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Duration of central venous catheter placement and central line-associated bloodstream infections after the adoption of prevention bundles: a two-year retrospective study



Central line–associated bloodstream infections (CLABSIs) remain a critical and possibly fatal outcome of hospitalization. Use of central venous catheter (CVC) bundles can considerably reduce CLABSI rates in hospitalized patients. However, despite widespread adoption of these bundles in hospitals worldwide, CLABSIs still remain prevalent. The aim of the present study was to determine whether longer duration of CVCs placement is related to CLABSIs in hospitalized adults, despite the implementation of preventive bundles. Also to analyse CLABSI pathogens distribution and antimicrobial resistance profiles in different time intervals of catheterization.


A retrospective study was performed among hospitalized patients who had a CVC inserted during a 24-month period (May 2017–May 2019) and developed CLABSIs. To evaluate the association between CVC placement duration and CLABSI events, we categorized events into three groups, each representing a 10-day time interval.


A total of 59 CLABSI cases were identified among 9774 catheter/days. The CLABSI incidence rate per 1000 catheter/days was 4.80 for duration of catheterization up to 10 days, 5.92 for duration of 11–20 days, and 8.64 for duration > 20 days(p = 0.007). The CLABSI incidence rate per 1000 catheter/days due to multidrug-resistant organisms (MDROs) among the three groups was 2.62 for catheter duration of up to 10 days, 3.83 for 11–20 days, and 3.46 for > 20 days (p = 0.14). Among CLABSIs, the most common microorganism identified was multidrug-resistant Acinetobacter baumannii, which accounted for 27.1% of the cases. There was no significant difference in the type of CLABSI pathogens isolated among the 3 groups.


Our findings suggest that duration of CVC placement remains an important risk factor for CLABSIs in hospitalized patients, even after the adoption of prevention bundles. The high prevalence of MDROs in our setting reflects the local epidemiology, highlighting a significant threat of urgent public health concern.


Central line-associated bloodstream infections (CLABSIs) remain important healthcare-associated infections leading to prolonged hospital stays and increased healthcare costs and mortality [1, 2]. Identified CLABSI risk factors before the adoption of preventive bundles include prolonged hospitalization before catheterization, femoral catheterization, longer catheterization duration, use of total parenteral nutrition, extensive catheter manipulations, and reduced nurse: patient ratio [3]. The implementation of central venous catheters (CVCs) bundles including avoidance of femoral sites for CVC insertion, strict adherence to hand hygiene protocols, use of full barrier precautions, chlorhexidine skin preparation, and removal of unnecessary catheters, considerably decreased CLABSI rates in hospitalized patients [4]. However, CLABSIs rates still remain at least 1 case per 1000 catheter-days in US hospitals, despite the broad and continuous implementation of these bundles [5].

With regards to the duration of catheterization, current guidelines recommend that catheter removal is required only if it is no longer needed [6]. On the basis of this recommendation, many patients who have limited vascular access and need prolonged parenteral treatment use CVCs for periods longer than 3 weeks, raising the concern for developing CLABSI events despite the implementation of CVC hygiene bundles. The existing literature on CLABSI prevention measures has yielded varying and opposing suggestions on the appropriate duration of catheterization, with some recommending optimal cut-offs to avoid CLABSIs and others supporting that an indefinite duration may be acceptable [7,8,9].

Most of the previous studies that examined the catheter duration as a risk factor for CLABSIs were performed in paediatric populations that mainly concerned peripheral inserted central catheters (PICCs) since they are more commonly used by clinicians in daily practice [8, 9].

The aim of the present study was to examine the association between duration of CVC placement and CLABSI rates in hospitalized adults during a period of prevention bundles adoption. The study was conducted in the context of investigating increased rates of CLABSIs in a tertiary large hospital with highly trained personnel. For this purpose, we categorized events into consecutive 10-day time intervals, divided into 3 groups. We also analysed and compared distribution of CLABSI pathogens and their resistance profiles between the three groups.

