Table 1.
Regimens and targets for prophylaxis in the posttransplant period
Infections | Target Groups | Prophylaxis Regimens/Comments | Suggested Duration of Prophylaxis |
---|---|---|---|
Bacterial infection (postoperative wound infection and sepsis) | All recipients | Perioperative antimicrobials regimens vary depending on organ, nature of surgery, and recipient factors (eg, selected regimens for cystic fibrosis) | 48–72 h |
Herpes simplex | Seropositive recipients | Acyclovir | 3 months |
CMV | Stratification of risk based on CMV donor/recipient serostatus | Intravenous ganciclovir (with/without intravenous immune globulin in some centers) Emerging data for valganciclovir in low- to intermediate-risk older children |
Typically 3 months; some centers use prophylactics for shorter periods (2 weeks) or longer (6 months) |
EBV | High-risk patients are D+R− patients | No established regimens; preemptive reduction in immune suppression in response to rising EBV load in peripheral blood in use by growing number of centers; ganciclovir with/without immune globulin used in some centers | Duration variable if antivirals with/without immune globulin used |
Candida species | All recipients | Fluconazole selectively; lipid amphoterin B products selectively; nystatin often used | Up to 4 weeks depending on risk factors |
Aspergillus | Lung/heart-lung recipients | Voriconazole; intraconazole; amphotericin B products | Duration variable; up to 4–6 months depending on risk |
Pneumocystis jiroveci | All recipients | Trimethoprim-sulfamethoxazole | Typically 6–12 months; for lung and small bowel transplant recipients, as well as any transplant patient with a history of prior PCP infection or chronic CMV disease, lifelong prophylaxis may be indicated |
Toxoplasma gondii | Heart/heart-lung recipients | Pyrimethamine/sulfa for D+R− patients Trimethoprim/sulfa of some value for R+ patients |
6 months |