Objective: To find the lowest effective injection dose of abobotulinum toxin A (Dysport) for allergic rhinitis.
Study Design: Dose-escalation randomized controlled trial.
Methods: We included all patients aged 18 years or older who had persistent allergic rhinitis and positive allergy skin prick test. The patients were randomly allocated to receive 40, 30, or 20 U of abobotulinum toxin A by injection at the inferior turbinate. We followed up on patients for 12 weeks to evaluate nasal symptoms, ocular symptoms, minimum nasal cross-sectional area as measured using acoustic rhinometry, and complications.
Results: Seventeen patients were included in this study, with 7 receiving 20 U of abobotulinum toxin A and 5 each receiving 30 U and 40 U. Abobotulinum toxin A significantly improved nasal congestion, rhinorrhea, sneezing, and loss of smell at 40 U ( < .05) and nasal congestion, sneezing, and loss of smell at 30 U ( < .05). However, at a dose of 20 U, only nasal congestion and loss of smell improved ( < .05). Nasal patency had also significantly improved two weeks after treatment at doses of 40 and 30 U ( < .05). Complications included epistaxis (11.8%) and nasal dryness (23.5%).
Conclusion: Abobotulinum toxin A at a dose of at least 30 U effectively reduced most nasal symptoms.
Level Of Evidence: 2.
Trial Registration: Clinicaltrials.in.th/ TCTR20200526014.
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http://dx.doi.org/10.1002/lio2.499 | DOI Listing |
Ophthalmic Plast Reconstr Surg
December 2024
Department of Ophthalmology and Visual Sciences, Montefiore Medical Center, Albert Einstein College of Medicine.
Purpose: Thyroid eye disease-related retraction and strabismus treatment is complicated by the activity level of the disease. Botulinum toxin injection can provide relief of symptoms in lieu of, or while waiting for surgery, radiation, or alternative medications. This study reviews techniques, outcomes, and effectiveness of botulinum toxin usage in thyroid eye disease.
View Article and Find Full Text PDFBr J Pharmacol
February 2025
Department of Biomedical Sciences, University of Padova, Padova, Italy.
Background And Purpose: Botulinum neurotoxin type A1 (BoNT/A) is one of the most potent neurotoxins known. At the same time, it is also one of the safest therapeutic agents used for the treatment of several human disorders and in aesthetic medicine. Notwithstanding great effectiveness, strategies to accelerate the onset and prolong BoNT/A action would significantly ameliorate its pharmacological effects with beneficial outcomes for clinical use.
View Article and Find Full Text PDFToxins (Basel)
June 2024
Movement Disorders Center, Department of Neurology, School of Medicine, University of São Paulo, São Paulo 05403-000, Brazil.
Sci Rep
June 2024
Department of Dentistry, Ingá University Center, Uningá, Paraná, Brazil.
The present study aimed to assess the effectiveness and functional adverse effects of a single and multiple injections of botulinum toxin A (BoNT-A) for masseter hypertrophy (MH). Twenty-six women complaining about lower third facial enlargement due to MH, received 75 U of BoNT-A (abobotulinum toxin) in each masseter muscles. After 3 months, patients were randomly assigned to receive a second treatment session of Saline Solution: (G1; n = 11) or BoNT-A: (G2; n = 12).
View Article and Find Full Text PDFToxins (Basel)
March 2024
Doctoral School, Carol Davila University of Medicine and Pharmacy, 020021 Bucharest, Romania.
Introduction: The rehabilitation medical team is responsible for the therapeutic management of post-stroke patients and, therefore, for the complex therapeutic approach of spasticity. Considering the generous arsenal at our disposal in terms of both pharmacological treatment, through the possibility of administering botulinum toxin to combat spasticity, and in terms of accurate assessment through developed functional scales such as the GAS (Goal Attainment Scale), one of our purposes is to monitor the parameters that influence the achievement of functional goals set by patients together with the medical team in order to render the patients as close as possible to achieving their proposed functional goals, thus enhancing their quality of life. By assessing and establishing statistical and clinical correlations between the GAS and quantifiable parameters related to the affected post-stroke upper limb, namely degree of spasticity, motor control, pain level and evolution of pain under treatment with BoNT-A (abobotulinum toxin A), and patients' overall response to BoNT-A treatment, we aim to quantify the improvement of the therapeutic management of post-stroke patients with spasticity and develop a more personalized and effective approach to their disability and impairment.
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