Materials and methods

We performed a retrospective analysis of data collected from consecutive admissions to Metropolitan Hospital, a large tertiary care hospital of Piraeus, Attica Prefecture, covering a 24-month period from May 2017 to May 2019. This observational study was approved by the institutional review board.

Data collection

After insertion, catheters were checked using a check-box form containing the patient’s diagnosis, operator’s name, site chosen, date placed and removed, date of intensive care units (ICU) discharge or death, mechanical ventilation, arterial catheters, parenteral nutrition, and daily clinical assessment (e.g., discharge, erythema, and tenderness) of possible catheter infection. The operator inserting the catheter entered the initial data; nurse personnel entered data the following days while the infection control nurse monitored data collection 3–4 times per week. We retrospectively collected study data from three different sources where information was completed: 1) ICU database (for demographic and clinical data related to the patient’s admission and clinical course); 2) and 3) Clinical Laboratory and hospital infection control team database (for blood culture and antibiotic susceptibility results).

Catheterization protocol

In our hospital triple lumen, non-antibiotic impregnated catheters (Arrow model, total provided by Arrow®/Teleflex®, Wayne, USA) are mainly used. Double lumen catheters (Arrow®/Teleflex®, Wayne, USA), are also used but in a lower percentage, particularly in patients that do not require complex therapeutic interventions. The choice of the site of insertion was left to the discretion of the physician caring for the patient. Maximal sterile barrier precautions (large sterile drape; surgical hand antisepsis; and mask, cap, sterile gloves, and gown) were used at catheter insertion according to CDC recommendations.

Catheter care protocol

Standardized CVC care practices were implemented by a highly proficient nursing staff. Every couple of days or earlier if clinically required, the nursing staff changed the dressing, cleaned the skin site and the catheter hub with iodine solution, and changed the intravenous accessory tubing. CVCs were removed when (a) there was evidence or suspicion of infection, (b) when the catheter was no longer required.

Culture techniques

All catheters were examined for the presence of pathogens either as a routine after removal or after suspicion of infection. After disinfecting skin around the CVC entry site, the proximal 4–5 cm part of the tip was cut off using sterile scissors. The specimen was placed in a sterile container and transported to the microbiology laboratory within 15 min at room temperature. The intradermal and intravascular portion of the catheter was analyzed by the semiquantitative culture technique described by Maki et al. [10]. According to Maki’s technique, catheter-tip culture is considered positive in the presence of ≥ 15 colony-forming units (CFU) growth of any organism.

Blood cultures were incubated in Becton Dickinson Bactec (BD Bio-sciences, USA) in aerobic and anaerobic broth media. Identification of isolates and antimicrobial resistance patterns were determined by the VITEK®2Automated Compact System (BioMérieux Co., France). E-test (BioMérieux Co., France) was performed as an additional test, in order to confirm the resistance phenotypes reported by the VITEK System, according to the standard laboratory procedures.


Catheter infection and colonization definitions were based on the Centers for Disease Control bloodstream infection guidelines and the semi-quantitative culture technique by Maki et al.

Catheter associated BSI (CLABSI) was defined as a laboratory confirmed BSI (a positive blood culture with no other apparent source of infection) occurring in the presence of a CVC or within 48 h of CVC removal.

Catheter/days was defined as the number of CVCs presents among all units’ patients at 08:00 h each morning. When more than one concurrent CVC was present in the patient, they were counted as one CVC.

Multidrug-resistant organisms (MDROs) were defined as species of microorganisms that exhibit antimicrobial resistance to at least one antimicrobial drug in three or more antimicrobial categories. This definition concerns both gram-positive and gram-negative bacteria [11].

Statistical analysis

Descriptive analysis to characterize patients’ population were reported as count (percent) or mean value (+ / − standard deviation) for qualitative and quantitative variables, respectively, and were compared between the three groups using Chi-square or one-way ANOVA test, as appropriate. A p-value of ≤ 0.05 was considered as statistically significant.


