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Rev. bras. ter. intensiva ; 27(3): 260-265, jul.-set. 2015. tab, ilus
Article in Portuguese | LILACS | ID: lil-761667

ABSTRACT

RESUMOObjetivo:Avaliar a concordância entre um novo método de vigilância epidemiológica do Center for Disease Control and Prevention e o Clinical Pulmonary Infection Score para detecção de pneumonia associada à ventilação mecânica.Métodos:Coorte prospectiva que avaliou pacientes internados nas unidades de terapia intensiva de dois hospitais que permaneceram intubados por mais de 48 horas no período de agosto de 2013 a junho de 2014. Os pacientes foram avaliados diariamente pelos fisioterapeutas com o Clinical Pulmonary Infection Score. De forma independente, um enfermeiro aplicou o novo método de vigilância proposto pelo Center for Disease Control and Prevention. Avaliou-se a concordância diagnóstica entre os métodos. Clinical Pulmonary Infection Score ≥ 7 foi considerado diagnóstico clínico de pneumonia associada à ventilação mecânica, considerando-se diagnóstico definitivo a associação de Clinical Pulmonary Infection Score ≥ 7 com germe isolado em cultura semiquantitativa ≥ 104 unidades formadoras de colônias.Resultados:De 801 pacientes admitidos nas unidades de terapia intensiva, 198 estiveram sob ventilação mecânica. Destes, 168 permaneceram intubados por mais de 48 horas. Identificaram-se 18 (10,7%) condições infecciosas associadas à ventilação mecânica e 14 (8,3%) pneumonias associadas à ventilação mecânica possíveis ou prováveis, representando 35% (14/38) diagnósticos clínicos de pneumonia associada à ventilação mecânica. O método do Center for Disease Control and Prevention identificou casos de pneumonia associada à ventilação mecânica com sensibilidade de 0,37 e especificidade de 1,0, com valor preditivo positivo de 1,0 e negativo de 0,84. As diferenças implicaram em discrepâncias na densidade de incidência de pneumonia associada à ventilação mecânica (CDC: 5,2/1000 dias de ventilação mecânica; Clinical Pulmonary Infection Score ≥ 7: 13,1/1000 dias de ventilação mecânica).Conclusão:O método do Center for Disease Control and Prevention falhou na detecção de casos de pneumonia associada à ventilação mecânica e pode não ser satisfatório como método de vigilância.Objective: To evaluate the agreement between a new epidemiological surveillance method of the Center for Disease Control and Prevention and the clinical pulmonary infection score for mechanical ventilator-associated pneumonia detection.


ABSTRACTObjective:>To evaluate the agreement between a new epidemiological surveillance method of the Center for Disease Control and Prevention and the clinical pulmonary infection score for mechanical ventilator-associated pneumonia detection.Methods:This was a prospective cohort study that evaluated patients in the intensive care units of two hospitals who were intubated for more than 48 hours between August 2013 and June 2014. Patients were evaluated daily by physical therapist using the clinical pulmonary infection score. A nurse independently applied the new surveillance method proposed by the Center for Disease Control and Prevention. The diagnostic agreement between the methods was evaluated. A clinical pulmonary infection score of ≥ 7 indicated a clinical diagnosis of mechanical ventilator-associated pneumonia, and the association of a clinical pulmonary infection score ≥ 7 with an isolated semiquantitative culture consisting of ≥ 104 colony-forming units indicated a definitive diagnosis.Results:Of the 801 patients admitted to the intensive care units, 198 required mechanical ventilation. Of these, 168 were intubated for more than 48 hours. A total of 18 (10.7%) cases of mechanical ventilation-associated infectious conditions were identified, 14 (8.3%) of which exhibited possible or probable mechanical ventilatorassociated pneumonia, which represented 35% (14/38) of mechanical ventilator-associated pneumonia cases. The Center for Disease Control and Prevention method identified cases of mechanical ventilator-associated pneumonia with a sensitivity of 0.37, specificity of 1.0, positive predictive value of 1.0, and negative predictive value of 0.84. The differences resulted in discrepancies in the mechanical ventilator-associated pneumonia incidence density (CDC, 5.2/1000 days of mechanical ventilation; clinical pulmonary infection score ≥ 7, 13.1/1000 days of mechanical ventilation).Conclusion:The Center for Disease Control and Prevention method failed to detect mechanical ventilatorassociated pneumonia cases and may not be satisfactory as a surveillance method.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Intensive Care Units , Pneumonia, Ventilator-Associated/diagnosis , Population Surveillance/methods , Respiration, Artificial/adverse effects , Centers for Disease Control and Prevention, U.S. , Cohort Studies , Incidence , Predictive Value of Tests , Prospective Studies , Pneumonia, Ventilator-Associated/epidemiology , Respiration, Artificial/statistics & numerical data , Sensitivity and Specificity , United States
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