Pub Date : 2025-10-24DOI: 10.3171/2025.7.PEDS25242
Alejandro Enriquez-Marulanda, Marcella Ruppert-Gomez, Patrisha Lazatin, Steven Staffa, Shivani D Rangwala, Darren B Orbach, Alfred P See, Edward R Smith, Christopher S Ogilvy
Objective: The Matsushima grading system is widely used to evaluate angiographic revascularization outcomes after pial synangiosis for moyamoya vasculopathy by quantifying collateral ingrowth. The authors hypothesized that the orbital grading system (OGS), a new scale developed for adults to measure collateral ingrowth, would provide greater consistency and interrater reliability. They aimed to compare the performance of these scales for the first time in the pediatric population.
Methods: The authors performed a retrospective analysis of patients with moyamoya vasculopathy with follow-up catheter angiography after indirect revascularization at a single major pediatric center from 2006 to 2023. An interrater reliability analysis was performed using 5 raters with varying levels of training, who provided scores for 30 blinded cases. Fleiss' kappa coefficient (κ) was calculated as a measure of agreement beyond chance.
Results: A total of 101 patients with a median age of 9 years, of predominantly female sex (56.4%) who were mostly affected by moyamoya disease (71.3%) were included. A total of 158 cerebral hemispheres were treated with pial synangiosis (57 patients had bilateral surgeries). Most hemispheres were categorized as Suzuki stage 3 or above (82.9%). At a median of 12.4 months postoperatively, collateral growth was classified as Matsushima grade A in 57.6%, B in 24.1%, C in 14.6%, and as borderline grades in 3.8%. The OGS scores were grade 0 in 7.0%, grade 1 in 8.9%, grade 2 in 43.7%, and grade 3 in 40.5%. Interrater agreement evaluation revealed that the OGS had a superior κ value compared with the Matsushima scale (0.51 vs 0.15, p < 0.001).
Conclusions: The OGS had higher interrater agreement rates than the Matsushima scale for identifying postoperative collateral ingrowth in children after pial synangiosis. This scale provides a more consistent method for evaluating angiographic outcomes after indirect revascularization in the pediatric population.
目的:Matsushima分级系统被广泛应用于通过量化侧枝向内生长来评价烟雾病合并血管病后血管造影重建效果。作者假设,轨道分级系统(OGS),一种为成人开发的测量侧枝生长的新量表,将提供更大的一致性和相互可靠性。他们的目的是第一次在儿科人群中比较这些量表的表现。方法:作者对2006年至2023年在一家主要儿科中心进行间接血运重建术后随访导管血管造影的烟雾病患者进行回顾性分析。使用5名不同训练水平的评分者进行了一项评分者间信度分析,他们为30例盲法病例提供了评分。Fleiss的kappa系数(κ)被计算为超越偶然的一致性的度量。结果:共纳入101例患者,中位年龄9岁,以女性为主(56.4%),以烟雾病为主(71.3%)。共158个大脑半球被治疗了头髓合并症(57例患者进行了双侧手术)。大部分大脑半球属于铃木3期以上(82.9%)。术后中位12.4个月,侧枝生长分为松岛a级(57.6%)、B级(24.1%)、C级(14.6%)和边缘级(3.8%)。OGS评分为0级者占7.0%,1级者占8.9%,2级者占43.7%,3级者占40.5%。研究者间一致性评价显示,OGS量表的κ值优于Matsushima量表(0.51 vs 0.15, p < 0.001)。结论:OGS量表在鉴别小儿椎体粘连症术后侧支生长方面比Matsushima量表具有更高的一致性。该量表为评估儿童间接血运重建术后的血管造影结果提供了更一致的方法。
{"title":"The orbital grading system in pediatric moyamoya: an interrater reliability analysis of angiographic outcomes.","authors":"Alejandro Enriquez-Marulanda, Marcella Ruppert-Gomez, Patrisha Lazatin, Steven Staffa, Shivani D Rangwala, Darren B Orbach, Alfred P See, Edward R Smith, Christopher S Ogilvy","doi":"10.3171/2025.7.PEDS25242","DOIUrl":"10.3171/2025.7.PEDS25242","url":null,"abstract":"<p><strong>Objective: </strong>The Matsushima grading system is widely used to evaluate angiographic revascularization outcomes after pial synangiosis for moyamoya vasculopathy by quantifying collateral ingrowth. The authors hypothesized that the orbital grading system (OGS), a new scale developed for adults to measure collateral ingrowth, would provide greater consistency and interrater reliability. They aimed to compare the performance of these scales for the first time in the pediatric population.</p><p><strong>Methods: </strong>The authors performed a retrospective analysis of patients with moyamoya vasculopathy with follow-up catheter angiography after indirect revascularization at a single major pediatric center from 2006 to 2023. An interrater reliability analysis was performed using 5 raters with varying levels of training, who provided scores for 30 blinded cases. Fleiss' kappa coefficient (κ) was calculated as a measure of agreement beyond chance.</p><p><strong>Results: </strong>A total of 101 patients with a median age of 9 years, of predominantly female sex (56.4%) who were mostly affected by moyamoya disease (71.3%) were included. A total of 158 cerebral hemispheres were treated with pial synangiosis (57 patients had bilateral surgeries). Most hemispheres were categorized as Suzuki stage 3 or above (82.9%). At a median of 12.4 months postoperatively, collateral growth was classified as Matsushima grade A in 57.6%, B in 24.1%, C in 14.6%, and as borderline grades in 3.8%. The OGS scores were grade 0 in 7.0%, grade 1 in 8.9%, grade 2 in 43.7%, and grade 3 in 40.5%. Interrater agreement evaluation revealed that the OGS had a superior κ value compared with the Matsushima scale (0.51 vs 0.15, p < 0.001).</p><p><strong>Conclusions: </strong>The OGS had higher interrater agreement rates than the Matsushima scale for identifying postoperative collateral ingrowth in children after pial synangiosis. This scale provides a more consistent method for evaluating angiographic outcomes after indirect revascularization in the pediatric population.</p>","PeriodicalId":16549,"journal":{"name":"Journal of neurosurgery. Pediatrics","volume":" ","pages":"69-76"},"PeriodicalIF":2.1,"publicationDate":"2025-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145368080","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-17DOI: 10.3171/2025.7.PEDS25119
Michael J Feldman, Hailey Jensen, Anastasia Arynchyna-Smith, Ron W Reeder, Curtis J Rozzelle, Jennifer M Strahle, William E Whitehead, Jonathan Pindrik, Albert M Isaacs, Jason S Hauptman, Marcie Langley, Patrick J McDonald, Mandeep S Tamber, Ian F Pollack, Eric M Jackson, John C Wellons, Robert Naftel, Todd C Hankinson, Abhaya V Kulkarni, Jay Riva-Cambrin, John R W Kestle, Brandon G Rocque
Objective: Endoscopic third ventriculostomy (ETV), an alternative to ventriculoperitoneal shunt (VPS) placement, is associated with a higher risk of early failure, sometimes necessitating subsequent VPS insertion. The authors evaluated the impact of ETV prior to VPS placement on the risk of VPS failure by using the Hydrocephalus Clinical Research Network (HCRN) Core Data Project.
