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Systematic scoping review of automated systems for the surveillance of healthcare-associated bloodstream infections related to intravascular catheters

Abstract

Introduction

Intravascular catheters are crucial devices in medical practice that increase the risk of healthcare-associated infections (HAIs), and related health-economic adverse outcomes. This scoping review aims to provide a comprehensive overview of published automated algorithms for surveillance of catheter-related bloodstream infections (CRBSI) and central line-associated bloodstream infections (CLABSI).

Methods

We performed a scoping review based on a systematic search of the literature in PubMed and EMBASE from 1 January 2000 to 31 December 2021. Studies were included if they evaluated predictive performance of automated surveillance algorithms for CLABSI/CRBSI detection and used manually collected surveillance data as reference. We assessed the design of the automated systems, including the definitions used to develop algorithms (CLABSI versus CRBSI), the datasets and denominators used, and the algorithms evaluated in each of the studies.

Results

We screened 586 studies based on title and abstract, and 99 were assessed based on full text. Nine studies were included in the scoping review. Most studies were monocentric (n = 5), and they identified CLABSI (n = 7) as an outcome. The majority of the studies used administrative and microbiological data (n = 9) and five studies included the presence of a vascular central line in their automated system. Six studies explained the denominator they selected, five of which chose central line-days. The most common rules and steps used in the algorithms were categorized as hospital-acquired rules, infection rules (infection versus contamination), deduplication, episode grouping, secondary BSI rules (secondary versus primary BSI), and catheter-associated rules.

Conclusion

The automated surveillance systems that we identified were heterogeneous in terms of definitions, datasets and denominators used, with a combination of rules in each algorithm. Further guidelines and studies are needed to develop and implement algorithms to detect CLABSI/CRBSI, with standardized definitions, appropriate data sources and suitable denominators.

Background

Intravascular catheters (IVC) are essential devices in medical practice; however, they increase the risk of healthcare-associated infections (HAI). HAI are among the most common adverse events in healthcare settings with a mean prevalence of 6.5% in Europe [1, 2]. Central-line associated bloodstream infections (CLABSI) contribute significantly, accounting for 14.2% of all HAIs [3]. In European intensive care units (ICU), catheter-related bloodstream infection (CRBSI) represents 36.5% of acquired bloodstream infections [4]. CLABSI and CRBSI are preventable HAI, which result in increases in mortality rates, duration of hospitalization and healthcare expenditure [5,6,7,8,9,10].

Surveillance activities are deemed crucial to reduce HAI as they provide necessary information to identify problems and priorities [1]. Surveillance of bloodstream infections (BSI) related to IVC allows to quantify the burden of disease and to assess the effectiveness of interventions to prevent these infections. With this regards, the Center for Disease Control and Preventions (CDC) National Healthcare Safety Network (NHSN) has proposed to use the CLABSI definition criteria for surveillance purposes while including only central venous catheters, whereas CRBSI is a clinical definition mostly used for research investigations or clinical practice [11, 12].

Evidence suggests that automated algorithms can improve the efficiency of CLABSI/CRBSI surveillance compared to conventional “manual” surveillance, which is time consuming and resource intensive [13,14,15]. When designing an automated surveillance system, different points should be considered, such as definitions of HAI, data sources, algorithm development and validation against the best reference standard [14]. In our recent publication, we evaluated the predictive performance of automated algorithms for CLABSI/CRBSI detection, and we found that the performance of automated algorithms for detection of intravascular catheter infections in comparison to manual surveillance seems encouraging. In this scoping review, we aimed to provide a comprehensive overview of the relevant algorithms reported in the literature for automated surveillance of CLABSI/CRBSI surveillance.

