Skip to content

Medication Incidents in Primary Care Medicine

Medication Incidents in Primary Care Medicine: A Study by the Swiss Federal Sentinel Reporting System

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02295371
Acronym
MIPC
Enrollment
213
Registered
2014-11-20
Start date
2015-01-31
Completion date
2016-01-31
Last updated
2016-01-12

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

Conditions

Medication Incidents

Keywords

Drug therapy, Patient safety, Polydrug therapy

Brief summary

Prospective reporting of safety incidents concerning drug treatment by approximately 120 primary care physicians or pediatricians during 2015.

Detailed description

Objectives: Patient safety is a major concern in healthcare systems worldwide. Although most safety research has been conducted in the inpatient setting, evidence indicates that medical errors and adverse events pose a serious threat for patients in the primary care setting as well, since most patients receive ambulatory care. Information about frequency and outcomes of safety incidents in primary care is required to identify risks or hot spots, to prioritize them and to take the action as needed. Methods: Participants: Patients undergoing drug treatment by approximately 120 primary care physicians or pediatricians reporting to the Sentinel system. Collection of data: Questionnaires for cases, for clinical denominator data, and for physician practice specification. Study intervention: none. Primary outcome: ● To describe the type, frequency, seasonal and regional distribution of medication incidents Secondary outcomes: ● To elucidate risk factors like age, gender, poly-medication, morbidity, foreign care, hospitalization. Statistics: Descriptive statistics, logistic regression. Estimated sample size: 500. Flow chart: January 2015: Baseline physicians questionnaire. May 2015: Denominator data collection during 14 d. December 2015: Final physicians questionnaire. January to December 2015: Collection of case questionnaires / Counting of daily patient-to-physician contacts. After December 2015: Statistical Evaluation of data, publication.

Interventions

None listed

Sponsors

University of Lausanne
CollaboratorOTHER
University of Zurich
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Any erroneous event (as defined by the physician) related to the medication process interfering with normal treatment course

Exclusion criteria

* Lacking treatment effect, adverse drug reactions or drug-drug or drug-disease interactions, without detectable treatment error. * Refusal of patients to refer data to the Sentinel system.

Design outcomes

Primary

MeasureTime frameDescription
type, frequency, seasonal and regional distribution of medication incidents12 monthesDescriptives

Secondary

MeasureTime frameDescription
possible risk factors for medication incidents like age, gender, poly-medication, morbidity, previous hospitalization12 monthesLogistic regression

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026