Klin Padiatr 2020; 232(04): 203-209
DOI: 10.1055/a-1128-0524
Original Article

Screening for Third-Generation Cephalosporin-Resistant Bacteria Reduces the Incidence on Late-Onset Sepsis and Antibiotic use in Neonates

Screening auf Drittgeneration-Cephalosporin-resistente Bakterien reduziert Inzidenz von late-onset Infektion und Antibiotikaverbrauch bei Neugeborenen
Ann Carolin Longardt
1   Neonatology, Charité Universitätsmedizin Berlin, Berlin
,
Brar Piening
2   Institute of Hygiene and Environmental Medicine, Charité University Medicine Berlin, Berlin
,
Katharina von Weizsäcker
3   Obstetrics, Charité Universitätsmedizin Berlin, Berlin
,
Christof Dame
1   Neonatology, Charité Universitätsmedizin Berlin, Berlin
,
Christoph Bührer
1   Neonatology, Charité Universitätsmedizin Berlin, Berlin
,
Lars Garten
1   Neonatology, Charité Universitätsmedizin Berlin, Berlin
› Author Affiliations
Funding: No specific funding has been received for this work. The data have been generated as part of our clinical routine work and quality assessment.

Abstract

Background The extensive use of antibiotics is reflected by an increasing prevalence of infections with multidrug-resistant bacteria, including third-generation cephalosporin-resistant bacteria (3GCRB). For neonatal intensive care units screening and enhanced barrier precautions are recommended to control the spread of multidrug-resistant Gram-negative bacteria, while evidence for efficacy of barrier precautions remains scarce in a non-outbreak setting.

Objective To determine the impact of a screening program for maternal 3GCRB colonization and the effects of contact precautions and cohort nursing, concerning the risk of neonatal late-onset sepsis (LOS) and antibiotic use rates (AURs).

Study Design In a retrospective matched-pair cohort study, data of neonates exposed to maternal 3GCRB colonization were compared with findings in non-exposed neonates.

Results Of 3,144 neonates admitted, 184 neonates born to 3GCRB-positive mothers were eligible. Among them, 37 (20%) became 3GCRB positive during hospital stay. 3GCRB-exposed infants had a lower rate of LOS (6.5 vs. 14.1%, p=0.03) and lower AURs in that time period compared to controls (mean 0.009 vs. 0.025, p=0.006). When started within the first 72h after birth, days of therapy with meropenem were significantly lower in non-exposed vs. 3GCRB-exposed infants (mean 0.13 vs. 0.42; p=0.002). No invasive infections with 3GCRB occurred.

Conclusions Neonates of 3GCRB-positive mothers do not have an increased a priori risk for invasive 3GCRB infection and may benefit from enhanced contact precautions measures.

Zusammenfassung

Hintergrund Der zunehmende Einsatz von Antibiotika führt zu einem Anstieg von Infektionen mit multiresistenten Erregern wie z. B. Drittgeneration Cephalosporin-resistenten Bakterien (3GCRB). Empfehlungen zu Screening- und Kohortierungsmaßnahmen auf neonatologischen Intensivstationen zielen auf die Prävention von horizontaler Transmission und invasiven Infektionen ab. Für Nicht-Ausbruchssituationen ist die Evidenz für Hygienemaßnahmen und Screeningprogrammen unzureichend.

Ziel Evaluation eines Screening für mütterliche 3GCRB-Besiedlung mit nachfolgender Isolation bzw. Kohortenpflege des Neugeborenen (NG) unter Bezug auf das Risiko einer Late-Onset-Sepsis (LOS) und die Anzahl der Antibiotika-Tage (AUR).

Studiendesign In einer retrospektiven Fall-Kontroll-Kohortenstudie wurden Daten von NG mit maternaler 3GCRB-Besiedelung im Vergleich zu einer Kontrollgruppe mit unauffälligem Screening analysiert.

