Complications of cranioplasty following decompressive craniectomy for traumatic brain injury: systematic review and meta-analysis

被引:21
|
作者
Henry, Jack [1 ,2 ]
Amoo, Michael [1 ,3 ]
Murphy, Adam [1 ]
O'Brien, David P. [1 ,3 ]
机构
[1] Beaumont Hosp, Natl Ctr Neurosurg, Dublin, Ireland
[2] Univ Coll Dublin, Sch Med, Dublin, Ireland
[3] Royal Coll Surgeons Ireland, Dublin, Ireland
关键词
Cranioplasty; Decompressive craniectomy; Traumatic brain injury; Aseptic bone flap resorption; CEREBRAL-ARTERY INFARCTION; AUTOLOGOUS BONE; RISK-FACTORS; MALIGNANT INFARCTION; CONTROLLED-TRIAL; RESORPTION; INFECTION; SURGERY; POLYMETHYLMETHACRYLATE; CONSEQUENCES;
D O I
10.1007/s00701-021-04809-z
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Decompressive craniectomy (DC) is a common neurosurgical intervention for severe traumatic brain injury (TBI), as well as malignant stroke, malignancy and infection. DC necessitates subsequent cranioplasty. There are significant demographic differences between TBI and non-TBI patients undergoing cranioplasty, which may influence their relative risk profiles for infection, aseptic bone flap resorption (aBFR) and re-operation. Objective Perform a meta-analysis to determine the relative infection, aBFR and re-operation risk profiles of TBI patients as compared to other indications for DC. Methods A systematic review and meta-analysis was performed in accordance with the PRISMA guidelines. PubMed, MEDLINE, EMBASE and Google Scholar were searched until 26/11/2020. Studies detailing rates of infection, re-operation and/or aBFR in specific materials and the post-TBI population were included, while studies in paediatrics or craniosynostosis repair were excluded. Results Twenty-six studies were included. There was no difference in relative risk of infection between TBI and non-TBI cohorts (RR 0.81, 95% CI 0.57-1.17), with insignificant heterogeneity (I-2 = 33%). TBI was a risk factor for aBFR (RR 1.54, 95% CI 1.25-1.89), with no significant heterogeneity (I-2 = 13%). TBI was a risk factor for re-operation in the autologous sub-group (RR 1.49, 95% CI 1.05-2.11) but not in the alloplastic sub-group (RR = 0.86, 95% CI 0.34-2.18). Heterogeneity was insignificant (I-2 = 11%). Conclusion TBI is a risk factor for aBFR and re-operation following cranioplasty. Use of an alloplastic graft for primary cranioplasty in these patients may partially mitigate this increased risk.
引用
收藏
页码:1423 / 1435
页数:13
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