Please login or create an account. If you do not have access to this content, you will be shown a 30 second preview and licensing options.
- Presentation
Complications of Dermal Fillers in Autoimmune and Immuno-mediated Diseases
Description
In a presentation on the complications of dermal fillers in patients with autoimmune and immuno-mediated diseases, dermatologist Maya Yanis discusses the risks and challenges faced by these patients when considering filler injections. Engaging the audience, she highlights that while some guidelines suggest avoiding fillers in cases of active autoimmune diseases, patients with inactive conditions may be treated at the physician's discretion. A significant finding from her research, involving 338 patients, reveals an 8% complication rate and a 6.1% rate of disease reactivation, although the latter's direct causation by fillers remains uncertain. She emphasizes that complications associated with hyaluronic acid fillers are comparable to those involving collagen biostimulators and that current treatments such as biologics do not seem to increase risk. The discussion includes the potential benefits of immunosuppressants and biologics, suggesting they may help manage filler complications. However, the risk of infections, particularly in patients on corticosteroids and certain biologics, calls for careful monitoring and infection prevention strategies. Ultimately, she underscores the importance of informed decisions between physicians and patients, advocating individualized approaches based on disease status and treatment history.
View moreConclusions
- Dermal fillers can be injected in patients with inactive autoimmune and immune-mediated diseases at physician's discretion.
- 6.8% of patients with autoimmune diseases experienced disease reactivation after dermal filler injections, but it is unclear if this is due to the fillers or disease flare-up.
- The complication rate for dermal fillers in patients with autoimmune diseases is 8%, which is higher than in healthy individuals.
- Non-permanent fillers, collagen biostimulators, and hyaluronic acid have similar complication risks.
- Biologics for psoriasis do not influence complication rates in patients receiving dermal fillers.
- Corticosteroids, methotrexate, and JAK inhibitors may effectively treat complications arising from dermal fillers but carry a risk of infections, so proper antiseptic techniques should be adhered to.
- De Boulle K, Heydenrych I. Patient factors influencing dermal filler complications: prevention, assessment, and treatment. Clin Cosmet Investig Dermatol.
- lanhez M, Luz ARCA, Palermo EC, Miot HA. Dermal Filler Injections in Patients with Autoimmune and Immune-Mediated Diseases: A Survey with Dermatologists. Aesthetic Plast Surg. 2023 Sep 13. doi: 10.1007/s00266-023-03639-x. Online ahead of print.
- Alijotas-Reig J, et al. Semin Arthritis Rheum. 2013 Oct;43(2):241-58.
- Owczarczyk-Saczonek A, et al. The Immunogenicity of Hyaluronic Fillers and Its Consequences. Clin Cosmet Investig Dermatol. 2021;14:921-34.
- Broly M, et al. Management of granulomatous foreign body reaction to fillers with methotrexate. J Eur Acad Dermatol Venereol. 2020;34(4):817-20.
- Miot HA, Criado PR, de Castro CCS, lanhez M, et al. JAK-STAT pathway inhibitors in dermatology. An Bras Dermatol. 2023;98(5):656-77.
- Ianhez M, et al. Frequency of complications of aesthetic facial fillers in Brazil. Plast Reconstr Surg. 2022;149(3):599e-601e.
- Davies E, et al. Guideline Acute Bacterial Soft Tissue Infections Following Nonsurgical Cosmetic Procedures. J Clin Aesthet Dermatol. 2021;14(9 Suppl 1):S29-S35.
- Penso L, et al. Association Between Biologics Use and Risk of Serious Infection in Patients With Psoriasis. JAMA Dermatol. 2021;157(9):1056-65.
- Conway R, et al. Risk of Infection with Methotrexate Therapy in Inflammatory Diseases: A Systematic Review and Meta-Analysis. J Clin Med. 2018;8(1):15.
- Adas MA, et al. The infection risks of JAK inhibition. Expert Rev Clin Immunol. 2022;18(3):253-61.
- Henkle E, et al. Nontuberculous mycobacteria infections in immunosuppressed hosts. Clin Chest Med. 2015;36(1):91-9.