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脊髓损伤患者多汗症的患病率及盐酸右丙氧芬治疗效果评估。

The prevalence of hyperhidrosis in patients with spinal cord injuries and an evaluation of the effect of dextropropoxyphene hydrochloride in therapy.

作者信息

Andersen L S, Biering-Sørensen F, Müller P G, Jensen I L, Aggerbeck B

机构信息

Department of Rheumatology, Viborg Hospital, Denmark.

出版信息

Paraplegia. 1992 Mar;30(3):184-91. doi: 10.1038/sc.1992.53.

Abstract

The prevalence of annoying hyperhidrosis (HH) in patients with spinal cord traumatic lesions was investigated by a questionnaire. A total of 192 patients were sent the questionnaire, 154 patients answered, and 41 patients reported annoying sweating. Of these 41 patients, 13 had a somatic underlying cause and 28 indicated having annoying HH without a contributing somatic cause. Twenty-five patients with spinal cord injury (SCI) were included in a double-blind, randomized, placebo-controlled, crossover trial using dextropropoxyphene hydrochloride (DP) in a slow release form (Abalgin Retard 150 mg Benzon Pharma A/S, Copenhagen) twice a day, for the treatment of annoying HH. Nineteen patients with lesions between C4 and L4 completed the study. Eight found the active drug to be so effective that they wanted to continue the treatment while 3 preferred placebo. Six patients dropped out, 5 due to adverse effects. There was a trend towards an effect on sweating in daytime (p = 0.08-0.14). Given that the patients had a preference, which 15 of 19 had, the true frequency of patients preferring active treatment ranged from 32 to 84% (95% exact confidence limits). For those with SCI above T6 level the limits ranged from 40 to 97%. We conclude that in spite of the lack of statistically significant effect, it seems worthwhile to try DP for annoying HH, especially in patients with lesions above T6 level.

摘要

通过问卷调查对脊髓创伤性损伤患者中令人烦恼的多汗症(HH)患病率进行了调查。共向192名患者发放了问卷,154名患者进行了回复,其中41名患者报告有令人烦恼的出汗情况。在这41名患者中,13名有躯体潜在病因,28名表示有令人烦恼的HH但无相关躯体病因。25名脊髓损伤(SCI)患者被纳入一项双盲、随机、安慰剂对照、交叉试验,使用缓释型盐酸右丙氧芬(DP)(Abalgin Retard 150 mg,Benzon Pharma A/S,哥本哈根),每日两次,用于治疗令人烦恼的HH。19名C4至L4节段损伤的患者完成了研究。8名患者发现活性药物非常有效,希望继续治疗,而3名患者更喜欢安慰剂。6名患者退出,5名是由于不良反应。白天出汗方面有疗效趋势(p = 0.08 - 0.14)。鉴于19名患者中有15名有偏好,偏好活性治疗的患者的真实频率范围为32%至84%(95%精确置信区间)。对于T6水平以上的SCI患者,该区间范围为40%至97%。我们得出结论,尽管缺乏统计学上的显著效果,但对于令人烦恼的HH尝试使用DP似乎是值得的,尤其是对于T6水平以上损伤的患者。

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