International Journal of Medical and Pharmaceutical Research
2026, Volume-7, Issue 4 : 1038-1045
Research Article
Catheter-Related Bloodstream Infections in Patients Undergoing Hemodialysis through Non-Tunneled Catheters: Incidence, Microbiological Profile, Antimicrobial Susceptibility, and Clinical Outcomes
 ,
 ,
 ,
 ,
Received
May 4, 2026
Accepted
June 6, 2026
Published
July 13, 2026
Abstract

Background: Catheter-related bloodstream infections (CRBSIs) remain one of the most serious complications associated with non-tunneled hemodialysis catheters, leading to increased morbidity, mortality, and healthcare utilization among patients with end-stage kidney disease. Limited Indian data are available regarding their incidence, microbiological profile, and clinical outcomes.

Aim: To evaluate the incidence, microbiological characteristics, antimicrobial susceptibility pattern, and clinical outcomes of CRBSIs in patients with stage V chronic kidney disease (CKD-V) undergoing hemodialysis through non-tunneled catheters.

Materials and Methods: This prospective observational study was conducted in the Departments of Nephrology and Microbiology at Geetanjali Medical College and Hospital, Udaipur, India, between January 2024 and June 2025. Eighty-two adult CKD-V patients with CRBSIs associated with non-tunneled hemodialysis catheters were enrolled. Demographic characteristics, clinical features, laboratory parameters, microbiological findings, antimicrobial susceptibility, and treatment outcomes were recorded. Blood cultures were processed using the BACT/Alert automated system, and antimicrobial susceptibility testing was performed according to Clinical and Laboratory Standards Institute (CLSI) guidelines. Statistical analysis was performed using IBM SPSS version 21.0, with p<0.05 considered statistically significant.

Results: Among 560 patients undergoing non-tunneled catheterization, 82 developed CRBSIs, yielding an incidence of 14.64% and an incidence density of 7.66 episodes per 1,000 catheter-days. Most patients were male (64.6%) and aged <50 years (59.8%). Fever with chills (69.5%) was the most common presenting feature. Gram-positive cocci (34.2%) were the predominant isolates, with methicillin-resistant Staphylococcus aureus (MRSA) accounting for 39.3% of Gram-positive infections, whereas Escherichia coli and Klebsiella species were the leading Gram-negative pathogens (29.2% each). Vancomycin (89.3%) demonstrated the highest susceptibility among Gram-positive isolates, while colistin/polymyxin (83.3%) and amikacin (75.0%) showed the greatest activity against Gram-negative organisms. Patients with previous CRBSI had significantly higher diastolic blood pressure (p=0.009) and respiratory rate (p=0.021). Following treatment, significant improvements were observed in hemoglobin, serum albumin, total leukocyte count, random blood sugar, alanine aminotransferase, procalcitonin, and C-reactive protein (all p<0.001). Overall survival was 96.3%, with a mortality rate of 3.7%.

Conclusion: Catheter-related bloodstream infections remain a major complication of non-tunneled hemodialysis catheters. Gram-positive organisms, particularly MRSA, predominated, although multidrug-resistant Gram-negative pathogens were also common. Early diagnosis, adherence to catheter-care protocols, and culture-guided antimicrobial therapy are essential to reduce infection-related morbidity and improve clinical outcomes.

Keywords
INTRODUCTION

Chronic kidney disease (CKD) is a progressive disorder that may advance to end-stage renal disease (ESRD), requiring renal replacement therapy, with hemodialysis (HD) being the most commonly used modality.1 Although arteriovenous fistulas are the preferred vascular access due to their superior long-term outcomes, central venous catheters (CVCs), particularly non-tunneled catheters, are frequently used when urgent or temporary vascular access is required.1,2However, non-tunneled catheters are associated with a significantly higher risk of catheter-related bloodstream infections (CRBSIs), which are a major cause of morbidity and mortality among HD patients.3,4 The risk of CRBSIs is influenced by several patient- and catheter-related factors, including diabetes mellitus, prolonged catheter dwell time, insertion site, and inadequate infection control practices.5-9 These infections often result in sepsis, prolonged hospitalization, interruption of dialysis, and increased healthcare costs.10,11 Despite their clinical significance, data regarding the incidence and risk factors of CRBSIs in patients undergoing hemodialysis through non-tunneled catheters in the Indian population remain limited. Therefore, the present study was undertaken to assess the incidence of catheter-related bloodstream infections and identify the associated risk factors among patients undergoing hemodialysis using non-tunneled catheters.

