Morbidity after Hemorrhage in Children with Untreated Brain Arteriovenous Malformation

Li Ma1, Helen Kim, Xiao-Lin Chen

  • 1Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, PR China.

Insights

Untreated pediatric brain arteriovenous malformations (bAVM) carry a high risk of severe hemorrhage. Key predictors of severe bleeding include periventricular location, non-temporal lobe location, and long draining veins, aiding risk assessment.

Area of Science:

  • Neurology
  • Pediatric Neurosurgery
  • Vascular Malformations

Background:

  • Untreated pediatric brain arteriovenous malformations (bAVM) pose a significant risk of life-threatening hemorrhage.
  • Understanding bAVM hemorrhage morbidity is crucial for balancing risks of untreated bAVM versus invasive treatment.

Purpose of the Study:

  • To assess clinical outcomes following bAVM rupture in children.
  • To identify predictors of severe hemorrhage in pediatric bAVM patients.

Main Methods:

  • Retrospective analysis of 134 pediatric bAVM patients (July 2009-December 2014).
  • Clinical outcomes evaluated using the pediatric modified Rankin Scale (mRS).
  • Regression analyses identified demographic and morphological predictors of severe hemorrhage (mRS >3 or requiring evacuation).

Main Results:

  • Of 83 ruptured bAVMs, 49% experienced severe hemorrhage, with 24% resulting in disability (mRS ≥3).
  • Predictors of severe hemorrhage included periventricular location, non-temporal lobe location, and long draining veins.
  • A predictive nomogram demonstrated good calibration (C-statistic, 0.72) for individual hemorrhage risk.

Conclusions:

  • Morbidity and morphological features of pediatric bAVM hemorrhage are critical for risk assessment.
  • Predictive tools based on bAVM morphology can aid in weighing treatment risks for pediatric patients.
Abstract

Related Concept Videos

Ischemic Stroke ll: Pathophysiology01:15

Ischemic Stroke ll: Pathophysiology

An ischemic stroke occurs when a cerebral blood vessel becomes obstructed, most often by a thrombus or embolus, interrupting the delivery of oxygen and glucose to brain tissue. Because neurons rely on continuous aerobic metabolism, energy failure begins within minutes of reduced perfusion. The region receiving the least blood flow becomes the infarct core, an area of irreversible cellular death. Surrounding this core lies the penumbra, a zone of hypoperfused but still viable tissue that is...
Hemorrhagic Stroke l: Introduction01:17

Hemorrhagic Stroke l: Introduction

A hemorrhagic stroke is an acute neurological event that occurs when a weakened cerebral blood vessel ruptures, allowing blood to accumulate within or around the brain. The sudden release of blood forms a focal hematoma that increases intracranial pressure, displaces neural tissue, and can obstruct cerebrospinal fluid pathways. These effects may be compounded by intraventricular extension of the hemorrhage, cerebral edema, or compression of adjacent structures, all of which contribute to...
Hemorrhagic Stroke ll: Pathophysiology01:29

Hemorrhagic Stroke ll: Pathophysiology

A hemorrhagic stroke develops when a cerebral blood vessel ruptures, allowing blood to escape into the surrounding brain tissue, as in intracerebral hemorrhage (ICH), or into the subarachnoid space, as in subarachnoid hemorrhage (SAH). Because the skull is a rigid compartment, the sudden presence of extravascular blood rapidly increases intracranial pressure and compresses adjacent neural structures, leading to immediate tissue injury and impaired cerebral perfusion.Mass Effect and Primary...
Increased Intracranial Pressure l: Introduction01:14

Increased Intracranial Pressure l: Introduction

Intracranial hypertension is a sustained elevation of intracranial pressure (ICP) above 22 mm Hg. In supine adults, normal ICP is ~7–15 mm Hg.The rigid, nonexpandable cranium contains three components—brain tissue, blood, and cerebrospinal fluid (CSF)—that total ~1,700 mL in a typical adult: 1,400 mL brain (~80%), 150 mL blood (~10%), and 150 mL CSF (~10%). According to the Monro–Kellie doctrine, total intracranial volume is effectively fixed. When one component expands, CSF and venous blood...
Increased Intracranial Pressure ll: Pathophysiology01:29

Increased Intracranial Pressure ll: Pathophysiology

Increased intracranial pressure (ICP) refers to a potentially life-threatening rise in pressure inside the skull. This usually happens when there is a major change in the volume of brain tissue, blood, or cerebrospinal fluid (CSF) — the three components inside the skull. According to the Monro-Kellie doctrine, if the volume of one component increases, the volumes of the other components must decrease to maintain normal pressure. If this does not happen, ICP rises.The process often begins with...
Cerebral Edema ll: Pathophysiology01:22

Cerebral Edema ll: Pathophysiology

Vasogenic edema is a major form of cerebral edema characterized by abnormal accumulation of fluid in the brain’s extracellular space due to disruption of the blood–brain barrier (BBB). The BBB is a specialized structure composed of endothelial cells connected by tight junctions, supported by astrocytic endfeet and a basement membrane. Under normal conditions, it tightly regulates the movement of ions, proteins, and solutes between the bloodstream and brain parenchyma. When this barrier loses...