Methods: The authors retrospectively reviewed prospectively collected data from the HCRN Core Data Project (registry) on all children who underwent VPS surgery between April 2008 and July 2023. Children who had undergone VPS placement as initial treatment for hydrocephalus were compared with those who had undergone ETV prior to VPS insertion. The primary outcome was initial VPS survival, with failure defined as any subsequent hydrocephalus procedure. Kaplan-Meier and Cox proportional hazards analyses were performed to assess the effect of prior ETV, controlling for age at the first permanent procedure (ETV or VPS placement), hydrocephalus etiology, and complex chronic conditions (CCCs).
Results: VPS placement was performed in 6206 children, of whom 642 underwent VPS placement after failed ETV. VPS insertion after ETV improved shunt survival at 1 year (74.3% vs 67.8%, p < 0.001). Unadjusted analysis showed improved VPS survival after ETV (HR 0.78, 95% CI 0.68-0.90, p = 0.001). Corrected age ≥ 30 days at the time of the first permanent procedure, choroid plexus cauterization, etiology of hydrocephalus other than intraventricular hemorrhage of prematurity, and the absence of a CCC were also associated with improved shunt survival on univariable analysis. Multivariable analysis revealed that hydrocephalus etiology, the absence of a CCC, corrected age ≥ 30 days at the time of the first permanent procedure, and ETV prior to VPS insertion (HR 0.85, 95% CI 0.74-0.98) remained associated with shunt survival (all p < 0.05).
Conclusions: This analysis demonstrates an association between ETV prior to VPS placement and improved VPS survival, even when controlling for age, comorbid conditions, and hydrocephalus etiology. Further work is needed to understand the mechanism of this effect.
目的:内镜下第三脑室造口术(ETV)是脑室腹腔分流术(VPS)放置的一种替代方法,与早期失败的高风险相关,有时需要后续的VPS插入。作者通过脑积水临床研究网络(HCRN)核心数据项目评估了VPS放置前ETV对VPS失效风险的影响。方法:作者回顾性地回顾了HCRN核心数据项目(registry)收集的2008年4月至2023年7月期间所有接受VPS手术的儿童的数据。将接受VPS植入作为脑积水初始治疗的儿童与在VPS植入之前接受ETV治疗的儿童进行比较。主要结局是初始VPS存活,失败定义为任何后续脑积水手术。Kaplan-Meier和Cox比例风险分析评估了既往ETV的影响,控制了首次永久性手术(ETV或VPS放置)时的年龄、脑积水病因和复杂慢性疾病(CCCs)。结果:6206例患儿行VPS置入术,其中642例患儿在ETV失败后行VPS置入术。在ETV后插入VPS提高了1年的分流生存率(74.3% vs 67.8%, p < 0.001)。未经校正分析显示,ETV后VPS生存率提高(HR 0.78, 95% CI 0.68-0.90, p = 0.001)。单变量分析显示,第一次永久性手术时的矫正年龄≥30天、脉络膜丛火化、脑积水的病因(非脑室内出血的早产儿)和无CCC也与分流术生存率的提高有关。多变量分析显示,脑积水病因、无CCC、首次永久性手术时矫正年龄≥30天以及VPS插入前的ETV (HR 0.85, 95% CI 0.74-0.98)仍与分流术存活相关(均p < 0.05)。结论:该分析表明,即使在控制年龄、合并症和脑积水病因的情况下,放置VPS前的ETV与改善的VPS存活率之间存在关联。需要进一步的工作来了解这种效应的机制。
{"title":"Effect of endoscopic third ventriculostomy on subsequent shunt failure: a Hydrocephalus Clinical Research Network study.","authors":"Michael J Feldman, Hailey Jensen, Anastasia Arynchyna-Smith, Ron W Reeder, Curtis J Rozzelle, Jennifer M Strahle, William E Whitehead, Jonathan Pindrik, Albert M Isaacs, Jason S Hauptman, Marcie Langley, Patrick J McDonald, Mandeep S Tamber, Ian F Pollack, Eric M Jackson, John C Wellons, Robert Naftel, Todd C Hankinson, Abhaya V Kulkarni, Jay Riva-Cambrin, John R W Kestle, Brandon G Rocque","doi":"10.3171/2025.7.PEDS25119","DOIUrl":"10.3171/2025.7.PEDS25119","url":null,"abstract":"<p><strong>Objective: </strong>Endoscopic third ventriculostomy (ETV), an alternative to ventriculoperitoneal shunt (VPS) placement, is associated with a higher risk of early failure, sometimes necessitating subsequent VPS insertion. The authors evaluated the impact of ETV prior to VPS placement on the risk of VPS failure by using the Hydrocephalus Clinical Research Network (HCRN) Core Data Project.</p><p><strong>Methods: </strong>The authors retrospectively reviewed prospectively collected data from the HCRN Core Data Project (registry) on all children who underwent VPS surgery between April 2008 and July 2023. Children who had undergone VPS placement as initial treatment for hydrocephalus were compared with those who had undergone ETV prior to VPS insertion. The primary outcome was initial VPS survival, with failure defined as any subsequent hydrocephalus procedure. Kaplan-Meier and Cox proportional hazards analyses were performed to assess the effect of prior ETV, controlling for age at the first permanent procedure (ETV or VPS placement), hydrocephalus etiology, and complex chronic conditions (CCCs).</p><p><strong>Results: </strong>VPS placement was performed in 6206 children, of whom 642 underwent VPS placement after failed ETV. VPS insertion after ETV improved shunt survival at 1 year (74.3% vs 67.8%, p < 0.001). Unadjusted analysis showed improved VPS survival after ETV (HR 0.78, 95% CI 0.68-0.90, p = 0.001). Corrected age ≥ 30 days at the time of the first permanent procedure, choroid plexus cauterization, etiology of hydrocephalus other than intraventricular hemorrhage of prematurity, and the absence of a CCC were also associated with improved shunt survival on univariable analysis. Multivariable analysis revealed that hydrocephalus etiology, the absence of a CCC, corrected age ≥ 30 days at the time of the first permanent procedure, and ETV prior to VPS insertion (HR 0.85, 95% CI 0.74-0.98) remained associated with shunt survival (all p < 0.05).</p><p><strong>Conclusions: </strong>This analysis demonstrates an association between ETV prior to VPS placement and improved VPS survival, even when controlling for age, comorbid conditions, and hydrocephalus etiology. Further work is needed to understand the mechanism of this effect.</p>","PeriodicalId":16549,"journal":{"name":"Journal of neurosurgery. Pediatrics","volume":" ","pages":"669-676"},"PeriodicalIF":2.1,"publicationDate":"2025-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145313098","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-17DOI: 10.3171/2025.7.PEDS25208
Mandeep S Tamber, Hailey Jensen, Ron Reeder, Jason Clawson, Nichol Nunn, John R W Kestle
Objective: The Hydrocephalus Clinical Research Network-Quality (HCRNq) was established to encourage adoption of evidence-based best practices for the care of children with hydrocephalus. A shunt infection prevention initiative is ongoing within the network, and an analysis of baseline data suggested important practice variation with respect to shunt infection prevention practices. In a first attempt to standardize care, the authors recommended adoption of an endorsed shunt infection prevention protocol within the network, and now present information related to protocol adoption, compliance, and its effect on shunt infection rates.