Methods

Overview

This study was designed as a systematic scoping review following the Preferred Items for Systematic Reviews and Meta-Analysis guidelines extension for Scoping Reviews (PRISMA-ScR) [16]. We performed a scoping review because this type of review is appropriate when knowledge on a specific topic has not been comprehensively reviewed, as it is the case with automated algorithms for the detection of CLABSI/CRBSI in hospitalized patients. This study was registered within the PROSPERO international prospective register of systematic reviews (CRD42022299641) on January 21, 2022 [17].

Eligibility criteria

We limited our search to studies published between January 2000 and December 2021. Eligible study designs were observational (e.g., case–control, case series, and cross-sectional studies), experimental (e.g., randomized control trials), and quasi-experimental (e.g., controlled before and after studies, interrupted time series) studies. We included studies reporting fully automated surveillance or semiautomated surveillance (including a manual determination part) of CLABSI/CRBSI. For the sake of simplicity, we opted to use the term “automated” instead of “automated and semiautomated” throughout the manuscript. Studies were excluded if they lacked direct relevance to automated surveillance or did not address CLABSI/CRBSI.

Information sources

We systematically searched two electronic databases, PubMed and EMBASE, for relevant articles published between 1 January 2000 and 31 December 2021. The search was limited to articles published in English. We searched for studies that reported on automated surveillance of CLABSI/CRBSI. We performed two different searches. A search for studies that reported on the predictive performance of automated algorithms for the detection of any type of HAI (to increase the sensitivity of the search strategy) and a search for studies on the detection of IVC infections specifically (to increase the specificity of the search strategy). The records from the two searches were merged, and duplicates were removed using the EndNote program (Thomson Reuters, NY, USA).

Search

The search for studies reporting on surveillance outcomes was performed in PubMed and EMBASE. Briefly, we included terms related to intravascular catheters, BSI or CRBSI/CLABSI, automation and surveillance. Search strategy details are illustrated in the supplementary material.

Selection of sources of evidence

Two investigators (N.L. and J.M.J.) screened titles and abstracts and examined the full text of original articles selected for study inclusion independently and in duplicate. We resolved disagreements on study selection and data extraction by consensus and discussion with other authors if needed.

Data charting process

Data from studies retrieved through the systematic search were extracted using Microsoft Excel. A data-charting form was jointly developed by two reviewers to determine which variables to extract. Any disagreements were resolved through discussion between the two reviewers or further adjudication by a third reviewer.

Data items

We abstracted data on article characteristics (e.g., publication year, country of study) and on surveillance system characteristics including definitions of CLABSI/CRBSI, datasets used for the numerators and denominators, and algorithm rules. When multiple algorithms (i.e., algorithms with different definitions for identifying intravascular catheters infections) were evaluated in a single study, we defined each individual rule or combination of rules as a single observation in our study. The total number of algorithms evaluated was therefore higher than the number of included studies.

Synthesis of results

Study characteristics were tabulated and narratively summarized. Data on definitions of CLABSI/CRBSI were summarized in the text. Data on datasets used for numerators and denominators were tabulated and narratively summarized. Algorithm rules were grouped by rule categories as ‘hospital acquisition’, ‘infection’, ‘duplication’, ‘secondary BSI’, and ‘catheter associated’. Quantitative meta-analysis of the predictive performance of these algorithms was performed, and published elsewhere [18].

Results

Selection of sources of evidence

After duplicates were removed, we identified 586 non-redundant study records (Fig. 1). Based on the title and abstract screening, 487 records were excluded, with 99 full text articles to be retrieved and assessed for eligibility. Of these, 90 were excluded: 48% (n = 43) of studies did not report automated surveillance data for CLABSI/CRBSI.

Fig. 1
figure 1

Study flow-chart

Characteristics of individual sources of evidence

The characteristics of the nine included studies are presented in Table 1. Most studies (n = 6) were conducted in the United States. Five of the studies included in the scoping review were monocentric and the remaining four were multicentric. All studies were observational and mostly focused on central venous catheters (CVC).Two studies used a surveillance based on culture-positive catheter tips; none of them specified which type of peripheral catheters they used [19, 20]. A total of 46 different automated algorithms or study populations were identified.

