Epidemiology and complications of late-onset sepsis: an Italian area-based study
Autoři:
Alberto Berardi aff001; Francesca Sforza aff002; Lorenza Baroni aff003; Caterina Spada aff002; Simone Ambretti aff004; Giacomo Biasucci aff005; Serenella Bolognesi aff006; Mariagrazia Capretti aff007; Edoardo Carretto aff008; Matilde Ciccia aff009; Marcello Lanari aff010; Maria Federica Pedna aff011; Vittoria Rizzo aff012; Claudia Venturelli aff013; Crisoula Tzialla aff014; Laura Lucaccioni aff001; Maria Letizia Bacchi Reggiani aff015
Působiště autorů:
Unità Operativa di Terapia Intensiva Neonatale, Dipartimento Integrato Materno-Infantile, Azienda Ospedaliero-Universitaria Policlinico, Modena, Italy
aff001; Medico in formazione, Scuola di Specializzazione in Pediatria, Università degli Studi di Modena e Reggio, Modena, Italy
aff002; Terapia Intensiva Neonatale, Dipartimento Ostetrico e Pediatrico, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Arcispedale Santa Maria Nuova, Reggio Emilia, Italy
aff003; Unità Operativa di Microbiologia, Azienda Ospedaliero-Universitaria S. Orsola-Malpighi, Bologna, Italy
aff004; Unità Operativa di Pediatria, Ospedale G da Saliceto, Piacenza, Italy
aff005; Unità Operativa di Terapia Intensiva Neonatale, Ospedale Infermi, Rimini, Italy
aff006; Unità Operativa di Neonatologia, Dipartimento Del Bambino, Della Donna E Delle Malattie Urologiche, Azienda Ospedaliero-Universitaria Sant’Orsola–Malpighi, Bologna, Italy
aff007; Laboratorio di Microbiologia, Dipartimento Interaziendale di Diagnostica per Immagini e Medicina di Laboratorio, Istituto di Ricovero e Cura a Carattere Scientifico IRCCS, Arcispedale Santa Maria Nuova, Reggio Emilia, Italy
aff008; Unità Operativa di Terapia Intensiva Neonatale, Dipartimento Materno Infantile, Ospedale Maggiore, Bologna, Italy
aff009; Unità Operativa di Pediatria, Dipartimento Del Bambino, Della Donna E Delle Malattie Urologiche, Azienda Ospedaliero-Universitaria Sant’Orsola–Malpighi, Bologna, Italy
aff010; Unità Operativa di Microbiologia, Laboratorio Unico Ausl della Romagna, Pievesestina Cesena, Italy
aff011; Unità Operativa di Terapia Intensiva Neonatale e Pediatrica, Ospedale Civile M. Bufalini, Cesena, Italy
aff012; Struttura Complessa di Microbiologia e Virologia, Azienda Ospedaliero-Universitaria Policlinico, Modena, Italy
aff013; Neonatologia, Patologia Neonatale e Terapia Intensiva Neonatale, Fondazione IRCCS Policlinico “San Matteo”, Pavia, Italy
aff014; Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale, Azienda Ospedaliero-Universitaria S. Orsola-Malpighi—Università di Bologna, Bologna, Italy
aff015
Vyšlo v časopise:
PLoS ONE 14(11)
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pone.0225407
Souhrn
Background
Most studies regarding late-onset sepsis (LOS) address selected populations (i.e., neonates with low birth weight or extremely preterm neonates). Studying all age groups is more suitable to assess the burden of single pathogens and their clinical relevance.
Methods
This is a retrospective regional study involving paediatric departments and NICUs in Emilia-Romagna (Italy). Regional laboratory databases were searched from 2009 to 2012. Records of infants (aged 4 to 90 days) with a positive blood or cerebrospinal fluid (CSF) culture were retrospectively reviewed and analysed according to acquisition mode (whether hospital- or community-acquired).
