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Clinical Decision Support System for Quality Assurance in Potassium-Increasing Drug-Drug-Interactions

Clinical Decision Support System for Quality Assurance in Potassium-Increasing Drug-Drug-Interactions

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02020317
Enrollment
3341
Registered
2013-12-24
Start date
2014-01-31
Completion date
2015-01-31
Last updated
2015-06-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hyperkalemia

Keywords

drug interactions, Drug Monitoring, Potassium, Hyperkalemia

Brief summary

To investigate the impact of reminders for serum potassium monitoring and of hyperkalemia alerts during potassium-increasing drug-drug-interactions.

Detailed description

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.

Interventions

BEHAVIORALdecision support in potassium-inc. drug-drug-interactions

display of computer-based reminders for serum potassium monitoring and hyperkalemia alerts

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* in-patients treated with concurrent potassium-increasing drugs

Exclusion criteria

* outpatients; in-patients on wards without computerized physician order entry (i.e. patients treated in the ICU)

Design outcomes

Primary

MeasureTime frameDescription
Impact on serum potassium monitoring during potassium-increasing drug-drug-interactions1 yearRate 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

Secondary

MeasureTime frame
Frequency of potassium-increasing drug-drug-interactions ordered in the presence of hyperkalemia1 year
Frequency of transfers to the ICU during potassium-increasing drug-drug-interactions in function of the serum potassium level1 year
Frequency of hyperkalemia during potassium-increasing drug-drug-interactions1 year
Change in frequency distribution of serum potassium monitoring intervals1 year
Response of physicians to the computer-based alerts and reminders1 year
Frequency of death during potassium-increasing drug-drug-interactions in the presence or absence of hyperkalemia1 year

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026