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(Chest. 2006;130:1293-1296.)
© 2006 American College of Chest Physicians

Time To Get Serious About Infection Prevention in the ICU

Marin H. Kollef, MD, FCCP

St. Louis, MO
Dr. Kollef is Professor of Medicine, Washington University School of Medicine; Director, Medical Intensive Care Unit; and Director, Respiratory Care Services, Barnes-Jewish Hospital.

Correspondence to: Marin H. Kollef, MD, FCCP, Campus Box 8052, Washington University School of Medicine, 660 South Euclid Ave, St. Louis, MO 63110; e-mail: mkollef{at}im.wustl.edu

ICUs are an important area for the emergence and spread of nosocomial infections due to the frequent use of broad-spectrum antibiotics; the crowding of patients with high levels of disease acuity within relatively small specialized areas; reductions in nursing staff and other support staff due to economic pressures that increase the likelihood of person-to-person transmission of microorganisms; and the presence of more chronically and acutely ill patients who require prolonged hospitalizations and often harbor antibiotic-resistant bacteria.123 Increasingly nosocomial infections, especially those acquired in the ICU setting, are caused by antimicrobial-resistant pathogens. Therefore, clinicians need to be aware of strategies that are not only aimed at prevention of nosocomial infections but the prevention of antimicrobial resistance as well. Many of the available prevention strategies are described in the Centers for Disease Control and Prevention 12-step program for the prevention of antimicrobial resistance (http://www.cdc.gov/drugresistance/healthcare/). One of the key elements in this strategy is to consult experts in the field of nosocomial infections and antimicrobial resistance (eg, infectious disease experts, infection control practitioners, microbiologists) when designing interventions aimed at minimizing the emergence and spread of antibiotic resistant pathogens.

ICUs worldwide are faced with increasingly rapid emergence and spread of antibiotic-resistant bacteria. Both antibiotic-resistant Gram-negative bacilli and Gram-positive bacteria are reported as important causes of hospital-acquired infections.45678910 In many circumstances, particularly with methicillin-resistant Staphylococcus aureus and Enterococcus faecium and Gram-negative bacteria producing extended-spectrum ß-lactamases and carbapenemases with resistance to multiple antibiotics, few antimicrobial agents remain for effective treatment.1112131415161718 The emergence of new strains of existing pathogens within the community setting has created additional stressors favoring the entry of resistant microorganisms into the hospital setting. This has most recently been demonstrated by the identification and spread of community-associated methicillin-resistant S aureus (MRSA).192021 These community strains of MRSA have made their way into the hospital setting, representing an important potential source of additional nosocomial infections.2223

The prolonged administration of antimicrobial regimens appears to be the most important factor promoting the emergence of antibiotic resistance that is potentially amenable to intervention.24 Other factors promoting infection with antimicrobial-resistant bacteria include prolonged hospitalization; the presence of invasive devices, such as endotracheal tubes and intravascular catheters, possibly due to the formation of biofilms on the surfaces of these devices; residence in long-term treatment facilities; and inadequate infection control practices.3 Spread of antibiotic-resistant bacteria from patient to patient represents the main pathway for the development of infection due to antibiotic-resistant bacteria among hospitalized patients.1 Antibiotic-resistant nosocomial infections are an important source of patient morbidity and health-care costs. Nosocomial infections caused by antibiotic-resistant microorganisms are frequently treated with antimicrobial regimens lacking activity against the subsequently identified microorganisms (ie, inappropriate antimicrobial therapy).25

Administration of inappropriate initial antimicrobial therapy is associated with greater hospital mortality.262728 In addition to increased hospital mortality, antimicrobial resistance is associated with excess costs. Most of the cost excess is simply associated with the acquisition of a nosocomial infection, much of which is due to potentially resistant antibiotic-resistant bacteria.2930 However, antibiotic resistance may also confer added morbidity and costs. For example, prior reports have indicated that MRSA infections as compared to those due to methicillin-sensitive S aureus are associated with worse clinical outcomes. Cosgrove et al,31 in a metaanalysis of 30 investigations focusing on bacteremia, concluded that MRSA bacteremia independently increased the risk for death. Shorr et al32 recently conducted a retrospective analysis of a large cohort of subjects with bronchoscopically confirmed ventilator-associated pneumonia (VAP) due to S aureus, suggesting that MRSA infection has important effects on ICU length of stay and health-care costs. Conservatively assuming that the costs per day of ICU care equal $2,000 in the United States, one can compute that each case of MRSA, VAP amplified hospital costs by at least $10,000 to $15,000. Similar findings have been described for infections due to antibiotic-resistant Gram-negative infections.3334 Therefore, there is an economic motive in addition to clinical efficacy for attempting to minimize the emergence and spread of antibiotic resistant infections.

In this issue of CHEST (see page 1346), Estivariz et al35 describe an outbreak of infections attributed to Burkholderia cepacia in the ICU of a hospital with contaminated nasal spray. Although the nasal spray was contaminated, these authors linked the outbreak to extrinsic contamination of multidose albuterol used for nebulization treatments. This study has similar characteristics to other outbreaks of nosocomial infection linked to contaminated equipment or medications.363738 In general, there is often a delay in the recognition of an outbreak, significant patient morbidity can occur, and medical costs are increased as a result of the acquired infections. More challenging are the routine type of nosocomial infections occurring in the ICU setting not linked to a specific outbreak of contaminated equipment or medication. Many hospitals do not have systematic efforts in place to recognize and prevent these infections. This has lead organizations such as the Institute for Healthcare Improvement and the Keystone Project to partner with hospitals in order to enhance their infection prevention practices in addition to other practice improvements.3940

Hospitals caring for seriously ill patients need to develop and implement programs aimed at the prevention of nosocomial infections. There are many examples demonstrating the efficacy of such interventions and their impact on local health-care costs.4142434445 In addition to such interventions, hospitals should have active and accurate microbial surveillance programs in place to develop accurate antibiograms and to detect changing patterns and incidences of nosocomial infections.13 Unfortunately, such efforts can be viewed by hospital administration as cost centers without realizing their potential to improve outcomes and reduce hospital expenditures.45 Therefore, local demonstration projects may have to occur, based on prior successful interventions from other hospitals, to illustrate the potential role of infection control and surveillance.46

In summary, the prevention of nosocomial infections is an important practice in ICUs. Unfortunately, a single element or protocol is unlikely to suffice in most hospitals. Table 1 provides an outline of tasks that can assist clinicians in developing local infection control programs that also limit the emergence of antibiotic resistance.47


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Table 1.. Strategies To Prevent Resistance in the ICU*

 

Footnotes

The author has no conflicts of interest to declare on this topic.

References

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SMART Approaches for Reducing Nosocomial Infections in the ICU
Chest, August 1, 2008; 134(2): 447 - 456.
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