 

AIM AND OBJECTIVES

The present study aimed to evaluate the incidence, microbiological profile, and clinical outcomes of catheter-related bloodstream infections (CRBSIs) in patients with stage V chronic kidney disease undergoing hemodialysis through non-tunneled catheters. The primary objectives were to determine the incidence of CRBSIs, identify the causative microorganisms and their antimicrobial susceptibility patterns, and assess the clinical outcomes of patients who developed these infections. The secondary objective was to describe the demographic and clinical characteristics of patients who developed CRBSIs associated with non-tunneled hemodialysis catheters.

 

MATERIALS AND METHODS

This prospective observational study was conducted in the Departments of Nephrology and Microbiology at Geetanjali Medical College and Hospital, Udaipur, Rajasthan, over an 18-month period (January 2024 to June 2025). Adult patients (≥18 years) with stage V chronic kidney disease (CKD-V) undergoing hemodialysis through non-tunneled central venous catheters inserted at the study center were consecutively enrolled after obtaining written informed consent. Patients with catheters inserted elsewhere, tunneled catheters, acute kidney injury, active non-catheter-related infections, pediatric patients, and those unwilling to participate were excluded. Based on an expected CRBSI prevalence of 30.7%, 95% confidence level, and 10% allowable error, the calculated sample size was 82 patients.

 

Catheter-related bloodstream infection (CRBSI) was suspected according to Centers for Disease Control and Prevention (CDC) criteria in patients presenting with fever, chills or rigors, hypotension, or local catheter-site infection. Under aseptic precautions, 10 mL of blood was collected from the catheter venous hub before initiation of antimicrobial therapy for culture and sensitivity testing. Empirical broad-spectrum antibiotics were started and subsequently modified according to culture susceptibility results. Catheters were removed in patients with persistent symptoms or hemodynamic instability despite appropriate antibiotic therapy.

 

Demographic characteristics, clinical history, comorbidities, laboratory parameters, and microbiological findings were recorded using a structured case record form. Blood cultures were processed using the BACT/Alert automated culture system, organisms were identified by standard microbiological methods, and antimicrobial susceptibility testing was performed using the Kirby–Bauer disk diffusion method according to Clinical and Laboratory Standards Institute (CLSI) guidelines. Patients were followed for two weeks to assess clinical outcomes. The incidence of CRBSI was calculated as the number of CRBSI episodes per total catheter-days × 100. Statistical analysis was performed using IBM SPSS version 21.0. Continuous variables were expressed as mean ± standard deviation, categorical variables as frequencies and percentages, and comparisons were made using the independent t-test or Chi-square test as appropriate. A p-value <0.05 was considered statistically significant.

 

RESULTS

A total of 560 patients underwent non-tunneled hemodialysis catheterization during the study period, of whom 82 developed catheter-related bloodstream infections (CRBSIs), resulting in an incidence proportion of 14.64%. The cumulative catheter exposure was 1,070 catheter-days, with a mean catheter duration of 14.79 ± 8.96 days(range: 8–33 days), corresponding to an incidence density of 7.66 episodes per 1,000 catheter-days.

 

The baseline characteristics of patients with CRBSIs are shown in Table 1. Most patients were aged <50 years (59.8%) and were male (64.6%). Chronic glomerulonephritis (46.3%) was the most common underlying kidney disease, followed by diabetic nephropathy (28.1%) and chronic interstitial nephritis (20.7%). Comorbidities were present in 96.3% of patients, with hypertension (69.6%) and diabetes mellitus (63.3%) being the most frequent. Most patients underwent twice-weekly hemodialysis (86.6%), while catheter insertion was elective in 59.8% and emergency in 40.2% of cases. Right-sided catheter placement was performed in 84.2% of patients, and 13.4% had a previous history of CRBSI.

 

As shown in Table 2, fever with chills (69.5%) and rigors (62.2%) were the most common clinical manifestations, followed by hypotension (35.4%) and exit-site redness or purulent discharge (18.3%). Shortness of breath (15.9%) and generalized weakness (14.6%) were the most frequent associated symptoms. During follow-up, 41.5% of patients were transitioned to an arteriovenous fistula, whereas 58.5% continued dialysis through catheter access. The overall mortality rate was 3.7%.

