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Case report
Late-onset neonatal sepsis: A cinetobacter ursingii as an infectious agent
  1. Mariana Barros,
  2. Raquel Garrido,
  3. Ana Tavares and
  4. Manuel Sousa Cunha
  1. Neonatology Functional Unit, Children Department, Hospital de Cascais, Dr José de Almeida, Cascais, Portugal
  1. Correspondence to Dr Mariana Barros; marianaantunesbarros{at}gmail.com

Abstract

The authors report a case of a premature male newborn admitted to the neonatal intensive care unit after an emergent caesarean due to maternal pre-eclampsia and foetal bradycardia at 32 weeks of gestational age and birth weight of 1440 g. There were no infection risk factors reported. On day 3 his clinical condition deteriorated, with tachycardia and subfebrile temperature and C-reactive protein at 1.25 mg/dL. Empirical antibiotics (flucloxacillin and gentamicin) were started, with no clinical improvement and C-reactive protein increasing to a maximum of 19 mg/dL (upper normal level of 1 mg/dL) after 3 days. Blood cultures from the third to the eighth day of life were positive for Acinetobacter ursingii. Targeted therapy was administered for 14 days with clinical and laboratorial improvement and he was discharged on the 28th day of life without any known sequelae. A. ursingii is emerging as an infectious agent of late-onset sepsis in immunosuppressed neonates.

  • infectious diseases
  • neonatal intensive care

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Footnotes

  • Contributors MB, RG, AT and MSC were all present in the daily approach and management of the patient to whom the case report refers to. AT and MSC planned and conducted the initial design of the present case report, pointing out the main bullet points to transmit as well as relevant references to cite. MB and RG then proceeded with acquisition and analysis of data regarding the clinical and laboratory evolution of the patient as well as additional research concerning neonatal sepsis and Acinetobacter ursingii reports. MB and RG drafted the initial manuscript. AT and MSC then revised the work. All authors approved the final version.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient consent for publication Parental/guardian consent obtained.

  • Provenance and peer review Not commissioned; externally peer reviewed.