Associated Urinary Tract Infection in a SICU of a Tertiary Care Rural Hospital of India

Similar documents
Bacterial Pathogens in Urinary Tract Infection and Antibiotic Susceptibility Pattern from a Teaching Hospital, Bengaluru, India

Int.J.Curr.Microbiol.App.Sci (2017) 6(3):

Int.J.Curr.Microbiol.App.Sci (2017) 6(11):

Bacteriological Study of Catheter Associated Urinary Tract Infection in a Tertiary Care Hospital

Bacteriological Profile and Antimicrobial Sensitivity of DJ Stents

Aerobic bacterial infections in a burns unit of Sassoon General Hospital, Pune

Detection of ESBL Producing Gram Negative Uropathogens and their Antibiotic Resistance Pattern from a Tertiary Care Centre, Bengaluru, India

Biofilm Producing Uropathogens and Drug Resistance: Dual Foe for Patients on Urinary Catheter

Surveillance of Antimicrobial Resistance among Bacterial Pathogens Isolated from Hospitalized Patients at Chiang Mai University Hospital,

Isolation of Urinary Tract Pathogens and Study of their Drug Susceptibility Patterns

Antimicrobial Susceptibility Profile of E. coli Isolates Causing Urosepsis: Single Centre Experience

Intrinsic, implied and default resistance

A retrospective analysis of urine culture results issued by the microbiology department, Teaching Hospital, Karapitiya

Mili Rani Saha and Sanya Tahmina Jhora. Department of Microbiology, Sir Salimullah Medical College, Mitford, Dhaka, Bangladesh

Prevalence of Pseudomonas aeruginosa in Surgical Site Infection in a Tertiary Care Centre

Detection and Quantitation of the Etiologic Agents of Ventilator Associated Pneumonia in Endotracheal Tube Aspirates From Patients in Iran

Study of drug resistance pattern of principal ESBL producing urinary isolates in an urban hospital setting in Eastern India

Prevalence of Metallo-Beta-Lactamase Producing Pseudomonas aeruginosa and its antibiogram in a tertiary care centre

2012 ANTIBIOGRAM. Central Zone Former DTHR Sites. Department of Pathology and Laboratory Medicine

Prevalence of Extended Spectrum Beta- Lactamase Producers among Various Clinical Samples in a Tertiary Care Hospital: Kurnool District, India

Antimicrobial Susceptibility Testing: Advanced Course

جداول میکروارگانیسم های بیماریزای اولویت دار و آنتی بیوتیک های تعیین شده برای آزمایش تعیین حساسیت ضد میکروبی در برنامه مهار مقاومت میکروبی

Original Article. Hossein Khalili a*, Rasool Soltani b, Sorrosh Negahban c, Alireza Abdollahi d and Keirollah Gholami e.

Available online at ISSN No:

Aerobic Bacterial Profile and Antimicrobial Susceptibility Pattern of Pus Isolates in a Tertiary Care Hospital in Hadoti Region

Research Article. Antimicrobial sensitivity profile of nosocomial uropathogens in a tertiary care hospital of South India

Concise Antibiogram Toolkit Background

Aerobic bacteriological profile of urinary tract infections in a tertiary care hospital

BACTERIOLOGICAL PROFILE OF OSTEOMYELITIS IN A TERTIARY CARE HOSPITAL AT VISAKHAPATNAM, ANDHRA PRADESH

The Basics: Using CLSI Antimicrobial Susceptibility Testing Standards

International Journal of Pharma and Bio Sciences ANTIMICROBIAL SUSCEPTIBILITY PATTERN OF ESBL PRODUCING GRAM NEGATIVE BACILLI ABSTRACT

Antimicrobial Susceptibility Patterns

Isolation, identification and antimicrobial susceptibility pattern of uropathogens isolated at a tertiary care centre

Safe Patient Care Keeping our Residents Safe Use Standard Precautions for ALL Residents at ALL times

Original Articles. K A M S W Gunarathne 1, M Akbar 2, K Karunarathne 3, JRS de Silva 4. Sri Lanka Journal of Child Health, 2011; 40(4):

SCREENING OF URINARY ISOLATES FOR THE PREVALENCE AND ANTIMICROBIAL SUSCEPTIBILITY OF ENTEROBACTERIA OTHER THAN ESCHERICHIA COLI.

