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Aesthetic Plastic Surgery

, Volume 29, Issue 1, pp 34–48 | Cite as

Adverse Reactions to Injectable Soft Tissue Permanent Fillers

  • Lise ChristensenEmail author
  • Vibeke Breiting
  • Martin Janssen
  • Jens Vuust
  • Estrid Hogdall
Article

Abstract

Background

Synthetic injectable facial fillers with a permanent effect are widely atoxic and nonimmunogenic, but they differ with respect to composition and in chemical and biologic characteristics. Yet, they all act as foreign bodies in the tissues eliciting a host response that try to remove the gel. Inflammatory nodules may develop at the sites of injection-for some fillers, many years later, for others, not. Why is that?

Methods

Biopsies were contributed by various plastic surgeons from Europe and Australia after requests were made at international congresses and workshops. The study was based on (a) 5 biopsies from unreactive tissue obtained at different times after injection of polyacrylamide hydrogel (Aquamid); (b) 28 biopsies from intermediate or late inflammatory nodules after injection of polyacrylamide hydrogel (Aquamid) (20 cases), a hyaluronic acid-polyhydroxyethylmethacrylate/ethylmethacrylate gel (Dermalive) (2 cases), and a gel consisting of polylactic acid in mannitol/carbomethoxycellulose (New-Fill) (6 cases); and (c) a review of the literature on adverse reactions after injection with permanent fillers.

Results

Clinically unreactive tissues after injection with Aquamid showed modest or no host reaction. Inflammatory nodules showed an increased foreign body reaction and a bacterial infection after injection with Aquamid, and a combination of moderate foreign body reaction, fibrosis, and in some cases also bacterial infection after injection with Dermalive and New-Fill. According to the literature, inflammatory nodules occur no later than 1 year after injection with polyacrylamide hydrogel, but up to 6 years after injection of combination gels (Artecol), and up to 28 years after injection of silicone gel.

Conclusions

Inflammatory nodules are likely to be caused by a low-grade infection maintained within a biogfilm surrounding the hydrophobic silicone gel and the combination gels. Aquamid gel may prevent formation of a biofilm through its high water-binding capacity, explaining why late inflammatory nodules are not seen after injection of this polyacrylamide hydrogel product.

Keywords

Adverse reactions Facial augmentation Literature review Permanent effect Synthetic injectable fillers 

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Copyright information

© Springer Science+Business Media, Inc. 2005

Authors and Affiliations

  • Lise Christensen
    • 1
    Email author
  • Vibeke Breiting
    • 2
  • Martin Janssen
    • 3
  • Jens Vuust
    • 4
  • Estrid Hogdall
    • 5
  1. 1.Department of Pathology, RigshospitaletUniversity Hospital of CopenhagenDenmark
  2. 2.Holte Clinic of Plastic SurgeryHolteDenmark
  3. 3.Esthetische HoeveHelvoirtThe Netherlands
  4. 4.Department of Clinical BiochemistryStatens Serum InstituteCopenhagenDenmark
  5. 5.Department of Virus, Hormones and CancerDanish Cancer SocietyCopenhagenDenmark

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