Ergebnisse In einer Kohorte von 3144 NG fanden sich 184 NG von 3GCRB-besiedelten Müttern. Bei 37 (20%) wurde im Verlauf eine Besiedelung mit 3GCRB nachgewiesen. In der Gruppe der 3GCRB-exponierten NG kam es seltener zu einer LOS (6,5 vs. 14,1%, p=0,03). Zwischen dem 4. Lebenstag und der Entlassung hatten 3GCRB-exponierte NG eine niedrigere AUR (Mittelwert 0,009 vs. 0,025, p=0,006) als die Kontrollgruppe. Die Behandlungstage mit Meropenem (Start in den ersten 3 Lebenstagen), war in der Kontrollgruppe signifikant geringer als in der 3GCRB-exponierten Gruppe (Mittelwert 0,13 vs. 0,43 Tage; p=0,002). In beiden Gruppen trat keine invasive Infektion mit 3GCRB auf.

Schlussfolgerung Neugeborene, deren Mütter 3GCRB besiedelt sind, haben kein erhöhtes a priori Risiko für eine invasive Infektion mit 3GCRB Erregern und profitieren wahrscheinlich von erweiterten Kohortierungs- und Isolationsmaßnahmen.



Publication History

Article published online:
14 April 2020

© Georg Thieme Verlag KG
Stuttgart · New York

 
  • References

  • 1 Abdel-Hady H, Hawas S, El-Daker M. et al. Extended-spectrum beta-lactamase producing Klebsiella pneumoniae in neonatal intensive care unit. J Perinatol 2008; 28: 685-690
  • 2 Benenson S, Levin PD, Block C. et al. Continuous surveillance to reduce extended-spectrum beta-lactamase Klebsiella pneumoniae colonization in the neonatal intensive care unit. Neonatology 2013; 103: 155-160
  • 3 Biehl LM, Bertz H, Bogner J. et al. Screening and contact precautions – A survey on infection control measures for multidrug-resistant bacteria in German university hospitals. Antimicrob Resist Infect Control 2017; 6: 37
  • 4 Birgy A, Mariani-Kurkdjian P, Bidet P. et al. Characterization of extended-spectrum-beta-lactamase-producing Escherichia coli strains involved in maternal-fetal colonization: prevalence of E. coli ST131. J Clin Microbiol 2013; 51: 1727-1732
  • 5 Cantey JB, Sreeramoju P, Jaleel M. et al. Prompt control of an outbreak caused by extended-spectrum beta-lactamase-producing Klebsiella pneumoniae in a neonatal intensive care unit. J Pediatr 2013; 163: 672-679 e671-673
  • 6 Chereau F, Herindrainy P, Garin B. et al. Colonization of extended-spectrum-beta-lactamase- and NDM-1-producing Enterobacteriaceae among pregnant women in the community in a low-income country: a potential reservoir for transmission of multiresistant Enterobacteriaceae to neonates. Antimicrob Agents Chemother 2015; 59: 3652-3655
  • 7 Cizman M, Plankar Srovin T. Antibiotic consumption and resistance of gram-negative pathogens (collateral damage). GMS Infect Dis 2018; 6: Doc05
  • 8 Cohen CC, Cohen B, Shang J. Effectiveness of contact precautions against multidrug-resistant organism transmission in acute care: a systematic review of the literature. J Hosp Infect 2015; 90: 275-284
  • 9 Denkel LA, Schwab F, Kola A. et al. The mother as most important risk factor for colonization of very low birth weight (VLBW) infants with extended-spectrum beta-lactamase-producing Enterobacteriaceae (ESBL-E). J Antimicrob Chemother 2014; 69: 2230-2237
  • 10 Dubois V, De Barbeyrac B, Rogues AM. et al. CTX-M-producing Escherichia coli in a maternity ward: a likely community importation and evidence of mother-to-neonate transmission. J Antimicrob Chemother 2010; 65: 1368-1371
  • 11 E. D. Categories of Care 2011 In www.bapm.org/publications/documents/ guidelines/CatsofcarereportAug11.pdf; British Assocation of Perintal Care; 2011.
  • 12 Franz AR, Bauer K, Schalk A. et al. Measurement of interleukin 8 in combination with C-reactive protein reduced unnecessary antibiotic therapy in newborn infants: a multicenter, randomized, controlled trial. Pediatrics 2004; 114: 1-8