Clinico-Microbiological Profile of Urinary Tract Infection in Tertiary Care Hospital in Ahmedabad, Gujarat, India

Bacteriological profile of blood stream infections at a Rural tertiary care teaching hospital of Western Uttar Pradesh

Microbial Profile and Antimicrobial Susceptibility Pattern of Uropathogens Isolated From Catheter Associated Urinary Tract Infection (CAUTI)

Study of biofilm production and antimicrobial sensitivity pattern of uropathogens in a tertiary care hospital in North India

ESBL Producers An Increasing Problem: An Overview Of An Underrated Threat

Understanding the Hospital Antibiogram

Detection of Inducible AmpC β-lactamase-producing Gram-Negative Bacteria in a Teaching Tertiary Care Hospital in North India

Comparison of Antibiotic Resistance and Sensitivity with Reference to Ages of Elders

Study of Methicillin-resistant Staphylococcus aureus in indoor patients of a tertiary care hospital in North India

Key words: Urinary tract infection, Antibiotic resistance, E.coli.

Microbial Profile and Antibiotic Susceptibility Pattern of Surgical Site Infections in Orthopedic Patients at a Tertiary Hospital in Bilaspur

ALARMING RATES OF PREVALENCE OF ESBL PRODUCING E. COLI IN URINARY TRACT INFECTION CASES IN A TERTIARY CARE NEUROSPECIALITY HOSPITAL

European Committee on Antimicrobial Susceptibility Testing

Study of Bacteriological Profile of Corneal Ulcers in Patients Attending VIMS, Ballari, India

EUCAST recommended strains for internal quality control

1/30/ Division of Disease Control and Health Protection. Division of Disease Control and Health Protection

Detection of ESBL, MBL and MRSA among Isolates of Chronic Osteomyelitis and their Antibiogram

Swarnatrisha Saha*, Ksh Mamta Devi, Shan Damrolien, Kh. Sulochana Devi, Krossnunpuii, Kongbrailatpam Tharbendra Sharma

Service Delivery and Safety Department World Health Organization, Headquarters

International Journal of Health Sciences and Research ISSN:

Volume-7, Issue-2, April-June-2016 Coden IJABFP-CAS-USA Received: 5 th Mar 2016 Revised: 11 th April 2016 Accepted: 13 th April 2016 Research article

a. 379 laboratories provided quantitative results, e.g (DD method) to 35.4% (MIC method) of all participants; see Table 2.

BACTERIOLOGICAL PROFILE AND ANTIMICROBIAL SUSCEPTIBILITY PATTERN OF ISOLATES OF NEONATAL SEPTICEMIA IN A TERTIARY CARE HOSPITAL

Antibiotic susceptibility pattern of Pseudomonas aeruginosa at the tertiary care center, Dhiraj Hospital, Piparia, Gujarat

Prevalence of Urinary Tract Infections and Susceptibily Pattern of Uropathogens in Women of Reproductive age Group from North India

BACTERIOLOGICALL STUDY OF MICROORGANISMS ON MOBILES AND STETHOSCOPES USED BY HEALTH CARE WORKERS IN EMERGENCY AND ICU S

Appropriate antimicrobial therapy in HAP: What does this mean?

RETROSPECTIVE STUDY OF GRAM NEGATIVE BACILLI ISOLATES AMONG DIFFERENT CLINICAL SAMPLES FROM A DIAGNOSTIC CENTER OF KANPUR

Does Screening for MRSA Colonization Have A Role In Healthcare-Associated Infection Prevention Programs?

