Roodbol Joyce, de Wit Marie-Claire Y, Aarsen Femke K, Catsman-Berrevoets Coriene E, Jacobs Bart C
Department of Pediatric Neurology, Erasmus MC and Erasmus MC-Sophia Children's Hospital, University Medical Center Rotterdam, Rotterdam, The Netherlands; Department of Neurology, Erasmus MC and Erasmus MC-Sophia Children's Hospital, University Medical Center Rotterdam, Rotterdam, The Netherlands; Department of Immunology, Erasmus MC and Erasmus MC-Sophia Children's Hospital, University Medical Center Rotterdam, Rotterdam, The Netherlands.
J Peripher Nerv Syst. 2014 Jun;19(2):121-6. doi: 10.1111/jns5.12068.
The objective of this study is to determine the long-term outcome and consequences of Guillain-Barré syndrome (GBS) in children. This is an observational cross-sectional cohort study of children diagnosed with GBS (0-18 years old) at the Sophia Children's Hospital in Rotterdam from 1987 to 2009. All patients were invited for a structured interview, questionnaires, and full neurologic exam to record their current clinical condition focused on complaints and symptoms, neurological deficits, disabilities, behavior, and quality of life. Thirty-seven patients participated, 23 were now adults, with a median age of 20 years (range 4-39 years) and a median follow-up time of 11 years (range 1-22 years). Residual complaints were reported by 24 (65%) patients, including paresthesias (38%), unsteadiness of gait in the dark (37%), painful hands or feet (24%), and severe fatigue (22%). Four patients had severe neurological deficits, including facial diplegia and limb weakness. Two patients had had a recurrence of GBS. In 10 patients (26%), GBS had a negative impact on their school career. Questionnaires identified a wide range of behavioral problems. Quality of life was below normal on the subscale vitality, and above normal on the subscales social functioning and positive emotions in the adult group. Most children show good recovery of neurological deficits after GBS, but many have persisting long-term residual complaints and symptoms that may lead to psychosocial problems interfering with participation in daily life.
本研究的目的是确定儿童吉兰-巴雷综合征(GBS)的长期预后及后果。这是一项对1987年至2009年在鹿特丹索菲亚儿童医院确诊为GBS(0至18岁)的儿童进行的观察性横断面队列研究。所有患者均受邀参加结构化访谈、问卷调查及全面的神经学检查,以记录他们当前的临床状况,重点关注主诉和症状、神经功能缺损、残疾、行为及生活质量。37名患者参与,其中23名已成年,中位年龄为20岁(范围4至39岁),中位随访时间为11年(范围1至22年)。24名(65%)患者报告有残留症状,包括感觉异常(38%)、黑暗中步态不稳(37%)、手足疼痛(24%)及严重疲劳(22%)。4名患者有严重的神经功能缺损,包括双侧面瘫和肢体无力。2名患者出现GBS复发。10名患者(26%)中,GBS对其学业有负面影响。问卷调查发现了广泛的行为问题。成年组在活力子量表上生活质量低于正常,在社会功能和积极情绪子量表上高于正常。大多数儿童GBS后神经功能缺损恢复良好,但许多人有持续的长期残留症状,可能导致心理社会问题,影响日常生活参与。