Table 1 Study characteristics

Definitions used to develop algorithms

Seven out of nine studies used CLABSIs and only two studies used CRBSIs as outcome. All studies adapted the CDC NHSN definitions to develop automated algorithms. It is noteworthy that the NHSN CLABSI definition has been modified over the years. One of the major changes since 2008 was the removal of the criterion considering a single positive blood culture with a common skin contaminant (CSC) as a CLABSI in the presence of relevant clinical symptoms and antimicrobials. Three studies used the pre-2008 definition and the four others used the post-2008 definition. Two studies used CRBSI as the outcome [19, 20]. One of the studies defined CRBSI with a positive quantitative tip culture growing ≥ 103 CFU/mL with the presence of local signs of infection at the catheter insertion site and systemic signs of infection (such as fever or increased white blood cell count), or both [20]. Bellini et al. defined CRBSIs as simultaneous isolation of the same organism from blood and catheter tip culture (> 15 CFU/catheter tip) [19]. Clinical or therapeutic criteria were not included in these two CRBSI automated systems, because they were not available in their local hospital’s information system.

Dataset used for indicators and denominators

Table 2 describes the type of data used in each study. All studies used administrative data in their automated algorithms, including admission dates (all studies) and discharge dates [21,22,23,24]. Microbiological data were automatically extracted in eight out of the nine studies [19,20,21,22, 24,25,26,27], with dates of blood culture sampling in fours studies [20, 22, 25, 26]. Only one study used a semi-automated CLABSI surveillance system with manual extraction of microbiological results [23]. The two studies evaluating an automated CRBSI detection system used blood and catheter tip culture results. Microorganisms were considered identical if the species identification and antimicrobial susceptibility profile matched [19, 20]. Snyders et al. evaluated the addition of cultures from other body sites (a sterile site, skin, wound, respiratory tract) in the algorithm [26]. Hota et al. included all positive and negative cultures from blood and other body sites, except catheter tips and surveillance cultures [24]. Lin et al. included wound or any non-blood cultures to identify primary BSI [27].

Table 2 Type of data automatically extracted and integrated in the different algorithms

The presence of a central line was included in the dataset of five studies [22, 23, 25,26,27]. Four studies included clinical data, such as fever (> 38.0 °C) [22, 23, 25, 26] or blood pressure [23], in their automated system. Only one study used machine learning to convert free text data into structured data to be used for automated surveillance [24]. Four studies included antimicrobial therapy data in their automated system, and all of these studies used vancomycin prescription data as an indicator for CLABSIs [21,22,23,24]. Kaiser et al. added other relevant antimicrobials to their automated system [23]. Six studies provided details of the denominator used, five of which chose central line-days (e.g., CLABSI rate per 1000 central line-days) and one study used patient-days (CLABSI rate per 1000 patient-days) as the denominator.

Algorithms

Four studies reported a single algorithm [20, 23, 24, 27], while five studies evaluated more than one combination of algorithm rules. All studies compared the performance of the automated algorithms with the reference standard, defined as manual chart review. The most common rules used in the different algorithms were categorized as hospital-acquired rules, infection rules (infection versus contamination), deduplication, secondary BSI rules (secondary versus primary BSI), and catheter-related rules (Table 3). Most of the studies defined a hospital-acquisition rule, as blood culture collected more than 48 h after hospital admission [20, 22, 24,25,26].The majority of the studies defined infection rule as: ≥1 blood culture with non-CSC organism(s), ≥ 2 blood cultures with CSC organisms (same species), and ≥ 1 of the following signs or symptoms: fever (> 38.0 °C), chills, or hypotension. Three studies defined the secondary BSI rule as positive culture of the same organism identified in blood from another body site [20, 22, 25]. Different deduplication and catheter associated rules were applied in the included studies.

