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

Drug Dosing: Infants and Children01:29

Drug Dosing: Infants and Children

120
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...
120
Aryldiazonium Salts to Azo Dyes: Diazo Coupling01:11

Aryldiazonium Salts to Azo Dyes: Diazo Coupling

3.4K
The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the para...
3.4K
Drug Delivery: Enteral Route01:18

Drug Delivery: Enteral Route

1.2K
The enteral drug administration involves three primary routes: oral, sublingual, and buccal. Oral ingestion is the most prevalent, safe, economical, and convenient method for drug administration. However, it has certain drawbacks, including limited absorption due to the drug's low water solubility or poor membrane permeability, possible emesis from GI mucosa irritation, destruction of drugs by digestive enzymes or low gastric pH, and irregular absorption along with food or other drugs.
1.2K

You might also read

Related Articles

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

Sort by
Same author

Safety and Efficacy of a Novel Aerosolized Surfactant (APC-0101) for the Treatment of Respiratory Distress Syndrome in Preterm Infants: A Randomized Phase 2b Study.

The Journal of pediatrics·2026
Same author

Pharmacologic Therapies for Patent Ductus Arteriosus in Extremely Preterm Infants.

JAMA network open·2026
Same author

Selective early medical treatment of the patent ductus arteriosus in extremely low gestational age infants: a pilot randomised controlled trial (SMART-PDA).

Archives of disease in childhood. Fetal and neonatal edition·2026
Same author

Outcomes after ventricular tachycardia ablation in patients with left ventricular assist device: a retrospective multicenter cohort study.

Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing·2026
Same author

Machine learning models for crude protein prediction in Tamani grass pastures.

Scientific reports·2026
Same author

Can N-terminal pro-brain natriuretic peptide accurately diagnose chronic pulmonary hypertension among extremely low gestational age neonates: A Retrospective Cohort Study.

Journal of perinatology : official journal of the California Perinatal Association·2025

Related Experiment Video

Updated: Dec 1, 2025

Breast Milk Enhances Growth of Enteroids: An Ex Vivo Model of Cell Proliferation
09:02

Breast Milk Enhances Growth of Enteroids: An Ex Vivo Model of Cell Proliferation

Published on: February 15, 2018

19.8K

Necrotising enterocolitis in newborns receiving diazoxide.

Laura A Prado1, Marina Castro2,3, Dany E Weisz2,3

  • 1Paediatrics, University of Toronto, Toronto, Ontario, Canada lauraalexiaprado@gmail.com.

Archives of Disease in Childhood. Fetal and Neonatal Edition
|November 11, 2020
PubMed
Summary

Diazoxide treatment for neonatal hypoglycemia may increase the risk of necrotizing enterocolitis (NEC). This study found a higher NEC incidence in diazoxide-exposed newborns, particularly premature infants.

Keywords:
intensive careneonatologypharmacology

More Related Videos

A Neonatal BALB/c Mouse Model of Necrotizing Enterocolitis
05:39

A Neonatal BALB/c Mouse Model of Necrotizing Enterocolitis

Published on: November 30, 2021

3.9K
Author Spotlight: Enhancing Understanding and Treatment Strategies with the NEC-on-a-Chip Model
06:51

Author Spotlight: Enhancing Understanding and Treatment Strategies with the NEC-on-a-Chip Model

Published on: July 28, 2023

1.6K

Related Experiment Videos

Last Updated: Dec 1, 2025

Breast Milk Enhances Growth of Enteroids: An Ex Vivo Model of Cell Proliferation
09:02

Breast Milk Enhances Growth of Enteroids: An Ex Vivo Model of Cell Proliferation

Published on: February 15, 2018

19.8K
A Neonatal BALB/c Mouse Model of Necrotizing Enterocolitis
05:39

A Neonatal BALB/c Mouse Model of Necrotizing Enterocolitis

Published on: November 30, 2021

3.9K
Author Spotlight: Enhancing Understanding and Treatment Strategies with the NEC-on-a-Chip Model
06:51

Author Spotlight: Enhancing Understanding and Treatment Strategies with the NEC-on-a-Chip Model

Published on: July 28, 2023

1.6K

Area of Science:

  • Neonatalogy
  • Pediatric Gastroenterology
  • Clinical Pharmacology

Background:

  • Gastrointestinal issues are common with diazoxide in older patients.
  • Necrotizing enterocolitis (NEC) incidence in newborns exposed to diazoxide is unknown.

Purpose of the Study:

  • To investigate the potential link between diazoxide treatment for neonatal hypoglycemia and NEC development.

Main Methods:

  • A multicenter retrospective cohort study was conducted in three Toronto NICUs.
  • Data from 55 neonates treated with diazoxide for hypoglycemia (July 2012-June 2017) were analyzed.
  • NEC incidence in exposed infants was compared to non-exposed infants using Canadian Neonatal Network data.

Main Results:

  • Seven of 55 (13%) diazoxide-exposed neonates developed NEC.
  • NEC was significantly more prevalent in diazoxide-exposed infants (OR 5.07).
  • The risk was highest in infants born at 33-36 weeks' gestation (OR 13.76), with most cases occurring within 7 days of diazoxide initiation.

Conclusions:

  • Findings suggest a possible association between diazoxide exposure and NEC in neonates.
  • Further research is needed to confirm the diazoxide-associated NEC risk in infants treated for persistent hypoglycemia.