The Role of Ketamine as an Adjuvant Therapy for Children With Acute Status Asthmaticus
Status Asthmaticus
About this trial
This is an interventional treatment trial for Status Asthmaticus focused on measuring ketamine, pediatric status asthmaticus
Eligibility Criteria
Inclusion Criteria:
- Pediatric patients (≥2 years and ≤ 18 years old)
Patients presenting in status asthmaticus:
- Patients with a CAS of greater than or equal to 10 on presentation that have received at least two (appropriately dosed based on weight) albuterol treatments prior to arrival
OR
- Patients with a CAS of greater than or equal to 10 that have not received treatment prior to arrival and after 1 hour of treatment per the severe asthma pathway do not have a decrease in CAS of greater than 2
OR
- Patients with a CAS above 6 but less than 10 as measured 1 hour after initiation of standard treatment per AU's moderate asthma pathway
Exclusion Criteria:
- Pregnancy
- Congestive Heart Failure or prior diagnosis of cardiovascular disease (congenital or acquired)
- Chronic lung disease outside of a previous diagnosis of Asthma
- Seizure disorder
- Liver disease
- History of hypertension greater than 95% for age
- Obstructive Sleep Apnea with AHI greater than 5
- History of allergic or serious reaction to Ketamine
- Significant history of psychiatric illness defined as any patient with a diagnosis of psychiatric illness meeting the Diagnostic and Statistical Manual of Mental Disorders V criteria (severe Autism)
Sites / Locations
Arms of the Study
Arm 1
Experimental
Ketamine Treatment
Everyone enrolled in study presenting in status asthmaticus to pediatric emergency department at Augusta University will receive a ketamine treatment, who include: Patients with a Clinical Asthma SCore (CAS) of greater than or equal to 10 on presentation and have received at least two (appropriately dosed based on weight) albuterol treatments prior to arrival OR Patients with a CAS of ≥ greater than or equal to 10 that have not received treatment prior to arrival and after receiving 1 hour of treatment per the severe asthma pathway do not have a decrease in CAS of greater than 2 OR Patients with a CAS above > 6 but less than < 10 when as measured 1 hour after initiation of standard treatment per Augusta University's moderate asthma pathway