Methods: A memorandum was circulated to HCRNq sites endorsing and recommending adoption of a 7-step shunt infection prevention protocol. Patient and procedural data relevant to shunt surgery and infection prevention were then prospectively collected from 31 network sites. The relationship between the infection outcome and patient and procedural variables, including protocol adoption, was modeled using uni- and multivariable statistics.
Results: An unadjusted infection rate of 3.6% was observed over nearly 3500 shunt procedures, similar to what was observed at baseline, but with a narrower range, suggesting that some outlying sites were brought closer to the network average. An increased infection risk was associated with shunt placement for preterm posthemorrhagic hydrocephalus, the occurrence of prior shunt surgery within 6 months of the index procedure, and the use of antibiotic ointment. A reduced infection risk with the use of antibiotic-impregnated catheters was suggested. Adoption of the recommended protocol was modest, and as a result, significant practice variation continued to be observed. In this analysis, no relationship was observed between infection risk and the use of an infection prevention protocol.
Conclusions: This first attempt to encourage standardization of perioperative practices for shunt infection prevention, by endorsing an evidence-based shunt infection prevention protocol for use at network sites, resulted in incremental protocol adoption. Many shunt procedures continue to occur without the cover of a protocol. Although adherence to a protocol did not appear to influence infection risk in the present analysis, an opportunity to improve remains, with a potential beneficial effect on infection rates to follow. The authors continue to work toward further improvement in this regard.
{"title":"Effect of a recommended shunt infection prevention protocol on perioperative practices and infection rates in the Hydrocephalus Clinical Research Network-Quality.","authors":"Mandeep S Tamber, Hailey Jensen, Ron Reeder, Jason Clawson, Nichol Nunn, John R W Kestle","doi":"10.3171/2025.7.PEDS25208","DOIUrl":"10.3171/2025.7.PEDS25208","url":null,"abstract":"<p><strong>Objective: </strong>The Hydrocephalus Clinical Research Network-Quality (HCRNq) was established to encourage adoption of evidence-based best practices for the care of children with hydrocephalus. A shunt infection prevention initiative is ongoing within the network, and an analysis of baseline data suggested important practice variation with respect to shunt infection prevention practices. In a first attempt to standardize care, the authors recommended adoption of an endorsed shunt infection prevention protocol within the network, and now present information related to protocol adoption, compliance, and its effect on shunt infection rates.</p><p><strong>Methods: </strong>A memorandum was circulated to HCRNq sites endorsing and recommending adoption of a 7-step shunt infection prevention protocol. Patient and procedural data relevant to shunt surgery and infection prevention were then prospectively collected from 31 network sites. The relationship between the infection outcome and patient and procedural variables, including protocol adoption, was modeled using uni- and multivariable statistics.</p><p><strong>Results: </strong>An unadjusted infection rate of 3.6% was observed over nearly 3500 shunt procedures, similar to what was observed at baseline, but with a narrower range, suggesting that some outlying sites were brought closer to the network average. An increased infection risk was associated with shunt placement for preterm posthemorrhagic hydrocephalus, the occurrence of prior shunt surgery within 6 months of the index procedure, and the use of antibiotic ointment. A reduced infection risk with the use of antibiotic-impregnated catheters was suggested. Adoption of the recommended protocol was modest, and as a result, significant practice variation continued to be observed. In this analysis, no relationship was observed between infection risk and the use of an infection prevention protocol.</p><p><strong>Conclusions: </strong>This first attempt to encourage standardization of perioperative practices for shunt infection prevention, by endorsing an evidence-based shunt infection prevention protocol for use at network sites, resulted in incremental protocol adoption. Many shunt procedures continue to occur without the cover of a protocol. Although adherence to a protocol did not appear to influence infection risk in the present analysis, an opportunity to improve remains, with a potential beneficial effect on infection rates to follow. The authors continue to work toward further improvement in this regard.</p>","PeriodicalId":16549,"journal":{"name":"Journal of neurosurgery. Pediatrics","volume":" ","pages":"677-682"},"PeriodicalIF":2.1,"publicationDate":"2025-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145313097","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-10DOI: 10.3171/2025.6.PEDS25109
Diwas Gautam, Michael T Bounajem, Monica-Rae Owens, Allison Liang, Luke Silveira, Craig J Kilburg, Ramesh Grandhi, Robert C Rennert, Douglas L Brockmeyer, Robert J Bollo, William T Couldwell, Karol P Budohoski
Objective: Children with cerebral arteriovenous malformation (AVM) have a high risk of spontaneous intracerebral hemorrhage. The identification of patients at risk for AVM rupture and accurate prediction of outcomes are critical to guide management strategies. The authors examined the angioarchitectural features of pediatric AVMs associated with hemorrhagic presentation and reviewed the utility of the Ruptured AVM Grading Scale (RAGS) for outcome prognostication in pediatric patients treated surgically at a single institution.
Methods: The authors retrospectively reviewed the records of pediatric (age ≤ 18 years) patients who underwent resection of AVMs at their institution between 1998 and 2023. Demographic factors, clinical presentation, and angioarchitectural details including nidus size, location, venous drainage, presence of flow-related aneurysm, presence of an en passage vessel, and perforator vessel supply were collected. Clinical presentation and angioarchitecture were compared in patients with ruptured and unruptured AVMs. In patients with ruptured AVMs, the area under the receiver operating characteristic curve (AUROC) was calculated based on their RAGS scores at 3 follow-up time points using dichotomous analysis of the modified Rankin Scale score as the response variable.
Results: Of the 62 patients included in this study, 59.7% presented after rupture. Patients with ruptured AVMs had, on average, a smaller nidus (24.84 vs 38.24 mm, p < 0.001) and a higher percentage of deep venous drainage (64.9% vs 32.0%, p = 0.009). Multivariable logistic regression analysis confirmed smaller nidus diameter (OR 0.93, 95% CI 0.87-0.98, p = 0.016) and presence of deep venous drainage (OR 10.78, 95% CI 1.73-42.94, p = 0.011) as independent predictors of hemorrhagic presentation. Good clinical outcomes (modified Rankin Scale [mRS] score ≤ 2) at last follow-up were similar for the unruptured and ruptured cohorts (85.5% vs 88.0%, p = 0.230). For patients with ruptured AVMs, the AUROC values for the RAGS scoring system were 0.48 at 3 months, 0.67 at 1 year, and 0.70 at the last known follow-up.
Conclusions: Smaller AVM nidus size and deep venous drainage were associated with hemorrhagic presentation in children with AVMs. Although the AUROC for RAGS improved with longer follow-up periods, it did not reach the 0.8 threshold needed for clinical utility.
