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1.
J Infect Dis ; 185(10): 1395-400, 2002 May 15.
Artículo en Inglés | MEDLINE | ID: mdl-11992273

RESUMEN

Critically ill surgery patients are susceptible to pulmonary reactivation of latent cytomegalovirus (CMV), but what triggers this reactivation is unknown. Immunosuppression and bacterial sepsis are thought to stimulate reactivation of CMV, and in this study it was hypothesized that immunosuppressive effects of surgery with or without concomitant bacterial infection may reactivate latent CMV. Mice infected with CMV were allowed to develop latent infections. Latently infected mice underwent a laparotomy with cecal ligation and puncture (CLP; n=30), a laparotomy alone (sham; n=10), or no surgery (control; n=5). Lung tissue homogenates were evaluated for viral activity, and, 2 and 3 weeks after CLP, lungs of 7 of 7 and 5 of 5 mice, respectively, showed reactivation of latent CMV. In contrast, lungs from all sham-operated animals and controls showed no viral reactivation. These findings demonstrate that surgery with subsequent intra-abdominal bacterial infection reactivated CMV in lungs of latently infected mice. The mechanism of this reactivation is unknown but likely involves cytokines induced by sepsis.


Asunto(s)
Infecciones por Herpesviridae/complicaciones , Pulmón/virología , Muromegalovirus , Neumonía Viral/complicaciones , Complicaciones Posoperatorias , Sepsis/complicaciones , Abdomen , Animales , Ciego/microbiología , Ciego/cirugía , Modelos Animales de Enfermedad , Femenino , Infecciones por Herpesviridae/virología , Inmunocompetencia , Laparotomía , Ratones , Ratones Endogámicos BALB C , Muromegalovirus/fisiología , Neumonía Viral/virología , Sepsis/microbiología , Activación Viral , Latencia del Virus
2.
Crit Care Med ; 31(7): 1923-9, 2003 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-12847384

RESUMEN

OBJECTIVE: Herpes family viruses have been recognized as pathogens for many years in immunosuppressed transplant or human immunodeficiency virus patients, but they have garnered little attention as potential pathogens in the nonimmunosuppressed critically ill. The objective of this study was to define the prevalence of and risk factors for development of herpes family virus infection in chronic critically ill surgical patients. DESIGN: Prospective epidemiologic study. SETTING: A 38-bed surgical intensive care unit in a major university hospital. PATIENTS: Nonimmunosuppressed intensive care unit patients in intensive care unit for >/=5 days. INTERVENTIONS: None; patients received no antiviral treatment during the study. MEASUREMENTS AND MAIN RESULTS: Weekly cultures for cytomegalovirus (CMV) and herpes simplex virus, viral serologies, and T-cell counts were performed. The prevalence (95% confidence interval) of positive respiratory cultures for herpes simplex or CMV was 35% (22-49%); 15% (5-25%) cultured positive for CMV, 23% (11-35%) cultured positive for herpes simplex virus, and one patient's respiratory secretions culturing positive for both CMV and herpes simplex virus. The prevalence of CMV viremia was only 5.8% (1-10%). CMV+ patients had longer hospital admissions, intensive care unit admissions, and periods of ventilator dependence than CMV- patients, despite having comparable severity of illness scores. CMV+ patients also had significantly higher numbers of blood transfusions, prevalence of steroid exposure, and prevalence of hepatic dysfunction, and all were immunoglobulin G positive at the beginning of the study. In contrast, herpes simplex virus-positive patients had lengths of hospital admissions, lengths of intensive care unit admissions, and periods of ventilator dependence comparable with patients without viral infections (p >.05). CONCLUSIONS: There is a significant prevalence (22-49%) of occult active herpes family viruses in chronic critically ill surgical patients. The clinical significance of these viral infections is unknown, although CMV+ patients have significantly higher morbidity rates than CMV- patients. Several factors suggest pathogenicity, but further study is needed to define causality.


Asunto(s)
Cuidados Críticos/estadística & datos numéricos , Enfermedad Crítica/epidemiología , Infección Hospitalaria/epidemiología , Infecciones por Citomegalovirus/epidemiología , Enfermedades Endémicas , Herpes Simple/epidemiología , APACHE , Relación CD4-CD8 , Causalidad , Infección Hospitalaria/inmunología , Estudios Transversales , Infecciones por Citomegalovirus/inmunología , Femenino , Herpes Simple/inmunología , Humanos , Masculino , Persona de Mediana Edad , Estudios Prospectivos
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