4.6 Article

Infants Born Late/Moderately Preterm Are at Increased Risk for a Positive Autism Screen at 2 Years of Age

期刊

JOURNAL OF PEDIATRICS
卷 166, 期 2, 页码 269-+

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MOSBY-ELSEVIER
DOI: 10.1016/j.jpeds.2014.10.053

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资金

  1. National Institute for Health Research (NIHR) under its Programme Grants for Applied Research (PGfAR) [RP-PG-0407-10029]
  2. Department of Health's NIHR biomedical research centers funding scheme at UCLH/UCL
  3. National Institute for Health Research [RP-PG-0407-10029] Funding Source: researchfish
  4. National Institutes of Health Research (NIHR) [RP-PG-0407-10029] Funding Source: National Institutes of Health Research (NIHR)

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Objectives To assess the prevalence of positive screens using the Modified Checklist for Autism in Toddlers (M-CHAT) questionnaire and follow-up interview in late and moderately preterm (LMPT; 32-36 weeks) infants and term-born controls. Study design Population-based prospective cohort study of 1130 LMPT and 1255 term-born infants. Parents completed the M-CHAT questionnaire at 2-years corrected age. Parents of infants with positive questionnaire screens were followed up with a telephone interview to clarify failed items. The M-CHAT questionnaire was rescored, and infants were classified as true or false positives. Neurosensory, cognitive, and behavioral outcomes were assessed using parent report. Results Parents of 634 (57%) LMPT and 761 (62%) term-born infants completed the M-CHAT questionnaire. LMPT infants had significantly higher risk of a positive questionnaire screen compared with controls (14.5% vs 9.2%; relative risk [RR] 1.58; 95% CI 1.18, 2.11). After follow-up, significantly more LMPT infants than controls had a true positive screen (2.4% vs 0.5%; RR 4.52; 1.51, 13.56). This remained significant after excluding infants with neurosensory impairments (2.0% vs 0.5%; RR 3.67; 1.19, 11.3). Conclusions LMPT infants are at significantly increased risk for positive autistic screen. An M-CHAT follow-up interview is essential as screening for autism spectrum disorders is especially confounded in preterm populations. Infants with false positive screens are at risk for cognitive and behavioral problems.

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