Journal List > J Korean Ophthalmol Soc > v.56(8) > 1010058

Kim and Moon: Analysis of Clinical Changes in Pediatric Low Vision Patients

Abstract

Purpose

To analyze the clinical changes in pediatric low-vision patients under 15 years of age. Methods: We compared pediatric low-vision patients under 15 years of age with subjects from 1995 to 2000 (past group, sub-jects from our previous study) and from 2004 to 2014 (present group). A retrospective chart review was performed of 109 pa-tients from the present group, including epidemiological characteristics and prescribed aids.

Results

The mean age in the present group was 8.6 years and decreased by 1.1 years compared with the past group. The per-centage of pediatric patients under 15 years of age increased from 31.9% to 36.1%; however, there was no statistical sig-nificance ( p = 0.241). The treatable or preventable diseases including congenital cataract and glaucoma decreased significantly from 23.4% to 11.9% ( p = 0.021). The percentage of 0.1 or better in near and distant visual acuity increased significantly from 60.5% and 54.0% to 85.4% and 67.9%, respectively ( p = 0.027 and p < 0.001, respectively). The number of subjects prescribed 2 or more low vision aids and new portable electronic magnifying devices was significant.

Conclusions

Recent changes including decreased mean age, reduced treatable or preventable diseases, and increased per-centage of pediatric patients might correlate to social services. Early detection is important for rehabilitation and quality of life in low vision patients, thus promotion and expansion of social services is necessary. In addition, because the proportion of novel low vision aids has increased, ophthalmologists should stay current on technology improvements.

References

1. World Health Organization. Developing an action plan to prevent blindness at national, provincial and district levels. 2nd. Geneva: World Health Organization and International Agency for the prevention of blindness;2004. p. 43–4.
2. Pascolini D, Mariotti SP. Global estimates of visual impairment: 2010. Br J Ophthalmol. 2012; 96:614–8.
crossref
3. Chiang PP, Marella M, Ormsby G, Keeffe J. Critical issues in im-plementing low vision care in the Asia-Pacific region. Indian J Ophthalmol. 2012; 60:456–9.
crossref
4. Park JH. The relationships between low vision and socioeconomic status in Korean adults. J Korean Ophthalmic Opt Soc. 2011; 16:319–25.
5. Bodeau-Livinec F, Surman G, Kaminski M. . Recent trends in visual impairment and blindness in the UK. Arch Dis Child. 2007; 92:1099–104.
crossref
6. Lee HI, Song KS, Moon NJ. Clinical Analysis of 350 low vision patients. J Korean Ophthalmol Soc. 2000; 41:2391–400.
7. Kim YD, Park SC, Kim DH. Epidemiological analysis and study of social welfare of low vision patients. J Korean Ophthalmol Soc. 2007; 48:111–6.
8. Keen DV. Helping the young visually impaired: a view from the community. Arch Dis Child. 1993; 69:467–9.
crossref
9. Park MG, Moon NJ. Analysis of 137 pediatric low vision patients. J Korean Ophthalmol Soc. 2001; 42:1194–201.
10. Aghaji A, Okoye O, Bowman R. Causes and emerging trends of childhood blindness: findings from schools for the blind in Southeast Nigeria. Br J Ophthalmol. 2015; 99:727–31.
crossref
11. Patel DK, Tajunisah I, Gilbert C, Subrayan V. Childhood blindness and severe visual impairment in Malaysia: a nationwide study. Eye (Lond). 2011; 25:436–42.
crossref
12. Sarvananthan N, Surendran M, Roberts EO. . The prevalence of nystagmus: the Leicestershire nystagmus survey. Invest Ophthalmol Vis Sci. 2009; 50:5201–6.
crossref
13. Haji SA, Sambhav K, Grover S, Chalam KV. Evaluation of the iPad as a low vision aid for improving reading ability. Clin Ophthalmol. 2014; 9:17–20.
14. Hakobyan L, Lumsden J, O'Sullivan D, Bartlett H. Mobile assis-tive technologies for the visually impaired. Surv Ophthalmol. 2013; 58:513–28.
crossref
15. Chadha RK, Subramanian A. The effect of visual impairment on quality of life of children aged 3-16 years. Br J Ophthalmol. 2011; 95:642–5.
crossref
16. Gyawali R, Paudel N, Adhikari P. Quality of life in Nepalese pa-tients with low vision and the impact of low vision services. J Optom. 2012; 5:188–95.
crossref
17. Oh DH, Park SH, Lee JK, Moon NJ. Clinical findings and results of low vision devices in pediatric patients with albinism. J Korean Ophthalmol Soc. 2011; 52:466–71.
crossref
18. Çalik BB, Kitiş A, Cavlak U, Oğ uzhanoğ lu A. The impact of atten-tion training on children with low vision: a randomized trial. Turk J Med Sci. 2012; 42:(Suppl 1). 1186–93.

