Trending Topic

23 mins

Trending Topic

Developed by Touch
Mark CompleteCompleted
BookmarkBookmarked
Luke G Qin, Michael T Pierce, Rachel C Robbins

The uvea is a vascular stratum that includes the iris, ciliary body and choroid. Uveitis is defined as inflammation of a part of the uvea or its entirety, but it is also used to describe inflammatory processes of any part of the eye, such as the vitreous or peripheral retina. The clinical taxonomy of uveitis […]

Comparison of Contact Lens and Intraocular Lens Correction of Monocular Aphakia During Infancy

Natalie Weil, Scott R Lambert
Share
Facebook
X (formerly Twitter)
LinkedIn
Via Email
Mark CompleteCompleted
BookmarkBookmarked
Copy LinkLink Copied
Download as PDF
Published Online: Feb 9th 2015 US Ophthalmic Review, 2015;8(1):21–2 DOI: http://doi.org/10.17925/usor.2015.8.1.21
Select a Section…
1

Abstract

Overview

The Infant Aphakia Treatment Study recommended primary intraocular lens (IOL) implantation be reserved for infants with parents unable to manage contact lenses. The best baseline predictor of a good visual outcome was private health insurance. IOL implantation was associated with more adverse events, but lower direct costs to parents.

Keywords

Infant Aphakia Treatment Study, primary intraocular lens, total direct costs, congenital cataracts, contact lens, iris prolapse, pupillary membranes

2

Article

The Infant Aphakia Treatment Study (IATS) was a randomized, multicenter clinical trial that compared visual outcomes at age 4.5 years with or without intraocular lens (IOL) implantation in 114 children who underwent unilateral cataract surgery at 1 to <7 months of age. The study concluded that the visual outcomes were similar in both treatment groups, but there were more intraoperative and postoperative adverse events in the IOL group and, as a result, IOL implantation was only recommended if it was deemed likely that the parents of a child would not be able to manage contact lenses (CTLs). The most common adverse events in the IOL group were intraoperative iris prolapse (11 %), lens reproliferation into the visual axis (40 %), pupillary membrane (28 %), and postoperative correctopia (28 %). Nearly five times more patients in the IOL group required an additional intraocular surgery to clear the visual axis in comparison to the CTL group (68 % versus 14 %).1,2 The majority of these adverse events occurred during the first year after cataract surgery.3 We also found the prevalence of glaucoma, strabismus, and stereopsis to be similar in the two treatment groups at age 5 years.2,4

While 1 year after cataract surgery, the total direct costs were 37 % higher in the IOL group, by age 5 the total direct costs were nearly the same for both treatment groups. The higher costs in the IOL group at 1 year after cataract surgery were primarily due to the increased costs of additional intraocular surgeries. However, after the first postoperative year the costs were higher in the CTL group so that by age 5, the costs in the IOL group were only 7 % higher than the CTL group. Most of the increased costs after the first postoperative year in the CTL group were due to the replacement of CTLs. Both groups of patients wore bifocal spectacles at age 2 andonward. The total cost of supplies (spectacles, CTLs, and occlusive patches) were nearly twice as high in the CTL group ($7,728) compared with the IOL group ($3,204). So while the total direct costs were still slightly higher at age 5 in the IOL group, the supply costs, which in most cases are borne by parents since most medical insurance policies do not cover these costs, were more than $4,000 higher in the CTL group.5,6

We also analyzed whether there were baseline factors that could predict visual outcome. We found the age at which cataract surgery was performed to only be weakly associated with the age 4.5 visual outcome. Overall, while patients <3 months of age at the time of cataract surgery had an improved median visual acuity, the strongest predictor of visual outcome was whether the patient had private insurance.7 Patients covered by private insurance had a significantly better visual outcome compared with children covered by Medicaid.

