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Year : 2010  |  Volume : 54  |  Issue : 6  |  Page : 535-540 Table of Contents     

A study of ventilator-associated pneumonia: Incidence, outcome, risk factors and measures to be taken for prevention

Department of Anaesthesiology, M P Shah Medical College, Jamnagar, Gujarat - 361 008, India

Date of Web Publication22-Nov-2010

Correspondence Address:
Hina Gadani
501, Sumeru Apartment, Opp. Manusmruthi, Opp. Palace Ground, Jamnagar - 361 008, Gujarat
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0019-5049.72643

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Ventilator-associated pneumonia (VAP) is a major cause of hospital morbidity and mortality despite recent advances in diagnosis and accuracy of management. However, as taught in medical science, prevention is better than cure is probably more appropriate as concerned to VAP because of the fact that it is a well preventable disease and a proper approach decreases the hospital stay, cost, morbidity and mortality. The aim of the study is to critically review the incidence and outcome, identify various risk factors and conclude specific measures that should be undertaken to prevent VAP. We studied 100 patients randomly, kept on ventilatory support for more than 48 h. After excluding those who developed pneumonia within 48 h, VAP was diagnosed when a score of ≥6 was obtained in the clinical pulmonary infection scoring system having six variables and a maximum score of 12. After evaluating, the data were subjected to univariate analysis using the chi-square test. The level of significance was set at P<0.05. It was found that 37 patients developed VAP. The risk factor significantly associated with VAP in our study was found to be duration of ventilator support, reintubation, supine position, advanced age and altered consciousness. Declining ratio of partial pressure to inspired fraction of oxygen (PaO 2 /FiO 2 ratio) was found to be the earliest indicator of VAP. The most common organism isolated in our institution was Pseudomonas. The incidence of early-onset VAP (within 96 h) was found to be 27% while the late-onset type (>96 h) was 73%. Late-onset VAP had poor prognosis in terms of mortality (66%) as compared to the early-onset type (20%). The mortality of patients of the non-VAP group was found to be 41% while that of VAP patients was 54%. Targeted strategies aimed at preventing VAP should be implemented to improve patient outcome and reduce length of intensive care unit stay and costs. Above all, everyone of the critical care unit should understand the factors that place the patients at risk of VAP and utmost importance must be given to prevent VAP.

Keywords: Intensive care unit, mechanical ventilation, ventilator-associated pneumonia

How to cite this article:
Gadani H, Vyas A, Kar AK. A study of ventilator-associated pneumonia: Incidence, outcome, risk factors and measures to be taken for prevention. Indian J Anaesth 2010;54:535-40

How to cite this URL:
Gadani H, Vyas A, Kar AK. A study of ventilator-associated pneumonia: Incidence, outcome, risk factors and measures to be taken for prevention. Indian J Anaesth [serial online] 2010 [cited 2020 Oct 19];54:535-40. Available from: https://www.ijaweb.org/text.asp?2010/54/6/535/72643

   Introduction Top

Ventilator-associated pneumonia (VAP) refers to bacterial pneumonia developed in patients who have been mechanically ventilated for a duration of more than 48 h. [1] It ranges from 6 to 52% and can reach 76% in some specific settings. [2] Hospital-acquired pneumonia (HAP) is the pneumonia after 48 h or more after admission, which did not appear to be incubating at the time of admission. The presence of HAP increases hospital stay by an average of 7-9 days per patient [3],[4] also imposes an extra financial burden to the hospital. The risk of VAP is highest early in the course of hospital stay, and is estimated to be 3%/day during the first 5 days of ventilation, 2%/day during days 5-10 of ventilation and 1%/day after this. [5]

Lack of a gold standard for diagnosis is the major culprit of poor outcome of VAP. The clinical diagnosis based on purulent sputum may follow intubation or oropharyngeal secretion leakage around airway, chest X-ray changes suspected of VAP may also be a feature of pulmonary oedema, pulmonary infarction, atelectasis or acute respiratory distress syndrome. Fever and leukocytosis are non-specific and can be caused by any condition that releases cytokines. Although microbiology helps in diagnosis, it is not devoid of pitfalls. In fact, it was proven that colonization of airway is common and presence of pathogens in tracheal secretions in the absence of clinical findings does not suggest VAP. [6],[7] The Clinical Pulmonary Infection Scoring (CPIS) system originally proposed by Pugin and others helps in diagnosing VAP with better sensitivity (72%) and specificity (80%). This study aims to critically review the incidence and outcome, identify various risk factors and to conclude specific measures that should be undertaken to prevent VAP.

