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Traumatic posterior fossa extradural hematoma in children: a meta-analysis and institutional experience of its clinical course, treatment and outcomes
被引:0
|作者:
Lee, Keng Siang
[1
,2
,3
]
Ong, Shi Hui
[3
]
Gillespie, Conor S.
[4
]
Ng, Lee Ping
[3
,5
]
Seow, Wan Tew
[3
,5
]
Low, Sharon Y. Y.
[3
,5
,6
,7
]
机构:
[1] Kings Coll Hosp London, Dept Neurosurg, London, England
[2] Kings Coll London, Maurice Wohl Clin Neurosci Inst, Inst Psychiat Psychol & Neurosci IoPPN, Dept Basic & Clin Neurosci, London, England
[3] KK Womens & Childrens Hosp, Neurosurg Serv, Singapore, Singapore
[4] Univ Cambridge, Dept Neurosurg, Dept Clin Neurosci, Cambridge, England
[5] Natl Neurosci Inst, Dept Neurosurg, Singapore, Singapore
[6] SingHlth Duke NUS, Neurosci Acad Clin Program, Singapore, Singapore
[7] SingHealth Duke NUS, Paediat Acad Clin Program, Singapore, Singapore
关键词:
Extradural;
Hematoma;
Pediatric;
Posterior fossa;
Traumatic;
EPIDURAL HEMATOMAS;
COMPUTED-TOMOGRAPHY;
CRANIAL FOSSA;
HEAD-INJURY;
MANAGEMENT;
PATTERNS;
SERIES;
RULES;
D O I:
10.1007/s10143-024-03089-2
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Posterior fossa extradural hematoma (PFEDH) is rare but has a greater incidence amongst children. It is also associated with a rapid deterioration. The aim of this study was to present the management of PFEDH through our institutional experience and a meta-analysis. A retrospective single institution review of all children from 2004 to 2024 who underwent craniotomy for PFEDH was undertaken. The collected variables included: demographics, type of trauma, clinical findings, computed tomography findings, and clinical course. A systematic review using Ovid Medline, Ovid Embase, and Cochrane Central Register of Controlled Trials (CENTRAL), and meta-analysis were performed. Nineteen children with PFEDH who underwent surgery were identified. All 19 (100%) patients benefited from good Glasgow Outcome Scale (GOS) score 4-5, and there were no incidences of in-hospital mortality. From the systematic review, 391 patients, across twenty-four studies and our series, were included. A total of 308 were treated with surgery, whereas 83 patients were treated conservatively. A comparative meta-analysis was not performed as the two groups were deemed too heterogeneous in clinical characteristics. Instead, single-arm meta-analyses were performed. The pooled incidence of patients initially under conservative management requiring surgery was 9.90% (95%CI 1.61;22.21%, I2 = 35.2). The incidence of good functional outcomes in patients managed surgically and conservatively were 93.68% (95%CI: 88.69;97.57%, I2 = 0.0%), and 99.99% (95%CI: 96.53;100%, I2 = 0.0%), respectively. Overall pooled of mortality in patients managed surgically and conservatively were 0.57% (95%CI: 0.00;2.87%, I2 = 0.0%) and 0.00% (95%CI: 0.00;1.18%, I2 = 0.0%). Overall, our study reiterates that pediatric PFEDH is uncommon, and patients often present atypically. Based on our institutional experience and extrapolating data from our meta-analysis of the wider literature, neurosurgical intervention is a reliable therapeutic option with good clinical outcomes.
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