A total of 9774 catheter/days were reported and analyzed during the 2-years period. Among them, a total of 59 CLABSI cases were identified. The total patients’ demographic characteristics are presented in Table 1. Distribution of CLABSI events among hospital units was as follows: Oncology Unit 3%; ICU 43%; Surgery Unit 14%; Pathology Unit 35%; other units 5%. The mean duration of catheter placement was 16, 2 ± 10.1 days (Range: 2–56 days). In order to evaluate the association between CVC duration and incidence rate of CLABSIs, we categorized events into three groups, each representing a 10-day time interval of catheterization. In the group of up to 10 days (group 1) 22 CLABSI cases were included, 17 cases in the group of 11–20 days’duration (group 2) and 20 cases in the group of > 20 days’ duration (group 3). The mean age of the participants in each group was 52.7 ± 16.7 for group 1, 63.3 ± 22.7 for group 2 and 50.6 ± 19.2 for group 3 (ANOVA, p = 0.1). The male/female analogy was 14/8 in the group 1, 12/5 in group 2 and 15/5 in group 3 (X2, p = 0.72). No significant differences in demographic characteristics were determined among the 3 groups (data not shown). No differences also existed in the proportion of catheterization site (femoral, internal jugular and subclavian) among the 3 groups (Table 2).

Table 1 Study populations’ demographic and clinical characteristics
Table 2 Site of catheter insertion among the CLABSI groups

The CLABSI rates were 4.80 in group 1, 5.92 in group 2, and 8.64 in group 3 (ANOVA, p = 0.007). The CLABSI rate due to multidrug-resistant organisms (MDROs) among the 3 groups was 2.62 in group 1, 3.83 in group 2, and 3.46 in group 3 (ANOVA, p = 0.14) (Table 3).

Table 3 Incidence rate of CLABSIs and MDROs among the CLABSI groups

Within CLABSI events, the most common microorganism identified was MDR Acinetobacter baumannii (n = 27.1%). Among the 3 groups, MDR A. baumannii was the predominant pathogen in group 1 (36.4%), MDR K. pneumoniae (35.3%) for group 2 and both pathogens equally for group 3 (20%) (Table 4). No significant difference in the type of isolated CLABSIs pathogens between the 3 groups was detected.

Table 4 Pathogen distribution among the CLABSI groups


CVCs are important in managing many clinical practices such as blood sampling and infusion of medications, particularly in ICUs. Therefore, in the real world setting, a CVC can remain even for months [12, 13]. Prior to the widespread implementation of CVC bundles, longer duration of catheterization was listed as an identified and significant CLABSI risk factors among others such as use of total parenteral nutrition and extensive catheter manipulation [14]. However, these risk factors refer to practices from a long-gone period [15].

In our setting, CLABSI prevention bundles were adopted in 2009, and included avoidance of femoral sites for CVC insertion, strict adherence to hand hygiene, use of full barrier precautions, chlorhexidine skin preparation, and removal of unnecessary catheters. However, despite the widespread adoption of these bundles and high compliance, CLABSIs still continued to occur in rates that were not negligible. Therefore, we conducted the present study to further investigate the risk factors for these events by analyzing the clinical characteristics of patients, focusing on duration of catheters maintenance and the pathogen distribution associated with CLABSIs after the bundle adoption. Certain limitations should be acknowledged at this point. They mainly concern the short study time-period and the small sample size. More specifically, we present an observational study through a retrospective analysis of two years’ period-due to the lack of complete epidemiological data from previous years- in which only 59 CLABSI cases were identified and analyzed. However, despite these limitations, we have managed to yield additional valuable information that will provide the opportunity for future modifications of our hospital’s CLABSI prevention bundles.

Our analysis showed that an increased duration of central venous access was associated with a gradually higher rate of CLABSI events, in a statistically significant level. In fact, although an increase in CLABSI rate was already noticed during the first ten days of catheterization (group 1), the rate value had almost doubled after 20 days (group 3). Overall, there was no significant difference in patients’ clinical characteristics, including sex, age, underlying diseases, risk factors for CLABSI, laboratory findings, or clinical outcomes, between the 3 groups.

We have considered time as a categorical variable to assess the existing risk over the duration of the catheterization, similarly to other studies [16]. Taking into consideration the existing bibliography referring to the selection of appropriate time thresholds for catheter replacement [17, 18], we set cut-points at 10 days following catheter insertion for each of the 3 groups [19].