Some have questioned whether there would have been fewer postoperative adverse events in the IOL group if steroids had been prescribed to be administered more frequently. It is unlikely that the more frequent instillation of topical corticosteroids would have affected the incidence of lens reproliferation into the visual axis. While it is possible that the more frequent administration of corticosteroids would have reduced the incidence of certain inflammatory complications such as pupillary membranes, we were unable to find an association between the frequency topical corticosteroids were prescribed and the prevalence of inflammatory membranes.8 It is possible that the incidence of adverse events would have been lower if more experienced pediatric cataract surgeons had performed the surgeries. However, it should be emphasized that all of the investigators participating in the Infant Aphakia Treatment Study were experienced pediatric cataract surgeons who were selected to participate in the clinical trial because of the high volume of pediatric cataract surgery at their clinical site. The decision to implant an IOL in an infant <7 months of age with a visually significant unilateral congenital cataract is complicated. If parents have the financial resources to purchase CTLs and it is deemed that they can likely manage them, the IATS supports leaving these patients aphakic and correcting them optically with a CTL. However, there is still a subset of these patients who would likely benefit from IOL implantation. This decision must be carefully considered and made through an established patient–doctor relationship on an individual basis.

2

References

  1. Infant Aphakia Treatment Study Group. A randomized clinical
    trial comparing contact lens and intraocular lens correction of
    monocular aphakia during infancy: Grating acuity and adverse
    events at age 1 year, Arch Ophthalmol, 2010;128:810–8.

  2. Infant Aphakia Treatment Study Group. A randomized clinical
    trial comparing contact lens to intraocular lens correction of
    monocular aphakia during infancy: HOTV optotype acuity at age
    4.5 years and clinical findings at age 5 years, JAMA Ophthalmol,
    2014;132:676–82.

  3. Plager DA, Lynn MJ, Buckley EG, et al., Complications in the first
    5 years following cataract surgery in infants with and without
    IOL in the IATS, Am J Ophthalmol, 2014;158:892–8.

  4. Hartmann EE, Stout AU, Lynn MJ, et al.; Infant Aphakia
    Treatment Study Group, Stereopsis results at 4.5 years of
    age in the Infant Aphakia Treatment Study, Am J Ophthalmol,
    2015;159:64–70.

  5. Carrigan AK, DuBois LG, Becker ER, Lambert SR, Cost of
    intraocular lens vs contact lens treatment after unilateral
    congenital cataract surgery: Retrospective analysis at age 1
    year, Ophthalmology, 2013;120:14–9.

  6. Kruger S, DuBois L, Becker ER, et al.; Infant Aphakia Treatment
    Study, Cost of intraocular lens vs. contact lens treatment after
    unilateral congenital cataract surgery in the Infant Aphakia
    Treatment Study: Retrospective analysis at age 5 years,
    Ophthalmology, 2015;122:288–92.

  7. Hartmann EE, Lynn MJ, Lambert S, Baseline characteristics
    of the Infant Aphakia Treatment Study population: Predicting
    recognition acuity at 4.5 years of age, Invest Ophthalmol Vis Sci,
    2015;56:388–95.

  8. Lambert SR, Plager DA, Buckley EG, et al.; Infant Aphakia
    Treatment Study, The Infant Aphakia Treatment Study: Was the
    high rate of intraoperative and postoperative adverse events in
    the intraocular lens group preventable?, J AAPOS, In Press.

3

Article Information

Disclosure

Natalie Weil, MD, and Scott R Lambert, MD, have no conflicts of interest to declare.

Correspondence

Scott R Lambert, MD, R Howard Dobbs Professor of Ophthalmology and Pediatrics, Emory University, Atlanta, GA, US. E: scott.lambert@emory.edu

Support

Supported by National Institutes of Health (NIH) Grants U10 EY13272 and U10 EY013287 and in part by NIH Departmental Core Grant EY006360 and Research to Prevent Blindness, Inc., New York, New York.

Access

This article is published under the Creative Commons Attribution Noncommercial License, which permits any noncommercial use, distribution, adaptation, and reproduction provided the original author(s) and source are given appropriate credit.

Received

2015-01-10T00:00:00

4

Further Resources

Share
Facebook
X (formerly Twitter)
LinkedIn
Via Email
Mark CompleteCompleted
BookmarkBookmarked
Copy LinkLink Copied
Download as PDF
Close Popup