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1.
Dermatol Ther (Heidelb) ; 13(7): 1603-1610, 2023 Jul.
Article in English | MEDLINE | ID: mdl-37316750

ABSTRACT

INTRODUCTION: Randomized controlled trials (RCTs) suggested that liquid formulation of botulinum toxin type A (aboBoNT-A) is safe and effective, but data confirming these characteristics in a real-life heterogenous set of patients are currently lacking. This study aimed to assess the efficacy and safety of the ready-to-use aboBoNT-A solution in adults with moderate-to-severe glabellar wrinkles. METHODS: In this real-life, multicenter, retrospective, observational study, healthy adults were treated at baseline only with aboBoNT-A solution on the glabellar area and followed up for 24 weeks. Re-treatment after 20-24 weeks could also be combined with other aesthetic procedures. Family history of immune-mediated inflammatory diseases (IMIDs) was not an exclusion criterion. Patient-reported outcomes (patient's satisfaction and injection-related pain) and physician-reported outcomes (Physician Global Assessment, PGA) were collected. RESULTS: Of the 542 patients enrolled in the study, 38 had IMID family history. Injection-related pain was reported in 128 (23.62%) as mild (pain VAS = 1.34 ± 0.87) mainly by non-botulinum toxin treatment-naïve women under 50 years of age. At 48 h, physicians rated the clinical result as "improved" in 64% of patients, conversely 264 patients (48.71%) self-evaluated as "satisfied"/"very satisfied". At 4 weeks a touch-up (< 10 units) was performed in 11 (2.03%) patients and 98.2% were "highly satisfied". Re-treatment was performed in 330 (61.45%) patients, mainly botulinum-experienced, at 20 weeks and in 207 (38.55%), mainly botulinum naïve, at 24 weeks. A total of 403 (74.35%) patients were re-treated with the three-point technique and 201 (37.08%) also received hyaluronic acid filler in the lower central face and middle third. There were no cases of de novo IMIDs. CONCLUSIONS: Real-world data confirmed that aboBoNT-A is a fast, efficient, durable, reproducible, and easy-to-use drug which is also well tolerated in patients with family history of IMID.

2.
J Drugs Dermatol ; 17(1): 83-88, 2018 Jan 01.
Article in English | MEDLINE | ID: mdl-29320592

ABSTRACT

Hyaluronic acid (HA) is used extensively in aesthetic medicine thanks to its documented role in skin rejuvenation. The specific applications of HA-based products are not always fully acknowledged due to a lack of consistent recommendations. In this paper, the authors have summarized available published data on the range of applications of non-animal stabilized hyaluronic acid (NASHA®) gel skin boosters (NSBs) in several anatomical areas and types of patient, as well as their own recommendations. Overall, the panel agreed that a standard initial protocol treatment of up to 3 sessions, followed by a maintenance schedule, would allow patients to improve and then preserve skin quality over time. Indeed, distinct effects are evident after the first session, but a progressive enhancement of skin texture is detectable for up to 12 months after repeat treatment at 4 to 6 month intervals. Moreover, the authors agreed that the NASHA gel, reaching the dermis, is able to reestablish a greater degree of hydration and stimulate collagen that, in turn, restores the volume and density of the skin. Thus, a strong consensus was reached that NSB procedures are minimally invasive, safe, and effective, and designed to improve skin texture and maintain skin quality.

J Drugs Dermatol. 2018;17(1):83-88.

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Subject(s)
Dermatologic Agents/pharmacology , Dermis/physiology , Hyaluronic Acid/pharmacology , Skin Aging , Skin Physiological Phenomena/drug effects , Consensus , Dermatologic Agents/administration & dosage , Drug Administration Schedule , Face , Gels , Hand , Humans , Hyaluronic Acid/administration & dosage , Injections, Intradermal , Rejuvenation
3.
Am J Ther ; 23(5): e1202-4, 2016.
Article in English | MEDLINE | ID: mdl-26164023

ABSTRACT

Drug-induced bullous pemphigoid (DIBP) has been reported to be an autoimmune bullous disease induced or precipitated by several drugs, immunopathologically similar to classic bullous pemphigoid. Several medications may not only cause DIBP, including diuretics, antiarrythmics-antihypertensives, and recently antitumor necrosis factor agents, other drugs as chloroquine, but also rarely by antibiotics as amoxicillin and penicillin. The authors present the third case of DIBP induced by quinolones and the second case of localized DIBP triggered by oral ciprofloxacin. A DIBP can be suspected in old patients when they add or change some drugs in their normal medication regimen.


Subject(s)
Ciprofloxacin/adverse effects , Drug Eruptions/etiology , Pemphigoid, Bullous/chemically induced , Administration, Oral , Aged, 80 and over , Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/adverse effects , Ciprofloxacin/administration & dosage , Drug Eruptions/pathology , Female , Humans , Pemphigoid, Bullous/diagnosis
4.
Clin Dermatol ; 26(2): 123-59, 2008.
Article in English | MEDLINE | ID: mdl-18472056

ABSTRACT

This article is aimed at providing information about the cross-linked hyaluronic acid marketing at present. It is also aimed at helping the lectors improve their knowledge about injection modalities and patient manage.


Subject(s)
Dermatologic Agents/pharmacology , Hyaluronic Acid/therapeutic use , Rejuvenation , Skin Aging/drug effects , Cosmetic Techniques/adverse effects , Dermatologic Agents/administration & dosage , Dermatologic Agents/chemistry , Esthetics , Face , Humans , Hyaluronic Acid/administration & dosage , Hyaluronic Acid/analogs & derivatives , Hyaluronic Acid/chemistry , Hyaluronic Acid/pharmacology , Injections, Intradermal , Skin Aging/physiology
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