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Clinical science
Presenting features and early management of childhood intermittent exotropia in the UK: inception cohort study
  1. D Buck1,
  2. C Powell2,
  3. P Cumberland3,
  4. H Davis4,
  5. E Dawson5,
  6. J Rahi3,6,
  7. J Sloper5,
  8. R Taylor7,
  9. P Tiffin8,
  10. M P Clarke2,9,
  11. on behalf of the Improving Outcomes in Intermittent Exotropia Study Group
  1. 1
    Institute of Health and Society, Newcastle University, Newcastle upon Tyne, UK
  2. 2
    Royal Victoria Infirmary Eye Department, Newcastle upon Tyne Hospitals NHS Trust, Newcastle upon Tyne, UK
  3. 3
    Institute of Child Health, University College London, London, UK
  4. 4
    Academic Unit of Ophthalmology & Orthoptics, University of Sheffield, Sheffield, UK
  5. 5
    Moorfields Eye Hospital, London, UK
  6. 6
    Institute of Ophthalmology, University College London, London, UK
  7. 7
    York Hospitals NHS Trust, York, UK
  8. 8
    Sunderland Eye Infirmary, Sunderland, UK
  9. 9
    Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK
  1. Correspondence to Dr M P Clarke, Claremont Wing Eye Department, Royal Victoria Infirmary, Queen Victoria Road, Newcastle upon Tyne NE1 4LP, UK; m.p.clarke{at}ncl.ac.uk

Abstract

Aim: To investigate factors associated with early management of intermittent exotropia (X(T)) in hospital eye departments in the UK in a prospective cohort study.

Methods: An inception cohort of 460 children aged <12 years with previously untreated X(T) (mean age 3.6 years, 55.9% girls) was recruited from 26 UK hospital children’s eye clinics and orthoptic departments. Participants received a standard ophthalmic examination at recruitment and orthoptic assessment at three-monthly intervals thereafter. The influence of severity of exotropia (control measured by Newcastle Control Score (NCS), and angle of strabismus, visual acuity and stereoacuity) and age on the type of management was investigated.

Results: Within the first 12 months following recruitment, 297 (64.6%) children received no treatment, either for impaired visual acuity or for strabismus. Ninety-six (21%) children had treatment for impaired visual acuity. Eighty-nine (19.4%) received treatment for strabismus (22 of whom also received treatment for defective visual acuity); in 54 (11.7%) treatment was non-surgical and in 35 (7.6%) eye muscle surgery was performed. Children with poor (score 7–9) control of strabismus at recruitment were more likely to have surgery than children with good (score 1–3) control (p<0.001). Children who had no treatment were younger (mean age 3.38 years) than those who were treated (mean 4.07 years) (p<0.001). Stereoacuity and size of the angle of strabismus did not influence the type of management received.

Conclusions: X(T) can be a presenting sign of reduced visual acuity. Most children with well controlled X(T) receive no treatment within 12 months following presentation.

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Footnotes

  • Competing interests H Davis has a financial interest in the Frisby Davis Distance Stereotest (FD2TM). None of the other authors has any competing financial interest.

  • Ethics approval The study was approved by the UK North West Multi Centre Research Ethics Committee. Each collaborating centre obtained local approval from their relevant NHS Trust R&D (Research and Development) Department. The study was conducted in accordance with the tenets of the Declaration of Helsinki.

  • Patient consent Obtained

  • Provenance and peer review Not commissioned; externally peer reviewed.

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