Sepsis-related Pediatric Acute Respiratory Distress Syndrome: A Multicenter Observational Study

Completed

• Conditions: pediatric acute respiratory distress syndrome; sepsis; pediatric; outcomes

• Registration Number: TCTR20220705008
• Lead Sponsor: Ramathibodi Hospital

Brief Summary

Sepsis-related PARDS patients had more severe illness and higher morbidities and mortality than non-sepsis PARDS patients.

Detailed Description

Not available

Study Timeline

• Study Completion: 2019-06-30
• Study Start: 2022-07-05
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 132

Inclusion Criteria

The screened patients were children 1 month to 18 years old who required intubation during the study period

Exclusion Criteria

The exclusion criteria were premature neonates with a corrected age less than 35 weeks, PARDS established outside of our centers, congestive heart failure, or perinatal-related lung disease

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
organ dysfunction 30 day %

Secondary Outcome Measures

Name	Time	Method
mortality 30 day %