The Food and Drug Administration’s (FDA) Mini-Sentinel is a pilot program that aims to conduct active surveillance to detect and refine safety signals that emerge for marketed medical products. The purpose of this Mini-Sentinel AMI Validation project was to: (a) develop and design an abstraction and adjudication process to use when full text medical record review is required to confirm a coded diagnosis; and (b) to test this approach by validating a code algorithm for acute myocardial infarction (AMI)
Objective: Numerous studies have shown that a substantial number of patients suffer from adverse eve...
a<p>Validation was conducted amongst a coronary care unit population.</p>b<p>Eight algorithms were e...
audit of the care of patients with myocardial infarction, with little guidance on how to achieve the...
PURPOSE: To validate an algorithm based upon International Classification of Diseases, 9(th) revisio...
PURPOSE: To describe the acute myocardial infarction (AMI) validation project, a test case for healt...
BackgroundHealthcare administrative claims data hold value for monitoring drug safety and assessing ...
Though administrative databases are increasingly being used for research related to myocardial infar...
AbstractElectronic health records (EHRs) offer the opportunity to ascertain clinical outcomes at lar...
Purpose: To assess whether acute myocardial infarction (MI) diagnoses in national health registers a...
Drug-related adverse events remain an important cause of morbidity and mortality and impose huge bur...
Background:Drug-related adverse events remain an important cause of morbidity and mortality and impo...
Background: The availability of hospital cardiac services may vary between hospitals and influence c...
Purposes: We aimed to evaluate the Global Registry of Acute Cardiac Events (GRACE) and Thrombolysis ...
The U.S. Food and Drug Administration (FDA)\u27s Mini-Sentinel pilot has created a distributed data ...
Background: Drug-related adverse events remain an important cause of morbidity and mortality and imp...
Objective: Numerous studies have shown that a substantial number of patients suffer from adverse eve...
a<p>Validation was conducted amongst a coronary care unit population.</p>b<p>Eight algorithms were e...
audit of the care of patients with myocardial infarction, with little guidance on how to achieve the...
PURPOSE: To validate an algorithm based upon International Classification of Diseases, 9(th) revisio...
PURPOSE: To describe the acute myocardial infarction (AMI) validation project, a test case for healt...
BackgroundHealthcare administrative claims data hold value for monitoring drug safety and assessing ...
Though administrative databases are increasingly being used for research related to myocardial infar...
AbstractElectronic health records (EHRs) offer the opportunity to ascertain clinical outcomes at lar...
Purpose: To assess whether acute myocardial infarction (MI) diagnoses in national health registers a...
Drug-related adverse events remain an important cause of morbidity and mortality and impose huge bur...
Background:Drug-related adverse events remain an important cause of morbidity and mortality and impo...
Background: The availability of hospital cardiac services may vary between hospitals and influence c...
Purposes: We aimed to evaluate the Global Registry of Acute Cardiac Events (GRACE) and Thrombolysis ...
The U.S. Food and Drug Administration (FDA)\u27s Mini-Sentinel pilot has created a distributed data ...
Background: Drug-related adverse events remain an important cause of morbidity and mortality and imp...
Objective: Numerous studies have shown that a substantial number of patients suffer from adverse eve...
a<p>Validation was conducted amongst a coronary care unit population.</p>b<p>Eight algorithms were e...
audit of the care of patients with myocardial infarction, with little guidance on how to achieve the...