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1.
Hum Exp Toxicol ; 37(2): 107-117, 2018 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-29233028

RESUMO

BACKGROUND: In aluminum phosphide (AlP) poisoning, death is mainly due to cardiovascular failure and refractory acute heart failure. There is a lot of evidence showing thyroid hormones have cardioprotective effects. OBJECTIVE: The purpose of this study was to evaluate the effect of oral liothyronine in the treatment of AlP poisoning. METHODS: Twenty-four patients from intensive care unit of Baharloo Hospital, Tehran, Iran, were included based on the inclusion and exclusion criteria. They were randomly divided into two parallel groups of 12 cases and 12 controls. Intervention in the case group was administration of 50 µg liothyronine via nasogastric tube after gastric lavage, in the first 6 h of poisoning. In both groups, the routine treatment of AlP poisoning was performed. Blood samples were prepared at the beginning of the study and after 12 h. Patients were followed up till discharge from the hospital or death. RESULTS: The findings demonstrated that oral liothyronine was able to significantly improve systolic blood pressure, arterial blood pH, and total thiol molecules and also could decrease lipid peroxidation, increase catalase activity, and prevent further decline in total antioxidant capacity. CONCLUSION: Liothyronine administration is effective in controlling AlP poisoning and can improve patients' outcome.


Assuntos
Compostos de Alumínio/intoxicação , Antídotos/administração & dosagem , Doenças Cardiovasculares/tratamento farmacológico , Praguicidas/intoxicação , Fosfinas/intoxicação , Tri-Iodotironina/administração & dosagem , Administração Oral , Adulto , Antídotos/efeitos adversos , Biomarcadores/sangue , Pressão Sanguínea/efeitos dos fármacos , Doenças Cardiovasculares/induzido quimicamente , Doenças Cardiovasculares/mortalidade , Doenças Cardiovasculares/fisiopatologia , Feminino , Humanos , Concentração de Íons de Hidrogênio , Irã (Geográfico) , Peroxidação de Lipídeos/efeitos dos fármacos , Masculino , Estresse Oxidativo/efeitos dos fármacos , Fatores de Tempo , Resultado do Tratamento , Tri-Iodotironina/efeitos adversos
2.
Hum Exp Toxicol ; 34(5): 445-59, 2015 May.
Artigo em Inglês | MEDLINE | ID: mdl-25378092

RESUMO

Several studies have indicated the harmful effect of flare-up periods in pregnant women with inflammatory bowel disease (IBD) on their newborns. Therefore, an effective and safe medical treatment during pregnancy is of great concern in IBD patients. The aim of this study was to perform a meta-analysis on the outcomes of thiopurines use and a systematic review of antitumor necrosis factor (anti-TNF) drugs used during pregnancy in women with IBD. The results of cohorts evaluating the safety of anti-TNF drugs during pregnancy up to July 2013 were collected and analyzed. In the meta-analysis, a total of 312 pregnant women with IBD who used thiopurines were compared with 1149 controls (women with IBD who were not treated with any medication and women who were exposed to drugs other than thiopurines) to evaluate the drug effect on different pregnancy outcomes, including prematurity, low birth weight, congenital abnormalities, spontaneous abortion, and neonatal adverse outcomes. Results of statistical analysis demonstrated that congenital abnormalities were increased significantly in thiopurine-exposed group in comparison with control group who did not receive any medicine for IBD treatment. The summary odds ratio was 2.95 with 95% confidence interval = 1.03-8.43 (p = 0.04). We observed no significant differences in occurrence of other adverse pregnancy outcomes between compared groups. The results of cohorts evaluated the safety of anti-TNF drugs during pregnancy demonstrated no increase in occurrence of adverse pregnancy outcomes in comparison with controls except for the significant decrease in gestational age of newborns of drug-exposed mothers in one trial. In conclusion, a benefit-risk ratio should be considered in prescribing or continuing medicinal therapy during pregnancy of IBD patients.


