Variability of Pneumocystis jirovecii prophylaxis use among pediatric solid organ transplant providers

Grant Paulsen1,2, Marian G Michaels3, Lara Danziger-Isakov1,2

  • 1Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.

Pediatric Transplantation
|November 13, 2019
PubMed

Insights

Pediatric solid organ transplant recipients commonly receive Pneumocystis jirovecii pneumonia (PJP) prophylaxis. However, prophylaxis practices and durations vary significantly by transplant center and organ type, with most centers reporting low PJP incidence.

Area of Science:

  • Pediatric Solid Organ Transplantation
  • Infectious Disease Prophylaxis
  • Immunocompromised Patient Management

Background:

  • Pneumocystis jirovecii pneumonia (PJP) prophylaxis is standard post-pediatric solid organ transplant (SOT), yet clinical practices exhibit considerable variation.
  • Understanding current prophylaxis strategies is crucial for optimizing patient care and preventing PJP in this vulnerable population.

Purpose of the Study:

  • To investigate current practices regarding PJP prophylaxis in pediatric SOT recipients.
  • To identify variations in prophylaxis protocols based on organ type, duration, and institutional guidelines.

Main Methods:

  • An online survey was distributed in 2018 to 707 members of the International Pediatric Transplant Association.
  • Responses from 105 participants representing 47 institutions across 18 countries were analyzed.

Main Results:

  • 88% of institutions reported routine PJP prophylaxis; 12% did not, primarily for renal transplants due to perceived low PJP incidence.
  • Trimethoprim/sulfamethoxazole was the predominant first-line agent (95%).
  • Prophylaxis durations varied: 4-6 months for kidney, liver, and heart transplants; 10-12 months or lifelong for abdominal multivisceral; and lifelong for most lung transplants.

Conclusions:

  • PJP prophylaxis is widely implemented in pediatric SOT, but significant variability exists in its application and duration.
  • Prophylaxis strategies should be tailored to organ type, considering local PJP incidence and patient risk factors.
  • Further standardization may improve PJP prevention in pediatric SOT recipients.

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