Severity of retinopathy of prematurity was associated with a higher risk of cerebral dysfunction in young adults born extremely preterm

被引:6
|
作者
Jacobson, Lena [1 ]
Vollmer, Brigitte [2 ,3 ]
Kistner, Anna [4 ,5 ]
Bohm, Birgitta [3 ]
机构
[1] Karolinska Inst, Dept Clin Neurosci, Stockholm, Sweden
[2] Univ Southampton, Fac Med, Clin & Expt Sci, Southampton, Hants, England
[3] Karolinska Inst, Dept Womens & Children S Hlth, Stockholm, Sweden
[4] Karolinska Univ Hosp, Med Radiat Phys & Nucl Med, Stockholm, Sweden
[5] Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden
关键词
adult outcome; cerebral dysfunction; cognition; cryo-treatment; retinopathy of prematurity; CHILDREN BORN; AGE; STRENGTHS; BLINDNESS; VOLUMES; DAMAGE; TERM;
D O I
10.1111/apa.15461
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Aim This Swedish study evaluated whether the severity of retinopathy of prematurity (ROP) in extremely preterm infants was related to their overall outcome in young adulthood. Methods We followed 39 individuals born between 1988 and 1993 at less than 28 gestational weeks, included in the Stockholm Neonatal Project. A total of 19 were treated for severe ROP, and 20 had no or mild ROP. They were assessed for general cognitive abilities and mental health at 18 years of age and compared with 23 term-born controls. Visual acuity was examined at 21-25 years. They were asked about their education and everyday life. Results The 19 individuals with severe treated ROP had lower visual acuity and higher risk for intellectual deficits, cerebral palsy and neuropsychiatric diagnoses than those with no or mild ROP and the term controls. Three were visually impaired, none were blind. They were less physically active than the other groups and had more problems finding their way around. However, nine were at university. Conclusion Young adults treated for severe ROP had more problems resulting from cerebral dysfunction than those with no or mild ROP and term-born controls. Retinal and brain pathologies in the extremely preterm infant constitute different expressions of neurovascular disease.
引用
收藏
页码:528 / 536
页数:9
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