Table 3 Rules categories and most common rules applied

Discussion

Summary of evidence

Our scoping review identified nine studies from 2000 to 2021 on automated CLABSI/CRBSI surveillance. The automated surveillance systems were heterogeneous in terms of the definitions of CLABSI and CRBSI, the datasets and denominators used, and the combination of rules in each algorithm. This highlights the necessity for more research and alignment regarding definitions suitable for large-scale automated surveillance, appropriate data sources, methods for estimating denominators, and the development and implementation of algorithms across various contexts.

Overall, CLABSI was the most frequent outcome used in the included studies. Interestingly, long-term, midlines and PICC lines were disregarded in automated surveillance systems. CRBSI definition requires catheter removal and catheter tip culture. Therefore, CRBSI surveillance allows a higher degree of certainty in attributing the catheter as the source of the BSI [28], compared to the conventional CLABSI definition. However, catheter tip cultures are not commonly performed in many countries [29]. In spite of the fact that peripheral intravenous catheter associated BSI is a rare event, the frequent use of these catheters in healthcare makes this outcome relevant. In the majority of the studies, the adoption of fully automated systems required adjustments to the surveillance definitions, potentially resulting in information loss. Furthermore, over the years, distinct definitions for CLABSI and CRBSI surveillance have been changed, making it challenging to compare the results generated by the various automated systems. For instance, Lin et al. modified their categorization of blood culture episodes during their study due to the removal of the NHSN CLABSI criterion that classified a single positive blood culture with a CSC as a CLABSI in the presence of clinical symptoms [27]. Fully automated systems generally require adaptation of definitions used in the context of manual surveillance, which could lead to loss of clinical relevance. Consensus should be reached on surveillance definitions that are suitable for automated surveillance, and based in priority on data that are readily available in the electronic health records.

All studies used algorithms that combined multiple data sources to identify CLABSI/CRBSI. The majority of studies relied on admission data and microbiology culture results, which are usually in a structured format. Many of the studies included the presence of IVC in their automated system. Only few studies included antimicrobial use and clinical data such as vital signs. Bouam et al. presumed that the lower sensitivity of their automated system could be explained with the lack of automated clinical signs and symptoms [20]. When developing an automated surveillance, a minimal dataset that include the most important variables of interest should be developed, and it should carefully include details of the data sources. The minimal dataset should allow extraction of data from electronic health records [14]. Higher specificity of these automated surveillance systems could be achieved in the future by better capturing the data included in the electronic health records using more advanced IT process, such as text mining [14].

When computing rates of CLABSI, catheter-days is calculated as a denominator. Patient-days allows to calculate CVC utilization [11, 25, 30]. Four studies calculated their denominator as catheter-days [22, 23, 25, 27]. Automation of denominator calculation for CLABSI has not been explained in some of the included studies, as device use was not documented in a structured format. None of the studies discussed denominator calculations for CRBSI. To correctly measure incidence densities, we recommend both patient-days and catheter-days data to be extracted and used as denominator.

Based on the surveillance definitions recommended during the time of each study, different algorithms have been developed and assessed on various study populations. We categorized the most frequent rules and steps used in the algorithms as hospital-acquired rule, infection rule (infection versus contamination), deduplication, secondary BSI rule (secondary versus primary BSI), and catheter-associated rule. Most of the studies reported an overestimation of CLABSI/CRBSI with automated surveillance compared with manual surveillance. Bellini et al. observed that prolonged BSI episodes such as Candida sp. fungemia could be counted multiple times; therefore, these investigators improved their algorithm performance by considering only one episode of Candida sp. fungemia for the entire hospital stay [19]. Woeltje et al. observed that some infections classified as CLABSI by the automated system were secondary infections with a site culture that was not included in the automated algorithms [25]. The differential time to positivity, which is an important criterion to identify CRBSI, was not included in any of the algorithms. Translating manual surveillance definitions into automated rules may lead to a great variety of algorithms, and therefore different CLABSI rates were produced by these algorithms. As part of a standardization initiative, it is essential to create guidelines and establish a standardized approach in order to provide valid results. Additionally, a comprehensive report detailing the application of these rules and the combinations of rules applied to the data should be provided [18].

