Retrospective Analysis of Blood Stream Infections and Antibiotic Susceptibility Pattern of Gram Negative Bacteria in a Tertiary Care Cancer Hospital

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International Journal of Medical Research & Health Sciences Available online at www.ijmrhs.com ISSN No: 2319-5886 International Journal of Medical Research & Health Sciences, 2017, 6(12): 19-26 I J M R H S Retrospective Analysis of Blood Stream Infections and Antibiotic Susceptibility Pattern of Gram Negative Bacteria in a Tertiary Care Cancer Hospital Radha Rani D 1 *, Sridevi Chaitanya B 1, Senthil Rajappa J 2, Basanth Kumar R 3, Krishna Prabhakar K 4, Krishna Mohan MVT 2, Vibhavari Nayak K 3, Pavan Kumar 2, Ayyagari Santa 2 and T. Subramanyeshwara Rao 5 1 Department of Microbiology, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India 2 Department of Medical Oncology, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India 3 Department of Anaesthesiology, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India 4 Department of Critical Care Medicine, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India 5 Department of Surgical Oncology, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, India *Corresponding e-mail: dradharani@gmail.com ABSTRACT Background: Bacterial bloodstream infections are important causes of morbidity and mortality globally. The aim of the present study was to determine the bacterial profile of bloodstream infections and their antibiotic susceptibility pattern among the clinically diagnosed cases of sepsis in cancer patients. Methods: In the present study, etiological and antimicrobial susceptibility profile of blood cultures over a period of 1 year at a tertiary cancer care hospital was done. Blood culture positive isolates were identified using standard microbiological methods and by Fully automated BD Phoenix 100. The antibiotic susceptibility pattern of the organisms was performed by Kirby-Bauer disc diffusion method and MIC (Minimum inhibitory concentration) was done by Fully automated BD Phoenix 100. Results: There were 1178 blood culture samples, of which 327 (27.7%) were identified to be culture positive. Out of 327 positive cultures, 299 (91.4%) showed bacterial growth, Gram negative were 161 (53.8%) and Gram positive were 138 (46.1%). Candida species were isolated from 13 (3.97%) of positive samples and 15 samples showed contamination. The most common Gram-negative isolate was. Escherichia coli (37.80%) and Gram-positive isolate was coagulasenegative staphylococci (52.80%). Escherichia coli showed highest sensitivity to amikacin (83.60%) and sensitivity to piperacillin+ tazobactum and cefaperazone+sulbactam was 54.09% and 52.45% respectively. High degree of resistance was found to cephalosporins and levofloxacin. Conclusion: The results indicate high level of antimicrobial resistance among Gram negative bacilli in septicemic patients. The results warrant continuous monitoring of antimicrobial pattern so as to build geographical epidemiological data. Keywords: Blood stream infections (BSI), Antimicrobial susceptibility, Bacteremia, Resistance INTRODUCTION Infectious complications consequent to the immunosuppressive therapy has become a major cause of morbidity and mortality in cancer patients [1]. The cancer patient is immunocompromised due to nature of the disease and due to interventions in the form of chemotherapy. Other associated risk factors for acquiring infection are long term catheterization, mucositis due to cytotoxic agents, neutropenia, and stem cell transplantation [2]. Blood stream infections increase the length of hospital stay, cause significant morbidity and mortality and increase the cost of care. 19