Our study indicated that Acinetobacter spp., K. pneumoniae, coagulase-negative staphylococci and Candida albicans were the most common microorganisms isolated from CVCs. Acinetobacter is an important nosocomial pathogen that can be found in many health care environments, on the environment and hands of ICU staff. It frequently colonizes hospitalized patients, especially those with mechanical ventilation in ICU and patients with indwelling catheters [20]. Similarly, to our findings, another retrospective study in an adult ICU in a tertiary care hospital has also showed that the most frequently isolated organism was A. baumannii [21].

In consistence with the international CLABSI pathogen distribution patterns available from numerous studies, causative microorganisms typically originate from the normal resident flora of the skin present at the insertion site, which are mostly consisting by gram-positives such as Staphylococcus spp, Streptococcus spp., Corynebacterium spp., and Candida spp.[22,23,24].However, later studies and data from our previous survey, support that CLABSIs caused by Gram-negatives either predominated in the panel of isolated organisms or exhibited growing trends [25,26,27]. In our study the epidemiology profile of CLABSI pathogens reflects the recently published Greek ICU pathogen profile, where MDR A. baumannii is frequently isolated [28]. This emergence of MDR pathogens has created a great concern on medical care in Greek hospitals, especially for ICU patients [29].

Based on the annual data of antimicrobial resistance rates reported by our hospital’s clinical laboratory, the rates of the 3 most commonly isolated MDR Gram-negatives (A. baumannii, K. pneumoniae, P. aeruginosa) isolated from nosocomial patients was 21.6% for the same time period, 63.3% of which were isolated from ICU. Moreover, 43% of CLABSIs by MDROs were recovered from ICU patients, whereas all patients from other hospital units had a history of previous admission to our ICU prior to the MDROs isolation. This fact, combined with the endemicity of Gram-negative MDROs in our hospital has led to the domination of these pathogens in the microbial profile of CLABSIs.


The findings of the present study displayed that longer duration of catheter placement was associated with an increase in CLABSI rates, supporting the need for continuous training of personnel regarding the proper implementation of bundles, continuous measurement of compliance indicators and probably reassessment of the bundles strategy. Most attention should be focused not only on improving catheter insertion procedures but also and most importantly on maintenance of anaseptic setting during the postinsertion care of the CVCs, a period that seems most likely that infection prevention lapses occur.

In patients with a CVC who develop a CLABSI, the catheter is regularly removed, especially if the causative pathogen is a Gram-negative pathogen or Candida. On this basis, an approach of preventive catheter replacement if intravascular access beyond a specific time period is required, should be considered necessary. However, future studies should determine the total cost–benefit of preventive catheter replacement and the optimal time cut-offs. Moreover, a substantial swift in the epidemiological profile of CLABSIs pathogens towards a high proportion of Gram-negative pathogens and specifically MDROs was noted. Since multidrug-resistant Gram-negative infections are associated with considerable mortality, empirical treatment should be focused on their increasing prevalence and be directed by regional epidemiology reports.

Availability of data and materials

All data generated or analyzed during this study are included in this published article.



Central-line associated bloodstream infection


Catheter-related infection


Central venous catheter


Intensive care unit


Multidrug-resistant organism


  1. Magill SS, O’Leary E, Janelle SJ, Thompson DL, Dumyati G, Nadle J, et al. Changes in prevalence of health care–associated infections in U.S. hospitals. N Engl J Med. 2018;379(18):1732–44.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Stevens V, Geiger K, Concannon C, Nelson RE, Brown J, Dumyati G. Inpatient costs, mortality and 30-day re-admission in patients with central-line-associated bloodstream infections. Clin Microbiol Infect. 2014;20(5):O318–24.

    CAS  Article  PubMed  Google Scholar 

  3. Cardo D, Dennehy PH, Halverson P, Fishman N, Kohn M, Murphy CL, et al. HAI elimination white paper writing group. Moving toward elimination of healthcare-associated infections: a call to action. Am J Infect Control. 2010;38(9):671–5.

