Difference between revisions of "Clinical Users~"
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| − | ; Clinical Users | + | ; [[Clinical Users~|Clinical Users]] |
| − | : These are the doctors, nurses, other clinicians, and clerks entering the data into [[Allergy~|Allergy]] Tracking . They are required to enter data pertinent for a particular [[allergy~|Allergy]]/adverse reaction. If the [[allergy~|Allergy]]/adverse reaction was observed at the site, data pertaining to any possible legal action could be tracked. This data would then be made available to users of any service using the Reporting options, thus avoiding any errors in care. Two other data elements that are tracked are the date/time that the patient chart was marked and the date/time that the patient ID band was marked, indicating the patient’s reaction to the particular [[causative agent~|Causative Agent]]. Automated mail bulletins are sent to the appropriate users when the date/time patient chart marked data field has not been recorded. | + | : These are the doctors, nurses, other clinicians, and clerks entering the data into [[Allergy~|Allergy]] Tracking . They are required to enter data pertinent for a particular [[allergy~|Allergy]]/adverse reaction. If the [[allergy~|Allergy]]/adverse reaction was [[observed~|Observed]] at the site, data pertaining to any possible legal [[action~|Action]] could be tracked. This data would then be made available to users of any service using the Reporting options, thus avoiding any errors in care. Two other data elements that are tracked are the date/time that the patient chart was marked and the date/time that the patient ID band was marked, indicating the patient’s reaction to the particular [[causative agent~|Causative Agent]]. Automated mail bulletins are sent to the appropriate users when the date/time patient chart marked data field has not been recorded. |
Latest revision as of 17:36, 17 July 2012
- Clinical Users
- These are the doctors, nurses, other clinicians, and clerks entering the data into Allergy Tracking . They are required to enter data pertinent for a particular Allergy/adverse reaction. If the Allergy/adverse reaction was Observed at the site, data pertaining to any possible legal Action could be tracked. This data would then be made available to users of any service using the Reporting options, thus avoiding any errors in care. Two other data elements that are tracked are the date/time that the patient chart was marked and the date/time that the patient ID band was marked, indicating the patient’s reaction to the particular Causative Agent. Automated mail bulletins are sent to the appropriate users when the date/time patient chart marked data field has not been recorded.
Source: Adverse Reaction Tracking User Manual Version 4.0
| This is a Glossary term from the VistA Documentation Library |