Figure 1.
Electronic magnifying device (mouse type).
jkos-56-1256f1.tif
Table 1.
Demographics of participants
Past (1995-2000) Present (2004-2014) p-value
Total subjects 137 109
M:F 85:52 59:50 1.567 ( p = 0.211)
Mean age (years)
 Male 9.8 8.7 ± 3.4 p = 0.337
 Female 9.5 8.6 ± 3.8
Total 9.7 8.6 ± 3.6
Percentage of ≤15 years old 31.9% 36.1% 1.372 ( p = 0.241)

Values are presented as mean ± SD unless otherwise indicated.

Chi-square ( p-value);

Student’s t-test between male and female of the present group.

Table 2.
Distribution of diagnosis
Diagnosis Past (1995-2000) Present (2004-2014)
Preventable or treatable (n, %)
 Retinopathy of prematurity 10 (7.3) 7 (6.4)
 Congenital cataract 17 (12.4) 6 (5.5)
 Congenital glaucoma 2 (1.5) 0
 Retinal detachment 2 (1.5) 0
 Retinoblastoma 1 (0.7) 0
 Total 32 (23.4) 13 (11.9)
Unpreventable or untreatable
 Optic atrophy 57 (41.6) 30 (27.5)
 Albinism 10 (7.3) 18 (16.5)
 Macular dystrophy and degeneration 13 (9.5) 17 (15.6)
 Nystagmus 0 13 (11.9)
 Retinitis pigmentosa 1 (0.7) 4 (3.6)
 Morning glory syndrome 0 3 (2.8)
 LHON 0 3 (2.8)
 Optic nerve hypoplasia 0 3 (2.8)
 Cortical visual impairment 0 3 (2.8)
 Aniridia 6 (4.4) 1 (0.9)
 Stargardt’s disease 2 (1.5) 1 (0.9)
 PHPV 6 (4.4) 0
 Corneal opacity 3 (2.2) 0
 Micropthalmos 3 (2.2) 0
 Peter’s anomaly 1 (0.7) 0
 Sixth nerve palsy 1 (0.7) 0
 Retinal dystrophy 1 (0.7) 0
 FEVR 1 (0.7) 0
 Total 105 (76.6) 96 (88.1)
 Chi-square test ( p-value) 5.307 ( p = 0.021)

LHON = Leber’s hereditary optic neuropathy; PHPV = persistent hyperplastic primary vitreous; FEVR = familial exudative vitreoretinopathy.

Between ‘Preventable or Treatable’ and ‘Unpreventable or Untreatable’ of the past and the present.

Table 3.
Distribution of distant and near visual acuity
Visual acuity Distant Near
Visual acuity Past (1995-2000) Present (2004-2014) Past (1995-2000) Present (2004-2014)
L.P(+)-0.01 18 (13.1%) 4 (3.7%) 2 (1.5%) 2 (1.8%)
0.02-0.04 19 (13.9%) 23 (21.1%) 13 (9.5%) 2 (1.8%)
0.05-0.09 26 (19.0%) 8 (7.3%) 39 (28.5%) 12 (11.0%)
0.1-0.29 64 (46.7%) 72 (66.1%) 65 (47.4%) 57 (52.3%)
0.3-0.5 10 (7.3%) 2 (1.8%) 18 (13.1%) 36 (33.1%)
Total 137 (100%) 109 (100%) 137 (100%) 109 (100%)
Chi-square test ( p-value) 4.8796 ( p = 0.027) 17.103 ( p < 0.001)

L.P = light perception.

Between L.P(+)-0.09 and 0.1-0.5 of the past and the present.

Table 4.
Low vision aids for near vision
Past (1995-2000) Present (2004-2014)
Conventional low vision aids
 Magnifier (n, %)
  Light gathering magnifier 41 (36.9) 26 (23.0)
  Hand-held magnifier 21 (18.9) 41 (36.3)
  Stand magnifier 12 (10.8) 4 (3.5)
 Glasses (n, %)
  Prismatic glasses 5 (4.5) 2 (1.8)
  High plus reading glasses 2 (1.8) 1 (0.9)
  Clip-on microscope 2 (1.8) 6 (5.3)
  Clear image (n, %) 14 (12.6) 7 (6.2)
  Telemicroscope (n, %) 12 (10.8) 0
  CCTV (n, %) 2 (1.8) 3 (2.6)
 Newly prescribed aids (n, %)
  Electronic magnifying device (Pocket viewer) 15 (13.3)
  Electronic magnifying device (mouse type) 2 (1.8)
  Electronic magnifying device (other type) 5 (4.4)
  Portable CCTV 1 (0.9)
  Total (n, %) 111 (100) 113 (100)

CCTV = closed-circuit television.

TOOLS
Similar articles