Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 9 de 9
Filtrar
1.
Contact Dermatitis ; 89(6): 471-479, 2023 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-37667591

RESUMO

BACKGROUND: Allergic contact dermatitis from (meth)acrylic monomers (ACDMA) in manicure products is increasing. OBJECTIVE: To evaluate the prognosis, work performance impairment and sequelae of a cohort of beauticians and manicure consumers with ACDMA sensitized from the exposure to manicure products. METHODS: We conducted a telephone survey with patients diagnosed with ACDMA. RESULTS: One hundred and six patients were evaluated, including 75 (70.8%) beauticians and 31 (29.2%) consumers. All were women with a mean age of 39 (19-62). Thirty-seven of 75 beauticians (49.3%) continued to work. Twenty-seven of 106 (25.5%) patients continued to use manicure products with (meth)acrylates regularly. Seventeen of 51 (33.3%) patients who discontinued the exposure described ongoing nail/periungual changes. Nine of 58 (15.5%) patients who required dental restoration, orthodontic or occlusal splint materials recalled reactions from them; and, 25 of 96 (26%) who used sanitary napkins recalled intolerance to them starting after the diagnosis of ACDMA. Fifteen of 25 (60%) discontinued the use of sanitary napkins. CONCLUSION: 49.3% beauticians continued to work; most patients stopped wearing acrylic manicure materials; reactions from dental materials were not uncommon, however, removal of dental materials was never required; and, reactions to sanitary napkins developing after the diagnosis of ACDMA were common most leading to discontinuation of use.


Assuntos
Dermatite Alérgica de Contato , Dermatite Ocupacional , Humanos , Feminino , Adulto , Masculino , Dermatite Alérgica de Contato/diagnóstico , Acrilatos/efeitos adversos , Testes do Emplastro , Prognóstico , Materiais Dentários , Metacrilatos/efeitos adversos
4.
Cir. Esp. (Ed. impr.) ; 100(12): 768-771, dic. 2022. ilus, tab
Artigo em Espanhol | IBECS | ID: ibc-212489

RESUMO

Introducción: La estenosis aórtica severa es una enfermedad mortal en caso de no ser intervenida. Este estudio pretende conocer el impacto de la pandemia por COVID-19 en la mortalidad de pacientes con estenosis severa durante la primera ola y compararlo con el mismo período del año anterior. Métodos: Se analizaron mediante software basado en inteligencia artificial todos los pacientes que acudieron al hospital en una región española durante la primera ola y en el año anterior, evaluándose la mortalidad comparada entre pacientes con estenosis aórtica severa con y sin COVID-19 durante la pandemia y la era pre-COVID. Se comparó la mortalidad en tres grupos diferentes. En cuanto al número de cirugías cardiacas, se observó una tendencia a la baja en los pacientes sin COVID-19 con respecto al mismo período del año anterior (p = 0,07), y un descenso significativo entre pacientes COVID-19 positivo y COVID-19 negativo. Resultados: Durante la primera ola, acudieron un 13,82% menos de pacientes. Un total de 1.112 tenían estenosis aórtica, de los cuales un 5,48% fueron COVID-19 positivo. La mortalidad fue mayor (p=0,01) en COVID-19 negativo durante la pandemia (4,37%) frente a los de la era pre-COVID-19 (2,57%); también lo fue en el grupo COVID-19 positivo (11,47%) frente a los COVID-19 negativo (4,37%) durante la primera ola (p=0,01). Se observó una tendencia a la disminución de cirugías (p=0,07) en los pacientes COVID-19 negativo durante la pandemia y disminuyeron significativamente en pacientes COVID-19 positivo, frente a los COVID-19 negativo (p=0,04). Conclusiones: El estudio reveló una disminución de los pacientes que acudieron al hospital y un exceso de mortalidad en pacientes con estenosis aórtica severa sin la infección durante la primera ola, frente al mismo período del año anterior; y también, en los pacientes COVID-19 positivo, frente a los COVID-19 negativo. (AU)