 

The microbiological profile is summarized in Table 3. Gram-positive cocci were the predominant isolates (34.2%), followed by Gram-negative bacilli (29.3%), while non-pathogenic organisms and culture-negative samples each accounted for 18.3%. Among Gram-positive isolates, methicillin-resistant Staphylococcus aureus (MRSA) was the commonest pathogen (39.3%), whereas Escherichia coli and Klebsiella species were the leading Gram-negative organisms (29.2% each).

 

The antimicrobial susceptibility patterns of CRBSI isolates are presented in Table 4. Among Gram-positive isolates, the highest susceptibility was observed for vancomycin (89.3%), followed by linezolid (71.4%), teicoplanin (67.9%), and gentamicin (67.9%). In contrast, low susceptibility was noted for doxycycline (10.7%), penicillin G (3.6%), azithromycin/erythromycin (3.6%), and daptomycin (3.6%). Among Gram-negative isolates, colistin/polymyxin demonstrated the highest susceptibility (83.3%), followed by amikacin (75.0%) and imipenem/meropenem (66.7%). Lower susceptibility rates were observed for ciprofloxacin (16.7%) and ceftriaxone (4.2%).

 

Comparison of patients with and without previous CRBSI demonstrated significantly higher diastolic blood pressure (87.91 ± 21.96 vs. 76.86 ± 10.90 mmHg; p=0.009) and respiratory rate (22.64 ± 4.78 vs. 19.96 ± 3.28 breaths/min; p=0.021) among patients with prior infection. No significant differences were observed for age, body mass index, systolic blood pressure, pulse rate, or body temperature (Table 5).

 

Changes in laboratory parameters following treatment are presented in Table 6. At two-week follow-up, hemoglobin and serum albumin increased significantly, while total leukocyte count, random blood sugar, alanine aminotransferase, procalcitonin, and C-reactive protein showed significant reductions (all p<0.001). No significant changes were observed in aspartate aminotransferase or alkaline phosphatase levels (p>0.05).

 

Table 1. Baseline Characteristics of Patients with Catheter-Related Bloodstream Infections (CRBSIs) (n = 82)

Characteristic

Category

Frequency (n)

Percentage (%)

Age (years)

<50

49

59.76

≥50

33

40.24

Gender

Male

53

64.63

Female

29

35.37

Native kidney disease

Chronic glomerulonephritis

38

46.34

Diabetic nephropathy

23

28.05

Chronic interstitial nephritis

17

20.73

Obstructive uropathy

3

3.66

Autosomal dominant polycystic kidney disease

1

1.22

Presence of comorbidity

Yes

79

96.34

No

3

3.66

Comorbidities

Hypertension

55

69.62

Diabetes mellitus

50

63.29

Hypothyroidism

8

10.13

Ischemic heart disease

5

6.33

Chronic liver disease

4

5.06

Tuberculosis

2

2.53

Cerebrovascular accident

2

2.53

Chronic obstructive pulmonary disease

1

1.27

Hepatitis B

1

1.27

Hepatitis C

1

1.27

Malignancy

1

1.27

Hemodialysis frequency

Once weekly

1

1.22

Twice weekly

71

86.59

Thrice weekly

10

12.20

Indication for catheter insertion

Elective

49

59.76

Emergency

33

40.24

Catheter insertion side

Right

69

84.15

Left

13

15.85

Previous history of CRBSI

Yes

11

13.41

No

71

86.59

 

Table 2:Clinical presentation, associated symptoms, and clinical outcomes among patients with CRBSI undergoing hemodialysis through non-tunneled catheters.

Variable

Frequency (n)

Percentage (%)

Clinical presentation

Fever with chills

57

69.51

Rigors

51

62.19

Hypotension

29

35.37

Exit-site redness/purulent discharge

15

18.29

Associated clinical features

Shortness of breath

13

15.85

Generalized weakness

12

14.63

Generalized edema

6

7.32

Loss of appetite

3

3.66

Cough

3

3.66

Loose motions

1

1.22

Clinical outcomes

Transition to arteriovenous fistula (AVF)

34

41.46

Continued catheter use

48

58.54

Survived

79

96.34

Death

3

3.66

 

Table 3: Microbiological Profile of Catheter-Related Bloodstream Infections (CRBSIs) (n = 82)

Microbiological Profile

Frequency (n)

Percentage (%)

Gram-positive isolates

(n = 28)

Methicillin-resistant Staphylococcus aureus (MRSA)

11

39.29

Staphylococcus haemolyticus

8

28.57

Staphylococcus epidermidis

7

25.00

Enterococcus faecium

1

3.57

Enterococcus faecalis

1

3.57

Gram-negative isolates (n = 24)

Escherichia coli

7

29.17

Klebsiella spp.