A Study on Bacterial Flora on the Finger printing Surface of the Biometric Devices at a Tertiary Care Hospital

Antimicrobial Stewardship/Statewide Antibiogram. Felicia Matthews Senior Consultant, Pharmacy Specialty BD MedMined Services

Suggestions for appropriate agents to include in routine antimicrobial susceptibility testing

An Approach to Appropriate Antibiotic Prescribing in Outpatient and LTC Settings?

Prevalence and Resistance pattern of Pseudomonas strains isolated from ICU Patients

International Journal of Health Sciences and Research ISSN:

Antimicrobial Susceptibility Testing: The Basics

INCIDENCE OF BACTERIAL COLONISATION IN HOSPITALISED PATIENTS WITH DRUG-RESISTANT TUBERCULOSIS

ESBL Positive E. coli and K. pneumoneae are Emerging as Major Pathogens for Urinary Tract Infection

PrevalenceofAntimicrobialResistanceamongGramNegativeIsolatesinanAdultIntensiveCareUnitataTertiaryCareCenterinSaudiArabia

Acinetobacter species-associated infections and their antibiotic susceptibility profiles in Malaysia.

2016 Antibiotic Susceptibility Report

Antimicrobial resistance at different levels of health-care services in Nepal

European Committee on Antimicrobial Susceptibility Testing

Emergence of multi-drug resistant strains among bacterial isolates in burn wound swabs in a tertiary care centre, Nanded, Maharashtra, India

MICRONAUT MICRONAUT-S Detection of Resistance Mechanisms. Innovation with Integrity BMD MIC

2017 Antibiogram. Central Zone. Alberta Health Services. including. Red Deer Regional Hospital. St. Mary s Hospital, Camrose

Nosocomial Infections: What Are the Unmet Needs

Internationally indexed journal

Int.J.Curr.Microbiol.App.Sci (2017) 6(11):

Evaluation of Bacterial Contamination of Old and New Indian Paper Currency Notes

GENERAL NOTES: 2016 site of infection type of organism location of the patient

Help with moving disc diffusion methods from BSAC to EUCAST. Media BSAC EUCAST

Multi-Drug Resistant Organisms (MDRO)

Antimicrobial Resistance Pattern of Bacterial Isolates from Urinary Tract Infections at a Tertiary Care Centre

High Antibiotic Resistance Pattern Observed in Bacterial Isolates from a Tertiary Hospital in South East Nigeria

Other Enterobacteriaceae

2015 Antibiotic Susceptibility Report

Antibiotic Susceptibility of Common Bacterial Pathogens in Canine Urinary Tract Infections

2015 Antibiogram. Red Deer Regional Hospital. Central Zone. Alberta Health Services

Routine internal quality control as recommended by EUCAST Version 3.1, valid from

Detection of inducible clindamycin resistance among clinical isolates of Staphylococcus aureus in a tertiary care hospital

ESBL Producing Gram Negative Bacteria-A Cause of Concern in Neonatal Septicemia in a Tertiary Care Hospital

Florida Health Care Association District 2 January 13, 2015 A.C. Burke, MA, CIC

Biofilm eradication studies on uropathogenic E. coli using ciprofloxacin and nitrofurantoin

Transcription:

