首页> 美国卫生研究院文献>Morbidity and Mortality Weekly Report >Health Status and Health Care Use Among Adolescents Identified With and Without Autism in Early Childhood — Four U.S. Sites 2018–2020
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Health Status and Health Care Use Among Adolescents Identified With and Without Autism in Early Childhood — Four U.S. Sites 2018–2020

机译:在幼儿期内发现和没有自闭症的青少年的健康状况和医疗保健 - 四个美国网站2018-2020

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摘要

Persons identified in early childhood as having autism spectrum disorder (autism) often have co-occurring health problems that extend into adolescence (1–3). Although only limited data exist on their health and use of health care services as they transition to adolescence, emerging data suggest that a minority of these persons receive recommended guidance* from their primary care providers (PCPs) starting at age 12 years to ensure a planned transition from pediatric to adult health care (4,5). To address this gap in data, researchers analyzed preliminary data from a follow-up survey of parents and guardians of adolescents aged 12–16 years who previously participated in the Study to Explore Early Development (https://www.cdc.govcbddd/autism/seed.html). The adolescents were originally studied at ages 2–5 years and identified at that age as having autism (autism group) or as general population controls (control group). Adjusted prevalence ratios (aPRs) that accounted for differences in demographic characteristics were used to compare outcomes between groups. Adolescents in the autism group were more likely than were those in the control group to have physical difficulties (21.2% versus 1.6%; aPR = 11.6; 95% confidence interval [CI] = 4.2–31.9), and to have additional mental health or other conditions† (one or more condition: 63.0% versus 28.9%; aPR = 1.9; 95% CI = 1.5–2.5). Adolescents in the autism group were more likely to receive mental health services (41.8% versus 22.1%; aPR = 1.8, 95% CI = 1.3–2.6) but were also more likely to have an unmet medical or mental health service need§ (11.0% versus 3.2%; aPR = 3.1; 95% CI = 1.1–8.8). In both groups, a small percentage of adolescents (autism, 7.5%; control, 14.1%) received recommended health care transition (transition) guidance. These findings are consistent with previous research (4,5) indicating that few adolescents receive the recommended transition guidance and suggest that adolescents identified with autism in early childhood are more likely than adolescents in the general population to have unmet health care service needs. Improved provider training on the heath care needs of adolescents with autism and coordination of comprehensive programs¶ to meet their needs can improve delivery of services and adherence to recommended guidance for transitioning from pediatric to adult health care.
机译:童年早期确定的人,因为具有自闭症谱系障碍(自闭症)通常具有延伸到青春期(1-3)的共同健康问题。虽然只有有限的数据存在健康和使用医疗服务,但在他们到青春期时,新兴数据表明,这些人的少数群体从12年开始的主要护理提供者(PCP)接受推荐的指导*,以确保计划从儿科过渡到成人保健(4,5)。为了解决数据中的这种差距,研究人员分析了在12-16岁的青少年的父母和监护人的后续调查中分析了初步数据,该父母和12-16岁以前参加了研究,探讨了早期发展(https://www.cdc.govcbddd / autism/seed.html)。青少年最初在2-5岁上学年学习,并在该年龄确定具有自闭症(自闭症组)或作为一般人口控制(对照组)。调整的患病率比率(APRS)占人口特征差异的差异用于比较组之间的结果。自闭症组中的青少年比对照组的青少年更有可能具有物理困难(21.2%,而不是1.6%; APR = 11.6; 95%置信区间[CI] = 4.2-31.9),并具有额外的心理健康或其他条件†(一个或多个条件:63.0%与28.9%; APR = 1.9; 95%CI = 1.5-2.5)。自闭症集团的青少年更有可能接受心理健康服务(41.8%,与22.1%; APR = 1.8,95%CI = 1.3-2.6),但也有可能需要未满足的医疗或心理健康服务§(11.0 %与3.2%; APR = 3.1; 95%CI = 1.1-8.8)。在两组中,少量青少年(自闭症,7.5%;控制,14.1%)接受了建议的医疗经理转型(转型)指导。这些发现与之前的研究(4,5)一致,表明少数青少年获得推荐的过渡指导,并表明在幼儿期内发现的青少年比一般人群中的青少年更有可能具有未满足的医疗保健服务需求。改进了对综合计划的自闭症和协调的青少年的荒地护理需求的提供商培训,以满足他们的需求,可以改善提供服务和依从性的推荐指导,从儿科对成人保健的转换。

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