   Methods Top

The study was conducted over a period of 1.5 years, extending from July 2008 to December 2009, in an intensive care unit (ICU) of a tertiary care centre. A total of 100 patients who were kept on mechanical ventilator were randomly selected. Cases included were patients of both sexes who were kept on mechanical ventilator for more than 48 h, having the age of >15 years. Patients who died or developed pneumonia within 48 h or those who were admitted with pneumonia at the time of admission and patients of ARDS (Acute Respiratory Distress Syndrome) were excluded from the study. Most of the patients put of ventilator support were primarily treated elsewhere with antibiotics either in the indoor ward or in other health care centres that was not traceable. A questionnaire was prepared and each patient selected to be included in the study was screened and monitored according to the questionnaire. Age, sex, date of admission to ICU, date of initiating mechanical ventilation and mode of assess to the patients' airway, i.e. orotracheal or tracheostomy, were recorded. Indication of mechanical ventilation was noted. In each patient, ventilator mode and settings were recorded and any change in setting was recorded daily. Patients' vitals, general and physical examination, oxygen saturation and position of the patients were monitored regularly. During the initial stage of ventilation, patients were adequately sedated. All necessary measures were taken for prevention of hospital-acquired infections. A battery of routine investigations was performed and special investigations, like culture of tracheal tube, blood and urine and others like serum cholinesterase levels when needed, were performed. Sputum from the patients were collected from the tip of the suction catheter and transported to the laboratory in a sterile tube. Patients were monitored from the date of inclusion in the study to the final outcome in the ICU. VAP was diagnosed on clinical grounds based on the modified CPIS system [Table 1] originally developed by Pugin and others, [1] giving 0-2 points each for fever, leukocyte count, oxygenation status, quantity and purulence of tracheal secretions, type of radiographic abnormality and result of sputum culture and Gram stain. The VAP group was classified into two groups, early-onset type (within 48-96 h) and late-onset type (>96 h). Once the clinical suspicion was established, empirical antibiotic therapy was initiated based on guidelines prescribed by the American Thoracic Society. Patients were routinely screened by arterial blood gas (ABG) analysis every 12 hourly and appropriate steps were taken to correct any change.
Table 1: Clinical pulmonary infection scoring system

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Statistical analysis

The study cohort was classified into two groups, "early-onset VAP (onset after 48 h but within 96 h)" and "late-onset VAP (onset after 96 h)". With a sample size of 70, calculated based the results of a previous study, [8] the power of the study was set at 80%. After evaluating, the data were subjected to univariate analysis using the chi-square test. The level of significance was set at P<0.05.

   Results Top

The study cohort comprised of 100 patients of various cases of poisoning, neurological disorders, sepsis and others. The mean age of the patients was 34 years, having a predominance of male population. Of the 100 patients, 37 patients developed VAP during the ICU stay. The mean duration of mechanical ventilation was found to be 11 days for the non-VAP group and 19 days for the VAP group. It was analysed in our study that those requiring prolonged ventilator support (>15 days) had a significantly higher incidence of VAP (P-value, 0.001). Supine position and stuporous, comatose patients were found to be risk factors, having a high incidence of VAP, and proved to be statistically significant (P-value, 0.003 and 0.0023, respectively). The PaO 2 /FiO 2 ratio was analysed in VAP patients and was found to be <240 mmHg in 86% of the cases. In the remaining 14%, the ratio was higher (>240 mmHg). Of the 37 patients who developed VAP, 10 patients developed early-onset (27.02%) VAP and 27 patients developed the late-onset type (72.97%). The overall mortality was found to be 46%, while mortality in the VAP patients was found to be 54%. The mortality of the early-onset type was found to be 20%. In case of the late-onset type, it was found to be 66.67%. Late-onset VAP had a significantly high association (P=0.0234) as far as mortality was concerned in comparison with early-onset pneumonia. The order of prevalence of organism in our study was found to be Pseudomonas (43.2%), Klebsiella (18.91%), followed by MRSA, E. coli, Acinetobacter, MSSA and S. pneumoniae.