ISSN: 2319-7706 Volume 4 Number 12 (2015) pp. 194-199 http://www.ijcmas.com Original Research Article Catheter Associated Urinary Tract Infection in a SICU of a Tertiary Care Rural Hospital of India Seema Bose* and Atindra Krishna Ghosh Rural medical college, Pravara institute of medical sciences, Loni, Maharashtra, India *Corresponding author A B S T R A C T K e y w o r d s Catheter associated UTI Intensive care unit Multi drug resistant Catheter associated urinary tract infection is one of the major causes of health care associated infection. Due to serious ailments, intensive care unit patients are more prone to have health care associated infections. Patients staying more than 2 days in surgical intensive care unit were included in this study. Urine samples were processed from those patients and cases with urinary tract infection were established on the basis of clinical and microbiological findings. Number of cases with urinary tract infection were 21 (6%). Maximum number of isolates was Escherichia coli (28.57%). All isolates were multidrug resistant. Following simple and well-established guidelines regarding device associated infections and preventing indiscriminate use of antibiotics can control catheter associated urinary tract infection. Introduction Incidence of indwelling drainage device associated urinary tract infection (UTI) is increasing steadily in health care facilities, especially in intensive care units. Rate of infection is directly proportional to the days of catheterization. Microorganisms get adhered to the surface of the catheter and there they colonize and form biofilm. It has been observed that colonization and biofilm formation on device usually occur within three days of catheterization(singh et al., 2010; Annaissie et al., 1995). McLean et al., 1995; in their study described that up to 7 days catheterization, 10 50% patients develop UTI, whereas catheterization for more than 28 days may lead to 100% UTI. The risk of UTI in a catheterized patient increases by approximately 10% for each day. Microorganisms may reach the urinary tract by three possible ways, such as; during insertion of catheter, through coat of exudate surrounding the catheter and intraluminally from tube or collection bag.if there is breach in closed drainage system microbes that enter into drainage bag are soon travel into bladder. Catheter associated UTI (CA UTI) is one of the major causes of health care associated infection (HAI). This adds to patient s morbidity and mortality (Donlan et al., 2002). 194

This study was undertaken to evaluate the incidence of CA UTI, in a surgical ICU(SICU) of a rural tertiary care hospital of western Maharashtra, India. The microorganisms isolated were identified and antibiotic susceptibility tests were done against them. Materials and Methods A prospective study of CA - UTI was done for one year. All patients, who stayed for longer than two days in SICU were included in this study (Suka et al., 2004).Patients admitted in SICU for less than two days or without complete data records were not included in this study. In suspected cases of CA UTI, urine was collected from sampling port of indwelling catheter with sterile syringe and needle. Clinically patients were labeled as suffering from CA UTI, if they fulfill one or more of the following criteria, such as; temperature > 38 0 C, urgency, supra pubic tenderness, pyuria (>10 5 CFU/ml of urine) in centrifuged urine and isolation of not more than two organisms on culture(catheter tip culture, Rush University Medical Centre, Chicago). Urine from the suspectedpatient was cultured on blood agar and MacConkey s agar and incubated for 24 48 hours. The microorganisms thus isolated were identified by conventional methods (Collee et al., 2008). Device - associated infection (DAI rate) was calculated by following formula: Number of DAI/1000 device days = Number of persons developing DAI x 1000/ Total number of device days (HAI programme). Device days are calculated by total number of days a device is in place for each patient (Eggleman et al., 2001; Bose et al., 2014). Antibiotic sensitivity of all the isolates were done using modified Kirby Bauer disk diffusion method. Antibiotic disks used for this study were following ampicillin (10 g), ceftazidime (10 g), Amikacin (30 g), Netilmycin (30 g), ciprofloxacin (5 g), ticarcillin (75 g), cefepime (30 g), piperacillin/tazobactam (100/10 g), Imipenem (10 g), aztreonam (30 g), colistin (10 g), polymyxin B (50 g), nitrofurantoin (300 g), vancomycin (30 g),cefoxitin (30 g)and tigecycline (15 g). Antibiotic sensitivity test was performed by following clinical and laboratory standard institute (CLSI) guidelines (CLSI guideline., 2013). MIC (minimum inhibitory concentration) of Imipenem was also detected in Imipenem - resistant isolates using E strip. All antibiotic disks were obtained from Hi - media private Limited, India and the E strips for MIC detection was obtained from AB BioMerieux. Results and Discussion Total 350 urine samples from catheterized patients were processed within a period of six month in the microbiology department. Out of 350 urine samples, 21 were culture positive. Out of 350 patients, 21(6%) were culture positive and diagnosed as CA UTI cases. Infection rate per 1000 device day was 13.8. The commonest organism isolated from urine of CA UTI patients were E. coli, 6 (28.7%), followed by P. aeruginosa, 4 (19.04%), K. pneumoniae, 3 (14.28%) and S.aureus, CONS, Enterococcus and Acinetobacter spp, 2 (9.52%) each. All isolates were resistant to ampicillin. Tigecycline and nitrofurantoin show high degree of susceptibility against all isolates. Colistin and polymyxin were used against P. aeruginosa and A. baumannii and found to 195

