Mostrar mensagens com a etiqueta pneumonia nosocomial. Mostrar todas as mensagens
Mostrar mensagens com a etiqueta pneumonia nosocomial. Mostrar todas as mensagens

04 junho 2009

E O PANTOPRAZOL?

Acid-Suppressive Medication Use and the Risk for Hospital-Acquired Pneumonia

Shoshana J. Herzig, MD; Michael D. Howell, MD, MPH; Long H. Ngo, PhD; Edward R. Marcantonio, MD, SM

JAMA. 2009;301(20):2120-2128.


Quase todo paciente que interna no hospital ganha um pantoprazol (ou ranitidina), não é verdade? Afinal de contas, mal não faz, e podemos estar prevenindo o risco de hemorragia digestiva... Pois é, esse artigo recente publicado no JAMA avaliou 63878 admissões hospitalares (pacientes de baixo risco para hemorragia digestiva - internados fora do CTI e fora de ventilação mecânica) e descobriu que o uso de pantoprazol aumentava em 30% o risco de pneumonia nosocomial, principalmente por broncoaspiração. A ranitidina não apresentou essa associação, provavelmente porque o número de pacientes em uso de ranitidina era menor.

Cássia Righy



18 novembro 2008

Conhecendo melhor as infecções por bactérias multiresistentes

Para aumentar nosso conhecimento sobre infecções por Multiresistentes.


Research

Determinants and impact of multidrug antibiotic resistance in pathogens causing ventilator-associated-pneumonia

Pieter Depuydt et al

Critical Care 2008, 12:R142doi:10.1186/cc7119


Published: 17 November 2008

Abstract (provisional)

Introduction

It is still debated whether multidrug antibiotic resistance (MDR) in pathogens causing ventilator-associated pneumonia (VAP) is an independent risk factor for adverse outcome. We aimed to identify the determinants of multidrug antibiotic resistance (MDR) versus non-MDR microbial etiology in VAP and assessed whether MDR versus non-MDR VAP was independently associated with increased 30 days mortality.

Methods

We performed a retrospective analysis of a prospectively registered cohort of adult patients with microbiologically confirmed VAP, diagnosed at a university hospital intensive care unit during a three-year period. Determinants of MDR as compared to non-MDR microbial etiology and impact of MDR versus non-MDR etiology on mortality were investigated using multivariate logistic and competing risk regression analysis.

Results

MDR pathogens were involved in 52 of 192 episodes of VAP (27%): methicillin-resistant Staphylococcus aureus in 12 (6%), extended-spectrum beta-lactamase producing Enterobacteriaceae in 28 (15%), MDR Pseudomonas aeruginosa and other non-fermenting pathogens in 12 (6%). Multivariable logistic regression identified the Charlson index of comorbidity (OR 1.38, 95% CI 1.08-1.75, p=0.01) and previous exposure to more than two different antibiotic classes (OR 5.11, 95% CI 1.38-18.89, p=0.01) as predictors of MDR etiology. 30 days mortality following VAP caused by MDR versus non-MDR was 37% and 20% (p=0.02) respectively. A multivariate competing risk regression analysis showed that renal replacement therapy prior to VAP (Standardized Hazard Ratio (SHR) 2.69, 95% CI 1.47-4.94, p=0.01), the Charlson index of comorbidity (SHR 1.21, 95% CI 1.03 -1.41, p=0.03) and septic shock upon ICU admission (SHR 1.86, 95% CI 1.03 - 3.35, p=0.03), but not MDR etiology of VAP, were independent predictors of mortality.

Conclusions

The risk of MDR pathogens causing VAP was mainly determined by comorbidity and prior exposure to more than two antibiotics. The increased mortality of VAP caused by MDR as compared to non-MDR pathogens was explained by more severe comorbidity and organ failure prior to VAP.

07 fevereiro 2008

O Novo número da RBTI está online- clique nesse título

O Novo número da RBTI está online- siga o link no titulo acima!


ARTIGOS DA REVISTA RBTI VOLUME 19 EDIÇÃO 4

TÍTULO: Como Melhorar a Comunicação e Prevenir Conflitos nas Situações de Terminalidade na Unidade de Terapia Intensiva
AUTOR: RACHEL DUARTE MORITZ

TÍTULO: Cuidando da Família de Pacientes em Situação de Terminalidade Internados na Unidade de Terapia Intensiva
AUTOR: MARCIO SOARES

TÍTULO: Como Avaliar Criticamente Revisões Sistemáticas e Metanálises?
AUTOR: OTÁVIO BERWANGER

TÍTULO: Fator de Inibição da Migração de Macrófagos e Interleucina-6 na Síndrome de Esmagamento: Analogia com Gravidade? Relato de Casos
AUTOR: RITA VIANNA DE AZEVEDO

TÍTULO: Síndrome Pulmonar por Hantavírus com Disfunção de Múltiplos Órgãos. Relato de Caso
AUTOR: SUZANA MARGARETH AJEJE LOBO

TÍTULO: Necrose Isquêmica Hepática e Diabete Melito. Relato de Caso
AUTOR: TICIANA PAES

TÍTULO: Entendendo os Mecanismos Determinantes da Lesão Pulmonar Induzida pela Ventilação Mecânica
AUTOR: PATRÍCIA RIEKEN MACEDO ROCCO

TÍTULO: Estrongiloidíase Disseminada: Diagnóstico e Tratamento
AUTOR: JORGE IBRAIN FIGUEIRA SALLUH

