Catheter-Related Bloodstream Infections
 

Introduction

The progress of modern medicine has been advanced, in part, by the wide use of invasive medical devices, including IV catheters. However,  IV catheters are often associated with serious infectious complications, such as catheter-related bloodstream infection (CRBSI).[1] In fact, CRBSI is considered to be the most common type of nosocomial bloodstream infection, a finding that has been attributed to the wide use of intravascular catheters in hospitalized patients.[2,3]

It is estimated that 7 million central venous catheters (CVCs) will be inserted annually in the United States . Even with the best available aseptic techniques being used during insertion and maintenance of the catheter, 1 of every 20 CVCs inserted will be associated with at least 1 episode of bloodstream infection. [4]

Therefore, it is estimated that more than 300,000 episodes of CVC-related bloodstream infections will occur annually in the United States over the next few years.[5] Pittet and colleagues[6] recently estimated the attributable mortality rate of such infections in critically ill patients to be 25%. Each episode of CRBSI will cost $30,000-56,000 per survivor and result in an additional average stay of 6.5 days in the ICU.

The high morbidity, mortality, and cost attributed to CRBSI are the driving forces underlying the search for new preventive approaches to reduce BSI’s.

Catheter-related bloodstream infections (CRBSI) resulting from bacterial colonization of an central venous catheter are a significant clinical problem, magnified in recent years by the increasing use of central venous catheters in intensive care, chemotherapy and total parental nutrition (TPN). In particular, central venous catheter-related infections are a common cause of bacteraemia and sepsis.

There are three routes by which infection can occur:

  • Intraluminal : situated within, occurring within, or introduced from internal lumen (catheter)
  • Extraluminal: situated outside, occurring from outside, tracked down outside of catheter
  • Hematogenous: occurring from blood

Diagnosis of CRBSI

Clinical
The symptoms and signs of catheter-related infection may be localized to the insertion site or track of a tunneled device. Alternatively, manifestations may be systemic and possibly complicated by bacterium.

Local infection

Systemic infection

  • Local inflammation
  • Discharge around the line
  • Erythematic
  • Pain
  • Fever
  • Rigors when the line is used
  • Tachycardia
  • Metastatic infection

Pathogenesis
Several factors pertaining to the pathogenesis of CRBSI have been identified during the last decade. These are:

Skin and Hub
The skin and the hub are the most common sources of colonization of percutaneous vascular catheters (Figure). For short-term, nontunneled, noncuffed catheters, the organisms migrate from the skin insertion site along the intercutaneous segment, eventually reaching the intravascular segment or the tip. [7, 8]

For long-term catheters (particularly those that are cuffed or surgically implanted), the hub is a major source of colonization of the catheter lumen, which ultimately leads to bloodstream infections through luminal colonization of the intravascular segment. [9-11]

The skin and the hub are the most common sites for bacterial migration resulting in infection.

Catheter Surface
Organisms that adhere to the catheter surface maintain themselves by producing an "extracellular slime," a substance rich in exopolysaccharides, often referred to as fibrous glycocalyx or microbial biofilm.[12,13] The organisms embed themselves in the biofilm layer, becoming more resistant to the antimicrobial activity of glycopeptide antibiotics.[14,15]

Thrombin Sheath
Following insertion, a thrombin sheath rich in host proteins covers the internal and external surface of the intravascular segment of the catheter. The proteins in the thrombin sheath -- such as fibrin, fibrinogen, fibronectin, laminin, thrombospondin, and collagen -- act as adhesins. Organisms, such as coagulase-negative staphylococci, bind to fibronectin. Staphylococcus aureus binds strongly to both fibronectin and fibrinogen,[16,17] while Candida albicans binds well to fibrin.[18] This process, observed at the molecular level, is translated into a correlation at the clinical level between thrombogenesis and infection.[19]  As such, reduction in thrombus formation in the catheter will reduce the formation of a thrombin sheath and reduce the formation of biofilm.

Colonization of CVCs
The colonization of CVCs is almost universal. Electron microscopy studies show that all catheters eventually become colonized after insertion.[7] However, the risk of infection is directly proportional to the quantitative level of organisms multiplying on the surface of the intravascular segment of the catheter. Therefore, factors that would potentiate the multiplication and spread of organisms from the biofilm environment would increase the risk of bloodstream infections.

