秒前
艺阳完成签到,获得积分10
11秒前
Agoni完成签到,获得积分10
11秒前
傻傻的小刺猬完成签到,获得积分10
12秒前
12秒前
漂泊的思绪完成签到,获得积分10
14秒前
14秒前
16秒前
研友_VZG7GZ应助谦让的靖巧采纳,获得10
16秒前
yookia应助雪白蚂蚁采纳,获得10
16秒前
zhouxiuman完成签到,获得积分10
17秒前
SYLH应助cc采纳,获得10
18秒前
zyj完成签到,获得积分10
18秒前
lmg发布了新的文献求助10
19秒前
CometF完成签到 ,获得积分10
21秒前
猪猪hero发布了新的文献求助10
21秒前
22秒前
22秒前
李爱国应助吖吖草采纳,获得30
22秒前
高分求助中
The Mother of All Tableaux Order, Equivalence, and Geometry in the Large-scale Structure of Optimality Theory 2400
Ophthalmic Equipment Market by Devices(surgical: vitreorentinal,IOLs,OVDs,contact lens,RGP lens,backflush,diagnostic&monitoring:OCT,actorefractor,keratometer,tonometer,ophthalmoscpe,OVD), End User,Buying Criteria-Global Forecast to2029 2000
Optimal Transport: A Comprehensive Introduction to Modeling, Analysis, Simulation, Applications 800
Official Methods of Analysis of AOAC INTERNATIONAL 600
ACSM’s Guidelines for Exercise Testing and Prescription, 12th edition 588
A new approach to the extrapolation of accelerated life test data 500
T/CIET 1202-2025 可吸收再生氧化纤维素止血材料 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 3954275
求助须知:如何正确求助?哪些是违规求助? 3500311
关于积分的说明 11098873
捐赠科研通 3230815
什么是DOI,文献DOI怎么找? 1786149
邀请新用户注册赠送积分活动 869840
科研通“疑难数据库(出版商)”最低求助积分说明 801651