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对阿巴丁毒素 A 耐药患者换用低剂量利马肉毒毒素后短暂改善。

Transient Improvement after Switch to Low Doses of RimabotulinumtoxinB in Patients Resistant to AbobotulinumtoxinA.

机构信息

Department of Neurology, University of Düsseldorf, Moorenstraße 5, D-40225 Düsseldorf, Germany.

出版信息

Toxins (Basel). 2020 Oct 27;12(11):677. doi: 10.3390/toxins12110677.

Abstract

BACKGROUND

Botulinum toxin type B (BoNT/B) has been recommended as an alternative for patients who have become resistant to botulinum toxin type A (BoNT/A). This study aimed to compare the clinical effect, within a patient, of four injections with low doses of rimabotulinumtoxinB with the effect of the preceding abobotulinumtoxinA (aboBoNT/A) injections.

METHODS

In 17 patients with cervical dystonia (CD) who had become resistant to aboBoNT/A, the clinical effect of the first four rimabotulinumtoxinB (rimaBoNT/B) injections was compared to the effect of the first four aboBoNT/A injections using a global assessment scale and the TSUI score.

RESULTS

After the first two BoNT/B injections, all 17 patients responded well and to a similar extent as to the first two BoNT/A injections, but with more side effects such as dry mouth and constipation. After the next BoNT/B injection, the improvement started to decline. The response to the fourth BoNT/B injection was significant ( < 0.048) lower than the fourth BoNT/A injection. Only three patients developed a complete secondary treatment failure (CSTF) and five patients a partial secondary treatment failure (PSTF) after four BoNT/B injections. In nine patients, the usual response persisted.

CONCLUSION

With the use of low rimaBoNT/B doses, the induction of CSTF and PSTF to BoNT/B could not be avoided but was delayed in comparison to the use of higher doses. In contrast to aboBoNT/A injections, PSTF and CSTF occurred much earlier, although low doses of rimaBoNT/B had been applied.

摘要

背景

肉毒毒素 B 型(BoNT/B)已被推荐用于对肉毒毒素 A 型(BoNT/A)产生耐药的患者。本研究旨在比较 17 例对 aboBoNT/A 产生耐药的颈肌张力障碍(CD)患者,低剂量瑞马肉毒毒素 B(rimaBoNT/B)的 4 次注射的临床效果与之前的 aboBoNT/A 注射效果。

方法

在 17 例对 aboBoNT/A 产生耐药的颈肌张力障碍(CD)患者中,使用整体评估量表和 TSUI 评分比较了 rimaBoNT/B 前 4 次注射的临床效果与前 4 次 aboBoNT/A 注射的效果。

结果

在接受前 2 次 BoNT/B 注射后,所有 17 例患者的反应均良好,与前 2 次 BoNT/A 注射相似,但副作用更多,如口干和便秘。在接受下一次 BoNT/B 注射后,改善开始下降。第四次 BoNT/B 注射的反应明显(<0.048)低于第四次 BoNT/A 注射。在 4 次 BoNT/B 注射后,仅 3 例患者出现完全二次治疗失败(CSTF),5 例患者出现部分二次治疗失败(PSTF)。在 9 例患者中,通常的反应仍然存在。

结论

与使用较高剂量的 rimaBoNT/B 相比,低剂量 rimaBoNT/B 诱导 CSTF 和 PSTF 不能避免,但会延迟。与 aboBoNT/A 注射相比,尽管使用了低剂量的 rimaBoNT/B,但 PSTF 和 CSTF 发生得更早。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2671/7693617/3a07b609fd41/toxins-12-00677-g001.jpg

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