Department of Paediatrics and Adolescent Medicine, Centre for Rare Diseases, Aarhus University Hospital, Palle Juul-Jensens Boulevard 99, 8200, Aarhus N, Denmark.
Department of Paediatrics and Adolescent Medicine, Center of Paediatric Pulmonology and Allergology, Aarhus University Hospital, Palle Juul-Jensens Boulevard 103, 8200, Aarhus N, Denmark.
Orphanet J Rare Dis. 2022 May 21;17(1):208. doi: 10.1186/s13023-022-02356-z.
The transition of adolescents to adult care is known to be challenging. Studies indicate that patients with a chronic disease and cognitive deficits are at risk of inadequate transition to adult care, which eventually may result in disease deterioration. This study investigated the transition process for patients with neurofibromatosis type 1 (NF1) and discussed whether patients with NF1 and cognitive deficits should receive additional attention in their transitional period.
A self-reported online questionnaire assessing disease severity, cognitive deficits, psychiatric diagnoses as well as transition experiences was completed by patients with NF1 aged 15-25-years. Patients were assigned to a national NF1 expert centre covering the western part of Denmark. Furthermore, a retrospective medical chart review was performed, and data were collected to estimate the prevalence of psychiatric diagnoses.
The questionnaire was completed by 41/103 (39%), median age 20 [range 15; 25] years. Medical chart review was performed in 103 patients, median age 20 [range 15; 25]. Participants reporting the transition as difficult all received special needs education, six reported executive function deficits and three out of seven had a psychiatric diagnosis. Fifteen (37%) questionnaire participants reported a wish for more information about the natural history and the prognosis of NF1. The prevalence of psychiatric diagnoses was 24% in the questionnaire survey and 30% in the medical chart review.
This study suggests a need of additional care for patients with NF1 and cognitive deficits including psychiatric disorders during their transition to adult care. In addition, it suggests a need for more information on and education in long-term prospects and mental health issues for patients with NF1.
青少年向成人护理的过渡众所周知具有挑战性。研究表明,患有慢性疾病和认知障碍的患者有过渡到成人护理不足的风险,这最终可能导致疾病恶化。本研究调查了 1 型神经纤维瘤病(NF1)患者的过渡过程,并讨论了是否应在过渡期间给予 NF1 和认知障碍患者额外关注。
通过自我报告的在线问卷评估疾病严重程度、认知障碍、精神科诊断以及过渡经历,由 15-25 岁的 NF1 患者完成。患者被分配到一个覆盖丹麦西部的国家 NF1 专家中心。此外,还进行了回顾性病历审查,并收集数据以估计精神科诊断的患病率。
共完成了 41/103(39%)份问卷,中位年龄 20 [范围 15;25] 岁。对 103 名患者进行了病历审查,中位年龄 20 [范围 15;25] 岁。报告过渡困难的参与者均接受了特殊需求教育,6 名报告存在执行功能障碍,7 名中有 3 名存在精神科诊断。15(37%)名问卷参与者表示希望获得更多关于 NF1 的自然史和预后的信息。问卷调查中的精神科诊断患病率为 24%,病历审查中的患病率为 30%。
本研究表明,NF1 患者和认知障碍患者在过渡到成人护理时需要额外的护理,包括精神障碍。此外,还需要为 NF1 患者提供更多关于长期前景和心理健康问题的信息和教育。