目的:儿童脑动静脉畸形(AVM)是发生自发性脑出血的高危患者。识别有AVM破裂风险的患者和准确预测结果对指导治疗策略至关重要。作者检查了与出血表现相关的儿童动静脉畸形的血管结构特征,并回顾了在单一机构接受手术治疗的儿童患者破裂动静脉畸形分级量表(RAGS)的预后预测的效用。方法:作者回顾性回顾了1998年至2023年在该院接受动静脉畸形切除术的儿童(年龄≤18岁)患者的记录。收集人口统计学因素、临床表现和血管建筑学细节,包括病灶大小、位置、静脉引流、血流相关动脉瘤的存在、通道血管的存在和穿支血管的供应。比较破裂和未破裂的动静脉畸形患者的临床表现和血管结构。在avm破裂患者中,根据随访3个时间点的RAGS评分计算受试者工作特征曲线下面积(AUROC),采用修正Rankin量表评分的二分类分析作为反应变量。结果:在本研究的62例患者中,59.7%的患者在破裂后出现。avm破裂的患者平均病灶较小(24.84 mm vs 38.24 mm, p < 0.001),深静脉引流比例较高(64.9% vs 32.0%, p = 0.009)。多变量logistic回归分析证实,较小的病灶直径(OR 0.93, 95% CI 0.87-0.98, p = 0.016)和存在深静脉引流(OR 10.78, 95% CI 1.73-42.94, p = 0.011)是出血表现的独立预测因素。最后随访时,未破裂组和破裂组的良好临床结果(改良Rankin量表[mRS]评分≤2)相似(85.5% vs 88.0%, p = 0.230)。对于avm破裂的患者,rag评分系统的AUROC值在3个月时为0.48,1年时为0.67,最后一次已知随访时为0.70。结论:较小的动静脉畸形病灶大小和深静脉引流与儿童动静脉畸形出血有关。虽然随着随访时间的延长,RAGS的AUROC有所改善,但仍未达到临床应用所需的0.8阈值。
{"title":"Rupture-associated angioarchitectural features and assessment of the Ruptured Arteriovenous Malformation Grading Scale in surgically treated pediatric patients.","authors":"Diwas Gautam, Michael T Bounajem, Monica-Rae Owens, Allison Liang, Luke Silveira, Craig J Kilburg, Ramesh Grandhi, Robert C Rennert, Douglas L Brockmeyer, Robert J Bollo, William T Couldwell, Karol P Budohoski","doi":"10.3171/2025.6.PEDS25109","DOIUrl":"10.3171/2025.6.PEDS25109","url":null,"abstract":"<p><strong>Objective: </strong>Children with cerebral arteriovenous malformation (AVM) have a high risk of spontaneous intracerebral hemorrhage. The identification of patients at risk for AVM rupture and accurate prediction of outcomes are critical to guide management strategies. The authors examined the angioarchitectural features of pediatric AVMs associated with hemorrhagic presentation and reviewed the utility of the Ruptured AVM Grading Scale (RAGS) for outcome prognostication in pediatric patients treated surgically at a single institution.</p><p><strong>Methods: </strong>The authors retrospectively reviewed the records of pediatric (age ≤ 18 years) patients who underwent resection of AVMs at their institution between 1998 and 2023. Demographic factors, clinical presentation, and angioarchitectural details including nidus size, location, venous drainage, presence of flow-related aneurysm, presence of an en passage vessel, and perforator vessel supply were collected. Clinical presentation and angioarchitecture were compared in patients with ruptured and unruptured AVMs. In patients with ruptured AVMs, the area under the receiver operating characteristic curve (AUROC) was calculated based on their RAGS scores at 3 follow-up time points using dichotomous analysis of the modified Rankin Scale score as the response variable.</p><p><strong>Results: </strong>Of the 62 patients included in this study, 59.7% presented after rupture. Patients with ruptured AVMs had, on average, a smaller nidus (24.84 vs 38.24 mm, p < 0.001) and a higher percentage of deep venous drainage (64.9% vs 32.0%, p = 0.009). Multivariable logistic regression analysis confirmed smaller nidus diameter (OR 0.93, 95% CI 0.87-0.98, p = 0.016) and presence of deep venous drainage (OR 10.78, 95% CI 1.73-42.94, p = 0.011) as independent predictors of hemorrhagic presentation. Good clinical outcomes (modified Rankin Scale [mRS] score ≤ 2) at last follow-up were similar for the unruptured and ruptured cohorts (85.5% vs 88.0%, p = 0.230). For patients with ruptured AVMs, the AUROC values for the RAGS scoring system were 0.48 at 3 months, 0.67 at 1 year, and 0.70 at the last known follow-up.</p><p><strong>Conclusions: </strong>Smaller AVM nidus size and deep venous drainage were associated with hemorrhagic presentation in children with AVMs. Although the AUROC for RAGS improved with longer follow-up periods, it did not reach the 0.8 threshold needed for clinical utility.</p>","PeriodicalId":16549,"journal":{"name":"Journal of neurosurgery. Pediatrics","volume":" ","pages":"729-737"},"PeriodicalIF":2.1,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145274845","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Benjamin A Brakel, Mandeep S Tamber, Annika Weir, Isabella Watson, A Hana Miller, Patrick J McDonald, Ash Singhal, Faizal A Haji
Objective: The treatment of sagittal craniosynostosis typically involves endoscopic suturectomy (ES) to allow skull expansion, followed by postoperative helmet orthosis, resulting in an improvement in cranial deformity as assessed using the cephalic index (CI). The impact of variations in surgical technique on long-term CI outcomes is not well understood, and there is controversy regarding whether adding barrel stave osteotomy (BSO) to standard ES leads to greater improvement in the CI postoperatively. This combined approach is thought to improve cranial shape and overall clinical outcomes but may increase operative burden. The aim of this study was to investigate the impact of BSO during ES on operative outcomes and postoperative cranial deformity in patients who underwent surgical correction of sagittal craniosynostosis.
Methods: The authors conducted a retrospective chart review of children who had been treated with ES for sagittal craniosynostosis between 2010 and 2021 at British Columbia Children's Hospital. Demographics, operative outcomes, and postoperative longitudinal CI measurements were collected and compared between patients who had undergone ES with BSO (ES+BSO) and those who had undergone ES alone. Operative outcomes related to anesthesia and surgical time, blood loss, and hospital length of stay were analyzed, as were changes in the CI at various follow-up times. A mixed-effects model was used to compare longitudinal CI measurements between treatment groups, controlling for patient age, preoperative CI, and duration of helmet therapy.
Results: Eighty-five patients were included in the analysis, 67 treated with ES+BSO and 18 treated with ES. Operative outcomes, including length of hospital stay, operative time, time under anesthesia, blood loss, and need for transfusion did not differ significantly between treatment groups (p > 0.05). The mean follow-up for the last CI measurements was 56.0 months. While preoperative CI was similar for the two groups (mean 67.4 for ES+BSO vs 66.8 for ES, p = 0.61), CI was significantly higher in the ES+BSO group immediately postoperatively (p = 0.004) and at the 6-month (p = 0.01), 2-year (p = 0.02), and final (p = 0.002) follow-ups. A mixed-effects model revealed that the addition of BSO led to significantly greater CI measurements independent of age, preoperative CI, and helmeting duration (estimated effect size 2.21, p = 0.001).
Conclusions: In this series, the addition of BSO to ES significantly improved immediate and long-term cranial deformity in patients with sagittal craniosynostosis, without increasing the operative burden.