be very effective. Vancomycin was used only for gram-positive cocci. All Staphylococci were sensitive to vancomycin and one of the Enterococci was vancomycin resistant. All Staphylococci were methicillin sensitive as detected by cefoxitin disk ((CLSI guideline., 2013). The ICU patients are usually in critical health conditions and can easily acquire HAI. This causes prolonged hospital stay, thereby imposing burden on both patients and the health care facilities. UTI is the second most common cause of HAI. Globally, the incidence of UTI in an ICU is more than 15%(Singh et al., 2010).In CA UTI patient, the person is either currently catheterized or has been catheterized within the previous 48 hours. The most successful treatment of CA UTI is removal of the catheter if possible and by restricting it s use only where it is clearly indicated. Urinary catheterization is the commonest predisposing factor for nosocomial UTI. Catheterization disturbs host defense mechanisms and creates easier access of uropathogens from urethral meatus to urinary bladder. It has been observed that causative uropathogens for UTI was present in the urethral meatus in 67% women and 29% men just prior to development of CA bacteriuria.(hootan TM et al, 2009)Microorganisms may reach the urinary tract by three possible ways, such as; during insertion of catheter, through coat of exudate surrounding the catheter and intraluminally from tube or collection bag. If there is breach in closed drainage system microbes that enter into drainage bag are soon travel into bladder. It has also been observed that uroepithelial cells from catheterized patients are more susceptible to binding of microorganisms. (Barford JMT et al, 2009). Over the period of one year, we processed 350 urine samples from suspected cases of CA UTI patients, admitted in a SICU. Outof which, 21(6%) were culture positive. Infection rate/1000 urinary device days were 13.8. Researchers from different region of India observed different rates of CA UTI in their health care facilities. Datta et al., 2014 reported 10.75%, Singh et al.,2010;observed 0.23% and Prasanna et al.,2008 described 95% of CA UTI incidences from different parts of India. Habibi et al., 2008;observed incidence of HAI/1000 urinary catheter dayto be 11.3. Greene et al, (2008) reported that 36% of cases of UTI were found in acute healthcare setting. Xie DS et al (2011) isolated fungi (21.28%), followed by E.coli (17.02%) and P.aeruginosa (10.64%) from cases of UTI admitted in ICU. In our study, maximum number of isolation was of E. coli, 6 (28.57%), followed by P. aeruginosa, Klebsiella spp, S. aureus, CONS and Acinetobacter spp. We found multi drug resistance among various hospital strains. One of the isolates of A.baumannii was resistant to Imipenem by Kirby Bauer disk diffusion method but was found to be susceptible for the same by MIC detection. Sinha et al., 2007;also reported similar observation. In our study, all isolates were resistant to ampicillin. We found that, all non-fermentinggramnegative bacilli were 100% susceptible against colistin, polymyxin B and tigecycline. While using colistin and polymyxin B, one has to be careful, because of side effects, such as, nephrotoxicity (27 58%). Tigecycline (Gar 936) is a new glycylcycline derivative of tetracycline, bacteriostatic in nature and effective against both gram- positive as well as gram-negative organisms. This can be used against multidrug resistant organisms (Levin et al., 2003; Pachon Ibanez et al., 2004). 196