7

29.17

Acinetobacterbaumannii

4

16.67

Ralstoniamannitolilytica

1

4.17

Pseudomonas aeruginosa

1

4.17

Raoultellaornithinolytica

1

4.17

Serratiamarcescens

1

4.17

Enterobacter cloacae

1

4.17

Burkholderia spp.

1

4.17

Non-pathogenic organisms (n = 15)

Staphylococcus hominis

5

33.33

Staphylococcus warneri

3

20.00

Staphylococcus pseudointermedius

3

20.00

Kocuriakristinae

2

13.33

Non-pathogenic coagulase-negative Staphylococcus (CONS)

2

13.33

 

 

 

Table 4. Antimicrobial Susceptibility Pattern of CRBSI Isolates

Type of isolates

Antibiotic

Total (Sensitivity%)

Gram-positive isolates

(n = 28)

Vancomycin

25 (89.29)

Linezolid

20 (71.43)

Teicoplanin

19 (67.86)

Gentamicin

19 (67.86)

Rifampicin

14 (50.00)

Clindamycin

11 (39.29)

Ciprofloxacin/Ofloxacin

11 (39.29)

Doxycycline

3 (10.71)

Penicillin G

1 (3.57)

Azithromycin/Erythromycin

1 (3.57)

Daptomycin

1 (3.57)

Gram-negative isolates

(n = 24)

Colistin/Polymyxin

20 (83.33)

Amikacin

18 (75.00)

Imipenem/Meropenem

16 (66.67)

Piperacillin/Tazobactam

13 (54.17)

Ceftazidime

12 (50.00)

Trimethoprim/Sulfamethoxazole

11 (45.83)

Cefepime

9 (37.50)

Cefoperazone/Sulbactam

9 (37.50)

Ciprofloxacin

4 (16.67)

Ceftriaxone

1 (4.17)

 

Table 5:Clinical risk indicators of CRBSI

Clinical risk indicators

(Mean ± SD)

Prior CRBSI

(n = 11)

No Prior CRBSI (n = 71)

t value

p-value

Body mass index (kg/m²)

24.18 ± 4.85

27.04 ± 14.78

-0.63

0.528

Age (years)

53.64 ± 21.09

51.75 ± 15.83

0.35

0.726

Systolic blood pressure (mmHg)

130.82 ± 35.91

122.68 ± 19.50

1.31

0.262

Diastolic blood pressure (mmHg)

87.91 ± 21.96

76.86 ± 10.90

2.66

0.009*

Pulse rate (beats/min)

100.55 ± 15.80

93.41 ± 15.20

1.44

0.153

Respiratory rate (breaths/min)

22.64 ± 4.78

19.96 ± 3.28

2.36

0.021*

Body temperature (°F)

99.09 ± 1.04

98.80 ± 0.95

0.92

0.359

 

Table 6: Comparison of laboratory parameters at the time of diagnosis of CRBSI and at two-week follow-up after treatment in patients undergoing hemodialysis through non-tunneled catheters

Laboratory Parameter

(Mean ± SD)

At Diagnosis of CRBSI

At 2-Week Follow-up

t-value

p-value

Hemoglobin (g/dL)

8.13 ± 1.65

8.62 ± 1.96

−4.002

<0.001*

Total leukocyte count (×10⁹/L)

15.04 ± 5.84

9.71 ± 2.63

8.441

<0.001*

Random blood sugar (mg/dL)

127.75 ± 51.73

111.57 ± 44.70

4.500

<0.001*

Aspartate aminotransferase (U/L)

75.84 ± 116.89

64.98 ± 171.90

0.729

0.468

Alanine aminotransferase (U/L)

79.31 ± 189.56

57.59 ± 162.55

11.974

<0.001*

Alkaline phosphatase (U/L)

143.36 ± 72.53

128.34 ± 70.28

1.932

0.057

Serum albumin (g/dL)

2.45 ± 0.49

2.72 ± 0.42

−6.513

<0.001*

Procalcitonin (ng/mL)

