Effects of Preoperative Child and Parental Anxiety on Emergence Agitation

Ondokuz Mayıs University

Status: Completed

Conditions: Emergence Agitation

Treatments: Other: No intervention - observational study

Study type: Observational

Funder types: Other

Identifiers

NCT07486427

EA140324

Details and patient eligibility

About

Investigation of the effect of preoperative parental anxiety and sociodemographic characteristics on emergence agitation in patients undergoing pediatric adenotonsil surgery

Full description

Adenotonsillectomy, with or without adenoidectomy, is one of the most commonly performed surgical procedures worldwide in pediatric patients. Despite its widespread application, this surgery presents significant challenges for both surgeons and anesthesiologists due to the associated increased risks of morbidity and mortality. Safe administration of anesthesia is critical in avoiding complications and alleviating not only patient distress but also parental anxiety.

Preoperative anxiety in pediatric patients is influenced by several factors, including young age and parental concerns. Additionally, longer surgery durations (>30 minutes) and previous hospitalizations are known risk factors for heightened anxiety. Several previous studies have explored the relationship between parental stress levels and postoperative complications, including emergence agitation and pain. Research indicates a significant association between parental anxiety and postoperative behavioral disturbances in children.

The primary objective of this study is to evaluate the impact of preoperative parental anxiety and sociodemographic characteristics on the incidence and severity of emergence agitation in pediatric patients undergoing adenotonsillectomy.

Enrollment: 99 patients

Sex: All

Ages: 3 to 7 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients aged 3-7 years who will undergo adenoidectomy, adenotonsillectomy or tonsillectomy surgery and their parents
• Patients with ASA (American Society of Anesthesiologists) physical status I/II

Exclusion criteria

• Patients with ASA score III and above
• Conditions that prevent communication with the patient or parent (mental retardation, disability etc.)
• Patients in whom routinely scheduled anesthetic and analgesic drugs cannot be administered due to allergy or contraindication
• Patients who have previously received anesthesia or entered the operating room for a surgical procedure

Trial design

99 participants in 1 patient group

observational

Description:

No intervention - cross sectional analysis

Treatment:

Other: No intervention - observational study