Potentially resistant microorganisms in intubated patients with hospital-acquired pneumonia: the interaction of ecology, shock and risk factors

被引:109
作者
Martin-Loeches, Ignacio [1 ,2 ,3 ,12 ]
Deja, Maria [4 ]
Koulenti, Despoina [5 ]
Dimopoulos, George [6 ]
Marsh, Brian [3 ]
Torres, Antonio [7 ,12 ]
Niederman, Michael S. [8 ]
Rello, Jordi [9 ,10 ,11 ,12 ]
机构
[1] Coporacio Sanitaria Parc Tauli, Crit Care Ctr, Sabadell, Spain
[2] Inst Univ UAB, Barcelona, Spain
[3] Mater Misericordiae Univ Hosp, Crit Care Dept, Dublin, Ireland
[4] Charite Med Ctr, Campus Virchow Clin, Dept Anesthesiol & Crit Care Med, D-13353 Berlin, Germany
[5] Univ Hosp Attikon, Crit Care Dept, Athens 12462, Greece
[6] Univ Athens, Sch Med, Univ Hosp ATTIKON, Dept Crit Care Med, GR-11527 Athens, Greece
[7] Hosp Clin Barcelona, Dept Pneumol, Barcelona, Spain
[8] Winthrop Univ Hosp, Dept Med, Mineola, NY 11501 USA
[9] Hosp Valle De Hebron, Crit Care Dept, Barcelona, Spain
[10] VHIR, Barcelona, Spain
[11] Univ Autonoma Barcelona, E-08193 Barcelona, Spain
[12] CIBERES, Barcelona, Spain
关键词
HAP; VAP; Multidrug-resistant organisms; Septic shock; Guidelines; Antibiotic treatment; VENTILATOR-ASSOCIATED PNEUMONIA; NOSOCOMIAL PNEUMONIA; THERAPY; MORTALITY; IMPACT; SCORE; DETERMINANTS; COMBINATION; INFECTIONS; PATHOGENS;
D O I
10.1007/s00134-012-2808-5
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
As per 2005 American Thoracic Society and Infectious Disease Society of America (ATS/IDSA) guidelines for managing hospital-acquired pneumonia, patients with early-onset pneumonia and without risk factors do not need to be treated for potentially resistant microorganisms (PRM). This was a secondary analysis of a prospective, observational, cohort, multicentre study conducted in 27 ICUs from nine European countries. From a total of 689 patients with nosocomial pneumonia who required mechanical ventilation, 485 patients with confirmed etiology and antibiotic susceptibility were further analysed. Of these patients, 152 (31.3 %) were allocated to group 1 with early-onset pneumonia and no risk factors for PRM acquisition, and 333 (68.7 %) were classified into group 2 with early-onset pneumonia with risk factors for PRM or late-onset pneumonia. Group 2 patients were older and had more chronic renal failure and more severe illness (SAPS II score, 44.6 +/- A 16.5 vs. 47.4 +/- A 17.8, p = 0.04) than group 1 patients. Trauma patients were more frequent and surgical patients less frequent in group 1 than in group 2 (p < 0.01). In group 1, 77 patients (50.7 %) had PRM in spite of the absence of classic risk factors recognised by the current guidelines. A logistic regression analysis identified that presence of severe sepsis/septic shock (OR = 3.7, 95 % CI 1.5-8.9) and pneumonia developed in centres with greater than 25 % prevalence of PRM (OR = 11.3, 95 % CI 2.1-59.3) were independently associated with PRM in group 1 patients. In patients admitted to ICUs with a prevalence of PRM greater than 25 % or with severe sepsis/septic shock, empiric therapy for group 1 nosocomial pneumonia requiring mechanical ventilation should also include agents likely to be effective for PRM pathogens.
引用
收藏
页码:672 / 681
页数:10
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