| | Catheter-associated bloodstream infections: Looking outside of the ICUBackgroundCurrent recommendations for the prevention of central venous catheter-associated bloodstream infections (CA-BSIs) are mostly based on data from intensive care units (ICUs). The rates of CA-BSIs appear to be higher in non-ICU wards. Until this year, no published data were available on non-ICU CA-BSIs in the United States. This article is a summary of a talk given at an industry-sponsored conference on CA-BSIs. It summarizes an original article of ours previously published in a peer-reviewed journal. ObjectiveThe objective of this study was to determine the rate of CA-BSIs in non-ICU medical patients by developing a prospective surveillance program in a major tertiary care hospital. All positive blood cultures electronically detected from April 1, 2002, to April 30, 2003, were reviewed and clinical data collected by chart review. DefinitionsCatheter utilization ratio = total number of days with a central venous catheter (CVC)/total number of patient-days; catheter-associated BSIs = defined by Centers for Disease Control and Prevention criteria, eg, a patient had to have a catheter at least 48 hours before detection of infection; CA-BSI rate = CA-BSIs/1000 catheter-days. ResultsThe 13-month study included 7337 catheter-days and 33,174 patient-days. The overall catheter-utilization ratio was 0.22 (range, 0.19-0.25). Of 42 cases of CA-BSIs, gram-positive organisms were recovered in 24 (57%); gram-negative bacteria in 7 (17%); and Candida spp in 6 (14%). The CA-BSI rate was 5.7 (95% confidence interval: 3.4-8.0) and varied from 4.3 to 8.0. There were no significant differences in CA-BSI rates among the wards (χ2 for linear trend, 0.42; P = .52). The overall rate of CA-BSIs decreased steadily during the study period, from 7.8 during the first 6 months to 3.9 during the following 7 months, representing a rate ratio of 0.5 (95% confidence interval: 0.27-0.93). ConclusionBenchmark data for hospital infections in the non-ICU setting are starting to become available and efforts to improve care may have greater impact here than in the ICU. Upon patient transfer out of the ICU, it should be determined whether the catheter can be removed. Educational measures targeted at non-ICU wards are warranted. First results of computer-assisted methods to facilitate surveillance of larger number of patients are promising. The Healthcare Infection Control Practices Advisory Committee recommends that CA-BSIs be publicly reported. CA-BSIs in non-ICU patients could soon be part of a mandatory reporting. More than 5 million central venous catheters (CVC) are inserted each year in the United States, and there are approximately 200,000 cases of bloodstream infections (BSIs) related to the use of indwelling catheters.1 A high rate of morbidity and mortality is associated with catheter-associated (CA) BSIs.2 Extensive information is available about CA-BSIs in high-risk areas including intensive care units (ICUs) as shown by data from surveillance programs such as the National Nosocomial Infections Surveillance System (NNIS).3 Surveillance for nosocomial infections is an established method to measure hospital infection rates, to make rates comparable over time, and to serve as a quality indicator for infection control.4 For surveillance purposes, the ICU setting has been regarded as a good representation of the health care system because catheters are widely used in this setting, ICU patients have significant underlying diseases making them vulnerable to infections, and CA-BSIs rates are perceived as high. CA-BSIs rates in nonacute care settings have rarely been investigated. A search of the National Library of Medicine on November 3, 2007, for the words “non-ICU,” “catheter,” “bloodstream,” and “infection” resulted in the 4 studies discussed below. In addition, a few studies compared BSIs in ICU and non-ICU settings, but only one of these recorded the presence of a catheter.5 In that study, catheters were present in a smaller percentage of non-ICU patients (16/33) than ICU patients (36/45). A 1-day prevalence study of catheter use in adult inpatients in 6 medical centers found that the device utilization ratio (ie, catheter-days/patient-days) was lower for non-ICU