Results
During the study period, there were 146,682 live births (LBs), with 296 patients experiencing 331 episodes of LOS (incidence rate: 2.3/1000 LBs). Brain lesions upon discharge from the hospital were found in 12.3% (40/296) of cases, with death occurring in 7.1% (23/296; 0.14/1000 LBs). With respect to full-term neonates, extremely preterm or extremely low birth weight neonates had very high risk of LOS and related mortality (> 100- and > 800-fold higher respectively). Hospital-acquired LOS (n = 209) was significantly associated with very low birth weight, extremely preterm birth, pneumonia, mechanical ventilation, and death (p< 0.01). At multivariate logistic regression analysis, catecholamine support (OR = 3.2), central venous line before LOS (OR = 14.9), and meningitis (OR = 44.7) were associated with brain lesions or death in hospital-acquired LOS (area under the ROC curve 0.81, H-L p = 0.41). Commonly identified pathogens included coagulase-negative staphylococci (CoNS n = 71, 21.4%), Escherichia coli (n = 50, 15.1%), Staphylococcus aureus (n = 41, 12.4%) and Enterobacteriaceae (n = 41, 12.4%). Group B streptococcus was the predominant cause of meningitis (16 of 38 cases, 42%). Most pathogens were sensitive to first line antibiotics.
Conclusions
This study provides the first Italian data regarding late-onset sepsis (LOS) in all gestational age groups. Compared to full-term neonates, very high rates of LOS and mortality occurred in neonates with a lower birth weight and gestational age. Group B streptococcus was the leading cause of meningitis. Excluding CoNS, the predominant pathogens were Escherichia coli and Staphylococcus aureus. Neonates with hospital-acquired LOS had a worse outcome. Antibiotic associations, recommended for empirical treatment of hospital- or community-acquired LOS, were adequate.
Klíčová slova:
Bacterial pathogens – Fungal pathogens – Neonates – Blood – Birth weight – Nosocomial infections – Neonatal sepsis – Meningitis
Zdroje
1. Schlapbach LJ, Aebischer M, Adams M, Natalucci G, Bonhoeffer J, Latzin P et al. Swiss Neonatal Network and Follow-Up Group. Impact of sepsis on neurodevelopmental outcome in a Swiss National Cohort of extremely premature infants. Pediatrics. 2011 Aug;128(2):e348–57. doi: 10.1542/peds.2010-3338 21768312
2. Bizzarro MJ, Raskind C, Baltimore RS, Gallagher PG. Seventy-five years of neonatal sepsis at Yale: 1928–2003. Pediatrics. 2005 Sep;116(3):595–602. doi: 10.1542/peds.2005-0552 16140698
3. Stoll BJ, Hansen NI, Adams-Chapman I, Fanaroff AA, Hintz SR, Vohr B et al. National Institute of Child Health and Human Development Neonatal Research Network. Neurodevelopmental and growth impairment among extremely low-birth-weight infants with neonatal infection. JAMA. 2004 Nov 17;292(19):2357–65. doi: 10.1001/jama.292.19.2357 15547163
4. Payne NR, Carpenter JH, Badger GJ, Horbar JD, Rogowski J. Marginal increase in cost and excess length of stay associated with nosocomial bloodstream infections in surviving very low birth weight infants. Pediatrics. 2004 Aug;114(2):348–55. doi: 10.1542/peds.114.2.348 15286215
5. Hornik CP, Fort P, Clark RH, Watt K, Benjamin DK Jr, Smith PB, et al. Early and late onset sepsis in very-low-birth-weight infants from a large group of neonatal intensive care units. Early Hum Dev. 2012 May;88 Suppl 2:S69–74.
