Abstract

Introduction: Despite the advantages of umbilical cord blood culture (UCBC) use for diagnosis of early onset sepsis (EOS), contamination rates have deterred neonatologists from its widespread use. We aimed to implement UCBC collection in a level III neonatal intensive care unit (NICU) and apply quality improvement (QI) methods to reduce contamination in the diagnosis of early onset sepsis.Methods: Single-center implementation study utilizing quality improvement methodology to achieve 0% contamination rate in UCBC samples using the Plan-Do-Study-Act (PDSA) model for improvement. UCBC was obtained in conjunction with peripheral blood cultures (PBC) in neonates admitted to the NICU due to maternal chorioamnionitis. Maternal and neonatal characteristics between clinical sepsis and asymptomatic groups were compared. Process, outcome, and balancing measures were monitored.Results: Eighty-two UCBC samples were collected in addition to peripheral blood culture from neonates admitted due to maternal chorioamnionitis. Ten (12%) neonates had a diagnosis of clinical sepsis. All PBCs were negative and 5 UCBCs were positive in the study period. After 2 PDSA cycles, there was special cause variation with improvement in the percent of contaminated samples from 7.3 to 0%. There was no change in antibiotic duration among asymptomatic neonates.Conclusions: Implementation of UCBC for the diagnosis of EOS in term infants is feasible and contamination can be minimized with the implementation of a core team of trained providers and a proper sterile technique without increasing antibiotic duration.

Highlights

  • Despite the advantages of umbilical cord blood culture (UCBC) use for diagnosis of early onset sepsis (EOS), contamination rates have deterred neonatologists from its widespread use

  • A total of 82 out of 97 (84.5%) eligible neonates had both Umbilical cord blood culture (UCBC) samples and Peripheral blood culture (PBC) collected during the 22-month period

  • Reasons for missed opportunities to collect UCBC samples included: provider forgot to obtain UCBC (n = 7), inability to obtain consent (n = 4), unavailable UCBC kit in the delivery cart (n = 1), or post-natal diagnosis of chorioamnionitis after placenta was sent to pathology (n = 3)

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Summary

Introduction

Despite the advantages of umbilical cord blood culture (UCBC) use for diagnosis of early onset sepsis (EOS), contamination rates have deterred neonatologists from its widespread use. Utilizing cord blood in high-risk infants to obtain blood cultures has been shown to increase the etiological diagnosis of sepsis [7]. Umbilical cord blood culture (UCBC) has a sensitivity between 80 and 100% and specificity between 91.4 and 94.9% when compared to PBC for the diagnosis of sepsis in high-risk newborns [8]. The procedure is painless and technically less challenging when compared to peripheral vein or artery puncture in a term or preterm neonate and has been shown as a possible alternative for peripherally obtained infant blood in sepsis evaluation [9, 10]

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