Logo Logo
Hilfe
Hilfe
Switch Language to English

Gotkin, Robert H.; Gout, Uliana; Sattler, Sonja; Piansay-Soriano, Miriam Emily; Wanitphakdeedecha, Rungsima; Ghannam, Sahar; Rossi, Elena; Ferrariz, Teresita S.; Hexsel, Doris; Frank, Konstantin; Davidovic, Kristina; Sarnoff, Deborah S. und Cotofana, Sebastian (2021): Global Recommendations on COVID-19 Vaccines and Soft Tissue Filler Reactions: A Survey-Based Investigation in Cooperation With the International Society for Dermatologic and Aesthetic Surgery (ISDS). In: Journal of Drugs in Dermatology, Bd. 20, Nr. 4: S. 374-378

Volltext auf 'Open Access LMU' nicht verfügbar.

Abstract

Background: Recent reports have surfaced from the United States Food and Drug Administration hearings in December 2020 regarding the COVID-19 vaccines and study participants who developed facial and/or lip swelling after receiving the newly developed drug. Despite an incidence rate of 0.02% in the vaccine arm of the Moderna mRNA-1273 trial, concerns have been expressed about the association of adverse reactions following soft tissue filler injections and the COVID-19 vaccines. The International Society for Dermatologic and Aesthetic Surgery (ISDS) understands these concerns and has designed the following study. Methods: A global survey was designed to capture the incidence of adverse events related to: (1) previous soft tissue filler injections, (2) soft tissue filler injections during positive testing for COVID-19, and (3) soft tissue filler injections during and after receiving any of the COVID-19 vaccines globally available. Results: The information of 106 survey participants from 18 different countries was analyzed. 80.2% (n=85) never experienced any adverse reaction following their soft tissue filler injection whereas 15.1% (n=16) experienced swelling and 4.7% (n=5) experienced pain that lasted longer than two days. Of those who received at least one dose of the COVID-19 vaccine (n=78), 94.9% reported not to have experienced any adverse reaction related to their previous soft tissue filler injection, whereas 5.1% (n=4) reported to have perceived pain that lasted longer than two days. Conclusion:The data collected does not support the concern for an increased risk of developing adverse reactions following soft tissue filler injections associated with the COVID-19 vaccines compared to that risk associated with other previously described triggers or the default risk following soft tissue filler injections.

Dokument bearbeiten Dokument bearbeiten