The situation further deteriorates with increasing rate of multidrug resistance. The crude mortality rate due to BSIs in cancer patients ranges from 18% to 42% [3-6]. The organisms and their antibiotic susceptibility pattern varies among different healthcare facilities and geographical areas. Blood culture is the single most reliable procedure for bacterial isolation and detection. The aim of the present study was to determine the bacterial profile of bloodstream infections and to assess the antibiotic susceptibility pattern of the major pathogens among the clinically diagnosed cases of sepsis in cancer patients. MATERIALS AND METHODS This was a retrospective study conducted at a tertiary care hospital for cancer patients. We analyzed all blood samples sent for bacterial culture during the year 2016. A total of 1178 blood samples from clinically diagnosed cases of sepsis, received in the microbiology laboratory of a 450-bedded cancer hospital of south India over duration of one year, were included in the study. Blood samples were collected before the administration of antibiotics. Relevant details of the patients were recorded. Blood culture bottles from Biomerieux were inoculated with the sample and incubated in BACT/ALERT 3D. When the instrument signaled positive, sub cultures were done on blood agar, MacConkey agar and chocolate agar. The growth obtained was identified by colony morphology, Gram stain of the isolated colonies, standard microbiological, biochemical tests and by fully automated BD Phoenix 100. The antibiotic susceptibility pattern of the isolated organisms was performed by Kirby-Bauer disc diffusion method on Mueller-Hinton agar plates as well as MICs were done by fully automated BD Phoenix 100 and the results were interpreted as per the Clinical and Laboratory Standards Institute (CLSI) 2016 guidelines. Cefoxitin disc diffusion method was used to identify MRSA (Methicillin resistant Staphylococcus aureus) as per CLSI guidelines. MDR (Multi drug resistant) was defined as non-susceptibility to at least one agent in three or more antimicrobial categories. The antibiotic discs that were used to identify the susceptibility pattern of the gram-negative pathogens and their concentrations include amikacin (30 mcg), amoxicillin+clavulanic acid (20/10 mcg), ceftazidime (30 mcg), ceftriaxone (30 mcg), cefepime (30 mcg), cefoperazone+sulbactam (75/30 mcg), imipenem (10 mcg), meropenem (10 mcg), piperacillin+tazobactum (100/10 mcg), levofloxacin (5 mcg), cotrimoxazole (1.25/23.75). RESULTS This study was carried out from January 2016 to December 2016 with 1178 blood samples receive from patients suspected of having bloodstream infections attending and admitted in Basavatarakam Indo-American cancer Hospital, Hyderabad. Details like medical registration number, laboratory number, age and sex of the patients, and type and place of collection of specimen were recorded. Culture positivity was seen in 327 (27.35%) samples, and 851 (72.24%) samples were sterile (Table 1) as detected with the BACT/ALERT 3D (Biomerieux) blood culture system. Table 1 Ward wise distribution of blood cultures and positivity rate S. No Location Blood cultures received No Growth (%) Growth (%) 1 Wards 575 426 (74.08) 149 (25.9) 2 MICU 312 193 (61.8) 119 (38.14) 3 BMT 232 185 (79.74) 47 (20.25) 4 SICU 17 11 (64.7) 06 (35.2) 5 OP 42 36 (85.7) 06 (14.28) 6 TOTAL 1178 851 (72.24) 327 (27.75) Out of total 1178 samples received, 705 (59.84%) were males and 473 (40.15%) were females. Overall Blood culture positivity rate among males was 16.29% and 10.95% among females (Table 2). Table 2 Age wise and sex wise distribution (Blood cultures Jan 2016 - Dec 2016) Age group Males (705) Females (473) Growth No growth Growth No growth Total <20 28 98 21 65 212 21-40 57 121 29 92 299 41-60 69 179 58 124 430 >60 38 115 27 57 237 Total 192 (16.29%) 513 (43.54%) 135 (10.95%) 338 (29.20%) 1178 20

Out of 327 positive cultures, 299 (91.4%) showed bacterial growth, Gram-negative were 161 (53.8%) and Gram positive were 138 (46.1%). Candida species were isolated from 13 (3.97%) of positive samples and 15 samples showed contamination. Among Gram-negative isolates Escherichia coli (37.80%) was found to be most predominant followed by Klebsiella species (24.20%), Pseudomonas species (13.60%) and Acinetobacter species (6.80%) (Figure 1). Among Gram-positive isolates coagulase negative Staphylococci (52.80%) was most predominant followed by Staphylococcus aureus (14.40%) and Enterococcus species (10.14%) (Figure 2). 37.80% n = 161 24.20% 13.60% 6.80% 2.40% 1.20% 7.40% 2.40% 3.70% Figure 1 Percentage of gram negative isolates 52.80% n = 138 14.40% 6.50% 0.72% 10.14% 2.10% 8.69% 4.34% Figure 2 Percentage of gram positive isolates Antibiotic sensitivity pattern of Gram-negative and Gram-positive organisms was studied. Out of 61 Escherichia coli isolates 83.60% were sensitive to amikacin and 67.21% and 65.57% of isolates were sensitive to meropenem and imipenem respectively. Only 13.11% of isolates were sensitive to levofloxacin and 18.03% were sensitive to cefepime showing high degree of resistance to both the drugs (Figure 3). Klebsiella species showed lower sensitivity to amikacin (61.53%) and a higher sensitivity to levofloxacin (51.28%) and cefepime (25.64%) as compared to Escherichia coli. Sensitivity to imipenem and meropenem in Klebsiella species was 53.84% and 56.41% respectively (Figure 4). Non-fermenters Pseudomonas species and Acinetobacter species had a sensitivity of 81.8% and 72.70% to amikacin (Figures 5 and 6). Unlike Escherichia coli and Klebsiella species the non-fermenters Pseudomonas species and Acinetobacter species had 77.2% and 81.8% sensitivity to levofloxacin (Figures 5 and 6). Among 61 Escherichia coli isolates 80.30% were ESBL (extended spectrum beta lactamase) and 22.90% were MDR and among 39 Klebsiella isolates 64.10% were ESBL producers and 41.02% were 21

