A preliminary study of painless and effective transdermal botulinum toxin A delivery by jet nebulization for treatment of primary hyperhidrosis

被引:29
作者
Iannitti, Tommaso [1 ,2 ]
Palmieri, Beniamino [3 ]
Aspiro, Anna [3 ]
Di Cerbo, Alessandro [2 ,3 ]
机构
[1] Univ Leeds, Sch Biomed Sci, Leeds LS2 9JT, W Yorkshire, England
[2] Poliambulatorio Secondo Parere, Modena, Italy
[3] Univ Modena & Reggio Emilia, Sch Med, Dept Surg & Surg Specialties, Surg Clin, Modena, Italy
关键词
hyperhidrosis; JetPeel (TM)-3; botulinum toxin A; anesthesia; pain; sweating; transdermal drug delivery; jet nebulization; QUALITY-OF-LIFE; PRIMARY FOCAL HYPERHIDROSIS; PLACEBO-CONTROLLED TRIAL; AXILLARY HYPERHIDROSIS; DOUBLE-BLIND; MANAGEMENT; INJECTIONS; DIAGNOSIS;
D O I
10.2147/DDDT.S60389
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Background: Hyperhidrosis is a chronic disease characterized by increased sweat production. Local injections of botulinum toxin A (BTX-A) have been extensively used for treatment of primary hyperhidrosis (idiopathic). The current treatment for this condition involves several intradermal injections, resulting in poor patient compliance due to injection-related pain. Therefore, new protocols, including an improved anesthetic regimen, are required. Aim: We designed the present study to determine whether JetPeel (TM)-3, a medical device used for transdermal delivery of drugs by jet nebulization, could be used to deliver lidocaine prior to the standard multiple BTX-A injections or deliver lidocaine together with BTX-A in order to determine the protocol giving better results in terms of procedure-related pain, sweating, and patient satisfaction in subjects affected by primary axillary, palmar or plantar hyperhidrosis. Materials and methods: Twenty patients with a visual analog scale (VAS) sweating score >= 8 cm were randomized to receive lidocaine 2% (5 mL) delivered by JetPeel (TM)-3 followed by multiple injections of BTX-A (100 units) or lidocaine 2% (5 mL) and BTX-A (50 units) delivered together by JetPeel (TM)-3. Effect of treatment on sweating was measured by VAS (0= minimum sweating; 10= maximum sweating) at 3-month follow-up. Pain induced by the procedure was assessed by VAS (0= minimum pain; 10= maximum pain) immediately after the procedure. Patient satisfaction was assessed at 3-month follow-up using a 5-point scale (1= not at all satisfied; 2= not satisfied; 3= partially satisfied; 4= satisfied; 5= highly satisfied). Results: Both treatment modalities reduced sweating at 3-month follow-up, if compared with baseline (all P < 0.001). Delivery of lidocaine and BTX-A by JetPeel (TM)-3 resulted in lower procedure-related pain and reduced sweating, if compared with lidocaine delivered by JetPeel (TM)-3 followed by multiple BTX-A injections (all P < 0.001). Patient satisfaction with the procedure was higher in the group receiving lidocaine and BTX-A treatment by JetPeel (TM)-3, if compared with lidocaine delivered by JetPeel (TM)-3 followed by multiple BTX-A injections (P < 0.001). No side effects were observed in both groups. Conclusion: Lidocaine and BTX-A can be safely delivered together by JetPeel (TM)-3 to treat primary palmar, plantar and axillary hyperhidrosis, resulting in lower procedure-related pain, improved sweating and higher patient satisfaction, if compared with lidocaine delivered by JetPeel (TM)-3 followed by standard BTX-A injection therapy. Our protocol delivering lidocaine and BTX-A together by JetPeel (TM)-3 requires a reduced quantity of BTX-A, further supporting the use of the transdermal drug delivery by jet nebulization over standard injection therapy for treatment of primary hyperhidrosis.
引用
收藏
页码:931 / 935
页数:5
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