Skin Organisms
The skin is the major source of catheter colonization and infection, followed by the hub; the latter is often contaminated by the hands of medical personnel. Such skin organisms as coagulase-negative staphylococci and S aureus are the leading pathogens that cause vascular catheter-related infections.[1,20]C albicans and Candida parapsilosis have been shown to colonize the hands of medical personnel.[21]

In addition, C parapsilosis has been associated with total parenteral nutrition and glucose-containing infusions.[22] Both C albicans and C parapsilosis are emerging as important pathogens that cause catheter-related infections.[1,2] It should be noted that coagulase-negative staphylococci and C parapsilosis produce extracellular slime.[12,13,15]

 


 

Approaches to Prevention

Since skin flora, such as staphylococci, are the predominant organisms that cause CRBSI, antimicrobial agents that are highly active against such organisms should be employed. Antimicrobial agents used in the prevention of CRBSI should have broad-spectrum activity against gram-positive organisms, gram-negative organisms, and Candida species.

The complexity of catheter colonization and the infection process are caused by the formation of biofilm. Microorganisms bind to the surface of host proteins, such as fibrin and fibronectin, to produce biofilm; together they act as binding factors. Therefore, practices should be in place that reduce the formation and contamination of biofilm, such as effective flushing and swabbing techniques.

The following sections describe approaches for preventing CRBSI.

Prevention of CRBSI

Several factors affect the risk of CRBSI including:

  • Site of insertion
  • Type of devices and Hygiene and Aseptic Technique
  • Insertion and Maintenance Technique
  • Duration of Placement

Site of Catheter Insertion
The site at which the catheter is placed influences the subsequent risk for catheter related infection and phlebitis. This is directly related to the density of local skin flora. Catheters inserted into an internal jugular vein have been associated with higher risk for infection than those inserted into the subclavian or femoral vein.

Type of Device

Type of intravascular device Comments
Peripheral venous catheter Usually inserted into the veins of the forearm or the hand; most commonly used short-term intravascular device; rarely associated with bloodstream infection
Peripheral arterial catheter For short-term use; commonly used to monitor hemodynamic status and to determine blood gas levels of critically ill patients; risk of bloodstream infection may approach that of CVCs
Midline catheter Peripheral catheter (size, 7.6–20.3 cm) is inserted via the antecubital fossa into the proximalbasilic or cephalic veins, but it does not enter central veins; is associated with lower rates of phlebitis and infection than are CVCs
Nontunneled CVC Most commonly used CVC; accounts for an estimated 90% of all catheter-related bloodstream infections; increased risk of infection with internal jugular vein site ofinsertion
Pulmonary artery catheter Inserted through a Teflon introducer and typically remains in place for an average duration of only 3 days; most catheters are heparin bonded to reduce catheter thrombosis and microbial adherence to the catheter
Pressure-monitoring system Used in conjunction with arterial catheter; associated with both epidemic and endemic nosocomial bloodstream infections; source is often the fluid column in the tubing between the patient’s intravascular catheter and the pressure-monitoring apparatus, contaminated infusate,or nondisposable transducers
Peripherally inserted centra lCatheter Provides an alternative to subclavian or jugular vein catheterization; is inserted via the peripheral vein into the superior vena cava, usually by way of cephalic and basilar veins; is easier to maintain and is associated with fewer mechanical complications (e.g., hemothorax) than are nontunneled CVCs
Tunneled CVC Surgically implanted CVC (e.g., Hickman, Broviac, Groshong, or Quinton catheter) with the tunneled portion exiting the skin and a Dacron cuff just inside the exit site; the cuff inhibits migration of organisms into the catheter tract by stimulating growth of surrounding tissue, thus the sealing catheter tract; used to provide vascular access to patients who require prolonged iv chemotherapy, home-infusion therapy, or hemodialysis
Totally implantable device A subcutaneous port or reservoir with self-sealing septum is tunneled beneath the skin and is accessed by a needle through intact skin; low rates of infection
  NOTE. CVC, central venous catheter.

Table 3. Types of intravascular devices and comments on their use.

The type of catheter placed directly affects the patients risk of catheter related bloodstream infections.  Central Venous Catheters are most commonly associated with increased risk of infection.

Other devices that are available to assist in the prevention of Catheter Related Bloodstream Infections include:

Sutureless devices
Catheter Securement devices

Aseptic Hubs
Luer Activated Access ports that can be conpletely disinfected or that feature novel caps to automatically disinfect the hub.

Antimicrobial Catheters
Cook and Arrow feature Central Venous Catheters with Antimicrobial properties.

Hand Hygiene and Aspetic Technique
Surveys have revealed that near 30% of nurses do not follow appropriate hand hygiene regimen prior to catheter placement or maintenance.

The primary sources of most pathogens causing endemic catheter associated bloodstream infection are the catheter insertion site or the catheter hub. Contamination may result from the patient’s own flora or from the healthcare worker’s hands during insertion, manipulation, or both.   Following proper hand hygiene and aseptic technique is a key to prevention.

Insertion and Maintenance Technique
Catheters which are inserted and managed by specialized nursing teams assist in the prevention of catheter related infections. These teams follow the “Central-Line Bundle”, where each team member is trained on the proper insertion and care of the catheter, all components for maximal barrier sterile insertion are provided in one kit or cart for easy access, and a check list is provided and followed. By assuring that all prevention strategies are utilized appropriately during placement and care, the risk of infection has been shown to decrease.

Main factors for success with insertion and maintenance include:
Use of Chlorhexidine for disinfection of site before insertion and in follow up care
PICC Teams or IV Teams
Re-Education on the importance of Hand Hygiene and “Scrub the Hub” campaigns|
Catheter Site Dressing Regimens, Catheter Securement
Maximal Barrier Precaution Line Insertion Kits or Line Insertion Carts
These factors are so important that the Association for Vascular Access (AVA) has initiated a program called SAVE THAT LINE!

Scrupulous hand hygiene before and after contact with all vascular access devices and prior to insertion.

Aspetic technique during catheter insertion and care

Vigorous friction to hubs. Vigorous friction with alcohol wherever you make or break a connection to give medications, flush, change tubing or access injection port or add on device.

Ensure Patency- flush all lumens with adequate amount of saline or heparinized saline to maintain patency per institution policy.

Why are access ports so important?

Luer activated needleless access ports provide access to the intravascular system with a standard male luer from a syringe or IV tubing set. These ports act as entry points for potential bacteria ingress if they are not disinfected properly or if by design they can not be disinfected properly.

Air, Skin, Blood, and other bodily discharge can settle on injection ports. Airborne contaminants from a cough, sneeze, saliva, etc can settle on injection ports. Bodily discharge from the patient can contaminate clothing, bedding, dressings, and the floor. Intravenous tubing that is allowed to drape on the floor or next to the patient may inadvertently be contaminated where fecal mass or urine could contaminate the injection port or tubing exterior. The healthcare workers hands may become contaminated while bathing or cleaning the patient or during manipulation of dressing or devices. Subsequent manipulation of the intravenous tubing and access port without prior hand washing can lead to infection (20). The access port is the access site to the intravascular system. Anything that comes in contact with the port can subsequently be delivered directly into the intravascular system of the patient. The ability to disinfect the access port is of utmost importance.

Recently, press and presentations have concluded that some luer activated needleless access ports have been shown to increase the risk of catheter related bloodstream infections. Dr. Jarvis, previously a specialist for the CDC on the topic of Hospital Acquired Infections, has presented data at several conferences during 2005 - 2007 on this topic. He suggests that mechanical valves and positive pressure mechanical valves increase the risk of catheter related bloodstream infection due to the design of the product. The table lists the risk factors Dr. Jarvis presents related to mechanical valves:

Difficulty cleaning access surface HCW’s may not adequately clean the intricate surface details, leading to fluid path contamination.
Gap around plunger harbors bacteria Gap cannot be accessed for disinfection and can lead to fluid path contamination especially with repeated access such as SAS or SASH method.
Opaque housing hides incomplete flushing of media based fluids During the course of normal manipulation of the catheter small amounts of media like fluid contaminate the valve. If these organisms proliferate, then they can be infused with subsequent manipulations.
Internal mechanisms obscure fluid path Impossible to visually confirm complete flushing.

Obviously, the luer activated access port is extremely important and must be designed to allow appropriate disinfection and flushing of blood components from the device. With out complete flushing of the device and catheter, thrombus formation may occur. Multiple studies have shown that a decrease in blood accumulation in the line reduces the formation of biofilm and CRBSI’s. Devices should feature access ports that can be disinfected during normal swabbing. Devices should be clear to promote effective flushing.

Duration of Placement
The longer the catheter is indwelling the greater the risk of infection. Longer placement results in more chances for microbial ingress due to more contact, manipulation, etc.

Today, measures to prevent bloodstream infections are top priority for infection control practitioners and other health care workers. The Institute for Healthcare Improvement has a new program titled Save 5 Million lives. The 5 Million Lives Campaign is an initiative to engage U.S. hospitals in a commitment to implement changes in care proven to improve patient care and prevent avoidable deaths.  The Campaign is the first national effort to promote saving a specified number of lives by a certain date.

The program has a campaign to prevent central line associated bloodstream infections. You can review the details of this campaign by accessing the How to Guide for Central Line Infections at www.ihi.org/IHI/Programs/Campaign/.

The Center for Disease Control, CDC, also has a MMWR guideline which promotes proper technique for preventing Catheter Related Bloodstream Infections. This document titled Guidelines for the Prevention of Intravascular Catheter-Related Infections is in this manual under the section titled guidelines.

