Post-Pyloric Administration of Rivaroxaban With Therapeutic Monitoring in Pediatric Cardiac Patients: Experience in 3

Joshua W Branstetter1, Sarah Woodmansee2, Jordan Foland1

  • 1Department of Pharmacy (JWB, JF, HZ), Children's Healthcare of Atlanta, Atlanta, GA.

Insights

Rivaroxaban can be safely administered via post-pyloric feeding tubes in pediatric patients with congenital heart disease (CHD) and feeding intolerance. Therapeutic drug monitoring confirmed adequate absorption and consistent serum concentrations, supporting its use in this challenging population.

Area of Science:

  • Pediatric Cardiology
  • Pharmacology
  • Thrombosis Management

Background:

  • Thromboembolism is a significant complication in pediatric patients with congenital heart disease (CHD).
  • Feeding intolerance in CHD patients complicates anticoagulation choices due to variable gastrointestinal absorption.
  • Traditional anticoagulants include heparin, enoxaparin, and warfarin.

Purpose of the Study:

  • To evaluate the efficacy and safety of rivaroxaban in pediatric patients with complex CHD and feeding intolerance requiring therapeutic anticoagulation.
  • To assess rivaroxaban absorption and serum concentrations when administered via post-pyloric feeding tubes.

Main Methods:

  • Case series reporting on 3 pediatric patients with complex CHD and feeding intolerance.
  • Administration of rivaroxaban via post-pyloric feeding tubes.
  • Therapeutic serum concentration monitoring of rivaroxaban.

Main Results:

  • All reported rivaroxaban serum concentrations were within the therapeutic reference range.
  • Three out of four measured concentrations fell within the age-related geometric coefficient of variation.
  • Successful therapeutic anticoagulation was achieved in all patients.

Conclusions:

  • Rivaroxaban demonstrates adequate post-pyloric absorption in pediatric patients with CHD and feeding intolerance.
  • Serum concentration monitoring supports the safe and effective use of post-pyloric rivaroxaban in this population.
  • This approach offers a viable anticoagulation option for CHD patients with complex feeding challenges.

Related Concept Videos

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,...
240
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...
229
Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses...
174
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...
194
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...
231
Therapeutic Drug Monitoring: Affecting Factors01:29

Therapeutic Drug Monitoring: Affecting Factors

Therapeutic Drug Monitoring (TDM) is the clinical practice of measuring specific drug levels in a patient's blood or body tissues to manage and optimize therapy. TDM is crucial for drugs with narrow therapeutic windows, like warfarin and phenytoin, where incorrect doses can lead to treatment failure or severe side effects. This monitoring ensures the dosage administered is within a safe and effective range. The factors affecting therapeutic drug monitoring include:Patient-Specific Factors:a.
175