Non-operating Room Anesthesia Experiences in Pediatric Magnetic Resonance Imaging Cases

NCT ID: NCT05423821

Last Updated: 2022-06-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

350 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-06-14

Study Completion Date

2022-07-25

Brief Summary

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In recent years, out patient anesthesia applications have been increasing for diagnostic and interventional procedures for pediatric patients. In this study, we aimed to retrospectively analyze the anesthesia applications performed in pediatric MRI cases in our hospital.

It is a retrospective study

Detailed Description

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In recent years, applications with sedation and/or general anesthesia for diagnostic purposes in pediatric cases with Magnetic Resonance Imaging (MRI) method have been increasing. Although imaging methods are useful in diagnosis and treatment, they carry minimal risk for patients. As the demands for anesthesia increase during Magnetic Resonance Imaging, questions have arisen about what can be done safely in anesthesia management. The type of anesthesia applied for Magnetic Resonance Imaging is called non-operating room anesthesia.

Cross-sectional imaging techniques such as MRI require pediatric patients to remain calm for up to one hour, and thus these patients need anesthesia. In the induction of anesthesia with agents used in anesthesia outside the operating room, the patient sleeps quickly, the vital functions are stable in its maintenance, the patient recovers quickly after anesthesia, the physical and mental activities return to normal as soon as possible after recovery, and there are no side effects such as nausea, vomiting, dizziness and pain that will delay the discharge. is necessary. Sedation or general anesthesia carries risks and can have unintended consequences if poorly managed.

Conditions

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Magnetic Resonance Imaging Contrast Media Adverse Reaction Sedation Complication

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Interventions

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Anesthesia efficacy in patients undergoing MRI

atropine will be administered when bradycardia develops, oxygen will be given if hypoxia develops

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Elective cases under the age of 18 will be included in the study between 01.01.2020 and 01.01.2022.
* Patients to undergo elective magnetic resonance imaging

Exclusion Criteria

* Magnetic resonance without anesthesia will not be included. Over the age of 18 will be excluded from study
Minimum Eligible Age

1 Day

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Yunus Emre

OTHER

Sponsor Role lead

Responsible Party

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Yunus Emre

SPECIALIST DOCTOR

Responsibility Role SPONSOR_INVESTIGATOR

Other Identifiers

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ytuncdemir-MR

Identifier Type: -

Identifier Source: org_study_id

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