Prophylaxis of fungal infections in transplant patients.

Fungi are an important cause of infection in patients undergoing solid organ transplantation and bone marrow or hematopoietic stem cell transplantation (BMT/HSCT). The incidence and mortality of fungal infections differ according to the organ and the time since transplantation. In the first 30 days after transplantation, yeast (primarily Candida spp.) predominate. After the first month, filamentous fungi, such as Aspergillus spp., are the most frequent agents of infection (1-6).

In BMT/HSCT patients, however, invasive aspergillosis has two peaks of incidence: one at one month post-transplantation and another approximately 90 days after the transplant if the patient develops chronic graft versus host disease (7,8).

Among solid organ transplantation, liver and lung transplant have the highest risk for fungal infection due to underlying diseases, surgical techniques and the graft itself (4,9).

Antifungal prophylaxis use is well established following some transplant types, such as BMT/HSCT and liver (10,11). However, few studies have evaluated heart and pancreas transplants. One of the major challenges is the prevention of filamentous fungal infections, especially by Aspergillus spp., in high-risk patients, such as those who have undergone an allogeneic BMT and developed chronic graft versus host disease or undergone a lung transplantation (12,13).

To standardize the use of primary prophylaxis in transplant patients, we analyzed the literature related to the following transplants: liver, kidney, heart, lung, and HSCT. The IDSA (Infectious Diseases Society of America) system was used to determine the levels of evidence.

Liver transplantation (11,14-20)

Universal prophylaxis: no (CII)

Targeted prophylaxis: yes (AI)

- Fluconazole 400 mg/day for 21 days

Criterion 1 – at least one of the following risk factors: fulminant hepatitis, re-transplant requirement, post-tx hemodialysis, or the use of antibodies for rejection treatment.

Criterion 2 – at least two of the following risk factors: antibiotic prophylaxis for spontaneous bacterial peritonitis (SBP) pre-tx, reoperation, ICU admission in the 30 days before the tx, or antibiotic use in the 30 days before the tx.

Kidney transplantation

There are no studies on prophylaxis.

Prophylaxis is not recommended (DII).

Lung transplantation (12,21-24)

Universal prophylaxis: yes (AI)

- Inhaled amphotericin B deoxycholate for 3 months (50 mg + 50 ml of distilled water; 10 ml inhalation twice a day)

Targeted prophylaxis: yes, if the recipient or donor has airway colonization by Aspergillus spp. pre-tx or post-tx (associated with amphotericin B inhalation).

First choice*: 400 mg itraconazole orally for 3 months (BIII)

Second choice: IV voriconazole (6 mg/kg/day) or oral voriconazole (400 mg/day) for 3 months (CIII)

* Advised serum concentration.

Heart transplantation (22)

Prophylaxis not indicated (DII).

Hematopoietic stem cell transplant (HSCT)(10,25-28)

Universal prophylaxis: yes (AI)

Fluconazole 400 mg/day IV or oral for 100 days

Targeted prophylaxis: yes, for patients under treatment for GVHD

First option: amphotericin B deoxycholate 1 mg/kg/day (or equivalent doses of a lipidic formulation) for 100 days (CIII)

Second option: itraconazole* 400 mg/day, oral for 100 days (CIII)

Third option: EV voriconazole (6 mg/kg/day) or oral voriconazole (400 mg/day) for 100 days (CIII)

** Advised serum concentration.

Controlled and randomized studies have been registered with other azoles, but they were not standardized in the institution or perhaps they are not available in Brazil.

Pancreas transplant (29)

Universal prophylaxis: yes (CII)

Fluconazole 400 mg/day IV or VO for 7 days (surgical prophylaxis)

Targeted prophylaxis: no (DII)

Recommendations

Conflicts of interest: Edson Abdala - speaker for Bago, performs clinical research with Bristol. Sílvia Figueiredo Costa - speaker for Pfizer. Tania Mara Varejão Strabelli - speaker for Novartis, works with Novartis, performs clinical research with Merck.

ACKNOWLEDGMENTS

We thank the Clinical Directors from the Hospital das Clínicas da Faculdade de Medicina da USP for their support: Prof. Jose Otávio Costa Auler Junior, Prof. Tarcísio Eloi Pessoa de Barros Filho and Prof. Eloísa Bonfá.

Table 1

The incidence and mortality of fungal infections in patients who received a solid organ transplantation or BMT/HSCT (1,4).

Transplant	Incidence	Mortality
Liver	8-15%	50-60%
Lung	15-35%	30-75%
Kidney	3.5-6%	NR
Pancreas	9%	NR
Heart	2.2%	30%
HSCT	3.9% (AI)	50%

NR: not reported.

Tabela 1

Incidência e mortalidade das Infecções Fúngicas na população de pacientes submetidos a transplante de órgãos sólidos e TMO/TCTH [1,4].

Transplante	Incidência	Mortalidade
Fígado	8-15%	50-60%
Pulmão	15-35%	30-75%
Rim	3,5-6%	NR
Pâncreas	9%	NR
Coração	2,2%	30%
TCTH	3,9% (AI)	50%

NR: não relatado.