Risk Factors for Preoperative Developmental Delay in Patients with Nonsyndromic Sagittal Craniosynostosis.


Journal

Plastic and reconstructive surgery
ISSN: 1529-4242
Titre abrégé: Plast Reconstr Surg
Pays: United States
ID NLM: 1306050

Informations de publication

Date de publication:
01 2019
Historique:
entrez: 28 12 2018
pubmed: 28 12 2018
medline: 28 3 2019
Statut: ppublish

Résumé

Some patients with isolated sagittal craniosynostosis have demonstrated mild neurodevelopmental delays. This study examined potential preoperative risk factors for developmental delay. Patients completed preoperative Bayley Scales of Infant and Toddler Development, Third Edition, and medical records were reviewed. Multivariate analyses of covariance and correlations were calculated. Participants (n = 77) were predominantly male (77.9 percent) and were aged 2 to 12 months (mean, 5.1 ± 2.3 months). Patients were classified with no delays [n = 63 (82 percent)] or delays [n = 14 (18 percent)] in one or more developmental area(s). There were no group sociodemographic differences. Prenatally, patients with delays versus no delays had lower mean gestational age in weeks (36.9 ± 2.8 weeks versus 39.1 ± 1.7 weeks; p = 0.001) with higher rates of gestational diabetes (36 percent versus 5 percent; p = 0.006) and premature rupture of membranes (14 percent versus 2 percent; p = 0.026). At birth, patients with delays had lower mean birth weight (2982 ± 714 g versus 3374 ± 544 g; p = 0.053), higher rates of respiratory distress (29 percent versus 5 percent; p = 0.005), additional medical diagnoses (57 percent versus 13 percent; p = 0.001), and longer mean neonatal intensive care unit stays (1.4 ± 1.8 weeks versus 0.2 ± 0.9 week; p = 0.002). Variables differing by group had moderate correlations. Patients with nonsyndromic sagittal craniosynostosis that had delays in development had lower gestational age and birth weight, with more prenatal and birth complications. These factors can help identify patients who might be at risk for delay and need close monitoring. Risk, III.

Sections du résumé

BACKGROUND
Some patients with isolated sagittal craniosynostosis have demonstrated mild neurodevelopmental delays. This study examined potential preoperative risk factors for developmental delay.
METHODS
Patients completed preoperative Bayley Scales of Infant and Toddler Development, Third Edition, and medical records were reviewed. Multivariate analyses of covariance and correlations were calculated.
RESULTS
Participants (n = 77) were predominantly male (77.9 percent) and were aged 2 to 12 months (mean, 5.1 ± 2.3 months). Patients were classified with no delays [n = 63 (82 percent)] or delays [n = 14 (18 percent)] in one or more developmental area(s). There were no group sociodemographic differences. Prenatally, patients with delays versus no delays had lower mean gestational age in weeks (36.9 ± 2.8 weeks versus 39.1 ± 1.7 weeks; p = 0.001) with higher rates of gestational diabetes (36 percent versus 5 percent; p = 0.006) and premature rupture of membranes (14 percent versus 2 percent; p = 0.026). At birth, patients with delays had lower mean birth weight (2982 ± 714 g versus 3374 ± 544 g; p = 0.053), higher rates of respiratory distress (29 percent versus 5 percent; p = 0.005), additional medical diagnoses (57 percent versus 13 percent; p = 0.001), and longer mean neonatal intensive care unit stays (1.4 ± 1.8 weeks versus 0.2 ± 0.9 week; p = 0.002). Variables differing by group had moderate correlations.
CONCLUSIONS
Patients with nonsyndromic sagittal craniosynostosis that had delays in development had lower gestational age and birth weight, with more prenatal and birth complications. These factors can help identify patients who might be at risk for delay and need close monitoring.
CLINICAL QUESTION/LEVEL OF EVIDENCE
Risk, III.

