High
concentration capsaicin for treatment of peripheral neuropathic pain:
effect on somatosensory symptoms and identification of treatment
responders.
Abstract
BACKGROUND:
Pain
is usually assessed by spontaneous pain ratings. Time-dependent (brief
attacks) or evoked (allodynia) phenomena, common in neuropathic pain,
are not captured. To evaluate the overall effectiveness of a treatment,
improvement of all sensory symptoms should be measured. Since the
pattern of sensory abnormalities might hint at the underlying mechanisms
of pain, this baseline information may aid in predicting the treatment
effect. Data on sensory neuropathic abnormalities (painDETECT
questionnaire) were analyzed aiming to (1) evaluate the frequency of
neuropathic symptoms in different peripheral neuropathic pain syndromes,
(2) assess the effect of capsaicin 8% patch on neuropathic symptoms and
(3) identify treatment responders based on baseline values.
METHODS:
Data
analysis of a prospective 12 week non-interventional trial in
peripheral neuropathic pain treated with capsaicin 8% cutaneous patch.
Average pain intensity during the past 24 hours, pain descriptors and
qualities of neuropathic pain were assessed to characterize the
patients' sensory symptoms at baseline and to document changes.
RESULTS:
(1)
Characteristic symptoms of neuropathic pain were present in all
peripheral neuropathic pain syndromes, but frequencies varied in the
individual syndromes. (2) Topical capsaicin 8% treatment significantly
reduced the overall pain intensity and resulted in a reduction of
sensory abnormalities. (3) Short disease duration predicted a better
treatment effect. High painDETECT scores, the presence of burning and
pressure-evoked pain were weakly associated with treatment response.
CONCLUSIONS:
Topical
capsaicin 8% treatment effectively reduced sensory abnormalities in
peripheral neuropathic pain. The association of sensory symptoms and
treatment response aids in understanding the mechanism of action of high
concentration capsaicin. It is, however, not possible to use sensory
symptom patterns to predict treatment response to capsaicin on an
individual level.
LIMITATIONS:
Completion
of painDETECT was optional and therefore data was not available for all
patients. Further studies for confirmation of these results are needed.
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