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Temporal summation in children with a history of retinopathy of prematurity.
Hansen, Ronald M; Moskowitz, Anne; Tavormina, Jena L; Bush, Jennifer N; Soni, Garima; Fulton, Anne B.
Afiliação
  • Hansen RM; Department of Ophthalmology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, United States.
  • Moskowitz A; Department of Ophthalmology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, United States.
  • Tavormina JL; Department of Ophthalmology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, United States.
  • Bush JN; Department of Ophthalmology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, United States.
  • Soni G; Department of Ophthalmology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, United States.
  • Fulton AB; Department of Ophthalmology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, United States.
Invest Ophthalmol Vis Sci ; 56(2): 914-7, 2015 Jan 20.
Article em En | MEDLINE | ID: mdl-25604681
ABSTRACT

PURPOSE:

To assess temporal summation in children with a history of retinopathy of prematurity (ROP) by determining the critical duration (tCRIT) for complete temporal summation under rod-mediated conditions. From prior ERG studies, it is known that the kinetics of activation of phototransduction are prolonged in the ROP rod photoreceptor.

METHODS:

Dark-adapted thresholds for detecting 10° diameter stimuli with durations from 10 to 640 ms were measured. A two-alternative, spatial, forced-choice psychophysical procedure was used. The tCRIT for complete summation was estimated in former preterm subjects with a history of severe ROP (n = 7), mild ROP (n = 23), and no ROP (n = 15). The subjects ranged in age from 10.4 to 17.6 (median 15.6) years. Age-similar term-born control subjects (n = 5) were also tested.

RESULTS:

Critical duration was significantly longer in subjects with a history of ROP than in subjects who never had ROP or who were born at term. Mean tCRIT in the mild ROP group [127.5 (SD = 19.9) ms] and severe group [147.6 (SD = 18.9) ms] did not differ significantly, but both were significantly longer than in former preterms who never had ROP [101.1 (SD = 16.5) ms] and in term-born controls [101.0 (SD = 19.5) ms].

CONCLUSIONS:

In ROP subjects, tCRIT is significantly prolonged. This is likely due to abnormal kinetics in the rod outer segment.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Limiar Sensorial / Retinopatia da Prematuridade / Células Fotorreceptoras Retinianas Bastonetes / Adaptação à Escuridão Tipo de estudo: Prognostic_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Invest Ophthalmol Vis Sci Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Limiar Sensorial / Retinopatia da Prematuridade / Células Fotorreceptoras Retinianas Bastonetes / Adaptação à Escuridão Tipo de estudo: Prognostic_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Invest Ophthalmol Vis Sci Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos