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Related Concept Videos

What is Variation?01:14

What is Variation?

Apart from the measures of central tendency, distribution, outliers, and the changing characteristics of data with time, an important characteristic of any data set is its variation or spread. In some data sets, the data values are concentrated closely near the mean; in others, the data values are more widely spread out from the mean.
The range, standard deviation, standard error, and variance are the different measures of variation.
Range: The range is the difference between its maximum and...
Expected Value01:15

Expected Value

The expected value is known as the "long-term" average or mean. This means that over the long term of experimenting over and over, you would expect this average. The expected average is represented by the symbol μ. It is calculated as follows:In the equation, x is an event, and P(x) is the probability of the event occurring.The expected value has practical applications in decision theory.This text is adapted from Openstax, Introductory Statistics, Section 4.2 Mean or Expected Value and...
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Ovarian Cycle

The menstrual cycle includes a critical component known as the ovarian cycle, which undergoes two main phases each month—the follicular phase and the luteal phase. The follicular phase is variable and averaging around 14 days. Ovulation, triggered by a surge in luteinizing hormone (LH), marks the transition between the two phases. The second phase, the luteal phase, is relatively consistent, lasting approximately 14 days, and is marked by the activity of the corpus luteum. While a cycle length...
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Bioequivalence: Overview

Pharmaceutical equivalents, by definition, are drug products with the same active ingredient in the same quantities, encapsulated in identical dosage forms, and intended for the same administration routes. These pharmaceutical equivalents are deemed bioequivalent if the bioavailability of the active entity in the drug preparations is similar. Moreover, pharmaceutical equivalents demonstrating bioequivalence are also regarded as therapeutically equivalent. This means that when used as directed,...
Equivalence: In Vitro and In Vivo Bioequivalence01:17

Equivalence: In Vitro and In Vivo Bioequivalence

Bioequivalence studies are crucial in evaluating whether new drugs can match an approved one regarding pharmacological effects and clinical performance. These studies test if drugs, despite different dosage forms, share identical plasma concentration-time profiles. Three types of equivalence are central to these studies: chemical, pharmaceutical, and therapeutic. Chemical equivalence indicates that two or more drug products contain identical active ingredients in equal amounts. Pharmaceutical...
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In Vitro Fertilization

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Fertility Preservation Through Oocyte Vitrification: Clinical and Laboratory Perspectives
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Published on: September 16, 2021

Primovist, Eovist: what to expect?

Bernard E Van Beers1, Catherine M Pastor, Hero K Hussain

  • 1Laboratoire d'Imagerie Physiologique et Moléculaire de l'Abdomen et Service de Radiologie, Université Paris Diderot, Sorbonne Paris Cité, INSERM UMR 773, Hôpitaux Universitaires Paris Nord Val de Seine, Beaujon, Clichy, France. bernard.van-beers@bjn.aphp.fr

Journal of Hepatology
|April 17, 2012
PubMed
Summary

Gadolinium ethoxybenzyl dimeglumine (Gd-EOB-DTPA) is a liver-specific MRI contrast agent. It enhances liver lesion detection and characterization by providing both dynamic and hepatobiliary phase information.

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Area of Science:

  • Radiology
  • Hepatology
  • Medical Imaging

Background:

  • Liver-specific contrast agents improve diagnostic accuracy in liver imaging.
  • Gadolinium ethoxybenzyl dimeglumine (Gd-EOB-DTPA) offers unique hepatobiliary excretion properties.

Purpose of the Study:

  • To evaluate the diagnostic utility of Gd-EOB-DTPA in liver imaging.
  • To highlight the advantages of Gd-EOB-DTPA over non-specific contrast agents.

Main Methods:

  • Intravenous administration of Gd-EOB-DTPA.
  • Assessment of contrast distribution during dynamic and hepatobiliary phases.
  • Evaluation of hepatocyte uptake via OATP1B1/B3 and biliary excretion via MRP2.

Main Results:

  • Gd-EOB-DTPA shows similar distribution to non-specific agents in dynamic phases.
  • Significant hepatobiliary phase enhancement improves detection/characterization of focal and diffuse liver diseases.
  • Enhanced detection of metastases, cirrhotic nodules, and early hepatocellular carcinomas.

Conclusions:

  • Gd-EOB-DTPA-enhanced MRI provides unique anatomic and functional information unattainable with non-specific agents.
  • This agent improves the diagnosis of various liver conditions, including cancer.
  • Further research is needed to fully establish its potential in quantitative liver assessment.