首页> 外文期刊>Circulation. Cardiovascular quality and outcomes >Feasibility of a Team Approach to Complex Congenital Heart Defect Neurodevelopmental Follow-Up: Early Experience of a Combined Cardiology/Neonatal Intensive Care Unit Follow-Up Program
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Feasibility of a Team Approach to Complex Congenital Heart Defect Neurodevelopmental Follow-Up: Early Experience of a Combined Cardiology/Neonatal Intensive Care Unit Follow-Up Program

机译:复杂先天性心脏缺损神经发育后续随访的团队方法的可行性:联合心脏病学/新生儿重症监护室随访计划的早期经验

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摘要

Infants with complex congenital heart disease are at high risk for poor neurodevelopmental outcomes. However, implementation of dedicated congenital heart disease follow-up programs presents important infrastructure, personnel, and resource challenges. We present the development, implementation, and retrospective review of 1- and 2-year outcomes of a Complex Congenital Heart Defect Neurodevelopmental Follow-Up program. This program was a synergistic approach between the Pediatric Cardiology, Cardiothoracic Surgery, Pediatric Intensive Care, and Neonatal Intensive Care Unit Follow-Up teams to provide a feasible and responsible utilization of existing infrastructure and personnel, to develop and implement a program dedicated to children with congenital heart disease. Trained developmental testers administered the Ages and Stages Questionnaire-3 over the phone to the parents of all referred children at least once between 6 and 12 months' corrected age. At 18 months' corrected age, all children were scheduled in the Neonatal Intensive-Care Unit Follow-Up Clinic for a visit with standardized neurological exams, Bayley III, multidisciplinary therapy evaluations and continued follow-up. Of the 132 patients identified in the Cardiothoracic Surgery database and at discharge from the hospital, a total number of 106 infants were reviewed. A genetic syndrome was identified in 23.4% of the population. Neuroimaging abnormalities were identified in 21.7% of the cohort with 12.8% having visibly severe insults. As a result, 23 (26.7%) received first-time referrals for early intervention services, 16 (13.8%) received referrals for new services in addition to their existing ones. We concluded that utilization of existing resources in collaboration with established programs can ensure targeted neurodevelopmental follow-up for all children with complex congenital heart disease.
机译:具有复杂的先天性心脏病的婴儿具有较差的神经发育成果的高风险。然而,实施专门的先天性心脏病的后续计划具有重要的基础设施,人员和资源挑战。我们展示了复杂的先天性心脏缺陷神经发作后续行动计划的1比和2年结果的发展,实施和回顾性审查。该计划是儿科心脏病学,心胸外科手术,儿科重症监护和新生儿重症监护室后续队伍之间的协同方法,以提供现有基础设施和人员的可行和负责任,开发和实施致力于儿童的计划先天性心脏病。经过培训的发展测试人员将年龄和阶段调查问卷-3通过电话向所有转诊儿童的父母进行,至少在6到12个月之间的纠正年龄之间。在18个月的纠正年龄,所有儿童都安排在新生儿重症监护单位随访诊所,用于访问标准化的神经学检查,拜利III,多学科治疗评估和继续随访。在心胸外科手术数据库和医院排放中发现的132名患者中,审查了106名婴儿总数。遗传综合征以23.4%的人群鉴定出来。在21.7%的群组中确定了神经影像异常,12.8%具有明显严重的侮辱。因此,23(26.7%)收到了早期干预服务的首次推荐,16(13.8%)除了现有的人外,还收到了新服务的推荐。我们得出结论,利用与已建立的计划合作的现有资源可以确保所有患有复杂的先天性心脏病的儿童的靶向神经发育的随访。

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