Intracranial Hypotension and Intracranial Hypertension

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Intracranial pressure

Intracranial pressure (ICP) is the pressure within the intracranial space. In the steady state, pressure within the brain parenchyma and intracranial extra-axial spaces are equal. Normal values of ICP are 5 to 15 mm Hg (6–20 cm H2O) in adults and older children (ages 8 years and older) in the supine position, 1 to 7 mm Hg (1–10 cm H2O) in younger children, and up to 18 mm Hg (25 cm H2O) in obese patients.1, 2 ICP increases with Valsalva maneuver, and falls below atmospheric pressure in the

Intracranial hypotension

In intracranial hypotension, low CSF volume results in orthostatic headache, and, less commonly, nausea, vomiting, photophobia, and, rarely, decreased level of consciousness. Intracranial hypotension results from loss of CSF through a dural defect in the spine, cranial vault, or skull base. SIH refers loosely to cases of intracranial hypotension in which a dural defect is identified and cannot be attributed to a prior procedure or to trauma. Causes of secondary intracranial hypotension include

Symptoms

The most common symptom in intracranial hypotension is orthostatic, or postural, headache. The classic orthostatic headache commences within 15 minutes, but occasionally up to several hours, after assuming a standing or upright sitting position.4, 5 Improvement or resolution typically occurs within 15 to 30 minutes of lying down. Orthostatic headache in SIH is most likely caused by downward displacement of the brain and resulting traction on the richly innervated dura. Orthostatic headaches are

Pathophysiology

Most CSF is formed in the ventricular system through active secretion by the choroid plexus. The average CSF volume in adults is approximately 150 mL, and the rate of CSF formation in adults is approximately 500 mL/d.18, 19 The arachnoid granulations (projections of the arachnoid membrane into the venous sinuses) are the major site of CSF absorption.

Post–lumbar puncture headache was described as early as 1899 by Dr August Bier, a pioneer of spinal anesthesia, who stated after undergoing such a

Diagnosis

The diagnosis of SIH is based on a combination of clinical signs and symptoms, head and spine imaging, and intrathecal pressure measurements.

Treatment

Although recognition of SIH has increased in the past decade because of the increased sensitivity of MR imaging, SIH continues to be frequently misdiagnosed. Suboccipital craniotomies for Chiari 1 malformation, catheter angiography for unexplained headache, and craniotomies for meningeal biopsy or subdural hematoma evacuation have been performed in cases of undiagnosed SIH (Fig. 7). A 2003 study reported that 17 of 18 consecutive patients referred to a surgical practice for treatment of SIH

Intracranial hypertension

Intracranial hypertension can occur in chronic or acute forms in a large variety of neurologic and systemic disorders, including intracranial mass lesions such as tumor or abscess, traumatic brain injury, ischemic or hemorrhagic stroke, dural venous sinus thrombosis, dural arteriovenous fistula, hydrocephalus, or diffuse cerebral edema such as in liver failure. A diagnosis of IIH is made in the setting of chronic elevated ICP when a specific cause cannot be defined. Normal values of ICP in

Clinical presentation

Acute, abnormal increase of ICP results in headache, nausea and vomiting, blurred vision, and, in severe cases, reflex bradycardia and altered level of consciousness or death caused by cerebral hypoperfusion and/or brain herniation.

In IIH, characterized by mild to intermediate chronic increase of ICP, the most common presenting symptom is chronic daily headache.62, 63 Other common presenting symptoms in IIH are pulsatile tinnitus (60%) and transient visual obscurations (75%),64 the latter

Idiopathic Intracranial Hypertension

IIH, also known as pseudotumor cerebri, is chronically increased ICP in the absence of a specific known cause. Modified Dandy criteria for IIH66 include increased opening pressure on lumbar puncture, with normal CSF composition and no known specific cause of increased ICP. The overall annual incidence of IIH is 1 to 2 per 100,000,65, 67 although the incidence in women in the 20- to 44-year age range who are more than 20% heavier than ideal body weight is as much as 20 times higher.65 IIH is

Idiopathic Intracranial Hypertension: Lumbar Puncture

An increased CSF opening pressure is the essential diagnostic criterion for IIH; imaging studies may be normal despite markedly increased ICP. In contrast, in SIH, CSF pressures can be within the normal range and imaging tests frequently play a key and decisive role in both diagnosis and treatment. IIH is suspected when opening pressure is in excess of 20 cm H2O (10 cm H2O in young children, and 25 cm H2O in obese patients). Asymptomatic presentations of IIH are common, for example when

Acute Intracranial Hypertension

Treatment of acute intracranial hypertension has the following goals:

  • 1.

    Maintenance of ICP at <20 to 25 mm Hg

  • 2.

    Maintenance of cerebral perfusion pressure at greater than 60 mm Hg

  • 3.

    Avoidance of factors that exacerbate intracranial hypertension, including obstruction of venous return through head malpositioning or agitation, hypoxia/hypercarbia, fever, anemia, seizures, and hyponatremia

For patients with persistently increased ICP of more than 20 to 25 mm Hg, aggressive treatment, including hyperosmolar

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