Hoyt Drazen Catherine, Abel Regina, Lindsey Terianne, King Allison A
Washington University in St, Louis School of Medicine, Program in Occupational Therapy, 4444 Forest Park Pkwy, Box 8505, St, Louis, MO 63108, USA.
BMC Public Health. 2014 Feb 5;14:116. doi: 10.1186/1471-2458-14-116.
Children with sickle cell disease (SCD) commonly have cognitive deficits, even among toddlers. Much medical literature emphasizes disease-based factors to account for these deficits. However, the social environment plays a large role in child development. To address the specific needs of early childhood, a monthly hospital-based education program was initiated to educate parents about child development. Education sessions were poorly attended (20-25%) and deemed unsuccessful. This study describes the development and implementation of a home-based education service to teach parents about SCD, developmental milestones and positive parenting techniques.
This was a prospective, single-arm intervention to study the feasibility of a home-based caregiver education program for families with infants and toddlers with SCD. Parents of children aged 0-3 years with SCD from one Midwestern hospital were approached to participate in a home-based program. The program followed the Born to Learn™ curriculum provided through the Parents as Teachers™ National Center. Reminder calls or texts were provided the day before each visit. Results of the first twenty-six months of the program are presented.
A total of 62% (56 of 91) of families approached agreed to participate; all were African American. The majority of caregivers were single mothers with a high school education or less and whose children had Medicaid for health coverage. The phenotypes of SCD represented in this sample were similar to those in the general SCD population. Over 26 months, 39 families received at least one home visit. Parents of infants (younger than 8 months) were more likely to participate in the home-based education program than parents of older children, (Fisher's exact test, p < .001).
For participating families, home-based visits were a feasible method for reinforcing clinic education. About 43% of eligible families participated in the education, a two-fold increase in the poor attendance (20%) for a previous hospital-based program. A home visitation program for parents of infants with SCD could offer an effective approach to helping these children overcome adverse environmental conditions that are compounded by the complexities of a chronic health condition.
镰状细胞病(SCD)患儿普遍存在认知缺陷,即使是在幼儿中也是如此。许多医学文献强调基于疾病的因素来解释这些缺陷。然而,社会环境在儿童发育中起着很大的作用。为满足幼儿的特殊需求,启动了一项每月在医院开展的教育项目,向家长传授儿童发育知识。但教育课程的参与率很低(20%-25%),且被认为不成功。本研究描述了一项以家庭为基础的教育服务的开发与实施,该服务旨在向家长传授SCD、发育里程碑和积极育儿技巧。
这是一项前瞻性单臂干预研究,旨在探讨为患有SCD的婴幼儿家庭开展以家庭为基础的照顾者教育项目的可行性。来自一家中西部医院的0-3岁SCD患儿的家长被邀请参加一个以家庭为基础的项目。该项目遵循由“家长即教师”全国中心提供的“生来就会学”课程。每次家访前一天会进行提醒电话或短信通知。呈现了该项目前二十六个月的结果。
共有62%(91个家庭中的56个)被邀请的家庭同意参与;所有家庭均为非裔美国人。大多数照顾者是单身母亲,高中及以下学历,其子女通过医疗补助获得医保。该样本中SCD的表型与一般SCD人群相似。在26个月的时间里,39个家庭接受了至少一次家访。婴儿(8个月以下)的家长比大龄儿童的家长更有可能参与以家庭为基础的教育项目(Fisher精确检验,p<0.001)。
对于参与项目的家庭来说,家访是强化门诊教育的一种可行方法。约43%符合条件的家庭参与了教育,这比之前基于医院的项目中20%的低参与率提高了两倍。为患有SCD的婴儿家长开展家访项目可能是帮助这些儿童克服因慢性健康状况的复杂性而加剧的不利环境条件的有效途径。