Year : 2017 | Volume
| Issue : 4 | Page : 402-407
Epidemiology and characteristics of nosocomial infections in critically ill patients in a tertiary care intensive care unit of Northern India
Anirban Hom Choudhuri, Mitali Chakravarty, Rajeev Uppal
Department of Anaesthesiology and Intensive Care, GB Pant Institute of Postgraduate Medical Education and Research, New Delhi, India
Anirban Hom Choudhuri
Department of Anaesthesiology and Intensive Care, GB Pant Institute of Postgraduate Medical Education and Research, New Delhi - 110 002
Source of Support: None, Conflict of Interest: None
|Date of Web Publication||22-Sep-2017|
Background and Aims: The prevalence of nosocomial infection is higher in the Intensive Care Unit (ICU) than other areas of the hospital. The present observational study was undertaken to describe the epidemiology and characteristics of nosocomial infections acquired in a tertiary care ICU and the impact of the various risk factors in their causation.
Materials and Methods: A retrospective study was conducted on the prospectively collected data of 153 consecutive patients admitted in a tertiary care ICU between July 2014 and December 2015. The primary objective was to assess the epidemiology of ICU-acquired bacterial infections in terms of the incidence of new infections, causative organism, and site. The secondary end point was to assess the risk factors for developing ICU-acquired infections.
Results: Out of the 153 patients enrolled in the study, 87 had an ICU-acquired nosocomial infection (58.86%). The most common organism responsible for infection was Klebsiella pneumoniae (37%), and the most common infection was pneumonia (33%). The duration of mechanical ventilation and length of ICU stay were significantly prolonged in patients developing nosocomial infections. There was no difference in mortality between the groups. The multivariate analyses identified intubation longer than 7 days, urinary catheterization >7 days, duration of mechanical ventilation more than 7 days, and ICU length of stay longer than 7 days as independent risk factors for nosocomial infections.
Conclusion: The study demonstrated a high incidence of nosocomial infection in the ICU and identified the risk factors for acquisition of nosocomial infections in the ICU.
Keywords: Critically ill, ICU, nosocomial infection
|How to cite this article:|
Choudhuri AH, Chakravarty M, Uppal R. Epidemiology and characteristics of nosocomial infections in critically ill patients in a tertiary care intensive care unit of Northern India. Saudi J Anaesth 2017;11:402-7
|How to cite this URL:|
Choudhuri AH, Chakravarty M, Uppal R. Epidemiology and characteristics of nosocomial infections in critically ill patients in a tertiary care intensive care unit of Northern India. Saudi J Anaesth [serial online] 2017 [cited 2020 Jul 8];11:402-7. Available from: http://www.saudija.org/text.asp?2017/11/4/402/215409
| Introduction|| |
Nosocomial infections are a major threat to the patients' safety in any health-care facility. However, the prevalence is higher in the Intensive Care Units (ICUs) than other areas of the hospital.,, This increased prevalence of nosocomial infection not only influences the mortality and morbidity pattern of ICU but also poses a significant financial burden to the patient and the society.,
National nosocomial infections surveillance system has defined nosocomial infection as a localized or systemic condition that results from an adverse reaction to the presence of an infectious agent(s) or its toxin(s) that was not present or incubating at the time of admission to the hospital.
The important nosocomial infections in the ICU based on frequency and potential severity include urinary tract infection (UTI), pneumonia, bloodstream infections, skin and soft tissue infections, gastroenteritis, hepatitis, and meningitis.,,,
The aim of this observational study was to describe the epidemiology and characteristics of nosocomial infections in our ICU including risk factors, causative microorganisms and the impact of such nosocomial infections on the ICU mortality, and length of stay.
| Materials and Methods|| |
After seeking approval from the Institute Ethics Committee for waiver of informed consent, a retrospective observational study of prospectively collected data was conducted in a cohort of 153 consecutively admitted patients in the seven bedded mixed medical-surgical ICU between July 2014 and December 2015.
