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Related Concept Videos

Clinical Trials01:16

Clinical Trials

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Clinical trials are prospective experimental studies conducted on humans to determine the safety and efficacy of treatments, drugs, diet methods, and medical devices. Using statistics in clinical trials enables researchers to derive reasonable and accurate conclusions from the collected data, allowing them to make wise decisions in uncertain situations. In medical research, statistical methods are crucial for preventing errors and bias.
There are four phases in a clinical trial. A phase one...
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Clinical development focuses on how the drug will interact with the human body and encompasses four key phases of clinical trials, each serving a specific purpose in assessing the safety and effectiveness of new drugs. These phases overlap and build upon one another. Phase I involves a small group of healthy volunteers (typically 20-80 individuals) or, in cases where significant toxicity is expected, patients with the targeted disease, such as cancer or AIDS. The volunteers are tested for...
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Nursing Clinical Information System01:27

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Nursing Clinical Information System (NCIS)
A Nursing Clinical Information System (NCIS) is a specialized type of healthcare information system tailored to meet the unique needs of nursing practice. It incorporates the principles of nursing informatics to streamline information management and improve the quality of care delivery.
Critical attributes of NCIS include:
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Acute Coronary Syndrome III: Diagnostic Studies01:30

Acute Coronary Syndrome III: Diagnostic Studies

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Diagnosing acute coronary syndrome or ACS begins with a thorough patient history. Notable symptoms include central, crushing chest pain radiating to the left arm, neck, jaw, or back, along with shortness of breath, sweating (diaphoresis), nausea, vomiting, dizziness, and palpitations.It is crucial to note any history of cardiac illnesses and assess risk factors, including age, gender, smoking, hypertension, diabetes, hyperlipidemia, and a sedentary lifestyle.During physical examination, vital...
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Establishment of a Clinic-based Biorepository
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The Mid-South clinical Data Research Network.

S Trent Rosenbloom1, Paul Harris2, Jill Pulley3

  • 1Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee, USA Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, USA Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Journal of the American Medical Informatics Association : JAMIA
|May 14, 2014
PubMed
Summary

The Mid-South Clinical Data Research Network (CDRN) is expanding its data network to integrate three major health systems. This initiative aims to enhance clinical data research and data sharing capabilities nationwide.

Keywords:
Clinical ResearchData StandardsHealth Information ExchangeInteroperabilityResearch Network

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Area of Science:

  • Health Informatics
  • Clinical Research Networks
  • Data Science in Healthcare

Background:

  • The Mid-South Clinical Data Research Network (CDRN) currently comprises Vanderbilt Health System (VU), Vanderbilt Healthcare Affiliated Network (VHAN), and Greenway Medical Technologies.
  • These systems collectively manage electronic medical records for millions of patients, providing a substantial data resource.

Purpose of the Study:

  • To expand the existing VU data network to incorporate VHAN and Greenway systems.
  • To develop robust data integration and interoperability across these three health systems.
  • To enhance tools for clinical data extraction and patient-reported data collection, and expand clinical decision support.

Main Methods:

  • Integrating electronic medical record data from Vanderbilt Health System, Vanderbilt Healthcare Affiliated Network, and Greenway Medical Technologies.
  • Developing and optimizing data extraction and patient-reported data collection tools.
  • Expanding clinical decision support functionalities within the network.

Main Results:

  • Anticipated robust support for comparative effectiveness research and pragmatic clinical trials within 18 months.
  • Development of the capacity to share data and health information technology tools nationally.
  • Establishment of a comprehensive data network across multiple large health systems.

Conclusions:

  • The Mid-South CDRN is poised to become a significant national resource for clinical research.
  • Enhanced data integration and tool optimization will accelerate research and improve healthcare delivery.
  • The network's expansion will facilitate broader data sharing and collaborative research initiatives.