   Discussion Top

In the study of our set up, males predominated (62%). Although the incidence of VAP was also high in males, it was statistically not significant (P=0.2086) [Table 2]. The mean age group in our study was 34 years. The young population group in our set up is due to the number of cases of poisoning that predominated our study.
Table 2: Gender distribution

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The incidence of VAP in our setting was 37%. In the era of advanced diagnosis and early management of possible complications, the incidence tends to be lower. In recent studies, [9],[10] the reported incidence is very low, ranging from 15 to 30%. The high incidence in our study may be due to a lower number of cases (i.e., 100) and lack of adequate nursing staff (which should ideally be 1:1 as compared to 4:1 in our institute) which may have adversely affected the quality of care given to the patients. Another factor in our study was a higher number of cases of patients of Organo-phosphorous poisoning that required prolonged ventilation, which is proved to be a risk factor having a statistically significant relation (P-value, 0.001; [Table 3]) with incidence of VAP, and may have influenced the incidence. The mean duration of ventilation in our study for non-VAP patients was 11 days whereas it was almost 19 days for VAP patients, which almost matches other studies. [11] It was proved in our study that duration of mechanical ventilation is an important risk factor for VAP, which is similar to other studies [12] where the mean duration of ventilation was around 10 days and the incidence of VAP was found to be 9.3%.
Table 3: Comparison of duration of mechanical ventilation and incidence of VAP ventilator-associated pneumonia

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The mean duration of ventilation can effectively be reduced by administrating a proper weaning protocol. It was estimated that 42% of the time a medical patient spends on the mechanical ventilator is during the weaning process. [13] Among the various methods of weaning, spontaneous breath trial has been proved to be very effective as compared with the intermittent mandatory ventilation (IMV) because of the fact that IMV promotes respiratory fatigue. [14],[15] A once-daily trial of spontaneous breathing and a prolonged period of rest may be the most effective methods of weaning to recondition respiratory muscles that may have been weakened during mechanical ventilation. [16],[17]

Reintubation resulted in a very high incidence of VAP [18] and proved to be an independent risk factor in various studies. [19] This may be due to impaired reflexes after prolonged intubation or due to the altered level of consciousness, increasing the risk of aspiration. In our study, the number of patients reintubated were only five in number, but four patients developed VAP. This number is too less to compare with other studies. A recent case-control study of 135 patients following heart surgery also found reintubation to be a major risk factor as VAP occurred in 92% of the reintubated patients versus 12% of the control subjects. [20]

It was noted that patients having unaffected lung during admission, like snake bite and meningitis, have a considerably low incidence of VAP and a significantly higher incidence of VAP in supine positioning as compared with the semi-recumbent position (P=0.003) [Table 4] because it may facilitate aspiration, which may be decreased by a semi-recumbent positioning matches to the outcome of the other studies when position is considered as a risk factor. [21],[22],[23] In fact, it was proved using radioactive-labeled enteral feeding, that cumulative numbers of endotracheal counts were higher when patients were placed in the completely supine position (0°) as compared with a semi-recumbent position (45°). [21],[22] Infection in patients in the supine position was strongly associated with the simultaneous administration of enteral nutrition. Thus, intubated patients should be managed in a semi-recumbent position, particularly during feeding.
Table 4: Incidence of VAP in supine vs.semi-recumbent position