The data of all patients admitted in the ICU between July 2014 and December 2015 were extracted from the official database maintained for the clinical and administrative purpose. Patients whose length of stay in the ICU was more than 48 h were chosen for enrollment. “ICU-acquired infections” were defined as all new infections acquired in the ICU after 48 h of admission. The preexisting infections were distinguished from the ICU-acquired infections both clinically and microbiologically. Clinical diagnosis was made according to the criteria of the Center for Disease Control and Prevention National Healthcare Safety Network. All microbiological isolates of infected patients were evaluated.
The primary objective was to assess the epidemiology of ICU-acquired bacterial infections in terms of the incidence of new infections, causative organism, and site.
The secondary objective was to assess the risk factors for developing ICU-acquired infections. The group which acquired nosocomial infection (Group A) was compared to the group which did not acquire any nosocomial infection (Group B) according to a number of demographic and clinical factors including age, sex, disease severity at the time of admission (assessed from acute physiology and chronic health evaluation II [APACHE II] score), duration of mechanical ventilation, duration of stay in the ICU, duration of endotracheal intubation, central venous catheterization, and urinary catheterization. The other secondary objectives were to assess the outcome of patients with ICU-acquired infections in terms of mortality, duration of mechanical ventilation and length of ICU stay.
The incidence of ICU-acquired infections was described as a percentage. The data for continuous variables were presented in terms of mean ± standard deviation and data for categorical variables were indicated by frequency (%). The statistical significance of qualitative variables between the different groups was calculated using Chi-square or Fischer exact test. The statistical significance of quantitative variables was calculated by Student's t-test or Wilcoxon test. Mann–Whitney test was done where data did not follow a normal distribution. Independent risk factors for mortality and morbidity were analyzed by multivariate analysis. Results of multivariate analysis were presented as a P value and odds ratio (OR) with 95% confidence interval (CI). Data were analyzed using the STATA 9.1 software (STATA Corp, 4905, Lakeway Drive College Station, 77845, Texas, US).
| Results|| |
Of the 153 patients enrolled in our study, majority had stroke, liver diseases, and pancreatitis [Figure 1] and 87 had an ICU-acquired nosocomial infection (56.86%). The bacteria responsible for the infection were primarily Klebsiella pneumoniae and Escherichia More Details coli [Figure 2]. Majority of the infections were due to pneumonia followed by UTIs and blood stream spread [Figure 3]. The patients in the Group A (those who acquired nosocomial infection) and Group B (who did not acquire any nosocomial infection) showed no difference with regard to age, sex, disease severity, and comorbid conditions. The comparison of ICU length of stay (15.24 ± 10.9 vs. 4.46 ± 5.03) and duration of mechanical ventilation (11.9 ± 8.3 vs. 3.07 ± 2.25) showed that these were higher in Group A than in Group B (P< 0.001). There was no statistically significant difference in mortality between the groups (46.15% vs. 53.85%) [Table 1]. The multivariate analysis showed the following to be independent factors associated with nosocomial infections in the ICU: duration of stay (P< 0.001, OR 19.7, 95% CI 7.9-49.1), duration of mechanical ventilation (P< 0.001, OR: 37.9, 95% CI: 10.9–130.8), duration of tracheal intubation (P< 0.001, OR: 14.8, 95% CI: 2.56–86.12), and duration of urinary catheterization (P< 0.001, OR: 2.8, 95% CI: 0.71–11.6) [Table 2].
