Outcomes of cryptococcosis in renal transplant recipients in a less-resourced health care system.

Vinicius Ponzio, Luis Fernando Camargo, José Medina-Pestana, John Robert Perfect, Arnaldo Lopes Colombo
Author Information
  1. Vinicius Ponzio: Department of Medicine, Division of Infectious Diseases, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil. ORCID
  2. Luis Fernando Camargo: Department of Medicine, Division of Infectious Diseases, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.
  3. José Medina-Pestana: Discipline of Nephrology, Hospital do Rim Oswaldo Ramos Foundation, Universidade Federal de São Paulo, São Paulo, Brazil.
  4. John Robert Perfect: Division of Infectious Diseases, Department of Medicine, Duke University School of Medicine, Durham, NC, USA.
  5. Arnaldo Lopes Colombo: Department of Medicine, Division of Infectious Diseases, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.

Abstract

BACKGROUND: cryptococcosis is the second most common cause of invasive fungal infections in renal transplant recipients in many countries, and data on graft outcome after treatment for this infection is lacking in less-resourced health care settings.
METHODS: Data from 47 renal transplant recipients were retrospectively collected at a single institution during a period of 13 years. graft dysfunction, graft loss, and mortality rates were evaluated. Predictors of mortality and graft loss were estimated.
RESULTS: A total of 38 (97.4%) patients treated with amphotericin B deoxycholate (AMBd) showed graft dysfunction after antifungal initiation and 8 (18.2%) had kidney graft loss. graft loss within 30 days after cryptococcosis onset was significantly associated with disseminated infection, greater baseline creatinine levels, and graft dysfunction concomitant to AMBd therapy and an additional nephrotoxic condition. The 30-day mortality rate was 19.2% and it was significantly associated with disseminated and pulmonary infections, somnolence at admission, high CSF opening pressure, positive CSF India ink, creatinine levels greater than 2.0 mg/dL at admission, graft dysfunction in patients treated with AMBd and an additional nephrotoxic condition and graft loss within 30 days.
CONCLUSION: graft dysfunction was common in renal transplant recipients with cryptococcosis treated with AMBd. The rate of graft loss rate was high, most frequently in patients with concomitant nephrotoxic conditions. Therefore, the clinical focus should be on the use of less nephrotoxic lipid formulations of amphotericin B in this specific population requiring a polyene induction regimen for treatment of severe cryptococcosis in all health care systems caring for transplantation recipients.

Keywords

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Grants

  1. R01 AI028388/NIAID NIH HHS
  2. R01 AI073896/NIAID NIH HHS
  3. R01 AI093257/NIAID NIH HHS

MeSH Term

Adult
Aged
Allografts
Amphotericin B
Antifungal Agents
Brazil
Cryptococcosis
Deoxycholic Acid
Drug Combinations
Female
Graft Rejection
Humans
Invasive Fungal Infections
Kidney
Kidney Transplantation
Male
Middle Aged
Retrospective Studies
Transplant Recipients
Young Adult

Chemicals

Antifungal Agents
Drug Combinations
Deoxycholic Acid
Amphotericin B
amphotericin B, deoxycholate drug combination

Word Cloud

Created with Highcharts 10.0.0graftrenaldysfunctionlossrecipientscryptococcosistransplanthealthcareAMBdnephrotoxicless-resourcedGraftmortalitypatientstreatedamphotericinBratecommoninfectionstreatmentinfection2%within30 dayssignificantlyassociateddisseminatedgreatercreatininelevelsconcomitantadditionalconditionadmissionhighCSFtransplantationsystemBACKGROUND:CryptococcosissecondcauseinvasivefungalmanycountriesdataoutcomelackingsettingsMETHODS:Data47retrospectivelycollectedsingleinstitutionperiod13 yearsratesevaluatedPredictorsestimatedRESULTS:total38974%deoxycholateshowedantifungalinitiation818kidneyonsetbaselinetherapy30-day19pulmonarysomnolenceopeningpressurepositiveIndiaink20 mg/dLCONCLUSION:frequentlyconditionsThereforeclinicalfocususelesslipidformulationsspecificpopulationrequiringpolyeneinductionregimenseveresystemscaringOutcomes

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