Limitations

Our scoping review has limitations. First, the aim of the scoping review was to provide a broad overview of the literature, rather than a detailed synthesis of the outcomes. Therefore, our study group conducted a separate analysis to assess the performance of these algorithms [18]. Second, we only included peer-reviewed literature, including grey literature may have identified additional automated systems that have been implemented and evaluated, especially in commercially available packages. Third, we performed a scoping review and a critical appraisal of the included study was not performed. Finally, since we restricted our review to studies published in English, we might have missed relevant work published in other languages.

Conclusions

This scoping review sought to examine the current literature on the development of automated systems to monitor CLABSI/CRBSI through a systematic search of the literature. The findings suggest that, while efforts to shift from traditional to automated CLABSI/CRBSI surveillance have been made over the past two decades, a need for further research is required to optimize these automated surveillance methods. More extensive guidelines and studies are needed to create and deploy algorithms for CLABSI/CRBSI detection, with standardized definitions, appropriate data sources, and denominator calculations. Moreover, providing in-depth insights into the design of automated systems will help in continuously enhancing algorithm performance, thereby facilitating the widespread implementation of automated systems across diverse healthcare settings.

Data availability

No datasets were generated or analysed during the current study.

References

  1. Organization WH. Report on the burden of endemic health care-associated infection worldwide [Internet]. World Health Organization; 2011 [cited 2021 Apr 28]. Available from: https://apps.who.int/iris/handle/10665/80135.

  2. Suetens C, Latour K, Kärki T, Ricchizzi E, Kinross P, Moro ML, et al. Prevalence of healthcare-associated infections, estimated incidence and composite antimicrobial resistance index in acute care hospitals and long-term care facilities: results from two European point prevalence surveys, 2016 to 2017. Eurosurveillance. 2018;23(46):1800516.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Zarb P, Coignard B, Griskeviciene J, Muller A, Vankerckhoven V, Weist K, et al. The European centre for Disease Prevention and Control (ECDC) pilot point prevalence survey of healthcare-associated infections and antimicrobial use. Eurosurveillance. 2012;17(46):20316.

    Article  PubMed  Google Scholar 

  4. Healthcare-associated infections in intensive care units -. Annual Epidemiological Report for 2017 [Internet]. 2019 [cited 2023 May 23]. Available from: https://www.ecdc.europa.eu/en/publications-data/healthcare-associated-infections-intensive-care-units-annual-epidemiological-1.

  5. Schreiber PW, Sax H, Wolfensberger A, Clack L, Kuster SP, Swissnoso. The preventable proportion of healthcare-associated infections 2005–2016: systematic review and meta-analysis. Infect Control Hosp Epidemiol. 2018;39(11):1277–95.

    Article  PubMed  Google Scholar 

  6. Dimick JB, Pelz RK, Consunji R, Swoboda SM, Hendrix CW, Lipsett PA. Increased resource use associated with catheter-related bloodstream infection in the surgical intensive care unit. Arch Surg. 2001;136(2):229–34.

    Article  CAS  PubMed  Google Scholar 

  7. Olaechea PM, Palomar M, Álvarez-Lerma F, Otal JJ, Insausti J, López-Pueyo MJ, et al. Morbidity and mortality associated with primary and catheter-related bloodstream infections in critically ill patients. Rev Esp Quimioter. 2013;26(1):21–9.

    PubMed  Google Scholar 

  8. Ziegler MJ, Pellegrini DC, Safdar N. Attributable mortality of central line associated bloodstream infection: systematic review and meta-analysis. Infection. 2015;43(1):29–36.

    Article  PubMed  Google Scholar 

  9. Zimlichman E, Henderson D, Tamir O, Franz C, Song P, Yamin CK, et al. Health care-associated infections: a meta-analysis of costs and financial impact on the US health care system. JAMA Intern Med. 2013;173(22):2039–46.