patients (0.244) than for ICU patients (0.554).6 The ratio for non-ICU patients was also lower than the NNIS ratio for medical ICU patients (0.52).7 The absolute number of catheters used was higher in non-ICU than in ICU patients (523 vs 238, respectively). Non-ICU patients were more likely than ICU patients to have catheters placed in the subclavian vein (61% vs 47%, respectively, P < .001) or to have peripherally inserted central catheters (20% vs 6%, respectively, P < .001). Because the subclavian access site is associated with fewer infections than the jugular or femoral sites,8 fewer infections would be expected in non-ICU patients. A cross-sectional survey of all adult patients in a 600-bed teaching hospital on a single day also investigated catheter use.9 The subclavian access site was used more frequently in non-ICU than in ICU patients (36% vs 22%, respectively) in this study also. Criteria were developed to identify CVCs that were in place without justification. Results showed that 83% of catheters were used in non-ICU settings and that non-ICU patients were more likely to have a catheter that was clinically unjustified (33/388 [8.5%] vs 10/557 [1.8%], respectively). In a subset of patients from whom the access site dressing data were collected, non-ICU patients were less likely than ICU patients to have an intact dressing (6/13 [43%] vs. 17/19 [89%], respectively, P = .007). These 2 potential explanations for increased infection rates are discussed further below. In 2006, the first non-ICU surveillance data from a large German nosocomial surveillance system (the DEVICE-KISS substudy) were published.10 Centers for Disease Control and Prevention (CDC) surveillance criteria were used to determine CA-BSI rates for various types of non-ICU care settings in 42 community- and university-level hospitals. The minimum surveillance period per hospital was 3 months, and no peripherally inserted central catheters lines were used in any hospital. The non-ICU device-utilization ratio they reported (0.046)10 was considerably lower than that reported by Climo and Diekema for 6 United States hospitals (0.244).6 The CA-BSI rate for non-ICU settings (4.3/1000 catheter-days) was markedly higher than the rate for ICUs in their system (1.8/1000 catheter-days). In summary, non-ICU and ICU patients differ in terms of severity of illness, length of stay, and possibly level of care. The rate of catheter use in non-ICU wards is lower, whereas the absolute number of catheters is higher. The mix of catheter types encountered between units and the rates of nonjustified catheters in place differ between these 2 groups. The rates of CA-BSIs appear to be higher in non-ICU wards. Until 2007, no published data were available on non-ICU CA-BSI in the United States. Current recommendations for the prevention of CA-BSI are mostly based on studies done in the ICU setting.11 CA-BSI in non-ICU Settings  The objective of our previous study12 was to determine the rate of CA-BSIs in non-ICU medical patients by developing a prospective surveillance program in a major tertiary care hospital. The study was conducted at Barnes-Jewish Hospital, a 1250-bed teaching hospital in St. Louis, Missouri. Four general medical wards were selected for surveillance. Each ward had separate nursing staff; 2 wards shared a medical director, interns, residents, and a nurse manager. Three wards were 26-bed units, and 1 ward was a 27-bed unit (a total of 105 beds). All positive blood cultures reported by an electronic detection tool (GermWatcher, St. Louis, MO)13 were reviewed. The surveillance period was April 1, 2002, to April 30, 2003. A single infection control specialist collected data by chart review (catheter start and stop dates, ward admission and discharge dates, microbiology data). Any adult patient admitted to 1 of the 4 wards was included in the study as soon as a CVC was inserted. The following definitions were used: “Catheter utilization ratio” = total number of days with a CVC/total number of patient-days; “Catheter-associated BSI” = defined by CDC criteria14, eg, a patient had to have a catheter at least 48 hours before detection of infection; “CA-BSI rate” = CA-BSIs/1000 catheter-days. Results  The 13-month study included 7337 catheter-days and 33,174 