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1.
Drug Des Devel Ther ; 7: 1035-41, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24101860

RESUMO

BACKGROUND AND AIM: The use of transdermal therapeutic systems has spread worldwide since they allow effective local drug delivery. In the present study, we investigated the efficacy and safety of a new betamethasone valerate medicated plaster (Betesil®) to manage facial swelling, edema, inflammation, ecchymosis, and hematoma, when applied immediately after a facial rejuvenation procedure. MATERIALS AND METHODS: We applied the plaster to the skin of 20 healthy patients for 12 hours immediately after hyaluronic acid-based procedure performed with the aim of erasing facial wrinkles of perioral and nasolabial folds and improving chin and eye contour. A further 20 patients underwent the same cosmetic procedure, but they were treated with an aescin 10% cream (applied immediately after the procedure, in the evening, and the morning after) and served as control group. RESULTS: Betesil® application resulted in a significant improvement in swelling/edema/inflammation score, if compared with aescin 10% cream (P < 0.01). As for facial ecchymosis and hematoma around the needle injection track, only two patients in the active treatment group displayed minimal ecchymosis and hematoma. In the control group, two patients presented minimal ecchymosis and three slight hematoma. However, using the ecchymosis/hematoma score, no significant difference between Betesil® and aescin 10% cream groups was observed. Patients' satisfaction was significantly higher among subjects receiving Betesil®, if compared to patients receiving aescin 10% cream (P < 0.01). CONCLUSION: The present study supports the use of Betesil® plaster immediately after facial cosmetic procedures in order to safely control swelling, edema, and inflammation.


Assuntos
Valerato de Betametasona/uso terapêutico , Técnicas Cosméticas , Glucocorticoides/uso terapêutico , Envelhecimento da Pele/efeitos dos fármacos , Administração Cutânea , Adulto , Idoso , Valerato de Betametasona/administração & dosagem , Técnicas Cosméticas/efeitos adversos , Edema/etiologia , Edema/prevenção & controle , Escina/administração & dosagem , Escina/uso terapêutico , Feminino , Seguimentos , Glucocorticoides/administração & dosagem , Humanos , Ácido Hialurônico/administração & dosagem , Inflamação/etiologia , Inflamação/prevenção & controle , Masculino , Pessoa de Meia-Idade , Satisfação do Paciente , Rejuvenescimento , Resultado do Tratamento
2.
Int J Impot Res ; 25(3): 117-20, 2013 May.
Artigo em Inglês | MEDLINE | ID: mdl-23552577

RESUMO

Premature ejaculation is a sexual debilitating condition affecting a large number of men worldwide and leading to important dysfunctions influencing the patients' affective and emotional life. Hyaluronic acid is a natural and safe compound that has been widely used not only in the aesthetic medicine clinic, but also for treatment of osteoarthritis. The present study shows the effectiveness of a hyaluronic acid-based procedure for treatment of premature ejaculation. A hundred and ten male patients were treated with hyaluronic acid injections in the deep dermis of their glans penis to increase the volume and the circumference of their penis to prevent male premature ejaculation and improve the patients' and their partners' sexual satisfaction. The intravaginal ejaculation latency time increased significantly from a baseline value of 88.34±3.14 s to 293.14±8.16 s after 6 months from the procedure. Maximal glandular circumference increased from 98.51±0.71 mm to 114.35±0.66 mm after 6 months from the procedure. At 6-month follow-up, patients' self-rated satisfaction was 5.3±0.07 (range: 4-6). At the follow-up, partners' self-rated satisfaction was 5.1±0.09 (range: 3-6). The present clinical study showed that hyaluronic acid injection is a promising treatment for premature ejaculation. The effect of the procedure in the long-term follow-up needs to be clarified.


Assuntos
Ácido Hialurônico/administração & dosagem , Ejaculação Precoce/tratamento farmacológico , Adulto , Coito , Derme/efeitos dos fármacos , Humanos , Injeções , Masculino , Satisfação do Paciente , Pênis/efeitos dos fármacos
3.
Lasers Med Sci ; 28(3): 865-9, 2013 May.
Artigo em Inglês | MEDLINE | ID: mdl-22855380

