Respiratory failure associated with human metapneumovirus infection in an infant posthepatic transplant

K M A Evashuk1, S E Forgie, S Gilmour

  • 1Department of Pediatrics, Stollery Children's Hospital, Edmonton, Alberta, Canada.

Insights

This case study reports the first instance of respiratory failure from human metapneumovirus (hMPV) in a pediatric liver transplant patient. The infant recovered after intensive support, highlighting the risks of hMPV in immunocompromised children.

Area of Science:

  • Pediatric critical care medicine
  • Transplant infectious diseases
  • Virology

Background:

  • Liver transplant recipients and pediatric solid organ transplant recipients are at risk for severe infections.
  • Human metapneumovirus (hMPV) is a common respiratory pathogen, but its impact on immunocompromised pediatric populations is not well-defined.

Observation:

  • A 9-month-old female developed severe respiratory distress 8 days post-liver transplant.
  • hMPV infection was confirmed, necessitating mechanical ventilation and extracorporeal membrane oxygenation (ECMO) for 26 days.
  • The patient's immunosuppressive therapy was adjusted, and close monitoring for hepatic complications was performed.

Findings:

  • This is the first reported case of respiratory failure due to hMPV in a liver transplant recipient or a pediatric solid organ transplant recipient.
  • The patient successfully recovered from the hMPV infection with no evidence of allograft rejection or hepatic vessel thrombosis.
  • Pulmonary function was satisfactory post-recovery, with a noted possibility of mild developmental delay.

Implications:

  • hMPV infection poses a significant threat to immunocompromised pediatric transplant recipients, potentially causing severe respiratory compromise.
  • Management requires a multidisciplinary approach, including respiratory support, careful medication management, and vigilant monitoring for complications.
  • Further research is needed to understand the epidemiology and long-term outcomes of hMPV in this vulnerable population.

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