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croosh911 croosh911
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Posts: 908
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7 years ago
The Quality Improvement committee designed a global triggering tool to report the number of times an ampule of Dextrose 50% is prescribed. Once the trigger occurs through the electronic medical record which action would occur next?
1. Name of the physician would be reported
2. The name of the patient would be recorded
3. Further investigation for an adverse event would occur
4. The patient’s diagnosis would be matched for appropriateness
Correct
Textbook 
Quality and Safety for Transformational Nursing: Core Competencies

Quality and Safety for Transformational Nursing: Core Competencies


Edition: 1st
Author:
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wrote...
7 years ago
3
Rationale 1: A global triggering tool is a tool where a trigger for a mediation, discharge code, or lab result would be activated in order to call attention to a potential adverse event. The adverse event then could be analyzed. This process is more sensitive that voluntary reporting of adverse events. The name of the physician would not be a part of the analysis from a global triggering tool. (See Page 144 Global Trigger Tool)
Rationale 2: A global triggering tool is a tool where a trigger for a mediation, discharge code, or lab result would be activated in order to call attention to a potential adverse event. The adverse event then could be analyzed. This process is more sensitive that voluntary reporting of adverse events. The name of the patient may be needed for analysis but would not be recorded. (See Page 144 Global Trigger Tool)
Rationale 3: A global triggering tool is a tool where a trigger for a mediation, discharge code, or lab result would be activated in order to call attention to a potential adverse event. The adverse event then could be analyzed. This process is more sensitive that voluntary reporting of adverse events. (See Page 144 Global Trigger Tool)
Rationale 4: A global triggering tool is a tool where a trigger for a mediation, discharge code, or lab result would be activated in order to call attention to a potential adverse event. The adverse event then could be analyzed. This process is more sensitive that voluntary reporting of adverse events. This process does not include matching the patient’s diagnosis for appropriateness. (See Page 144 Global Trigger Tool)
croosh911 Author
wrote...
7 years ago
This answers my question perfectly
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