RESUMO

Outpatient laser ablation of palatine tonsils is a very interesting procedure that has been recently introduced as a routine in head and neck surgery departments. The aim of this study was to describe a new strategy using a Doppler-guided fibre optic neodymium-yttrium-aluminium-garnet (YAG) laser to remove up to 80 % of tonsillar tissue, as assessed in the long-term postoperative clinical evaluation of the volume of the tonsils at the follow-up, and leaving the capsule in place, thus avoiding any haemorrhagic complication and minimize pain. A total of 20 patients (men, n=13; women, n=7), aged between 6 and 63, were recruited for the procedure. They were affected by chronic hypertrophic tonsillitis with a recurrent fever and other symptoms that were related to oral inflammation. Among the 20 patients, no serious adverse events, including haemorrhage-related complications, were observed. Treatment was well tolerated, even in patients displaying an overall low pain threshold. No dropout or uncompleted procedure occurred in the present study. Minor complications included sore throat, moderate oedema, mild acute pharynx inflammation, slight peritonsillar exudate and local burning. The postoperative pain, measured by Scott-Huskisson visual analogue scale, was between 5 and 40 mm and was easily counteracted by means of external ice packages and nonsteroidal anti-inflammatory drugs, according to the individual patient's need. During the 12-36-month follow-up patients showed improved symptoms (n=7) and complete recovery (n=13). A relapse episode was observed in two patients. This study supports fibre optic laser neodymium-YAG tonsil surgery, named "cribriform intracapsular tonsillectomy" or "Swiss-cheese laser tonsillectomy", as an effective alternative to the traditional cold knife approach or electrosurgery. This approach could become the gold standard for tonsil surgery in the third millennium for safety reasons, acceptable cost-benefit ratio, the precise targeting of the beam across the affected tissues and the short- and long-term recovery.


Assuntos
Terapia a Laser/métodos , Tonsilectomia/métodos , Tonsilite/cirurgia , Adulto , Criança , Feminino , Humanos , Terapia a Laser/efeitos adversos , Terapia a Laser/instrumentação , Lasers de Estado Sólido/uso terapêutico , Masculino , Pessoa de Meia-Idade , Fibras Ópticas , Tonsila Palatina/diagnóstico por imagem , Tonsila Palatina/cirurgia , Tonsilectomia/efeitos adversos , Tonsilite/diagnóstico por imagem , Ultrassonografia Doppler , Adulto Jovem
4.
Eur Rev Med Pharmacol Sci ; 17(24): 3272-8, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-24379055

RESUMO

BACKGROUND: Proton pump inhibitors (PPIs) are a major breakthrough in the medical management of gastroesophageal reflux disease (GERD). In several patients with non erosive reflux disease symptoms (NERD) the response to PPIs is partial or limited and symptoms relief needs the administration of additional medications. AIM: The aim of this study was to evaluate the effect of a new medical device, based on an oral fixed combination of hyaluronic acid and chondroitin-sulphate (HA+CS), in a bioadhesive carrier, in adults with symptoms of non erosive gastroesophageal reflux and with a low response to PPIs. PATIENTS AND METHODS: Twenty patients who had experienced heartburn and/or acid regurgitation for at least 3 days during a 7 day run-in period, without endoscopic mucosal breaks, were randomized in a double blind crossover study to receive four daily doses of a fixed oral combination of HA+CS and placebo for 14 days. Relief of cardinal symptoms of GERD was evaluated at the end of each period. RESULTS: A significant greater Sum of Symptoms Intensity Difference, compared to placebo, was observed after HA+CS treatment (-2.7 vs 0.5 - p < 0.01), being both heartburn (-1.6 vs 0.5 - p < 0.03) and acid regurgitation (-1.1 vs 0.1 - p < 0.03) significantly improved by the medical device. A speed of action ≤ 30 min was significantly more frequently reported by patients during HA+CS administration than with placebo (60% vs 30% - p = 0.05). Total disappearance of symptoms was observed in 50% of the patients compared to 10% during placebo administration (p = 0.01 between group comparison). CONCLUSIONS: A fixed combination of HA+CS has demonstrated to be effective in gastroesophageal reflux control, with a rapid onset of action.