Table.1 Catheter associated UTI in SICU (n= 21) No. of cases No. of cases with UTI detected Total No. of device Infection rate/1000 (culture positive) days device days 350 21(6%) 1520 13.8 Table.2 Number and percentage of different isolates obtained from urine samples (n = 21) Organisms Number of Percentage isolates Escherichia coli 6 28.57 Pseudomonas aeruginosa 4 19.04 (P.aeruginosa) Klebsiella pneumoniae 3 14.28 (K. pneumoniae) Staphylococcus aureus (S. aureus) 2 9.52 Coagulase negative 2 9.52 staphylococci (CONS) Enterococcus spp 2 9.52 Acinetobacter spp 2 9.52 Table.3 Antibiotic sensitivity pattern of various clinical isolates from urine samples of CA UTI cases Antibiotics E.coli (n=6) P.aeruginosa (n=4) K. pneumoniae (n=3) S.aureus CONS Enterococcus Acinetobacter Ampicillin 0 0 0 0 0 0 0 Vancomycin - - - 2 1(50%) 1(50%) - (100%) Amikacin 5(83.3%) 3(75%) 2(66.66%) 2(100%) 1(50%) 1(50%) 1(50%) Ceftazidime 2(33.33%) 2(50%) 0 1(50%) 1(50%) 1(50%) 0(50%) Netilmycin 2(33.33%) 1(25%) 1(33.33%) 2(100%) 1(50%) 1(50%) 0(50%) Ciprofloxacin 2(33.33%) 1(25%) 1(33.33%) 1(50%) 1(50%) 1(50%) 0(50%) Ticarcillin 2(33.33%) 1(25%) 1(33.33%) - - - 0 Piperacillin/ 3(50%) 2(50%) 1(33.33%) - - - 0 Tazobactam Aztreonam 3(50%) 2(50%) 2(66.66%) - - - - Imipenem 4(66.66%) 3(75%) 2(66.66%) - - - 2(100%) Polymyxin B - 4(100%) - - - - 2(100%) Colistin - 4(100%) - - - - 2(100%) Tigecycline 6(100%) 4(100%) 3(100%) 2(100%) 2(100%) 1(50%) 2(100%) Cefoxitin 2(33.33%) 1(25%) 0 2(100%) 2(100%) 1(50%) 0 Nitrofurantoin 5(83.3%) 4(100%) 2(66.66%) 2(100%) 2(100%) 2(100%) 1(50%) However, some researchers found tigecycline resistant strains in their work (Neonakis et al., 2011). All our S.aureus and CONS were methicillin sensitive and 197

vancomycin sensitive. One strain of enterococcus spp was vancomycin resistant. Methicillin resistance was detected using 30 g cefoxitin disk, as per CLSI guideline, 2013. Cefoxitin has been recently recommended by CLSI for detection of methicillin resistant Staphylococci and is more reliable than oxacillin, 1 g (CLSI guideline, 2013). During their research, Xie DS et al (2011) found that 88% E.coli and 100% of P.aeruginosa isolated from ICU patients urine were resistant to ciprofloxacin. In their work P. aeruginosa also showed 100%( resistance to Amikacin ceftazidime and meropenem. According to some researchers, antibiotic treatment is controversial. Initially it reduces bacterial load in urine but there is always chances of development of resistant bacteria (Hootan TM et al, 2009). In conclusion, the SICU patients are usually admitted with serious health conditions. They can easily acquire HAI because of their low immune status. This prolongs their hospital stay, thereby imposing burden on both patients and the hospitals resources. To prevent CA UTI, simple measures, such as; proper hand washing should be followed meticulously. Health care associated workers should follow well-established guidelines on prevention of DAI. Use of antibiotic or antiseptic coated urinary catheters help to prevent CA UTI (CDC. NHSN manual, 2009). Acknowledgement Authors are grateful to Pravara Institute of Medical Sciences (Deemed University) for it s valuable support. References Annaissie, E., Samonis, G., Kontoyiannis, D., Costerton, J., Sabharwal, U., Bodey, G., Raad, I.1995. Role of catheter related infections. Eur JClin Microbiol Infect Dis.14,135 137. Bose, S., Saini, S., Deorukhkar, S., Kinikar, A. 2014. A study of device associated infection in an ICU of a teaching hospital of rural Maharashtra. Int J Infect Trop Dis. 1(2): 68 72. Barford, J.M.T., Coates, A.R.M. 2009. The pathogenesis of catheter associated urinary tract infection. J Infect Prevention. 10(2): 50 56. Catheter tip culture Rush university medical center (last updated: 19.05.2014): available in: http://www.rush.edu/webapps/rml/rm LTestEntryDtl.jsp?id=3225 (accessed on 27.05.2014). Collee, J.G., MilesR.S., Watt,B. 2008. Test for identification of bacteria. In Mackie and McCartney s Practical Medical Microbiology 14 th ed. J.G. Collee, A.G. Fraser, B.P. Marmion, and A. Simmons, Editors. Churchill Livingstone: Indian Reprints, 131 149. CDC, The national health care safety network (NHSN) manual: Patient safety component protocol 2009. Available in: https://www.premierinc.com/safety/to pics/guidelines/surveil.jsp (accessed on 27. 05.2014). Donlan, R.M., Costerton, J.W. 2002. Biofilms: Survival mechanisms of clinically relevant Microorganisms. Clin Microbiol Rev. 167 193. Datta,P., Rani,H., Chauhan, R., Gomber,V., Chander, J.2014.Health. 38:an intensive care unit in Northern India.Ind J Anaes. 58(1), 30 35. Eggleman, P., Pittet, D. 2001.Infection control in the ICU. Chest.120 (6): 2059. Greene, L., Marx, J., Oriola, S. 2008. Guide to the elimination of catheter 198

