Safety of micafungin in infants: insights into optimal dosing

Simon Ascher1, Phillip Brian Smith, Daniel K Benjamin

  • 1Duke University, Department of Pediatrics, 2400 Pratt St., Durham, NC 27715, USA. danny.benjamin@duke.edu

Abstract

Insights

Micafungin is a safe and effective treatment for invasive candidiasis in neonatal intensive care units (NICUs). A 10 mg/kg/day dose is recommended for both term and preterm infants, showing good tolerability.

Area of Science:

  • Neonatal Medicine
  • Pediatric Infectious Diseases
  • Pharmacology

Background:

  • Invasive Candida infections pose significant mortality risks in neonatal intensive care units (NICUs).
  • Micafungin presents a promising antifungal treatment option for infants, supported by its established safety in older populations.
  • Assessing micafungin safety is crucial for vulnerable premature infants with complex medical conditions.

Purpose of the Study:

  • To review existing literature on micafungin's safety profile in infants.
  • To provide dosing recommendations for treating invasive candidiasis in the NICU setting.

Main Methods:

  • A comprehensive Medline literature search was conducted up to September 2010.
  • Search terms included 'micafungin', 'safety', 'antifungal', 'candidiasis', 'drug toxicity', 'infant, premature', and 'infant, newborn'.
  • The review focused on studies evaluating micafungin's safety and efficacy in neonates.

Main Results:

  • Limited safety data are available for micafungin in the infant population.
  • Higher doses of micafungin demonstrated safety and good tolerability in the studied infants.

Conclusions:

  • Micafungin at a dose of 10 mg/kg/day is a viable option for invasive candidiasis in neonates.
  • This dosing regimen is recommended for both term and preterm infants in the NICU.
  • Further research is warranted to expand the safety data for micafungin in infants.

Related Concept Videos

Pharmacokinetics in Pediatric Patients: Drug Excretion01:26

Pharmacokinetics in Pediatric Patients: Drug Excretion

In pediatric medicine, understanding the renal function and drug elimination nuances is crucial for administering safe and effective treatments. Newborns, in particular, display markedly slower renal functions than adults, profoundly affecting how drugs are cleared from their bodies. This slower drug clearance requires clinicians to extend the dosing intervals for many medications to prevent drug accumulation and toxicity while ensuring therapeutic efficacy.One key area where these adjustments...
Drug Dosing: Infants and Children01:29

Drug Dosing: Infants and Children

Pediatric patient dosages diverge from adults due to disparities in body surface area, total body water, and extracellular fluid per kilogram of body weight. The dosing regimen considers the variations in pharmacokinetics and pharmacology across distinct age groups, encompassing preterm newborns, infants, young children, older children, and adolescents. Calculation of pediatric patient doses is predicated on determining body surface area, which exhibits a superior correlation with the child's...
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption01:23

Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption

Understanding the physiological differences in the pediatric population is crucial for effective pharmacotherapy. Neonates, infants, and children exhibit significant variations in gastric pH, gastric emptying time, intestinal transit time, and biliary function. These variations profoundly affect oral drug absorption, necessitating a nuanced approach to pediatric dosing.Neonates present with a unique physiological profile, having a gastric pH greater than 4 and faster and more irregular gastric...
Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations01:15

Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations

Gentamicin, an aminoglycoside antibiotic, is commonly administered via intermittent intravenous infusion to treat severe infections. An intermittent one-hour infusion of gentamicin, administered at eight-hour intervals, allows for precise control of plasma drug concentrations, minimizing toxicity while ensuring therapeutic efficacy. Pharmacokinetic principles govern the dynamics of plasma concentrations and can be mathematically described using specific equations.The plasma drug concentration...
Pharmacokinetics in Pediatric Patients: Drug Distribution01:17

Pharmacokinetics in Pediatric Patients: Drug Distribution

Drug distribution in the pediatric population exhibits unique challenges and considerations due to the physiological differences between children, particularly neonates and infants, and adults. A crucial aspect of pediatric pharmacology is understanding how these differences impact the pharmacokinetics of various drugs, necessitating age-specific dosing strategies to ensure efficacy and safety.Neonates and infants have a higher total body water content, ~75%–90% of their body weight, compared...
Impact of Pharmacokinetic–Pharmacodynamic Models: Regulatory Decisions01:15

Impact of Pharmacokinetic–Pharmacodynamic Models: Regulatory Decisions

PK–PD modeling has significantly influenced FDA regulatory decisions, particularly drug approval, dosage optimization, and labeling. These models integrate pharmacokinetics (PK) and pharmacodynamics (PD) to predict drug behavior and effects, aiding in optimizing dosing regimens and enhancing the probability of clinical trial success.One notable example is Nesiritide (Natrecor®), a recombinant human brain natriuretic peptide for treating acute decompensated congestive heart failure (CHF).