43.38 ± 37.40

9.05 ± 24.91

8.896

<0.001*

C-reactive protein (mg/L)

100.97 ± 70.45

16.77 ± 35.77

11.974

<0.001*

 

DISCUSSION

The incidence proportion of CRBSI in the present study was 14.64%, with an incidence density of 7.66 episodes per 1,000 catheter-days. These findings are consistent with recent reports demonstrating that non-tunneled hemodialysis catheters continue to carry a considerable risk of bloodstream infection despite improvements in infection-control practices. Bitunguramye et al. and Costantine et al. similarly reported a substantial burden of CRBSIs among patients receiving maintenance hemodialysis and emphasized that catheter-dependent dialysis remains an important contributor to infectious complications, particularly in resource-limited settings.12,13 Differences in incidence reported across studies may be explained by variations in catheter type, catheter dwell time, patient characteristics, adherence to aseptic protocols, and institutional infection-prevention measures.2-4

 

The demographic characteristics of our study demonstrated that nearly 60% of infected patients were younger than 50 years, while males constituted approximately two-thirds of the study population. Similar male predominance has been reported by Bhojaraja et al., Moin et al., and Agrawal et al., reflecting the greater proportion of male patients undergoing maintenance hemodialysis in many dialysis centers.14,15,16 Although advancing age has frequently been associated with increased susceptibility to infections because of immunosenescence and multiple comorbidities, our findings indicate that younger patients with end-stage kidney disease also remain vulnerable to CRBSIs, probably reflecting the demographic profile of patients attending our institution.

 

Chronic glomerulonephritis was the leading cause of underlying kidney disease, followed by diabetic nephropathy and chronic interstitial nephritis. This differs from several international studies in which diabetic nephropathy predominated among patients with catheter-related infections.12, 17These differences likely reflect regional variations in CKD etiology rather than differences in infection susceptibility.

 

Almost all patients had one or more associated comorbidities, with hypertension and diabetes mellitus being the most prevalent. Similar observations have been reported by Demirci et al., Weldetensae et al., and Matos et al., who identified diabetes and multiple comorbid conditions as important predictors of catheter-related infections because of impaired immune responses, vascular dysfunction, and repeated healthcare exposure.18, 19, 20 The coexistence of chronic illnesses further compromises host defense mechanisms and predisposes patients to bloodstream infections.

 

Most patients underwent twice-weekly hemodialysis, and catheter insertion was performed electively in nearly 60% of cases. Right-sided catheter placement was preferred in the majority of patients, consistent with current vascular access guidelines recommending the right internal jugular vein because of its favorable anatomy and lower complication rates.4, 21Only a small proportion of patients had a previous history of CRBSI; however, these patients require close surveillance because recurrent infections are associated with poorer vascular access outcomes.

 

Fever with chills and rigors were the most common presenting manifestations, followed by hypotension and exit-site inflammation. Similar findings have been reported by Pasilan et al., Bhojaraja et al., and Jose et al., who identified fever as the predominant clinical manifestation of CRBSI in hemodialysis patients.17, 15, 22 The relatively low frequency of exit-site infection observed in the present study supports previous evidence that bloodstream infections frequently occur without obvious local catheter-related signs, emphasizing the importance of maintaining a high index of suspicion whenever systemic symptoms develop during or after dialysis. Among associated manifestations, shortness of breath and generalized weakness were more frequent than gastrointestinal symptoms, reflecting the systemic inflammatory response accompanying bacteremia.

 

The overall clinical outcome was favorable, with more than 40% of patients successfully transitioned to an arteriovenous fistula and an overall survival of 96.34%. Early diagnosis, prompt initiation of empirical antimicrobial therapy, microbiological confirmation, and timely catheter removal in clinically unstable patients probably contributed to the relatively low mortality observed in our study. Similar observations have been reported by Pandit et al. and Almenara-Tejederas et al., who demonstrated that protocol-based management significantly improves patient outcomes following CRBSI.23, 24

 

Comparison of patients with and without previous CRBSI demonstrated significantly higher diastolic blood pressure and respiratory rate among patients with recurrent infection, whereas age, body mass index, systolic blood pressure, pulse rate, and body temperature were comparable between the groups. Although previous studies have identified prolonged catheter duration, diabetes, hypoalbuminemia, and previous catheter infections as important predictors of CRBSI,13, 18, 20 the higher respiratory rate observed in our cohort may represent an early clinical marker of systemic infection requiring prompt intervention.

