Assessment of Risk Factors for Ventilator Associated Pneumonia in the Medical Intensive Care Unit

被引:1
作者
Alp, Emine [1 ]
Gundogan, Kursat [2 ]
Guven, Muhammet [2 ]
Sungur, Murat [2 ]
机构
[1] Erciyes Univ, Tip Fak, Infeksiyon Hastaliklar Anabilim Dali, Kayseri, Turkey
[2] Erciyes Univ, Ic Hastaliklari, Tip Fak, Yogun Bakim Unit, Kayseri, Turkey
来源
JOURNAL OF MEDICAL AND SURGICAL INTENSIVE CARE MEDICINE | 2011年 / 2卷 / 02期
关键词
Ventilator-associated pneumonia; mechanical ventilation; ventilatory parameters and modes; risk factors;
D O I
10.5152/dcbybd.2011.08
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Aim: To detect the risk factors for ventilator associated pneumonia (VAP) and role of ventilator parameters in the development of VAP in a Medical Intensive Care Unit (MICU). Materials and Methods: This study was performed prospectively in Gevher Nesibe Hospital MICU of Erciyes University Medical Faculty between 1 January, 2003 and 1 April, 2004. The patients, who were 16 years old and over, who had been ventilated with a mechanical ventilator for more than 24 hours and who had no pulmonary infection, were included in the study. The patients' demographic characteristics, risk factors and ventilator parametres (PEEP, ventilation mode, tidal volume, FiO(2), PEAK, mean pressure, plateau pressure) were recorded. Also the hospitalization period before mechanical ventilation and up to pneumonia development, total time of ICU admission and the time of weaning were recorded. Results: A total of 106 patients were included in the study and VAP developed in 49 (46.2%) patients. When risk factors for VAP were evaluated in the univariate analysis, it was found that there was a statistically significant relationship between previous sepsis (OR= 2.557, 95% CI=1.153- 5.671, p=0.021), sedative drug usage (OR=2.876, 95% CI=1.168-7.075, p=0.021), tracheostomy (0R=3.602, 95% CI=1.446-8.972, p=0.006), PIP (OR=0.946, 95% CI=0.898-0.997, p=0.036), number of aspirations (OR=1.778, 95% CI=1.238-2.552, p=0.002), enteral nutrition (OR=5.440, 95% CI=2.197-13.471, p=0.000) and nasogastric tube (OR=2.510, 95% CI=1.138-5.537, p=0.023). When multivariate analysis was performed, previous sepsis (OR=6.291, 95% CI=1.944-20.356, p=0.002), sedative drug usage (OR=3.719, 95% CI=1.109-12.476, p=0.033), number of aspiration (OR=2.107, 95% CI=1.313-3.381, p=0.002) and enteral nutrition (OR=3.586, 95% CI=1.063-12.100, p=0.040) were determined to be independent risk factors. Ventilation modes and ventilation parameters had no effect on the development of pneumonia with multivariate logistic regression analysis. The duration of hospitalization in patients with VAP was longer than those who had no VAP (p<0.05). The crude mortality rate was 81.6%. There was no statistically significant relationship in mortality rates between the patients with VAP and those without VAP (p>0.05). Conclusion: Sepsis, sedative drug usage, number of aspirations and enteral nutrition were established as risk factors, whereas ventilation modes and ventilation parameters had no effect on the development of pneumonia. Avoiding unnecessary aspiration and sedation, rapid diagnosis and treatment of infections in other systems will be effective in the prevention of VAP.
引用
收藏
页码:34 / 38
页数:5
相关论文
共 25 条
[1]   Ventilator associated pneumonia and infection control [J].
Alp E. ;
Voss A. .
Annals of Clinical Microbiology and Antimicrobials, 5 (1)
[2]   Incidence, risk factors and mortality of nosocomial pneumonia in intensive care units: A prospective study [J].
Alp E. ;
Güven M. ;
Yildiz O. ;
Aygen B. ;
Voss A. ;
Doganay M. .
Annals of Clinical Microbiology and Antimicrobials, 3 (1)
[3]   AMERICAN-COLLEGE OF CHEST PHYSICIANS SOCIETY OF CRITICAL CARE MEDICINE CONSENSUS CONFERENCE - DEFINITIONS FOR SEPSIS AND ORGAN FAILURE AND GUIDELINES FOR THE USE OF INNOVATIVE THERAPIES IN SEPSIS [J].
BONE, RC ;
BALK, RA ;
CERRA, FB ;
DELLINGER, RP ;
FEIN, AM ;
KNAUS, WA ;
SCHEIN, RMH ;
SIBBALD, WJ ;
ABRAMS, JH ;
BERNARD, GR ;
BIONDI, JW ;
CALVIN, JE ;
DEMLING, R ;
FAHEY, PJ ;
FISHER, CJ ;
FRANKLIN, C ;
GORELICK, KJ ;
KELLEY, MA ;
MAKI, DG ;
MARSHALL, JC ;
MERRILL, WW ;
PRIBBLE, JP ;
RACKOW, EC ;
RODELL, TC ;
SHEAGREN, JN ;
SILVER, M ;
SPRUNG, CL ;
STRAUBE, RC ;
TOBIN, MJ ;
TRENHOLME, GM ;
WAGNER, DP ;
WEBB, CD ;
WHERRY, JC ;
WIEDEMANN, HP ;
WORTEL, CH .
CRITICAL CARE MEDICINE, 1992, 20 (06) :864-874
[4]  
Bouza E, 2003, CRIT CARE MED, V31, P1964, DOI [10.1097/01.ccm.0000084807.15352.93, 10.1097/01.CCM.0000084807.15352.93]
[5]   Influence of positive end-expiratory pressure (PEEP) on histopathological and bacteriological aspects of pneumonia during low tidal volume mechanical ventilation [J].
Charles, PE ;
Martin, L ;
Etienne, M ;
Croisier, D ;
Piroth, L ;
Lequeu, C ;
Pugin, J ;
Portier, H ;
Chavanet, P .
INTENSIVE CARE MEDICINE, 2004, 30 (12) :2263-2270
[6]   Mechanical ventilation modulates Toll-like receptor-3-induced lung inflammation via a MyD88-dependent, TLR4-independent pathway: a controlled animal study [J].
Chun, Carrie D. ;
Liles, W. Conrad ;
Frevert, Charles W. ;
Glenny, Robb W. ;
Altemeier, William A. .
BMC PULMONARY MEDICINE, 2010, 10
[7]   Incidence of and risk factors for ventilator-associated pneumonia in critically ill patients [J].
Cook, DJ ;
Walter, SD ;
Cook, RJ ;
Griffith, LE ;
Guyatt, GH ;
Leasa, D ;
Jaeschke, RZ ;
Brun-Buisson, C .
ANNALS OF INTERNAL MEDICINE, 1998, 129 (06) :433-440
[8]  
Craven DE, 1997, INFECT CONT HOSP EP, V18, P783
[9]  
George DL, 1996, HOSP EPIDEMIOLOGY IN, P175
[10]  
Integio EP, 1998, PRINCIPELS INTERNAL, P1486