Emergency. 2017; 5 (1): e26 OR I G I N A L RE S E A RC H Ventilator-Associated Pneumonia and Its Responsible Germs; an Epidemiological Study Rama Bozorgmehr1, Vanousheh Bahrani1, Alireza Fatemi2∗ 1. Clinical Research Development Unit, Shohadaye Tajrish Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran. 2. Infectious Diseases and Tropical Medicine Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Received: August 2016; Accepted: October 2016; Published online: 10 January 2017 Abstract: Introduction: Ventilator-associated pneumonia (VAP) is one of the most common hospital infections and a side effect of lengthy stay in intensive care unit (ICU). Considering the ever-changing pattern of common pathogens in infectious diseases and the raise in prevalence of hospital infections, the present study was designed aiming to determine the prevalence of VAP and its bacterial causes. Methods: In this cross-sectional study, the medical profiles of all the patients under mechanical ventilation, who had no symptoms of pneumonia at the time of in- tubation and developed new infiltration in chest radiography after 48 hours under mechanical ventilation along with at least 2 of the symptoms including fever, hypothermia, leukocytosis, leukopenia, or purulent discharge from the lungs, were evaluated. Demographic data, clinical and laboratory findings, and final outcome of the patients were extracted from the patient’s clinical profile and reported using SPSS version 20 and descriptive statistics. Results: 518 patients with the mean age of 62.3 ± 20.8 years were evaluated (50.9% female). Mean time interval between intubation and showing symptoms was 10.89 ± 12.27 days. Purulent discharges (100%), leukocytosis (71.9%), fever (49.1%), hypothermia (12.3%), and leukopenia (8.8%) were the most common clini- cal and laboratory symptoms and acinetobacter baumannii (31.58%) and klebsiella pneumoniae (29.82%) were the most common germs growing in sputum cultures. 19 (33.3%) cases of pan drug resistance (PDR) and 10 (17.5%) cases of extensive drug resistance (XDR) were seen. Mortality due to VAP was 78.9% and there was no significant correlation between age (p = 0.841), sex (p = 0.473), ICU admission (p = 0.777), duration of hospital- ization (p = 0.254), leukocytosis (p = 0.790), leukopenia (p = 0.952), fever (p = 0.171), hypothermia (p = 0.639), type of culture (p = 0.282), and type of antibiotic resistance (p = 0.066) with mortality. Conclusion: Prevalence of VAP and its associated mortality were 11% and 78.9%, respectively. The most common symptoms and signs were purulent discharge, leukocytosis, and fever. Acinetobacter baumannii and klebsiella pneumoniae were the most common germs in sputum cultures with 50% resistance to commonly used antibiotics. Keywords: Pneumonia, ventilator-associated; cross infection; drug resistance, microbial; intensive care units © Copyright (2017) Shahid Beheshti University of Medical Sciences Cite this article as: Bozorgmehr R, Bahrani V, Fatemi A. Ventilator-Associated Pneumonia and Its Responsible Germs; an Epidemiological Study. Emergency. 2017; 5(1): e26. 1. Introduction T he respiratory infection caused by micro-aspiration of organisms, 48 hours after going under mechanical ventilation is called ventilator-associated pneumonia (VAP) (1). Pneumonia is one of the most common hospital infections and a side effect of long stay in the intensive care ∗Corresponding Author: Alireza Fatemi; Infectious Diseases and Trop- ical Medicine Research Center, Koodakyar St., Daneshjoo Blv, Velenjak, Shahid Chamran Highway, Tehran, Iran. Tel: +989128949858 Email: dr_fatemi_alireza@yahoo.com unit (ICU) (2). This problem has a prevalence of 16 to 78%, while infections of urinary tract or skin have a prevalence of 1 - 4% (2-6). Due to the important role of antibiotic-resistant bacteria in these kinds of infection, with longer duration of hospital stay, the probability of mortality will rise (3, 7, 8). VAPis the reason