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The Swedish National Pediatric Cataract Register (PECARE): Coexisting systemic disorders 2007-2023
David Wackerberg1,2, Jenny Gyllén1,2, Birgitte Haargaard3
1Department of Ophthalmology, Västra Götalandsregionen, Sahlgrenska University Hospital, Mölndal, Sweden.
Insights
Systemic disorders coexist in children with cataracts, particularly bilateral cases. Further research and genetic screening guidelines are recommended for pediatric cataract patients.
Area of Science:
- Ophthalmology
- Pediatrics
- Genetics
Background:
- Pediatric cataract surgery is a critical intervention.
- Understanding coexisting systemic disorders is vital for comprehensive care.
Purpose of the Study:
- To determine the frequency and types of systemic disorders in Swedish children undergoing cataract surgery.
- To analyze the association between cataract laterality and systemic disorders.
Main Methods:
- Retrospective analysis of the Swedish National Pediatric Cataract Register (PECARE) from 2007-2023.
- Inclusion of 975 children, with exclusions for specific cataract causes.
- Follow-up data at ages 1, 2, 5, and 10 years.
Main Results:
- 15.1% of 872 children had coexisting systemic disorders.
- Systemic disorders were more prevalent in bilateral cataracts (27.6%) than unilateral (4.3%).
- Prevalence was higher in children with parental consanguinity (34.4%) and lower in hereditary cataracts (15.9%).
Conclusions:
- Systemic disorders are common in pediatric cataract patients, especially with bilateral cataracts.
- Laterality and parental consanguinity influence prevalence.
- A national consensus on genetic screening for systemic disorders is necessary.
Purpose:
To analyse the frequency and type of coexisting systemic disorders in children operated on for cataract in Sweden.
Methods:
Data were retrieved from the Swedish National Pediatric Cataract Register (PECARE) for children operated between January 1, 2007, and December 31, 2023 (n = 975), including follow-ups at age 1, 2, 5 and 10. Cataracts due to uveitis, trauma or radiation, and lens extraction due to luxation were excluded. Genetic screening was not mandatory during this period.
Results:
Of the 872 children who remained after exclusions, 466 (53.4%) had unilateral cataracts and 406 (46.6%) had bilateral cataracts. Coexisting systemic disorders were found in 132/872 (15.1%), of which 5/132 (3.8%) were strongly suspected, 64/132 (48.5%) defined and 63/132 (47.7%) undefined. Overall, 20/872 (2.3%) were developmentally delayed without any systemic disorder diagnosis. Systemic disorder was present in 20/466 (4.3%) with unilateral cataracts, 112/406 (27.6%) with bilateral cataracts, 22/138 (15.9%) with bilateral inherited cataracts and 11/32 (34.4%) with parental consanguinity.
Conclusion:
Coexisting systemic disorders were present regardless of laterality, but more common among children with bilateral cataracts. Prevalence was similar among children with consanguineous parents, and lower among children with hereditary cataracts. National consensus regarding genetic screening for systemic disorders is needed.
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