Hc. Hansen et K. Helmke, VALIDATION OF THE OPTIC-NERVE SHEATH RESPONSE TO CHANGING CEREBROSPINAL-FLUID PRESSURE - ULTRASOUND FINDINGS DURING INTRATHECAL INFUSION TESTS, Journal of neurosurgery, 87(1), 1997, pp. 34-40
Raised intracranial pressure leads to increased pressure around the op
tic nerve (ON), which underlies the formation of papilledema and the e
nlargement of the dural optic nerve sheath (ONS). In clinical practice
, the presence of widened ONSs is demonstrable on neuroimaging. but th
eir relationship to cerebrospinal fluid (CSF) pressure remains unknown
. The authors investigated the ONS response to pressure during CSF abs
orption studies in 12 patients undergoing neurological testing. The ON
S diameter was evaluated by serial B-mode ultrasound scans of the ante
rior ON near its, entry into the globe. All patients tested showed ONS
diameter changes that exhibited covariance with the alteration of lum
ber CSF pressure and were completely reversible during the infusion te
sts. The maximum difference in ONS diameter between baseline and peak
pressure conditions was 1.8 mm on average (range 0.7-3.1 mm). correspo
nding to an average ONS diameter variation of 45% (range 15-89%). Regr
ession analysis yielded a linear covariance between ONS diameter and C
SF pressure with different slopes across subjects (0.019-0.071 mm/mm H
g, mean r = 0.78). However, this linear relationship was only present
within a CSF pressure interval. This interval differed between patient
s: ONS dilation commenced at pressure thresholds between 15 mm Hg and
30 mm Hg and in some patients saturation of the response (constant ONS
diameter) occurred between 30 mm Hg and 10 mm Hg. With a single excep
tion, definitely enlarged ONS diameters (> 5 mm) were present when CSF
pressure exceeded levels of 30 mm Hg. Retrospectively. discrimination
between normal and elevated outflow resistance was possible on the ba
sis of the ONS response to intrathecal infusion alone. It is concluded
that the human ONS has sufficient elasticity to allow a detectable di
lation in response to intracranial hypertension. Because of a variable
pressure-diameter relationship. the subarachnoid pressure cannot be p
redicted exactly single scans, Therefore, the clinical relevance of th
is method relies on the demonstration of pathologically enlarged ;heat
hs or ongoing enlargement on serial ultrasonography studies.