- Open Access
The microbiological and clinical outcome of guide wire exchanged versus newly inserted antimicrobial surface treated central venous catheters
Critical Care volume 17, Article number: R184 (2013)
The management of suspected central venous catheter (CVC)-related sepsis by guide wire exchange (GWX) is not recommended. However, GWX for new antimicrobial surface treated (AST) triple lumen CVCs has never been studied. We aimed to compare the microbiological outcome of triple lumen AST CVCs inserted by GWX (GWX-CVCs) with newly inserted triple lumen AST CVCs (NI-CVCs).
We studied a cohort of 145 consecutive patients with GWX-CVCs and contemporaneous site-matched control cohort of 163 patients with NI-CVCs in a tertiary intensive care unit (ICU).
GWX-CVC and NI-CVC patients were similar for mean age (58.7 vs. 62.2 years), gender (88 (60.7%) vs. 98 (60.5%) male) and illness severity on admission (mean Acute Physiology and Chronic Health Evaluation (APACHE) III: 71.3 vs. 72.2). However, GWX patients had longer median ICU lengths of stay (12.2 vs. 4.4 days; P < 0.001) and median hospital lengths of stay (30.7 vs. 18.0 days; P < 0.001). There was no significant difference with regard to the number of CVC tips with bacterial or fungal pathogen colonization among GWX-CVCs vs. NI-CVCs (5 (2.5%) vs. 6 (7.4%); P = 0.90). Catheter-associated blood stream infection (CA-BSI) occurred in 2 (1.4%) GWX patients compared with 3 (1.8%) NI-CVC patients (P = 0.75). There was no significant difference in hospital mortality (35 (24.1%) vs. 48 (29.4%); P = 0.29).
GWX-CVCs and NI-CVCs had similar rates of tip colonization at removal, CA-BSI and mortality. If the CVC removed by GWX is colonized, a new CVC must then be inserted at another site. In selected ICU patients at higher central vein puncture risk receiving AST CVCs GWX may be an acceptable initial approach to line insertion.
Central venous catheters (CVCs) are commonly used in intensive care units. However, their use is not without risk [1–3] and line-related bacteraemia and sepsis remain significant problems [4–6]. Several studies in the 1990s suggested that regular line change does not decrease the risk of line-related sepsis and exposes patients to the risks associated with a new insertion (pneumothorax and arterial puncture) [7–9]. Thus, in the absence of clear identification of an alternative source of sepsis, clinicians currently respond to signs of possible or suspected CVC infection (new fever, increased white cell count, increased C-reactive protein or procalcitonin levels or a combination of these indicators) [10–12] by removing the CVC as the possible infective source [13, 14]. However, if a CVC continues to be required, the removed CVC can then be replaced by two techniques: either by inserting a new CVC at another site or by inserting the new CVC at the same site by guide wire exchange (GWX) [9–15]. Finally, if GWX is performed and the tip of the line so removed grows a pathogen, the CVC inserted by GWX is removed and a fresh CVC is inserted at another site.
Theoretically, a new CVC insertion at a new site exposes the patient to some risk of arterial or lung puncture while, logically, GWX will eliminate the risk associated with such a puncture [16–19]. However, GWX may expose patients to a greater risk of line contamination through inadequate protection of the insertion field with anti-bacterial solutions. This, in turn, could potentially increase the risk of subsequent line tip colonization and bacteraemia [20–23]. Regrettably, despite the relatively common occurrence of suspected line related sepsis and the importance of this issue in daily practice, little empirical data exist to guide clinical practice.
The last decade has seen the widespread introduction of antimicrobial surface treated (AST) CVCs [24–27]. These AST-CVCs are associated with less line-related colonization and sepsis [26, 27]. These CVCs may be logically expected to also diminish the risk of infection associated with GWX. Yet, to our knowledge, no studies have compared the risk of line colonization with pathogens and/or catheter-associated bloodstream infection (CA-BSI) when such surface treated CVCs are inserted by GWX. Accordingly, we conducted a retrospective study and estimated the incidence of subsequent line colonization and CA-BSI after GWX of AST-CVCs compared with a matched cohort of newly inserted AST-CVCs. We aimed to test the hypothesis that the incidence of CVC colonization with pathogens would still be much greater with GWX insertion.
Materials and methods
This study was approved by the Austin Hospital Human Research Ethics Committee (HREC). The Austin HREC waived the need for informed consent for this study because it involved no intervention and the use of routinely collected data which were also de-identified and made anonymous for the purpose of the investigation.
Our unit has exclusively used antimicrobial surface treated (chlorhexidine acetate and silver sulfadiazine) triple lumen CVCs (Arrowgard blue®, Arrow-Howes, Reading, PA, USA) since 2005. Thus, we conducted a retrospective study of all CVCs inserted in our ICU as consecutively recorded in our database since 2005.
All line insertion-related data are recorded prospectively in our database as part of an ongoing quality assurance process whenever an ICU doctor inserts a CVC, arterial line, dialysis catheter or other invasive lines. The database contains specific information regarding when the CVC was inserted, the reason and method of insertion, any complications and the reason and timing of removal.
We used this database to identify all patients who had a central line inserted by GWX and selected a control population. Controls were selected as the patients in the database who had a new CVC inserted in ICU but not by the GWX method on the same day or as close to the same day as possible and, whenever possible, at the same site. This matching approach was selected because the average time to GWX of a CVC was seven days after admission and matching by admission to characteristics did not appear logical. On the other hand, matching controls for date of CVC insertion was considered to decrease the more relevant risks of CVC-insertion doctor and time-related bias.
We excluded patients who had a new CVC inserted (non-GWX) within 72 hours of a GWX, to avoid possible difficulties in attributing any source of bacteraemia. The decision to perform a GWX insertion in the presence of suspected CVC infection was made by the treating clinician in consideration of all possible risks and benefits of such an approach following unit protocol (see below).
Approach to suspected line infection
During the study period, the approach to suspected line infection followed these unit guidelines:
Consider line infection if there is: a) a new fever or worsening fever not explained by likely infection elsewhere; b) an elevated white cell count or worsening white cell count not explained by likely infection elsewhere.
If line infection is suspected, inspect the insertion site. If there is redness or any suspicion of site infection, remove the line and insert a new CVC elsewhere. If there is no evidence of skin inflammation, consider the risks and benefits of GWX vs. new line insertion elsewhere.
If the patient has coagulopathy, thrombocytopenia, marked obesity, lack of other suitable sites for CVC insertion or other anatomical features that make new line insertion relatively contraindicated, proceed to GXW.
In all cases, send the line of the suspected tip for culture and obtain blood cultures, urine cultures and sputum cultures.
If GWX has been completed and the line tip of the removed CVC is subsequently found to be colonized, remove the GWX CVC and insert a new CVC elsewhere.
If a CVC is removed because it is no longer needed and there is no clinical suspicion of infection, do not send the tip for culture.
Patients with shock (vasopressor dependence) were excluded as they required continued infusion of vasopressors, which could not be maintained during the GWX of the line.
We then obtained data on CVC tip cultures for both the GWX and control groups using the hospital microbiology database, as well as blood cultures taken during the time the line was in situ and for 48 hours after line removal.
Once the intervention and control groups had been identified, we compared the two groups for patient characteristics as obtained by the ICU admissions and discharges database, which is part of the Australian and New Zealand adult patient database program . Such data included age, sex, admission diagnosis, Acute Physiology and Chronic Health Evaluation (APACHE) III score, use of mechanical ventilation and key outcomes. Similarly, we compared the two groups for microbiological outcomes including: a) the number of CVC tips that were sent for culture, b) the number which had a positive tip culture for a pathogen (exclusion of skin flora and skin commensal organisms unless isolated from two different blood cultures as per Centre for Disease Control guidelines), and c) the number of patients who had catheter-associated blood stream infection (CA-BSI) using the criteria described by the US National Nosocomial Infections Surveillance System of the Centers for Disease Control and Prevention as used in a recent multicentre study . Finally, we compared patient outcomes. For this comparison, we assessed the patients' length of stay in the ICU, the length of stay in hospital, and their survival status at ICU and hospital discharge.
Technique of guide wire exchange (GWX)
Since 1995, the technique employed at our institution for changing CVCs over a guide wire involves full aseptic precautions (gloves, gown, hat and mask). The steps used to insert the line by GWX are shown in a photographic sequence using a mannequin from Figure 1a-i.
In brief, the patient is positioned as for a new CVC insertion. Approximately 5 cm of the catheter external to the entry site are extensively prepared with chlorhexidine solution in 70% alcohol solution. Some parts of the catheter are more difficult to cover with the antiseptic solution. These, including the hub and connecting ports, are covered with drapes, which are later removed.
The skin surrounding the catheter insertion site is also treated with an alcohol and chlorhexidine solution, and sterile drapes are placed appropriately to cover the catheter except for the component under manipulation. The segment of catheter remaining uncovered is then covered with alcohol-chlorhexidine impregnated gauze. The catheter is clamped just above its point of entry in the skin and, using sterile scissors, the CVC is then cut below the hub and 3 to 4 cm from the skin. The external cut portion is covered with drapes. The operator then removes his/her gloves and changes to a new pair of sterile gloves.
The field is further covered so that only a small skin surface of 3 to 5 cm2 is exposed where the CVC enters the skin. The severed cross-section of the line shows the various lumens and the soft J tip of the guide wire is then inserted into the largest lumen (distal 16 gauge lumen) until it meets the resistance of the clamp. The clamp is removed with one hand, while the other holds the external part of the CVC.
The wire is then advanced to 20 cm and the 'old' CVC is removed over it. The removed CVC is placed onto the sterile drapes, the distal 5 cm portion is cut with sterile scissors, placed in a sterile container and sent for subsequent microbiological culture. The operator now has a wire in place for a new central line insertion. A new catheter can now be inserted over the wire and secured to the skin as would be the case for a new CVC.
All lines are inserted by a variable group of doctors (residents, fellows, specialists) during the study period. If junior doctors inserted the catheter, it is under supervision of a senior doctor.
Skin preparation is with 2% chlorhexidine in 70% alcohol. Protection of the CVC site after insertion is in the form of a "sandwich" cover with a transparent dressing (IV 300 Frame Delivery, Smith & Nephew, Hull, UK) and with a chlorhexidine impregnated antimicrobial disk (Biopatch, Ethicon Inc., Bridgewater, NJ, USA) around the skin entry site (Figure 2). The dressing is not changed until line removal; nursing care is given on a 1:1 ratio to all patients with no regular change to giving sets.
Line removal is decided upon by the treating clinicians with consideration of all relevant aspects of patient management.
In our microbiology lab, CVC tips are processed by first adding 2 ml of D/E Neutralizing Broth (Neogen, Lansing, MI, USA) to neutralize any residual disinfectants or antimicrobials. The tip and broth are vortexed for 30 seconds, then 100 μL of the fluid are inoculated onto a horse blood agar plate (BioMerieux, Marcy-l'Etoile, France). Plates are incubated at 36°C in a 5% CO2 incubator, and read at 24 and 48 hours. Any positive cultures are subsequently identified by routine laboratory methods, and reported as qualitative cultures only.
Blood samples are collected in aerobic and anaerobic bottles for culture (Bactec 9240, Becton Dickinson, Sparks, MD, USA), and cultured for five days. Positive bottles are then sub-cultured manually onto HBA, chocolate HBA and anaerobic HBA (plus Sabaraud dextrose agar if yeasts present in Gram stain) (BioMerieux), and incubated aerobically, anaerobically and in 5% CO2 for up to five days. Positive cultures are subsequently identified according to routine laboratory methods.
All analyses are performed using SAS version 9.2 (SAS Institute Inc., Cary, NC, USA). Group comparisons are made using chi-square tests for equal proportions of Fisher's exact test when appropriate for categorical data, Student's t-test and Wilcoxon rank sum test for continuous data. Results are reported as numbers (percentages), means (standard deviation) or medians (interquartile range) as appropriate. Due to the low number of outcomes, multivariable logistic regression was not performed. A two-sided P-value of 0.05 was considered to be statistically significant.
We compared microbiological data from the 145 patients with a GWX-CVC insertion with those of 163 control patients with a NI-CVC from December 2005 to February 2011 (Table 1). During this time a total of 2,378 CVCs were inserted in the unit. At the time of CVC insertion, all patients receiving GWX have suspected line infection. All lines replaced by GWX were sent for cultures and blood cultures were obtained. The line tips of the CVC removed by GWX grew coagulase negative staphylococci in 11 cases, enterococci in 1, gram negative bacilli in 1 and Candida albicans in 1. In all cases, the newly inserted GWX line was removed and a new CVC placed elsewhere. In two additional cases, both blood culture and CVC tip grew the same organisms (Klebsiella and Candida albicans). In both cases, the newly inserted GWX CVC was removed and a new CVC placed elsewhere.
Both groups were similar for gender distribution, mean age and APACHE III scores on admission. There was also no significant difference in APACHE III admission-related diagnostic groups and co-morbidities. However, 134 (92.4%) patients in the GWX group were mechanically ventilated compared with 127 (77.9%) in the control group (P = 0.005). There were no complications of GWX insertion. In the control group, there were two episodes of arterial puncture which required manual compression with one residual haematoma. There were no pneumothoraces. Microbiological data are presented in Table 2.
As expected given a period of pre-GWX cannulation, there was a significant difference in ICU length of stay between the two study groups. The GWX group had a longer ICU length of stay than the control group (median (IQR) of 12.2 (4.8 to 17.8) days compared to 4.4 (2.1 to 9.0) days in the control group; P < 0.001. This significant difference persisted for hospital length of stay with a median for the GWX group of 30.7 (17.3 to 56.7) days compared with 18.0 (8.5 to 37.7) days for the control group (P < 0.001). Median time from insertion to discharge from ICU was 5 (2 to 10) vs. 3 (2 to 7) days for the GWX and control group, respectively (P = 0.005); while time from insertion to hospital discharge was 19 (10 to 42) vs. 13 days (5 to 31) (P = 0.003).
The most common site for line insertion was the internal jugular vein in both groups (91 (62.7%) in the GWX group, vs. 96 (58.9%) in the control group; P = 0.49) followed by the femoral vein (25 (17.2%) in the GWX group vs. 42 (25.7%) in the control group; P = 0.07) and finally, the subclavian vein (8 (5.5%) in the GWX group vs. 9 (5.5%) in the control group; P = 0.99]
Tip cultures from the CVC were obtained in 81 (55.9%) GWX patients and in 95 (58.3%) of controls (P = 0.66). Pathogens were isolated from six (6.3%; 95% CI: 1.7 to 10.9) tips (three Gram negative organisms, two Staphylococcus isolates and one Candida) in six control patients compared with five (5.9%; 95% CI: 1.9 to 9.9%) tips in five GWX patients (five Gram negative isolates) (Table 2).
For the 13 patients who had a positive CVC tip culture and a positive blood culture during their ICU stay, the same organism was isolated in both cultures in two patients in the GWX group vs. three patients in the control group (Table 2). The overall incidence of CA-BSI was 2.6 events/1,000 catheter days (1.8 (0 to 5) for GWX vs. 3.5 (0 to 14) for controls. There was no significant difference between the two groups for ICU mortality (19 (13.1%) vs. 31 (19.0%); P = 0.15) and hospital mortality (35 (24.1%) vs. 48 (29.4%); P = 0.29).
In a clinical environment where all CVCs inserted are antimicrobial surface treated (AST) CVCs, we conducted a retrospective observational study to test the hypothesis that GWX would result in a major increased incidence of subsequent line colonization with pathogens compared with NI-CVCs. Our results suggest that, in selected ICU patients at higher central vein puncture risk, using AST-CVCs and the GWX method carries similar risks of subsequent line colonization with pathogens and CA-BSI as NI-CVCs. Survival to both hospital and ICU discharge were also similar for both groups.
GWX might increase the risk of catheter-related infections [30–32]. However, previous studies did not adjust for all relevant confounders or report how GWX was performed. Moreover, current guidelines on GWX  are based on data from studies published in the 1990s. In the most prominent of these studies , the GWX procedure was often performed with insertion via the most distal port and distal to the CVC hub (Sawyer R and Peled H, personal communication). In 2000, on the basis of such information, a review concluded that GWX might be associated with a higher rate of catheter colonisation and catheter-related bacteraemia . In addition, recent guidelines  imply that GWX would be the final step in the therapeutic process for a suspected CVC-related infection.
In contrast to the above positions, several other observational studies reported that GWX of a CVC was microbiologically safe [11, 15, 30, 34]. Unfortunately, in the absence of randomized trials or contemporaneous controls, these reports were confounded by selection bias and provided only weak evidence for or against GWX-CVCs. In the last 10 years, only two studies have assessed the potential relationship between GWX and microbiological outcome. One  reported a rate of colonization for newly inserted CVCs of 6.8% compared with 2.3% for GWX CVCs. No information was provided on the technique of GWX. The other found that GWX was associated with an increased risk of catheter-related bacteraemia . However, this latter study only assessed 76 CVCs inserted by GWX, with only half being triple lumen CVCs. Moreover, one-third was inserted outside the ICU, chlorhexidine preparation of the site was only used in less than 10% of insertions, and AST-CVCs were not used. Additionally, in contrast to our study, the process of GWX insertion was not described.
Implications of study findings
The results of our study suggest that, when using AST-CVCs and a sterile procedure for insertion of the guide wire below the hub and directly into the AST catheter, CVC replacement by GWX in the ICU is likely microbiologically equivalent to de novo CVC insertion. The information obtained in our study justifies the use of GWX as an acceptable approach to CVC replacement in selected ICU patients deemed at high risk from attempted central vein puncture because of coagulopathy, thrombocytopenia and/or anatomical characteristics (for example, extreme obesity, poor central vein visualization on ultrasound), provided that AST CVCs are used and a sterile technique with insertion of the wire below the hub is applied and there is no evidence of insertion site inflammation. It must be emphatically stated, however, that, if the line exchanged by the guide wire is found to be colonized, the GWX CVC must then be removed and a new CVC inserted at another site.
Strengths and limitations
This study has several strengths. It describes the largest cohort of GWX CVCs in the literature. It is the first to assess the microbiological outcome of GWX of AST-CVCs and to explicitly present the technique of GWX in detail. Nonetheless, our database provided only information on the admission diagnosis but not on the presence, degree and alternative sources of sepsis at the time of CVC removal. These shortcomings applied to both cohorts similarly, making the introduction of bias in favour or against GWX unlikely.
Our study compared microbiological outcomes and major clinical outcomes with those of contemporaneous newly inserted CVCs. However, the comparison with new CVCs inserted early in the course of the ICU admissions in a cohort of patients with a relatively short stay biased the study against GWX-CVCs. The fact that, despite such negative bias, there was no evidence of greater colonization rates after GWX supports the notion that GXW insertion of AST-CVCs is likely microbiologically similar to newly inserted CVCs.
Our study data were obtained from the ICU and microbiology databases. These were collected prospectively and electronically recorded and were not amenable to manipulation or post-hoc ascertainment bias. The study period was long, allowing the capture of data from many different clinicians (junior and senior), which suggests a degree of generalizability. However, our study was retrospective with all the inherent limitations associated with such design. Of technical importance, we applied a specific technique to GWX as illustrated in the figures. This technique may have decreased the risk of colonization. Unfortunately, all previous papers describing the microbiological outcome of GWX failed to report the details of the GWX technique.
Our findings are from an intensive care unit, which serves as a referral centre for liver transplantation and which, therefore, handles many immune-suppressed patients with advanced liver disease and coagulopathy, who require CVCs for extended periods and are at high risk of bleeding. Thus, our results may not apply to different patient populations. We acknowledge that CVC insertion in higher risk patients may still be safe under ultrasound guidance. However, logically the avoidance of puncture and dilatation must provide a greater degree of safety.
The rates of CA-BSI appear slightly higher than those reported in a recent multicentre study . However, the study population had twice our unit average stay among controls and six times the unit average among GWX patients. Our ICU applied all components of the bundle of line insertion care  during the entire study period in a strategic attempt to decrease noscomial infection associated with any cannulation in complex patients [36, 37].
Our findings could represent a type II error. However, ours is the largest cohort of patients receiving GWX of CVC where all catheters in question were triple lumen AST-CVCs catheters. Finally, the point estimate for line colonization with pathogens and CA-BSI was lower in the GWX cohort despite the illness duration related bias against them. Thus, within these statistical limitations, our study provides initial evidence for clinicians to estimate the microbiological risk of GWX insertion of CVCs in selected patients at higher risk of central vein cannulation.
In conclusion, GWX of an antimicrobial surface treated CVC in selected patients at high risk from central vein cannulation appears not to be associated with an increased rate of bacteraemia or pathogen colonization compared with a newly inserted CVC. Such GWX of a CVC is safe and easy to perform. Treatment of suspected CVC-related sepsis should include antibiotics and removal of the CVC. However, if the CVC needs replacement, in selected patients with severe coagulopathy or unfavourable anatomy or limited availability of other insertion sites, clinicians may now consider GWX using an AST-CVC with a clearer appreciation of its microbiological risk.
In selected patients, central venous catheter replacement by guide wire exchange is microbiologically associated with a low rate of line-related bacteraemia when using antimicrobial surface-treated catheters.
In selected patients, guide wire exchange of central venous catheters can be technically performed in a systematic way that minimizes risk of colonization.
In selected patients at high risk of bleeding or with anatomically unfavourable characteristics, replacement of a new central venous catheter by guide-wire exchange may be a safe and preferred approach when antimicrobial surface treated catheters are used.
If the CVC removed by GWX is found to have been colonized, however, the CVC inserted by GWX must be removed and a new CVC must be inserted at another site.
Acute Physiology and Chronic Health Evaluation
antimicrobial surface treated
catheter associated bloodstream infection
central venous catheter
guide wire exchange
CVCs inserted by GWX
Human Research Ethics Committee
newly inserted triple lumen AST CVCs.
Maki DG: Nosocomial bacteremia. An epidemiologic overview. Am J Med 1981, 70: 719-732. 10.1016/0002-9343(81)90603-3
Craven DE, Kunches LM, Lichtenberg DA, Kollisch NR, Barry MA, Heeren TC, McCabe WR: Nosocomial infection and fatality in medical and surgical intensive care patients. Arch Intern Med 1988, 148: 1161-1168. 10.1001/archinte.1988.00380050165024
Kaye CG, Smith DR: Complications of central venous cannulation. BMJ 1988, 297: 572-573. 10.1136/bmj.297.6648.572
Safdar N, Makdi DG: The pathogenesis of catheter-related bloodstream infection with noncuffed short-term central venous catheters. Intensive Care Med 2004, 30: 62-67. 10.1007/s00134-003-2045-z
Patil HV, Patil VC, Ramteerthkar MN, Kulkarni RD: Central venous catheter-related bloodstream infections in the intensive care unit. Indian J Crit Care Med 2011, 15: 213-223. 10.4103/0972-5229.92074
Pittet D, Tarara D, Wenzel R: Nosocomial bloodstream infection in critically ill patients: excess length of stay, extra costs, and attributable mortality. JAMA 2004, 271: 1598-1601.
Cobb D, High K, Sawyer R: A controlled trial of scheduled replacement of central venous and pulmonary artery catheters. N Engl J Med 1992, 327: 1062-1068. 10.1056/NEJM199210083271505
Cook D, Randolph A, Kernerman P, Cupido C, King D, Soukup C, Brun-Buisson C: Central venous catheter replacement strategies: a systematic review of the literature. Crit Care Med 1997, 25: 1417-1424. 10.1097/00003246-199708000-00033
Timsit JF: Scheduled replacement of central venous catheters is not necessary. Infect Control Hosp Epidemiol 2000, 21: 371-374. 10.1086/501775
Jeske C, Raedler C, von Goedecke A, Mayr A, Hinterberger G, Aspoeck Ch, Lass-Floerl C, Benzer A: Early identification of bacteria leading to central venous catheter contamination. Anesth Analg 2003, 97: 940-943.
Casey J, Davies J, Balshaw-Greer A, Taylor N, Crowe AV, McClelland P: Inserting tunnelled hemodialysis catheters using elective guidewire exchange from nontunnelled catheters: is there a greater risk of infection when compared with new-site replacement? Haemodial Int 2008, 12: 52-54. 10.1111/j.1542-4758.2008.00240.x
Cahill SL, Benotti PN: Catheter infection control in parenteral nutrition. Nutr Clin Pract 1991, 6: 65-67. 10.1177/011542659100600265
Mermel L, Farr B, Sherertz R, Raad II, O'Grady N, Harris JS, Craven DE, Infectious Diseases Society of America; American College of Critical Care Medicine; Society for Healthcare Epidemiology of America: Guidelines for management of intravascular catheter- related infections. Clin Infect Dis 2001, 32: 1249-1272. 10.1086/320001
Pagani JL, Eggimann P: Management of catheter-related infection. Expert Rev Anti Infect Ther 2008, 6: 31-37. 10.1586/1478718.104.22.168
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: 267-273.
