Early posterior vault distraction osteogenesis changes the syndromic craniosynostosis treatment paradigm: long-term outcomes of a 23-year cohort study.

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY Child's Nervous System Pub Date : 2024-09-01 Epub Date: 2024-06-21 DOI:10.1007/s00381-024-06465-x
Meagan Wu, Sarah L Barnett, Benjamin B Massenburg, Jinggang J Ng, Dominic J Romeo, Jesse A Taylor, Scott P Bartlett, Jordan W Swanson
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Abstract

Background: Early surgical management of syndromic craniosynostosis varies widely between centers, with patients typically undergoing multiple intracranial procedures through childhood. This study evaluates the long-term impact of early posterior vault distraction osteogenesis (PVDO) versus conventional treatment paradigms on the number and timing of subsequent craniofacial procedures.

Methods: We retrospectively analyzed the longitudinal operative patterns of patients with syndromic craniosynostosis treated from 2000 to 2023 with greater than five years of follow-up. Outcomes of patients who underwent early PVDO and conventional vault reconstruction were compared.

Results: Fifty-five patients met the inclusion criteria (30 PVDO and 25 conventional). Age at initial vault surgery was similar between the PVDO and conventional cohorts (7.6 vs. 8.8 months), as were baseline craniometrics (p > 0.05). Multiple fronto-orbital advancement (FOA) procedures were performed in only 1/30 (3%) PVDO-treated patient versus 12/25 (48%) conventionally-treated patients (p < 0.001). Twelve (40%) PVDO-treated patients did not undergo FOA at all. Among patients with Apert and Crouzon syndromes, fewer PVDO-treated patients required FOA prior to midface surgery (33% vs. 92%, p = 0.004) or repeat FOA (6% vs. 50%, p = 0.005) compared to conventionally-treated patients. Among patients with Muenke and Saethre-Chotzen syndromes, a similar proportion of patients required FOA in the PVDO and conventional cohorts (91% vs. 100%, p = 0.353), though no PVDO-treated patients required repeat FOA (0% vs. 44%, p = 0.018).

Conclusions: Early PVDO is associated with a reduction in the high burden of both FOA and, critically, revisionary frontal procedures which are commonly seen in conventionally-treated patients with syndromic craniosynostosis.

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早期后穹隆牵张成骨术改变了综合征颅骨发育不良的治疗模式:23 年队列研究的长期结果。
背景:综合征颅畸形的早期手术治疗在不同中心之间存在很大差异,患者通常在童年时期接受多次颅内手术。本研究评估了早期后穹隆牵张成骨术(PVDO)与传统治疗模式对后续颅颌面手术的次数和时间的长期影响:我们回顾性分析了2000年至2023年期间接受治疗且随访时间超过五年的综合征颅畸形患者的纵向手术模式。结果:55 名患者符合纳入标准:55名患者符合纳入标准(30名PVDO患者和25名传统患者)。PVDO和传统穹隆重建手术的初次手术年龄相似(7.6个月对8.8个月),基线头颅测量也相似(P > 0.05)。仅有 1/30 (3%)名 PVDO 治疗患者与 12/25 (48%)名常规治疗患者进行了多次眶前推进 (FOA) 手术(p 结论:PVDO 和常规治疗患者的颅底手术时间相差无几(7.6 个月与 8.8 个月):早期 PVDO 可减少 FOA 的高负担,更重要的是,可减少在接受常规治疗的综合征颅骨发育不良患者中常见的额部翻修手术。
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来源期刊
Child's Nervous System
Child's Nervous System 医学-临床神经学
CiteScore
3.00
自引率
7.10%
发文量
322
审稿时长
3 months
期刊介绍: The journal has been expanded to encompass all aspects of pediatric neurosciences concerning the developmental and acquired abnormalities of the nervous system and its coverings, functional disorders, epilepsy, spasticity, basic and clinical neuro-oncology, rehabilitation and trauma. Global pediatric neurosurgery is an additional field of interest that will be considered for publication in the journal.
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