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Patients seek consultations for various reasons. However, there is a new common factor that influences people’s decision to get a cosmetic treatment: social media. A person with social media dysmorphia (SMD), or selfie or Snapchat dysmorphia, may have a body dysmorphic disorder (BDD) that can be triggered or worsened by social media.
Many social media users are accustomed to sharing selfies that have been altered with filters to erase imperfections. Constant exposure to this enhanced version of oneself—combined with the positive feedback in the form of likes, shares, and follows—can make people feel their unedited selves aren’t enough. Some potential patients may even present a modified selfie to demonstrate aesthetic goals, regardless of whether or not they are realistic.
While social media dysmorphia isn’t a recognized diagnosis per the DSM-5, the term still reflects the way that social media can impact someone with BDD. A person with BDD is usually obsessed with self-perceived flaws that others likely do not notice. Too often, this psychological disorder is mis- or undiagnosed.
While social media doesn’t cause BDD, it can trigger or worsen it. Teenagers and influencers are often at higher risk for developing BDD because of their excessive use. Influencers may perceive their market value to directly correlate to the number and quality of their social media interactions.
There is a clear connection between social media use and demand for cosmetic enhancements. In fact, more than half of aesthetic surgeons say they’ve seen an increase in the number of patients who want treatments specifically to improve their selfies. However, it’s important to screen prospective patients for SMD and BDD for a number of reasons:
Researchers estimate that up to 15% of patients seeking cosmetic enhancement procedures have BDD, the majority of whom are women. Because SMD is a relatively new development, however, it isn’t clear yet how many people have it.
Symptoms of BDD include:
While it can be difficult to determine whether a patient’s perception of his or her flaws is warranted, medical aesthetic experts should screen clients for possible mental health concerns prior to administering treatment. One survey found that 84% of aesthetic practitioners had treated a person they considered an appropriate candidate and later determined that the recipient had BDD.
To better identify patients who may have BDD and/or social media dysmorphia, pay attention to their concerns. If someone presents edited selfies during a consultation, ask how much the pictures been edited. Be clear and firm about what aesthetic treatment can and can’t do. You can also ask a candidate to identify flaws in a mirror. This could help you get a better sense of his or her self-perception.
Another way to screen for BDD is to use a questionnaire that lists common symptoms. Have patients rate the severity of distress for each one. If a person has symptoms of BDD, you can then refer them to a mental health specialist.
Before treating any patient, you should address these questions:
With social media playing an ever-increasing role in people’s lives, it is imperative to keep BDD and SMD in mind during each consultation. To avoid dramatic surgical outcomes that may not be reversible, consider providing non-invasive solutions to better serve your patients.
Venus Concept offers an extensive lineup of cutting-edge, non-invasive medical aesthetic devices and post-sales support services. Contact us today for more information or download our report, “Filters and Fillers: The Growing Incidence of Social Media Dysmorphia in the Medical Aesthetics Space.”
For more information call: (+44) 208 748 2221 // info.uk@venusconcept.com
REGULATORY CLEARANCES [ More ]
Venus Versa™ has CE Mark as a multi-application device intended to be used in aesthetic and cosmetic procedures. The SR515 and SR580 applicators have CE Mark for the treatment of benign pigmented epidermal and cutaneous lesions and treatment of benign cutaneous vascular lesions. The HR650/HR650XL and HR690/HR690XL applicators have CE Mark for the removal of unwanted hair and to effect stable long-term or permanent hair reduction for Fitzpatrick. The AC Dual applicator has CE Mark for the treatment of acne vulgaris. The DiamondPolar™ applicator has CE Mark for non-invasive treatment of moderate to severe facial wrinkles and rhytides in Fitzpatrick skin types I-IV. The OctiPolar™ applicators on the Venus Versa™ system has CE Mark for temporary body contouring via skin tightening, circumferential reduction, and cellulite reduction. The NanoFractional RF™ (Viva) applicator has CE Mark for dermatological procedures requiring ablation and resurfacing of the skin.
Venus Bliss™ has CE Mark as a non-invasive medical aesthetic device enabling a comprehensive approach leading to body contouring, addressing fat reduction, skin tightening, circumference reduction, and cellulite reduction.
ARTAS iX™ has CE Mark with indication for use for harvesting hair follicles from the scalp in men diagnosed with androgenic alopecia (male pattern hair loss) who have black or brown straight hair. ARTAS iX™ is intended to assist physicians in identifying and extracting hair follicular units from the scalp during hair transplantation; creating recipient sites; and implanting harvested hair follicles.
NeoGraft® has CE Mark with indication for use in suction-assisted follicular extraction and re-implantation. NeoGraft® is an auto-graft system and can be used on both male and female patients.
Venus Legacy™ has CE Mark for the increase of skin tightening, temporary circumferential reduction, cellulite reduction, and wrinkle reduction.
Venus Velocity™ has CE Mark for treatment of hirsutism (hair removal), permanent hair reduction (defined as the long-term stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regimen), and the treatment of pseudofolliculitis barbae for all Fitzpatrick skin types.
Venus Viva™ has CE Mark for the use in dermatological procedures requiring ablation and resurfacing of the skin, and the treatment of moderate to severe facial wrinkles and rhytides in Fitzpatrick skin types I-IV with the DiamondPolar™ applicator.
Venus Epileve™ has CE Mark for hair removal, permanent hair reduction (defined as the long-term stable reduction in the number of hairs re-growing when measured at 6, 9 and 12 months after the completion of a treatment regimen), and the treatment of pseudofolliculitis barbae for all Fitzpatrick skin types. Venus Epileve™ is also CE-Marked for hirsutism.
Venus Freeze Plus™ has CE Mark for treatment of moderate to severe facial wrinkles and rhytides using the DiamondPolar™ applicator, and CE Mark for the treatment of cellulite reduction, increase of skin tightening, and temporary circumferential reduction on the OctiPolar™ applicator.
Venus Glow™ provides a dermal rejuvenation treatment that works to open up and deep-clean pores. Venus Concept is the exclusive distributor for Venus Glow™.
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