Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Vaccine Production01:23

Vaccine Production

Vaccine production involves a sequence of upstream and downstream processes to generate a safe and effective immunological product. It begins with cultivating microorganisms, such as viruses or bacteria, to obtain antigenic material. For viral vaccines, mammalian host cells are grown in bioreactors and subsequently infected with the target virus. The virus replicates within the host cells, which are lysed to release viral particles. This lysate is then clarified through filtration or...
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...
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...
Pharmaceutical Poisoning: Potential Scenarios01:26

Pharmaceutical Poisoning: Potential Scenarios

Pharmaceutical poisoning can occur through various channels, impacting an estimated 2 million hospitalized patients in the U.S. annually with serious adverse drug responses. These scenarios encompass both therapeutic uses, such as drug toxicity, where even standard dosages can lead to severe central nervous system depression, and non-therapeutic exposures, including accidental ingestion by children, and environmental and occupational exposures.Unintentional poisonings often involve exploratory...
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...
Vaccinations01:51

Vaccinations

Overview

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Integrated Scheduling and Capacity Planning with Considerations for Patients' Length-of-Stays.

Production and operations management·2020
Same author

Case Sequencing of Diagnostic Imaging Studies Performed Under General Anesthesia or Monitored Anesthesia Care During Nights and Weekends.

A & A case reports·2015
See all related articles

Related Experiment Video

Updated: May 19, 2026

Fabrication of Pulsatile Polymeric Microparticles Encapsulating Rabies Antigen
07:44

Fabrication of Pulsatile Polymeric Microparticles Encapsulating Rabies Antigen

Published on: May 12, 2023

The pediatric vaccine stockpiling problem.

Van-Anh Truong1

  • 1Industrial Engineering and Operations Research, Columbia University, 500 West 120th Street, New York, NY 10027, United States. vatruong@ieor.columbia.edu

Vaccine
|August 10, 2012
PubMed
Summary

Managing pediatric vaccine stockpiles is challenging due to production interruptions. This study introduces an efficient policy to optimize vaccine inventory, performing within 1% of optimal levels and reducing stock levels with multiple suppliers.

More Related Videos

Experimental Human Pneumococcal Carriage
07:47

Experimental Human Pneumococcal Carriage

Published on: February 15, 2013

Production of Near-Infrared Sensitive, Core-Shell Vaccine Delivery Platform
06:27

Production of Near-Infrared Sensitive, Core-Shell Vaccine Delivery Platform

Published on: October 20, 2020

Related Experiment Videos

Last Updated: May 19, 2026

Fabrication of Pulsatile Polymeric Microparticles Encapsulating Rabies Antigen
07:44

Fabrication of Pulsatile Polymeric Microparticles Encapsulating Rabies Antigen

Published on: May 12, 2023

Experimental Human Pneumococcal Carriage
07:47

Experimental Human Pneumococcal Carriage

Published on: February 15, 2013

Production of Near-Infrared Sensitive, Core-Shell Vaccine Delivery Platform
06:27

Production of Near-Infrared Sensitive, Core-Shell Vaccine Delivery Platform

Published on: October 20, 2020

Area of Science:

  • Operations Research
  • Public Health Policy
  • Supply Chain Management

Background:

  • The U.S. faces recurrent disruptions in pediatric vaccine production.
  • The Centers for Disease Control and Prevention (CDC) manages a national vaccine stockpile to mitigate shortages.
  • Stockpile management is complicated by limited production capacity and unpredictable interruptions.

Purpose of the Study:

  • To develop and evaluate optimal policies for managing the national pediatric vaccine stockpile.
  • To identify conditions under which a modified state-dependent base-stock policy is optimal.
  • To provide bounds for optimal decision-making in stockpile management.

Main Methods:

  • Formulation of inventory management policies for vaccine stockpiles.
  • Derivation of sufficient conditions for optimality of a modified base-stock policy.
  • Development of an efficient policy with performance bounds and simulation analysis.

Main Results:

  • An efficient policy was developed, achieving near-optimal performance (within 1% in simulations).
  • The study identified conditions for a modified state-dependent base-stock policy, decreasing with pipeline inventory.
  • Analysis showed that uniform stocking across vaccine types can be inefficient; multiple suppliers significantly reduce inventory levels.

Conclusions:

  • Optimized stockpile management policies are crucial for ensuring pediatric vaccine availability.
  • The proposed efficient policy offers a practical approach to near-optimal vaccine inventory management.
  • Diversifying suppliers can lead to substantial reductions in overall vaccine inventory requirements.