The Incidence of Artifacts in the Anesthesia Information Management System Database.

To Evaluate the Incidence of Artifacts in the Locally Developed AIMS Database.

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03814941

Enrollment

Registered

2019-01-24

Start date

2021-05-01

Completion date

2022-12-31

Last updated

2023-03-15

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

Conditions

Artifacts, Integrated Advanced Information Management Systems

Keywords

Artifacts, anesthesia information management system

Brief summary

The purpose of the study is to evaluate the incidence of artifacts in the developed AIMS database

Detailed description

At first, the authors evaluated the accuracy of the traditional, manually completed paper-based documentation, which sets a benchmark for the accuracy that the electronic documentation and database provides. At the second portion, the investigators used the paper-based documentation as a standard to compare the electronic documentation. The incidence of artifact was double checked by two investigators. At the third portion, the authors calculated the artifact incidence in the AIMS database, using paper based and electric document anesthesia records as the standard respectively.

Interventions

OTHERpaper-based anesthesia record

to evaluate the incidence of artifacts in the AIMS database by paper-based anesthesia record

OTHERelectronic documents

to evaluate the incidence of artifacts in the AIMS database by electronic documents anesthesia record

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 85 Years

Healthy volunteers

Yes

Inclusion criteria

* patient undergo general or regional anesthesia * elective surgery

Exclusion criteria

* emergency operation

Design outcomes

Primary

Measure	Time frame	Description
percentage of artifacts	intraoperative (from the beginning to the end of anesthesia record)	to evaluate how many percentage of artifacts for each of the included parameters

Secondary

Measure	Time frame	Description
deviating values	intraoperative (from the beginning to the end of anesthesia record)	to calculate the number of values deviating from the predefined baseline value
percentage of devotional artifacts	intraoperative (from the beginning to the end of anesthesia record)	to evaluate how many percentage of the deviations are artifacts
episodes of artifacts	intraoperative (from the beginning to the end of anesthesia record)	to find out the average of number of episodes across each artifact
causes of artifacts	intraoperative (from the beginning to the end of anesthesia record)	to find out the cause of the artifact and respective percentage

Countries

Taiwan

Outcome results

None listed

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