BACKGROUND/ PURPOSE: To evaluate growth and development in children with anorectal malformations and to analyze effects of type of malformation and comorbidities. METHODS: Non-syndromal children with anorectal malformations were prospectively evaluated at 0.5, 1, 2, and 5 years. Biometrics were obtained at all visits. Mental and psychomotor function development was determined. RESULTS: 108 children (59% male) were included. 49% had a high malformation, and 46% had ≥ 1 additional major comorbidity. All growth parameters were below the norm at all ages (p<0.01), irrespective of type of malformation. Children with ≥ 1 additional major anomaly had lower height at all ages; at 5 years, mean (95% CI) height was -1.83 (-2.7 to -1.1) and -0.70 (-1.3 to -0.1) in children with and without comorbidities, respectively (p=0.019). Mental development was normal, irrespective of the type of malformation or comorbidities. Motor development was delayed at all ages. At 5 years, motor development (n=30) was normal in 70%, borderline in 23%, and 7% had definitive motor problems (p=0.043). CONCLUSION: Non-syndromal children with anorectal malformations are at risk for growth impairment, especially those with additional major comorbidity. Mental development is normal. Motor development is slightly impaired. Supportive care should focus on growth, dietary management, and motor development besides defecation problems.
BACKGROUND/ PURPOSE: To evaluate growth and development in children with anorectal malformations and to analyze effects of type of malformation and comorbidities. METHODS: Non-syndromal children with anorectal malformations were prospectively evaluated at 0.5, 1, 2, and 5 years. Biometrics were obtained at all visits. Mental and psychomotor function development was determined. RESULTS: 108 children (59% male) were included. 49% had a high malformation, and 46% had ≥ 1 additional major comorbidity. All growth parameters were below the norm at all ages (p<0.01), irrespective of type of malformation. Children with ≥ 1 additional major anomaly had lower height at all ages; at 5 years, mean (95% CI) height was -1.83 (-2.7 to -1.1) and -0.70 (-1.3 to -0.1) in children with and without comorbidities, respectively (p=0.019). Mental development was normal, irrespective of the type of malformation or comorbidities. Motor development was delayed at all ages. At 5 years, motor development (n=30) was normal in 70%, borderline in 23%, and 7% had definitive motor problems (p=0.043). CONCLUSION: Non-syndromal children with anorectal malformations are at risk for growth impairment, especially those with additional major comorbidity. Mental development is normal. Motor development is slightly impaired. Supportive care should focus on growth, dietary management, and motor development besides defecation problems.
Authors: Marjolein Husen; Pauline C Schut; Adriana C H Neven; Nagma Yousoufi; Nanko de Graaf; Cornelius E J Sloots; Alex J Eggink; Titia E Cohen-Overbeek Journal: Fetal Diagn Ther Date: 2019-01-10 Impact factor: 2.587
Authors: Desiree van den Hondel; Charlotte H W Wijers; Yolande van Bever; Annelies de Klein; Carlo L M Marcelis; Ivo de Blaauw; Cornelius E J Sloots; Hanneke IJsselstijn Journal: Eur J Pediatr Date: 2015-10-24 Impact factor: 3.183