Brandon G Rocque, Hailey Jensen, Ron W Reeder, Curtis J Rozzelle, Abhaya V Kulkarni, Ian F Pollack, Michael M McDowell, Robert P Naftel, Eric M Jackson, William E Whitehead, Jonathan A Pindrik, Albert M Isaacs, Jennifer M Strahle, Patrick J McDonald, Mandeep S Tamber, Todd C Hankinson, Samuel R Browd, Jason S Hauptman, Mark D Krieger, Jason Chu, Jay Riva-Cambrin, David D Limbrick, Richard Holubkov, John R W Kestle, John C Wellons
{"title":"脑积水死亡率和分流术修正的种族差异:来自脑积水临床研究网络的研究。","authors":"Brandon G Rocque, Hailey Jensen, Ron W Reeder, Curtis J Rozzelle, Abhaya V Kulkarni, Ian F Pollack, Michael M McDowell, Robert P Naftel, Eric M Jackson, William E Whitehead, Jonathan A Pindrik, Albert M Isaacs, Jennifer M Strahle, Patrick J McDonald, Mandeep S Tamber, Todd C Hankinson, Samuel R Browd, Jason S Hauptman, Mark D Krieger, Jason Chu, Jay Riva-Cambrin, David D Limbrick, Richard Holubkov, John R W Kestle, John C Wellons","doi":"10.3171/2024.12.PEDS24371","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Several studies of administrative data have noted higher mortality rates for Black/African American children with shunted hydrocephalus. A longitudinal study of children with hydrocephalus secondary to myelomeningocele showed lower lifetime rates of shunt revision in minority children compared to White children, indicating a possible disparity in hydrocephalus treatment. The goal of this study is to identify racial and ethnic disparities in mortality or in shunt revision rates by using the Hydrocephalus Clinical Research Network (HCRN) hydrocephalus registry sample.</p><p><strong>Methods: </strong>The HCRN registry was queried for patients with shunted hydrocephalus for whom data on all lifetime hydrocephalus procedures were available. Patients with a primary shunt placement prior to 2023 were included, with follow-up extending through March 19, 2024. A Cox proportional hazards model was created to determine the effect of race and ethnicity on mortality while controlling for age at initial shunt placement, sex, hydrocephalus etiology, gestational age at birth, and presence of complex chronic conditions. Similarly, a proportional means model was used to evaluate association with lifetime number of shunt revision surgeries. The authors' hypothesis was that when controlling for other variables, minority children would have higher mortality and fewer shunt revision surgeries than White children.</p><p><strong>Results: </strong>A total of 5656 children were included in the analysis of mortality. There were 579 deaths. Race and ethnicity were independently associated with mortality, with Black (HR 1.32, 95% CI 1.05-1.65), other non-White (HR 1.39, 95% CI 1.03-1.86), and Hispanic (HR 1.50, 95% CI 1.22-1.84) children having a higher mortality rate than White children. In the analysis of 4081 children with shunts, Hispanic ethnicity was also independently associated with fewer total shunt revisions (HR 0.84, 95% CI 0.72-0.98).</p><p><strong>Conclusions: </strong>In children with hydrocephalus, when controlling for other factors, there is a higher mortality rate among Hispanic, Black, and other non-White children, and fewer shunt revisions among Hispanic children. These findings highlight important potential disparities in hydrocephalus treatment.</p>","PeriodicalId":16549,"journal":{"name":"Journal of neurosurgery. 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A longitudinal study of children with hydrocephalus secondary to myelomeningocele showed lower lifetime rates of shunt revision in minority children compared to White children, indicating a possible disparity in hydrocephalus treatment. The goal of this study is to identify racial and ethnic disparities in mortality or in shunt revision rates by using the Hydrocephalus Clinical Research Network (HCRN) hydrocephalus registry sample.