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1.
An. bras. dermatol ; 91(5): 652-654, Sept.-Oct. 2016. graf
Artigo em Inglês | LILACS | ID: biblio-827762

RESUMO

Abstract: Non-steroidal, anti-inflammatory drugs, followed by antibiotics, are the main causes of fixed drug eruption. They provoke one or several round erythematous or bullous lesions that recur in the same place after taking the causative medication. A positive patch test on residual, lesional skin can replace satisfactorily oral reintroduction. We describe the case of a 74-year-old woman with numerous, rounded, erythematous lesions on the trunk and recurrent blistering on the fifth right-hand finger, which developed a few hours after taking etoricoxib. Lesional patch testing with etoricoxib was positive and reproduced the typical pattern of a fixed drug eruption upon histopathology. We emphasize the specific reactivity of the etoricoxib patch test, and the capacity to reproduce the histologic pattern of the reaction.


Assuntos
Humanos , Feminino , Idoso , Piridinas/efeitos adversos , Sulfonas/efeitos adversos , Testes do Emplastro/métodos , Toxidermias/etiologia , Inibidores de Ciclo-Oxigenase 2/efeitos adversos , Toxidermias/patologia
2.
Braz. oral res. (Online) ; 30(1): e127, 2016. tab, graf
Artigo em Inglês | LILACS | ID: biblio-951983

RESUMO

Abstract The consumption of low-dose aspirin (LDA) to prevent cardiovascular disease continues to increase worldwide. Consequently, the number of chronic LDA users seeking dental procedures that require complementary acute anti-inflammatory medication has also grown. Considering the lack of literature evaluating this interaction, we analyzed the gastric and renal effects caused by a selective COX-2 inhibitor (etoricoxib) and a non-selective COX-2 inhibitor (ibuprofen) nonsteroidal anti-inflammatory drug (NSAID) in rats receiving chronic LDA therapy. Male Wistar rats were divided into six experimental groups (carboxymethylcellulose (CMC) - vehicle; LDA; LDA + ibuprofen; ibuprofen; LDA + etoricoxib; and etoricoxib) and submitted to long-term LDA therapy with a subsequent NSAID administration for three days by gavage. After the experimental period, we analyzed gastric and renal tissues and quantified serum creatinine levels. The concomitant use of LDA with either NSAID induced the highest levels of gastric damage when compared to the CMC group (F = 20.26, p < 0.05). Treatment with either LDA or etoricoxib alone was not associated with gastric damage. No significant damage was observed on kidney morphology and function (F = 0.5418, p > 0.05). These results suggest that even the acute use of an NSAID (regardless of COX-2 selectivity) can induce gastric damage when combined with the long-term use of low-dose aspirin in an animal model. Additional studies, including clinical assessments, are thus needed to clarify this interaction, and clinicians should be careful of prescribing NSAIDs to patients using LDA.


Assuntos
Animais , Masculino , Inibidores da Agregação Plaquetária/administração & dosagem , Anti-Inflamatórios não Esteroides/efeitos adversos , Aspirina/administração & dosagem , Inibidores de Ciclo-Oxigenase 2/efeitos adversos , Mucosa Gástrica/efeitos dos fármacos , Rim/efeitos dos fármacos , Piridinas/efeitos adversos , Gastropatias/induzido quimicamente , Sulfonas/efeitos adversos , Fatores de Tempo , Doenças Cardiovasculares/prevenção & controle , Distribuição Aleatória , Ibuprofeno/efeitos adversos , Fatores de Risco , Resultado do Tratamento , Ratos Wistar , Creatinina/sangue , Etoricoxib , Nefropatias/induzido quimicamente
3.
Journal of Korean Medical Science ; : 561-567, 2011.
Artigo em Inglês | WPRIM | ID: wpr-173905

RESUMO

This is a cross-sectional observational study undertaken to explore the current prescription pattern of non-steroidal anti-inflammatory drugs (NSAIDs) and the prevalence of NSAID-induced gastrointestinal (GI) risk factors of orthopaedic patients in real clinical practice in Korea. Study cohort included 3,140 orthopaedic outpatients at 131 hospitals and clinics between January 2008 and August 2008. A self-administered questionnaire was completed by each patient and physician. A simplified risk scoring scale (the Standardized Calculator of Risk for Events; SCORE) was used to measure patients' risk for GI complications. The pattern of NSAIDs prescription was identified from medical recordings. Forty-five percents of the patients belonged to high risk or very high risk groups for GI complications. The cyclooxygenase-2 enzyme (COX-2) selective NSAID showed a propensity to be prescribed more commonly for high/very high GI risk groups, but the rate was still as low as 51%. In conclusion, physician's considerate prescription of NSAIDs with well-understanding of each patient's GI risk factors is strongly encouraged in order to maximize cost effectiveness and to prevent serious GI complications in Korea. Other strategic efforts such as medical association-led education programs and application of Korean electronic SCORE system to hospital order communication system (OCS) should also be accompanied in a way to promote physician's attention.


Assuntos
Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Anti-Inflamatórios não Esteroides/efeitos adversos , Estudos de Coortes , Estudos Transversais , Ciclo-Oxigenase 2/metabolismo , Inibidores de Ciclo-Oxigenase 2/efeitos adversos , Prescrições de Medicamentos , Gastroenteropatias/induzido quimicamente , Doenças Musculoesqueléticas/complicações , Prevalência , Inquéritos e Questionários , República da Coreia , Fatores de Risco
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