Majnemer Annette, Mazer Barbara, Lecker Emily, Leduc Carter Alison, Limperopoulos Catherine, Shevell Michael, Rohlicek Charles, Rosenblatt Bernard, Tchervenkov Christo
School of Physical & Occupational Therapy, McGill University-MUHC Montreal Children's Hospital, Montreal, Canada.
Cardiol Young. 2008 Jun;18(3):288-96. doi: 10.1017/S1047951108002114. Epub 2008 Mar 7.
Infants with congenitally malformed hearts who require early open-heart surgery are at high risk for developmental, psychosocial, and academic difficulties. Our objective was to describe the pattern of use of educational supports and rehabilitation services in these children at early school age.
Parents of children who participated in a prospective study of developmental progress following open-surgery were contacted to participate in a telephone survey. The questionnaire included questions regarding current educational and rehabilitation resources their child was receiving, as well as the needs perceived by the parents for services, and obstacles to accessing services.
The survey was completed by 60 families, the mean age of the children being 8.1 years, with standard deviation of 1.1 years. Of the children, 22% received educational supports, which primarily included supplemental tutoring. Rehabilitation services were received by 23%, speech therapy for 9 children, psychologic support for 6, occupational therapy for 3, and physical therapy for 1. Children receiving these services were significantly more likely to have had low developmental scores in the expected domains, when compared to those not receiving services. The majority of developmentally delayed children were not receiving adequate, if any, resource support. Medical and surgical history was not associated with greater likelihood of receipt of services.
Children with congenitally malformed hearts who are now of school age are at risk for developmental challenges and academic difficulties, yet many do not receive services to optimize performance. Modification of current practice to include systematic, periodic screening, as well as the availability of a resource person for information and referral, may be warranted to meet the ongoing needs of these children and their families, and to optimize their health and well-being.
需要早期心脏直视手术的先天性心脏畸形婴儿面临发育、心理社会和学业困难的高风险。我们的目标是描述这些儿童在学龄早期使用教育支持和康复服务的模式。
联系参与心脏直视手术后发育进展前瞻性研究的儿童的家长,让他们参与电话调查。问卷包括关于他们孩子目前正在接受的教育和康复资源的问题,以及家长对服务的需求和获得服务的障碍。
60个家庭完成了调查,儿童的平均年龄为8.1岁,标准差为1.1岁。在这些儿童中,22%接受了教育支持,主要包括补习辅导。23%的儿童接受了康复服务,9名儿童接受了言语治疗,6名接受了心理支持,3名接受了职业治疗,1名接受了物理治疗。与未接受服务的儿童相比,接受这些服务的儿童在预期领域的发育得分显著更低。大多数发育迟缓的儿童没有得到足够的资源支持(如果有的话)。医疗和手术史与接受服务的可能性增加无关。
目前已到学龄期的先天性心脏畸形儿童面临发育挑战和学业困难的风险,但许多儿童没有接受优化表现的服务。可能有必要改变当前的做法,包括进行系统的定期筛查,以及提供一名资源人员负责信息提供和转诊,以满足这些儿童及其家庭的持续需求,并优化他们的健康和福祉。