ISSN: 0973-7510
E-ISSN: 2581-690X
Central venous catheters are commonly inserted to monitor patients with critical illnesses. Even when used to treat very ill patients, they are susceptible to widespread headaches, including central line-associated bloodstream infections (CLABSI). Central line-associated bloodstream infection (CLABSI) is one of the most significant HAIs, associated with excess mortality of 12–25%. To discover CLABSI cases, microbiological profiles, and their antimicrobial susceptibility. The study was conducted in an intensive care unit over a period of 12 months. 150 blood samples and catheter tips were collected for the culture of suspected or secondary bacteremia. CLABSI is described as being consistent with the CDC’s proposal. Automated VITEK 2 technology identifies bacterial isolates and investigates their antimicrobial susceptibility. Out of 150 samples, 50 showed no growth, 45 showed colonizers, 40 showed CLABSI, and 15 showed secondary infection. Fifty-five had positive blood cultures, 15 of whom had another source of infection. In our study, the CLABSI rate was 7.8/1000 central venous days. Rigorous implementation of the system and maintenance of the central line bundle are mandatory to prevent colonization.
Central Venous Catheter, Intensive Care Units, Sepsis
Central venous catheters (CVCs) are inserted in seriously ill patients. Its inevitable use makes patients more vulnerable to headaches, which consist of central line-related bloodstream infections (CLABSIs). The problem of CLABSIs has received increasing interest in recent years.1 The prevention of CLABSI consists of the development of information, guidelines, package care, the most sterile barrier, the use of 2% chlorhexidine, early catheter elimination, and the use of antimicrobial catheters and antimicrobial catheter lock solution.2 The main objective of the present study was to determine the microbiological profile and antimicrobial susceptibility pattern of isolated bacteria from CLABSIs in an intensive care unit. Central line-associated bloodstream infections (CLABSIs) are one of the most critical HAIs, with an excessive mortality rate of 12–25%.3
In general, 150 blood samples and catheter tips were collected for culture when primary or secondary bacteremia was suspected in patients admitted to the tertiary care centre’s intensive care unit over a one-year period. Central lines were inserted with strict aseptic precautions as consistent with the preferred protocol. Catheter tip specimens were processed using the conventional culture plate method; a 4 cm segment of the catheter tip was cut and kept in a sterile universal container. It was transported immediately, preventing drying and allowing it to be processed within two hours of being collected. Blood samples for a culture investigation have been collected using an ideal venepuncture technique and then processed as per standard technique by incubating the bottles in Bac T/Alert 3D.4-6 In positive cultures, bacterial colonies have been processed and identified. The phenotypic identity of pathogens and antimicrobial sensitivity were performed by way of an automatic approach, VITEK 2,7 as per Clinical and Laboratory Standard Institute (CLSI) guideline 2022.8 The CLABSI rate was calculated by means of the following equation9:
CLABSI rate per 1000 central line days
[ Number of CLABSI cases / Number of central line days ] X 1000
Statistical analysis
Statistical analysis was done using Microsoft Excel 2007 (Microsoft Corp., Redmond, WA, USA) and SPSS version 20 (IBM Corp., Somers, NY, USA). Frequencies and percentages were calculated. The Chi-square test was used to calculate the relationship between pathogens, isolated organisms, and infection. The significance level was set at P< 0.05.
The categorization of patients on the basis of CLABSI is shown in Table 1. A total of 150 tip cultures were acquired by means of the laboratory from intensive care unit patients with a clinical diagnosis of sepsis following central venous catheterization. Of the 150 patients, 45 (30%) had colonised catheter tips. Among the colonised catheters, Gram-positive cocci 17 (37.78%) had been the most common isolates observed, followed by Klebsiella pneumoniae 12 (26.67%), Escherichia coli 8 (17.78%), Acinetobacter baumanii 4 (8.89%), and Pseudomonas aeruginosa 4 (8.89%).
Table (1):
Categorization of patients on the basis of central line associated bloodstream infections.
