Am J Perinatol 2020; 37(S 02): S5-S9
DOI: 10.1055/s-0040-1715584
Review Article

Advances in Neonatal Infections

Avroy A. Fanaroff
1   Division of Neonatology, Department of Pediatrics, Rainbow Babies and Children's Hospital, Case Western Reserve University School of Medicine, Cleveland, Ohio
,
Jonathan M. Fanaroff
1   Division of Neonatology, Department of Pediatrics, Rainbow Babies and Children's Hospital, Case Western Reserve University School of Medicine, Cleveland, Ohio
› Author Affiliations

Abstract

Despite continued advances and developments in neonatal medicine, neonatal sepsis is the third leading cause of neonatal mortality and a major public health problem, especially in developing countries. Sepsis accounts for mortality for almost 50% of global children under 5 years of age.

Over the past 50 years, there have been many advances in the diagnosis, prevention, and treatment of neonatal infections. The diagnostic advances include better culture techniques that permit more rapid confirmation of the diagnosis, advent of polymerase chain reaction (PCR) to rapidly diagnose viral infections, use of biologic markers indicating evidence of infection, and a better understanding of immunoglobulin markers of infection. From a therapeutic stand point, there have been a variety of antibiotics, antifungals, and antiviral agents, better approaches to prevent sepsis, specific immunotherapy, for example, respiratory syncytial virus (RSV); bundled approach to prevention of deep-line infection and better antibiotic stewardship, leading to earlier discontinuation of antibiotic therapy.

Hand hygiene remains the benchmark and gold standard for late-onset sepsis prevention. The challenge has been that each decade, newer resistant bacteria dominate as the cause of sepsis and newer viruses emerge, for example, human immunodeficiency virus, zika virus, and novel coronavirus disease 2019.

Future treatment options might include stem cell therapy, other antimicrobial protein and peptides, and targeting of pattern recognition receptors in an effort to prevent and/or treat sepsis in this vulnerable population. Also, the microbiome of premature infants has a smaller proportion of beneficial bacteria and higher numbers of pathogenic bacteria compared with term infants, likely owing to higher frequencies of cesarean sections, antibiotic use, exposure to the hospital environment, and feeding nonhuman milk products. Modifying the microbiome with more mother's milk and shorter duration of antibiotics in noninfected babies should be a goal.

Key Points

  • Neonatal sepsis remains a leading cause of mortality.

  • Challenges include bacterial resistance and newer viruses.

  • Future treatments may include newer antibiotics/antivirals and stem cell therapy.



Publication History

Article published online:
08 September 2020

Thieme Medical Publishers
333 Seventh Avenue, New York, NY 10001, USA.

 
  • References

  • 1 Kadar N. Rediscovering Ignaz Philipp Semmelweis (1818-1865). Am J Obstet Gynecol 2019; 220 (01) 26-39
  • 2 Khalil N, Biunt H, Li Z, Hartman T. Neonatal early onset sepsis in Middle Eastern countries: a systematic review. Arch Dis Childl 2020; 105 (07) 639-647
  • 3 Mukhopadhyay S, Sengupta S, Puopolo KM. Challenges and opportunities for antibiotic stewardship among preterm infants. Arch Dis Child Fetal Neonatal Ed 2019; 104 (03) F327-F332
  • 4 Puopolo KM, Benitz WE, Zaoutis TE. Committee on Fetus and Newborn; Committee on Infectious Diseases. Management of neonates born at ≤34 6/7 weeks' gestation with suspected or proven early-onset bacterial sepsis. Pediatrics 2018; 142 (06) e20182896
  • 5 Dermyshi E, Wang Y, Yan C. , et al. The “golden age” of probiotics: a systematic review and meta-analysis of randomized and observational studies in preterm infants. Neonatology 2017; 112 (01) 9-23
  • 6 Pammi M, Suresh G. Enteral lactoferrin supplementation for prevention of sepsis and necrotizing enterocolitis in preterm infants. Cochrane Database Syst Rev 2017; 6 (06) CD007137
  • 7 Griffiths J, Jenkins P, Vargova M. , et al. The ELFIN trial investigators group enteral lactoferrin to prevent infection for very preterm infants. The ELFIN RCT Health Technol Assess 2018; 22: 1-60
  • 8 Russel NJ, Seale AC, O'Sullivan C. , et al. Risk of early-onset neonatal group B streptococcal disease with maternal colonization worldwide: systematic review and meta-analyses. Clin Infect Dis 2017; 65 (Suppl. 02) S152-S159
  • 9 Schrag SJ, Verani JR. Intrapartum antibiotic prophylaxis for the prevention of perinatal group B streptococcal disease: experience in the United States and implications for a potential group B streptococcal vaccine. Vaccine 2013; 31 (Suppl. 04) D20-D26
  • 10 Taylor JE, McDonald SJ, Earnest A. , et al. A quality improvement initiative to reduce central line infection in neonates using checklists. Eur J Pediatr 2017; 176 (05) 639-646
  • 11 Kimberlin DW, Brady MT, Jackson MA, Long SS. , eds. Committee on Infectious Diseases: Syphilis. Red book: 2018–2021 Report of the Committee on Infectious Diseases. 31st ed. Itasca, IL: American Academy of Pediatrics; 2018
  • 12 Manzoni P, Jacqz-Aigrain E, Rizzollo S. , et al. Antifungal prophylaxis in neonates. Early Hum Dev 2011; 87 (Suppl. 01) S59-S60
  • 13 Chuang Y-Y, Huang YC. Enteroviral infection in neonates. J Microbiol Immunol Infect 2019; 52 (06) 851-857
  • 14 Pevear DC, Tull TM, Seipel ME, Groarke JM. Activity of pleconaril against enteroviruses. Antimicrob Agents Chemother 1999; 43 (09) 2109-2115
  • 15 Abzug MJ, Michaels MG, Wald E. , et al; National Institute of Allergy and Infectious Diseases Collaborative Antiviral Study Group. A randomized, double-blind, placebo-controlled trial of pleconaril for the treatment of neonates with enterovirus sepsis. J Pediatric Infect Dis Soc 2016; 5 (01) 53-62
  • 16 Marsico C, Kimberlin DW. Congenital cytomegalovirus infection: advances and challenges in diagnosis, prevention and treatment. Ital J Pediatr 2017; 43 (01) 38
  • 17 Kimberlin DW, Jester PM, Sánchez PJ. , et al; National Institute of Allergy and Infectious Diseases Collaborative Antiviral Study Group. Valganciclovir for symptomatic congenital cytomegalovirus disease. N Engl J Med 2015; 372 (10) 933-943
  • 18 White MK, Wollebo HS, David Beckham J, Tyler KL, Khalili K. Zika virus: an emergent neuropathological agent. Ann Neurol 2016; 80 (04) 479-489
  • 19 James SH, Kimberlin DW. Neonatal herpes simplex virus infection: epidemiology and treatment. Clin Perinatol 2015; 42 (01) 47-59 , viii
  • 20 Schillie S, Vellozzi C, Reingold A. , et al. Prevention of hepatitis B virus infection in the United States: recommendations of the advisory committee on immunization practices. MMWR Recomm Rep 2018; 67 (01) 1-31
  • 21 Slogrove AL, Powis KM, Johnson LF, Stover J, Mahy M. Estimates of the global population of children who are HIV-exposed and uninfected, 2000-18: a modelling study. Lancet Glob Health 2020; 8 (01) e67-e75