 

The microbiological profile demonstrated that Gram-positive cocci constituted the largest proportion of isolates, followed by Gram-negative bacilli, while culture-negative and non-pathogenic isolates each accounted for approximately one-fifth of cases. These findings are comparable with those reported by Bhojaraja et al., Agrawal et al., Pansuriya et al., and Costantine et al., who also observed predominance of Gram-positive organisms in catheter-related infections because of colonization of the skin surrounding vascular access sites. 12, 15, 16, 25

 

Among Gram-positive pathogens, methicillin-resistant Staphylococcus aureus (MRSA) represented the commonest isolate, followed by Staphylococcus haemolyticus and Staphylococcus epidermidis. Similar observations have been reported by Pasilan et al., Jose et al., and Demirci et al., where Staphylococcus aureus and coagulase-negative staphylococci were identified as the principal pathogens responsible for CRBSIs because of their ability to adhere to catheter surfaces and produce biofilms.17, 20, 22 Biofilm formation contributes to persistent infection, antimicrobial resistance, and recurrent bacteremia.

 

Gram-negative bacilli accounted for nearly one-third of culture-positive infections, with Escherichia coli and Klebsiella species being the predominant organisms, followed by Acinetobacterbaumannii. Similar trends have been reported by Moin et al., Bitunguramye et al., and Costantine et al., suggesting an increasing contribution of multidrug-resistant Gram-negative organisms in dialysis-related infections.12, 13, 14 Isolation of less common pathogens including Ralstoniamannitolilytica, Raoultellaornithinolytica, Burkholderia species, and Serratiamarcescens further highlights the diverse microbiological spectrum encountered in patients with repeated healthcare exposure and prolonged catheter dependence.

 

Culture-negative infections accounted for 18.29% of cases, comparable to previous studies. Possible explanations include prior empirical antibiotic administration, low bacterial inoculum, fastidious organisms, or limitations of conventional microbiological methods.16, 17

 

The antimicrobial susceptibility profile provides important information for empirical management of CRBSIs. Among Gram-positive isolates, vancomycin demonstrated the highest susceptibility, followed by linezolid, teicoplanin, and gentamicin. Similar findings have been reported by Bhojaraja et al., Jose et al., and Pansuriya et al., supporting the continued effectiveness of glycopeptides against methicillin-resistant staphylococcal infections.15, 22, 25 However, poor susceptibility to penicillin, macrolides, and doxycycline reflects the growing burden of antimicrobial resistance among Gram-positive pathogens.

 

Among Gram-negative isolates, colistin/polymyxin, amikacin, and carbapenems demonstrated the highest susceptibility, whereas resistance was greatest against ceftriaxone and ciprofloxacin. Comparable resistance patterns have been reported by Costantine et al., Moin et al., and Bitunguramye et al., emphasizing the emergence of multidrug-resistant Gram-negative bacteria in dialysis units.12, 13, 14 These findings reinforce the importance of institution-specific antibiograms and culture-guided therapy to optimize antimicrobial stewardship and reduce inappropriate antibiotic use.

 

Serial laboratory evaluation demonstrated significant improvement in several hematological and inflammatory parameters following treatment. Hemoglobin increased significantly after two weeks, although anemia persisted because of the underlying chronic kidney disease. Total leukocyte count, procalcitonin, and C-reactive protein declined markedly, indicating effective resolution of infection. Similar findings have been reported by Bhojaraja et al., Costantine et al., and Demirci et al., who identified these biomarkers as valuable tools for diagnosis and monitoring therapeutic response in CRBSIs.12, 15, 20

 

Random blood sugar levels also decreased significantly following treatment, probably reflecting resolution of infection-associated stress hyperglycemia. Alanine aminotransferase showed significant improvement, whereas changes in aspartate aminotransferase and alkaline phosphatase were not statistically significant. Serum albumin increased significantly following treatment, although absolute levels remained low. Similar observations have been reported by Bitunguramye et al., Matos et al., and Weldetensae et al., who demonstrated that hypoalbuminemia is an important predictor of infection and adverse outcomes in hemodialysis patients.13, 18, 19

 

CONCLUSION

Catheter-related bloodstream infections remain a significant complication among patients undergoing hemodialysis through non-tunneled catheters. Gram-positive cocci, particularly methicillin-resistant Staphylococcus aureus, were the predominant pathogens, although Gram-negative organisms also contributed substantially to the infectious burden. Early diagnosis, strict adherence to catheter-care protocols, culture-guided antimicrobial therapy, regular surveillance of antimicrobial resistance, and timely transition to permanent vascular access are essential strategies for reducing infection-related morbidity and improving outcomes in this vulnerable patient population.