Blood culture |
Tip culture |
Impression |
No. of cases (%) |
Interpretation |
---|---|---|---|---|
Positive |
Positive (similar isolate) |
CLABSI |
40 (26.7%) |
CLABSI present |
Negative |
Positive |
Catheter tip colonization |
45 (30%) |
CLABSI absent |
Positive |
Negative |
Secondary infection |
3 (2%) |
CLABSI absent |
Positive |
Positive (different isolate) |
Secondary infection |
8 (5.33%) |
CLABSI absent |
Negative |
Negative |
Sterile |
50 (33.33%) |
CLABSI absent |
Positive |
Positive (similar isolate) |
Secondary infection |
4 (2.67%) |
CLABSI absent |
Table (2):
Shows the antibiotic sensitivity pattern of Gram-positive isolates in cases of central line-associated bloodstream infection.
Antibiotics | S/R (Sensitivity %) | ||
---|---|---|---|
Staphylococcus aureus (6) | Staphylococcus haemolyticus (4) | Staphylococcus epidermidis (3) | |
Cefoxitin | 2/4 (33.3%) | 2/2 (5%) | 2/1 (66.7%) |
Ciprofloxacin | 2/4 (33.3%) | 1/4 (25%) | 1/2 (33.3%) |
Clindamycin | 3/3 (50%) | 2/2 (5%) | 2/1 (66.7%) |
Cotrimoxazole | 4/2 (66.7%) | 3/1 (75%) | 3/0 (100%) |
Erythromycin | 2/4 (33.3%) | 2/2 (5%) | 1/2 (33.3%) |
Gentamicin | 4/2 (66.7%) | 3/1 (75%) | 3/0 (100%) |
Linezolid | 6/0 (100%) | 4/0 (100%) | 3/0 (100%) |
Vancomycin | 6/0 (100%) | 4/0 (100%) | 3/0 (100%) |
Tetracycline | 1/6 (16.7%) | 1/4 (25%) | 1/2 (33.3%) |
Penicillin G | 0/6 (0%) | 0/4 (0%) | 0/3 (0%) |
Of the 55 (36.7%) bloodstream infections, 40 (26.7%) had been diagnosed as CLABSI with a rate of 7.8/1000 central line days, and Klebsiella pneumoniae 10 (25%) was the most common isolate, followed by Escherichia coli 8 (20%) (Table 3), Staphylococcus aureus 6 (15%), Acinetobacter baumanii 5 (12.5%), Pseudomonas aeruginosa 4 (10%), Staphylococcus haemolyticus 4 (10%), and Staphylococcus epidermidis 3 (7.5%), and results of antibiotic susceptibility testing of the bacterial pathogens causing CLABSI are shown in Table 2 and Table 3.
Table (3):
Shows the antibiotic sensitivity pattern of Gram-negative isolates in cases of central line-associated bloodstream infection.
Antibiotics | S/R (Sensitivity %) | |||
---|---|---|---|---|
Klebsiella pneumoniae(10) | Escherichia coli (8) | Acinetobacter baumanii (5) | Pseudomonas aeruginosa (4) | |
Amikacin | 7/3 (70%) | 6/2 (75%) | 3/2 (60%) | 2/4 (50%) |
Amoxycillin/Clavulinic acid | 2/8 (20%) | 3/5 (37.5%) | 0/5 (0%) | – |
Ampicillin | 0/10 (0%) | 0/8 (0%) | 0/5 (0%) | – |
Cefipime | 3/7 (30%) | 3/5 (37.5%) | 1/4 (20%) | 1/4 (25%) |
Ceftriaxone | 1/9 (10%) | 2/6 (25%) | 0/5 (0%) | – |
Ciprofloxacin | 2/8 (20%) | 2/6 (25%) | 0/5 (0%) | 0/4 (0%) |
Imipenem | 4/6 (40%) | 5/3 (62.5%) | 2/3 (40%) | 3/4 (75%) |
Meropenem | 4/6 (40%) | 4/4 (50%) | 2/3 (40%) | 2/4 (50%) |
Ertapenem | 4/6 (40%) | 5/3 (62.5%) | 2/3 (40%) | – |
Piperacillin/Tazobactam | 4/6 (40%) | 4/4 (50%) | 2/3 (40%) | 2/4 (50%) |
Cefoperazone/Sulbactam | 4/6 (40%) | 4/4 (50%) | 4/1 (80%) | 2/4 (50%) |
Colistin | 10/0 (100%) | 8/0 (100%) | 5/0 (100%) | 4/0 (100%) |
Tigecycline | 8/2 (80%) | 7/1 (87.5%) | 5/0 (100%) | – |
Cotrimoxazole | 7/3 (70%) | 6/2 (75%) | 2/3 (40%) | 1/4 (25%) |
Among 6 isolates of Staphylococcus aureus, 4 (66.67%) had been methicillin-resistant Staphylococcus aureus (MRSA), and among 7 coagulase-negative Staphylococcus, 5 (71.5%) had been methicillin-resistant coagulase-negative Staphylococcus (MR-CoNS). Among 27 gram-negative isolates, 16 (59.25%) had been carbapenemase-producing strains, and 20 (74.07%) were extended-spectrum beta-lactamase-producing strains [Table 4].