{"title":"Impact of barrel stave osteotomy on cephalometric measurements in patients who have undergone endoscopic repair of sagittal craniosynostosis.","authors":"Benjamin A Brakel, Mandeep S Tamber, Annika Weir, Isabella Watson, A Hana Miller, Patrick J McDonald, Ash Singhal, Faizal A Haji","doi":"10.3171/2025.6.PEDS2523","DOIUrl":"10.3171/2025.6.PEDS2523","url":null,"abstract":"<p><strong>Objective: </strong>The treatment of sagittal craniosynostosis typically involves endoscopic suturectomy (ES) to allow skull expansion, followed by postoperative helmet orthosis, resulting in an improvement in cranial deformity as assessed using the cephalic index (CI). The impact of variations in surgical technique on long-term CI outcomes is not well understood, and there is controversy regarding whether adding barrel stave osteotomy (BSO) to standard ES leads to greater improvement in the CI postoperatively. This combined approach is thought to improve cranial shape and overall clinical outcomes but may increase operative burden. The aim of this study was to investigate the impact of BSO during ES on operative outcomes and postoperative cranial deformity in patients who underwent surgical correction of sagittal craniosynostosis.</p><p><strong>Methods: </strong>The authors conducted a retrospective chart review of children who had been treated with ES for sagittal craniosynostosis between 2010 and 2021 at British Columbia Children's Hospital. Demographics, operative outcomes, and postoperative longitudinal CI measurements were collected and compared between patients who had undergone ES with BSO (ES+BSO) and those who had undergone ES alone. Operative outcomes related to anesthesia and surgical time, blood loss, and hospital length of stay were analyzed, as were changes in the CI at various follow-up times. A mixed-effects model was used to compare longitudinal CI measurements between treatment groups, controlling for patient age, preoperative CI, and duration of helmet therapy.</p><p><strong>Results: </strong>Eighty-five patients were included in the analysis, 67 treated with ES+BSO and 18 treated with ES. Operative outcomes, including length of hospital stay, operative time, time under anesthesia, blood loss, and need for transfusion did not differ significantly between treatment groups (p > 0.05). The mean follow-up for the last CI measurements was 56.0 months. While preoperative CI was similar for the two groups (mean 67.4 for ES+BSO vs 66.8 for ES, p = 0.61), CI was significantly higher in the ES+BSO group immediately postoperatively (p = 0.004) and at the 6-month (p = 0.01), 2-year (p = 0.02), and final (p = 0.002) follow-ups. A mixed-effects model revealed that the addition of BSO led to significantly greater CI measurements independent of age, preoperative CI, and helmeting duration (estimated effect size 2.21, p = 0.001).</p><p><strong>Conclusions: </strong>In this series, the addition of BSO to ES significantly improved immediate and long-term cranial deformity in patients with sagittal craniosynostosis, without increasing the operative burden.</p>","PeriodicalId":16549,"journal":{"name":"Journal of neurosurgery. Pediatrics","volume":" ","pages":"683-688"},"PeriodicalIF":2.1,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145274799","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-10DOI: 10.3171/2025.5.PEDS24552
Jana H Badrani, Caroline Caudill, Kenneth S Paik, Luke Anderson, Tofey J Leon, Brandon G Rocque, Curtis J Rozzelle
Objective: Chiari malformation type I (CM-I) is a common condition characterized by the cerebellar tonsillar position below the foramen magnum. Radiographic measurements are important for diagnosing CM-I but have limited use in predicting the severity of the condition and the need for surgery. The fourth ventricle roof angle (FVRA), a measure of deformation or bowing of the roof of the fourth ventricle, has been presented as a tool for predicting brainstem dysfunction in patients with CM-I; however, this has not been validated. Utilizing a database of pediatric patients with CM-I from a large single center, this study aimed to validate the finding that the FVRA can serve as a predictor of brainstem dysfunction in pediatric CM-I and to present additional potential correlations of interest between the FVRA and symptoms and other radiographical measurements.
Methods: Radiographic measurements were retrospectively reviewed for 388 pediatric patients evaluated for CM-I at Children's of Alabama from November 2010 to 2017. Fourth ventricle bowing was determined to be present if the FVRA was > 65°. Univariate and multivariate logistic regression analyses were performed to identify significant associations with the FVRA, brainstem dysfunction, and surgery. Brainstem dysfunction was defined as the presence of lower cranial nerve dysfunction and/or sleep apnea.
Results: Multivariate logistic regression showed significant association of lower brainstem dysfunction with tonsillar position (OR 1.17, 95% CI 1.06-1.29), basilar invagination (OR 0.66, 95% CI 0.47-0.91), supraoccipital length (OR 0.86, 95% CI 0.77-0.96), and tussive headache (OR 6.62, 95% CI 1.95-22.46). The presence of bowing did not show a significant association with brainstem dysfunction in the multivariable model (OR 1.02, 95% CI 0.27-3.81), and it was not significantly associated with undergoing surgery after controlling for symptoms that always resulted in surgery (p = 0.483).
Conclusions: Univariate logistic regression analysis demonstrated that an FVRA greater than 65° is significantly associated with brainstem dysfunction. In a multivariate logistic regression model, however, the presence of bowing was not independently associated with brainstem dysfunction. As such, additional studies are needed before FVRA can be utilized clinically.
目的:I型Chiari畸形(CM-I)是一种以小脑扁桃体位于枕骨大孔以下为特征的常见病。放射测量对诊断CM-I很重要,但在预测病情严重程度和是否需要手术方面用处有限。第四脑室顶角(FVRA)是测量第四脑室顶变形或弯曲的一种方法,已被提出作为预测CM-I患者脑干功能障碍的工具;然而,这还没有得到证实。利用来自大型单一中心的小儿CM-I患者数据库,本研究旨在验证FVRA可以作为小儿CM-I脑干功能障碍的预测因子,并提出FVRA与症状和其他影像学测量之间的其他潜在相关性。方法:回顾性分析2010年11月至2017年在阿拉巴马州儿童医院接受CM-I评估的388名儿童患者的放射学测量结果。如果FVRA为bbb65°,则确定存在第四脑室弯曲。进行单因素和多因素logistic回归分析,以确定FVRA、脑干功能障碍和手术的显著相关性。脑干功能障碍被定义为存在下颅神经功能障碍和/或睡眠呼吸暂停。结果:多因素logistic回归显示,下脑干功能障碍与扁桃体位置(OR 1.17, 95% CI 1.06-1.29)、颅底内翻(OR 0.66, 95% CI 0.47-0.91)、枕上长度(OR 0.86, 95% CI 0.77-0.96)和咳嗽头痛(OR 6.62, 95% CI 1.95-22.46)有显著相关性。在多变量模型中,弓形现象的存在与脑干功能障碍无显著相关性(OR 1.02, 95% CI 0.27-3.81),在控制了总是导致手术的症状后,弓形现象与接受手术无显著相关性(p = 0.483)。结论:单因素logistic回归分析显示,FVRA大于65°与脑干功能障碍显著相关。然而,在多变量logistic回归模型中,弓形的存在与脑干功能障碍并不是独立相关的。因此,在临床应用FVRA之前,还需要进一步的研究。
