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Research from Stanford University confirms that corneal cross-linking (CXL) stabilizes and may improve visual and corneal parameters in children and young adults with keratoconus. This new evidence adds to that from previous studies supporting CXL as a safe, well-tolerated intervention in these younger patients with keratoconus.1
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CXL RESULTS. In this Pentacam set, the pre-op, post-op, and difference map images show the flattening that occurs following CXL.
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Reassuring outcomes in kids. Keratoconus typically starts at puberty but may also occur in younger children. “We were curious to see how well CXL worked in a cohort of young patients with keratoconus,” said study coauthor Edward E. Manche, MD. He added, “We were expecting to have similar results to previously published studies. Our results confirmed that the technique is safe and effective in this group of patients.”
Study details. The researchers retrospectively reviewed the medical records of 49 keratoconus patients (57 eyes) between the ages of 12 and 22 years who underwent CXL between January 2013 and November 2019 at Byers Eye Institute at Stanford University in Palo Alto, California. Eight of these patients underwent bilateral CXL.
Outcome measures included various visual and corneal parameters taken at baseline and at 12 and 24 months postoperatively. The researchers’ analysis revealed post-CXL improvement in corrected distance visual acuity (CDVA), with a mean CDVA of 0.38 ± 0.32 at baseline, a mean CDVA of 0.29 ± 0.31 at 12 months post-op, and a mean CDVA of 0.31 ± 0.31 at 24 months post-op. A significant improvement in maximum keratometry was seen at 12 and 24 months post-CXL.
Corneal thinning (as measured by minimum central corneal thickness) initially occurred but stabilized by 24 months post-CXL. The procedure was well-tolerated by all patients, with no lasting side effects reported. There were no cases of microbial keratitis or delayed epithelial healing beyond one month. Two eyes continued to have mild haze at the 24-month examination, but this was not visually significant.
A call for early intervention. CXL has become a first-line treatment for keratoconus in adults. Although the condition typically progresses more rapidly in children, standardization of its management in pediatric patients is lacking.
“I believe that we should implement topographic screening protocols for children and young adolescents in order to identify patients with keratoconus at an early stage,” said Dr. Manche. He added that earlier diagnosis and treatment of keratoconus “can prevent the long-term morbidity of the disease, including need for specialty contact lenses and corneal transplantation.”
—Patricia Weiser, PharmD
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1 Saleh S et al. Cornea. 2022;41(4):408-416.
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Relevant financial disclosures—Dr. Manche: NIH: S; Research to Prevent Blindness: S.
For full disclosures and the disclosure key, see below.
Full Financial Disclosures
Dr. Hwang Catholic University of Korea: P; Ministry of Education, Republic of Korea: S.
Dr. Manche Alcon: S; Allergan: S; Avedro: C,S; Carl Zeiss Meditec: S; Johnson & Johnson Vision: C,S; NIH: S; Novartis: S; Placid0: P,S; Presbia: S; Research to Prevent Blindness: S; RxSight: U,S; VacuMed: P,S.
Dr. Ten Hulzen None.
Dr. Wykoff Adverum: C,S; Aerie: S; Aldeyra: S; Alimera Sciences S; Allergan: C; Apellis: C,S; Bausch + Lomb: C; Bayer: C,S; Bionic Vision Technologies: C; Boehringer Ingelheim: S; Chengdu Kanghong: C,S; Clearside Biomedical: C,S; EyePoint: C; Gemini Therapeutics: S; Genentech: C,S; Graybug Vision: S; Gyroscope: C,S; Ionis Pharmaceutical: S; IVERIC Bio: C,S; Kato: C; Kodiak Sciences: C,S; LMRI: S; NGM Biopharmaceuticals: C,S; Novartis: C,S; OccuRx: C; Ocular Therapeutix: C; ONL Therapeutics: C,O; Opthea: C,S; Oxurion: C,S; Palatin: C; PolyPhotonix: C,O; RecensMedical: C,O,S; Regeneron: C,S; RegenXBio: C,S; Roche: C,S; Santen: S; Takeda: C; Visgenx: C,O: Xbrane Biopharma: S.
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