    Article  PubMed  Google Scholar 

  10. 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):O318–324.

    Article  CAS  PubMed  Google Scholar 

  11. BSI| PSC| NHSN| CDC [Internet]. 2023 [cited 2023 May 25]. Available from: https://www.cdc.gov/nhsn/psc/bsi/index.html.

  12. Mermel LA, Allon M, Bouza E, Craven DE, Flynn P, O’Grady NP, et al. Clinical practice guidelines for the diagnosis and management of intravascular catheter-related infection: 2009 update by the Infectious Diseases Society of America. Clin Infect Dis. 2009;49(1):1–45.

    Article  CAS  PubMed  Google Scholar 

  13. Bae S, Kim Y, Chang HH, Kim S, Kim HJ, Jeon H, et al. The effect of the multimodal intervention including an automatic notification of catheter days on reducing central line-related bloodstream infection: a retrospective, observational, quasi-experimental study. BMC Infect Dis. 2022;22(1):604.

    Article  PubMed  PubMed Central  Google Scholar 

  14. van Mourik MSM, van Rooden SM, Abbas M, Aspevall O, Astagneau P, Bonten MJM, et al. PRAISE: providing a roadmap for automated infection surveillance in Europe. Clin Microbiol Infect. 2021;27(Suppl 1):3–19.

    Article  Google Scholar 

  15. Verberk JDM, Aghdassi SJS, Abbas M, Nauclér P, Gubbels S, Maldonado N, et al. Automated surveillance systems for healthcare-associated infections: results from a European survey and experiences from real-life utilization. J Hosp Infect. 2022;122:35–43.

    Article  CAS  PubMed  Google Scholar 

  16. Tricco AC, Lillie E, Zarin W, O’Brien KK, Colquhoun H, Levac D, et al. PRISMA Extension for scoping reviews (PRISMA-ScR): Checklist and Explanation. Ann Intern Med. 2018;169(7):467–73.

    Article  PubMed  Google Scholar 

  17. crd [Internet]. [cited 2023 Sep 28]. Available from: https://www.crd.york.ac.uk/Prospero/display_record.php?RecordID=299641.

  18. Januel JM, Lotfinejad N, Grant R, Tschudin-Sutter S, Schreiber PW, Grandbastien B, et al. Predictive performance of automated surveillance algorithms for intravascular catheter bloodstream infections: a systematic review and meta-analysis. Antimicrob Resist Infect Control. 2023;12(1):87.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Bellini C, Petignat C, Francioli P, Wenger A, Bille J, Klopotov A, et al. Comparison of automated strategies for surveillance of nosocomial bacteremia. Infect Control Hosp Epidemiol. 2007;28(9):1030–5.

    Article  PubMed  Google Scholar 

  20. Bouam S, Girou E, Brun-Buisson C, Karadimas H, Lepage E. An intranet-based automated system for the surveillance of nosocomial infections: prospective validation compared with physicians’ self-reports. Infect Control Hosp Epidemiol. 2003;24(1):51–5.

    Article  PubMed  Google Scholar 

  21. Trick WE, Zagorski BM, Tokars JI, Vernon MO, Welbel SF, Wisniewski MF, et al. Computer algorithms to detect bloodstream infections. Emerg Infect Dis. 2004;10(9):1612–20.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Woeltje KF, Butler AM, Goris AJ, Tutlam NT, Doherty JA, Westover MB, et al. Automated surveillance for central line-associated bloodstream infection in intensive care units. Infect Control Hosp Epidemiol. 2008;29(9):842–6.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Kaiser AM, de Jong E, Evelein-Brugman SF, Peppink JM, Vandenbroucke-Grauls CM, Girbes AR. Development of trigger-based semi-automated surveillance of ventilator-associated pneumonia and central line-associated bloodstream infections in a Dutch intensive care. Ann Intensiv Care. 2014;4(1):40.