Identifiants

pubmed: 30589799
doi: 10.1097/PRS.0000000000005108
pii: 00006534-201901000-00044
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

133e-139e

Références

Knight SJ, Anderson VA, Spencer-Smith MM, Da Costa AC. Neurodevelopmental outcomes in infants and children with single-suture craniosynostosis: A systematic review. Dev Neuropsychol. 2014;39:159186.
Speltz ML, Kapp-Simon KA, Cunningham M, Marsh J, Dawson G. Single-suture craniosynostosis: A review of neurobehavioral research and theory. J Pediatr Psychol. 2004;29:651668.
Speltz ML, Kapp-Simon K, Collett B, et al. Neurodevelopment of infants with single-suture craniosynostosis: Presurgery comparisons with case-matched controls. Plast Reconstr Surg. 2007;119:18741881.
Panchal J, Amirsheybani H, Gurwitch R, et al. Neurodevelopment in children with single-suture craniosynostosis and plagiocephaly without synostosis. Plast Reconstr Surg. 2001;108:14921498; discussion 14991500.
Ruiz-Correa S, Starr JR, Lin HJ, Kapp-Simon KA, Cunningham ML, Speltz ML. Severity of skull malformation is unrelated to presurgery neurobehavioral status of infants with sagittal synostosis. Cleft Palate Craniofac J. 2007;44:548554.
Starr JR, Kapp-Simon KA, Cloonan YK, et al. Presurgical and postsurgical assessment of the neurodevelopment of infants with single-suture craniosynostosis: Comparison with controls. J Neurosurg. 2007;107(Suppl):103110.
Mackay DF, Smith GC, Dobbie R, Cooper SA, Pell JP. Obstetric factors and different causes of special educational need: Retrospective cohort study of 407,503 schoolchildren. BJOG 2013;120:297307; discussion 307308.
Schieve LA, Clayton HB, Durkin MS, Wingate MS, Drews-Botsch C. Comparison of perinatal risk factors associated with autism spectrum disorder (ASD), intellectual disability (ID), and co-occurring ASD and ID. J Autism Dev Disord. 2015;45:23612372.
Schieve LA, Tian LH, Rankin K, et al. Population impact of preterm birth and low birth weight on developmental disabilities in US children. Ann Epidemiol. 2016;26:267274.
Singh GK, Kenney MK, Ghandour RM, Kogan MD, Lu MC. Mental health outcomes in US children and adolescents born prematurely or with low birthweight. Depress Res Treat. 2013;2013:570743.
Woythaler M, McCormick MC, Mao WY, Smith VC. Late preterm infants and neurodevelopmental outcomes at kindergarten. Pediatrics 2015;136:424431.
Bayley N. Bayley Scales of Infant and Toddler Development, Third Edition. 2006.San Antonio, Texas: Psychological Corporation.
Acton BV, Biggs WS, Creighton DE, et al. Overestimating neurodevelopment using the Bayley-III after early complex cardiac surgery. Pediatrics 2011;128:e794e800.
Hollingshead AA. Four-Factor Index of Social Status. 1975.New Haven, Conn: Yale University.
Kapp-Simon KA, Leroux B, Cunningham M, Speltz ML. Multisite study of infants with single-suture craniosynostosis: Preliminary report of presurgery development. Cleft Palate Craniofac J. 2005;42:377384.
Arnaud E, Renier D, Marchac D. Prognosis for mental function in scaphocephaly. J Neurosurg. 1995;83:476479.
Barritt J, Brooksbank M, Simpson D. Scaphocephaly: Aesthetic and psychosocial considerations. Dev Med Child Neurol. 1981;23:183191.
Kapp-Simon KA. Mental development and learning disorders in children with single suture craniosynostosis. Cleft Palate Craniofac J. 1998;35:197203.
Kapp-Simon KA, Speltz ML, Cunningham ML, Patel PK, Tomita T. Neurodevelopment of children with single suture craniosynostosis: A review. Childs Nerv Syst. 2007;23:269281.
Shipster C, Hearst D, Somerville A, Stackhouse J, Hayward R, Wade A. Speech, language, and cognitive development in children with isolated sagittal synostosis. Dev Med Child Neurol. 2003;45:3443.
Bradley RH, Corwyn RF. Socioeconomic status and child development. Annu Rev Psychol. 2002;53:371399.
Bilder DA, Pinborough-Zimmerman J, Bakian AV, et al. Prenatal and perinatal factors associated with intellectual disability. Am J Intellect Dev Disabil. 2013;118:156176.
de Moura DR, Costa JC, Santos IS, et al. Risk factors for suspected developmental delay at age 2 years in a Brazilian birth cohort. Paediatr Perinat Epidemiol. 2010;24:211221.
Arcangeli T, Thilaganathan B, Hooper R, Khan KS, Bhide A. Neurodevelopmental delay in small babies at term: A systematic review. Ultrasound Obstet Gynecol. 2012;40:267275.
De Jesus LC, Pappas A, Shankaran S, et al.; Eunice Kennedy Shriver National Institute of Health and Human Development Neonatal Research Network. Outcomes of small for gestational age infants born at <27 weeks’ gestation. J Pediatr. 2013;163:5560.e1.
Geva R, Eshel R, Leitner Y, Valevski AF, Harel S. Neuropsychological outcome of children with intrauterine growth restriction: A 9-year prospective study. Pediatrics 2006;118:91100.
von Beckerath AK, Kollmann M, Rotky-Fast C, Karpf E, Lang U, Klaritsch P. Perinatal complications and long-term neurodevelopmental outcome of infants with intrauterine growth restriction. Am J Obstet Gynecol. 2013;208:130.e1130.e6.
Bolaños L, Matute E, Ramírez-Dueñas Mde L, Zarabozo D. Neuropsychological impairment in school-aged children born to mothers with gestational diabetes. J Child Neurol. 2015;30:16161624.
Daraki V, Roumeliotaki T, Koutra K, et al. Effect of parental obesity and gestational diabetes on child neuropsychological and behavioral development at 4 years of age: The Rhea mother-child cohort, Crete, Greece. Eur Child Adolesc Psychiatry 2017;26:703714.
Ornoy A, Wolf A, Ratzon N, et al. Neurodevelopmental outcome at early school age of children born to mothers with gestational diabetes. Arch Dis Child Fetal Neonatal Ed. 1999;81:F10F14.

