Tuğba Yeşilyurt Doğu
Istanbul, Istanbul, Fatih, 34098, Turkey (Türkiye)
NCT Number: NCT05852899
This study aimed to evaluate preoperative risk factors in pediatric patients and to determine their effectiveness in predicting intensive care unit admission within 72 hours. The study also aimed to better define the pediatric population and identify factors associated with perioperative risk.
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Notify Me0 year–17 year
All sexes
Observational
Istanbul, Istanbul, Fatih, 34098, Turkey (Türkiye)
The aim of this study was to evaluate preoperative risk factors and determine their effectiveness in predicting ICU admission after emergency or elective surgery in pediatric patients . To achieve this aim, data such as gender, age, height, weight, history of prematurity, post-conceptional week, ASA physical status (ASA-PS), comorbidites, history of previous anesthesia, type of surgery, tumor surgery, chemotherapy and radiotherapy history, surgical risk classification, and difficult airway were recorded.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Within 72 hours after surgery
Number of participants requiring admission to the pediatric intensive care unit (PICU) within 72 hours after surgery. PICU admission was recorded as a binary outcome (yes/no).
Time frame: postoperative follow-up ( in 72 hours)
Number of participants of Postoperative Pediatric Intensive Care Unit admission
Istanbul University - Cerrahpasa
Other
Preoperative Risk Factors for ICU Admission in Children
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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