MDR. MDR Pseudomonas and Acinetobacter were in the range of 13.60% and 18.18% respectively. Out of the total 20 Staphylococcus aureus isolates 15% were MRSA. 83.60% n = 61 65.57% 54.09% 67.21% 52.45% 31.14% 13.11% 18.03% Figure 3 Antibiotic sensitivity pattern of Escherichia coli isolates n = 39 61.53% 53.84% 56.41% 51.28% 48.71% 46.15% 25.64% Amikacin Imipenem Meropenm Levofloxacin Cefepime Cef + Sulbactum Pip+ Tazo Figure 4 Antibiotic sensitivity pattern of Klebsiella isolates n = 22 86.30% 86.30% 81.80% 77.20% 77.20% 77.20% 72.70% Amikacin Imipenem Meropenm Levofloxacin Cefepime Cef + Sulbactum Pip+ Tazo Figure 5 Antibiotic sensitivity pattern of Pseudomonas isolates 22

72.70% 72.70% 72.70% n = 11 81.80% 63.60% 72.70% 72.70% Amikacin Imipenem Meropenm Levofloxacin Cefepime Cef + Sulbactum Pip+ Tazo Figure 6 Antibiotic sensitivity pattern of Acinetobacter isolates DISCUSSION The present study provides information on the distribution of bacterial isolates causing bloodstream infections along with their antibiotic susceptibility pattern that plays a crucial role in effective management of septicemic cases. In our study, the blood culture positivity rate in clinically suspected septicemia cases was 27.35%, which was approximately similar to the studies by Venkatesh, et al. [7] which showed positivity of 27.16%, Wasihun, et al. [8] showed 28%, Ali, et al. [9] showed 24.2%, Nikita Vasudeva, et al. [10] showed 31.2% positivity. This is in contrast to other studies which have shown blood culture positivity rates between 9.94% to 11.2% [11-15]. Such differences in prevalence of BSI could be due to the different methodology used in blood culture system, the study design, geographical location, nature of patient population, epidemiological difference of the etiological agents and differences in the infection control policies [16-18]. In our study, Gram-negative and Gram-positive bacteria constituted 54.76% and 46.90% respectively. This finding was in accordance with other studies [13,19-24] where Gram-negative bacilli have taken over the Gram-positive organisms. In the present study, the predominant Gram-negative isolates were Escherichia coli (37.8%), followed by Klebsiella species (24.2%), Pseudomonas species (13.6%) and Acinetobacter species (6.8%) which was in concordance with other studies [25-29]. In contrast to this finding, a study from Mumbai revealed that, Pseudomonas species was the most common cause (30.37%) and Escherichia coli and Klebsiella species accounted to 16.06% and 10.61% respectively [23]. In a recent study from Lebanon, Escherichia coli represented 39.5% of all Gram-negative organisms [25]. In another study from Pakistan to evaluate drug resistance amongst bacteremic isolates of febrile neutropenic patients, Escherichia coli was found to be the most predominant organism of the Enterobacteriaceae group while P. aeruginosa and Acinetobacter species were the most common isolates among the non-enterobacteriaceae group [26]. In our study the predominant Gram-positive isolate was coagulase-negative Staphylococci (52.80%) followed by Staphylococcus aureus (14.40%) and Enterococcus species (10.14%). This finding is similar to other studies where coagulase-negative Staphylococci has contributed to blood stream infections in cancer patients [28,30,31]. Some authors have demonstrated that coagulase-negative Staphylococcus adheres to the catheter surface, and produces slime, which are risk factors for BSI [32]. This is in contrast to other studies where Staphylococcus aureus was the most common isolate [23,33,34]. The prevalence of ESBL producers among Escherichia coli and Klebsiella species was 80.30% and 64.10% in the present study which is higher than a study from Delhi published in 2010 where 70.7% of Klebsiella isolates and 41.7% of Escherichia coli isolates were ESBL producers [35]. This is somewhat similar to a study from Saudi Arabia where 79% of all Escherichia coli and K. pneumoniae isolated were ESBL (extended-spectrum β-lactamases) producing [36]. Hospitalization in the previous 3 months and co morbidity could be the risk factors associated with infections by the ESBL-producing Gram-negative bacteria [37]. Patients at high risk for developing colonization or infection 23