patient-days. Thirty-five patients (83%) had a nontunneled catheter, 3 (7%) had totally implanted ports, 2 (5%) had tunneled catheters, and 2 (5%) had more than 1 catheter in place. The overall catheter-utilization ratio was 0.22 (range, 0.19-0.25). Forty-two CA-BSIs were identified. Gram-positive organisms were recovered in 24 (57%) cases; gram-negative bacteria in 7 (17%); and Candida spp in 6 (14%). The CA-BSI rate was 5.7 (95% confidence interval: 3.4-8.0) and varied from 4.3 to 8.0 between the 4 wards. There was no significant difference in CA-BSI rates between the wards (χ2 for linear trend, 0.42; P = .52). The overall rate of CA-BSIs decreased steadily during the study period, from 7.8 during the first 6 months to 3.9 during the following 7 months, representing a rate ratio of 0.5 (95% confidence interval: 0.27-0.93). This may be partly due to an intervention that was started during the study period (a mandatory educational module for nurses on 2 of the 4 wards studied). Surveillance itself (and the feeding back of rates to wards) has also been shown to decrease infection rates.15 The catheter utilization ratio of 0.22 is similar to data reported by Climo et al6 for patients in the non-ICU setting, lower than NNIS ICU data (range, 0.51-0.69)3 but higher than what Vonberg and Behnke reported in German hospitals (0.046).10 It is unclear why US device utilization ratios should be higher, and this raises the question whether the United States has catheter policies different from those in other countries. At least for the ICU setting, the results of an international study on CA-BSIs argue against significant differences among countries. The multicenter prospective Evaluation of Processes and Indicators in Infection Control study compared CA-BSI rates in ICUs in the United States to rates in 14 other countries (3.82 vs 5.02, respectively; P = .27), and no significant difference was found.16 There may still be differences in the much more diverse non-ICU wards of hospitals. Vonberg and Behnke10 included community hospitals and documented longer hospital lengths of stay than we did, both indicating lower acuity of illness and possibly resulting in lower rates of catheter use and therefore nosocomial infections. Although catheter utilization was lower than for the ICUs in the NNIS system, the CA-BSI rate of 5.7 was similar to the 5.0 rate for NNIS ICUs and similar to the CA-BSI rate in ICUs at Barnes-Jewish Hospital during the same time period (5.2). This discrepancy is surprising, and we can only hypothesize what the reasons may have been. As discussed earlier, Trick et al pointed to an increased number of idle catheters outside the ICU and to possible deficits in optimal care.9 This suggests that patients in non-ICU wards might be at a higher rates of unnecessary catheters and/or suboptimal care and therefore at a high risk of catheter-associated infections. Both Trick et al9 and Climo et al6 showed differences in the types of catheters used in different settings within the hospital. Therefore, patients in non-ICU wards might have catheters that are more prone to infections. In a facility with shortage of ICU beds, Mnatzaganian et al examined ward patients who qualified as critically ill (by criteria derived from the Society of Critical Care Medicine) and reported lower rates of BSIs in critically ill patients admitted to regular wards compared with the ICU.17 This argues against severity of illness as the primary risk factor for BSI. Other factors may influence the pathogenesis of BSIs and lead to high rates outside the ICUs as encountered in our study. The Institute for Healthcare Improvement leads a campaign called “5 Million Lives,” referring to the number of lives that could be saved if infection control was optimized.18 The campaign Web site mentions CA-BSIs but only under the heading “intensive care.” On the other hand, the NNIS has recognized the need for surveillance data in other areas of the health care system. In 2004, Clinical Infectious Diseases published an article describing surveillance and surveillance systems in the United States.19 It was stated that the transformed NNIS system would also “expand surveillance beyond intensive care units.” The NHSN report for 2006 is the first article to provide