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Level of consciousness has a significant impact on the incidence of VAP. It was found in our study that the incidence of VAP in stuporous (62.5%) and comatose (50%) patients is significantly higher (P=0.0023) than that in conscious (35.75%) and drowsy (18.42%) patients [Table 5]. This may be due to the higher chances of aspiration in comatose patients. An early and planned tracheostomy was found to decrease the VAP significantly but could not be studied as it will take time to be accepted by one and all. When used for stress ulcer prophylaxis, Sucralfate appears to have a small protective effect against VAP because it does not raise the gastric pH like H 2 receptor antagonists. [11] Therefore, whenever feasible, Sucralfate should be used instead of H 2 receptor antagonists.
Table 5: Relation of VAP with consciousness status

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The PaO 2 /FiO 2 ratio was assessed during the course of ventilatory support and it was observed that the ratio dropped at least 12-24 h before the onset of the clinicoradiologic picture suggestive of VAP. Thus, a decline in the PaO 2 /FiO 2 ratio was found to be an early indicator of onset of VAP. Although fever was found almost in 100% of the patients, it was of no significance as far as diagnosis was concerned because most of the patients were of poisoning cases that required atropine in due course of time and, as such, fever is a non-specific sign itself.

The most common organism associated with VAP is Pseudomonas (43.24%), followed by Klebsiella (18.91%). Also, the overall mortality rate was high in the Pseudomonas group (62.5%). In other studies, [24],[25] isolation of Pseudomonas ranges from 15 to 25%. Susceptibility testing could not be studied in all patients due to a lack of clinical microbiologic support as it is not done routinely and sending samples outside is not allowed by the hospital authority except in special cases.

Early-onset VAP in our study was found to be 27.02% while in various study it was found to be around 40%. [26] The low incidence in our study may be due to antibiotic use before admission to the ICU. Studies [27] have shown that previous antibiotic use decreases early-onset VAP but markedly increases multidrug-resistant (MDR) pathogens, which is also reflected in our study. Our study also demonstrated that early-onset VAP had a good prognosis as compared with the late-onset type in terms of mortality, which is also statistically significant (P=0.0234) [Table 6]. Probably, the de-escaltation strategy [28] fully endorsed by the American Thoracic Society, which means initiation of a broad-spectrum antibiotic and changing to a narrow spectrum after the sensitivity results are made available, will reduce inappropriate antibiotic use and, subsequently, the drug-resistant pathogens. Although it is not performed in our ICU, invasive bronchoscopic sample collection and quantitative sample culture reduces inappropriate antibiotic use. [29]
Table 6: Outcome of patients ofventilator-associated pneumonia

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The mortality rate in our study was found to be 54.05% in the VAP group as compared to 41.2% in the non-VAP group. Although the incidence was slightly high in VAP, it is statistically not significant. [Table 6] implies that VAP as such does not increase the mortality in ICU patients.

Hand washing is widely recognized as an important but underused measure to prevent nosocomial infections. [30] According to the 2004 CDC (Center for Disease Control) guidelines, hands should be washed before and after patient contact and also in between patient contact. Chlorhexidine has been shown to be effective in the control of ventilator-circuit colonization and pneumonia caused by antibiotic-resistant bacteria. [31] Oropharyngeal decontamination with Chlorhexidine solution has also been shown to reduce the occurrence of VAP in patients undergoing cardiac surgery. [32]

   Conclusion Top

We arrive at the following conclusions:

  • Incidence is directly proportional to duration of mechanical ventilation and re-intubation is a strong risk factor for development of VAP. Therefore, duration of ventilation has to be reduced to get rid of morbidity and mortality associated with mechanical ventilation, which can be achieved by administering a proper weaning protocol and titrating sedation regimens as per the need of the patients.
  • Promoting nasogastric feeding. Although necessary for critically ill patients, it should be given keeping the patients in a semi-recumbent position with the head end elevated to 45° because the supine position promotes aspiration.
  • A decrease in the PaO 2 /FiO 2 ratio is an early predictor of VAP.
  • Pseudomonas is the most common organism in our institution.
  • Late-onset VAP is associated with poor prognosis as compared to the early-onset variety.
  • Inappropriate antibiotic use prior to ventilatory support decreases the early-onset variety but predisposes to a high incidence of MDR pathogens.

