What is the recommended dose of Micafungin (micafungin) for a lung transplant donor?

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Last updated: April 19, 2025View editorial policy

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From the Guidelines

Micafungin should be dosed at 100 mg intravenously once daily for antifungal prophylaxis in lung transplant donors, as this dose has been shown to be effective in preventing invasive candidiasis in high-risk patients [@7@]. For donors with suspected or confirmed fungal infections, the dose may be increased to 150 mg daily, as supported by studies such as the one by Pappas et al. [@7@], which demonstrated the efficacy of micafungin at this dose. The medication should be administered as a slow intravenous infusion over 1 hour. Duration of therapy depends on the clinical scenario, but typically continues until the donor organs are procured. Micafungin is preferred in this setting due to its broad-spectrum activity against Candida and Aspergillus species, which are common pathogens in lung transplantation, as noted in the guidelines by the Infectious Diseases Society of America 1. It has minimal drug interactions compared to azole antifungals, making it safer in the complex donor management setting. Micafungin also has good lung tissue penetration and a favorable safety profile with minimal renal or hepatic toxicity, as demonstrated in studies such as the one by Ostrosky-Zeichner et al. [@6@]. Dose adjustment is not typically required for renal impairment, though moderate hepatic impairment may warrant consideration of dose reduction to 100 mg daily if higher doses are being used. Some key points to consider when using micafungin in lung transplant donors include:

  • The importance of administering the medication as a slow intravenous infusion over 1 hour to minimize the risk of adverse reactions
  • The need to monitor patients closely for signs of fungal infection, such as fever, cough, and shortness of breath
  • The potential for drug interactions with other medications, such as sirolimus and tacrolimus, which are commonly used in transplant patients 1.

From the FDA Drug Label

The FDA drug label does not answer the question.

From the Research

Micafungin Dose for Donor on Lung Transplant

  • The optimal dose of micafungin for lung transplant donors is not explicitly stated in the provided studies 2, 3, 4, 5, 6.
  • However, study 5 mentions that living-donor liver transplant recipients received intravenous micafungin 100 mg/day, which may serve as a reference point.
  • Study 4 notes that micafungin is approved for the treatment of invasive candidiasis and as prophylactic treatment to prevent Candida infections in hematopoietic stem cell transplant recipients, but does not specify a dose for lung transplant donors.
  • Study 3 compared micafungin with fluconazole as prophylaxis against invasive fungal infections in hematopoietic stem cell transplant recipients, but does not provide information on lung transplant donors.
  • Study 2 evaluated targeted versus universal prophylaxis for the prevention of invasive fungal infections following lung transplantation, but does not mention the specific dose of micafungin used.
  • Study 6 conducted a meta-analysis of randomized controlled trials to examine the efficacy and safety of micafungin for invasive candida infections, but does not provide information on lung transplant donors.

Key Findings

  • Micafungin has been shown to be effective in preventing invasive fungal infections in various patient populations, including hematopoietic stem cell transplant recipients 3, 4, 6.
  • The drug has a good safety and tolerability profile, with an efficacy at least comparable to other antifungal agents 6.
  • However, the optimal dose and regimen of micafungin for lung transplant donors remain unclear due to the lack of specific studies on this population.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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