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1.
Gastroenterology ; 137(4): 1229-37; quiz 1518-9, 2009 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19549528

RESUMO

BACKGROUND & AIMS: Endoscopist-directed propofol sedation (EDP) remains controversial. We sought to update the safety experience of EDP and estimate the cost of using anesthesia specialists for endoscopic sedation. METHODS: We reviewed all published work using EDP. We contacted all endoscopists performing EDP for endoscopy that we were aware of to obtain their safety experience. These complications were available in all patients: endotracheal intubations, permanent neurologic injuries, and death. RESULTS: A total of 646,080 (223,656 published and 422,424 unpublished) EDP cases were identified. Endotracheal intubations, permanent neurologic injuries, and deaths were 11, 0, and 4, respectively. Deaths occurred in 2 patients with pancreatic cancer, a severely handicapped patient with mental retardation, and a patient with severe cardiomyopathy. The overall number of cases requiring mask ventilation was 489 (0.1%) of 569,220 cases with data available. For sites specifying mask ventilation risk by procedure type, 185 (0.1%) of 185,245 patients and 20 (0.01%) of 142,863 patients required mask ventilation during their esophagogastroduodenoscopy or colonoscopy, respectively (P < .001). The estimated cost per life-year saved to substitute anesthesia specialists in these cases, assuming they would have prevented all deaths, was $5.3 million. CONCLUSIONS: EDP thus far has a lower mortality rate than that in published data on endoscopist-delivered benzodiazepines and opioids and a comparable rate to that in published data on general anesthesia by anesthesiologists. In the cases described here, use of anesthesia specialists to deliver propofol would have had high costs relative to any potential benefit.


Assuntos
Anestesia , Anestésicos Intravenosos/efeitos adversos , Endoscopia , Propofol/administração & dosagem , Anestesia/efeitos adversos , Anestesia/economia , Anestésicos Intravenosos/administração & dosagem , Anestésicos Intravenosos/economia , Competência Clínica , Qualidade de Produtos para o Consumidor , Análise Custo-Benefício , Endoscopia/economia , Saúde Global , Custos de Cuidados de Saúde , Humanos , Intubação Intratraqueal , Máscaras , Guias de Prática Clínica como Assunto , Propofol/efeitos adversos , Propofol/economia , Respiração Artificial/instrumentação , Medição de Risco
2.
Dig Dis Sci ; 52(6): 1505-12, 2007 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-17464561

RESUMO

In this randomized, double-blind, multicenter study, H. pylori-positive patients with an active duodenal ulcer (DU) received esomeprazole, 20 mg twice daily (bid), or omeprazole, 20 mg bid, with amoxicillin, 1000 mg bid, and clarithromycin, 500 mg bid, for 1 week (EAC and OAC, respectively). Patients received an additional 3 weeks of either placebo or omeprazole, 20 mg once daily (od), in the EAC and OAC groups, respectively. The intent-to-treat population included 374 patients (EAC, 186; OAC, 188). Four-week DU healing rates were similar in the EAC+placebo and OAC+omeprazole groups: 74% and 76%, respectively. DU healing rates at 8 weeks were 87% for EAC+placebo and 88% for OAC+omeprazole. H. pylori eradication rates were 75% and 79% for EAC and OAC, respectively. Both regimens were well tolerated. A 1-week regimen of esomeprazole-based H. pylori eradication triple therapy was as effective for DU healing and eradication of H. pylori as omeprazole-based triple therapy followed by an additional 3 weeks of monotherapy.


Assuntos
Antiulcerosos/administração & dosagem , Úlcera Duodenal/tratamento farmacológico , Infecções por Helicobacter/tratamento farmacológico , Helicobacter pylori/efeitos dos fármacos , Omeprazol/administração & dosagem , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Antiulcerosos/efeitos adversos , Método Duplo-Cego , Úlcera Duodenal/microbiologia , Esomeprazol , Feminino , Infecções por Helicobacter/etnologia , Infecções por Helicobacter/microbiologia , Humanos , Masculino , Pessoa de Meia-Idade , Omeprazol/efeitos adversos
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