Table (4):
Distribution of MRSA, MRCoNS, ESBL in patients with central line associated bloodstream infection.
Isolates |
No. (%) |
---|---|
MRSA |
4 (66.67%) |
MR-CoNS |
5 (71.5%) |
Carbapenemase |
16 (59.25%) |
Klebsiella pneumoniae (ESBL) |
9 (90%) |
Escherichia coli (ESBL) |
2 (75%) |
Acinetobacter baumanii (ESBL) |
0 (100%) |
MRSA is methicillin-resistant Staphylococcus aureus.
MRCoNS is methicillin-resistant coagulase-negative Staphylococcus species.
ESBL stands for extended spectrum beta-lactamases.
The maximum number of underlying conditions for the CLABSI cases (n = 40) was chronic obstructive pulmonary disease (COPD) at 25 (62.5%), followed by renal failure at 10 (25%), and cerebrovascular accident at 5 (12.5%). [Table 5] Three (7.5%) out of the 40 CLABSI cases were fatal: one because of renal failure, one because of sepsis with multi-organ disorder syndrome (MODS), and two because of chronic obstructive pulmonary disorder [Table 6]. Mortality among jugular vein CLABSI was 0.67%. Mortality due to CLABSI with subclavian or femoral line catheterization was 0 and 1.33 percent, respectively [Table 7]. Out of 40 cases of CLABSI, the highest percentage of infection was observed in the femoral catheter (80%), followed by the jugular catheter (60%) and the subclavian catheter (30%). [Table 8].
Table (5):
Central line associated bloodstream infections in various clinical conditions.
Underlying condition |
No. (%) |
---|---|
Chronic obstructive pulmonary disease |
25 (62.5%) |
Renal failure |
10 (25%) |
Cerebrovascular accident |
5 (12.5%) |
Table (6):
Mortality in patients with central line associated bloodstream infection cases.
Outcome |
No. (%) |
---|---|
Death |
3 (7.5%) |
Survival |
37 (92.5%) |
Table (7):
Mortality in CLABSI in relation to central line catheters.
Central line catheter type |
No. (%) |
---|---|
Jugular |
|
CLABSI |
1 (0.67%) |
Non-CLABSI |
4 (2.67%) |
Femoral |
|
CLABSI |
2 (1.33%) |
Non-CLABSI |
5(3.33%) |
Subclavian |
|
CLABSI |
0 (0%) |
Non-CLABSI |
1 (0.67%) |
CLABSI: Central line associated blood stream infection
Table (8):
C LABSI rate in different catheter sites.
Site |
Overall Number of Patients (n = 150) |
Number of blood streams associated with catheters infection cases (n = 40). |
P-value |
---|---|---|---|
Jugular |
60 |
24 (60%) |
<0.0031 |
Femoral |
50 |
32 (80%) |
<0.0031 |
Subclavian |
40 |
12 (30%) |
<0.0031 |
P value by Chi-square test, statistically significant.
This study examined the incidence, clinical and microbiological characteristics of the development of catheter-related infections at a tertiary health care centre. Of the 150 patients, 40 (26.7%) developed a bloodstream infection 4-5 days after CVC insertion. The age group 50 to 60 years old had the highest number of CLABSI cases.10 In our study, catheter colonisation occurred at a rate of 30% (45). The incidence of catheter colonisation in various other studies ranged from 36% to 70%.11,12 which was co related to our study. Gram-positive Cocci colonised the catheters the most (17.78%), followed by Klebsiella pneumoniae12 (26.67%), Escherichia coli 8 (17.78%), Acinetobacter baumanii 4 (8.89%), and Pseudomonas aeruginosa 4 (8.89%). Gram-positive cocci were the most predominant colonisers of central lines, as said in other research.13,14 Among the 150 cases, the most common site for central line catheter insertion was subclavian (50%), followed by jugular (40%), and femoral (10%). Out of 40 cases of CLABSI, the highest percentage of infection was discovered in the femoral catheter (80%),15-17 followed by the jugular catheter (60%) and the subclavian catheter (30%), with a p-value of <0.0031, which was statistically significant and was calculated by the Chi-square test. The occurrence of CLABSI in different site reported by YazanHddadin et al.18 was related to our study.
