Zinc Oxide Patches Are a Highly Effective Treatment for Chronic Prurigo: A Randomized Split-Body Study

Author:

Schuermann Manuel,Richter Clara,Tanadini Matteo,Steigmiller Klaus,Burri Elias,Guillet Carole,Luchsinger Isabelle,Meier-Schiesser Barbara,Boesch Andrea,Nägeli Mirjam,Hafner Jürg

Abstract

Background: Chronic prurigo (CPG) presents with pruriginous lesions and reduced quality of life (QoL). Established treatment options are often unsatisfying. Little is known about the efficacy of topical occlusive treatments. Patients often report rapid relief of symptoms when using topical occlusive zinc oxide patches (ZOP). We, therefore, aimed to assess the efficacy of ZOP. Methods: In this randomized controlled split-body crossover study, 22 participants were analyzed, receiving three treatments sequentially: ZOP, topical betamethasone 17-valerate (topical glucocorticosteroids [TGCs]), and both ZOP and TGC combined (ZOP + TGC). Each intervention was applied to either the right or left side of the body for seven consecutive days. Outcomes were a count of active excoriated pruriginous lesions (APLs), itch, recurrence of APL, QoL, and treatment comfort. They were assessed through photographs and questionnaires: modified Prurigo Activity and Severity Score, modified Itchy Quality of Life Questionnaire, and Therapy Comfort Score. Results: We observed a significant reduction of 46% in APL count for ZOP (95% CI from 30% to 58%, p value: <0.0001). Similar reduction was seen for ZOP + TGC, and a lower reduction was seen for TGC alone (48% [95% CI from 33% to 60%, p value: <0.0001] vs. 26% [95% CI from 4% to 43%, p value: 0.02]). APL counts on the non-treated side remained stable. Significant reduction in itch was observed after all treatments, with the largest improvement for ZOP + TGC, followed by TGC and, lastly, ZOP alone (−2.3 units [95% CI from −3.5 to −1.1, p value: 0.00015] vs. −1.5 units [95% CI from −2.8 to −0.3, p value: 0.01 vs. −1.4 units [95% CI from −2.6 to −0.2, p value: 0.02]). QoL increased significantly after ZOP + TGC as well as after TGC (−8.3 units [95% CI from −13.6 to −3.1, p value: 0.0018] vs. −5.7 units [95% CI from −10.9 to −0.5, p value: 0.03]). A good subjective response concerning treatment comfort was observed. Conclusion: ZOP are effective in reducing APL after 1 week of treatment. Adding TGC to ZOP did not add considerable benefit in reducing APL. All three treatments reduced itch and improved QoL, with the largest improvement shown by ZOP combined with TGC. Patients tolerated ZOP well and reported no adverse events. We therefore suggest ZOP combined with TGC as an effective, fast-acting, low-cost treatment for reducing APL and itch in patients with CPG.

Publisher

S. Karger AG

Subject

Dermatology

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