Auteurs

Thomas A Imahiyerobo (TA)

From the Division of Plastic Surgery, New York Presbyterian Hospital-Columbia University Medical Center; the Divisions of Plastic and Maxillofacial Plastic Surgery and Neurosurgery, Children's Hospital Los Angeles; the Departments of Pediatrics, Neurological Surgery, and Pathology and Laboratory Medicine, and the Division of Plastic and Reconstructive Surgery, Keck School of Medicine at the University of Southern California.

Alexis L Johns (AL)

From the Division of Plastic Surgery, New York Presbyterian Hospital-Columbia University Medical Center; the Divisions of Plastic and Maxillofacial Plastic Surgery and Neurosurgery, Children's Hospital Los Angeles; the Departments of Pediatrics, Neurological Surgery, and Pathology and Laboratory Medicine, and the Division of Plastic and Reconstructive Surgery, Keck School of Medicine at the University of Southern California.

Eisha A Christian (EA)

From the Division of Plastic Surgery, New York Presbyterian Hospital-Columbia University Medical Center; the Divisions of Plastic and Maxillofacial Plastic Surgery and Neurosurgery, Children's Hospital Los Angeles; the Departments of Pediatrics, Neurological Surgery, and Pathology and Laboratory Medicine, and the Division of Plastic and Reconstructive Surgery, Keck School of Medicine at the University of Southern California.

Pedro A Sanchez-Lara (PA)

From the Division of Plastic Surgery, New York Presbyterian Hospital-Columbia University Medical Center; the Divisions of Plastic and Maxillofacial Plastic Surgery and Neurosurgery, Children's Hospital Los Angeles; the Departments of Pediatrics, Neurological Surgery, and Pathology and Laboratory Medicine, and the Division of Plastic and Reconstructive Surgery, Keck School of Medicine at the University of Southern California.

Mark D Krieger (MD)

From the Division of Plastic Surgery, New York Presbyterian Hospital-Columbia University Medical Center; the Divisions of Plastic and Maxillofacial Plastic Surgery and Neurosurgery, Children's Hospital Los Angeles; the Departments of Pediatrics, Neurological Surgery, and Pathology and Laboratory Medicine, and the Division of Plastic and Reconstructive Surgery, Keck School of Medicine at the University of Southern California.

J Gordon McComb (JG)

From the Division of Plastic Surgery, New York Presbyterian Hospital-Columbia University Medical Center; the Divisions of Plastic and Maxillofacial Plastic Surgery and Neurosurgery, Children's Hospital Los Angeles; the Departments of Pediatrics, Neurological Surgery, and Pathology and Laboratory Medicine, and the Division of Plastic and Reconstructive Surgery, Keck School of Medicine at the University of Southern California.

Mark M Urata (MM)

From the Division of Plastic Surgery, New York Presbyterian Hospital-Columbia University Medical Center; the Divisions of Plastic and Maxillofacial Plastic Surgery and Neurosurgery, Children's Hospital Los Angeles; the Departments of Pediatrics, Neurological Surgery, and Pathology and Laboratory Medicine, and the Division of Plastic and Reconstructive Surgery, Keck School of Medicine at the University of Southern California.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH