Ventilator-Associated Pneumonia due to Drug-Resistant Acinetobacter baumannii: Risk Factors and Mortality Relation with Resistance Profiles, and Independent Predictors of In-Hospital Mortality

被引:66
作者
Ciginskiene, Ausra [1 ]
Dambrauskiene, Asta [2 ]
Rello, Jordi [3 ,4 ,5 ,6 ,7 ]
Adukauskiene, Dalia [1 ]
机构
[1] Lithuanian Univ Hlth Sci, Med Acad, Dept Intens Care, LT-50161 Kaunas, Lithuania
[2] Lithuanian Univ Hlth Sci, Infect Control Serv, Med Acad, LT-50161 Kaunas, Lithuania
[3] Vall dHebron Univ Hosp, Dept Intens Care, Barcelona 08035, Spain
[4] CIBERES, Barcelona 08035, Spain
[5] Univ Autonoma Barcelona, E-08193 Barcelona, Spain
[6] Vall dHebron Inst Res, Barcelona 08035, Spain
[7] Vall dHebron Inst Res VHIR, CRIPS, Barcelona 08035, Spain
来源
MEDICINA-LITHUANIA | 2019年 / 55卷 / 02期
关键词
A; baumannii; ventilator-associated pneumonia (VAP); drug resistance; mortality; predictors; MULTIDRUG-RESISTANT; CRITICALLY-ILL;
D O I
10.3390/medicina55020049
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and objectives: High mortality and healthcare costs area associated with ventilator-associated pneumonia (VAP) due to Acinetobacter baumannii (A. baumannii). The data concerning the link between multidrug-resistance of A. baumannii strains and outcomes remains controversial. Therefore, we aimed to identify the relation of risk factors for ventilator-associated pneumonia (VAP) and mortality with the drug resistance profiles of Acinetobacter baumannii (A. baumannii) and independent predictors of in-hospital mortality. Methods: A retrospective ongoing cohort study of 60 patients that were treated for VAP due to drug-resistant A. baumannii in medical-surgical intensive care units (ICU) over a two-year period was conducted. Results: The proportions of multidrug-resistant (MDR), extensively drug-resistant (XDR), and potentially pandrug-resistant (pPDR) A. baumannii were 13.3%, 68.3%, and 18.3%, respectively. The SAPS II scores on ICU admission were 42.6, 48.7, and 49 (p = 0.048); hospital length of stay (LOS) prior to ICU was 0, one, and two days (p = 0.036), prior to mechanical ventilation (MV)-0, 0, and three days (p = 0.013), and carbapenem use prior to VAP-50%, 29.3%, and 18.2% (p = 0.036), respectively. The overall in-hospital mortality rate was 63.3%. In MDR, XDR, and pPDR A. baumannii VAP groups, it was 62.5%, 61.3%, and 72.7% (p = 0.772), respectively. Binary logistic regression analysis showed that female gender (95% OR 5.26; CI: 1.21-22.83), SOFA score on ICU admission (95% OR 1.28; CI: 1.06-1.53), and RBC transfusion (95% OR 5.98; CI: 1.41-25.27) were all independent predictors of in-hospital mortality. Conclusions: The VAP risk factors: higher SAPS II score, increased hospital LOS prior to ICU, and MV were related to the higher resistance profile of A. baumannii. Carbapenem use was found to be associated with the risk of MDR A. baumannii VAP. Mortality due to drug-resistant A. baumannii VAP was high, but it was not associated with the A. baumannii resistance profile. Female gender, SOFA score, and RBC transfusion were found to be independent predictors of in-hospital mortality.
引用
收藏
页数:13
相关论文
共 28 条
  • [2] [Anonymous], EUCAST BREAKP TABL I
  • [3] [Anonymous], EUR RESP J
  • [4] [Anonymous], ACINETOBACTER INFECT
  • [5] [Anonymous], 2016, ENFERM INFEC MICR CL, DOI DOI 10.1016/j.eimc.2015.11.018
  • [6] [Anonymous], 2017, SURV ANT RES EUR
  • [7] A Review of Acinetobacter baumannii as a Highly Successful Pathogen in Times of War
    Camp, Callie
    Tatum, Owatha L.
    [J]. LABMEDICINE, 2010, 41 (11): : 649 - 657
  • [8] Dellinger RP., 2013, CRIT CARE MED, V41
  • [9] European Centre for Disease Prevention and Control, 2016, SUMM LAT DAT ANT RES
  • [10] Treatment of multidrug-resistant Acinetobacter baumannii ventilator-associated pneumonia (VAP) with intravenous colistin:: A comparison with imipenem-susceptible VAP
    Garnacho-Montero, J
    Ortiz-Leyba, C
    Jiménez-Jiménez, FJ
    Barrero-Alodóvar, AE
    García-Garmendia, JL
    Bernabeu-Witteli, M
    Gallego-Lara, SL
    Madrazo-Osuna, J
    [J]. CLINICAL INFECTIOUS DISEASES, 2003, 36 (09) : 1111 - 1118