Early-onset neonatal sepsis: It is not only group B streptococcus
2011, Paediatrics & Child Health
https://doi.org/10.1093/PCH/16.5.269Abstract
A male infant was born at 35 weeks' gestational age. A spontaneous rupture of membranes occurred 22 h before delivery. At that time, the mother received three doses of intravenous penicillin. There was no fever during labour. The infant weighed 2.2 kg with an Apgar score of 7 at both 1 min and 5 min. The infant experienced mild respiratory distress at birth and was admitted to the level II neonatal intensive care unit. On admission, the infant's heart rate and respiratory rate were 185 beats/min and 86 breaths/min, respectively. His oxygen saturation was 94% with 30% oxygen and his temperature was 35.2°C. A complete blood count was performed and blood cultures were drawn. Ampicillin and gentamycin were started intravenously. At 4 h of age, the infant deteriorated, with increasing respiratory distress and poor perfusion followed by a drop in blood pressure. His complete blood count revealed a white blood cell count of 4.2×10 9 /L, with 40% neutrophils, 23% bands, 9% metamyelocytes and 4% myelocytes. An arterial blood gas analysis was performed (pH=7.12, PCO 2 =66 mmHg, PO 2 =58 mmHg, bicarbonate = 20 mmol/L, and base excess = -7). Low lung volumes, hazy opacification of both lung fields and air bronchograms were observed on the chest x-ray. At 6 h of age, the infant was intubated and given surfactant. At 20 h of age, the blood culture grew Escherichia coli. On day 2, a lumbar puncture was performed and the cerebrospinal fluid results were the following: three red blood cells, 10 white blood cells and no bacteria seen. Additionally, the cerebrospinal fluid culture revealed no growth. However, the E coli in the blood culture was resistant to penicillin and ampicillin, and sensitive to gentamycin. The infant remained ventilated for four days, treated with gentamycin for 14 days and then discharged home. At the six-month neonatal follow-up, the infant was doing well and developing normally.
References (10)
- Maayan-Metzger A, Barzilai A, Keller N, Kuint J. Are the "good old" antibiotics still appropriate for early-onset neonatal sepsis? A 10 year survey. Isr Med Assoc J 2009;11:138-42.
- Stroll BJ, Hansen N, Fanaroff AA, et al. Change in pathogens causing early-onset sepsis in very-low-birth-weight infants. N Engl J Med 2002;347:240-7.
- Edwards RK, Jamie WE, Sterner D, Gentry S, Counts K, Duff P. Intrapartum antibiotic prophylaxis and early-onset neonatal sepsis patterns. Infect Dis Obstet Gynecol 2003;11:221-6.
- Baltimore RS, Huie SM, Meek JI, Schuchat A, O'Brien KL. Early-onset neonatal sepsis in the era of group B streptococcal prevention. Pediatrics 2001;108:1094-8.
- Barrington KJ; Canadian Paediatric Society, Fetus and Newborn Committee. Management of the infant at increased risk for sepsis. Paediatr Child Health 2007;12:893-905.
- Sgro M, Shah PS, Campbell DM, Tenuta A, Shivananda S, Lee SK. Early onset neonatal sepsis: Rate and organism pattern between 2003 and 2008. J Perinatol 2011. (In press)
- Money DM, Dobson S. The prevention of early-onset neonatal group B streptococcal disease. J Obstet Gynaecol Can 2004;26:826-40.
- Bizzarro MJ, Dembry L-M, Baltimore RS, Gallagher PG. Changing patterns in neonatal Escherichia coli sepsis and ampicillin resistance in the era of intrapartum antibiotic prophylaxis. Pediatrics 2008;121:689-96.
- Aurangzeb B, Hameed A. Neonatal sepsis in hospital-born babies: Bacterial isolates and antibiotic susceptibility patterns. J Coll Physcians Surg Pak 2003;13:629-32.
- Puopolo KM, Eichewald EC. No change in the incidence of ampicillin-resistant, neonatal, early-onset sepsis over 18 years. Pediatrics 2010;125:e1031-8.