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1.
J Am Geriatr Soc ; 67(11): 2298-2304, 2019 11.
Artigo em Inglês | MEDLINE | ID: mdl-31335969

RESUMO

OBJECTIVES: Whether early medication reconciliation and integration can reduce polypharmacy and potentially inappropriate medication (PIM) in the emergency department (ED) remains unclear. Polypharmacy and PIM have been recognized as significant causes of adverse drug events in older adults. Therefore, this pilot study was conducted to delineate this issue. DESIGN: An interventional study. SETTING: A medical center in Taiwan. PARTICIPANTS: Older ED patients (aged ≥65 years) awaiting hospitalization between December 1, 2017, and October 31, 2018 were recruited in this study. A multidisciplinary team and a computer-based and pharmacist-assisted medication reconciliation and integration system were implemented. MEASUREMENTS: The reduced proportions of major polypharmacy (≥10 medications) and PIM at hospital discharge were compared with those on admission to the ED between pre- and post-intervention periods. RESULTS: A total of 911 patients (pre-intervention = 243 vs post-intervention = 668) were recruited. The proportions of major polypharmacy and PIM were lower in the post-intervention than in the pre-intervention period (-79.4% vs -65.3%; P < .001, and - 67.5% vs -49.1%; P < .001, respectively). The number of medications was reduced from 12.5 ± 2.7 to 6.9 ± 3.0 in the post-intervention period in patients with major polypharmacy (P < .001). CONCLUSION: Early initiation of computer-based and pharmacist-assisted intervention in the ED for reducing major polypharmacy and PIM is a promising method for improving geriatric care and reducing medical expenditures. J Am Geriatr Soc 67:2298-2304, 2019.


Assuntos
Revisão de Uso de Medicamentos/métodos , Serviço Hospitalar de Emergência/estatística & dados numéricos , Prescrição Inadequada/prevenção & controle , Reconciliação de Medicamentos/tendências , Serviço de Farmácia Hospitalar/organização & administração , Polimedicação , Lista de Medicamentos Potencialmente Inapropriados/tendências , Idoso , Idoso de 80 Anos ou mais , Feminino , Avaliação Geriátrica , Hospitalização , Humanos , Prescrição Inadequada/estatística & dados numéricos , Masculino , Reconciliação de Medicamentos/métodos , Conduta do Tratamento Medicamentoso/organização & administração , Estudos Prospectivos , Taiwan
2.
J Agric Food Chem ; 62(16): 3644-8, 2014 Apr 23.
Artigo em Inglês | MEDLINE | ID: mdl-24684565

RESUMO

The residues of four insecticides belonging to different families were studied on head lettuce (Lactuca sativa L. var. capitata L.), cabbage (Brassica oleracea Linn. var. capitata DC.), Chinese cabbage (Brassica pekinensis Skeels), and broccoli (Brassica oleracea var. italica) after pesticide application. To reduce application variability, a tank mix of acetamiprid 20% SP, chlorpyrifos 22.5% EC, deltamethrin 2.4% SC, and methomyl 40% SP was applied at recommended and double doses. Initial deposits of all pesticides on head lettuce were higher than those of the other three crops. The residues of chlorpyrifos and deltamethrin were higher than the maximum residue limits (MRLs) at recommended preharvest intervals (PHIs) on head lettuce and Chinese broccoli treated with higher doses. The residues of methomyl on head lettuce also showed the same phenomenon.


Assuntos
Brassica/química , Contaminação de Alimentos/análise , Inseticidas/análise , Lactuca/química , Resíduos de Praguicidas/análise , Brassica/crescimento & desenvolvimento , Clorpirifos/análise , Lactuca/crescimento & desenvolvimento , Neonicotinoides , Nitrilas/análise , Piretrinas/análise , Piridinas/análise
3.
Bioorg Med Chem ; 16(4): 1957-65, 2008 Feb 15.
Artigo em Inglês | MEDLINE | ID: mdl-18024043

RESUMO

A type of new 1,2,3,4-tetrahydroisoquinoline derivatives was synthesized via concise procedure from commercially available tetrahydroisoquinoline. These derivatives were delicately designed to possess propargyl-related pharmacophores simulated with a monoamine oxidase inhibitor rasagiline. We investigated the effect of these synthetic tetrahydroisoquinoline derivatives on the regulation of proteolytic processing of amyloid precursor protein (APP) by an ERK-dependent signaling pathway. Additionally, these compounds were also evaluated on the prevention of the proteolytic processing of C99 as gamma-secretase inhibitors by using a highly efficient cell-based reporter gene assay for gamma-secretase. The results suggested that certain compounds might be explored to possess both sAPPalpha-releasing stimulation and gamma-secretase inhibitory potency, which may reflect the synergetic potential of neuroprotective activities for the treatment of Alzheimer's disease as they possessed both ERK activation and inhibition of amyloidogenic Abeta release.


Assuntos
Precursor de Proteína beta-Amiloide/metabolismo , Peptídeo Hidrolases/metabolismo , Tetra-Hidroisoquinolinas/farmacologia , Doença de Alzheimer/tratamento farmacológico , Secretases da Proteína Precursora do Amiloide/antagonistas & inibidores , MAP Quinases Reguladas por Sinal Extracelular/metabolismo , Humanos , Hidrólise/efeitos dos fármacos , Fármacos Neuroprotetores , Tetra-Hidroisoquinolinas/química
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