Normal pressure hydrocephalus

Normal pressure hydrocephalus remains a controversial entity with often ambiguous imaging findings. It is classically characterized by the triad of gait apraxia, urinary incontinence, and dementia, although not all patients with the condition have all three.

On imaging, it can be characterized both on CT and MRI by enlarged lateral and third ventricles out of proportion to the cortical sulcal enlargement.

This article is focused on idiopathic cases. For a discussion of secondary causes of communicating hydrocephalus, please refer to the article hydrocephalus.

It is important to note that there are many causes of communicating hydrocephalus without elevated opening CSF pressures, such as trauma, prior subarachnoid hemorrhage, and meningitis. This is sometimes confusingly referred to as secondary normal pressure hydrocephalus 3. Most clinicians will assume that one is referring to idiopathic normal pressure hydrocephalus if no qualifier is used.

The majority of cases are idiopathic. The incidence is much higher in elderly populations. Exact epidemiology is difficult to establish, as the diagnosis is often not made in nursing home patients for the following reasons: 

  • approximately 20% of patients in nursing homes have gait impairment
  • approximately 10% of these patients also have dementia
  • 15% have incontinence 19

A large study in Norway found a striking increase in incidence with increasing age 3:

  • 3.3 per 100,000 for people 50 to 59 years of age
  • 49.3 per 100,000 for people 60 to 69 years of age
  • 181.7 per 100,000 for people 70 to 79 years of age

The classical clinical findings of normal pressure hydrocephalus are 1-3

  • urinary incontinence
  • deterioration in cognition (dementia)
  • gait disturbances

These can be remembered with the unkind mnemonic Wet, Wacky, and Wobbly

As the name suggests, mean CSF opening pressure is within the normal range  (<18 cmH2O or 13 mmHg) 3

A classic neurological sign in NPH is magnetic gait, where the patients' feet appear to be magnetically attached to the floor.

The underlying cause remains controversial. One theory is that the condition is an obstructive type of communicating hydrocephalus due to reduced of CSF resorption. A second theory suggests it results from weakening of the ventricular wall due to periventricular white matter ischemic damage 3. The periventricular white matter ischemic change has also been hypothesized to slow the flow of CSF through the extracellular spaces, resulting in a "back-pressure" effect, leading to ventricular enlargement.

Shearing forces are exerted on the periventricular white matter as the ventricles enlarge. As the corticospinal tracts to the legs run medially, these tangential shearing forces cause gait disturbance.

Although CT is able to visualize the anatomical changes, it is inferior to MRI. 

MRI is the best modality to image anatomical changes and can further support the diagnosis with CSF flow studies and magnetic resonance spectroscopy.

  • ventriculomegaly
  • disproportionate changes in subarachnoid spaces
    • dilated Sylvian fissures 2,24,25,28
    • tight high convexity (narrow sulci and subarachnoid spaces at the vertex and medial/parafalcine region) 1,24,25,28
    • cingulate sulcus sign: posterior half of cingulate sulcus is narrower than the anterior half 1,17
    • focal/isolated dilation of sulci over the medial surface or convexity (sometimes called transport sulci) 1,24,28,29

The combination of ventriculomegaly, Sylvian fissure widening, and crowding at the vertex has been termed disproportionately enlarged subarachnoid space hydrocephalus (DESH), reflecting disproportionality between the superior and inferior CSF spaces 1,23,27. The finding of DESH without neurologic symptoms has been termed asymptomatic ventriculomegaly with features of idiopathic normal pressure hydrocephalus on MRI (AVIM) 1.  It is felt by some authors that AVIM is actually a pre-clinical form of iNPH 30

Periventricular hypodensity (on CT) or high T2-FLAIR signal (on MRI) is supportive of changes in brain water content seen in NPH, but these findings can also be seen with microvascular ischemic changes or demyelination 2,25.

  • aqueductal flow void due to increased CSF velocity across the aqueduct in patients with NPH
    • best seen on T2 and PD spin echo sequences 14 but it is no longer a useful sign, as in modern high field strength MRI machines aqueductal CSF flow void is present in most of the normal subjects
    • there is a well-established correlation between higher flow velocities and the favourable outcome after ventriculoperitoneal (VP) shunting; hence, quantitative (rather than qualitative) methods have been developed which can be useful not only in patient selection for shunting but also in diagnosis and predicting prognosis 12-15
  • CSF flow studies 3
    • increased aqueductal CSF stroke volume
      • aqueductal CSF stroke volume is the average volume of CSF flowing through the cerebral aqueduct during both systole and diastole
    • increased aqueductal peak velocity
    • various publications have set various normal and abnormal ranges
      • flow rate of >24.5 mL/min 95% specific for NPH 9,11
      • stroke volume of ≥42 μL shown in one paper to predict a good response to shunting 10
      • stroke volume upper limit is now suggested to be variable between institutions due to intrinsic scanner differences; thus each center should obtain their own "normal values", with the upper limit being suggested as two times the normal value 16
    • studies have shown that aqueductal stroke volume decreases later in the disease process despite clinical progression
      • this has been theorized to be caused by cerebral atrophy, which indicates that the patient is unlikely to respond to shunt surgery 18
    • a recent paper has cast serious doubt on the usefulness of aqueduct stroke volume in patient selection for VP shunting 21

MRS has not been shown to have any added value for differentiating idiopathic NPH from other types of dementia, nor does it help in patient selection for VP shunting 22.

Nuclear medicine is less important in diagnosing NPH. Some of the features described are 13

  • early detection of the radiotracer into lateral ventricles giving a heart-shaped appearance of lateral ventricles rather than a normal trident pattern
  • persistence of radiopharmaceutical beyond 24-48 hours due to impaired absorption
  • radiotracer does not extend to the superior aspect of convexities of lateral ventricles
  • retrograde CSF flow into lateral ventricles

Treatment of normal pressure hydrocephalus, once the diagnosis is established, is with CSF shunting, usually a ventriculoperitoneal shunt (VP shunt). The challenge is identifying those patients which will benefit from shunting. Favourable prognostic factors include 3

  • short duration of presurgical symptoms (less than 6 months)
  • onset of gait disturbance before dementia
  • temporary symptom relief from a CSF tap test (removal of 40ml of CSF via lumbar puncture)
  • absence of significant cerebral vascular disease
  • presence of an aqueductal flow void on T2 imaging 10,14

It is thought to have been initially described by Colombian neurosurgeon Salomón Hakim and R D Adams in 1965, although it may actually have been described earlier under a different name by McHugh 4,6,7.

The possible imaging differential spectrum includes:

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Article information

rID: 6306
Synonyms or Alternate Spellings:
  • Idiopathic normal pressure hydrocephalus (iNPH)
  • Normal pressure hydrocephalus (NPH)

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Cases and figures

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    Case 1: showing a flow void at the aqueduct
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  • Case 11: narrowed callosal angle
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  • Case 12
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