  • 13 Goddard S, Muller MP. The efficacy of infection control interventions in reducing the incidence of extended-spectrum beta-lactamase-producing Enterobacteriaceae in the nonoutbreak setting: A systematic review. Am J Infect Control 2011; 39: 599-601
  • 14 Grace T, Oddy W, Bulsara M. et al. Breastfeeding and motor development: A longitudinal cohort study. Hum Mov Sci 2017; 51: 9-16
  • 15 Hawser SP, Bouchillon SK, Hoban DJ. et al. Incidence and antimicrobial susceptibility of Escherichia coli and Klebsiella pneumoniae with extended-spectrum beta-lactamases in community- and hospital-associated intra-abdominal infections in Europe: results of the 2008 Study for Monitoring Antimicrobial Resistance Trends (SMART). Antimicrob Agents Chemother 2010; 54: 3043-3046
  • 16 Kirkland KB. Taking off the gloves: toward a less dogmatic approach to the use of contact isolation. Clin Infect Dis 2009; 48: 766-771
  • 17 Kung E, Waldhor T, Rittenschober-Bohm J. et al. Increased nurse workload is associated with bloodstream infections in very low birth weight infants. Sci Rep 2019; 9: 6331
  • 18 Laux R, Wirtz S, Huggett S. et al. Bedeutung der Eltern als Quelle bei der Besiedelung von Neonaten mit multiresistenten gramnegativen Erregern (MRGN). Z Geburtshilfe Neonatol 2013; 217: 61-64
  • 19 Lowe C, Katz K, McGeer A. et al. Disparity in infection control practices for multidrug-resistant Enterobacteriaceae. Am J Infect Control 2012; 40: 836-839
  • 20 Manzur A, Tubau F, Pujol M. et al. Nosocomial outbreak due to extended-spectrum-beta-lactamase- producing Enterobacter cloacae in a cardiothoracic intensive care unit. J Clin Microbiol 2007; 45: 2365-2369
  • 21 NEO-KISS- German National Refernce System on Health-Care Associated Infection in Neonatology. www.nrz-hygiene.de/fileadmin/nrz/module/neo/201701_201812_NEO Ref.pdf; 09.07.2019
  • 22 Parm U, Metsvaht T, Sepp E. et al. Risk factors associated with gut and nasopharyngeal colonization by common Gram-negative species and yeasts in neonatal intensive care units patients. Early Hum Dev 2011; 87: 391-399
  • 23 Pelat C, Kardas-Sloma L, Birgand G. et al. Hand Hygiene, Cohorting, or Antibiotic Restriction to Control Outbreaks of Multidrug-Resistant Enterobacteriaceae. Infect Control Hosp Epidemiol 2016; 37: 272-280
  • 24 Peretz A, Skuratovsky A, Khabra E. et al. Peripartum maternal transmission of extended-spectrum beta-lactamase organism to newborn infants. Diagn Microbiol Infect Dis 2017; 87: 168-171
  • 25 Rettedal S, Lohr IH, Bernhoff E. et al. Extended-spectrum beta-lactamase-producing Enterobacteriaceae among pregnant women in Norway: prevalence and maternal-neonatal transmission. J Perinatol 2015; 35: 907-912
  • 26 Rodriguez-Bano J, Picon E, Gijon P. et al. Community-onset bacteremia due to extended-spectrum beta-lactamase-producing Escherichia coli: risk factors and prognosis. Clin Infect Dis 2010; 50: 40-48
  • 27 Rogowski JA, Staiger D, Patrick T. et al. Nurse staffing and NICU infection rates. JAMA Pediatr 2013; 167: 444-450
  • 28 Shakil S, Akram M, Ali SM. et al. Acquisition of extended-spectrum beta-lactamase producing Escherichia coli strains in male and female infants admitted to a neonatal intensive care unit: molecular epidemiology and analysis of risk factors. J Med Microbiol 2010; 59: 948-954
  • 29 Stapleton PJ, Murphy M, McCallion N. et al. Outbreaks of extended spectrum beta-lactamase-producing Enterobacteriaceae in neonatal intensive care units: a systematic review. Arch Dis Child Fetal Neonatal Ed 2016; 101: F72-78
  • 30 Ting JY, Synnes A, Roberts A. et al. Association Between Antibiotic Use and Neonatal Mortality and Morbidities in Very Low-Birth-Weight Infants Without Culture-Proven Sepsis or Necrotizing Enterocolitis. JAMA Pediatr 2016; 170: 1181-1187