Most hospitals track their bloodstream infection rate per 1000 catheter days and are actively pursuing methods to assist in reduction of bloodstream infections. We feel MaxPlus and MaxPlus Clear are both excellent devices to implement to assist in the reduction of bloodstream infections.

References:

  1. Raad II, Bodey GP. Infectious complications of indwelling vascular catheters. Clin Infect Dis. 1992;15:197-210.
  2. Maki DG. Infections due to infusion therapy. In: Bennett JV, Brachman PS, eds. Hospital Infections. Boston: Little Brown; 1992:849-898.
  3. Jarvis WR, Edwards JR, Culver DH, et al. Nosocomial infection rates in adult and pediatric intensive care units in the United States. Am J Med. 1991;9(suppl 3B):185S-191S.
  4. Maki DG, Cobb L, Garman JK, et al. An attachable silver impregnated cuff for prevention of infection with central venous catheters: a prospective randomized multicenter trial. Am J Med. 1988;85:307-314.
  5. Heiselman D. Nosocomial bloodstream infections in the critically ill. JAMA. 1994;272:1819-1820.
  6. Pittet D, Tarara D, Wenzel RP. Nosocomial bloodstream infection in critically ill patients: excess length of stay, extra costs, and attributable mortality. JAMA. 1994;272:1578-1601.
  7. Raad II, Costerton W, Sabharwal U, et al. Ultrastructural analysis of indwelling vascular catheters: a quantitative relationship between luminal colonization and duration of placement. J Infect Dis. 1993;168:400-407.
  8. Mermel LA, McCormick RD, Springman SR, Maki DG. The pathogenesis and epidemiology of catheter-related infection with pulmonary artery Swan-Ganz catheters: a prospective study utilizing molecular subtyping. Am J Med. 1991;92(suppl 3B):197S-205S.
  9. Linares J, Sitges-Serra A, Garau J, et al. Pathogenesis of catheter sepsis: a prospective study with quantitative and semiquantitative cultures of catheter hub and segment. J Clin Microbiol. 1983;21:357-360.
  10. Salzman MB, Isenberg HD, Shapiro JF, et al. A prospective study of the catheter hub as the portal of entry for microorganisms causing catheter-related sepsis in neonates. J Infect Dis. 1993;167:487-490.
  11. Sitges-Serra A, Puig P, Linares J, et al. Hub colonization as the initial step in an outbreak of catheter-related sepsis due to coagulase negative staphylococci during parenteral nutrition. JPEN. 1984;8:668-672.
  12. Costerton JW, Irvin RT, Cheng KR. The bacterial glycocalyx in nature and disease. Annu Rev Microbiol. 1981;35:299-324.
  13. Pfaller MA, Messer SA, Hollis RJ. Variations in DNA subtype, antifungal susceptibility, and slime production among clinical isolates of Candida parapsilosis. Diagn Microbiol Infect Dis. 1995;21:9-14.
  14. Sheth NK, Franson TR, Sohnle PG. Influence of bacterial adherence to intravascular catheters on in vitro antibiotic susceptibility. Lancet. 1985;2:1266-1268.
  15. Farber BF, Kaplan MH, Clogstron AG. Staphy- lococcus epidermidis extracted slime inhibits the antimicrobial action of glycopeptide antibiotics. J Infect Dis. 1990;161:37-40.
  16. Hawiger J, Timmons S, Strong DD, et al. Identification of a region of human fibrinogen interacting with staphylococcal clumping factor. Biochem J. 1982;21:1407-1413.
  17. Kuusela P. Fibronectin binds to Staphylococcus aureus. Nature. 1978;276:718-720.
  18. Bouali A, Robert R, Tronchin G, Senet JM. Characterization of binding of human fibrinogen to the surface of germ-tubes and mycelium of Candida albicans. J Gen Microbiol. 1987;133:545-551.
  19. Raad I, Luna M, Sayed-Ahmed MK, et al. The relationship between the thrombotic and infectious complications of central venous catheters. JAMA. 1994;271:1014-1016.
  20. Schmid, M. RN PHD CIC Preventing Intravenous Cather Associated Infections; An Update
 
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The MaxPlus Needleless Connector
The MaxPlus is the fastest growing needleless connector on the market today. As evidence to its success the MaxPlus is being utilized in a number of facilities who in 2006 were awarded Honor Roll status by the U.S. News and World Report as 'America's Best Hospitals." The nation's top facilities are using the MaxPlus for two main reasons; it significantly lowers Catheter Related Blood Stream infections CRBSIs and catheter line occlusions. Reducing these two complications improves patient outcomes.
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