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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, compared...
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: 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...
Rh Blood Group01:19

Rh Blood Group

The Rhesus (Rh) antigen is crucial in determining blood groups and ensuring compatibility during blood transfusions.
Oxygen Transport in the Blood01:27

Oxygen Transport in the Blood

Hemoglobin (Hb) is a crucial molecule in the human body, consisting of four polypeptide chains, each bound to an iron-containing heme group. This unique structure enables hemoglobin to bind to oxygen, with each molecule capable of combining with four molecules of oxygen, leading to rapid and reversible oxygen loading. When fully loaded with oxygen, it is called oxyhemoglobin, while hemoglobin that has released oxygen is called reduced hemoglobin or deoxyhemoglobin. As hemoglobin binds oxygen,...
Hemoglobin01:24

Hemoglobin

Hemoglobin is a globular protein made up of four subunits. Two of these subunits are alpha chains, and the other two are beta chains. Each subunit contains a molecule of heme, which has an iron atom and can bind to oxygen. When an oxygen molecule binds to one heme group, it changes the shape of hemoglobin, making it easier for the other heme groups to bind oxygen as well.
When all four heme groups are bound to oxygen, the resulting molecule is called oxyhemoglobin. As a result, arterial blood...

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Related Experiment Video

Updated: Jun 5, 2026

Development of a Neonatal Piglet Acute Lung Injury Model Recreating the Early Environment of Preterm Infant Lungs
08:58

Development of a Neonatal Piglet Acute Lung Injury Model Recreating the Early Environment of Preterm Infant Lungs

Published on: October 31, 2025

'Haptoglobin concentrations in preterm and term newborns'.

S Chavez-Bueno1, J A Beasley, J M Goldbeck

  • 1Department of Pediatrics, Section of Pediatric Infectious Diseases, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA. Susana-Chavez-Bueno@ouhsc.edu

Journal of Perinatology : Official Journal of the California Perinatal Association
|January 22, 2011
PubMed
Summary

Systemic haptoglobin (HPT) is detectable from birth in preterm and term newborns. HPT levels increase in newborns with bacteremia, suggesting its clinical utility in diagnosing neonatal sepsis.

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Last Updated: Jun 5, 2026

Development of a Neonatal Piglet Acute Lung Injury Model Recreating the Early Environment of Preterm Infant Lungs
08:58

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Published on: October 31, 2025

Biochemical Measurement of Neonatal Hypoxia
13:13

Biochemical Measurement of Neonatal Hypoxia

Published on: August 24, 2011

Transcutaneous Microcirculatory Imaging in Preterm Neonates
06:27

Transcutaneous Microcirculatory Imaging in Preterm Neonates

Published on: December 31, 2015

Area of Science:

  • Neonatal Medicine
  • Biochemistry
  • Clinical Diagnostics

Background:

  • Haptoglobin (HPT) is a protein involved in hemoglobin binding.
  • Understanding HPT dynamics in newborns is crucial for diagnosing inflammatory conditions.

Purpose of the Study:

  • To quantify systemic haptoglobin (HPT) concentrations from birth in preterm (PT) and term (T) neonates.
  • To compare HPT levels in healthy newborns versus those with bacteremia.

Main Methods:

  • HPT was measured via enzyme-linked immunosorbent assay in PT and T newborns.
  • Samples were collected at birth, days 2-4, and 1-2 weeks; bacteremic newborns were also assessed.

Main Results:

  • HPT was consistently detectable from birth in both PT and T neonates.
  • HPT concentrations significantly increased in newborns aged 2-4 days compared to birth.
  • Bacteremic newborns exhibited significantly higher HPT levels than non-infected newborns.

Conclusions:

  • Haptoglobin is a reliable biomarker detectable from birth in neonates.
  • Elevated HPT levels in newborns correlate with bacteremia.
  • HPT shows potential clinical utility for evaluating neonatal sepsis.