Introduction: Untreated, severe, symptomatic aortic stenosis is associated with an ominous diagnosis without intervention. This study aims to determine the impact of the COVID-19 pandemic on the mortality of patients with severe stenosis during the first wave and compare it with the same period last year. Methods: All patients who went to the hospitals in an Spanish region during the first wave, and in the same period of previous year, were analyzed using artificial intelligence-based software, evaluating the mortality of patients with severe aortic stenosis with and without COVID-19 during the pandemic and the pre-COVID era. Mortality of the 3 groups was compared. Regarding cardiac surgeries was a tendency to decrease (P=.07) in patients without COVID-19 between the pandemic and the previous period was observed. A significant decrease of surgeries between patients with COVID-19 and without COVID-19 was shown. Results: Data showed 13.82% less admitted patients during the first wave. A total of 1,112 of them had aortic stenosis and 5.48% were COVID-19 positive. Mortality was higher (P=.01), in COVID-19 negative during the pandemic (4.37%) versus those in the pre-COVID-19 era (2.57%); it was also in the COVID-19 positive group (11.47%), versus COVID-19 negative (4.37%) during the first wave (P=.01). Conclusions: The study revealed a decrease in patients who went to the hospital and an excess of mortality in patients with severe aortic stenosis without infection during the first wave, compared to the same period last year; and also, in COVID-19 positive patients versus COVID-19 negative. (AU)


Assuntos
Humanos , Pandemias , Infecções por Coronavirus/epidemiologia , Inteligência Artificial , Estenose da Valva Aórtica/mortalidade , Software , Cirurgia Torácica
5.
Cir Esp (Engl Ed) ; 100(12): 768-771, 2022 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-36064176

RESUMO

INTRODUCTION: Untreated, severe, symptomatic aortic stenosis is associated with an ominous diagnosis without intervention. This study aims to determine the impact of the COVID-19 pandemic on the mortality of patients with severe stenosis during the first wave and compare it with the same period last year. METHODS: All patients who went to the hospitals in a spanish region during the first wave, and in the same period of previous year, were analysed using Artificial Intelligence-based software, evaluating the mortality of patients with severe aortic stenosis with and without COVID-19 during the pandemic and the pre-COVID era. Mortality of the three groups were compared. Regarding cardiac surgeries was a tendency to decrease (p = .07) in patients without COVID-19 between the pandemic and the previous period was observed. A significant decrease of surgeries between patients with COVID-19 and without COVID-19 was shown. RESULTS: Data showed 13.82% less admitted patients during the first wave. 1112 of them, had aortic stenosis and 5.48% were COVID-19 positive. Mortality was higher (p = .01), in COVID-19 negative during the pandemic (4.37%) versus those in the pre-COVID19 era (2.57%); it was also in the COVID-19 positive group (11.47%), versus covid-19 negative (4.37%) during the first wave (p = .01). CONCLUSIONS: The study revealed a decrease in patients who went to the hospital and an excess of mortality in patients with severe AD without infection during the first wave, compared to the same period last year; and also, in COVID-19 positive patients versus COVID-19 negative.


Assuntos
Estenose da Valva Aórtica , COVID-19 , Humanos , Pandemias , Inteligência Artificial , Fatores de Risco , Estenose da Valva Aórtica/complicações , Estenose da Valva Aórtica/cirurgia , Estenose da Valva Aórtica/diagnóstico
6.
Cir Esp ; 100(12): 768-771, 2022 Dec.
Artigo em Espanhol | MEDLINE | ID: mdl-34393253

RESUMO

Introduction: Untreated, severe, symptomatic aortic stenosis is associated with an ominous diagnosis without intervention. This study aims to determine the impact of the COVID-19 pandemic on the mortality of patients with severe stenosis during the first wave and compare it with the same period last year. Methods: All patients who went to the hospitals in an Spanish region during the first wave, and in the same period of previous year, were analyzed using artificial intelligence-based software, evaluating the mortality of patients with severe aortic stenosis with and without COVID-19 during the pandemic and the pre-COVID era. Mortality of the 3 groups was compared. Regarding cardiac surgeries was a tendency to decrease (P = .07) in patients without COVID-19 between the pandemic and the previous period was observed. A significant decrease of surgeries between patients with COVID-19 and without COVID-19 was shown. Results: Data showed 13.82% less admitted patients during the first wave. A total of 1,112 of them had aortic stenosis and 5.48% were COVID-19 positive. Mortality was higher (P = .01), in COVID-19 negative during the pandemic (4.37%) versus those in the pre-COVID-19 era (2.57%); it was also in the COVID-19 positive group (11.47%), versus COVID-19 negative (4.37%) during the first wave (P = .01). Conclusions: The study revealed a decrease in patients who went to the hospital and an excess of mortality in patients with severe aortic stenosis without infection during the first wave, compared to the same period last year; and also, in COVID-19 positive patients versus COVID-19 negative.

7.
Br J Gen Pract ; 57(541): 653-4, 2007 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-17688761

RESUMO

This is a descriptive study designed to assess the predictive value of intraocular pressure (IOP) measurement in GPs' offices in an urban healthcare site using Tono-pen XL. A total of 2044 patients, aged > or =40 years, were enrolled by consecutive sampling from patients visiting the GP. Those participants who had IOP > or =21 mmHg were referred to the ophthalmologist. Of the 226 then tested, ocular hypertension was confirmed in 100 participants (4.89%, 95% CI [confidence interval] = 3.93 to 5.85%). Predictive value was 44.2%. These results suggest the validity of using Tono-pen XL in the GP's office to detect ocular hypertension.


