Risk factors for unchanged ventricles during pediatric shunt malfunction

被引:3
作者
Reynolds, Rebecca A. [1 ,2 ]
Ahluwalia, Ranbir [2 ]
Krishnan, Vishal [3 ]
Kelly, Katherine A. [4 ]
Lee, Jaclyn [4 ]
Waldrop, Raymond P. [5 ]
Guidry, Bradley [4 ]
Hengartner, Astrid C. [3 ]
McCroskey, Justin [8 ]
Arynchyna, Anastasia [8 ]
Staulcup, Susan [7 ]
Chen, Heidi [2 ,6 ]
Hankinson, Todd C. [3 ,7 ]
Rocque, Brandon G. [8 ]
Shannon, Chevis N. [1 ,2 ]
Naftel, Robert [1 ,2 ]
机构
[1] Vanderbilt Univ, Med Ctr, Dept Neurol Surg, Nashville, TN USA
[2] Monroe Carell Jr Childrens Hosp Vanderbilt, Surg Outcomes Ctr Kids, Nashville, TN USA
[3] Univ Colorado, Sch Med, Aurora, CO USA
[4] Vanderbilt Univ, Sch Med, Nashville, TN 37212 USA
[5] Univ Alabama Birmingham, Sch Med, Birmingham, AL USA
[6] Vanderbilt Univ, Med Ctr, Dept Biostat, Nashville, TN USA
[7] Childrens Hosp Colorado, Dept Neurol Surg, Aurora, CO USA
[8] Univ Alabama Birmingham, Dept Neurol Surg, Birmingham, AL USA
关键词
pediatric hydrocephalus; VP shunt; shunt failure; ventricular compliance; slit ventricle syndrome; OCCIPITAL HORN RATIO; VENTRICULOPERITONEAL SHUNT; HYDROCEPHALUS; BRAIN; SIZE; OBSTRUCTION; MANAGEMENT; EPENDYMA; SCORE;
D O I
10.3171/2021.6.PEDS2125
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE Children whose ventricles do not change during shunt malfunction present a diagnostic dilemma. This study was performed to identify risk factors for unchanged ventricular size at shunt malfunction. METHODS This retrospective 1:1 age-matched case-control study identified children with shunted hydrocephalus who underwent shunt revision with intraoperative evidence of malfunction at one of the three participating institutions from 1997 to 2019. Cases were defined as patients with a change of < 0.05 in the frontal-occipital horn ratio (FOR) between malfunction and baseline, and controls included patients with FOR changes >= 0.05. The presence of infection, abdominal pseudocyst, pseudomeningocele, or wound drainage and lack of baseline cranial imaging at the time of malfunction warranted exclusion. RESULTS Of 450 included patients, 60% were male, 73% were Caucasian, and 67% had an occipital shunt. The median age was 4.3 (IQR 0.97-9.21) years at malfunction. On univariable analysis, unchanged ventricles at malfunction were associated with a frontal shunt (41% vs 28%, p < 0.001), programmable valve (17% vs 9%, p = 0.011), nonsiphoning shunt (85% vs 66%, p < 0.001), larger baseline FOR (0.44 +/- 0.12 vs 0.38 +/- 0.11, p < 0.001), no prior shunt infection (87% vs 76%, p = 0.003), and no prior shunt revisions (68% vs 52%, p < 0.001). On multivariable analysis with collinear variables removed, patients with a frontal shunt (OR 1.67, 95% CI 1.08-2.70, p = 0.037), programmable valve (OR 2.63, 95% CI 1.32-5.26, p = 0.007), nonsiphoning shunt at malfunction (OR 2.76, 95% CI 1.63-4.67, p < 0.001), larger baseline FOR (OR 3.13, 95% CI 2.21-4.43, p < 0.001), and no prior shunt infection (OR 2.34, 95% CI 1.27-4.30, p = 0.007) were more likely to have unchanged ventricles at malfunction. CONCLUSIONS In a multicenter cohort of children with shunt malfunction, those with a frontal shunt, programmable valve, nonsiphoning shunt, baseline large ventricles, and no prior shunt infection were more likely than others to have unchanged ventricles at shunt failure.
引用
收藏
页码:703 / 709
页数:7
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