6. Dong Y, Speer CP. Late-onset neonatal sepsis: recent developments. Arch Dis Child Fetal Neonatal Ed. 2015 May;100(3):F257–63. doi: 10.1136/archdischild-2014-306213 25425653
7. Shah BA, Padbury JF. Neonatal sepsis: an old problem with new insights.Virulence. 2014 Jan 1;5(1):170–8. doi: 10.4161/viru.26906 24185532
8. Vergnano S, Menson E, Kennea N, Embleton N, Russell AB, Watts T et al. Neonatal infections in England: the NeonIN surveillance network. Arch Dis Child Fetal Neonatal Ed. 2011 Jan;96(1):F9–F14. doi: 10.1136/adc.2009.178798 20876594
9. Tsai MH, Hsu JF, Chu SM, Lien R, Huang HR, Chiang MC et al. Incidence, clinical characteristics and risk factors for adverse outcome in neonates with late-onset sepsis. Pediatr Infect Dis J. 2014 Jan;33(1):e7–e13. doi: 10.1097/INF.0b013e3182a72ee0 23899966
10. Bizzarro MJ, Shabanova V, Baltimore RS, Dembry LM, Ehrenkranz RA, Gallagher PG. Neonatal sepsis 2004–2013: the rise and fall of coagulase-negative staphylococci. J Pediatr. 2015 May;166(5):1193–9. doi: 10.1016/j.jpeds.2015.02.009 25919728
11. Gowda H, Norton R, White A, Kandasamy Y. Late-onset Neonatal Sepsis-A 10-year Review From North Queensland, Australia. Pediatr Infect Dis J. 2017 Sep;36(9):883–888. doi: 10.1097/INF.0000000000001568 28178107
12. Cailes B, Kortsalioudaki C, Buttery J, Pattnayak S, Greenough A, Matthes J et al. neonIN network. Epidemiology of UK neonatal infections: the neonIN infection surveillance network. Arch Dis Child Fetal Neonatal Ed. 2018 Nov;103(6):F547–F553. doi: 10.1136/archdischild-2017-313203 29208666
13. Didier C, Streicher MP, Chognot D, Campagni R, Schnebelen A, Messer J et al. Late-onset neonatal infections: incidences and pathogens in the era of antenatal antibiotics. Eur J Pediatr. 2012 Apr;171(4):681–7. doi: 10.1007/s00431-011-1639-7 22134805
14. Stoll BJ, Hansen N, Fanaroff AA, Wright LL, Carlo WA, Ehrenkranz RA et al. Late-onset sepsis in very low birth weight neonates: the experience of the NICHD Neonatal Research Network. Pediatrics. 2002 Aug;110(2 Pt 1):285–91.
15. Shah J, Jefferies AL, Yoon EW, Lee SK, Shah PS; Canadian Neonatal Network. Risk Factors and Outcomes of Late-Onset Bacterial Sepsis in Preterm Neonates Born at < 32 Weeks' Gestation. Am J Perinatol. 2015 Jun;32(7):675–82. doi: 10.1055/s-0034-1393936 25486288
16. Greenberg RG, Kandefer S, Do BT, Smith PB, Stoll BJ, Bell Ef et al. Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network. Late-onset Sepsis in Extremely Premature Infants: 2000–2011. Pediatr Infect Dis J. 2017 Aug;36(8):774–779. doi: 10.1097/INF.0000000000001570 28709162
17. Berardi A, Baroni L, Bacchi Reggiani ML, Ambretti S, Biasucci G, Bolognesi S et al. GBS Prevention Working Group Emilia-Romagna. The burden of early-onset sepsis in Emilia-Romagna (Italy): a 4-year, population-based study. J Matern Fetal Neonatal Med. 2016 Oct;29(19):3126–31. doi: 10.3109/14767058.2015.1114093 26515917
18. Berardi A, Lugli L, Rossi C, Guidotti I, Lanari M, Creti R et al. GBS Prevention Working Group, Emilia-Romagna. Impact of perinatal practices for early-onset group B Streptococcal disease prevention. Pediatr Infect Dis J. 2013 Jul;32(7):e265–71. doi: 10.1097/INF.0b013e31828b0884 23385951