Assuntos
Medicina de Família e Comunidade , Glaucoma/prevenção & controle , Pressão Intraocular/fisiologia , Hipertensão Ocular/diagnóstico , Tonometria Ocular/instrumentação , Adulto , Idoso , Estudos Transversais , Feminino , Glaucoma/complicações , Humanos , Masculino , Pessoa de Meia-Idade , Hipertensão Ocular/complicações , Valor Preditivo dos Testes , Espanha
8.
Exp Eye Res ; 82(4): 583-7, 2006 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-16256986

RESUMO

Lens autofluorescence originates from an accumulation of fluorescent substances such as the tryptophan-derived residues and protein aggregations, which are associated with the preclinical progress of cataractogenesis, diabetes and lens aging. Our purpose is to determine if pregnancy alters the typical constituents of the lens autofluorescence. Fifteen healthy pregnant women (22 eyes) who were in their third trimester of pregnancy and 23 age-matched healthy controls (37 eyes, non-pregnant females). Lens autofluorescence, lens transmission and corneal autofluorescence were studied with fluorophotometry. The lens autofluorescence values were 358+/-151 ng ml(-1) in the control group and 201+/-110 ng ml(-1) in the pregnants women. The difference was significant (p=0.0074). Lens transmission values were 0.93+/-0.02 ng ml(-1) in the control group and 0.94+/-0.02 ng ml(-1) in the pregnants women: the difference was not significant. Corneal autofluorescence values were 21.9+/-7.5 ng ml(-1) in the control group and 18.2+/-5.8 ng ml(-1) in the pregnant women. The difference was not significant. Our study showed a significant decrease in lens autofluorescence in pregnant women compared to a normal population. The decrease can be partly attributed to the aqueous component of the lens that increases significantly during the final trimester of pregnancy and that this provokes a dilution of the fluorescent substances.


Assuntos
Cristalino/fisiologia , Gravidez/fisiologia , Adulto , Córnea/fisiologia , Feminino , Fluorescência , Fluorofotometria/métodos , Humanos , Terceiro Trimestre da Gravidez
9.
J Rheumatol ; 31(2): 308-14, 2004 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-14760802

RESUMO

OBJECTIVE: Local corticosteroid injections, commonly accepted by rheumatologists to be effective treating painful shoulder, have shown controversial results. High frequency ultrasonography is an accurate and safe imaging modality for guiding musculoskeletal injections. We prospectively compared the short term response to randomized blind injection versus sonographic-guided injection of local corticosteroid in patients with painful shoulder. METHODS: We studied 41 consecutive patients with painful shoulder. Patients with previous trauma or chronic inflammatory arthritis were excluded. No patient had received previous physiotherapy or local steroid injection in the shoulder. Patients were randomized to receive either a blind subacromial injection of 20 mg triamcinolone (Group 1, n = 20) or a sonographic guided injection of 20 mg triamcinolone (Group 2, n = 21) by the same rheumatologist blinded to the clinical evaluation. In both groups we recorded shoulder abnormalities and the location of the steroid postinjection by ultrasound. Each patient was clinically assessed within 5 days before injection and 6 weeks after injection by another rheumatologist without knowledge of the injection technique performed. Clinical assessment included demographic and clinical data, a visual analog scale (VAS) for pain (0-100), the Shoulder Function Assessment (SFA) scale (0-70), and postinjection adverse effects. No patient received physical therapy during the followup period. Initially, demographic, clinical, and ultrasonographic findings in both groups showed no significant differences. RESULTS: Six weeks after injection, the VAS and the SFA score showed a significantly greater improvement in Group 2 compared with Group 1 (mean VAS score change 34.9 for Group 2 vs 7.1 for Group 1, p < 0.001; and mean SFA score change 15 for Group 2 vs 5.6 for Group 1, p = 0.012). One patient in Group 1 reported mild postinjection adverse effects. CONCLUSION: We suggest that sonographic-guided corticosteroid injections should be indicated, at least, in patients with poor response to previous blind injection to ensure accurate medication placement in order to improve therapeutic effectiveness.


Assuntos
Corticosteroides/administração & dosagem , Injeções Intra-Articulares/métodos , Dor/diagnóstico por imagem , Dor/tratamento farmacológico , Articulação do Ombro , Corticosteroides/efeitos adversos , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Medição da Dor , Palpação , Ultrassonografia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...