CSU
Unsolicited study data message
4 trigger events
Data are entered in the clinical trials system or may reside in laboratory, pathology, radiology, pharmacy and/or other clinical applications. Most clinical trials data - clinical observations and study variables - will be communicated in OBR and OBX segments. The CSR, CSP, and CSS segments will identify the specific association these OBR and OBX have to the clinical trial. Data can be broadcast or transmitted in batch mode to study sponsors or the data management center for collaborative studies.
The general acknowledgement message as defined in Chapter 2 should be used for any acknowledgements.
Code
C09 Automated time intervals for reporting, like monthlyC10 Patient completes the clinical trialC11 Patient completes a phase of the clinical trialC12 Update/correction of patient order/result information
CSU_C09
MSHSFTUAC[PATIENT]
4 events