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We read with great interest in the Archives “A Complication of Mesotherapy: Noninfectious Granulomatous Panniculitis” by Davis and colleagues,1 which describes the morbid outcome of a woman injected with a deoxycholate-containing solution for the treatment of cellulite. The patient was diagnosed with a “mesotherapy-induced noninfectious granulomatous panniculitis”1 (p809) in tissue obtained from numerous violaceous nodules and erosions on her thighs, buttocks, knees, and lower legs.
The volume and concentration of the deoxycholate injected and the injection technique used were not known despite the comprehensive investigation and workup of the patient (Mark D. P. Davis, MD, e-mail correspondence, June 30, 2008). Control of these factors is critical to ensure treatment success and minimize adverse events with deoxycholate-containing solutions for the reduction of adipose tissue.2 - 3 It is apparent from the article's accompanying photographs1 that the practitioner used an unorthodox injection technique, given the haphazard, closely spaced distribution and locations of the lesions. Perhaps the nurse injector was not aware that “mesotherapy ingredients phosphatidylcholine solubilized with deoxycholate . . . [are] meant primarily for localized fat ablation rather than as a treatment of cellulite,”4 (p148) which is emphasized in our group's recent review of injectable treatments for cellulite.4 In fact, we did not find any peer-reviewed literature substantiating the use of common mesotherapy ingredients as an effective means of reducing cellulite.4 Although there is evidence that some nondetergent medications (such as β-adrenergic agonists) may be effective for localized fat reduction, clinical trials investigating their use for cellulite are lacking.
Investigational uses of sodium deoxycholate injected deeply into subcutaneous fat2 and lipomas3 have been reported to reduce these fatty collections without the untoward events described by Davis et al.1 While this nonionic detergent possesses potent adipolytic activity, it is important to underscore that nonadipose tissue may similarly be affected, particularly if high concentrations (up to 5%) are used.3
According to the US Food and Drug Administration (FDA), injectable fat loss treatments (known colloquially as lipodissolve, lipolysis, or mesotherapy) are “unapproved drugs for unapproved purposes.”5 In light of the fact that standardized injection protocols using approved, pharmaceutical-grade formulations do not exist, it would be unremarkable if reports of adverse events like those reported by Davis et al1 increase in frequency.
As with other popular cosmetic procedures such as botulinum toxin injections, improper dose and technique can transform an otherwise very positive outcome into an avoidable adverse event. Until rigorous clinical trials are performed with FDA oversight, physicians and patients should be informed that the FDA considers localized fat ablation using fat-dissolving injections a “buyer beware situation.”5 We therefore urge caution in the use of these treatments.
Correspondence: Dr Rotunda, 1401 Avocado Ave, Ste 810, Newport Beach, CA 92660 (amr@drrotunda.com).
Financial Disclosure: Dr Rotunda has served as consultant to Kythera Biopharmaceuticals Inc, Calabasas, California, and has codeveloped a patent pending process that describes the use of detergents for the treatment of adipose tissue. Dr Avram owns stock options in Zeltiq Aesthetics Inc, Pleasanton, California.
Country-Specific Mortality and Growth Failure in Infancy and Yound Children and Association With Material Stature
Use interactive graphics and maps to view and sort country-specific infant and early dhildhood mortality and growth failure data and their association with maternal
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