Table 5.
Author & Year | N | Class | Agent | Dose | Primary outcome | Result | Side effects |
---|---|---|---|---|---|---|---|
Schnider et al., 1997 [12] | 11 | II | A/Abo | 120 U | DNSS | Mean reduction in sweat production: 26%, 26%, and 31% at w 3, 8, 13 (p < 0.001) and improvement in VAS 38%, 40%, and 35% at w 3, 8, 13 respectively (p = 0.002) for A/Abo group. | Minor , reversible weakness of handgrip lasting between 2 and 5 w, and minor hematoma at injection site |
Lowe et al., 2002 [25] | 19 | II | A/Ona | 100 U | Sweat production (gravimetric measurement) and physician’s and patient’s rating of severity. Safety evaluations via grip strength | Mean percentage change from baseline was significantly greater in the A/Ona-treated palms than in the PBO-treated palms at day 28 (p = 0.0037). Similar results found for Minor’s test. | Finger tingling and numbness in one A/Ona patient. One PBO patient with weakness of injected hand, one patient bilateral hand pain. |
Baumann et al., 2005 [18] | 20 | II | B/Rima | 5000 U | Efficacy, duration, safety, and patient and investigator assessment | Patient assessed efficacy showed significant difference in favor of B/Rima through day 120. Physician assessment did not show difference at day 30. Mean duration of effect; 3.8 months. Onset of effect: within 1 w. | Transient dry mouth in 18. Indigestion, dry hands. Muscle weakness in 12. Decreased grip strength in 10. |
A/Ona: Onabotulinumtoxin A (Botox); A/Inco: incobotulinumtoxinA (Xeomin); A/Abo: abobotulinumtoxinA (Dysport); B/Rima: RimabotulinumtoxinB (Myobloc); DNSS: digitized ninhydrin-stained sheets; VAS: Visual Analogue Scale; SAE: Serious Adverse Effect; GATS: Patients Global assessments of treatment satisfaction; PBO: placebo; QOL: Quality of life; HDSS: Hyperhidrosis Disease Severity Scale; w: week(s).