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Related Concept Videos

Pharmacovigilance01:19

Pharmacovigilance

Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
Dosage Regimens: Designs and Approaches01:28

Dosage Regimens: Designs and Approaches

Designing a dosage regimen, which refers to the manner of drug administration, is a complex process involving the selection of drug dose, route, and frequency. This process is underpinned by pharmacokinetic parameters derived from tests and population averages. These parameters are then tailored to patient-specific variables such as diagnosis, demographics, and allergy status. Once therapy commences, therapeutic response monitoring is critical and achieved through clinical and physical...
Therapeutic Drug Monitoring: Overview and Classification01:16

Therapeutic Drug Monitoring: Overview and Classification

Therapeutic Drug Monitoring (TDM) is a clinical practice that measures specific drug levels in a patient's blood at designated intervals to ensure the drug concentration stays within a therapeutic range. This monitoring is crucial for optimizing individual dosage regimens, enhancing therapeutic efficacy, and minimizing drug-related toxicity. TDM is vital for drugs with narrow therapeutic windows, significant variability in pharmacokinetics, and a clear correlation between plasma levels and...
Drug Administration and Therapy Phases: Overview01:26

Drug Administration and Therapy Phases: Overview

Drugs, the chemical agents used in diagnosing, treating, or preventing diseases, undergo a four-phase process of development: pharmaceutic, pharmacokinetics, pharmacodynamics, and therapeutic.
The pharmaceutical phase focuses on leveraging the physicochemical properties of the drug to design and manufacture an effective product. Variants include orally administered tablets or capsules, topical creams or ointments, and parenteral-delivery solutions or emulsions.
The pharmacokinetic phase...
Therapeutic Drug Monitoring: Drug Analysis Methods01:26

Therapeutic Drug Monitoring: Drug Analysis Methods

Therapeutic Drug Monitoring (TDM) is a clinical practice that measures specific drug levels in a patient's blood or body tissues to tailor drug therapy effectively. This monitoring is critical for managing drugs with narrow therapeutic indices like digoxin and phenytoin, ensuring they are both safe and effective. For instance, monitoring theophylline levels in asthma patients involves precision and sensitivity to adjust doses according to individual responses to therapy, ensuring efficacy and...
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...

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Related Experiment Video

Updated: May 23, 2026

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System
05:10

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System

Published on: December 11, 2016

A clinical data warehouse-based process for refining medication orders alerts.

Abdelali Boussadi1, Thibaut Caruba, Eric Zapletal

  • 1Paris Descartes University (Paris 5), Paris, France. abdelali.boussadi@egp.aphp.fr

Journal of the American Medical Informatics Association : JAMIA
|April 24, 2012
PubMed
Summary
This summary is machine-generated.

This study refined medication alerts using a clinical data warehouse and information system. Retrospective analysis optimized alerts, improving patient safety and reducing overridden alerts.

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Area of Science:

  • Clinical Informatics
  • Health Data Analytics

Background:

  • Medication order alerts are crucial for patient safety but can be burdensome if not optimized.
  • Clinical information systems generate numerous alerts, necessitating refinement before full implementation.

Purpose of the Study:

  • To evaluate the use of a clinical data warehouse (CDW) and clinical information system (CIS) for refining medication order alerts.
  • To test and optimize alert parameters prior to widespread clinical deployment.

Main Methods:

  • A clinical decision rule refinement process was employed to assess alert frequencies.
  • Retrospective analysis of physicians' medication orders from a CDW was conducted.
  • Alerts for 10 renal function-dependent medications were evaluated in multiple iterations.

Main Results:

  • Initial alert frequencies for 'exceeds maximum daily dose' were 7.10% and 'under dose' were 3.14%.
  • Across iterations, 16.07% of rules were removed, 37.5% were modified, and 37.5% were newly introduced.
  • Extensive data analysis facilitated significant alert optimization.

Conclusions:

  • Coupling a CDW with a CIS enables effective testing and refinement of medication alerts.
  • Retrospective analysis of medication orders is key to optimizing alert systems for enhanced patient safety.
  • Optimized alerts minimize overridden alerts, improving clinical workflow efficiency.