 

REFERENCES

  1. Navaneethan SD, Aloudat S, Singh S. A systematic review of patient and health system characteristics associated with late referral in chronic kidney disease. BMC Nephrol 2008;9:3.
  2. Lok CE, Mokrzycki MH. Prevention and management of catheter-related infection in hemodialysis patients. Kidney Int 2011;79:587-98.
  3. Ravani P, Palmer SC, Oliver MJ, et al. Associations between hemodialysis access type and clinical outcomes: a systematic review. J Am SocNephrol 2013;24:465-73.
  4. Lok CE, Huber TS, Lee T, et al. KDOQI Clinical Practice Guideline for Vascular Access: 2019 Update. Am J Kidney Dis 2020;75:S1-S164.
  5. Allon M, Imrey PB, Cheung AK, et al. Relationships Between Clinical Processes and Arteriovenous Fistula Cannulation and Maturation: A Multicenter Prospective Cohort Study. Am J Kidney Dis 2018;71:677-89.
  6. Lok CE, Sontrop JM, Tomlinson G, et al. Cumulative patency of contemporary fistulas versus grafts (2000-2010). Clin J Am SocNephrol 2013;8:810-8.
  7. Al-Balas A, Lee T, Young CJ, et al. The Clinical and Economic Effect of Vascular Access Selection in Patients Initiating Hemodialysis with a Catheter. J Am SocNephrol 2017;28:3679-87.
  8. Polkinghorne KR, McDonald SP, Atkins RC, et al. Vascular access and all-cause mortality: a propensity score analysis. J Am SocNephrol 2004;15:477-86.
  9. Harms JC, Rangarajan S, Young CJ, et al. Outcomes of arteriovenous fistulas and grafts with or without intervention before successful use. J VascSurg 2016;64:155-62.
  10. Dember LM. Fistulas first--but can they last?.Clin J Am SocNephrol 2011;6:463-4. 15. Allon M. Vascular Access for Hemodialysis Patients: New Data Should Guide Decision Making. Clin J Am SocNephrol 2019;14:954-61.
  11. Lee T, Qian J, Thamer M, et al. Tradeoffs in Vascular Access Selection in Elderly Patients Initiating Hemodialysis With a Catheter. Am J Kidney Dis 2018;72:509-18.
  12. Costantine AR, Urasa SJ, Sadiq AM, et al. Catheter-Related Bloodstream Infections Among Hemodialysis Patients in Northern Tanzania: Insights From a Single-Centre Retrospective Study. Health Sci Rep. 2025;8(1):e70338.
  13. Bitunguramye A, Nkundimana G, Aboubasha AM, Kabahizi J, Rutikanga W, Nshimiyimana L et al. Incidence, risk factors, organism types, and outcomes of catheter-related bloodstream infections in hemodialysis patients. Cureus. 2024;16(9):e69554.
  14. Moin S, Salman B, Ahmad A. Frequency Determination of Central Line Associated Bloodstream Infection at a Renal Care Centre.EML.2024;9(2):138-144.
  15. Bhojaraja MV, Prabhu RA, Nagaraju SP, Rao IR, Shenoy SV, Rangaswamy D, Krishna VN, Nayak MN. Hemodialysis catheter-related bloodstream infections: a single-center experience. J Nephropharmacol. 2023;12(2):e10475.
  16. Agrawal V , Valson AT, Mohapatra A , David VG , Alexander S, Jacob S. Fast and furious: a retrospective study of catheter-associated bloodstream infections with internal jugular nontunneled hemodialysis catheters at a tropical center. Clinical Kidney Journal. 2019; 12(5):737–744.
  17. Pasilan RM, Tomacruz-Amante ID, Dimacali CT. The epidemiology and microbiology of central venous catheter related bloodstream infections among hemodialysis patients in the Philippines: a retrospective cohort study. BMC Nephrol. 2024;25(1):331.
  18. Matos JC, Polsin LLM, Israel KCP, Cavalcante LP. Predictive factors of infection in patients with chronic kidney disease using hemodialysis catheters. J Vasc Bras. 2023;22:e20220098.
  19. Weldetensae MK, Weledegebriel MG, Nigusse AT, Berhe E, Gebrearegay H. Catheter-Related Blood Stream Infections and Associated Factors Among Hemodialysis Patients in a Tertiary Care Hospital. Infect Drug Resist. 2023;16:3145-3156. 
  20. Demirci R, Sahtiyancı B, Bakan A, Akyuz O. The predictors of catheter-related bloodstream infections in patients undergoing hemodialysis: A single center experience. J Vasc Access. 2023;24(1):76-81.
  21. Engstrom BI, Horvath JJ, Stewart JK, et al. Tunneled internal jugular hemodialysis catheters: impact of laterality and tip position on catheter dysfunction and infection rates. J VascIntervRadiol 2013;24:1295-302.
  22. Jose N, Manikantan S, John K, Prasad R, Jayakumar M. CLABSI in Hemodialysis– New Face to an Old Foe; A Look at Current Trends and a Review of Literature. The Open Urology & Nephrology Journal, 2022, 15: e1874303X2208180.
  23. Pandit N, Rao N, Ansari M, Chandra A, Saran S. Adverse Outcomes After Tunneled Dialysis Catheter-Related Bloodstream Infections-Too Dark at the End of This Tunnel?. Semin Dial. 2025;38(2):124-131.
  24. Almenara-Tejederas M, Rodríguez-Pérez MA, Moyano-Franco MJ, de Cueto-López M, Rodríguez-Baño J, Salgueira-Lazo M. Tunneled catheter-related bacteremia in hemodialysis patients: incidence, risk factors and outcomes. A 14-year observational study. J Nephrol. 2023;36(1):203-212.
  25. Pansuriya D, Bansal SB, Rana A, Mittal A, Lokkur P et al. A clinical and microbiological spectrum of catheter-related bloodstream infection (CRBSI) and its outcomes in chronic kidney disease patients on maintenance hemodialysis. WCN'25, New Delhi, India.

