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PEWS Implementation in an LMIC Setting

Not Applicable
Completed
Conditions
Oncology
Interventions
Other: pediatric early warning scoring system and resuscitation curriculum
Registration Number
NCT04180306
Lead Sponsor
Boston Children's Hospital
Brief Summary

The PEWS implementation study will be undertaken with the following objectives:

1. Assess the effectiveness of implementation of PEWS and resuscitation training to identify patients at risk for clinical deterioration and to impact the frequency of clinical interventions made by treating providers on these patients.

2. Assess the effectiveness of implementation of PEWS and resuscitation training to impact time sensitive clinical interventions made on patients at risk for clinical deterioration.

3. Assess the impact of implementation of PEWS and resuscitation training on length of stay for patients admitted to the pediatric oncology ward.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1850
Inclusion Criteria
  • Patients eligible for the study are defined as pediatric patients (between birth and 12 years of age) admitted and subsequently discharged from the pediatric oncology ward in Beit Jala, Palestine and Gaza City, Palestine between March 2019 to June 2020
Exclusion Criteria
  • Patients will be excluded if they are not admitted to inpatient status. No oncology outpatients such as those in the infusion program will be included.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Inpatient pediatric oncology patientspediatric early warning scoring system and resuscitation curriculumAll patients admitted to the pediatric oncology ward will be in the cohort
Primary Outcome Measures
NameTimeMethod
Elevated Pediatric Early Warning Score (PEWS)1 year

frequency of patients whose PEWS score indicates 'risk for clinical deterioration' and receive a clinical intervention. PEWS 3 or greater (Scale is PEWS 0-6) is defined as at risk for clinical deterioration with a higher score concerning for worse clinical outcome.

Secondary Outcome Measures
NameTimeMethod
Time to antibiotics1 year

Time to antibiotics defined as time from documented vital signs/PEWS to time of antibiotic administration measured in minutes

Volume of IV fluids1 year

Volume of fluids received defined as volume given up to 60 minutes after the initiation of the first fluid bolus measured in milliliters

Time to IV fluid bolus1 year

Time to fluids defined as time from documented vital signs/PEWS to time of documented IV fluid bolus measured in minutes

Length of stay1 year

Length of stay for all patients admitted to the inpatient ward

Trial Locations

Locations (2)

Rantisi Hospital

🇵🇸

Gaza City, Palestinian Territory, occupied

Beit Jala Hospital

🇵🇸

Bethlehem, Palestinian Territory, occupied

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