Examining the Association Between Anxiety Severity and Required Sedative Medication Dosage in Children Undergoing Upper Gastrointestinal Endoscopy

Background: With the advancement and widespread adoption of new technologies in recent decades, there has been an increased utilization of diagnostic and therapeutic methods, such as upper gastrointestinal endoscopy (UGE). UGE is a procedure commonly employed for the diagnosis and treatment of various digestive disorders; however, it can induce anxiety and fear in both children and their parents. Objectives: This study examines the association between anxiety severity and the necessary dosage of sedative medications in children undergoing UGE. Methods: This study assessed the anxiety levels in children aged 3-7 years undergoing diagnostic endoscopy of the upper gastrointestinal tract. Before the endoscopy procedure, the intensity of anxiety was measured using the preschool anxiety score questionnaire. Sedation was achieved using propofol, with an initial dose of 2 mg/kg and an additional dose of 0.5 mg/kg if necessary. The total dose of propofol required to achieve deep sedation, as well as the duration of the endoscopy procedure, recovery time, and any sedation-related complications, were assessed and recorded for each patient. Results: The present study included 50 children (48% boys, 52% girls) with a mean age of 5 years and 1 month, who were scheduled for UGE. There was no significant correlation between the intensity of anxiety and the variables of age and gender (P of 0.20 and 0.766, respectively). However, a significant relationship was observed between the intensity of anxiety and the following factors: The need for an additional dose of propofol, duration of the endoscopy procedure, recovery time, and sedation-related complications (P<0.001, 0.027, 0.048, and 0.001, respectively). Among the sedation-related complications, irritability was the most frequently reported, occurring in 19 cases (38% frequency). Conclusions: The findings of this study suggest a significant association between pre-endoscopy anxiety levels and several factors, including propofol dosage, endoscopy duration, recovery time, and sedation-related complications. These results indicate that implementing anxiety-reducing interventions may potentially reduce the requirement for high doses of anesthetics and mitigate associated side effects.

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Journal
Journal of Pediatrics Review
Published
2025-04-01
DOI
https://doi.org/10.32598/jpr.13.2.1185.1
Primary Topic
Anesthesia and Sedative Agents
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article
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article

Examining the Association Between Anxiety Severity and Required Sedative Medication Dosage in Children Undergoing Upper Gastrointestinal Endoscopy

Roohollah Edalatkhah, Naeimeh Sadatmoosavi, Fateme Pourshamsi
1 links
Journal of Pediatrics Review
Anesthesia and Sedative Agents
article

Examining the Association Between Anxiety Severity and Required Sedative Medication Dosage in Children Undergoing Upper Gastrointestinal Endoscopy

Roohollah Edalatkhah, Naeimeh Sadatmoosavi, Fateme Pourshamsi
article en

Abstract

Background: With the advancement and widespread adoption of new technologies in recent decades, there has been an increased utilization of diagnostic and therapeutic methods, such as upper gastrointestinal endoscopy (UGE). UGE is a procedure commonly employed for the diagnosis and treatment of various digestive disorders; however, it can induce anxiety and fear in both children and their parents. Objectives: This study examines the association between anxiety severity and the necessary dosage of sedative medications in children undergoing UGE. Methods: This study assessed the anxiety levels in children aged 3-7 years undergoing diagnostic endoscopy of the upper gastrointestinal tract. Before the endoscopy procedure, the intensity of anxiety was measured using the preschool anxiety score questionnaire. Sedation was achieved using propofol, with an initial dose of 2 mg/kg and an additional dose of 0.5 mg/kg if necessary. The total dose of propofol required to achieve deep sedation, as well as the duration of the endoscopy procedure, recovery time, and any sedation-related complications, were assessed and recorded for each patient. Results: The present study included 50 children (48% boys, 52% girls) with a mean age of 5 years and 1 month, who were scheduled for UGE. There was no significant correlation between the intensity of anxiety and the variables of age and gender (P of 0.20 and 0.766, respectively). However, a significant relationship was observed between the intensity of anxiety and the following factors: The need for an additional dose of propofol, duration of the endoscopy procedure, recovery time, and sedation-related complications (P<0.001, 0.027, 0.048, and 0.001, respectively). Among the sedation-related complications, irritability was the most frequently reported, occurring in 19 cases (38% frequency). Conclusions: The findings of this study suggest a significant association between pre-endoscopy anxiety levels and several factors, including propofol dosage, endoscopy duration, recovery time, and sedation-related complications. These results indicate that implementing anxiety-reducing interventions may potentially reduce the requirement for high doses of anesthetics and mitigate associated side effects.

Journal of Pediatrics ReviewVol. 13(02)
Shahid Sadoughi University of Medical Sciences and Health Services (IR)
Openalex Percentile: Top 78%
Anesthesia and Sedative Agents
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