Comparative therapeutic evaluation of intrathecal versus epidural methylprednisolone for long-term analgesia in patients with intractable postherpetic neuralgia
A. Kikuchi et al., Comparative therapeutic evaluation of intrathecal versus epidural methylprednisolone for long-term analgesia in patients with intractable postherpetic neuralgia, REG ANES PA, 24(4), 1999, pp. 287-293
Background and Objectives. The goal of this study was to evaluate the analg
esic effects of intrathecal versus epidural methylprednisolone acetate (MPA
) in patients with intractable postherpetic neuralgia (PHN). Methods. We st
udied 25 patients with a duration of PHN of more than 1 year. The patients
were randomly allocated to one of two groups: an intrathecal group (n = 13)
and an epidural group (n = 12). Sixty milligrams of MPA was administered e
ither into the intrathecal or the epidural space four times at 1-week inter
vals depending on the treatment group. Continuous and lancinating pain and
allodynia were evaluated by a physician unaware of group assignment with a
10-cm visual analogue scale before treatment, at the end of treatment, and
1 and 24 weeks after treatment. In addition, cerebrospinal fluid (CSF) ;was
obtained for measurement of interleukin (IL)-1 beta, -6, and -8 and tumor
necrosis factor-alpha before and 1 week: after treatment. Results. We found
marked alleviation of continuous and lancinating pain and allodynia in the
intrathecal group (P < .001). The improvements were much greater in the in
trathecal group than in the epidural group at all time points after the end
of treatment (P < .005). IL-8 in the CSF decreased significantly in the in
trathecal group as compared to the epidural group at the 1-week time point
(P < .01), whereas the other cytokines were undetectable. Conclusions. Our
results suggest the effectiveness of intrathecal as compared to epi dural M
PA for relieving the pain and allodynia associated with Pi-IN. Also, our fi
ndings, together with the decrease in IL-8, may indicate that intrathecal M
PA improves analgesia by decreasing an ongoing inflammatory reaction in the
CSF.