Cadaver-derived Implants

A summary of cadaver-derived implants is provided in Table 6.2.
     
 
Table 6.2. Cadaver-derived implants

  Implants   Indications   Treatment   Complications and potential adverse reactions
  AlloDerm   FDA-approved for lip augmentation in the USA [14]. The allograft scaffold is also used for understandburn
injuries and cancer excisions and to correct soft tissue defects [8]
  Tiny incisions are made at both corners of the lip.An instrument is passed from one incision to the other to make a tunnel. The implant is passed from one end of the incision toward the other end [14]. Reports of longevity vary, ranging from 6–12 months to several years [4]   The major complication is overcorrection. The risk of this is minimized by the physicianfully understanding the patient’s expectations [14]
  Acellular allogeneic dermis Cymetra   FDA-approved for treat ment of rhytids, nasolabial folds, and lips   Injection at the midreticular level is optimal until the majority of the gentian lines have been removed or the deepest plane has been reached [4]. Double allergy testing is recommended [15], and patients shown to be allergic to bovine collagen might find this preparation to be a feasible alternative. Its longevity is normally 3–6 months   Bruising, redness, swelling, and wrinkling of skin [8]
  Injectable, microparticulate acellular allogenic dermis Human cadaver tissue       Augmentation reportedly lasts longer than does bovine collagen [16].    
  Fascian Lyophilized human particulate
fascia lata Human cadaver tissue
  FDA-approved for stimu lation of cutaneous collagen formation [17]   Reports claim the effect lasts 3–6 months while the manufacturer states 6–8 months [4]   Complications may include edema, erythema, and ecchymosis, and later complications may include postinflammatory hyperpigmentation. The larger particle sizes appear to be associated with side effects that are more persistent [4]. Painful to inject; bruising [17]