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Predictors of Clinical Outcomes in Autologous Cranioplasty

颅骨成形术 医学 去骨瓣减压术 格拉斯哥结局量表 优势比 脑积水 外科 置信区间 回顾性队列研究 逻辑回归 创伤性脑损伤 格拉斯哥昏迷指数 内科学 颅骨 精神科
作者
Saleh Safi,Arshad Ali,Ibrahim Abdelhafez,Abdul Salam,Talal Alrabayah,Abdulnasser Thabet,Sirajeddin Belkhair
出处
期刊:World Neurosurgery [Elsevier]
卷期号:167: e561-e566 被引量:5
标识
DOI:10.1016/j.wneu.2022.08.043
摘要

Cranioplasty is a common neurosurgical procedure and autologous grafts are preferred due to their aesthetic and biocompatibility benefits. Multiple risk factors are implicated as predictors for neurologic outcome. This study focuses on risk factors that may be associated with complications and analyzes the predictors of neurologic outcomes after autologous cranioplasty. This is a retrospective observational study conducted at a tertiary care center between 2015 and 2021. Adults with autologous cranioplasty (n = 132) were recruited from procedure logs and the hospital electronic health record. Clinicodemographic parameters, risk factors, and complications were recorded. Neurologic outcomes were measured using the dichotomized Glasgow Outcome Scale (GOS). Primary outcome measure was pre- and post-cranioplasty GOS at the last follow up. Secondary outcome measures were the predicting factors that contributed to enhanced neurologic outcome post-cranioplasty. Mean age was 41.4 (standard deviation ± 13.5) years with male predominance (12.2:1). Complications developed in 12.9% (n = 17), with infections in 3.8% (n = 5) and hydrocephalus in 2.3% (n = 3). In bivariate analysis, pre-cranioplasty GOS good grades 4 and 5 (P < 0.001), trauma as an indication for decompressive craniectomy (DC) (P < 0.001), and early cranioplasty ≤12 weeks (P = 0.023) were statistically significant predictors for post-cranioplasty neurologic recovery at follow-up. In a multiple logistic regression model, adjusted odds ratio for pre-cranioplasty GOS was 28.77 (95% confidence interval [CI] 7.21–114.74, P < 0.001), for trauma as indication for DC was 5.15 (95% CI 1.65–16.05, P = 0.003), and for early cranioplasty ≤12 weeks was 3.04 (95% CI 1.12–8.27 P = 0.029). Autologous cranioplasty contributes to a quantifiable neurologic outcome. Pre-cranioplasty neurologic status, cranioplasty done for traumatic DC and early cranioplasty may have potential for enhanced neurologic recovery. Further clinical studies with better evidence may expound upon these findings.
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