Prevalence and Associated Factors of Anesthetic Drug Administration Error, a Web Based Crossectional Survey, 2022.

June 1, 2023 updated by: Meseret Firde, DebreTabor University

Prevalence and Associated Factors of Anesthetic Drug Administration Error Among Anesthetists Working in Teaching and Referral Hospitals of Ethiopia, a Web Based Crossectional Survey, 2022.

The operating room (OR) is a demanding and time-constrained setting, in comparison to primary care settings, where perioperative medication administration is more complicated and there is a high risk that the patient will experience a medication error.

Without consulting the pharmacist or seeking assistance from other staff members, anesthesia clinicians prepare, deliver, and monitor strong anesthetic drugs.

Study Overview

Detailed Description

The operating room (OR) is a demanding and time-constrained setting, in comparison to primary care settings, where perioperative medication administration is more complicated and there is a high risk that the patient will experience a medication error. Anesthesia clinicians prepare, deliver, and monitor strong anesthetic drugs without consulting pharmacists or seeking assistance from other staff members.

The aim of this study was to determine the prevalence of medication administration errors by anesthetists and associated factors in referral and teaching hospitals in the Amhara region of, Ethiopia.

Study Type

Observational

Enrollment (Actual)

255

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Debre Tabor, Ethiopia, 271
        • Debre Tabor University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

all volunteer anesthetists with a minimum of six months of working experience and able to respond to the questionnaire using the listed online choices.

Description

Inclusion Criteria:

  • all anesthetists with a minimum of six months of working experience, the ability to respond to the questionnaire using the listed online choices, and involvement in direct patient care to be included in the study.

Exclusion Criteria:

  • Anesthetists who were not involved in medication administration and those serving in administrative positions were excluded from the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
anesthesia professionals
anesthetists working at teaching and referral hospitals of north west Ethiopia
since this is a cross sectional observational study any form of intervention was not applicable

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prevalence of anesthetics drug administration error by anesthetists working in Amhara region, Ethiopia
Time Frame: October 1-November 30, 2022

This study aimed to determine the type, frequency, and factors that lead to medication errors in patients under anesthesia.

This study aimed to determine the type, frequency, and factors that lead to medication errors in patients under anesthesia.

This study aimed to determine the type, frequency, and factors that lead to medication errors in patients under anesthesia

October 1-November 30, 2022

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
factors associated with medication administration errors by anesthetists
Time Frame: October 1-November 30, 2022
This study aimed to determine the type, frequency, and factors that lead to medication errors in patients under anesthesia
October 1-November 30, 2022

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 1, 2022

Primary Completion (Actual)

October 20, 2022

Study Completion (Actual)

November 20, 2022

Study Registration Dates

First Submitted

June 1, 2023

First Submitted That Met QC Criteria

June 1, 2023

First Posted (Actual)

June 12, 2023

Study Record Updates

Last Update Posted (Actual)

June 12, 2023

Last Update Submitted That Met QC Criteria

June 1, 2023

Last Verified

June 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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