NiPPV in the Treatment of Acute Asthma Exacerbations

Overview

Study Summary: Title: A Randomized Controlled Trial of Noninvasive Positive Airway Pressure in the Pediatric Emergency Department for the Treatment of Acute Asthma Exacerbations Principal Investigator: Thomas J. Abramo, MD Hypothesis: For acute moderate to severe pediatric asthma exacerbations the use of NIPPV/BiPAP, in conjunction with current standard of care therapies, will lead to a more rapid improvement in patient ventilation, faster resolution of respiratory distress and result in improved ventilatory parameters, secondary outcomes and pediatric asthma scores. Study Design: Prospective, randomized controlled trial Study Duration: This study will be conducted over a 36 month period. Sample Size: 240 subjects Population: Children ages 2-17 years of age presenting to the ED with Acute asthma exacerbation and a Pediatric Asthma Score (PAS) ≥ 8. Synopsis: Eligible subjects will be randomized to either a control group or study groups. The study groups will be either a NIPPV/BiPAP group. The subjects in the study groups will continue to receive all standard of care therapies per the asthma severity protocols. All nebulized therapies will be given through the NIPPV circuit. Patients will be assessed by the pediatric asthma score (PAS), measured respiratory parameters, volumetric end tidal carbon dioxide monitoring and measured cardiac parameters. Objectives: A. Evaluate if the use of NIPPV/BiPAP in conjunction with traditional inhaled beta-agonists improves the outcome in pediatric patients with acute moderate to severe asthma in the acute setting. B. Describe the physiology of NIPPV/BiPAP by measuring cardiac parameters in children randomized to a NIPPV group. C. Monitor safety of NIPPV/BiPAP use for acute asthma exacerbations in children. Safety A.: The study must be IRB approved. B.: Appropriate consent and assent documents will be obtained prior to enrolling the subject in the study. C.: A clear safety plan including DSMB will be established to monitor for adverse events. D.: Confidentiality will be ensured for all subjects enrolled in the study.

