Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Blekinge Hospital, Karlskrona, Sweden.
J Bone Joint Surg Am. 2018 Apr 18;100(8):640-647. doi: 10.2106/JBJS.17.00851.
Children with idiopathic toe-walking, a common pediatric condition, walk some or all of the time on their toes. This condition often causes parental concern, with repeated medical contacts and a range of interventions including stretching, casts, injection of botulinum toxin A, and surgical procedures. The purpose of this cohort study was to document the natural history of this condition.
In a population-based cohort of 1,401 healthy 5.5-year-old Swedish children, we found the prevalence of idiopathic toe-walking to be approximately 5% (63 of 1,401). Of the 63 children who had ever been a toe-walker, 26 still were at the age of 5.5 years and were followed in the current study at 8 and 10 years of age. At the 8-year follow-up, parents were asked by telephone whether their child had received any treatment or diagnosis since the 5.5-year assessment, as well as to what extent (approximately 25%, 50%, 75%, or 100% of the time) the child still walked on the toes. At the visit when the children were 10 years of age, their parents were asked the same questions. All 26 children also underwent a neurological examination and an orthopaedic examination focusing on the lower extremities.
At 8 years of age, 6 of 26 children had ceased toe-walking, and by the age of 10 years, 50 (79%) of the original 63 patients had spontaneously ceased toe-walking. Idiopathic toe-walking did not result in contractures of the triceps surae. One subgroup of children displayed early contracture of the ankle and should thus not be considered idiopathic toe-walkers. Four of the children who still toe-walked at the age of 10 years demonstrated some neurodevelopmental comorbidity.
By the age of 10 years, 79% of the children who have ever been a toe-walker spontaneously develop a typical gait, without intervention or contractures of the ankle dorsiflexion. The diagnosis of short tendo Achilles should be retained as a separate diagnosis as there is a subset of children with this entity who should be treated early in childhood. Neurodevelopmental comorbidities are common among those who continue to toe-walk.
Prognostic Level I. See Instructions for Authors for a complete description of levels of evidence.
儿童特发性踮脚行走是一种常见的儿科疾病,他们在行走时会部分或全部时间用脚尖着地。这种情况通常会引起家长的担忧,导致他们反复寻求医疗帮助并采取多种干预措施,包括拉伸、打石膏、注射肉毒杆菌毒素 A 以及手术。本队列研究的目的是记录这种情况的自然病史。
在一项基于人群的研究中,我们对 1401 名 5.5 岁健康的瑞典儿童进行了研究,发现特发性踮脚行走的患病率约为 5%(1401 名儿童中有 63 名)。在 63 名曾经踮脚行走的儿童中,有 26 名在 5.5 岁时仍存在该情况,并在当前的研究中分别于 8 岁和 10 岁时进行了随访。在 8 岁的随访中,我们通过电话询问父母自 5.5 岁评估以来,孩子是否接受过任何治疗或诊断,以及孩子踮脚行走的程度(大约 25%、50%、75%或 100%的时间)。当孩子 10 岁时,他们的父母也被问到同样的问题。所有 26 名儿童还接受了神经学检查和重点检查下肢的骨科检查。
在 8 岁时,26 名儿童中有 6 名已经停止踮脚行走,而到 10 岁时,最初的 63 名患者中有 50 名(79%)已经自然停止踮脚行走。特发性踮脚行走不会导致跟腱后肌挛缩。有一个亚组的儿童在踝关节早期出现挛缩,因此不应被视为特发性踮脚行走。在 10 岁时仍踮脚行走的 4 名儿童表现出一些神经发育合并症。
到 10 岁时,曾经踮脚行走的儿童中有 79%会自发地形成典型的步态,无需干预或踝关节背屈挛缩。作为一个单独的诊断,应保留短跟腱的诊断,因为有一部分患有这种疾病的儿童需要在儿童早期进行治疗。那些持续踮脚行走的儿童中,神经发育合并症很常见。
预后水平 I。请参阅作者说明,以获取完整的证据水平描述。