|Figure 2: Organisms responsible for causing nosocomial infections in the Intensive Care Unit|
Click here to view
|Table 1: Comparison between patients developing (Group A) and not developing (Group B) nosocomial infections|
Click here to view
|Table 2: Multivariate analysis showing independent predictors of Intensive Care Unit acquired nosocomial infections|
Click here to view
| Discussion|| |
Despite contributing to only 15%–20% of the hospital beds, ICUs account for more than 50% of the life-threatening nosocomial infections.,, The incidence of nosocomial infection found in our study is higher than some studies reported from other parts of the world., In India, studies reporting nosocomial infections in ICU have ranged from 11% to 60%., The wide variance in the prevalence is because of the presence or absence of various risk factors distributed unevenly across the health care settings. Our study found the highest incidence of nosocomial infection to be due to K. pneumoniae. Klebsiella accounts for approximately 8% of all hospital-acquired infections and as many as 14% of cases of primary bacteremia. The role of extended-spectrum beta-lactamase (ESBL) produced by Klebsiella strains in outbreaks of drug-resistant infections has been a major concern since the past decade. It is well known that the ESBLs increase affinity and hydrolytic activity for third generation cephalosporins and monobactams and aggravate cross-resistance among aminoglycosides.,, The outbreaks of K. pneumoniae occur most commonly in the ICU because of the presence of the potential risk factors for colonization and infection. The factors such as disease severity, extreme age, long duration antibiotic usage, and the high prevalence of invasive procedure contribute to their increased colonization and infection., Xiong et al. from China had reported a 51% K. pneumoniae incidence in the neurosurgical intensive care patients with a greater preponderance of the ESBL producing strains. Although we did not measure the ESBL producing strains in our study, our overall incidence is similar to Xiong et al. It was found in another multihospital study that when patients are admitted to acute care hospitals from high acuity long-term care facilities, they are more likely to be colonized with carbapenemase-producing K. pneumoniae carbapenemase. Many of our patients were initially admitted to other health-care facilities and later shifted to our center for advanced therapies. This can explain the risk of higher colonization and infection due to K. pneumoniae in our patients. Studies have reported K. pneumoniae outbreaks with a wide variety of objects such as ultrasonography gel, intravenous solutions containing dextrose, contaminated breast milk, and bath soap.,,, Since some of these factors can be relevant in our ICU, their identification and prevention can be useful to reduce the K. pneumoniae infections in our patients. Our study also showed a high incidence of Klebsiella in the UTIs and the same has also been described in studies reported from other parts of the world. It has been shown in many studies that asymptomatic bacteriuria should be differentiated from symptomatic UTI and only the later should be subjected to antibiotic treatment. This can prevent antibiotic-associated complications and reduce antibiotic misuse., The early identification of Pseudomonas and E. coli can make the patients amenable to treatment for UTI before they become more critical in the ICU and a good number of such patients existed in our ICU.
In our study, about 39% patients developed multiple infections due to two or more organisms at more than one site. It has been reported in studies that mortality associated with multiple organism bacteremia is 48% as against 25% in single organism bacteremia. However, such a correlation was beyond the scope of observation in our study.
Our study did not find any difference in mortality between the group which developed nosocomial infection in the ICU and the group which did not. There was also no difference in age, sex, and severity of disease based on APACHE II between the groups. This is because of the complex mix of heterogeneous cases and their inherent differences having a variable effect on all-cause mortality. However, there was a difference in ICU length of stay and duration of mechanical ventilation which has been corroborated in several other studies.,,
Our study has identified duration of intubation, duration of urinary catheterization, duration of mechanical ventilation, and duration of ICU stay as independent predictors of nosocomial infection in the ICU. In a similar study as ours, age, simplified acute physiology score II score at onset of blood stream infection, colistin resistance, and aminoglycoside were identified as independent predictors of K. pneumoniae infection in the ICU. Another study conducted in surgical ICU found admission APACHE II score, presence of peritonitis, pancreatitis, aminoglycoside use, and mechanical ventilation as independent risk factors for nosocomial infection. A retrospective cohort study conducted in a mixed ICU found the need for mechanical ventilation on ICU day 1 and transfer to the ICU from another unit as independent predictors of ICU-attributable nosocomial infections. No study has, however, shown the direct association between a particular organism and a particular infection site on mortality.
However, our study had some limitations. One, the observed variables are simple with regard to the complex nature of their outcomes. Two, since many patients had multi-organ dysfunction at the time of ICU admission, the addition of MODS score or SOFA score to APACHE II could have improved the evaluation. Three, many physiological determinants of outcomes are addressed before ICU admission in the emergency department which impacts the nosocomial infection. These factors were not addressed in our study. Finally, all inherent drawbacks of a retrospective study can limit our observation and interpretation.
| Conclusion|| |
Our study found a high incidence of nosocomial infections in the ICU which did not affect overall ICU mortality. The main cause of ICU infection was pneumonia caused by K. pneumoniae. The duration of mechanical ventilation, duration of urinary catheterization, duration of endotracheal intubation, and length of ICU stay were independent predictors of ICU-acquired nosocomial infections. More prospective observational and multicentric studies are necessary to enrich our understanding of the various risk factors and their associations.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Allegranzi B, Bagheri Nejad S, Combescure C, Graafmans W, Attar H, Donaldson L, et al.