{"title":"Validation of fourth ventricle roof angle as a measure of brainstem dysfunction in pediatric Chiari malformation type I.","authors":"Jana H Badrani, Caroline Caudill, Kenneth S Paik, Luke Anderson, Tofey J Leon, Brandon G Rocque, Curtis J Rozzelle","doi":"10.3171/2025.5.PEDS24552","DOIUrl":"10.3171/2025.5.PEDS24552","url":null,"abstract":"<p><strong>Objective: </strong>Chiari malformation type I (CM-I) is a common condition characterized by the cerebellar tonsillar position below the foramen magnum. Radiographic measurements are important for diagnosing CM-I but have limited use in predicting the severity of the condition and the need for surgery. The fourth ventricle roof angle (FVRA), a measure of deformation or bowing of the roof of the fourth ventricle, has been presented as a tool for predicting brainstem dysfunction in patients with CM-I; however, this has not been validated. Utilizing a database of pediatric patients with CM-I from a large single center, this study aimed to validate the finding that the FVRA can serve as a predictor of brainstem dysfunction in pediatric CM-I and to present additional potential correlations of interest between the FVRA and symptoms and other radiographical measurements.</p><p><strong>Methods: </strong>Radiographic measurements were retrospectively reviewed for 388 pediatric patients evaluated for CM-I at Children's of Alabama from November 2010 to 2017. Fourth ventricle bowing was determined to be present if the FVRA was > 65°. Univariate and multivariate logistic regression analyses were performed to identify significant associations with the FVRA, brainstem dysfunction, and surgery. Brainstem dysfunction was defined as the presence of lower cranial nerve dysfunction and/or sleep apnea.</p><p><strong>Results: </strong>Multivariate logistic regression showed significant association of lower brainstem dysfunction with tonsillar position (OR 1.17, 95% CI 1.06-1.29), basilar invagination (OR 0.66, 95% CI 0.47-0.91), supraoccipital length (OR 0.86, 95% CI 0.77-0.96), and tussive headache (OR 6.62, 95% CI 1.95-22.46). The presence of bowing did not show a significant association with brainstem dysfunction in the multivariable model (OR 1.02, 95% CI 0.27-3.81), and it was not significantly associated with undergoing surgery after controlling for symptoms that always resulted in surgery (p = 0.483).</p><p><strong>Conclusions: </strong>Univariate logistic regression analysis demonstrated that an FVRA greater than 65° is significantly associated with brainstem dysfunction. In a multivariate logistic regression model, however, the presence of bowing was not independently associated with brainstem dysfunction. As such, additional studies are needed before FVRA can be utilized clinically.</p>","PeriodicalId":16549,"journal":{"name":"Journal of neurosurgery. Pediatrics","volume":" ","pages":"694-701"},"PeriodicalIF":2.1,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145274868","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sebastian M Toescu, Barry Pizer, William Gump, Kristian Aquilina, Shivaram Avula, Conor Mallucci, Christopher Parks, Andrea Carai, Giles Robinson, Guillermo Aldave, Lissa Baird, Toba Niazi, Robert Keating, Paul Klimo
{"title":"Toward reducing the risk of cerebellar mutism syndrome: consensus statement from the Posterior Fossa Society.","authors":"Sebastian M Toescu, Barry Pizer, William Gump, Kristian Aquilina, Shivaram Avula, Conor Mallucci, Christopher Parks, Andrea Carai, Giles Robinson, Guillermo Aldave, Lissa Baird, Toba Niazi, Robert Keating, Paul Klimo","doi":"10.3171/2025.5.PEDS2593","DOIUrl":"10.3171/2025.5.PEDS2593","url":null,"abstract":"","PeriodicalId":16549,"journal":{"name":"Journal of neurosurgery. Pediatrics","volume":" ","pages":"789-797"},"PeriodicalIF":2.1,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145274824","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objective: The role of timely nutritional support in the recovery of pediatric traumatic brain injury (PTBI) patients is crucial yet underexplored. The authors planned a retrospective study to investigate the timing of feeding initiation (early feeding [≤ 48 hours] or delayed feeding [> 48 hours]), feeding pattern, and causes of feeding delay/interruption in this cohort and studied the association of delayed feeding with outcomes in PTBI from a single center in a lower-middle-income country.
Methods: This retrospective, single-center study included PTBI patients ≤ 15 years of age admitted to the neurotrauma intensive care unit (NICU) within 24 hours of head injury over a period of 1 year. Demographic data, injury characteristics, and nutritional data were recorded from hospital electronic records. The outcome was measured in terms of NICU length of stay (LOS) and hospital LOS, infectious complications, neurological recovery at discharge, and mortality.
Results: One hundred PTBI patients were included, with mild (n = 28, 28%), moderate (n = 28, 28%), and severe (n = 44, 44%) traumatic brain injury (TBI). Patients had a median Glasgow Coma Scale (GCS) score of 9 (IQR 7, 13) at admission. Enteral nutrition was initiated early in 48% (n = 48) of patients. Only 39 of 100 patients reached 70% of their caloric target within 7 days. Causes of feeding interruption were planned surgical/radiological and airway procedures (n = 89, 59.0%), feed intolerance (n = 25, 16.6%), feed refusal (n = 22, 14.6%), and hemodynamic instability (n = 15, 9.9%). Early initiation of enteral feeding was positively associated with reduced NICU LOS (r = 0.25) and overall hospital LOS (r = 0.33). Patients receiving early nutrition had a shorter hospital LOS (5.5 vs 10 days, p = 0.043) and higher GCS score at discharge (15 vs 13, p = 0.002). In mild TBI cases, early feeding significantly reduced NICU (2.5 vs 7.5 days, p = 0.01) and hospital (3.5 vs 13 days, p = 0.002) LOSs and improved discharge GCS score (15 vs 14.5, p = 0.02). These benefits were not observed in moderate or severe TBI patients. In multivariate analysis, undergoing neurosurgery influenced hospital LOS and discharge GCS score, and admission GCS score predicted mortality. The in-hospital mortality rate was 17%.
Conclusions: Early enteral feeding was initiated in 48% of PTBI patients. Common delays/interruptions were due to planned procedures. Early enteral feeding was associated with shorter NICU and hospital LOSs. However, a definite association of early enteral feeding with improved neurological outcomes could not be established.
