HYBRID EVENT: You can participate in person at Boston, Massachusetts, USA or Virtually from your home or work.

13th Edition of International Conference on Neurology and Brain Disorders

October 19-21, 2026

October 19 -21, 2026 | Boston, Massachusetts, USA
INBC 2026

What we don’t know about hydrocephalus and It’s management

Speaker at Brain Disorders Conference - Daniel Curry
Texas Children’s Hospital, United States
Title : What we don’t know about hydrocephalus and It’s management

Abstract:

Symptomatic hydrocephalus has been treated with cerebrospinal fluid (CSF) diverting shunts since their introduction in the 1950s. These systems have played a critical role in relieving life-threatening elevations in intracranial pressure (ICP), transforming hydrocephalus from a uniformly fatal diagnosis into a manageable chronic condition. However, despite their ubiquity in neurosurgical practice, shunt systems remain fundamentally crude in their regulation of CSF dynamics, focusing primarily on gross volume diversion rather than nuanced pressure control across varying physiologic states.
One of the most significant and underrecognized limitations in current shunt management is its failure to adapt to the evolving ICP requirements across the continuum of neurodevelopment, from neonatal to adolescent and adult physiology. In this respect, the traditional shunt acts as a static solution for a dynamic problem. There is little consensus on what constitutes “optimal” ICP in pediatric hydrocephalus, how that target may shift with age, sleep-wake cycles, posture, or comorbidities, and whether current shunt technologies can (or should) attempt to mimic native CSF autoregulation mechanisms.
Moreover, while acute shunt malfunction is well-recognized and typically results in prompt imaging and surgical intervention, there exists a large population of patients with so-called “functional” shunts who suffer from symptoms suggestive of ICP dysregulation but without clear radiographic findings. These symptoms, headaches, cognitive fog, gait instability, fatigue, are often intermittent, difficult to quantify, and frequently misattributed to other causes. This mismatch between clinical reality and diagnostic capability highlights the absence of continuous, physiologically informed monitoring.
Environmental influences on ICP, including altitude, barometric pressure fluctuations, and sleep positioning, are similarly underexplored, despite growing anecdotal and survey-based evidence suggesting their relevance in symptom generation. We remain largely reactive in hydrocephalus care, lacking real-time data that could empower earlier interventions or personalized adjustments in management strategy.
This presentation will review the current landscape of hydrocephalus treatment and highlight emerging technologies, including efforts toward ambulatory ICP monitoring, smart shunt systems with closed-loop feedback, and computational modeling of CSF flow dynamics. Finally, it will discuss the critical gaps that remain, particularly around dynamic ICP targets, individualized pressure modulation, and integration of environmental and physiological inputs into real-time decision-making frameworks.
Bridging these gaps will require interdisciplinary collaboration across neurosurgery, neurology, biomedical engineering, and data science. But the opportunity is clear: by moving from episodic, radiographically driven care to a data-enabled, precision-guided paradigm, we stand to transform the trajectory of hydrocephalus management for generations of patients.

Biography:

Daniel J. Curry, MD is an academic pediatric neurosurgeon and director of the Pediatric Functional Neurosurgery Program at Texas Children’s Hospital. He work spans surgical treatment of epilepsy, movement disorders, pain, and hydrocephalus. His lead the nation’s largest pediatric SEEG and RNS program, pioneered MR-guided laser ablation for hypothalamic hamartomas, and launched the first intracranial gene therapy at our institution. He advancing real-time, ambulatory ICP monitoring and closed-loop shunt systems for hydrocephalus. His translational efforts also include DBS in Rett syndrome models and focused ultrasound initiatives. He founded the TCH Neuroinfusion Center for enzyme therapy in Batten disease and NIH-directed intrathecal drug delivery research.

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