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4.
An. bras. dermatol ; 93(2): 299-301, Mar.-Apr. 2018. graf
Article Dans Anglais | LILACS | ID: biblio-1038267

Résumé

Abstract: Diphencyprone has been reported as a local immunotherapy for cutaneous melanoma metastases. We aim to report cases of melanoma patients treated with diphencyprone in a single Brazilian institution and highlight their outcomes. Since 2012, we have treated 16 melanoma patients with cutaneous metastases with topical diphencyprone. To date, we have had 37.5% of complete response, 25% of partial responses, and 31.25% patients without any response. Treatment was well tolerated and local toxicity was easily controlled. We believe topical diphencyprone is a feasible treatment that can be another option for treating melanoma patients, especially in cases of in-transit or extensive disease.


Sujets)
Humains , Mâle , Femelle , Adulte , Adulte d'âge moyen , Sujet âgé , Sujet âgé de 80 ans ou plus , Jeune adulte , Tumeurs cutanées/traitement médicamenteux , Cyclopropanes/usage thérapeutique , Mélanome/traitement médicamenteux , Mélanome/secondaire , Antinéoplasiques/usage thérapeutique , Tumeurs cutanées/anatomopathologie , Tumeurs cutanées/secondaire , Biopsie , Administration par voie cutanée , Brésil , Résultat thérapeutique , Mélanome/anatomopathologie
5.
Braz. j. med. biol. res ; 49(6): e4806, 2016. tab, graf
Article Dans Anglais | LILACS | ID: biblio-951682

Résumé

New generation antidepressant therapies, including serotonin-norepinephrine reuptake inhibitor (SNRIs), were introduced in the late 1980s; however, few comprehensive studies have compared the benefits and risks of various contemporary treatments for major depressive disorder (MDD) in young patients. A comprehensive literature search of PubMed, Cochrane, Embase, Web of Science, and PsycINFO databases was conducted from 1970 to January 2015. Only clinical trials that randomly assigned one SNRI or placebo to patients aged 7 to 18 years who met the diagnostic criteria for major depressive disorder were included. Treatment success, dropout rate, and suicidal ideation/attempt outcomes were measured. Primary efficacy was determined by pooling the risk ratios (RRs) of treatment response and remission. Acceptability was determined by pooling the RRs of dropouts for all reasons and for adverse effects as well as suicide-risk outcomes. Five trials with a total of 973 patients were included. SNRIs were not significantly more effective than placebo for treatment response but were for remission. The comparison of patients taking SNRIs that dropped out for all reasons and those taking placebo did not reach statistical significance. Significantly more patients taking SNRIs dropped out for adverse effects than those taking placebo. No significant difference was found in suicide-related risk outcomes. SNRI therapy does not display a superior efficacy and is not better tolerated compared to placebo in these young patients. However, duloxetine has a potential beneficial effect for depression in young populations, showing a need for further research.


Sujets)
Humains , Mâle , Femelle , Enfant , Adolescent , Essais contrôlés randomisés comme sujet , Trouble dépressif majeur/traitement médicamenteux , Inhibiteurs de la recapture de la sérotonine et de la noradrénaline/usage thérapeutique , Antidépresseurs/usage thérapeutique , Placebo/usage thérapeutique , Cyclopropanes/usage thérapeutique , Succinate de dèsvenlafaxine/usage thérapeutique , Chlorhydrate de duloxétine/usage thérapeutique , Milnacipran
6.
Yonsei Medical Journal ; : 928-935, 2016.
Article Dans Anglais | WPRIM | ID: wpr-63330

Résumé

PURPOSE: Roflumilast is the only oral phosphodiesterase 4 inhibitor approved to treat chronic obstructive pulmonary disease (COPD) patients [post-bronchodilator forced expiratory volume in 1 second (FEV1) <50% predicted] with chronic bronchitis and a history of frequent exacerbations. This study evaluated the efficacy and safety of roflumilast in Korean patients with COPD and compared the efficacy based on the severity of airflow limitation. MATERIALS AND METHODS: A post-hoc subgroup analysis was performed in Korean COPD patients participating in JADE, a 12-week, double-blinded, placebo-controlled, parallel-group, phase III trial in Asia. The primary efficacy endpoint was the mean [least-squares mean adjusted for covariates (LSMean)] change in post-bronchodilator FEV1 from baseline to each post-randomization visit. Safety endpoints included adverse events (AEs) and changes in laboratory values, vital signs, and electrocardiograms. RESULTS: A total of 260 Korean COPD patients were recruited, of which 207 were randomized to roflumilast (n=102) or placebo (n=105) treatment. After 12 weeks, LSMean post-bronchodilator FEV1 increased by 43 mL for patients receiving roflumilast and decreased by 60 mL for those taking placebo. Adverse events were more common in the roflumilast group than in the placebo group; however, the types and frequency of AEs were comparable to those reported in previous studies. CONCLUSION: Roflumilast significantly improved lung function with a tolerable safety profile in Korean COPD patients irrespective of the severity of airflow limitation.


Sujets)
Sujet âgé , Femelle , Humains , Mâle , Adulte d'âge moyen , Aminopyridines/usage thérapeutique , Asiatiques , Benzamides/usage thérapeutique , Cyclopropanes/usage thérapeutique , Méthode en double aveugle , Inhibiteurs de la phosphodiestérase-4/usage thérapeutique , Broncho-pneumopathie chronique obstructive/traitement médicamenteux , République de Corée , Tests de la fonction respiratoire , Résultat thérapeutique
10.
Rev. chil. dermatol ; 22(1): 18-23, 2006. ilus, tab, graf
Article Dans Espagnol | LILACS | ID: lil-433894

Résumé

Estudio retrospectivo de pacientes atendidos con diagnóstico de Alopecia Areata en el Servicio de Dermatología del Centro de Diagnóstico de la Pontificia Universidad Católica de Chile. Se revisaron las fichas de 77 pacientes con diagnóstico de Alopecia Areata, 38 por ciento hombres, 62 por ciento mujeres, con un promedio de edad de 26.7 (DSI 15.7; rango 2-65): 15 por ciento presentaron depresión, 11 por ciento rinitis alérgica, 6,5 por ciento presentaron ansiedad, 3,9 por ciento hipotiroidismo y 2,6 por ciento, vitíligo. La Alopecia Areata se asocia a un evento estresante en 27 por ciento de los pacientes. Dentro de los exámenes solicitados, un 2/26 tuvieron anticuerpos antitiroídeos positivos y 2/27, TSH alterada. Se discuten las diversas modalidades terapéuticas para tratar la Alopecia Areata.


Sujets)
Mâle , Adolescent , Adulte , Humains , Femelle , Enfant d'âge préscolaire , Enfant , Adulte d'âge moyen , Pelade/complications , Pelade/étiologie , Pelade/traitement médicamenteux , Cyclopropanes/usage thérapeutique , Hormones corticosurrénaliennes/usage thérapeutique , Association de médicaments , Maladies de la peau/complications , Maladies de la thyroïde/complications , Immunothérapie , Événements de vie , Minoxidil/usage thérapeutique , Études rétrospectives , Troubles mentaux/complications
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