    Article  Google Scholar 

  4. Pronovost P, Needham D, Berenholtz S, Sinopoli D, Haitao C, Cosgrove S, et al. An intervention to decrease catheter-related bloodstream infections in the ICU. N Engl J Med. 2006;355:2725–32.

    CAS  Article  Google Scholar 

  5. Callister D, Limchaiyawat P, Eells S, Miller L. Risk factors for central line–associated bloodstream infections in the era of prevention bundles. Infect Control Hosp Epidemiol. 2015;36(2):214–6.

    Article  PubMed  Google Scholar 

  6. O’Grady NP, Alexander M, Burns LA, Dellinger EP, Garland J, Heard SO, et al. Guidelines for the prevention of intravascular catheter-related infections. Clin Infect Dis. 2011;52(9):e162–93.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Park S, Moon S, Pai H, Kim B. Appropriate duration of peripherally inserted central catheter maintenance to prevent central line-associated bloodstream infection. PLoS ONE. 2020;15(6): e0234966.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  8. Ullman AJ, Bernstein SJ, Brown E, Aiyagari R, Doellman D, Faustino EVS, et al. The michigan appropriateness guide for intravenous catheters in pediatrics: miniMAGIC. Pediatrics. 2020;145(Suppl 3):S269–84.

    Article  PubMed  Google Scholar 

  9. Greenberg RG, Cochran KM, Smith PB, Edson BS, Schulman J, Lee HC, et al. Effect of catheter dwell time on risk of central line-associated bloodstream infection in infants. Pediatrics. 2015;136(6):1080–6.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Maki DG, Weise CE, Sarafin HW. A semiquantitative culture method for identifying intravenous-catheter-related infection. New Engl J Med. 1977;296:1305–9.

    CAS  Article  Google Scholar 

  11. Magiorakos AP, Srinivasan A, Carey RB, Carmeli Y, Falagas ME, Giske CG, et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect. 2012;18(3):268–81.

    CAS  Article  PubMed  Google Scholar 

  12. Seo HK, Hwang JH, Shin MJ, Kim SY, Song KH, Kim ES, et al. Two-year hospital-wide surveillance of central line-associated bloodstream infections in a Korean hospital. J Korean Med Sci. 2018;33(45): e280.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Chopra V, Kuhn L, Coffey CE Jr, Salameh M, Barron J, Krein S, et al. Hospitalist experiences, practice, opinions, and knowledge regarding peripherally inserted central catheters: a Michigan survey. J Hosp Med. 2013;8:309–14.

    Article  PubMed  Google Scholar 

  14. Marschall J, Mermel LA, Fakih M, Hadaway L, Kallen A, O’Grady NP, et al. Society for healthcare epidemiology of America. Strategies to prevent central line-associated bloodstream infections in acute care hospitals: update. Infect Control Hosp Epidemiol. 2014;35(7):753–71.

    Article  PubMed  Google Scholar 

  15. Casado-Flores J, Barja J, Martino R, Serrano A, Valdivielso A. Complications of central venous catheterization in critically ill children. Pediatr Crit Care Med. 2001;2(1):57–62.

    CAS  Article  Google Scholar 

  16. Cobb DK, High KP, Sawyer RG, et al. A controlled trial of scheduled replacement of central venous and pulmonary-artery catheters. N Engl J Med. 1992;327(15):1062–8.

    CAS  Article  Google Scholar 

  17. Castelli GP, Pognani C, Stuani A, Cita M, Paladini R. Central venous catheter replacement in the ICU: new site versus guidewire exchange. Minerva Anestesiol. 2007;73(5):267–73.

    CAS  PubMed  Google Scholar 

  18. McLaws ML, Burrell AR. Zero risk for central line–associated bloodstream infection: are we there yet? Crit Care Med. 2012;40:388–93.

    Article  Google Scholar 

  19. Sengupta A, Lehmann C, Diener-West M, Perl TM, Milstone AM. Catheter duration and risk of CLA-BSI in neonates with PICCs. Pediatrics. 2010;125(4):648–53.