for increased length of stay in ICU and is responsible for about 50% of antibiotic prescriptions in this unit. The risk of this infection has been reported to be 3% for each day of intubation during the first 5 days, 2% for each day during 5thto 10th day, and 1% after 10 days of intubation (9). Among the most common germs responsible for VAP are staphylococcus aureus, pseudomonas aeruginosa, klebsiella This open-access article distributed under the terms of the Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0). Downloaded from: www.jemerg.com R. Bozorgmehr et al. 2 pneumoniae, and acinetobacter (4, 10). In a study on 107 patients under mechanical ventilation, prevalence of VAP was calculated to be 28.54%, with pseudomonas aeruginosa, meticillin resistant staphylococcus aureus, klebsiella pneu- moniae, and acinetobacter baumannii (6). In another study, the total rate of hospital pneumonia was found to be 26.2% and its mortality rate was estimated to be 78.8% (11). A study in Shiraz, Iran, also reported a 10.2% VAP rate and acineto- bacter baumannii as the most common responsible organ- ism (12). 2 other studies reported prevalence of VAP to be 21.6% and 16% in 2013 and 2014, respectively (13, 14). Con- sidering the changes in pattern of common pathogens in in- fectious diseases and raise in hospital infection rates shown in various studies, identifying the pathogens responsible for infections can be of great help in selecting the proper treat- ment for VAP and is therefore a requirement and research priority all over the world. The importance of this issue is emphasized when we note that most of these patients have been intubated in emergency department and stayed there for a while. Therefore, the present study aimed to determine the rate of VAP and its bacterial causes. 2. Methods 2.1. Study design and setting The present study is a retrospective cross-sectional one car- ried out on patients under mechanical ventilation in ICU or other departments of Shohadaye Tajrish Hospital, Tehran, Iran, during 2014-2016, aiming to determine the prevalence of VAP and its bacterial causes in these patients. Protocol of this study was approved by the ethics committee of Shahid Beheshti University of Medical Sciences. The researchers ad- hered to confidentiality of patient data and Declaration of Helsinki principles. 2.2. Participants All the patients that had no signs of pneumonia at the time of intubation who developed new infiltration in chest radio- graphy after 48 hours of intubation along with at least 2 of the symptoms including fever, hypothermia, leukocytosis, leukopenia, or purulent discharge from the lungs were con- sidered VAP cases and included in the study. If the patients had pneumonia before going under ventilation or during the initial 48 hours or their clinical data were not available, they were excluded. No age or sex limitation was applied and the reason for intubation was not considered in exclusion crite- ria. Consecutive sampling was used. 2.3. Data gathering Demographic data of the patients (age, sex, admission ward), results of blood cell count, smear and culture of respiratory secretions, type of microorganism that grow, antibiotic resis- Table 1: Demographic and clinical data of studied patients Variable Number (%) Age (year) 15 - 29.9 6 (11.32) 30 - 44.9 4 (7.55) 45 - 59.9 12 (22.64) 60 -74.9 15 (28.30) >75 16 (30.19) Sex Female 29 (50.88) Male 28 (49.12) Hospitalized in Intensive care unit 21 (36.64) Other departments 36 (63.16) Fever Yes 28 (49.12) No 29 (50.88) Hypothermia Yes 7 (12.28) No 50 (87.72) Purulent discharge Yes 57 (100) No 0 (0) Leukocytosis Yes 41 (71.93) No 16 (28.07) Leukopenia Yes 5 (8.77) No 52 (91.23) Drug resistance Pan drug resistance (PDR) 19 (65.52) Extensive drug resistance (XDR) 10 (34.48) Final outcome Recovery 12 (21.05) Death 45 (78.95) tance, clinical symptoms, chest radiography findings, com- puted tomography (CT) scan of lungs, if present, and final outcome of