TÍTULO: Medicina Intensiva na Graduação Médica: Perspectiva do Estudante
AUTOR: ALESSANDRO DE MOURA ALMEIDA

TÍTULO: Central de Ventiladores Mecânicos: Organização, Segurança e Qualidade
AUTOR: LILIAN KHELLEN GOMES DE PAULA

TÍTULO: Estudo Comparativo entre Traqueostomia Precoce e Tardia em Pacientes sob Ventilação Mecânica
AUTOR: SYLVIA CAROLINA ARANHA

TÍTULO: Determinantes da Evolução do Standard Base Excess em Pacientes com Choque Séptico
AUTOR: MARCELO PARK

TÍTULO: Déficit de Base à Admissão na Unidade de Terapia Intensiva. Um Indicador de Mortalidade Precoce
AUTOR: FRANCISCO ALBANO DE MENESES

TÍTULO: A Presença de Patógenos Respiratórios no Biofilme Bucal de Pacientes com Pneumonia Nosocomial
AUTOR: LUIZ CLÁUDIO BORGES SILVA DE OLIVERIA

TÍTULO: Pseudomonas Aeruginosa: Freqüência de Resistência a Múltiplos Fármacos e Resistência Cruzada entre Antimicrobianos no Recife/PE
AUTOR: EDUARDO ANDRADA PESSOA DE FIGUEIREDO

TÍTULO: Prevalência de Infecção Nosocomial em Unidades de Terapia Intensiva do Rio Grande do Sul
AUTOR: GILBERTO FRIEDMAN

06 fevereiro 2008

Tratamento de "traqueobronquite-associada a ventilação mecânica

Uma discussão que dura décadas sobre a importância das traqueobronquites em pacientes submetidos a VM pode estar cheando ao fim. O estudo de Pastores et al (apresentado no SCCM 2008) demonstra redução de morbi-mortalidade nessa população de pacientes. Certamente ainda vai haver muita discussão e temos de ler o paper antes de tirar conclusões definitivas, mas as impressões iniciais são boas.

vejam abaixo...



Antibiotics Decrease Mortality in Ventilator-Associated Tracheobronchitis

Antibiotic treatment significantly reduces rates of pneumonia infection and subsequent mortality in patients with ventilator-associated tracheobronchitis (VAT), according to an interim analysis of the first prospective randomized multicenter study to examine this issue, presented here at the Society of Critical Care Medicine 37th Critical Care Congress.

"We expected that the duration of mechanical ventilation but not mortality would decrease with treatment of VAT," noted the lead author, Saad Nseir, MD, from the Centre Hospitalier Régional Universitaire, Lille, France. "However, this result is logical since subsequent ventilator-associated pneumonia rate was also significantly different between the 2 groups," he told Medscape Critical Care.

A total of 44 patients with a first episode of VAT diagnosed at least 48 hours after starting mechanical ventilation were randomly assigned to receive either intravenous antibiotics (n = 22) for 8 days or no antibiotics (n = 36). VAT was identified by the presence of a purulent tracheal aspirate, a fever of at least 38°C with no other recognizable cause, a positive tracheal aspirate culture with more than 1 × 106 colony-forming units/mL, and the absence of new infiltrate on chest radiograph.

Patient characteristics were similar between the groups. The most common infection was with Pseudomonas aeruginosa, which was present in 36% of the patients. Other causative organisms included Staphylococcus aureus and Escherichia coli.

Subsequent ventilator-associated pneumonia infections decreased significantly in the group receiving antibiotics compared with the control group (3% vs 17%; P = .011). Likewise, intensive care unit mortality rates decreased with antibiotic treatment (4% vs 17%; P = .047).

The duration of mechanical ventilation was not significantly different between groups (29 days with antibiotics vs 26 days without), although more ventilation-free days were observed in the group receiving treatment (12 vs 2 days; P < .001). Because of the significant differences in mortality between the groups, the study was terminated for ethical reasons after the first interim analysis.

According to Dr. Nseir, remaining questions include the optimal duration of antibiotic use and whether aerosolized antibiotics might be useful in this setting.

Stephen M. Pastores, MD, from the Memorial Sloan-Kettering Cancer Center, New York City, who moderated the session, noted that this is a first-of-a-kind prospective study and has important clinical implications. "Since VAT can lead to pneumonia and mortality, these study results suggest that more attention should be given to screening for VAT — which I think makes sense. These researchers reported a prevalence of 3% to 10%, so VAT may be more common than we like to think."

However, he added that "it is very difficult to determine the exact incidence and importance of VAT, as the definition of VAT has not been validated and the use of 'new or increased sputum production' and 'absence of infiltrates on a chest radiograph' are rather imprecise." One question that arises with the study is whether patients with VAT were truly negative for ventilator-associated pneumonia at baseline, he told Medscape Critical Care. "If some patients were positive for pneumonia and received appropriate antimicrobial treatment, this may have been the reason for the decreased mortality rates."

According to Dr. Pastores, additional studies are needed with more precise and objective criteria for the diagnosis of VAT to determine the real effect of antibiotic treatment on outcome in these patients.

The funding for this study was provided by the University Hospital of Lille, France. Dr. Nseir and Dr. Pastores have disclosed no relevant financial relationships.

Society of Critical Care Medicine 37th Critical Care Congress: Abstract 62. Presented February 3, 2008.

Transfusão de hemácias na UTI: após 20 anos

  Título: Red Blood Cell Transfusion in the Intensive Care Unit. Autores: Raasveld SJ, Bruin S, Reuland MC, et al for the InPUT Study Group....