Post-transplant infections

Post-transplant infections

Post-transplant infections

On this page

Infection Timeline - The Risky Calendar

  • <1 Month (Immediate): Hospital-acquired infections dominate. Think bacterial sources from the surgical wound, IV lines (catheter-related), or ventilator-associated pneumonia. Candida infections are also frequent.

  • 1-6 Months (Delayed): Corresponds to peak immunosuppressive therapy. This is the prime window for opportunistic pathogens normally controlled by T-cells (e.g., Pneumocystis jirovecii, Aspergillus).

  • >6 Months (Late): As immunosuppression is reduced, the risk profile shifts. Patients are more susceptible to common community-acquired pathogens and reactivation of chronic viruses like BK virus (nephropathy).

⭐ Cytomegalovirus (CMV) is the quintessential opportunistic infection of the 1-6 month period. It can manifest as pneumonitis, colitis, retinitis, or a mono-like syndrome.

Opportunistic Bugs - The Usual Suspects

  • CMV (Cytomegalovirus): The most significant pathogen in the 1-6 month window.
    • Presents as pneumonitis, esophagitis/colitis, hepatitis, or retinitis.
    • Biopsy reveals characteristic "owl's eye" intranuclear inclusions.
    • CMV owl's eye inclusion bodies in histology
  • Pneumocystis jirovecii (PJP):
    • Causes diffuse interstitial pneumonia; diagnosed via bronchoalveolar lavage (BAL).

    ⭐ Prophylaxis is crucial, typically with Trimethoprim-Sulfamethoxazole (TMP-SMX) for the first 6-12 months post-transplant.

  • Other Key Pathogens:
    • Fungi: Aspergillus fumigatus (invasive disease, "halo sign" on chest CT), Candida species.
    • Bacteria: Nocardia (cavitary lung lesions, brain abscesses), Listeria monocytogenes (meningitis).
    • Viruses: EBV (risk of Post-Transplant Lymphoproliferative Disorder - PTLD), VZV.

Prophylaxis & Tx - The Protective Shield

  • Universal Prophylaxis (First 6-12 months):

    • PJP/PCP: Lifelong TMP-SMX. Alternatives: atovaquone, dapsone.
    • CMV: Valganciclovir for high-risk (D+/R-). Others monitored with PCR (pre-emptive therapy).
    • Fungal (Candida): Fluconazole or nystatin, especially with high steroid use.
    • HSV/VZV: Acyclovir or valacyclovir if seropositive.
  • Treatment Approach:

    • Guided by pathogen identification (culture, PCR, biopsy).
    • Crucial first step: Reduce immunosuppression if feasible, balancing rejection risk.

⭐ For febrile neutropenia post-transplant, initial treatment requires broad-spectrum coverage against Pseudomonas, like cefepime or piperacillin-tazobactam.

High‑Yield Points - ⚡ Biggest Takeaways

  • Infection timing is the most crucial diagnostic clue.
  • <1 month post-transplant: Think nosocomial bacterial infections from the surgical site, catheters, or aspiration.
  • 1-6 months: This is the classic window for opportunistic infections (e.g., CMV, PJP, Aspergillus) due to peak immunosuppression.
  • >6 months: The risk profile shifts towards community-acquired pathogens and chronic viral infections like BK virus nephropathy.
  • Universal prophylaxis with TMP-SMX (for PJP) is standard.

Practice Questions: Post-transplant infections

Test your understanding with these related questions

A 26-year-old man comes to the physician for a follow-up examination. He was diagnosed with HIV infection 2 weeks ago. His CD4+ T-lymphocyte count is 162/mm3 (N ≥ 500). An interferon-gamma release assay is negative. Prophylactic treatment against which of the following pathogens is most appropriate at this time?

1 of 5

Flashcards: Post-transplant infections

1/4

In addition to medical treatment, _____ will need to be surgically removed

TAP TO REVEAL ANSWER

In addition to medical treatment, _____ will need to be surgically removed

aspergillomas (which complication of Aspergillus fumigatus)

browseSpaceflip

Enjoying this lesson?

Get full access to all lessons, practice questions, and more.

Start Your Free Trial