the patients were extracted from their medical profile and recorded in a checklist designed for this purpose. Data were gathered by a senior resident of internal medicine and when in doubt, an infectious disease specialist or an in- ternal medicine specialist was consulted. The findings of pa- tients’ radiography were reported by the center’s radiologist or the pulmonologist in charge of patient management in ICU. 2.4. Statistical Analysis Required sample size for this study was calculated to be 456 cases considering the 5% probability of VAP (3% for each day in the initial 5 days and 2% for each day 5-10 days after in- tubation), α = 5% and desired precision of 2% (15). Finally, data were analyzed using SPSS version 20 and Chi square and t-test. Qualitative data were reported as percentage and fre- quency, and quantitative ones as mean ± standard deviation This open-access article distributed under the terms of the Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0). Downloaded from: www.jemerg.com 3 Emergency. 2017; 5 (1): e26 (SD). To evaluate the correlation between studied variables and final outcome (mortality) chi-square test was used. P < 0.05 was considered as significance level. 3. Results 3.1. Baseline characteristics 518 patients with the mean age of 62.3 ± 20.8 (range: 15 - 97) years underwent mechanical ventilation via orotracheal in- tubation during the study period (50.9% female). 57 (11%) of cases developed VAP. Demographic data, clinical symp- toms, and laboratory findings of the studied patients are summarized in table 1. The highest frequency of patients belonged to ≥ 75 years age group (30.19%). Mean time in- terval between intubation and showing symptoms was 10.89 ± 12.27 days (range: 2 – 80). Only 21 (36.8%) patients were hospitalized in ICU and others were admitted to other departments. Purulent discharges with 100%, leukocytosis with 71.9%, fever with 49.1%, hypothermia with 12.3%, and leukopenia with 8.8% were the most common clinical and laboratory findings in the studied patients. 3.2. Cultures Tables 2 and 3 depict the most common germ growths in sputum culture and the results of antibiogram done for pa- tients with VAP. The most common germ growths belonged to acinetobacter baumannii with 31.58%, and klebsiella pneu- moniae with 29.82%, respectively. Rate of resistance to ciprofloxacin, doxycycline, cotrimoxazole, ceftazidime, and cefotaxime were reported to be more than 50%. Finally, 19 (33.3%) cases of pan drug resistance (PDR) and 10 (17.5%) cases of extensive drug resistance (XDR) were reported. No significant correlation was detected between the type of germ growth in sputum culture and presence of PDR or XDR (p = 0.931). Radiography of 100% of the patients included tur- bidity in 1 or multiple lobes. 3.3. Outcome Mortality due to VAP in the present study was estimated to be 78.9% (45 cases). No significant correlation was seen be- tween age (p = 0.841), sex (p = 0.473), ICU admission (p = 0.777), duration of hospitalization (p = 0.254), leukocytosis (p = 0.790), leukopenia (p = 0.952), fever (p = 0.171), hypother- mia (p = 0.639), type of culture (p = 0.282), and type of antibi- otic resistance (p = 0.066) with mortality. 4. Discussion Based on our findings, prevalence of VAP was 11% among the studied patients and mortality due to it was estimated to be 78.9%. The most common clinical and laboratory symptoms and signs of this type of pneumonia were purulent discharge, Table 2: Frequency of germs’ growth in studied patients’ sputum culture Growing germ Number (%) Acinetobacter Baumannii 18 (31.6) Klebsiella Pneumoniae 17 (29.8) Enterobacteriaceae 7 (12.3) Candida Albicans 4 (7) Pseudomonas Aeruginosa 4 (7) Staphylococcus Aureus 3 (5.3) Escherichia Coli 2 (3.5) Proteus Mirabilis 1 (1.8) Negative 1 (1.8) Table 3: Frequency of antibiotic resistance in studied patients Type of antibiotic Number (%) Ciprofloxacin 42 (73.7) Doxycycline 36 (63.2) Cotrimoxazole 32 (56.1) Ceftazidime 