Assuntos
Azatioprina/efeitos adversos , Doenças Inflamatórias Intestinais/tratamento farmacológico , Infliximab/efeitos adversos , Complicações na Gravidez/tratamento farmacológico , Resultado da Gravidez/epidemiologia , Efeitos Tardios da Exposição Pré-Natal/epidemiologia , Fator de Necrose Tumoral alfa/imunologia , Adulto , Azatioprina/administração & dosagem , Azatioprina/uso terapêutico , Feminino , Humanos , Doenças Inflamatórias Intestinais/epidemiologia , Doenças Inflamatórias Intestinais/imunologia , Infliximab/administração & dosagem , Infliximab/uso terapêutico , Gravidez , Complicações na Gravidez/epidemiologia , Complicações na Gravidez/imunologia , Efeitos Tardios da Exposição Pré-Natal/induzido quimicamente
4.
East Mediterr Health J ; 10(3): 406-15, 2004 May.
Artigo em Inglês | MEDLINE | ID: mdl-16212218

RESUMO

Prescribing, dispensing, availability and affordability of drugs were evaluated in 100 primary health care centres in 5 provinces of the Islamic Republic of Iran using WHO indicators. On average, 92% of the 12 essential drugs monitored were available in the health centre pharmacies and 95% of the drugs prescribed by the physician were dispensed by the health centre pharmacy. The stock-out duration was less than 1 month on average. A complete treatment for pneumonia cost only 2% of the lowest weekly government salary. The national average number of drugs per prescription was 3.4. Prescription of antibiotics and injectable drugs was very high (58% and 41% respectively). Although availability and affordability of essential drugs is good in this country, rational use of drugs needs to be emphasized.


Assuntos
Prescrições de Medicamentos/estatística & dados numéricos , Medicamentos Essenciais , Acessibilidade aos Serviços de Saúde/estatística & dados numéricos , Padrões de Prática Médica/estatística & dados numéricos , Antibacterianos/economia , Antibacterianos/uso terapêutico , Custos de Medicamentos/estatística & dados numéricos , Armazenamento de Medicamentos/estatística & dados numéricos , Uso de Medicamentos/economia , Medicamentos Essenciais/economia , Medicamentos Essenciais/provisão & distribuição , Medicamentos Essenciais/uso terapêutico , Eficiência Organizacional , Fidelidade a Diretrizes/estatística & dados numéricos , Pesquisas sobre Atenção à Saúde , Política de Saúde , Necessidades e Demandas de Serviços de Saúde , Humanos , Irã (Geográfico) , Programas Nacionais de Saúde/organização & administração , Farmácias/organização & administração , Farmacopeias como Assunto , Pneumonia/tratamento farmacológico , Pneumonia/economia , Guias de Prática Clínica como Assunto , Indicadores de Qualidade em Assistência à Saúde , Salários e Benefícios/estatística & dados numéricos
5.
Gen Pharmacol ; 25(1): 139-42, 1994 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-8026698

RESUMO

1. Subcutaneous (s.c.) administration of morphine to mice induced a dose-dependent antinociception. 2. Pretreatment of animals with adenosine receptor antagonists NECA (5'-N-ethylcarboxamide-adenosine) and L-PIA (N6-phenylisopropyladenosine) potentiated, while adenosine agonist CHA (N6-cyclohexyladenosine) decreased the morphine response. 3. Adenosine antagonist theophylline decreased, but adenosine receptor antagonist 8-PT (8-phenyltheophylline) increased the antinociception effect of morphine. Inhibitory effect of CHA on morphine antinociception was also reversed by 8-PT pretreatment. 4. NECA or L-PIA induced a high degree of antinociceptive effect in animals pretreated with 8-PT. 5. Dipyridamole pretreatment did not alter the effect of morphine. 6. It is concluded that A-1 and/or A-2 adenosine receptors are involved in morphine antinociception and the adenosine mechanism(s) may exert a modulatory role in this respect.


Assuntos
Morfina/farmacologia , Nociceptores/efeitos dos fármacos , Antagonistas de Receptores Purinérgicos P1 , Antagonistas do Receptor Purinérgico P2 , Receptores Purinérgicos P1/fisiologia , Receptores Purinérgicos P2/fisiologia , Adenosina/análogos & derivados , Adenosina/farmacologia , Adenosina-5'-(N-etilcarboxamida) , Animais , Dipiridamol/farmacologia , Relação Dose-Resposta a Droga , Masculino , Camundongos , Fenilisopropiladenosina/farmacologia , Cauda/efeitos dos fármacos , Cauda/fisiologia , Teofilina/análogos & derivados , Teofilina/farmacologia
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