Newsome HH Jr, Armstrong CW, Mayhall GC, Sugerman HJ, Miller K, Rich A, Dalton H: Mechanical complications from insertion of subclavian venous feeding catheters: comparison of de novo percutaneous venepuncture to change of catheter over guidewire. JPEN J Parenter Enteral Nutr 1984, 8: 560-562. 10.1177/0148607184008005560
Milner P: Complications of pulmonary artery balloon flotation catheters. Lancet 1983, 1: 37-38.
Mitchell SE, Clark RA: Complications of central venous catheterisation. Am J Roentgenol 1979, 133: 467-476. 10.2214/ajr.133.3.467
Borja AR: Current status of infraclavicular subclavian vein catheterisation. Ann Thorac Surg 1972, 13: 615-624. 10.1016/S0003-4975(10)65181-8
Pettigrew RA, Lang SD, Haydock DA, Parry BR, Bremner DA, Hill GL: Catheter-related sepsis in patients on intravenous nutrition: a prospective study of quantitative catheter cultures and guidewire changes for suspected sepsis. Br J Surg 1985, 72: 52-55. 10.1002/bjs.1800720121
Robinson D, Suhocki P, Schwab S: Treatment of infected tunnelled venous access haemodialysis catheters with guidewire exchange. Kidney Int 1998, 53: 1792-1794. 10.1046/j.1523-1755.1998.00954.x
Snyder RH, Archer FJ, Endy T, Allen TW, Condon B, Kaiser J, Whatmore D, Harrington G, McDermott CJ: Catheter infection: a comparison of two catheter maintenance techniques. Ann Surg 1988, 208: 651-653. 10.1097/00000658-198811000-00018
Graeve Ah, Carpenter CM, Schiller WR: Management of central venous catheters using a wire introducer. Am J Surg 1981, 142: 752-755. 10.1016/0002-9610(81)90327-5
Chatzinikolau I, Raad II: Intravascular catheter-related infections: a preventable challenge in the critically ill. Semin Respir Infect 2000, 15: 264-271. 10.1053/srin.2000.20943
Rupp ME, Lisco SJ, Lipsett PA, Perl TM, Keating K, Civetta JM, Mermel LA, Lee D, Dellinger EP, Donahoe M, Giles D, Pfaller MA, Maki DG, Sherertz R: Effect of a second generation venous catheter impregnated with chlorhexidine and silver sulfadiazine on central catheter-related infections: a randomized, controlled trial. Ann Intern Med 2005, 143: 570-580. 10.7326/0003-4819-143-8-200510180-00007
Brun-Buisson C, Doyon F, Sollett JP, Cochard JF, Cohen Y, Nitenberg G: Prevention of intravascular catheter-related infection with newer chlorhexidine-silver sulfadiazine-coated catheters: a randomized controlled trial. Intensive Care Med 2004, 30: 837-843. 10.1007/s00134-004-2221-9
Heard SO, Wagle M, Vijayakumar E, McLean S, Brueggemann A, Napolitano LM, Edwards LP, O'Connell FM, Puyana JC, Doern GV: Influence of triple-lumen central venous catheters coated with chlorhexidine and silver sulfadiazine on the incidence of catheter-related bacteremia. Arch Intern Med 1998, 158: 81-87. 10.1001/archinte.158.1.81
Stow PJ, Hart GK, Higlett T, George C, Herkes R, McWilliam D, Bellomo R, ANZICS Database Management Committee: Development and implementation of a high-quality clinical database: the Australian and New Zealand Intensive Care Society Adult Patient Database. J Crit Care 2006, 21: 133-141. 10.1016/j.jcrc.2005.11.010
Pronovost P, Needham D, Berenholtz S, Sinopoli D, Chu H, Cosgrove S, Sexton B, Hyzy R, Welsh R, Roth G, Bander J, Kepros J, Goeschel C: An intervention to decrease catheter-related bloodstream infections in the ICU. N Engl J Med 2006, 355: 2725-2732. Erratum in N Engl J Med 2007, 356:2660 10.1056/NEJMoa061115
Michel LA, Bradpiece HA, Randour P, Pouthier F: Safety of central venous catheter change over a guidewire for suspected catheter related sepsis. A prospective randomised trial. Int Surg 1988, 73: 180-186.
