Cost Analysis of Fluconazole Prophylaxis for Prevention of Neonatal Invasive Candidiasis

Jonathan R Swanson1, Jeff Vergales, David A Kaufman

  • 1From the *Division of Neonatology, Department of Pediatrics, and †Division of Cardiology, Department of Pediatrics, University of Virginia, Charlottesville, VA.

Insights

Fluconazole prophylaxis (FP) in premature infants is cost-beneficial, preventing invasive candidiasis (IC). The cost-benefit is maintained as long as the invasive candidiasis rate remains below 2.8%.

Area of Science:

  • Neonatal Medicine
  • Pharmacoeconomics
  • Infectious Disease Prevention

Background:

  • Invasive candidiasis (IC) in neonates incurs significant healthcare costs.
  • Fluconazole prophylaxis (FP) is established to reduce IC rates in premature infants.
  • Cost-benefit analysis of FP can further justify its targeted use in high-risk neonates.

Purpose of the Study:

  • To determine the threshold rate of invasive candidiasis (IC) at which fluconazole prophylaxis (FP) becomes cost-beneficial in premature infants.
  • To evaluate the economic impact of FP in preventing IC in neonatal intensive care units.

Main Methods:

  • A decision tree cost-analysis model was employed, comparing FP costs with IC-associated costs.
  • Literature review of PubMed for studies on intravenous FP and IC rates in very low birth weight neonates.
  • Sensitivity analysis and Monte Carlo simulation were used to assess cost-effectiveness across various IC rates and patient populations.

Main Results:

  • The average cost per patient due to IC was significantly lower with FP ($785) compared to no FP ($2617).
  • FP remains cost-beneficial if the IC rate is below 2.8%.
  • Targeting infants under 1000g with FP could result in an estimated $50.3 million annual cost savings in the US.

Conclusions:

  • Fluconazole prophylaxis offers a significant cost advantage for the youngest premature infants across a wide range of invasive candidiasis rates.
  • A threshold IC rate of 2.8% can guide healthcare providers in deciding the cost-effectiveness of FP for individual high-risk neonatal intensive care unit patients.
Abstract

Related Concept Videos

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...
726
Antifungal Agents01:15

Antifungal Agents

Amphotericin B is a broad-spectrum antifungal agent that exploits structural differences between fungal and mammalian cell membranes. Its amphipathic structure—featuring a hydrophobic polyene-lactone ring and a hydrophilic region containing mycosamine and carboxylic acid groups—enables selective binding to ergosterol, a sterol predominantly found in fungal plasma membranes. This selective interaction underlies the drug’s antifungal activity, although weak binding to...
34
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...
369
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...
65