Update on Febrile Neutropenia in Pediatric Oncological Patients Undergoing Chemotherapy

Federica Cennamo1, Riccardo Masetti2, Prisca Largo1

  • 1Pediatric Clinic, Pietro Barilla Children's Hospital, Department of Medicine and Surgery, University of Parma, Via Gramsci 14, 43126 Parma, Italy.

Insights

Febrile neutropenia (FN) in pediatric cancer patients is a serious chemotherapy complication. Early bacteremia detection and treatment are vital, but more research is needed to identify risk factors and improve diagnosis.

Area of Science:

  • Pediatric Oncology
  • Infectious Diseases
  • Hematology

Background:

  • Febrile neutropenia (FN) is a frequent and serious complication in children undergoing chemotherapy.
  • It significantly contributes to morbidity and mortality in pediatric cancer patients.
  • Prompt identification and treatment of bacteremia are critical for improving patient outcomes.

Purpose of the Study:

  • To review the epidemiology of FN in pediatric cancer patients.
  • To identify factors associated with negative outcomes.
  • To evaluate the utility of biological markers for early diagnosis and infection monitoring.

Main Methods:

  • Literature analysis of studies on FN in pediatric oncology.
  • Examination of epidemiological data, risk factors, etiology, and diagnostic markers.
  • Assessment of evidence for clinical practice guidelines and predictive tools.

Main Results:

  • Heterogeneity in studies limits definitive conclusions on risk factors.
  • Current evidence is insufficient to establish the role of specific risk factors in clinical practice.
  • Validated predictive scores and algorithms for FN management in pediatrics are lacking.

Conclusions:

  • Further research is mandatory to clarify FN epidemiology and risk factors in pediatric oncology.
  • Development of evidence-based guidelines and validated predictive tools for FN is urgently needed.
  • Improved diagnostic and monitoring strategies are essential for better patient outcomes.

Related Concept Videos

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...
20
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...
15
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,...
12
Chemotherapy-Induced Nausea and Vomiting: Neurokinin-1 Receptor Antagonists01:28

Chemotherapy-Induced Nausea and Vomiting: Neurokinin-1 Receptor Antagonists

Neurokinin 1 (NK1) receptors are distributed across the GI tract, vagal afferents, and key CNS regions including the central vomiting center and chemoreceptor trigger zone (CTZ) Chemotherapy agents stimulate enterochromaffin cells in the gastrointestinal (GI) tract to release large amounts of substance P (SP). SP is a neuropeptide released by specific sensory nerves in response to many different stressors, including those in the GI mucosa affected by chemotherapy.  SP binds and activates...
289
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...
14
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...
24