19. Verani JR, McGee L, Schrag SJ. Division of Bacterial Diseases, National Center for Immunization and Respiratory Diseases, Centres for Disease Control and Prevention (CDC). Prevention of perinatal group B streptococcal disease—revised guidelines from CDC, 2010. MMWR Recomm Rep 2010;59(RR-10):1–36 21088663
20. Schrag S, Gorwitz R, Fultz-Butts K, Schuchat A. Prevention of perinatal group B streptococcal disease. Revised guidelines from CDC. MMWR Recomm Rep. 2002 Aug 16;51(RR-11):1–22. 12211284
21. Berardi A, Di Fazzio G, Gavioli S, Di Grande E, Groppi A, Papa I, et al. Universal antenatal screening for group B streptococcus in Emilia-Romagna. J Med Screen. 2011;18:60–4 doi: 10.1258/jms.2011.011023 21852697
22. Berardi A, Rossi C, Bacchi Reggiani ML, Bastelli A, Capretti MG, Chiossi C, et al. An area-based study on intrapartum antibiotic prophylaxis for preventing group B streptococcus early-onset disease: advances and limitations. J Matern Fetal Neonatal Med. 2017;30:1739–1744. doi: 10.1080/14767058.2016.1224832 27593156
23. Vermont-Oxford Network Database Manual of Operations, Part 2, Release 22.1, VT: Vermont Oxford Network; 2017 Apr.
24. Ku LC, Boggess KA, Cohen-Wolkowiez M. Bacterial meningitis in infants. ClinPerinatol. 2015 Mar;42(1):29–45, vii-viii.
25. Brodie SB, Sands KE, Gray JE, Parker RA, Goldmann DA, Davis RB et al. Occurrence of nosocomial bloodstream infections in six neonatal intensive care units. Pediatr Infect Dis J. 2000 Jan;19(1):56–65. doi: 10.1097/00006454-200001000-00012 10643852
26. Giannoni E, Agyeman PKA, Stocker M, Posfay-Barbe KM, Heininger U, Spycher BD et al. Swiss Pediatric Sepsis Study. Neonatal Sepsis of Early Onset, and Hospital-Acquired and Community-Acquired Late Onset: A Prospective Population-Based Cohort Study. J Pediatr. 2018 Oct;201:106-114.e4.
27. Berardi A, Cattelani C, Creti R, Berner R, Pietrangiolillo Z, Margarit I et al. Group B streptococcal infections in the newborn infant and the potential value of maternal vaccination. Expert Rev Anti Infect Ther. 2015;13(11):1387–99. doi: 10.1586/14787210.2015.1079126 26295167
28. Boghossian NS, Page GP, Bell EF, Stoll BJ, Murray JC, Cotten CM et al. Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network. Late-onset sepsis in very low birth weight infants from singleton and multiple-gestation births. J Pediatr. 2013 Jun;162(6):1120–4,1124.e1. doi: 10.1016/j.jpeds.2012.11.089 23324523
29. Perlman SE, Saiman L, Larson EL. Risk factors for late-onset healthcare-associated bloodstream infections in patients in neonatal intensive care units. Am J Infect Control. 2007 Apr;35(3):177–82. doi: 10.1016/j.ajic.2006.01.002 17433941
30. Gkentzi D, Kortsalioudaki C, Cailes BC, Zaoutis T, Kopsidas J, Tsolia M et al. Epidemiology of infections and antimicrobial use in Greek Neonatal Units. Arch Dis Child Fetal Neonatal Ed. 2019 May;104(3):F293–F297 doi: 10.1136/archdischild-2018-315024 29954881
31. Jiang JH, Chiu NC, Huang FY, Kao HA, Hsu CH, Hung HY et al. Neonatal sepsis in the neonatal intensive care unit: characteristics of early versus late onset. J Microbiol Immunol Infect. 2004 Oct;37(5):301–6. 15497012
32. Berardi A, Ficara M, Pietrella E, Boncompagni A, Toffoli C, Bianchini A et al. Stewardship antimicrobica nel neonato e nel piccolo lattante. Perchè e come praticarla. Medico E Bambino. 2017;493–501.
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