    Article  PubMed  Google Scholar 

  20. Rebic V, Masic N, Teskeredzic S, Aljicevic M, Abduzaimovic A, Rebic D. The importance of Acinetobacter species in the hospital environment. Med Arch. 2018;72(5):325–9.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Kamolvit W, Sidjabat HE, Paterson DL. Molecular epidemiology and mechanisms of Carbapenem resistance of Acinetobacter spp. Asia Oceania Microb Drug Resist. 2015;21(4):424–34.

    CAS  Article  PubMed  Google Scholar 

  22. Sohail M, Latif Z. Molecular analysis, biofilm formation, and susceptibility of methicillin-resistant staphylococcus aureus strains causing community- and health care-associated infections in central venous catheters. Rev Soc Bras Med Trop. 2018;51(5):603–9.

    Article  PubMed  Google Scholar 

  23. Wright MO, Decker SG, Allen-Bridson K, Hebden JN, Leaptrot D. Healthcare-associated infections studies project: an American journal of infection control and national healthcare safety network data quality collaboration: location mapping. Am J infect Control. 2018;46(5):577–8.

    Article  Google Scholar 

  24. Alonso B, Latorre MC, Cruces R, Ampuero D, Haces L, Martín-Rabadán P, et al. Evaluation of the Alfred™ turbidity monitoring system (Alifax®) following sonication in the diagnosis of central venous catheter colonization. Eur J Clin Microbiol Infect Dis. 2019;38(9):1737–42.

    Article  PubMed  Google Scholar 

  25. He Y, Zhao H, Wei Y, Gan X, Ling Y, Ying Y. Retrospective analysis of microbial colonization patterns in central venous catheters, 2013–2017. J Healthc Eng. 2019;2019:8632701.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Weiner LM, Webb AK, Limbago B, Dudeck MA, Patel J, Kallen AJ, et al. Antimicrobial-resistant pathogens associated with healthcare-associated infections: Summary of data reported to the national healthcare safety network at the centers for disease control and prevention, 2011–2014. Infect Control Hosp Epidemiol. 2016;37(11):1288–301.

    Article  Google Scholar 

  27. Pitiriga V, Kanellopoulos P, Bakalis I, Kampos E, Sagris I, Saroglou G, et al. Central venous catheter-related bloodstream infection and colonization: the impact of insertion site and distribution of multidrug-resistant pathogens. Antimicrob Resist Infect Control. 2020;9(1):189.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Arvaniti K, Lathyris D, Clouva-Molyvdas P, Haidich AB, Mouloudi E, Synnefaki E, et al. Comparison of Oligon catheters and chlorhexidine-impregnated sponges with standard multilumen central venous catheters for prevention of associated colonization and infections in intensive care unit patients: a multicenter, randomized, controlled study. Crit Care Med. 2012;40(2):420–9.

    Article  Google Scholar 

  29. Moschou A, Ioannou P, Moraitaki E, Stafylaki D, Maraki S, Samonis G, et al. Rectal colonization by drug resistant bacteria in nursing home residents in Crete, Greece. Trop Med Infect Dis. 2021;6(3):123.

    Article  PubMed  PubMed Central  Google Scholar 

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We acknowledge the contribution of the hospital healthcare workers who participated in this study. We would also like to acknowledge the contribution of Mr. Pavlos Mariatos, Director of Quality Management Department in data recording and analysis.


No specific funding was received for this study.

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Authors and Affiliations



VP, PK, GS, AT designed and set up methodology, VP, JB, EK, PK performed the study, VP, PK, GS, AT analyzed the data, all authors contributed to read and approved the final manuscript.

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Correspondence to Athanasios Tsakris.

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Pitiriga, V., Bakalis, J., Kampos, E. et al. Duration of central venous catheter placement and central line-associated bloodstream infections after the adoption of prevention bundles: a two-year retrospective study. Antimicrob Resist Infect Control 11, 96 (2022).

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  • Catheterization
  • Central venous catheter
  • Sepsis
  • Colonization
  • Bloodstream infection
  • Insertion site
  • Central line-associated bloodstream infection
  • Peripherally inserted central catheter