This study is a prospective and randomized clinical trial to investigate the utility of BiPAP therapy for the pediatric patient in an acute moderate to severe asthma exacerbation. The study will be conducted in the pediatric emergency department at Arkansas Children's Hospital. Patients between 2-17 years old will be identified to participate based on the past medical history, history of present illness and PAS and the consent process will begin immediately. All patients will be started on standard of care therapies including continuous albuterol and atrovent aerosols, intravenous corticosteroids, intravenous magnesium sulfate and a normal saline fluid bolus. Additional therapies with subcutaneous epinephrine or terbutaline will be given at the discretion of the treating physician in the first 20 minutes. Further escalation of asthma therapy, for example administration of IV bronchodilators, ketamine, terbutaline and/or epinephrine will be at the discretion of the treating physician. The history of present illness, past medical history, triage information and initial physical exam information will be collected by the study investigator in the first hour and marked on the data sheet. Once consented, participants will be randomized to one of two groups by selection of an opaque folder by the study investigator. A PAS will be assigned at 1 hour after only having received traditional standard of care therapies and before placing the subject on the therapy determined by the randomization. If the child receives a score of 7 or less, he/she will not be placed on NIPPV; however, they will be analyzed in this group based on intention to treat. i. Group #1: This group will receive all standard of care therapies as per the pediatric ED Asthma Severity Protocol. Will be referred to as the control group. ii. Group #2: This group will receive all standard of care therapies as per the pediatric ED Asthma Severity Protocol. All nebulized treatments will be given via the NIPPV/BiPAP machine via the Servo i Ventilator. The treating PED Attending and treating PED respiratory therapist will be blinded to the BiPAP/NIPPV settings during the study period. The PED clinical trial research assistant and in conjunction with one of the study investigators will adjust the BiPAP settings in concert with the treating physician. The discussion will be about either increasing or decreasing the IPAP or EPAP not the true number changes to keep it blinded, will be as follows: The inspiratory positive airway pressure (IPAP) will be started at 10 cm H2O for all patients. The patient will be observed clinically by a PED respiratory therapist in conjunction with the treating pediatric ED attending and/or fellow. The IPAP will be increased as needed by 2 cm H2O up to a maximum IPAP of 16 cm H2O for patients 2-6 years of age, 20 cm H2O for patients 7-12 years of age, and 24 cm H2O for patients older than 12 years. The expiratory positive airway pressure (EPAP) will be set at 5 cm H2O. If the IPAP settings are maximized based on age and the respiratory distress score continues to be 5 or greater, the EPAP can be increased by 1 cm H2O to a maximum of 8 cm H2O for all patients less than 12 years and 10 cm H2O for all patients older than 12 years. The I:E setting will be 1.75 seconds. Optimal settings for each participant should be achieved within 20 minutes of initiation of BiPAP and respiratory distress scores should recorded at least every 5 minutes or with every BiPAP settings change during this period. Pediatric asthma scores will continue to be recorded at least every 30 minutes or with every physician suggested NIPPV ventilator setting change for an 8 hour period. Furthermore, the NIPPV ventilator, Servo i ventilator, has volumetric end tidal CO2 monitoring capabilities and will record ventilatory data in this NIPPV/BiPAP group and will be compared to other study groups. The subjects will remain in the study for minimum of 4 hrs NIPPV therapy and total of 8 hours unless clinically still needing the NIPPV therapy. The first hour they will all receive the same standard therapies, followed by 7 hours of the therapies from the group in which they were randomized. Each 30 minutes in the study, the subject will be assessed by treating PED/PICU attending as to whether to continue the patient on the study arm, switch to a rescue arm or discontinue the patient from the study. This reassessment will be facilitated by the study investigator via a direct discussion with the treating attending physician. Furthermore, every 30 minutes the treating RT, treating PED attending or fellow, or study investigator will perform a PAS. Based on the PAS, the treating PED attending will be asked if patient needs further adjustment of the EnVe or continue present therapy. Once a subject in the NIPPV arm reaches a PAS of less than or equal to 7, the NIPPV settings may be weaned per the ACH PED NIPPV/BiPAP weaning protocol. i. Rescue Arm A: If at any point during the treatment it is deemed medically necessary by the treating PED attending that a subject from the control arm, Group 1, requires an escalation of therapy, they may be moved from the group to the NIPPV/BiPAP group, Group 2, or be removed from the study i.e. if intubated. ii. Rescue Arm B: If at any point during the treatment it is deemed medically necessary by the treating PED attending that a subject from a NIPPV/BiPAP group,Group 2, is not tolerating NIPPV they may be removed from the study. Patients may not tolerate NIPPV due to agitation, vomiting or need for escalation of care. Additionally, in an attempt to better understand the physiology of NIPPV/BiPAP parameters of cardiac output, aortic flow and pulmonary flow, will be measured using the USCOM. This will assist us in understanding the physiological effects of the setting choices. Subjects in Group 2 will be kept on the NIPPV machine for 4 hours minimum, unless the PED or PICU treating attending deems the patient has dramatically improved to take off the machine. The study investigator will collect information regarding medications given and any complications. At the end of the 8 hour study period, a PAS score will be calculated, and the study investigator will ask the PED or PICU treating attending whether to continue present therapy or switch to another therapy. After the study time has completed, the study investigator will collect information such as PED/PICU diagnosis, disposition from PED/PICU and related information based on disposition, length of hospital stay and 72 hour returns from PED and mark it on the data sheet. VII. Selection and enrollment of subjects Inclusion criteria 2-17 years old For subjects 3 years and older, a known history of asthma as diagnosed by the PCP or per the ACH problem list For children ages 2-3 years, four or more episodes of wheezing in the past year that lasted more than 1 day and affected sleep AND one of the following: parental history of asthma, a physician diagnosis of atopic dermatitis, or evidence of sensitization to aeroallergens Acute asthma exacerbation Pediatric Asthma Score (PAS) ≥ 8 Parents willing and able to sign consent Children over the age of 6 willing to provide assent Exclusion criteria History of congenital heart disease, chronic respiratory disease including bronchopulmonary dysplasia, cystic fibrosis, pulmonary hypertension or any chronic lung disease other than asthma History of sickle cell disease Recently diagnosed pneumonia Current tracheostomy, on home ventilator or home oxygen requirement Recent diabetic ketoacidosis Requiring immediate intubation Weight less than 5 kilograms Any contraindication to BiPAP use including altered mental status, recent bowel surgery, intractable vomiting, inability to protect airway A history of prematurity of ≤ 30 weeks gestation N/A