   References Top

1.Davis KA. Ventilator-associated pneumonia: a review. J Intensive Care Med 2006;21:211-26.   Back to cited text no. 1
2. Koenig SM, Truwit JD. Ventilator-associated pneumonia: diagnosis, treatment, and prevention. Clin Microbiol Rev 2006;19:637-57.  Back to cited text no. 2
3.Chastre J, Fagon JY. Ventilator-associated pneumonia. Am J Respir Crit Care Med 2002;165:867-903.  Back to cited text no. 3
4.Rello J, Ollendorf DA, Oster G, Montserrat V, Bellm L, Redman R, et al. Epidemiology and outcomes of ventilator-associated pneumonia in a large US database. Chest 2002;122:2121.  Back to cited text no. 4
5.Cook DJ, Walter SD, Cook RJ, Griffith LE, Guyatt GH, Leasa D, et al. Incidence of and risk factors for ventilator-associated pneumonia in critically ill patients. Ann Intern Med 1998;129:440.  Back to cited text no. 5
6.Niederman MS. Gram-negative colonization of the respiratory tract: pathogenesis and clinical consequences. Semin Respir Infect 1990;5:173-84.  Back to cited text no. 6
7.Diaz E, Rodriguez AH, Rello J. Ventilator-associated pneumonia: issues related to the artificial airway. Respir Care 2005;50:900-6.  Back to cited text no. 7
8.Apostolopoulou E, Bakakos P, Katostaras T, Gregorakos L. Incidence and risk factors for ventilator-associated pneumonia in 4 multidisciplinary intensive care units in Athens, Greece. Respir Care 2003;48:681-8.  Back to cited text no. 8
9.Kollef MH. Ventilator-associated pneumonia: A multivariate analysis. JAMA 1993;270:1965-70.  Back to cited text no. 9
10.Fagon JY, Chastre J, Vuagnat A, Trouillet JL, Novara A, Gibert C. Nosocomial pneumonia and mortality among patients in intensive care units. JAMA 1996;275:866-9.  Back to cited text no. 10
11.Cook DJ, Reeve BK, Guyatt GH, Heyland DK, Griffith LE, Buckingham L, et al. Stress ulcer prophylaxis in critically ill patients. Resolving, discordant meta-analyses. JAMA 1996;275:308-14.  Back to cited text no. 11
12.Rello J, Sa-Borges M, Correa H, Leal SR, Baraibar J. Variations in etiology of ventilator-associated pneumonia across four treatment sites: Implications for antimicrobial prescribing practices. Am J Respir Crit Care Med 1999;160:608-13.  Back to cited text no. 12
13.Esteban A, Alνa I, Ibaρez J, Benito S, Tobin MJ. Modes of mechanical ventilation and weaning: a national survey of spanish hospitals: The Spanish Lung Failure Collaborative group. Chest 1994;106:1188-93.  Back to cited text no. 13
14.Marini JJ, Smith TC, Lamb VJ. External work output and force generation during synchronized intermittent mandatory ventilation: effect of machine assistance on breathing effort. Am Rev Respir Dis 1988;138:1169-79.  Back to cited text no. 14
15.Imsand C, Feihl F, Perret C, Fitting JW. Regulation of inspiratory neuromuscular output during synchronized intermittent mechanical ventilation. Anesthesiology 1994;80:13-22.  Back to cited text no. 15
16.Faulkner JA. Structural and functional adaptations of skeletal muscle. In: Roussos C, Macklem PT, editors. The thorax. Part B. Vol. 29 of Lung biology in health and disease. New York: Marcel Dekker; 1985. p. 1329-51.  Back to cited text no. 16
17.Rochester DF. Does respiratory muscle rest relieve fatigue or incipient fatigue? Am Rev Respir Dis 1988;138:516-7.  Back to cited text no. 17