Burden of endemic health-care-associated infection in developing countries: Systematic review and meta-analysis. Lancet 2011;377:228-41.
Magill SS, Edwards JR, Bamberg W, Beldavs ZG, Dumyati G, Kainer MA, et al.
Multistate point-prevalence survey of health care-associated infections. N
Engl J Med 2014;370:1198-208.
Richards MJ, Edwards JR, Culver DH, Gaynes RP. Nosocomial infections in combined medical-surgical Intensive Care Units in the United States. Infect Control Hosp Epidemiol 2000;21:510-5.
NNIS System. National Nosocomial Infections Surveillance (NNIS) System Report, data summary from January 1992 through June 2003, issued August 2003. Am J Infect Control 2003;31:481-98.
Inan D, Saba R, Yalcin AN, Yilmaz M, Ongut G, Ramazanoglu A, et al.
Device-associated nosocomial infection rates in Turkish medical-surgical Intensive Care Units. Infect Control Hosp Epidemiol 2006;27:343-8.
Richards M, Thursky K, Buising K. Epidemiology, prevalence, and sites of infections in Intensive Care Units. Semin Respir Crit Care Med 2003;24:3-22.
Horan TC, Andrus M, Dudeck MA. CDC/NHSN surveillance definition of health care-associated infection and criteria for specific types of infections in the acute care setting. Am J Infect Control 2008;36:309-32.
Bearman GM, Munro C, Sessler CN, Wenzel RP. Infection control and the prevention of nosocomial infections in the Intensive Care Unit. Semin Respir Crit Care Med 2006;27:310-24.
Smith RL. Prevention of infection in the Intensive Care Unit. Curr Opin Infect Dis 2006;19:323-6.
Ramritu P, Halton K, Cook D, Whitby M, Graves N. Catheter-related bloodstream infections in Intensive Care Units: A systematic review with meta-analysis. J Adv Nurs 2008;62:3-21.
Ak O, Batirel A, Ozer S, Çolakoglu S. Nosocomial infections and risk factors in the Intensive Care Unit of a teaching and research hospital: A prospective cohort study. Med Sci Monit 2011;17:PH29-34.
Aly NY, Al-Mousa HH, Al Asar el SM. Nosocomial infections in a medical-surgical Intensive Care Unit. Med Princ Pract 2008;17:373-7.
Mythri H, Kashinath K. Nosocomial infections in patients admitted in Intensive Care Unit of a tertiary health center, India. Ann Med Health Sci Res 2014;4:738-41.
] [Full text]
Dasgupta S, Das S, Chawan NS, Hazra A. Nosocomial infections in the Intensive Care Unit: Incidence, risk factors, outcome and associated pathogens in a public tertiary teaching hospital of Eastern India. Indian J Crit Care Med 2015;19:14-20.
] [Full text]
Peña C, Pujol M, Ricart A, Ardanuy C, Ayats J, Liñares J, et al.
Risk factors for faecal carriage of Klebsiella pneumoniae
producing extended spectrum beta-lactamase (ESBL-KP) in the Intensive Care Unit. J Hosp Infect 1997;35:9-16.
Lucet JC, Chevret S, Decré D, Vanjak D, Macrez A, Bédos JP, et al.
Outbreak of multiply resistant enterobacteriaceae in an Intensive Care Unit: Epidemiology and risk factors for acquisition. Clin Infect Dis 1996;22:430-6.
Pessoa-Silva CL, Meurer Moreira B, Câmara Almeida V, Flannery B, Almeida Lins MC, Mello Sampaio JL, et al.
Extended-spectrum beta-lactamase-producing Klebsiella pneumoniae
in a neonatal Intensive Care Unit: Risk factors for infection and colonization. J Hosp Infect 2003;53:198-206.
Yuan M, Aucken H, Hall LM, Pitt TL, Livermore DM. Epidemiological typing of klebsiellae with extended-spectrum beta-lactamases from European Intensive Care Units. J Antimicrob Chemother 1998;41:527-39.
