Woda A, Navez M L, Picard P, Gremeau C, Pichard-Leandri E
Université d'Auvergne, Faculté de Chirurgie Dentaire, Clermont-Ferrand, France.
J Orofac Pain. 1998 Fall;12(4):272-8.
Stomatodynia is a difficult disease for both patients and clinicians. When facing true stomatodynia, i.e., idiopathic burning mouth, patients are offered poorly effective treatment. This open study reports the results of local application of clonazepam (0.5 or 1 mg) two or three times daily in 25 subjects who suffered from idiopathic stomatodynia. At the first evaluation, 4 weeks after the beginning of treatment, a visual analogue scale (VAS) that represented the intensity of pain decreased significantly from 6.2 +/- 0.3 to 3.0 +/- 0.5. At the second evaluation, 3 to 29 months after the first consultation, the VAS scores dropped significantly further to 2.6 +/- 0.5. Analysis of the individual results showed that 10 patients were totally cured and needed no further treatment, 6 patients had no benefit at all, and the remaining 9 patients had some improvement but were not considered to be cured since they did not wish to stop the treatment. Blood level tests that were performed 1 and 3 hours after the topical application revealed the presence of small amounts of the drug (3.3 ng/mL +/- 0.66 and 3.3 ng/mL +/- 0.52, respectively). The hypothesis that clonazepam acts locally to disrupt the neuropathologic mechanism that underlies stomatodynia is proposed. The risk factors that are recognized for this condition could decrease the density and/or ligand affinity of peripheral benzodiazepine receptors. This, in turn, could cause spontaneous pain from the tissues concerned.
口腔疼痛对患者和临床医生来说都是一种棘手的疾病。当面对真正的口腔疼痛,即特发性灼口综合征时,患者所接受的治疗效果不佳。这项开放性研究报告了25例患有特发性口腔疼痛的受试者每天局部应用氯硝西泮(0.5或1毫克)两到三次的结果。在首次评估时,治疗开始4周后,代表疼痛强度的视觉模拟量表(VAS)评分从6.2±0.3显著降至3.0±0.5。在第二次评估时,即首次就诊后3至29个月,VAS评分进一步显著降至2.6±0.5。对个体结果的分析表明,10例患者完全治愈,无需进一步治疗,6例患者完全没有受益,其余9例患者有一定改善,但由于他们不想停止治疗,所以不被认为已治愈。局部应用药物1小时和3小时后进行的血药浓度检测显示存在少量药物(分别为3.3纳克/毫升±0.66和3.3纳克/毫升±0.52)。提出了氯硝西泮通过局部作用破坏口腔疼痛潜在神经病理机制的假说。这种情况公认的危险因素可能会降低外周苯二氮䓬受体的密度和/或配体亲和力。反过来,这可能会导致相关组织出现自发疼痛。