with ESBL-producing organisms are often seriously ill patients with prolonged hospital stays and in whom invasive medical devices are present (urinary catheters, endotracheal tubes, central venous lines) for a prolonged duration. Heavy antibiotic use is also a risk factor for acquisition of an ESBL-producing organism [38]. The high isolation rates of ESBL producers in our hospital could be because our hospital being a cancer hospital most of our patients require repeated hospitalization, also have invasive devices and are often seriously ill patients who require prolonged hospital stays. Among Escherichia coli and Klebsiella species Imipenem sensitivity was seen in 65.57% and 53.84% respectively. All showed 100% susceptibility to colistin. Sensitivity to β-lactam/β-lactamase inhibitors (piperacillin+tazobactam, cefoperazone+sulbactam) among Escherichia coli was 54% and 53% and among Klebsiella species was 46% and 49% respectively. This is similar to a study from Mumbai where susceptibility to carbapenems was 70% and, β-lactam/β-lactam inhibitors (piperacillin+tazobactam, cefoperazone+sulbactam) were 56.5% [39]. Both Escherichia coli and Klebsiella showed highest activity to amikacin, 83.60% and 61.53% respectively. This high resistance to carbapenems could be because majority of the patients reported to us are referred by other specialists or hospitals and these patients were offered antibiotics elsewhere before they reached our hospital. With this observation on emergence of carbapenem-resistant Enterobacteriaceae it is important to give due attention to infection control and antibiotic stewardship. A high degree of resistance to cephalosporins among Enterobacteriaceae in the present study could be due to the fact that cephalosporins are one of the most commonly used antibiotics for inpatients as well as for outpatients in developing countries and other reason is that in most of the cases self-medication is very common as the medicines are available at the counter [40]. Among non-fermenters, Pseudomonas showed highest sensitivity to β-lactam/β-lactam inhibitors and amikacin and Acinetobacter species showed highest sensitivity to levofloxacin and amikacin. Sensitivity to Imipenem was 77% in Pseudomonas species and 73% in Acinetobacter species. All our isolates were sensitive to colistin. This is in contrast to a study from Mumbai where imipenem sensitivity was (91.82%) followed by piperacillin+tazobactum sensitivity (67.27%) and amikacin sensitivity was (50%). Colistin showed (94.55%) sensitivity [22]. The high resistance rate of non-fermenters to imipenem in the present study is of concern. CONCLUSION This study provides information on antibiotic resistance of blood isolates which may be a useful guide for physicians initiating empiric therapy. The high prevalence of antimicrobial resistance in Gram-negative isolates is alarming. Routine surveillance of baseline resistance, formulation of hospital antibiotic policy and compliance with existing guidelines will go long way in reducing drug resistance in pathogens. Specific antibiotic utilization strategies like antibiotic restriction, combination therapy and usage according to the standard antimicrobial susceptibility testing may help to decrease or prevent the emergence of resistance. Conflict of Interest DECLARATIONS The authors and planners have disclosed no potential conflicts of interest, financial or otherwise. REFERENCES [1] Nucci, Marcio, et al. Risk factors for death among cancer patients with fungemia. Clinical Infectious Diseases Vol. 27, No. 1, 1998, pp. 107-11. [2] Bhat, Vivek, et al. Bacteriological profile and antibiotic susceptibility patterns of clinical isolates in a tertiary care cancer center. Indian Journal of Medical and Paediatric Oncology: Official Journal of Indian Society of Medical & Paediatric Oncology Vol. 37, No. 1, 2016, p. 20. [3] Collin, Berjan A., et al. Evolution, incidence, and susceptibility of bacterial bloodstream isolates from 519 bone marrow transplant patients. Clinical Infectious Diseases Vol. 33, No. 7, 2001, pp. 947-53. [4] Krupova, I., et al. Bacteremia and fungemia in pediatric versus adult cancer patients after chemotherapy: comparison of etiology, risk factors and outcome. Journal of Chemotherapy Vol. 10, No. 3, 1998, pp. 236-42. 24

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