</p><p><strong>Methods: </strong>The HCRN registry was queried for patients with shunted hydrocephalus for whom data on all lifetime hydrocephalus procedures were available. Patients with a primary shunt placement prior to 2023 were included, with follow-up extending through March 19, 2024. A Cox proportional hazards model was created to determine the effect of race and ethnicity on mortality while controlling for age at initial shunt placement, sex, hydrocephalus etiology, gestational age at birth, and presence of complex chronic conditions. Similarly, a proportional means model was used to evaluate association with lifetime number of shunt revision surgeries. The authors' hypothesis was that when controlling for other variables, minority children would have higher mortality and fewer shunt revision surgeries than White children.</p><p><strong>Results: </strong>A total of 5656 children were included in the analysis of mortality. There were 579 deaths. Race and ethnicity were independently associated with mortality, with Black (HR 1.32, 95% CI 1.05-1.65), other non-White (HR 1.39, 95% CI 1.03-1.86), and Hispanic (HR 1.50, 95% CI 1.22-1.84) children having a higher mortality rate than White children. 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引用次数: 0
摘要
目的:几项行政数据研究表明,黑人/非裔美国儿童的分流性脑积水死亡率较高。一项对脊髓脊膜膨出继发脑积水儿童的纵向研究显示,与白人儿童相比,少数民族儿童的终生分流修复率较低,这表明脑积水治疗可能存在差异。本研究的目的是通过使用脑积水临床研究网络(HCRN)脑积水登记样本,确定死亡率或分流修复率的种族和民族差异。方法:查询HCRN登记的分流性脑积水患者,这些患者一生中所有脑积水手术的数据都是可用的。纳入了2023年之前进行初级分流术的患者,随访时间延长至2024年3月19日。建立了Cox比例风险模型,以确定种族和民族对死亡率的影响,同时控制初始分流器放置时的年龄、性别、脑积水病因、出生时胎龄和是否存在复杂的慢性疾病。同样,采用比例平均模型来评估与一生中分流翻修手术次数的关系。作者的假设是,在控制其他变量的情况下,少数族裔儿童的死亡率会比白人儿童高,分流修复手术也会比白人儿童少。结果:共有5656名儿童被纳入死亡率分析。共有579人死亡。种族和民族与死亡率独立相关,黑人儿童(HR 1.32, 95% CI 1.05-1.65)、其他非白人儿童(HR 1.39, 95% CI 1.03-1.86)和西班牙裔儿童(HR 1.50, 95% CI 1.22-1.84)的死亡率高于白人儿童。在对4081例分流患儿的分析中,西班牙裔也与分流术的总改进量较少独立相关(HR 0.84, 95% CI 0.72-0.98)。结论:在脑积水儿童中,在控制其他因素后,西班牙裔、黑人和其他非白人儿童的死亡率较高,西班牙裔儿童的分流术改进率较低。这些发现突出了脑积水治疗的重要潜在差异。
Racial disparities in hydrocephalus mortality and shunt revision: a study from the Hydrocephalus Clinical Research Network.
Objective: Several studies of administrative data have noted higher mortality rates for Black/African American children with shunted hydrocephalus. A longitudinal study of children with hydrocephalus secondary to myelomeningocele showed lower lifetime rates of shunt revision in minority children compared to White children, indicating a possible disparity in hydrocephalus treatment. The goal of this study is to identify racial and ethnic disparities in mortality or in shunt revision rates by using the Hydrocephalus Clinical Research Network (HCRN) hydrocephalus registry sample.
Methods: The HCRN registry was queried for patients with shunted hydrocephalus for whom data on all lifetime hydrocephalus procedures were available. Patients with a primary shunt placement prior to 2023 were included, with follow-up extending through March 19, 2024. A Cox proportional hazards model was created to determine the effect of race and ethnicity on mortality while controlling for age at initial shunt placement, sex, hydrocephalus etiology, gestational age at birth, and presence of complex chronic conditions. Similarly, a proportional means model was used to evaluate association with lifetime number of shunt revision surgeries. The authors' hypothesis was that when controlling for other variables, minority children would have higher mortality and fewer shunt revision surgeries than White children.
Results: A total of 5656 children were included in the analysis of mortality. There were 579 deaths. Race and ethnicity were independently associated with mortality, with Black (HR 1.32, 95% CI 1.05-1.65), other non-White (HR 1.39, 95% CI 1.03-1.86), and Hispanic (HR 1.50, 95% CI 1.22-1.84) children having a higher mortality rate than White children. In the analysis of 4081 children with shunts, Hispanic ethnicity was also independently associated with fewer total shunt revisions (HR 0.84, 95% CI 0.72-0.98).
Conclusions: In children with hydrocephalus, when controlling for other factors, there is a higher mortality rate among Hispanic, Black, and other non-White children, and fewer shunt revisions among Hispanic children. These findings highlight important potential disparities in hydrocephalus treatment.