nationwide surveillance data for non-ICU units.20 Unfortunately, compared with the large number of ICUs described, only 18 inpatient medical wards were included. Catheter utilization was similar to what we found (0.24 vs 0.22, respectively), but CA-BSI rates were much lower (2.1 vs 5.7, respectively). However, no range was given because of the low number of wards studied, and there is no information readily available to determine whether these were wards in community or teaching hospitals. Conclusions  Benchmark data for hospital infections in the non-ICU setting are starting to become available. If maintenance of insertion-site dressings is less stringent outside ICUs, efforts to improve care may have greater impact here than in the ICU. When a patient is transferred out of the ICU, it should be determined whether the catheter can be removed. Educational measures targeted at non-ICU wards are needed. Computer-assisted surveillance has been proposed as a means to facilitate surveillance of larger number of patients because manual chart review—the gold standard—to determine CA-BSIs is time-consuming.21 First results of computer-assisted surveillance are promising.22 Mandatory public reporting of hospital-acquired infections is becoming more common as more states in the United States adopt such legislation.23 The Healthcare Infection Control Practices Advisory Committee recommends that CA-BSIs be reported but, again, reporting limited to ICUs.24 Soon, reportage of CA-BSIs in non-ICU patients could become mandatory.  The author thanks David K Warren, MD, MPH, for his mentorship during the original study. References  1. 1Mermel LA, Farr BM, Sherertz RJ, Raad , O'Grady N, Harris JS, et al. Guidelines for the management of intravascular catheter-related infections. Clin Infect Dis. 2001;32:1249–1272. MEDLINE |
CrossRef
2. 2Pittet D, Wenzel RP. Nosocomial bloodstream infections. Arch Intern Med. 1995;155:1177–1184. MEDLINE 3. 3NNIS System . National Nosocomial Infections Surveillance (NNIS) System report, data summary from January 1992 through June 2003, issued August 2003. Am J Infect Control. 2003;31:481–498. Full Text |
Full-Text PDF (218 KB)
|
CrossRef
4. 4Pittet D. Infection control and quality health care in the new millennium. Am J Infect Control. 2005;33:258–267. Abstract | Full Text |
Full-Text PDF (352 KB)
|
CrossRef
5. 5Suljagic V, Cobeljic M, Jankovic S, Mirovic V, Markovic-Denic L, Ronic P, et al. Nosocomial bloodstream infections in ICU and non-ICU patients. Am J Infect Control. 2005;33:333–340. Abstract | Full Text |
Full-Text PDF (185 KB)
|
CrossRef
6. 6Climo M, Diekema D, Mermel LA, Farr BM, Sherertz RJ, Raad , et al. Prevalence of the use of central venous access devices within and outside of the intensive care unit: results of a survey among hospitals in the prevention epicenter program of the Centers for Disease Control and Prevention. Infect Control Hosp Epidemiol. 2003;24:942–945.
CrossRef
7. 7NNIS System . National Nosocomial Infections Surveillance (NNIS) System report, data summary from January 1992 through June 2004, issued October 2004. Am J Infect Control. 2004;32:470–485. Full Text |
Full-Text PDF (229 KB)
|
CrossRef
8. 8Merrer J, De Jonghe B, Golliot F, Lefrant JY, Raffy B, Barre E, et al. Complications of femoral and subclavian venous catheterization in critically ill patients. J Am Med Assoc. 2001;286:700–707. 9. 9Trick WE, Vernon MO, Welbel SF, Wisniewski MF, Jernigan JA, Weinstein RA. Unnecessary use of central venous catheters: the need to look outside the intensive care unit. Infect Control Hosp Epidemiol. 2004;25:266–268.
CrossRef
10. 10Vonberg R, Behnke M, Geffers C, Sohr D, Ruden H, Dettenkofer M, et al. Device associated infection rates for non-intensive care unit patients. Infect Control Hosp Epidemiol. 2006;27:357–361.
CrossRef
11. 11Berenholtz S, Pronovost P, Lipsett PA, Hobson D, Earsing K, Farley JE, et al. Eliminating catheter-related bloodstream infections in the intensive care unit. Crit Care Med. 2004;32:2014–2020. MEDLINE |
CrossRef
12. 12Marschall J, Leone C, Jones M, Nihill D, Fraser VJ, Warren DK. Catheter-associated bloodstream infections in general medical patients outside the intensive care unit: a surveillance study. Infect Control Hosp Epidemiol. 2007;28:905–909.
