Coronial
SAhospital

Coroner's Finding: KISON Trinity Isabel

Deceased

Trinity Isabel Kison

Demographics

0y, female

Date of death

2008-10-28

Finding date

2012-07-31

Cause of death

respiratory failure due to congenital pneumonia with hyaline membrane disease caused by streptococcus pneumoniae

AI-generated summary

Trinity Kison, a 21-hour-old neonate born at 35 weeks gestation, died from respiratory failure due to congenial pneumonia caused by streptococcus pneumoniae. The maternal high vaginal swab taken one week before delivery was positive for streptococcus pneumoniae but this critical result was not properly communicated or understood. Prophylactic antibiotics were not administered to the mother despite clear guideline recommendations for preterm rupture of membranes. Post-delivery, despite respiratory distress, Trinity was not prescribed antibiotics until 12:30am on day of death—far too late. Multiple missed opportunities for intervention existed: failure to appreciate vaginal swab significance, failure to administer maternal prophylaxis, failure to recognise risk factors in neonatal management, reliance on falsely reassuring early FBE, and failure to escalate clinical deterioration. Evidence suggests Trinity would likely have survived with timely antibiotic administration at birth or within hours thereafter.

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Specialties

obstetricsneonatologymicrobiologypathology

Error types

diagnosticcommunicationsystemdelay

Drugs involved

benzylpenicillinpenicillinerythromycingentamicinsurfactant

Clinical conditions

congenital pneumoniastreptococcus pneumoniae infectionhyaline membrane diseaseearly onset neonatal sepsisrespiratory distresspreterm deliverypreterm rupture of membranespneumothorax

Procedures

caesarean sectionendotracheal intubationmechanical ventilationhigh vaginal swabblood culturefull blood examinationchest X-ray

Contributing factors

  • failure to administer prophylactic intrapartum antibiotics to mother despite preterm rupture of membranes
  • failure to recognise and communicate significance of positive streptococcus pneumoniae in maternal high vaginal swab
  • failure to administer antibiotics to neonate despite multiple clinical indications
  • attribution of respiratory distress to hyaline membrane disease rather than considering early onset sepsis
  • reliance on early FBE (taken 1 hour post-delivery) as reassurance without repeat testing
  • failure to escalate clinical deterioration observed from 7pm onwards
  • communication breakdown between obstetric and neonatal teams
  • failure to appreciate significance of 8pm chest X-ray showing consolidation consistent with pneumonia
  • delayed recognition that mother had received no intrapartum antibiotics
  • inadequate understanding by clinicians of guidelines regarding organisms other than GBS

Coroner's recommendations

  1. Multi-disciplinary review of sepsis prevention guidelines to define symptoms of sepsis, criteria for repeating FBE, and emphasise importance of administering antibiotics in preterm delivery even when time to delivery is short
  2. Develop standardised policy for nurses to escalate concerns to consultant
  3. Implement structured and standardised handover between obstetric and neonatal staff encompassing doctor-to-doctor/nurse practitioner and nurse-to-nurse handover
  4. Microbiology laboratory to verbally notify streptococcus pneumoniae and other significant HVS organisms to requesting clinician with clinical significance comment
  5. Communication between microbiology laboratory to extend to both obstetric and neonatal departments, not only obstetricians
  6. Disseminate these findings to all antenatal and neonatal clinical staff at public hospitals
  7. Ensure revised guidelines emphasise need for practitioners to be certain baby's symptoms are not due to early onset sepsis before deciding not to administer antibiotics
  8. Emphasise importance of considering risk factors such as prematurity alongside clinical presentation
  9. Deliver education to junior practitioners concerning potential effects of neonatal pathogens other than Group B Streptococcus
  10. Remind clinicians of importance of handovers and need for full information to be imparted during handovers
  11. Implement FMC protocol of routine antibiotic administration for unresolved respiratory distress after 4 hours with consideration of preterm risk factors
Full text

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