Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 10 de 10
Filter
Add more filters










Publication year range
2.
J Eur Acad Dermatol Venereol ; 35(3): 693-700, 2021 Mar.
Article in English | MEDLINE | ID: mdl-32916767

ABSTRACT

BACKGROUND: Brodalumab was efficacious and safe in moderate-to-severe plaque-type psoriasis in the AMAGINE trials; published reports under real-life conditions are limited. OBJECTIVES: To evaluate the effectiveness and safety of brodalumab in patients with moderate-to-severe plaque-type psoriasis in a real-world setting. METHODS: This observational, retrospective study enrolled adult patients (≥18 years) with moderate-to-severe plaque-type psoriasis who underwent 24 weeks of treatment with brodalumab at 17 Italian dermatological centres. Baseline data included demographics, comorbidities, age of onset and duration of psoriasis and previous treatments. Psoriasis Area and Severity Index (PASI), Physician Global Assessment (PGA), static PGA of Genitalia, Dermatology Life Quality Index and patient satisfaction were assessed at weeks 0, 4, 12 and 24; adverse events were recorded. RESULTS: Seventy-eight patients (mean age 47.9 years, 71.8% male, average disease duration 16.8 years) were enrolled. A rapid and significant reduction in mean PASI score was observed after 4 weeks of treatment, decreasing further at weeks 12 and 24 (all P < 0.0001 vs. baseline). A higher number of cardiometabolic comorbidities and previous therapies were negatively associated with the achievement of PASI 90 at all assessments. Brodalumab was effective in bio-experienced patients, including those who had failed on anti-interleukin (IL)-17 therapies. Quality of life and patient satisfaction increased significantly during treatment (P < 0.0001 and P < 0.01 vs. baseline, respectively). Treatment was interrupted in 9 (11.5%) patients due to adverse events (n = 4), lack of efficacy (n = 3), lost to follow-up (n = 1) and surgical procedure (n = 1). CONCLUSIONS: Brodalumab is effective and safe in the treatment of moderate-to-severe psoriasis in a real-world setting, including in patients with failure to anti-IL17 therapies.


Subject(s)
Psoriasis , Quality of Life , Adult , Antibodies, Monoclonal , Antibodies, Monoclonal, Humanized , Female , Humans , Male , Middle Aged , Psoriasis/drug therapy , Retrospective Studies , Severity of Illness Index , Treatment Outcome
4.
Mol Biochem Parasitol ; 31(1): 19-26, 1988 Oct.
Article in English | MEDLINE | ID: mdl-3054539

ABSTRACT

Concentrates of the epimastigote stage of Trypanosoma cruzi stocks derived from single cell clones and cultured under identical conditions display a spectrum of 'colors' varying from dark brown to milk white. The color of the concentrate is reproducible for a parasite stock. An essential component of the culture medium for epimastigote growth is hemin, an iron-containing compound. Consequently, it seemed possible that the color spectrum of the epimastigote stocks reflected differences in the uptake, concentration or utilization of iron. This report describes the quantitative studies utilizing electron probe X-ray elemental mapping, energy dispersive X-ray microanalysis, and energy dispersive X-ray fluorescence spectrometry of the epimastigote stage of two T. cruzi stocks (CA-I/72 and HO-3/15) which display extreme color differences. Striking and statistically significant quantitative differences were found in the levels of Fe, Zn, and K between the two stocks. On the basis of atomic ratios, the CA-I/72 stock contains approximately two-fold more Fe per cell than the HO-3/15 stock. However, in the case of Zn the ratio is reversed; the HO-3/15 stock contains approximately two-fold more Zn per cell than the CA-I/72 stock. The marked inter-stock differences which exist in the levels of several elements could modulate the pathogenicity, survival, or adaptability of T. cruzi and, consequently, be important factors in our understanding of the complex problem of Chagas' disease.


Subject(s)
Trypanosoma cruzi/analysis , Animals , Color , Electron Probe Microanalysis , Trypanosoma cruzi/ultrastructure
9.
Am Ind Hyg Assoc J ; 36(10): 755-9, 1975 Oct.
Article in English | MEDLINE | ID: mdl-1180209

ABSTRACT

Preparation of samples of known concentration of hydrogen fluoride, arsine and phosgene in air from 0.5 to 10 times the TLV is described. These are required to evaluate and calibrate analytical monitoring devices used for measuring these gases in work atmospheres. Dynamic gas-blending systems have been constructed and evaluated at the National Bureau of Standards for preparing these samples. Measurements to estimate the long term concentration stability of these gases are also included.


Subject(s)
Acids/analysis , Air Pollutants, Occupational/analysis , Air Pollutants/analysis , Arsenic/analysis , Hydrofluoric Acid/analysis , Occupational Medicine/instrumentation , Phosgene/analysis , Maximum Allowable Concentration , Methods
SELECTION OF CITATIONS
SEARCH DETAIL
...