In our observation, the CLABSI rate per 1000 days on the central line was 7.8, which was consistent with SZ Bukhari et al. benchmark of 6.8.18 Fluctuation in the rates of CLABSI could be attributed to differences in methods employed for blood culture (manual or automated), volume of blood used (5 or 10 ml), number of blood cultures taken (2 or 3 sets), and the lack of clinical indications (variations in clinical signs and symptoms of BSI), eventually increasing the proportion of negative results.19 Besides, the sample size, nature of patients, design of study, geographical locations, blood culturing rates as well as infection control strategies followed in different countries might have also contributed.20-22 Above all, infections caused by anaerobes and other etiological agents would had add to this disparity, with respect to the rate of isolation of cultures.23 When calculating the incidence density of CLABSIs, the device associated infection guidelines of National Healthcare Safety network (NHSN)24 endorse that we take “central-line days” as the denominator for the calculation. “Central line days” were calculated using a day-by-day count of patients on a central line who were admitted to a healthcare facility. This adjusts the risk of CLABSI with respect to the duration that the central line was in place.
Gram-negative bacteria were the most common isolates in our study, with 27 (67.5%), followed by gram-positive bacteria 13 (32.5%), which correlated with Aneta Guzeket al’s study.25-27 whereas gram-positive cocci were the most common pathogens causing CLABSI in the Zeng C et al. study.28
Among the gram-negative bacteria, carbapenemase-producing strains included Klebsiella pneumoniae (40%), Escherichia coli (62.5%), Acinetobacter baumanii (40%) and Pseudomonas aeruginosa (75%)which is co relating with other study Montrucchio, G et al study.29,30 While 90% of Klebsiella pneumoniae, 75% of Escherichia coli, and 100% of Acinetobacter baumanii were ESBL producers, All gram-negative bacteria were sensitive to polymyxin Bwhich is co relating with other studyKhodare A et al.31-33
Among the gram-positive cocci isolates, 66.67% of staphylococci were methicillin-resistant Staphylococcus aureus (MRSA) and 71.5% were methicillin-resistant coagulase-negative staphylococci (MR-CoNS). MRSA and MR-CoNS were both susceptible to vancomycin and linezolide; similar findings were reported in different studies.33
Out of 40 cases of CLABSI, three patients died: one from renal failure, one from sepsis with multi-organ disorder syndrome (MODS), and two from chronic obstructive pulmonary disease.
The presence of such a resistant strain in our hospitals has grave implications. It is time to establish antibiotic surveillance systems, with each country having its own antibiotic policy and adhering to good infection control practices, including hand hygiene.34 The colonisation of the catheter with organisms and the production of biofilm play an important role in the development of CLABSI-associated septicaemia and multi-organ failure.35 Thereby, both central line insertion and maintenance bundle have to be followed strictly to reduce the CLABSI in intensive care units.36,37
Active participation of clinicians in the early diagnosis of sepsis and proper collection of samples at an appropriate time for the early diagnosis of sepsis will thereby decrease morbidity and mortality associated with CLABSI.38,39 More emphasis on teaching and education of medical and paramedical staff regarding the insertion and maintenance bundle for the central line, catheter hub care and after-wound care aids in the prevention of catheter colonisation and thus reduces CLABSI. Adequate hand hygiene is the most important preventive step for the transmission of multidrug-resistant (MDR) organisms among patients with central lines.40-42
Limitations
Due to the small sample size confined to one hospital, our study’s ability to generalise current findings was limited. As a result, our study recommended that the study be replicated on a larger probability sample from different geographical locations.
ACKNOWLEDGMENTS
The authors would like to thank all critical care nursing staff and infection control staff at our hospital.
CONFLICT OF INTEREST
The authors declare that there is no conflict of interest.
AUTHORS’ CONTRIBUTION
Both authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.
FUNDING
None.
DATA AVAILABILITY
All datasets generated or analyzed during this study are included in the manuscript.
ETHICS STATEMENT
Not applicable.
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