Careers in Clinical Research

May 16, 2008

Google Health is now Live !!!

Filed under: EHR — clinnovo @ 10:13 pm

Google enters into the health care records race to stay in close reach to Microsoft which has launched a web-based medical record management. This system is close to the EHR post that was discussed previously on this blog.

you can get to google health at https://www.google.com/health/p/
Import of health records is a great feature, allows linking to some providers for direct import of clinical records

The search for clinicians and doctors was quite googlish, very smart search

May 14, 2008

Electronic Health Records (EHR) in clinical trials

Filed under: EHR, EMR, Enrollment — clinnovo @ 3:06 pm

Electronic Health Records (EHR) are standard instruments used to capture patient encounter data in clinical practice. They offer some key benefits in relation to clinical trials by supporting : 1. Increased patient recruitment, 2. Increased physician participation.

Study Set-up
  • Query EHR database to establish number of potential study candidates. 
  • Incorporate study manual or special instructions into EHR “clinical content”for study encounters 
Study execution
  • Incorporate study-specific data capture (just as you would do with a CRF in a clinical trial) as part of routine clinical care / clinical documentation workflow.
  • Auto-populate study data elements (for example demographics) into CRFs from other parts of the EHR database. 
  • Embed study-specific data requirements (modules not already included in the EHR) as special tabs/documentation templates using structured data entry. 
  • Implement rules/alerts to ensure compliance with study data collection requirements (EHR systems have inbuilt validation checks) 
  • Create range checks and structured documentation checks to ensure valid data entry

Study Enrollment

  • Implement study screening parameters into patient registration and scheduling. 
  • Query EHR database to contact/recruit potential candidates and notify the patient’s provider(s) of potential study eligibility. 
Submission & Reporting
  • Provide data extraction formats that support data exchange standards (for example CDISC)
  • Document and report adverse events (Note : EHRs often use ICD-9/10 coding, while CRFs would need MedDRA codes)

Theme: Silver is the New Black. Blog at WordPress.com.

Follow

Get every new post delivered to your Inbox.