18.Torres A, Gatell JM, Aznar E, el-Ebiary M, Puig de la Bellacasa J, Gonzalez J, et al. Re-intubation increases the risk of nosocomial pneumonia in patients needing mechanical ventilation. Am J Respir Crit Care Med 1995;152:137-41.  Back to cited text no. 18
19.Kollef MH, Von Harz B, Prentice D, Shapiro SD, Silver P, St John R, et al. Patient transport from intensive care increases the risk of developing ventilator-associated pneumonia. Chest 1997;112:765-73.  Back to cited text no. 19
20.Leal-Noval SR, Marquez-Vacaro JA, Garcia-Curiel A, Camacho-Larana P, Rincon-Ferrari MD, Ordonez-Fernandez A, et al. Nosocomial pneumonia in patients undergoing heart surgery. Crit Care Med 2000;28:935-40.  Back to cited text no. 20
21.Torres A, Serra-Batlles J, Ros E, Piera C, Puig de la Bellacasa J, Cobos A, et al. Pulmonary aspiration of gastric contents in patients receiving mechanical ventilation: the effect of body position. Ann Intern Med 1992;116:540-3.  Back to cited text no. 21
22.Orozco-Levi M, Torres A, Ferrer M, Piera C, El-Ebiary M, de la Bellacasa JP, et al. Semirecumbent position protects from pulmonary aspiration but not completely from gastroesophageal reflux in mechanically ventilated patients. Am J Respir Crit Care Med 1995;152:1387-90.  Back to cited text no. 22
23.Davis K Jr, Johannigman JA, Campbell RS, Marraccini A, Luchette FA, Frame SB, et al. The acute effects of body position strategies and respiratory therapy in paralyzed patients with acute lung injury. Crit Care 2001;5:81-7.  Back to cited text no. 23
24.Chastre J, Fagon JY. Ventilator associated pneumonia. Am J Respir Crit Care Med 2002;165:872.   Back to cited text no. 24
25.Kollef MH. Ventilator-associated pneumonia: A multivariate analysis. JAMA 1993;270:1965-70.  Back to cited text no. 25
26.Kollef MH. What is ventilator-associated pneumonia and why is it important? Respir Care 2005;50:714-21.  Back to cited text no. 26
27.Park DR. The microbiology of ventilator-associated pneumonia. Respir Care 2005;50:742-63.  Back to cited text no. 27
28.Guidelines for the management of adults with hospital-acquired, ventilator-associated, and healthcare-associated pneumonia. Am J Respir Crit Care Med 2005;171:388-416.  Back to cited text no. 28
29.Fagon JY, Chastre J, Wolff M, Gervais C, Parer-Aubas S, Stephan F, et al. Invasive and noninvasive strategies for management of suspected ventilator-associated pneumonia: a randomized trial. Ann Intern Med 2000;132:621-30.  Back to cited text no. 29
30.Doebbeling BN, Stanley GL, Sheetz CT, Pfaller MA, Houston AK, Annis L, et al. Comparative efficacy of alternative hand-washing agents in reducing nosocomial infections in intensive care units. N Engl J Med 1992;327:88-93.  Back to cited text no. 30
31.Rumbak MJ, Cancio MR. Significant reduction in methicillin-resistant Staphylococcus aureus ventilator-associated pneumonia associated with the institution of a prevention protocol. Crit Care Med 1995;23:1200-3.  Back to cited text no. 31
32.DeRiso AJ 2nd, Ladowski JS, Dillon TA, Justice JW, Peterson AC. Chlorhexidine gluconate 0.12% oral rinse reduces the incidence of total nosocomial respiratory infection and nonprophylactic systemic antibiotic use in patients undergoing heart surgery. Chest 1996;109:1556-61.  Back to cited text no. 32


  [Table 1], [Table 2], [Table 3], [Table 4], [Table 5], [Table 6]

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