Hilton E, Haslett TM, Borenstein MT, Tucci V, Isenberg HD, Singer C: Central catheter infections: single versus triple lumen catheters. Influence of guidewires on infection rates when used for replacement of catheters. Am J Med 1988, 84: 667-672. 10.1016/0002-9343(88)90102-7
Almuneef MA, Memish ZA, Blakhy HH, Hijazi O, Cunningham G, Francis C: Rate, risk factors and outcomes of catheter-related bloodstream infection in a paediatric intensive care unit in Saudi Arabia. J Hosp Infect 2006, 62: 207-213. 10.1016/j.jhin.2005.06.032
O'Grady NP, Alexander M, Burns LA, Dellinger EP, Garland J, Heard SO, Lipsett PA, Masur H, Mermel LA, Pearson ML, Raad II, Randolph AG, Rupp ME, Saint S, Healthcare Infection Control Practices Advisory Committee (HICPAC):: Summary of recommendations: guidelines for the prevention of intravascular catheter-related infections. Clin Infect Dis 2011, 52: 1087-1099. 10.1093/cid/cir138
Erbay A, Ergonul O, Stoddard GJ, Samore MH: Recurrent catheter-related bloodstream infections: risk factors and outcome. Int J Infect Dis 2006, 10: 396-400. 10.1016/j.ijid.2005.08.002
Garnacho-Montero J, Aldabó-Pallás T, Palomar-Martínez M, Vallés J, Almirante B, Garcés R, Grill F, Pujol M, Arenas-Giménez C, Mesalles E, Escoresca-Ortega A, de Cueto M, Ortiz-Leyba C: Risk factors and prognosis of catheter-related bloodstream infection in critically ill patients: a multicenter study. Intensive Care Med 2008, 34: 2185-2193. 10.1007/s00134-008-1204-7
Conrick-Martin I, O'Gorman J, Lenehan D, Oshodi D, Scanlon N, O'Brien S, Hannan M, Lynch M, Carton E: Nosocomial infections in a cohort of extracorporeal life support patients. Crit Care Resusc 2012, 14: 198-201.
Mullany DV, Bull TN, Hunt W, Shekar K, Thomson B, Fraser JF, Ziegenfuss M: Outcomes of the first 30 cases of an adult extracorporeal membrane oxygenation program: strategies to manage the "learning curve" and implications for intensive care unit risk adjustment models. Crit Care Resusc 2012, 14: 119-129.
This work was performed at the Department of Intensive Care, Austin Hospital, Heidelberg, Melbourne, Australia. This study was supported by the Austin Hospital Intensive Care Trust Fund.
No reprints will be ordered.
The authors declare that they have no competing interests.
All authors made substantial contributions to the conception and design of the study, or to the acquisition of data or analysis and interpretation of data. NP was in charge of the clinical data collection and wrote the first draft of the manuscript. NS was in charge of the microbiological data collection. RB was in charge of the design of the study, assisted with analysis and revised and critiqued the manuscript until ready. AGS was in charge of assisting with the clinical data collection and manuscript development. NJG assisted with the clinical outcome data collection and manuscript development. PDRJ assisted with the microbiological data collection and manuscript development and revision from a microbiological point of view. MB was in charge of the statistical analysis and study design development from a statistical point of view and reviewed the manuscript for content and accuracy. All authors have given final approval of the manuscript version to be published.
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Parbat, N., Sherry, N., Bellomo, R. et al. The microbiological and clinical outcome of guide wire exchanged versus newly inserted antimicrobial surface treated central venous catheters. Crit Care 17, R184 (2013). https://doi.org/10.1186/cc12867
- central venous catheters
- catheter related blood stream infection
- intensive care
- Gram negative bacteria