Ultrasound diagnosis and neurodevelopmental outcome of localised and extensive cystic periventricular leucomalacia

Citation
V. Pierrat et al., Ultrasound diagnosis and neurodevelopmental outcome of localised and extensive cystic periventricular leucomalacia, ARCH DIS CH, 84(3), 2001, pp. F151-F156
Citations number
37
Categorie Soggetti
Pediatrics,"Medical Research General Topics
Journal title
ARCHIVES OF DISEASE IN CHILDHOOD
ISSN journal
00039888 → ACNP
Volume
84
Issue
3
Year of publication
2001
Pages
F151 - F156
Database
ISI
SICI code
0003-9888(200105)84:3<F151:UDANOO>2.0.ZU;2-I
Abstract
Aims-To compare the ultrasound (US) evolution and neurodevelopmental outcom e of infants with localised (grade II) and extensive (grade III) cystic per iventricular leucomalacia (c-PVL). Methods-Over a nine year period, c-PVL was diagnosed in 96/3451 (2.8%) infa nts in two hospital cohorts. Eighteen were excluded from the study. Thirty nine infants with grade II PVL were compared with 39 infants with grade III PVL. Results-The two populations were com:parable for gestational age and birth weight. In infants with grade II PVL, cysts were noted to develop more ofte n after the first month of life (53%) in contrast with grade III PVL (22%) (odds ratio (OR) 3.81 (95% confidence interval (CI) 1.19 to 12.63)). Cysts were also more often unilateral in grade II (54%) than in grade III PVL (0% ) (OR indefinite; RR 3.17 (95% CI 2.16 to 4.64)). At 40 weeks postmenstrual age (PMA), cysts were no longer seen on US in 13/38 infants with grade II PVL, with ventriculomegaly being the only visible sequel in nine cases. In grade III PVL, cysts were still present in 25 of the 27 surviving infants. Nine infants with grade II PVL were free of motor sequelae at follow up com pared with one infant with grade III PVL (OR 8.07 (95% CI 0.92 to 181.66)). Twenty-two out of 29 children with grade II PVL who developed cerebral pal sy achieved independent walking compared with 3/26 with grade III PVL (OR 7 5 (95% CI 11.4 to 662)). Conclusions-In the cohort studied, 50% of the infants with c-PVL had a more localised form (grade II). In grade II PVL, the cysts developed beyond the first month of life in more than half of the cases and were often no longe r visible, on US, at 40 weeks PMA. In order not to miss this diagnosis, seq uential US should also be performed beyond the first month of life. Mild ve ntriculomegaly noted at term can sometimes be due to grade II c-PVL. Cerebr al palsy was slightly less common and tended to be less severe in infants w ith grade II PVL than in those with grade III PVL.