Papilledema surgery

Jump to navigation Jump to search

Papilledema

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Papilledema from other Diseases

Epidemiology and Demographics

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

CT

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Papilledema surgery On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Papilledema surgery

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Papilledema surgery

CDC on Papilledema surgery

Papilledema surgery in the news

Blogs on Papilledema surgery

Directions to Hospitals Treating Papilledema

Risk calculators and risk factors for Papilledema surgery

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Kalsang Dolma, M.B.B.S.[2]

Overview

Surgical treatment of papilledema depends on the underlying cause. Various surgeries including shunt surgeries, craniotomies and optic nerve sheath fenestration can be done depending on the cause.

Surgery

Shunting

It involves the placement of a ventricular catheter (a tube made ofsilastic), into the cerebral ventricles to bypass the flow obstruction/malfunctioning arachnoidal granulations and drain the excess fluid into other body cavities, from where it can be resorbed. Most shunts drain the fluid into the peritoneal cavity (ventriculo-peritoneal shunt), but alternative sites include the right atrium (ventriculo-atrial shunt), pleural cavity (ventriculo-pleural shunt), and gallbladder. There is some risk of infection being introduced into the brain through these shunts, however, and the shunts must be replaced as the person grows. More recently developed technologies using advanced imaging as well as endoscopic operative techniques have improved the ability of surgeons to place catheters in the ventricles of patients with IIH who do not have ventricular enlargement. [1]

Craniotomies

Holes are drilled in the skull to remove intracranial hematomas or relieve pressure from parts of the brain. As raised ICP's may be caused by the presence of a mass, removal of this via craniotomy will decrease raised ICP's.

Optic Nerve Sheath Fenestration

Optic nerve sheath fenestration is a procedure that is advocated for the treatment of certain types of optic nerve dysfunction associated with progressive decline in visual function. Optic nerve sheath fenestration can stabilize or improve visual loss due to papilledema in idiopathic intracranial hypertension. However, it may fail at any time after surgery. Patients with pseudotumor cerebri need to be followed up routinely with automated perimetry to detect deterioration of visual function.[2]

References

  1. {{cite journal |author=McGirt MJ, Woodworth G, Thomas G, Miller N, Williams M, Rigamonti D |title=Cerebrospinal fluid shunt placement for pseudotumor cerebri-associated intractable headache: predictors of treatment response and an analysis of long-term outcomes |journal=J. Neurosurg. |volume=101 |issue=4 |pages=627–32 |year=2004 |month=October |pmid=15481717 |doi=10.3171/jns.2004.101.4.0627 |url=}
  2. Spoor TC, McHenry JG (1993). "Long-term effectiveness of optic nerve sheath decompression for pseudotumor cerebri". Arch. Ophthalmol. 111 (5): 632–5. PMID 8489443. Unknown parameter |month= ignored (help)

Template:WikiDoc Sources