Aim Steady progress in intensive treatment worldwide has increased the survival of immature neonates, but with multiple invasive procedures, which have increased the risk of infection, thus the bacterial resistance to antibiotics. The aim of this study was to analyse the epidemiology of multidrug resistance pathogens as causative agents of neonatal sepsis in the neonatal intensive care unit. Methods A retrospective cohort study conducted at the Intensive care unit of the Paediatric Clinic of Tuzla over a three-year period (2016-2018) analysed epidemiology of neonatal sepsis caused by multidrug resistance pathogens. Statistical analysis applied standard methods, and the research was approved by the Ethics Committee of the institution. Results Of the total of 921 treated neonates, multidrug resistance (MDR) pathogens among causative agents of neonatal sepsis were found in 22 neonates (2.38%) with no gender difference. Prematurity and low birth weight were confirmed as the most significant risk factors. From the maternal risk factors a significant difference was found in the first birth and in vitro fertilization. Clinically, MDR sepsis manifested frequently as late onset sepsis, with longer hospital stay and higher mortality. The findings of leukopenia, thrombocytopenia and coagulation disorders were significant. Gram negative bacteria were frequently isolated, in particular Acinetobacter, which showed the greatest resistance to antibiotics. Conclusion Neonatal MDR sepsis is a threat to life, it complicates the treatment, increases costs and mortality. Outcomes can be improved by preventive strategies, earlier and more accurate diagnosis and rational use of antibiotics.
Rhodesa, Evans L, Alhazzani W, Levy M, Antonelli M, Ferrer R, et al. Surviving sepsis campaign: international guidelines for management of sepsis and septic shock. Intensive Care Med. 2016;304–77.
2.
Blair J, Webber M, Baylay A, Ogbolu D, Piddock L. Molecular mechanisms of antibiotic resistance. Nat Rev Microbiol. 2015;42–51.
3.
Laxminarayan R, Duse A, Wattal C, Zaidi A, Wertheim H, Sumpradit N, et al. Antibiotic resistance-the need for global solutions. Lancet. 2013;1057–98.
4.
Graham C. The global threat of antibiotic resistance: what can be done? JoGHR. 2017;
5.
Combating antibiotic-resistant bacteria. Federal Register. 13676;56931–5.
6.
Laxminarayan R, Matsoso P, Pant S, Brower C, Rottingen J, Klugman K, et al. Access to effective antimicrobials: a worldwide challenge. Lancet. 2016;168–75.
7.
Bandyopadhyay T, Kumar A, Saili A, Randhawa V. Distribution, antimicrobial resistance and predictors of mortality in neonatal sepsis. J Neonatal Perinatal Med. 2018;145–53.
8.
Raymond S, Stortz J, Mira J, Larson S, Wynn J, Moldawer L. Immunological defects in neonatal sepsis and potential therapeutic approaches. Front Pediatr. 2017;14.
9.
Mcpherson C, Liviskie C, Zeller B, Nelson M, Newland J. Antimicrobial stewardship in neonates: challenges and opportunities. Neonatal Netw. 2018;116–23.
10.
Shane A, Sanchez P, Stoll B. Neonatal sepsis. Lancet. 2017;1770–80.
11.
Behmadi H, Borji A, Taghavi-Rad A, Soghandi L, Behmadi R. Prevalence and antibiotic resistance of neonatal sepsis pathogen in Neyshabour, Iran. Arch Pediatr Dis. 2016;33818.
12.
Dorling J, Field D, Manktelow B. Neonatal disease severity scoring systems. Arch Dis Child Fetal Neonatal Ed. 2005;11–6.
13.
Afonso E, Blot S. Effect of gestational age on the epidemiology of late-onset sepsis in neonatal intensive care units -a review. Expert Rev Anti Infect Ther. 2017;917–24.
14.