31 (54.4) Cefotaxime 31 (54.4) Meropenem 28 (49.1) Imipenem 28 (49.1) Amikacin 26 (45.6) Clindamycin 22 (38.6) Tobramycin 21 (35.1) Cefepime 20 (31.8) Colistin 18 (31.6) Ampicillin sulbactam 13 (22.8) Levofloxacin 9 (15.8) Cephalexin 6 (10.5) Piperacillin 6 (10.5) Gentamicin 5 (8.8) Ceftriaxone 4 (7) Cefixime 3 (5.3) Azithromycin 2 (3.5) Ofloxacin 1 (1.8) leukocytosis, and fever. Acinetobacter baumannii and kleb- siella pneumonia were the most common germs growing in sputum cultures that showed resistance to commonly used antibiotics in more than 50% of cases. In a study by Nadi et al. mean age of the population affected with pneumonia in 353 patients who were hospitalized in ICU of Be’sat and Ek- batan Hospitals, Hamedan, Iran, was 51.2 ± 21.9 years, only 36 (10.2%) of which were affected with VAP (16). As men- tioned before, health care providers should face a big chal- lenge named hospital infections. In the United States, every year, an average of about 2 million people are affected with this kind of infection and 90000 die, which makes hospital in- fections the 5th most common cause of death in health cen- ters (15). The most common hospital infections are reported to be respiratory (65%), urinary tract (17%), and blood (12%) infections (15). Ventilator associated infections have the highest rate of mortality among hospital acquired infections, This open-access article distributed under the terms of the Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0). Downloaded from: www.jemerg.com R. Bozorgmehr et al. 4 90% of which occur during mechanical ventilation and 50% in the initial 4 days of going under mechanical ventilation (15). In 2009, it was estimated that VAP increases days in need of ventilator by 9.6 days, length of stay in ICU by 6.1 days, and hospitalization duration by 11.5 days, which inflicts physi- cal and financial burdens on the patient and health care sys- tem (17). Despite measures taken and recent advances in treatment, prevention, and management of pathogens as- sociated with ventilator, pneumonia is still a major cause of death in hospitalized patients. Since multi-drug resistant pathogens play a major role in VAP, currently antibiotics that properly cover these pathogens are used. These antibiotics include 3rd or 4th generation of cephalosporin (ceftazidime, cefepime), Κ-lactamase inhibitors (piperacillin, tazobac- tam), carbapenems (imipenem, meropenem) in combi- nation with an aminoglycoside (gentamicin, tobramycin, amikacin) or an anti-peseudomonas fluoroquinolone (lev- ofloxacin, ciprofloxacine) (15). In the present study, VAP had a prevalence of 11% among patients under mechanical ven- tilation. This rate was reported to be 19% in ICU of Shahid Beheshti Hospital, Kashan, Iran, during 2009-2010. In that study, a significant correlation was found between age, Glas- gow coma scale, positioning patient’s head in 30 or more de- grees, oral hygiene, and training the staff regarding infec- tion control with hospital pneumonia; and continuous train- ing of staff and taking complete and regular care of oral hy- giene of patients under mechanical ventilation were recom- mended (18). In a study by Chung et al., 77.3% of intubated patients admitted to ICU had VAP (19). In a similar study, Klompas et al. reported the prevalence of VAP to be 9.5% among 599 patients who were hospitalized in ICU of a hos- pital in America (20). This difference in prevalence may be due to the method of care given, the skill and experience of nurses, adhering to standards and beds being physically standard, positioning of patient’s head, space between beds and their rate of occupation, use of gloves and gowns by staff, oral hygiene, prevention of stomach distension, and method of prophylactic antibiotic use. Therefore, the higher the rate of standard treatments carried out for intubated patients, the lower the rate of pneumonia. In the present study, there was no significant difference between ICU of departments (in- ternal medicine and surgery) regarding incidence of pneu- monia or final outcome of mortality. In a study in Arak car- ried out in 2011, there was a significant difference between ICU of internal medicine and surgery wards (21). In addi- tion, in the Klompas et al. study, prevalence of pneumonia was 33% in internal medicine ward and 61% in surgery wad. This difference might be due to more invasive procedures, catheterization, intubation duration, and higher length of stay in surgery ward compared to internal medicine ward (20). The most common pathogens extracted from patients in the present study were acinetobacter baumannii and kleb- siella pneumoniae, while in another study the most common pathogens were acinetobacter, staphylococcus aureus, and pseudomonas aeruginosa (21). In 2 separate studies, com- mon germs responsible for pneumonia were staphylococcus aureus, pseudomonas aeruginosa, klebsiella pneumoniae, andacinetobacter, which is somehow similar to the present study (4, 10). In addition, in pediatric ICU, the most common germs in sputum of pneumonia patients were staphylococ- cus aureus, pseudomonas aeruginosa, and enterobacter (22). Regarding resistance to antibiotics in this study, pathogens were resistant to ciprofloxacin, doxycycline, cotrimoxazole, ceftazidime, and cefotaxime more than 50%. In a similar study, acinetobacter had the most resistance to gentamicin and was most sensitive to imipenem (21). Sadly, 78.9% of our studied patients died because of VAP. In a study by Zarin- far, 11.7% of the patient fully recovered, 18.3% were relatively better, 20% did not get better, and 50% died, which is lower than the rate in our study. As mentioned before, this might be due to the procedures done, method of intubation, physical health, positioning of patient’s head, and type of antibiotic prescribed (21). 5. Limitation Among the limitations of this study were its retrospective de- sign and extracting data from patients’ medical profile, which increase the probability of losing some information due to careless profile recording. In addition, data regarding the un- derlying disease and cause of intubation were not consid- ered, while they may play a role in increasing mortality due to ventilation. 6. Conclusion Based on our findings, prevalence of VAP and its associated mortality were 11% and 78.9%, respectively. The most com- mon symptoms and signs were purulent discharge, leuko- cytosis, and fever. Acinetobacter baumannii and klebsiella pneumoniae were the most common germs in sputum cul- tures with 50% resistance to commonly used antibiotics. 7. Appendix 7.1. Acknowledgements This article is derivated from Dr. Vanoushe Bahrani’s thesis for achieving her specialist degree in internal medicine. 7.2. Author contribution All the authors have contributed to drafting/revising the manuscript, study concept, or design, as well as data collec- tion and interpretation. This open-access article distributed under the terms of the Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0). Downloaded from: www.jemerg.com 5 Emergency. 2017; 5 (1): e26 7.3. Funding/Support None. 7.4. Conflict of interest All authors declare that there is no conflict of interest in this study. References 1. Nseir S, Zerimech F, Fournier C, Lubret R, Ramon P, Durocher A, et al. Continuous control of tracheal cuff pressure and microaspiration of gastric contents in criti- cally ill patients. American journal of respiratory and crit- ical care medicine. 2011;184(9):1041-7. 2. Chastre J, Fagon J-Y. Ventilator-associated pneumo- nia. American journal of respiratory and critical care medicine. 2002;165(7):867-903. 3. Valles J, Mesalles E, Mariscal D, del Mar Fernandez M, Pena R, Jimenez JL, et al. A 7-year study of severe hospital-acquired pneumonia requiring ICU admission. Intensive care medicine. 2003;29(11):1981-8. 4. Sopena N, Sabria M. Multicenter study of hospital- acquired pneumonia in non-ICU patients. Chest Journal. 2005;127(1):213-9. 