目的:及时的营养支持在儿童创伤性脑损伤(PTBI)患者康复中的作用至关重要,但尚未得到充分的探讨。作者计划进行一项回顾性研究,调查该队列中开始喂养的时间(早期喂养[≤48小时]或延迟喂养[> 48小时])、喂养方式和喂养延迟/中断的原因,并研究延迟喂养与中低收入国家单一中心PTBI结局的关系。方法:这项回顾性的单中心研究纳入了1年内头部损伤后24小时内入住神经外伤重症监护病房(NICU)的年龄≤15岁的PTBI患者。从医院电子病历中记录人口统计数据、损伤特征和营养数据。结果是根据NICU的住院时间(LOS)和医院LOS、感染并发症、出院时神经系统恢复和死亡率来衡量的。结果:纳入100例PTBI患者,分别为轻度(n = 28, 28%)、中度(n = 28, 28%)和重度(n = 44, 44%)创伤性脑损伤(TBI)。患者入院时格拉斯哥昏迷评分(GCS)中位数为9 (IQR 7,13)。48% (n = 48)的患者早期开始肠内营养。100名患者中只有39人在7天内达到了热量目标的70%。导致进食中断的原因包括计划中的外科/放射学和气道手术(n = 89, 59.0%)、食物不耐受(n = 25, 16.6%)、拒绝进食(n = 22, 14.6%)和血流动力学不稳定(n = 15, 9.9%)。早期开始肠内喂养与降低NICU LOS (r = 0.25)和整体医院LOS (r = 0.33)呈正相关。接受早期营养的患者住院时间较短(5.5 vs 10天,p = 0.043),出院时GCS评分较高(15 vs 13, p = 0.002)。在轻度TBI病例中,早期喂养显著减少NICU (2.5 vs 7.5天,p = 0.01)和住院(3.5 vs 13天,p = 0.002)损失和出院GCS评分(15 vs 14.5, p = 0.02)。在中度或重度TBI患者中未观察到这些益处。在多因素分析中,接受神经外科手术影响医院LOS和出院GCS评分,入院GCS评分预测死亡率。住院死亡率为17%。结论:48%的PTBI患者开始了早期肠内喂养。常见的延误/中断是由于计划好的程序。早期肠内喂养与较短的NICU和医院LOSs相关。然而,早期肠内喂养与神经预后改善之间的确切联系尚不能确定。
{"title":"Enteral feeding initiation and feeding practices in pediatric traumatic brain injury patients admitted to the neurotrauma intensive care unit.","authors":"Ashish Bindra, Mohamed Salih Mohamed Samsudeen, Richa Jaiswal, Preeti Gupta, Gyaninder P Singh, Manoj Phalak, Deepak Gupta","doi":"10.3171/2025.6.PEDS24640","DOIUrl":"10.3171/2025.6.PEDS24640","url":null,"abstract":"<p><strong>Objective: </strong>The role of timely nutritional support in the recovery of pediatric traumatic brain injury (PTBI) patients is crucial yet underexplored. The authors planned a retrospective study to investigate the timing of feeding initiation (early feeding [≤ 48 hours] or delayed feeding [> 48 hours]), feeding pattern, and causes of feeding delay/interruption in this cohort and studied the association of delayed feeding with outcomes in PTBI from a single center in a lower-middle-income country.</p><p><strong>Methods: </strong>This retrospective, single-center study included PTBI patients ≤ 15 years of age admitted to the neurotrauma intensive care unit (NICU) within 24 hours of head injury over a period of 1 year. Demographic data, injury characteristics, and nutritional data were recorded from hospital electronic records. The outcome was measured in terms of NICU length of stay (LOS) and hospital LOS, infectious complications, neurological recovery at discharge, and mortality.</p><p><strong>Results: </strong>One hundred PTBI patients were included, with mild (n = 28, 28%), moderate (n = 28, 28%), and severe (n = 44, 44%) traumatic brain injury (TBI). Patients had a median Glasgow Coma Scale (GCS) score of 9 (IQR 7, 13) at admission. Enteral nutrition was initiated early in 48% (n = 48) of patients. Only 39 of 100 patients reached 70% of their caloric target within 7 days. Causes of feeding interruption were planned surgical/radiological and airway procedures (n = 89, 59.0%), feed intolerance (n = 25, 16.6%), feed refusal (n = 22, 14.6%), and hemodynamic instability (n = 15, 9.9%). Early initiation of enteral feeding was positively associated with reduced NICU LOS (r = 0.25) and overall hospital LOS (r = 0.33). Patients receiving early nutrition had a shorter hospital LOS (5.5 vs 10 days, p = 0.043) and higher GCS score at discharge (15 vs 13, p = 0.002). In mild TBI cases, early feeding significantly reduced NICU (2.5 vs 7.5 days, p = 0.01) and hospital (3.5 vs 13 days, p = 0.002) LOSs and improved discharge GCS score (15 vs 14.5, p = 0.02). These benefits were not observed in moderate or severe TBI patients. In multivariate analysis, undergoing neurosurgery influenced hospital LOS and discharge GCS score, and admission GCS score predicted mortality. The in-hospital mortality rate was 17%.</p><p><strong>Conclusions: </strong>Early enteral feeding was initiated in 48% of PTBI patients. Common delays/interruptions were due to planned procedures. Early enteral feeding was associated with shorter NICU and hospital LOSs. However, a definite association of early enteral feeding with improved neurological outcomes could not be established.</p>","PeriodicalId":16549,"journal":{"name":"Journal of neurosurgery. Pediatrics","volume":" ","pages":"747-754"},"PeriodicalIF":2.1,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145274862","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-10DOI: 10.3171/2025.6.PEDS25132
David S Hersh, David J Daniels, Ruth E Bristol, Susan R Durham, Todd C Hankinson, Abhaya V Kulkarni, Howard L Weiner, Bradley Weprin, John C Wellons, Shenandoah Robinson
Objective: Neurosurgeon scientists play a unique role in advancing neuroscience research. While previous publications have explored trends in federal and foundation funding among neurosurgeons, funding is often dominated by neurosurgical oncologists and functional neurosurgeons. Less is known about the research efforts of pediatric neurosurgeons. The aim of this study was to survey the members of the American Society of Pediatric Neurosurgeons (ASPN) to provide an overview of past research experience, current involvement, funding, and research priorities among pediatric neurosurgeons, and to gather insights that could shape future efforts to advance pediatric neurosurgical research.
Methods: A survey was developed using the REDCap platform and distributed to all ASPN members via email. Survey questions used branching logic and were organized into 5 sections: 1) demographics, 2) research experience during training, 3) research experience as an attending physician, 4) research priorities, and 5) multicenter consortiums.
Results: One hundred thirty-nine respondents completed more than half of the survey, for an overall response rate of 52.1%. Most respondents (96.4%) participated in research during their training, but only 38.1% had received a grant during training. In contrast, 83.9% of respondents were actively engaged in research as an attending physician, and 48.7% reported active funding (60.7% federal, 41.8% from foundations, and 42.9% internal). Furthermore, 74.8% of respondents reported being a member of a multicenter research consortium, and 82.4% agreed that multicenter research is important. Seventy percent of respondents agreed that the ASPN should facilitate multicenter consortium-based pediatric neurosurgical research, offering free-text responses with the following suggestions: 1) set aside time at the annual meeting to discuss multicenter research (22.9%); 2) encourage collaboration and facilitate networking (42.9%); 3) provide centralized core services such as a data coordinator and biostatistician (12.9%); and 4) provide training, education, and mentoring (7.1%).
Conclusions: The survey provided a cross-sectional analysis of the pediatric neurosurgical research landscape, highlighting the current state of research experience, funding, and the perspectives of pediatric neurosurgeons regarding research priorities. Despite the challenges, there is clear recognition of the importance of multicenter research collaboration. These findings reinforce the ongoing necessity of organized initiatives to support pediatric neurosurgical research and offer actionable insights into how organized pediatric neurosurgery can contribute to this critical endeavor.