Cailes B, Kortsalioudaki C, Buttery J, Pattnayak S, Greenough A, Matthes J, et al. Antimicrobial resistance in UK neonatal units: neonIN infection surveillance network. Arch Dis Child Fetal Neonatal Ed. 2018;474–8.
15.
Black C, Tavares L, Stachel A, Ratner A, Randis T. Distribution of late-onset neonatal sepsis pathogens differs in inpatient and outpatient settings. Am J Perinatol. 2018;38–43.
16.
Ozkan H, Cetinkaya M, Koksal N, Celebi S, Hacimustafaoglu M. Culture-proven neonatal sepsis in preterm infants in a neonatal intensive care unit over a 7 year period: coagulase-negative Staphylococcus as the predominant pathogen. Pediatrics International. 2014;60–6.
17.
Klingenberg C, Kornelisse R, Buonocore G, Maier R, Stocker M. Culture-negative early-onset neonatal sepsis -at the crossroad between efficient sepsis care and antimicrobial stewardship. Front Pediatr. 2018;285.
18.
Townsel C, Emmer S, Campbell W, Hussain N. Gender differences in respiratory morbidity and mortality of preterm neonates. Front Pediatr. 2017;6.
19.
Roy P, Kumar A, Kaur I, Faridi M. Gender differences in outcomes of low birth weight and preterm neonates: the male disadvantage. J Trop Pediatr. 2014;480–5.
20.
Tsai M, Chu S, Hsu J, Huang L, Chiang H, Fu M, et al. Risk factors and outcomes for multidrug-resistant Gram-negative bacteremia in the NICU. Pediatrics. 2014;322–9.
21.
Nour I, Eldegla H, Nasef N, Shouman B, Hady A, Shabaan H, et al. Risk factors and clinical outcomes for carbapenem-resistant Gram-negative late-onset sepsis in a neonatal intensive care unit. J Hosp Infect. 2017;52–8.
22.
Jajoo M, Manchanda V, Chaurasia S, Sankar M, Gautam H, Agarwal R, et al. Alarming rates of antimicrobial resistance and fungal sepsis in outborn neonates in North India. PLoS One. 2018;180705.
23.
Garcia H, Torres-Gutierrez J, Peregrino-Bejarano L, Ma CC. Risk factors for nosocomial infection in a level III neonatal intensive care unit. Gac Med Mex. 2015;711–9.
24.
Verstraete E, De Coen K, Vogelaers D, Blot S. Risk factors for health care-associated sepsis in critically Ill neonates stratified by birth weight. Pediatr Infect Dis J. 2015;1180–6.
25.
Yusef D, Shalakhti T, Awad S, Algharaibeh H. Khasawneh W. Clinical characteristics and epidemiology of sepsis in the neonatal intensive care unit in the era of multi-drug resistant organisms: A retrospective review. Pediatr Neonatol. 2018;35–41.
26.
Hornik C, Benjamin D, Becker K, Benjamin D, Jr, Li J, et al. Use of the complete blood cell count in late-onset neonatal sepsis. Pediatr Infect Dis J. 2012;803–7.
27.
Vecchio D, A. Evaluation and management of thrombocytopenic neonates in the intensive care unit. Early Hum Dev. 2014;51–5.
28.
Perrone S, Lotti F, Longini M, Rossetti A, Bindi I, Bazzini F, et al. C reactive protein in healthy term newborns during the first 48 hours of life. Arch Dis Child Fetal Neonatal Ed. 2018;163–6.
29.
Gkentzi D, Kortsalioudaki C, Cailes B, Zaoutis T, Kopsidas J, Tsolia M, et al. Neonatal infection surveillance network in Greece. Epidemiology of infections and antimicrobial use in Greek neonatal units. Arch Dis Child Fetal Neonatal Ed. 2019;293–7.
The statements, opinions and data contained in the journal are solely those of the individual authors and contributors and not of the publisher and the editor(s). We stay neutral with regard to jurisdictional claims in published maps and institutional affiliations.