Clinical experience with linezolid in infants and children

Silvia Garazzino1, Pier-Angelo Tovo

  • 1Department of Paediatrics, University of Turin, Regina Margherita Children's Hospital, Infectious Diseases Unit, Piazza Polonia 94, Turin, Italy.

Insights

Linezolid is a safe and effective antibiotic for treating serious Gram-positive bacterial infections in children, especially for multidrug-resistant tuberculosis. Careful monitoring is recommended for prolonged treatments to avoid resistance.

Area of Science:

  • Infectious Diseases
  • Pediatric Pharmacology
  • Antimicrobial Resistance

Background:

  • The rise of multidrug-resistant organisms necessitates novel antimicrobial agents.
  • Linezolid, an oxazolidinone, exhibits broad-spectrum activity against Gram-positive bacteria, including resistant strains.
  • Pediatric clinical experience with linezolid remains limited, with off-label use common in many regions.

Observation:

  • This paper reviews existing evidence on the clinical use of linezolid in pediatric populations.
  • Data encompasses both approved and off-label indications, evaluating efficacy, safety, and tolerability.
  • Heterogeneous clinical trials and reports were considered, acknowledging potential biases.

Findings:

  • Available literature suggests linezolid is a safe and effective treatment for severe Gram-positive bacterial infections in neonates and children.
  • Linezolid is currently reserved for pediatric patients intolerant to or failing conventional therapies.
  • Linezolid-containing regimens show promise for treating pediatric multidrug-resistant and extensively drug-resistant tuberculosis, and disseminated non-tuberculous mycobacterial infections.

Implications:

  • Careful monitoring of hematological, neurological, and drug interaction parameters is crucial, particularly for prolonged linezolid treatments in children.
  • Appropriate dosing and infection control are vital to prevent the emergence of linezolid resistance.
  • Further research is needed to explore new pediatric indications and assess long-term tolerability.

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...
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 a challenge in...
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...
Factors Affecting Drug Response: Overview01:21

Factors Affecting Drug Response: Overview

When it comes to infants and young children, they are typically administered smaller doses of medication in comparison to adults. This is primarily because their organ functions still need to fully develop, meaning their bodies are not as efficient at metabolizing or eliminating drugs. Additionally, their blood-brain barrier is more permeable than in adults. As a result, high concentrations of drugs can easily penetrate the central nervous system (CNS), potentially leading to neurological...