Livermore DM, Yuan M. Antibiotic resistance and production of extended-spectrum beta-lactamases amongst Klebsiella
spp. from Intensive Care Units in Europe. J Antimicrob Chemother 1996;38:409-24.
Xiong Z, Zhu D, Wang F, Zhang Y, Okamoto R, Inoue M. Investigation of extended-spectrum beta-lactamase in Klebsiellae pneumoniae
and Escherichia coli
from China. Diagn Microbiol Infect Dis 2002;44:195-200.
Won SY, Munoz-Price LS, Lolans K, Hota B, Weinstein RA, Hayden MK; Centers for Disease Control and Prevention Epicenter Program. Emergence and rapid regional spread of Klebsiella pneumoniae
. Clin Infect Dis 2011;53:532-40.
Gaillot O, Maruéjouls C, Abachin E, Lecuru F, Arlet G, Simonet M, et al.
Nosocomial outbreak of Klebsiella pneumoniae
producing SHV-5 extended-spectrum beta-lactamase, originating from a contaminated ultrasonography coupling gel. J Clin Microbiol 1998;36:1357-60.
Lalitha MK, Kenneth J, Jana AK, Jesudason MV, Kuruvilla KA, Jacobson K, et al.
Identification of an IV-dextrose solution as the source of an outbreak of Klebsiella pneumoniae
sepsis in a newborn nursery. J Hosp Infect 1999;43:70-3.
Donowitz LG, Marsik FJ, Fisher KA, Wenzel RP. Contaminated breast milk: A source of Klebsiella bacteremia
in a newborn Intensive Care Unit. Rev Infect Dis 1981;3:716-20.
Szabó D, Filetóth Z, Szentandrássy J, Némedi M, Tóth E, Jeney C, et al.
Molecular epidemiology of a cluster of cases due to Klebsiella pneumoniae
producing SHV-5 extended-spectrum beta-lactamase in the premature Intensive Care Unit of a Hungarian hospital. J Clin Microbiol 1999;37:4167-9.
Zilberberg MD, Shorr AF. Secular trends in gram-negative resistance among urinary tract infection hospitalizations in the United States, 2000-2009. Infect Control Hosp Epidemiol 2013;34:940-6.
Shilo S, Assous MV, Lachish T, Kopuit P, Bdolah-Abram T, Yinnon AM, et al.
Risk factors for bacteriuria with carbapenem-resistant Klebsiella pneumoniae
and its impact on mortality: A case-control study. Infection 2013;41:503-9.
Ing AF, McLean AP, Meakins JL. Multiple-organism bacteremia in the surgical Intensive Care Unit: A sign of intraperitoneal sepsis. Surgery 1981;90:779-86.
Laupland KB, Zygun DA, Davies HD, Church DL, Louie TJ, Doig CJ. Population-based assessment of Intensive Care Unit-acquired bloodstream infections in adults: Incidence, risk factors, and associated mortality rate. Crit Care Med 2002;30:2462-7.
Laupland KB, Kirkpatrick AW, Church DL, Ross T, Gregson DB. Intensive-Care-Unit-acquired bloodstream infections in a regional critically ill population. J Hosp Infect 2004;58:137-45.
Erbay H, Yalcin AN, Serin S, Turgut H, Tomatir E, Cetin B, et al.
Nosocomial infections in Intensive Care Unit in a Turkish university hospital: A 2-year survey. Intensive Care Med 2003;29:1482-8.
Papadimitriou-Olivgeris M, Marangos M, Christofidou M, Fligou F, Bartzavali C, Panteli ES, et al.
Risk factors for infection and predictors of mortality among patients with KPC-producing Klebsiella pneumoniae
bloodstream infections in the Intensive Care Unit. Scand J Infect Dis 2014;46:642-8.
Markogiannakis H, Pachylaki N, Samara E, Kalderi M, Minettou M, Toutouza M, et al.
Infections in a surgical Intensive Care Unit of a university hospital in Greece. Int J Infect Dis 2009;13:145-53.
McCusker ME, Périssé AR, Roghmann MC. Severity-of-illness markers as predictors of nosocomial infection in adult Intensive Care Unit patients. Am J Infect Control 2002;30:139-44.
[Figure 1], [Figure 2], [Figure 3]
[Table 1], [Table 2]