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Skin tone representation in dermatologic direct-to-consumer advertisements: a cross-sectional analysis and call to action.

Direct-to-consumer advertisements (DTCAs) in medical marketing serve as a prominent modality to deliver information to an increasingly diverse audience of consumers and increase prescription sales. In dermatology, advertisements have the potential to shape the public's opinions, aid in the understanding of skin conditions, and raise awareness of available treatments. To investigate and characterize the representation of skin tones in DTCAs. Nielsen ratings were utilized to identify the networks most watched by Black viewers in 2022. Programming on NBCUniversal, ABC, CBS, and FOX that aired in the District of Columbia, suburban Maryland, and Northern Virginia from June 2022 to July 2022 was reviewed for DTCAs. DTCAs were then analyzed to determine the skin tones of models and skin conditions depicted on models with darkly pigmented skin. Of the 106 DTCAs related to dermatologic conditions, there were 13 unique advertisements featuring 32 unique models. Four advertisements depicted the skin condition on darkly pigmented skin tones. Using the Monk Skin Tone (MST) scale to assess the 32 unique individuals, only 25% (n = 8) were rated at an MST 7 or above, and 6.25% (n = 2) were rated at an MST 10. This study has the limitation of only sampling DTCAs from Washington, District of Columbia which does not fully represent all dermatology-related DTCAs in the United States. Results of this content analysis demonstrate that the number of persons of color within dermatologic DTCAs is 23%, whereas there are 13.6% Black individuals in the 2021 US census. This suggests that DTCAs are becoming more diverse since 2018. However, findings also show that the vast majority of DTCAs do not include models with darkly pigmented skin, and there remains a lack of advertisements depicting skin disease among people of color. Given the role of DTCAs in informing and aiding patients' requests for prescription drugs, representation of all skin tones is essential for this communication to be effective, especially in the field of dermatology.

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Efficacy and Safety of DaxibotulinumtoxinA for Injection in the Treatment of Glabellar Lines by Age and Race: Subgroup Analysis of the SAKURA Clinical Trials.

DaxibotulinumtoxinA for Injection (DAXI) is a novel botulinum toxin type A formulation approved for the treatment of glabellar lines. The efficacy, safety, and extended duration of response of DAXI 40 U for glabellar lines were demonstrated in 2 Phase 3, randomized, double-blind studies (SAKURA 1 and 2) and a Phase 3 open-label trial (SAKURA 3). The aim of this study was to evaluate the efficacy and safety of the first DAXI 40 U treatment received in SAKURA 1, 2, or 3 across age and race subgroups. Adults with moderate-to-severe glabellar lines (Investigator Global Assessment-Frown Wrinkle Severity [IGA-FWS] and Patient FWS [PFWS] scales) were evaluated for glabellar line severity for ≤36 weeks after the first DAXI treatment. Efficacy and safety were analyzed by age (18-45, >45-55, and >55 years) and race (Asian, Black and African American, and White). Overall, 2785 patients were included in the efficacy analysis. The proportion of patients achieving none or mild glabellar line severity at maximum frown (IGA-FWS) after DAXI treatment was high in all age and race subgroups (>96% at Week 4). Glabellar line severity of none or mild by composite IGA-FWS and PFWS rating was maintained for a median of 24.0 weeks in all age subgroups, and for 27.0, 25.3, and 24.0 weeks in the Asian, Black and African American, and White subgroups, respectively. Treatment-emergent adverse events were similar across all subgroups. Consistent with the overall study population, DAXI 40 U demonstrated a high response rate and duration of effect of ≥24 weeks across all age and race subgroups.

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62 - Compression Force Testing of Veneer-Retained Anterior Fixed Partial Dentures

The focus of this study is twofold; the first objective is to evaluate the resistance of veneer-retained anterior fixed partial dentures to compression testing. The second objective is to determine if veneer retainers with these axial grip extensions improve the restorations resistance to compressive forces as demand for biomaterial and access to care is often globally differentiated. Two maxillary typodont models with edentulous spaces in the left lateral incisor area were obtained. On each typodont model, the central incisor and canine neighbouring the edentulous space were given veneer-type preparations with a chamfer finish line. On one model, 2-mm axial grip extensions were added to the prepared facial surface of the abutment teeth. Metal duplicates of the prepared abutment teeth and edentulous spaces of each typodont model were produced using the lost wax casting technique. The two metal duplicates were scanned, and ten identical CAD/CAM restorations were produced for each metal duplicate. The restorations were cemented to metal duplicates and were subjected to compressive strength testing using a universal testing machine. Compressive forces were applied from the incisal margin towards the cervical in order to determine the force at which the restorations undergo debonding or fracture. Subject specimen N tested totalled 20. The veneer-retained restorations without axial grip extensions all underwent debonding but none fractured. In the veneer-retained restorations with axial grip extensions retention, nine cases of debonding (90%) were recorded and one case of fracture (10%) was recorded. The veneer-retained restorations with axial grip extensions (M = 302 N, SD = 79) compared to the restorations without axial grip extensions (M = 228 N, SD = 60) withstood significantly higher compressive forces (p < 0.05). This study shows that veneer-retained anterior fixed partial dentures with axial grip extensions can withstand higher compression forces than veneer-retained anterior fixed partial dentures without axial grip extensions. Veneer-retained anterior bridges can be useful in addressing esthetic concerns in a minimally invasive manner. This study shows that axial grip extensions can play a crucial and important role in addressing concerns about resistance and long-term success of this type of restoration. An important clinical relevance will be highlighted for endodontically treated dentition versus non-endodontic treated dentition. Additionally, there will be reporting on intersectional pending studies regarding custom geo-position of axial grip extensions preparation design.

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Alternative Cosmetic and Medical Applications of Injectable Deoxycholic Acid: A Systematic Review.

Beyond submental fat reduction, injectable deoxycholic acid (DCA) has gained popularity in recent years for various minimally invasive lipolysis applications. To summarize and evaluate the evidence of off-label uses of injectable DCA. MEDLINE, Embase, CINAHL, Web of Science, and CENTRAL were searched. The outcomes measured included applications of DCA, treatment regimen, and its efficacy. An overall success rate for each condition was calculated based on the improvement defined in the included studies. Eleven studies evaluated the cosmetic use of DCA for excess adipose tissue on various anatomical locations. The outcomes were evaluated at time points ranging from 1 to 21 months post-treatment, with overall success rates over 85%. Eight case reports and series reported the success of using DCA treating lipomas, xanthelasmas, paradoxical adipose hyperplasia, fibrofatty residue of infantile hemangioma, piezogenic pedal papules, and HIV-associated lipohypertrophy. Although the preliminary efficacies were high, the overall recommendations for off-label uses are weak because of the lack of high-level studies. The review emphasizes the diversity of injectable DCA as a minimally invasive technique for lipolysis. Further high-level studies demonstrating consistent treatment regimens and methods of evaluation are warranted to make more definitive recommendations regarding off-label DCA use.

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