Assuntos
Sulfatos de Condroitina/administração & dosagem , Refluxo Gastroesofágico/tratamento farmacológico , Fármacos Gastrointestinais/administração & dosagem , Ácido Hialurônico/administração & dosagem , Administração Oral , Adulto , Idoso , Análise de Variância , Distribuição de Qui-Quadrado , Estudos Cross-Over , Método Duplo-Cego , Esquema de Medicação , Combinação de Medicamentos , Quimioterapia Combinada , Feminino , Refluxo Gastroesofágico/diagnóstico , Antagonistas dos Receptores H2 da Histamina/administração & dosagem , Humanos , Itália , Masculino , Pessoa de Meia-Idade , Inibidores da Bomba de Prótons/administração & dosagem , Fatores de Tempo , Resultado do Tratamento
5.
J Oral Pathol Med ; 41(9): 649-61, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22494322

RESUMO

Free radicals play a key role in the development of several pathological conditions. Therefore, several methods have been developed to measure oxidative stress from bodily fluids including blood, urine and, more recently, saliva. Free radical and antioxidant defences within the oral cavity may play a key role in odontostomatological pathologies. This review provides an update of the literature concerning the association of oxidative stress with pathological conditions associated with the oral cavity. It focuses on the diagnostic and therapeutic importance of the tests based on saliva specimens in a preventive perspective.


Assuntos
Antioxidantes/farmacologia , Radicais Livres/efeitos adversos , Doenças da Boca/etiologia , Estresse Oxidativo/fisiologia , Antioxidantes/análise , Radicais Livres/análise , Humanos , Neoplasias Bucais/etiologia , Oxirredução , Doenças Periodontais/etiologia , Saliva/química
6.
Int J Immunopathol Pharmacol ; 25(4): 1093-8, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23298499

RESUMO

Osteoarthritis is characterized by progressive articular cartilage degeneration, changes in subchondral bone and synovial inflammation, leading to pain and disability. Viscosupplementation with hyaluronic acid has been widely investigated due to the viscoelastic properties of this compound to manage pain improving the ability to perform daily activities in patients affected by osteoarthritis. In the present study we investigated the clinical effectiveness of viscosupplementation with a new highly cross-linked hyaluronic acid, Variofill, in patients affected by bilateral knee osteoarthritis in comparison with the widely used Synvisc. A total of 20 patients, aged between 24-74 years and affected by bilateral knee osteoarthritis, participated in this pilot randomized triple-blind clinical study. They received two injections (2 ml each) of Synvisc in their left knee and 2 injections (2 ml each) of Variofill in their right knee spaced 15 days apart. Visual Analogue Scale and Western Ontario McMaster Universities Osteoarthritis Index score were used to evaluate the efficacy of hyaluronic acid injections before and 3 and 6 months after treatment. Both treatment regimens resulted in a significant improvement vs baseline in all endpoints at 3 and 6 months (p less than 0.001). Treatment with Variofill resulted in a high percentage improvement in Visual Analogue Scale pain, Western Ontario McMaster universities Osteoarthritis Index score pain and physical activity, when compared to Synvisc viscosupplementation, at 6 months (p less than 0.05). These results are encouraging for larger clinical trials with Variofill in larger cohorts of patients affected by osteoarthritis of the knee.


Assuntos
Ácido Hialurônico/análogos & derivados , Osteoartrite do Joelho/tratamento farmacológico , Adulto , Idoso , Feminino , Humanos , Ácido Hialurônico/uso terapêutico , Masculino , Pessoa de Meia-Idade , Medição da Dor , Projetos Piloto
7.
Clin Ter ; 162(5): 473-86, 2011.
Artigo em Italiano | MEDLINE | ID: mdl-22041807

RESUMO

Authors describe Er:YAG laser interaction with tissues, in particular their histomorphological characteristics to identify a specific clinic area for laser application through the examination of different clinical international trials. This study includes experimental trials about pig and rat skin laser application to know laser Er: YAG capability and limits; investigation is extended to laser application in human soft tissues as mucosa, periosteum and bones, its utility in cutaneous pathologies and in antiageing treatments.


Assuntos
Terapia a Laser , Lasers de Estado Sólido , Animais , Osso e Ossos/efeitos da radiação , Queimaduras/etiologia , Cicatriz/terapia , Colágeno/análise , Dermabrasão/instrumentação , Dermabrasão/métodos , Temperatura Alta/efeitos adversos , Humanos , Terapia a Laser/efeitos adversos , Lasers de Estado Sólido/efeitos adversos , Lasers de Estado Sólido/uso terapêutico , Terapia com Luz de Baixa Intensidade , Mucosa Bucal/efeitos da radiação , Músculos/efeitos da radiação , Tecido Nervoso/efeitos da radiação , Transtornos da Pigmentação/terapia , Lesões Experimentais por Radiação/etiologia , Pele/efeitos da radiação , Lesões dos Tecidos Moles/etiologia
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