 

Recommended Articles
Research Article Open Access
Medical Students Concerns and Apprehensions in their transition from Preclinical to Clinical Phase - A Cross-sectional observational study
2026, Volume-7, Issue 4 : 1063-1066
Research Article Open Access
Use of Focus groups for Obtaining Feedback from III Year Undergraduate Medical students for Evaluating Module on Electives in the New Competency Driven Medical Curriculum
2026, Volume-7, Issue 4 : 1053-1062
Research Article Open Access
Antimicrobial Resistance Pattern Among Patients with Complicated Urinary Tract Infection.
2026, Volume-7, Issue 4 : 1030-1037
Research Article Open Access
The Role of Portfolio-Based Reflective Learning in Teaching the AETCOM Module to Second-Year Medical Students within India's Competency-Based Curriculum
2026, Volume-7, Issue 4 : 1046-1052
International Journal of Medical and Pharmaceutical Research journal thumbnail
Volume-7, Issue 4
Citations
5 Views
2 Downloads
Share this article
License
Copyright (c) International Journal of Medical and Pharmaceutical Research
Creative Commons Attribution License Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.
All papers should be submitted electronically. All submitted manuscripts must be original work that is not under submission at another journal or under consideration for publication in another form, such as a monograph or chapter of a book. Authors of submitted papers are obligated not to submit their paper for publication elsewhere until an editorial decision is rendered on their submission. Further, authors of accepted papers are prohibited from publishing the results in other publications that appear before the paper is published in the Journal unless they receive approval for doing so from the Editor-In-Chief.
IJMPR open access articles are licensed under a Creative Commons Attribution-ShareAlike 4.0 International License. This license lets the audience to give appropriate credit, provide a link to the license, and indicate if changes were made and if they remix, transform, or build upon the material, they must distribute contributions under the same license as the original.
Logo
International Journal of Medical and Pharmaceutical Research
About Us
The International Journal of Medical and Pharmaceutical Research (IJMPR) is an EMBASE (Elsevier)–indexed, open-access journal for high-quality medical, pharmaceutical, and clinical research.
Follow Us
facebook twitter linkedin mendeley research-gate
© Copyright | International Journal of Medical and Pharmaceutical Research | All Rights Reserved