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Intensive Care Med ; 22(11): 1244-9, 1996 Nov.
Article in English | MEDLINE | ID: mdl-9120120

ABSTRACT

OBJECTIVE: The study was undertaken to determine if critically ill patients under mechanical ventilation could reactivate latent cytomegalovirus (CMV) in either lung or blood. DESIGN: Prospective study in critically ill patients was performed in a multidisciplinary intensive care unit in a university hospital. PATIENTS: 23 non-immunocompromised, mechanically ventilated patients who were anti-CMV immunoglobulin G-positive. Ten immunocompromised patients with active CMV infection and 16 asymptomatic CMV seropositive non-immunocompromised patients constituted the positive and negative control groups. MEASUREMENTS AND RESULTS: The presence of CMV in blood and bronchoalveolar lavage (BAL) was evaluated by both viral cultures and polymerase chain reaction (PCR). Thirty-seven blood and 22 BAL samples were investigated. Sequential samples were evaluated in 8 patients. For PCR, a 290 bp fragment in the first exon of the immediate early 1 gene was amplified. In order to exclude inhibitors of PCR amplification, a 268 bp fragment of the beta-globin gene was concurrently amplified in all samples. Viral cultures of blood and BAL were negative in all 23 non-immunocompromised, mechanically ventilated patients. Moreover, no CMV DNA could be amplified in blood BAL samples, whereas a beta-globin amplification was observed in all samples. CONCLUSION: In a series of 23 critically ill patients under mechanical ventilation who were seropositive for CMV, no reactivation of CMV in blood or lung was demonstrated.


Subject(s)
Critical Care , Cross Infection/virology , Cytomegalovirus Infections/diagnosis , Lung Diseases/virology , Respiration, Artificial , Adult , Aged , Aged, 80 and over , Bronchoalveolar Lavage Fluid/virology , Case-Control Studies , Critical Illness , Cross Infection/immunology , DNA Probes , DNA, Viral/genetics , Female , Humans , Leukocytes/virology , Lung Diseases/immunology , Male , Middle Aged , Polymerase Chain Reaction , Respiratory Distress Syndrome/immunology , Respiratory Distress Syndrome/virology , Systemic Inflammatory Response Syndrome/immunology , Systemic Inflammatory Response Syndrome/virology
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