associated infection. In An Epic Guide. Association professionals infect control epidemiol. pp. 5. Health care associated infections (HAI programme). Glossary of key terms and definitions. Available in: http://www.ct.gov/dph/lib/dph/hai/p DF/HAI_Glossary_of_Terms.pdf (accessed on 28.05.2014). 12. Hootan, T.M., Bradley, S.F., Cardenas, D.D., Colgan, R., Geerlings, S.E., Rice, J.C., Saint, S, et al. 2009. Diagnosis, prevention and treatment of catheter associated urinary tract infection in adults. 13.Habibi, S., Wig, N., Agarwal, S et al. 2008. Epidemiology of nosocomial infections in medicine intensive care unit at a tertiary care hospital in northern India. Trop Doc. 38(8): 233 235. Levin, A.S. 2003. Treatment of Acinetobacter spp infections. Expert Opinion Pharmacother. 4: 1289 1296. McLean, R. J. C., Nickel, J.C., Olson, M.E. Biofilm associated urinary tract infections. In Microbial Biofilms. 1995. H.M. Lappin Scott and J.W. Costerton (eds), 261 273, Neonakis, I.K., Stylianou, K., Daphnis E., Maraki, S. 2011. First case of resistance to tigecycline by Klebsiella pneumonia in a European university hospital. Ind J Med Microbiol. 29: 78 79. Performance standard for antimicrobial susceptibility testing; twenty-third informational supplements (M 100 S23).2013. 33 (1): 34 37. Prasanna, S., Doble,M.2008. Medical biofilm its formation and prevention using organic molecules. J Ind Inst Sci. 88 (1): 27 36. Pachon Ibanez,M.E., Jimenez Mejias., M.E., Pichardo,C., Llanos, A.C., Pachon, J. 2004.Activity of tigecycline (Gar 936) against Acinetobacter baumannii strains including those resistant to Imipenem. Antimicrob AgentsChemother. 48 (11): 4479 4481. Singh, S., Pandya, Y., Patel, R., Paliwal, M., Wilson, A., Trivedi, S. 2010. Surveillance of device associated infections at a teaching hospital in rural Gujarat, India. Ind JMed Microbiol. 28 (4): 342 347. Suka,M., Yoshida,K., Takezawa, J. 2004.Association between APACHE II score and nosocomial infections in intensive care unit patients: A multicenter cohort study. Environ health preventive med. 9 (6: 262 265, Sinha,M., Srinivasa,H. 2007.Mechanisms of resistance to carbapenems in meropenem resistant Acinetobacter isolates from clinical samples. Ind JMed Microbiol. 25: 121 125. Xie, D.S., Lai, R. P., Nie, S.F. 2011. Surveys of catheter associated urinary tract infection in a university hospital intensive care unit in China. Braz J Infect Dis. 15(3): 296 297. 199