    Article  Google Scholar 

  24. Hota B, Lin M, Doherty JA, Borlawsky T, Woeltje K, Stevenson K, et al. Formulation of a model for automating infection surveillance: algorithmic detection of central-line associated bloodstream infection. J Am Med Inf Assoc. 2010;17(1):42–8.

    Article  Google Scholar 

  25. Woeltje KF, McMullen KM, Butler AM, Goris AJ, Doherty JA. Electronic surveillance for healthcare-associated central line-associated bloodstream infections outside the intensive care unit. Infect Control Hosp Epidemiol. 2011;32(11):1086–90.

    Article  PubMed  Google Scholar 

  26. Snyders RE, Goris AJ, Gase KA, Leone CL, Doherty JA, Woeltje KF. Increasing the Reliability of Fully Automated Surveillance for Central Line-Associated Bloodstream Infections. Infect Control Hosp Epidemiol. 2015;36(12):1396–400.

    Article  PubMed  Google Scholar 

  27. Lin MY, Woeltje KF, Khan YM, Hota B, Doherty JA, Borlawsky TB, et al. Multicenter evaluation of computer automated versus traditional surveillance of hospital-acquired bloodstream infections. Infect Control Hosp Epidemiol. 2014;35(12):1483–90.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Buetti N, Timsit JF. Management and Prevention of central venous catheter-related infections in the ICU. Semin Respir Crit Care Med. 2019;40(4):508–23.

    Article  PubMed  Google Scholar 

  29. Peterson LR, Smith BA. Nonutility of catheter tip cultures for the diagnosis of central line-associated bloodstream infection. Clin Infect Dis. 2015;60(3):492–3.

    Article  PubMed  Google Scholar 

  30. Tejedor SC, Garrett G, Jacob JT, Meyer E, Reyes MD, Robichaux C, et al. Electronic documentation of central venous catheter-days: validation is essential. Infect Control Hosp Epidemiol. 2013;34(9):900–7.

    Article  PubMed  Google Scholar 

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Acknowledgements

We thank all members of Swissnoso. Collaborators: For Swissnoso, the National Center for Infection Control: Carlo Balmelli, Niccolò Buetti, Delphine Berthod, Stephan Harbarth, Philipp Jent, Jonas Marschall, Hugo Sax, Matthias Schlegel, Alexander Schweiger, Laurence Senn, Rami Sommerstein, Sarah Tschudin-Sutter, Nicolas Troillet, Danielle Vuichard Gysin, Andreas F Widmer, Aline Wolfensberger, Walter Zingg. This review was a part of the development module of the nationwide surveillance system of intravascular catheter infections in Switzerland, financed by the NOSO strategy of the Federal Office of Public Health of Switzerland.

Swissnoso group:

For Swissnoso, the National Center for Infection Control: Carlo Balmelli, Niccolò Buetti, Delphine Berthod, Stephan Harbarth, Philipp Jent, Jonas Marschall, Hugo Sax, Matthias Schlegel, Alexander Schweiger, Laurence Senn, Rami Sommerstein, Sarah Tschudin-Sutter, Nicolas Troillet, Danielle Vuichard Gysin, Andreas F Widmer, Aline Wolfensberger, Walter Zingg

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Open access funding provided by University of Geneva

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N.L., G.C. and N.B. wrote the main manuscript. J.M.J., S.T.S., P.W.S., B.G., L.D., E.L.P., A.S., and S.H. reviewed the manuscript.

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Correspondence to Nasim Lotfinejad.

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Supplementary Material 1: Search strategy.

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Lotfinejad, N., Januel, JM., Tschudin-Sutter, S. et al. Systematic scoping review of automated systems for the surveillance of healthcare-associated bloodstream infections related to intravascular catheters. Antimicrob Resist Infect Control 13, 25 (2024). https://doi.org/10.1186/s13756-024-01380-x

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