Ashayeri Kimberly, M Jackson Eric, Huang Judy, Brem Henry, Gordon Chad R
*Albert Einstein College of Medicine, New York, New York; ‡Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, Maryland; §Department of Plastic and Reconstructive Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Neurosurgery. 2016 Oct;79(4):525-34. doi: 10.1227/NEU.0000000000001366.
Syndrome of the trephined (SoT) is a rare, important complication of a craniectomy characterized by neurological dysfunction that improves with cranioplasty. Its varied symptoms include motor, cognitive, and language deficits. Its exact characterization appears suboptimal, with differing approaches of evaluation. Accordingly, this topic is in great need of further investigation.
To accurately describe SoT and explore methods of an objective diagnosis/evaluation.
Electronic searches of PubMed, MEDLINE, Web of Knowledge, and PsycINFO databases used the key words "syndrome of the trephined" and "sinking skin flap." Non-English-language and duplicate articles were eliminated. Title and abstract reviews were selected for relevance. Full-text reviews were selected for articles providing individual characteristics of SoT patients.
This review identified that SoT most often occurs in male patients (60%) at 5.1 ± 10.8 months after craniectomy for neurotrauma (38%). The average reported craniectomy is 88.3 ± 34.4 cm and usually exists with a "sunken skin flap" (93%). Symptoms most commonly include motor, cognitive, and language deficits (57%, 41%, 28%, respectively), with improvement after cranioplasty within 3.8 ± 3.9 days. Functional independence with activities of daily living is achieved by 54.9% of patients after 2.9 ± 3.4 months of rehabilitation. However, evaluation of SoT is inconsistent, with only 53% of reports documenting objective studies.
SoT is a variable phenomenon associated with a prolonged time to cranioplasty. Due to current weaknesses in objectivity, we hypothesize that SoT is often underdiagnosed and recommend a multifaceted approach for consistent evaluation.
SoT is a serious complication that lacks exact characterization and deserves future investigation. Improved understanding and recognition have important implications for early intervention and patient outcomes.
ADLs, activities of daily livingCBF, cerebral blood flowSoT, syndrome of the trephinedVP, ventriculoperitoneal.
环锯术后综合征(SoT)是颅骨切除术后一种罕见但重要的并发症,其特征为神经功能障碍,颅骨修补术后可改善。其症状多样,包括运动、认知和语言功能缺陷。由于评估方法不同,其确切特征尚不明确。因此,该主题急需进一步研究。
准确描述SoT并探索客观诊断/评估方法。
通过电子检索PubMed、MEDLINE、Web of Knowledge和PsycINFO数据库,使用关键词“环锯术后综合征”和“头皮下陷皮瓣”。剔除非英文和重复文章。筛选标题和摘要以确定相关性。选择提供SoT患者个体特征的文章进行全文阅读。
本综述发现,SoT最常发生于男性患者(60%),在因神经创伤行颅骨切除术后5.1±10.8个月(38%)。报告的平均颅骨切除面积为88.3±34.4平方厘米,通常伴有“头皮下陷皮瓣”(93%)。最常见的症状包括运动、认知和语言功能缺陷(分别为57%、41%、28%),颅骨修补术后3.8±3.9天内症状改善。2.9±3.4个月的康复治疗后,54.9%的患者实现了日常生活活动的功能独立。然而,对SoT的评估并不一致,只有53%的报告记录了客观研究。
SoT是一种与颅骨修补延迟相关的可变现象。由于目前在客观性方面存在不足,我们推测SoT常被漏诊,并建议采用多方面方法进行一致评估。
SoT是一种缺乏确切特征的严重并发症,值得未来进一步研究。更好的理解和认识对早期干预和患者预后具有重要意义。
ADLs,日常生活活动;CBF,脑血流量;SoT,环锯术后综合征;VP,脑室腹腔分流术