先天性肌性斜颈:临床危险因素和手术率。

Akshitha Adhiyaman, Emilie Lijesen, Olivia C Tracey, Ruth H Jones, Keza E Levine, Shevaun M Doyle
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引用次数: 0

摘要

背景:先天性肌性斜颈(CMT)是一种罕见的胸锁乳突肌缩短,导致颈椎侧向屈曲和旋转。非手术治疗最为常见;然而,挛缩解决失败可能导致手术。本研究的目的是确定CMT的临床危险因素,探讨不同治疗途径的手术矫正率、消退率和颈椎活动度。方法:本回顾性研究回顾了2016年1月1日至2023年7月31日在同一机构诊断为CMT的所有患者。收集患者人口统计资料、危险因素和临床记录。进行了两次分析,以临床记录的充分性分开。结果:共有171例患者被纳入最终评估。初诊时平均年龄5.0±8.7个月,52%为女性,51.1%为右侧CMT。在初步分析的171例患者中,47.3%的患者在诊断CMT之前没有其他病史,12.3%的患者有髋关节发育不良史(DDH), 20.5%的患者有斜头畸形。其中,40.9%的患者通过剖宫产分娩,41.5%的患者通过阴道自然分娩。纳入治疗和活动度(ROM)分析的110例患者,平均随访时间为9.6±13.0个月。平均侧屈度改善为11.6±20.4°(P P)结论:大多数CMT患儿在其他方面健康,可迅速改善,无需手术治疗。同时,对于长期治疗和/或手术干预的患者,本研究显示出良好的结果。关键概念:(1)诊断为先天性肌性斜颈(CMT)的患者通常有髋关节发育不良和斜头畸形的病史。(2)长期治疗CMT的婴儿很少需要手术干预,但如果有必要,结果是良好的,没有并发症。(3)总的来说,父母和照顾者可以放心,大多数患有CMT的婴儿是健康的儿童,没有明显的危险因素,可以迅速改善。证据水平:III。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital Muscular Torticollis: Clinical Risk Factors and Rates of Surgery.

Background: Congenital muscular torticollis (CMT) is a rare shortening of the sternocleidomastoid muscle leading to lateral flexion and rotation of the cervical spine. Nonoperative treatment is most common; however, failure of contracture resolution may result in surgery. The aim of this study was to determine the clinical risk factors for CMT, exploring surgical correction rates, resolution rates, and cervical range of motion surrounding various treatment paths.

Methods: This retrospective study reviewed all patients diagnosed with CMT at a single institution from January 1, 2016, to July 31, 2023. Patient demographics, risk factors, and clinical notes were collected. Two analyses were performed, separated by sufficiency of the clinical note.

Results: A total of 171 patients were included in the final evaluation. Mean age was 5.0 ± 8.7 months at initial visit, 52% were female and 51.1% of patients had right-sided CMT. Of the 171 patients included in the initial analysis, 47.3% of patients had no other medical history prior to diagnosis of CMT, 12.3% had a history of developmental dysplasia of the hip (DDH), and 20.5% had plagiocephaly. Of all, 40.9% of patients were delivered via Cesarean section and 41.5% via normal spontaneous vaginal delivery. For the 110 patients included in treatment and range of motion (ROM) analysis, the mean follow-up time was 9.6 ± 13.0 months. Average lateral flexion improvement was 11.6 ± 20.4° (P < .0001). Average axial rotation improvement was 10.8 ± 23.1° (P < .0001). Eight patients underwent surgery; these patients' average length of physical therapy (PT) before surgery was 42.3 ± 14.3 months. By the last clinical visit, 87 patients had resolved CMT and 4 patients had resolving CMT.

Conclusions: Most infants with CMT who are healthy otherwise will improve rapidly and not undergo surgery. Meanwhile, for patients with longer treatment and/or surgical intervention, this study demonstrates favorable outcomes.

Key concepts: (1)History of developmental dysplasia of the hip and plagiocephaly were common in patients diagnosed with congenital muscular torticollis (CMT).(2)Rarely, infants with long treatment regimens for CMT will need surgical intervention, but, if indicated, the outcomes are favorable with no complications.(3)Overall, parents and caregivers can be reassured that most infants who have CMT are healthy children without significant risk factors that improve rapidly.

Level of evidence: III.

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