Evaluation of Efficacy and Safety of miraDry® Procedure in the Treatment of Primary Axillary Hyperhidrosis

被引:1
|
作者
Wimmer, Florian [1 ,2 ]
Ramic, Anika [1 ]
Nolte, Jan Philipp [3 ]
Djedovic, Gabriel [1 ]
Dietl, Marion [1 ]
机构
[1] Acad Hosp Feldkirch, Dept Plast Reconstruct & Aesthet Surg, Carinagasse 47, A-6807 Feldkirch, Austria
[2] Paracelsus Med Univ Salzburg, Hosp Bros St John God, Dept Plast Reconstruct & Aesthet Surg, A-5020 Salzburg, Austria
[3] Innsbruck Med Univ, Dept Med Stat Informat & Hlth Econ, Schoepfstr 41, A-6020 Innsbruck, Austria
关键词
Axillary hyperhidrosis; Hyperhidrosis severity scale; HDSS; Minor test; Iodine starch test; Microwave thermolysis; miraDry (R); TOXIN TYPE-A; MICROWAVE DEVICE; CLINICAL-EVALUATION; DOUBLE-BLIND; OSMIDROSIS; CURETTAGE; RECOGNITION; LIPOSUCTION; REDUCTION; DIAGNOSIS;
D O I
10.1007/s00266-024-04558-1
中图分类号
R61 [外科手术学];
学科分类号
摘要
IntroductionPrimary axillary hyperhidrosis significantly impacts the quality of life of affected individuals. miraDry (R), a non-invasive local precisely controlled thermal energy procedure, represents a promising treatment option. This retrospective analysis aimed to evaluate the treatment success and patient safety following miraDry (R) procedure in the treatment of primary axillary hyperhidrosis. Material and MethodsA total of 139 patients receiving miraDry (R) procedure from 2019 to 2023 with miraDry (R) fresh protocol for treatment of excessive axillary hyperhidrosis were analyzed. Subjective assessment was performed before and after treatment using hyperhidrosis disease severity scale (HDSS). Minor test (iodine starch test) was done before treatment and 6 months after treatment to objectively quantify sweat severity. Patients with subjective or objective unsatisfied results after first procedure were scheduled for a second treatment. ResultsThe majority of treated patients (84%) could effectively be treated with one single treatment, while only 16% (n = 22) required a secondary intervention. HDSS after treatment completion (single and double treatment) showed a significant improvement (p < 0.001) in subjective evaluation of the treatment success. Minor tests demonstrated a significant reduction in sweat severity (p < 0.001), with 95% of patients experiencing no or minimal sweating after treatment completion. The miraDry (R) procedure demonstrated a favorable safety profile with typical and transient treatment reactions that mostly resolved within 6 months (94.2%) ConclusionOur data demonstrate that miraDry (R) procedure is an effective and safe treatment option for primary axillary hyperhidrosis, which results in an immense improvement in quality of life and high satisfaction of affected individuals. Level of Evidence IIThis journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266.
引用
收藏
页码:2545 / 2551
页数:8
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