{"title":"Research experience, goals, and priorities of pediatric neurosurgeons: a survey of the American Society of Pediatric Neurosurgeons.","authors":"David S Hersh, David J Daniels, Ruth E Bristol, Susan R Durham, Todd C Hankinson, Abhaya V Kulkarni, Howard L Weiner, Bradley Weprin, John C Wellons, Shenandoah Robinson","doi":"10.3171/2025.6.PEDS25132","DOIUrl":"10.3171/2025.6.PEDS25132","url":null,"abstract":"<p><strong>Objective: </strong>Neurosurgeon scientists play a unique role in advancing neuroscience research. While previous publications have explored trends in federal and foundation funding among neurosurgeons, funding is often dominated by neurosurgical oncologists and functional neurosurgeons. Less is known about the research efforts of pediatric neurosurgeons. The aim of this study was to survey the members of the American Society of Pediatric Neurosurgeons (ASPN) to provide an overview of past research experience, current involvement, funding, and research priorities among pediatric neurosurgeons, and to gather insights that could shape future efforts to advance pediatric neurosurgical research.</p><p><strong>Methods: </strong>A survey was developed using the REDCap platform and distributed to all ASPN members via email. Survey questions used branching logic and were organized into 5 sections: 1) demographics, 2) research experience during training, 3) research experience as an attending physician, 4) research priorities, and 5) multicenter consortiums.</p><p><strong>Results: </strong>One hundred thirty-nine respondents completed more than half of the survey, for an overall response rate of 52.1%. Most respondents (96.4%) participated in research during their training, but only 38.1% had received a grant during training. In contrast, 83.9% of respondents were actively engaged in research as an attending physician, and 48.7% reported active funding (60.7% federal, 41.8% from foundations, and 42.9% internal). Furthermore, 74.8% of respondents reported being a member of a multicenter research consortium, and 82.4% agreed that multicenter research is important. Seventy percent of respondents agreed that the ASPN should facilitate multicenter consortium-based pediatric neurosurgical research, offering free-text responses with the following suggestions: 1) set aside time at the annual meeting to discuss multicenter research (22.9%); 2) encourage collaboration and facilitate networking (42.9%); 3) provide centralized core services such as a data coordinator and biostatistician (12.9%); and 4) provide training, education, and mentoring (7.1%).</p><p><strong>Conclusions: </strong>The survey provided a cross-sectional analysis of the pediatric neurosurgical research landscape, highlighting the current state of research experience, funding, and the perspectives of pediatric neurosurgeons regarding research priorities. Despite the challenges, there is clear recognition of the importance of multicenter research collaboration. These findings reinforce the ongoing necessity of organized initiatives to support pediatric neurosurgical research and offer actionable insights into how organized pediatric neurosurgery can contribute to this critical endeavor.</p>","PeriodicalId":16549,"journal":{"name":"Journal of neurosurgery. Pediatrics","volume":" ","pages":"779-788"},"PeriodicalIF":2.1,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145274895","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-03DOI: 10.3171/2025.7.PEDS25256
Amanda N Stanton, Mallory R Dacus, Macey Martin, Heidi Chen, Alice P Lawrence, Elizabeth N Martin, Robert P Naftel
Objective: Selective dorsal rhizotomy (SDR) is a proven surgical treatment of spastic diplegia to improve function in patients suffering from spasticity compared to physical therapy alone. Few studies have addressed the benefit for those with spastic hemiplegia. The aim of this study was to describe and evaluate the efficacy of SDR in patients with spastic hemiplegia.
Methods: A retrospective chart review was performed on pediatric patients (< 18 years of age) who underwent SDR at Monroe Carell Jr. Children's Hospital from July 2013 through January 2024 with a diagnosis of spastic hemiplegic cerebral palsy. Patients underwent pre- and postoperative physical therapy testing at approximately 1 year. Any patients found to have spastic triplegia with asymmetrical hypertonia in the lower extremities, or those without postoperative evaluations, were excluded. Outcome measures included the modified Ashworth Scale (mAS), Gross Motor Function Measure-66 (GMFM-66), timed (10 m) walk test, Gross Motor Function Classification System (GMFCS), and the Pediatric Quality of Life Cerebral Palsy (PedsQL CP) module. Pre- versus postoperative comparisons were performed using a Wilcoxon signed-rank test and the differences were considered statistically significant when p values were < 0.05.
Results: Twenty-one patients underwent SDR for spastic hemiplegic cerebral palsy with pre- and postoperative physical therapy assessments. The patients were 52.4% male, 81.0% White, with a median age of 5 years at the time of surgery. The most common etiology for spastic hemiplegia was stroke (52.4%). All patients had a preoperative GMFCS level of I (85.7%) or II (14.3%). The median percentage of rootlets cut during the procedure was 60% on the affected side. The sum of the mAS extremity score was improved by 5 points (p < 0.001), the GMFM-66 score was improved by a median of 3.1 (p = 0.002), while the PedsQL CP module improved by a median of 12.3 percentage points (p = 0.003). Orthotic use was reduced from 90.5% preoperatively to 66.7% at follow-up.
Conclusions: SDR is an effective treatment in patients with spastic hemiplegia resulting in significant improvement in motor function, quality of life, and tone.
{"title":"Selective dorsal rhizotomy for spastic hemiplegic cerebral palsy.","authors":"Amanda N Stanton, Mallory R Dacus, Macey Martin, Heidi Chen, Alice P Lawrence, Elizabeth N Martin, Robert P Naftel","doi":"10.3171/2025.7.PEDS25256","DOIUrl":"10.3171/2025.7.PEDS25256","url":null,"abstract":"<p><strong>Objective: </strong>Selective dorsal rhizotomy (SDR) is a proven surgical treatment of spastic diplegia to improve function in patients suffering from spasticity compared to physical therapy alone. Few studies have addressed the benefit for those with spastic hemiplegia. The aim of this study was to describe and evaluate the efficacy of SDR in patients with spastic hemiplegia.</p><p><strong>Methods: </strong>A retrospective chart review was performed on pediatric patients (< 18 years of age) who underwent SDR at Monroe Carell Jr. Children's Hospital from July 2013 through January 2024 with a diagnosis of spastic hemiplegic cerebral palsy. Patients underwent pre- and postoperative physical therapy testing at approximately 1 year. Any patients found to have spastic triplegia with asymmetrical hypertonia in the lower extremities, or those without postoperative evaluations, were excluded. Outcome measures included the modified Ashworth Scale (mAS), Gross Motor Function Measure-66 (GMFM-66), timed (10 m) walk test, Gross Motor Function Classification System (GMFCS), and the Pediatric Quality of Life Cerebral Palsy (PedsQL CP) module. Pre- versus postoperative comparisons were performed using a Wilcoxon signed-rank test and the differences were considered statistically significant when p values were < 0.05.</p><p><strong>Results: </strong>Twenty-one patients underwent SDR for spastic hemiplegic cerebral palsy with pre- and postoperative physical therapy assessments. The patients were 52.4% male, 81.0% White, with a median age of 5 years at the time of surgery. The most common etiology for spastic hemiplegia was stroke (52.4%). All patients had a preoperative GMFCS level of I (85.7%) or II (14.3%). The median percentage of rootlets cut during the procedure was 60% on the affected side. The sum of the mAS extremity score was improved by 5 points (p < 0.001), the GMFM-66 score was improved by a median of 3.1 (p = 0.002), while the PedsQL CP module improved by a median of 12.3 percentage points (p = 0.003). Orthotic use was reduced from 90.5% preoperatively to 66.7% at follow-up.</p><p><strong>Conclusions: </strong>SDR is an effective treatment in patients with spastic hemiplegia resulting in significant improvement in motor function, quality of life, and tone.</p>","PeriodicalId":16549,"journal":{"name":"Journal of neurosurgery. Pediatrics","volume":" ","pages":"714-718"},"PeriodicalIF":2.1,"publicationDate":"2025-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145225758","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}