5. Vincent J-L, Rello J, Marshall J, Silva E, Anzueto A, Mar- tin CD, et al. International study of the prevalence and outcomes of infection in intensive care units. Jama. 2009;302(21):2323-9. 6. Gupta A, Agrawal A, Mehrotra S, Singh A, Malik S, Khanna A. Incidence, risk stratification, antibiogram of pathogens isolated and clinical outcome of ventilator associated pneumonia. Indian Journal of Critical Care Medicine. 2011;15(2):96. 7. Herzig SJ, Howell MD, Ngo LH, Marcantonio ER. Acid- suppressive medication use and the risk for hospital- acquired pneumonia. Jama. 2009;301(20):2120-8. 8. Safdar N, Dezfulian C, Collard HR, Saint S. Clinical and economic consequences of ventilator-associated pneu- monia: a systematic review. Critical care medicine. 2005;33(10):2184-93. 9. Nomellini V, Chen H. Murray and Nadel’s Textbook of Respiratory Medicine. Academic Press; 2012. 10. Dore P, Robert R, Grollier G, Rouffineau J, Lanquetot H, Charriere J-M, et al. Incidence of anaerobes in ventilator- associated pneumonia with use of a protected specimen brush. American journal of respiratory and critical care medicine. 1996;153(4):1292-8. 11. Resende MM, Monteiro SG, Callegari B, Figueiredo PM, Monteiro CR, Monteiro-Neto V. Epidemiology and out- comes of ventilator-associated pneumonia in northern Brazil: an analytical descriptive prospective cohort study. BMC infectious diseases. 2013;13(1):1. 12. Japoni A, Vazin A, Davarpanah MA, Ardakani MA, Alborzi A, Japoni S, et al. Ventilator-associated pneumonia in Ira- nian intensive care units. The Journal of Infection in De- veloping Countries. 2011;5(04):286-93. 13. Hamishekar H, Shadvar K, Taghizadeh M, Golzari SE, Mojtahedzadeh M, Soleimanpour H, et al. Ventilator- Associated Pneumonia in Patients Admitted to Intensive Care Units, Using Open or Closed Endotracheal Suction- ing. Anesthesiology and pain medicine. 2014;4(5). 14. Afhami S, Hadadi A, Khorami E, Seifi A, Bazaz NE. Ventilator-associated pneumonia in a teaching hospi- tal in Tehran and use of the Iranian Nosocomial In- fections Surveillance Software. Eastern Mediterranean Health Journal. 2013;19(10):883. 15. Bennett JE, Dolin R, Blaser MJ. Principles and practice of infectious diseases: Elsevier Health Sciences; 2014. 16. Nadi E, Nekoie B, Mobaien A, Moghimbeigi A, Nekoie A. Evaluation of the Etiology of Nosocomial Pneumonia in the ICUs of the Teaching Hospitals of Hamadan Univer- sity of Medical Sciences. Scientific Journal of Hamadan University of Medical Sciences. 2011;18(1):26-32. 17. Carlson KK, Louis S. Advanced critical care nursing. St Louis. 2009. 18. Sabery M, Shiri H, Moradiance v, Taghadosi M, Gilasi HR, Khamechian M. The frequency and risk factors for early- onset ventilator-associated pneumonia in intensive care units of Kashan Shahid-Beheshti hospital during 2009- 2010. KAUMS Journal ( FEYZ ). 2013;16(6):560-9. 19. Chung DR, Song J-H, Kim SH, Thamlikitkul V, Huang S-G, Wang H, et al. High prevalence of multidrug- resistant nonfermenters in hospital-acquired pneumo- nia in Asia. American journal of respiratory and critical care medicine. 2011;184(12):1409-17. 20. Klompas M, Kleinman K, Khan Y, Evans RS, Lloyd JF, Stevenson K, et al. Rapid and reproducible surveillance for ventilator-associated pneumonia. Clinical infectious diseases. 2012;54(3):370-7. 21. Zarinfar N, Sharafkhah M, Bayat B, sgharFarazi A, Ma- soomehSoofian. Epidemiological Factors of Ventilator- Associated Pneumonia (VAP) among ICU patients in Valiasr Hospital of Arak. 2012. Iranian Journal of Infec- tious Diseases and Tropical Medicine. 2014;19(64). 22. Nateghian A, Omrani A, Alipour Z, Haerinejad M. Causes of ventilator associated pneumonia in pediatrics ICU. Iranian South Medical Journal. 2016;19(1):98-105. This open-access article distributed under the terms of the Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0). Downloaded from: www.jemerg.com Introduction Methods Results Discussion Limitation Conclusion Appendix References