CrossRef
13. 13Kahn M, Steib S, Dunagan WC. An expert system for culture-based infection control surveillance. Proc Ann Symp Comput Appl Med Care. 1993;171–175. 14. 14Garner JS, Jarvis WR, Emori TG, Horan TC, Hughes JM. CDC definitions for nosocomial infections, 1988. Am J Infect Control. 1988;16:128–140. Abstract |
Full-Text PDF (1309 KB)
|
CrossRef
15. 15Gastmeier P, Geffers C, Brandt C, Vonberg RP, Halle H, Ruden H, et al. Effectiveness of a nationwide nosocomial infection surveillance system for reducing nosocomial infections. J Hosp Infect. 2006;64:16–22. 16. 16Memish Z, Arabi Y, Cunningham G, Kritchevsky S, Braun B, Richards C, et al. Comparison of US and non-US central venous catheter infection rates: evaluation of processes and indicators in infection control study. Am J Infect Control. 2003;31:237. Abstract | Full Text |
Full-Text PDF (110 KB)
|
CrossRef
17. 17Mnatzaganian G, Galai N, Sprung CL, Zitser-Gurevich Y, Mandel M, Ben-Hur D, et al. Increased risk of bloodstream and urinary infections in intensive care unit (ICU) patients compared with patients fitting ICU admission criteria treated in regular wards. J Hosp Infect. 2005;59:331–342. Abstract | Full Text |
Full-Text PDF (287 KB)
|
CrossRef
18. 18Institute for Healthcare Improvement. 5 Million Lives Campaign. Available at: http://www.ihi.org/ihi/programs/campaign. Accessed November 4, 2007. 19. 19Tokars J, Richards C, Andrus M, Klevens M, Curtis A, Horan T, et al. The changing face of surveillance for health care-associated infections. Clin Infect Dis. 2004;39:1347–1352.
CrossRef
20. 20Edwards JR, Peterson KD, Andrus ML, Tolson JS, Goulding JS, Dudeck MA, et al. National Healthcare Safety Network (NHSN) Report, data summary for 2006, issued June 2007. Am J Infect Control. 2007;35:290–301. Full Text |
Full-Text PDF (150 KB)
21. 21Trick WE, Zagorski BM, Tokars JI, Vernon MO, Weibel SF, Wisniewski MF, et al. Computer algorithms to detect bloodstream infections. Emerg Infect Dis. 2004;10:1612–1620. MEDLINE 22. 22Woeltje KF, Butler AM, Goris AJ, Tutlam NT, Doherty JA, Westover MB. Abstract 293, Medinfo. Brisbane: Australia; 2007;. 23. 23Association for Professionals in Infection Control and Epidemiology. Healthcare-associated reporting laws and regulations. Available at: www.apic.org/am/images/maps/mandrpt_map.gif. Accessed November 3, 2007. 24. 24McKibben L, Horan T, Tokars JI, Fowler G, Cardo DM, Pearson ML, et al. Guidance on public reporting of healthcare-associated infections: recommendations of the Healthcare Infection Control Practices Advisory Committee. Am J Infect Control. 2005;33:217. Abstract | Full Text |
Full-Text PDF (149 KB)
|
CrossRef
Division of Infectious Diseases, Washington University School of Medicine, St. Louis, MO Address correspondence to Jonas Marschall, MD, Division of Infectious Diseases, Washington University School of Medicine, 660 S Euclid Ave, Campus Box 8051, St. Louis, MO 63110.
Disclosures: Dr. Marschall received an honorarium for participating in the symposium and writing this article. The author reports no conflicts of interest. PII: S0196-6553(08)00790-6 doi:10.1016/j.ajic.2008.10.005 © 2008 Association for Professionals in Infection Control and Epidemiology, Inc. Published by Elsevier Inc All rights reserved. | |
|