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To investigate the impact of reminders for serum potassium monitoring and of hyperkalemia alerts during potassium-increasing drug-drug-interactions.
The development of hyperkalemia during potassium-increasing drug-drug-interactions (DDIs) is associated with (i) unknown or elevated serum potassium level at onset of treatment and (ii) insufficient monitoring of serum potassium during therapy. However, potassium-increasing DDIs are frequently started despite an unknown or elevated serum potassium level, and monitoring intervals often exceed 48 hours.
This study investigates the impact of reminders for serum potassium monitoring and hyperkalemia alerts. Both reminders and alerts are displayed in the electronic patient chart of in-patients treated with potassium-increasing DDIs.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| computer-based reminders and alerts | Active Comparator | Behavioral: display of computer-based reminders for serum potassium monitoring and hyperkalemia alerts (decision support in potassium-inc. drug-drug-interactions) |
|
| no computer-based reminders or alerts | No Intervention | Behavioral: no display of computer-based reminders for serum potassium monitoring and hyperkalemia alerts |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| decision support in potassium-inc. drug-drug-interactions | Behavioral | display of computer-based reminders for serum potassium monitoring and hyperkalemia alerts |
|
| Measure | Description | Time Frame |
|---|---|---|
| Impact on serum potassium monitoring during potassium-increasing drug-drug-interactions | Rate of serum potassium monitoring intervals of < = 72 hours during potassium-increasing drug-drug-interactions in proportion to all serum potassium monitoring intervals during potassium-increasing drug-drug-interactions | 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| Frequency of hyperkalemia during potassium-increasing drug-drug-interactions | 1 year | |
| Frequency of potassium-increasing drug-drug-interactions ordered in the presence of hyperkalemia | 1 year | |
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Inclusion criteria:
Exclusion criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Juerg Blaser, PhD, Prof | University Hospital Zurich, Center for Clinical Research, Research Center for Medical Informatics | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University Hospital Zurich, Center for Clinical Research, Research Center for Medical Informatics | Zurich | Canton of Zurich | 8091 | Switzerland |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 24150532 | Background | Eschmann E, Beeler PE, Kaplan V, Schneemann M, Zund G, Blaser J. Patient- and physician-related risk factors for hyperkalaemia in potassium-increasing drug-drug interactions. Eur J Clin Pharmacol. 2014 Feb;70(2):215-23. doi: 10.1007/s00228-013-1597-2. Epub 2013 Oct 23. | |
| 23920830 | Background | Eschmann E, Beeler PE, Zund G, Blaser J. Evaluation of alerts for potassium-increasing drug-drug-interactions. Stud Health Technol Inform. 2013;192:1056. |
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| ID | Term |
|---|---|
| D006947 | Hyperkalemia |
| ID | Term |
|---|---|
| D014883 | Water-Electrolyte Imbalance |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
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| Frequency of transfers to the ICU during potassium-increasing drug-drug-interactions in function of the serum potassium level |
| 1 year |
| Frequency of death during potassium-increasing drug-drug-interactions in the presence or absence of hyperkalemia | 1 year |
| Change in frequency distribution of serum potassium monitoring intervals | 1 year |
| Response of physicians to the computer-based alerts and reminders | 1 year |