General information
- The exact definition of this term is not generally agreed upon, and some use the term “compensated hydrocephalus” interchangeably.
- Most clinicians use these terms to refer to a situation where there is no progression or deleterious sequelae due to hydrocephalus that would require the presence of a CSF shunt.
- Patients and families should be advised to seek medical attention if they develop symptoms of intracranial hypertension (decompensation), which may include: headaches, vomiting, ataxia or visual symptoms.
Arrested hydrocephalus satisfies the following criteria in the absence of a CSF shunt
- Near normal ventricular size
- Normal head growth curve
- Continued psychomotor development
- Shunt independence
- Shunt independence is controversial
- Some feel that shunt independence occurs more commonly when the HCP is due to a block at the level of the arachnoid granulations (communicating hydrocephalus), but others have shown that it can occur regardless of the etiology.
- These patients must be followed closely, as there are reports of death as late as 5 years after apparent shunt independence, sometimes without warning.
When to remove a disconnected or non-functioning shunt?
- A disconnected shunt may continue to function by CSF flow through an endothelialized subcutaneous tract. → never remove a shunt UNLESS it is infected
- Recommendations on whether or not to repair vs. remove a disconnected or nonfunctioning shunt
- When in doubt, shunt
- Indications for shunt repair (vs. removal)
- Marginally functioning shunts
- The presence of any signs or symptoms of increased ICP (vomiting, upgaze palsy, sometimes H/A alone…)
- Changes in cognitive function, ↓ attention span, or emotional changes
- Patients with aqueductal stenosis or spina bifida: most are shunt-dependent
- Because of risks associated with shunt removal, surgery for this purpose alone should be performed only in the situation of a shunt infection (and then, and EVD is usually placed)
- Patients with a nonfunctioning shunt should be followed closely with serial CTs, and possibly with serial neuropsychological evaluations