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Non Invasive Positive Pressure Ventilation in Status Asthmaticus

Primary Purpose

Status Asthmaticus

Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Noninvasive positive pressure ventilation
Sponsored by
Southern Illinois University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Status Asthmaticus focused on measuring Asthma, non invasive ventilation, pediatrics, noninvasive positive pressure ventilation (NPPV)

Eligibility Criteria

1 Year - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 1-18 years old
  • Known H/O asthma
  • With status asthmaticus
  • CAS score 2-8 after one dose of systemic steroid, 1 hour of continuous albuterol and 3 doses of ipratropium bromide.

Exclusion Criteria:

  • No previous history of asthma.
  • Absence of airway protective reflexes.
  • Absence of respiratory drive.
  • Problems with clearing oral secretions.
  • Need for emergent intubation as determined by the attending physician.
  • Facial or airway anomaly or injury precluding the use of tight fitting mask.
  • Discretion of the attending physician depending on the severity of illness

Sites / Locations

  • Southern Illinois University School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

NPPV plus standard of care

Standard of care

Arm Description

Noninvasive positive pressure ventilation (NPPV) plus standard of care in the management of children admitted to the hospital with status asthmaticus

standard of care treatment in the management of children admitted to the hospital with status asthmaticus

Outcomes

Primary Outcome Measures

length of stay
Number of hours patient hospitalized in PICU

Secondary Outcome Measures

clinical asthma score
Clinical asthma score (CAS) will be recorded in 2 hour segments by clinical evaluation of 5 items-respiratory rate, inspiratory-expiratory ratio, retractions, adequacy of air exchange and wheezing-on a 3-point scale. A higher score indicates worsening respiratory status.
tolerability
Number of hours patient able to wear the NPPV mask will be recorded in 2 hour segments.
patient care costs
Actual costs accrued during PICU stay.
safety
measure of clinical monitoring parameters: Respiratory rate pH PaCO2

Full Information

First Posted
July 25, 2011
Last Updated
December 11, 2014
Sponsor
Southern Illinois University
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1. Study Identification

Unique Protocol Identification Number
NCT01403428
Brief Title
Non Invasive Positive Pressure Ventilation in Status Asthmaticus
Official Title
Effect Of Early Initiation Of Noninvasive Positive Pressure Ventilation On ICU Length Of Stay In Children With Status Asthmaticus, A Prospective Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2014
Overall Recruitment Status
Withdrawn
Why Stopped
In a pilot of early noninvasive positive pressure ventilation, the children did so well that early NPPV is now used in all children who meet criteria.
Study Start Date
June 2011 (undefined)
Primary Completion Date
January 2014 (Actual)
Study Completion Date
March 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Southern Illinois University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Status Asthmaticus is recognized as a common cause of morbidity in children in the United States (CDC). In recent years, hospitalization rates have reached an all time high. This study will evaluate the effect of early use of noninvasive positive pressure ventilation (NPPV) in children admitted to the pediatric intensive care unit (PICU) with moderate to moderately severe status asthmaticus to test the hypothesis that early initiation of NPPV plus standard of care will result in decreased length of PICU stay, significant improvement in clinical asthma score (CAS) and reduced patient care costs when compared to standard of care alone.
Detailed Description
Asthma is a common, chronic and complex disorder of the airways, with symptoms that are variable and recurring. It is characterized by bronchial hyper-responsiveness to various stimuli, airflow obstruction that is often reversible, and underlying inflammation. Conventional therapy for status asthmaticus is directed at relieving broncho-constriction, decreasing airway inflammation and clearing airway mucus. However, in some patients, maximal standard therapies are inadequate and can lead to prolonged hospitalization. Intubation and mechanical ventilation in patients with asthma is associated with significant risks. NPPV has several advantages over invasive intubation and mechanical ventilation. It leaves the upper airway intact, and avoids the risks associated with endotracheal intubation including upper airway trauma, laryngeal swelling, postextubation vocal cord dysfunction, and nosocomial infections. This study will be a prospective, open-labeled, randomized clinical trial comparing the use of NPPV plus standard of care versus standard of care alone in children admitted for status asthmaticus. A simple random numbers table will be used to assign subjects to either the NPPV plus standard of care group or standard of care alone group. In the first hour, all patients in both groups will receive a 2mg/kg dose of systemic steroid, continuous albuterol at 0.5mg/kg/hr (max of 15mg/hr) with 3 doses of 0.25-0.5 mg nebulized ipratropium bromide, and supplemental oxygen keep saturation >92%. Patients on both therapeutic arms will continue to receive 2mg/kg dose of systemic steroid per day, continuous albuterol at 0.5mg/kg/hr (max of 15mg/hr) and supplemental oxygen to keep saturation >92%. Patients randomized to the NPPV plus standard of care group will be fitted with a nasal or face mask and placed on the Respironics V60 bilevel positive airway pressure (BiPAP) Ventilator 33. Masks with gel seals at different pressure points will be used to prevent skin breakdown. To optimize patient cooperation, the mask will initially be applied manually to the patient's face. After a short adaptation period for the patient to feel comfortable, the mask will be firmly applied with head straps to minimize air leak without causing skin injury. Pressures will initially be low for comfort and acceptance while being placed on the machine. Patients randomized to the standard of care group will be placed on a similar continuous nebulizer attached to a similar oxygen blender as the ones used with the V60 unit set-up, using the same liter flow (11 liters per minute). An aerosol mask will be placed on the patient to aid in the delivery of the medication. The oxygen will be analyzed at the site of this mask with the initial set-up and any time the oxygen is decreased or increased. Data will be collected at baseline as soon as the patient is enrolled in the study. It will include: demographic variables, medical record number, age, race, gender; history and physical findings, other medical conditions, vital signs, oxygen saturation at baseline, CAS, peak flow in children >6 years of age, asthma severity prior to admission, NPPV settings, length of stay in the PICU, side effect profiles (tremor, tachycardia, agitation, nausea, nasal bridge pain, skin irritation/ulceration, gastric distension, dry eyes/mucosal dryness, sinus/ear pain, aspiration pneumonia, hypotension and pneumothorax). Each child's participation in the study will end when the child is transferred from the PICU.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Status Asthmaticus
Keywords
Asthma, non invasive ventilation, pediatrics, noninvasive positive pressure ventilation (NPPV)

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
NPPV plus standard of care
Arm Type
Experimental
Arm Description
Noninvasive positive pressure ventilation (NPPV) plus standard of care in the management of children admitted to the hospital with status asthmaticus
Arm Title
Standard of care
Arm Type
No Intervention
Arm Description
standard of care treatment in the management of children admitted to the hospital with status asthmaticus
Intervention Type
Other
Intervention Name(s)
Noninvasive positive pressure ventilation
Intervention Description
Noninvasive positive pressure ventilation (NPPV) will deliver pressurized gas through a nasal or oronasal mask, connected to a pressure targeted ventilator. NPPV provides ventilator support without the use of an endotracheal tube. Standard of care includes use of corticosteroids, oxygen, short acting β-agonist and inhaled ipratropium bromide.
Primary Outcome Measure Information:
Title
length of stay
Description
Number of hours patient hospitalized in PICU
Time Frame
baseline until transfer from PICU
Secondary Outcome Measure Information:
Title
clinical asthma score
Description
Clinical asthma score (CAS) will be recorded in 2 hour segments by clinical evaluation of 5 items-respiratory rate, inspiratory-expiratory ratio, retractions, adequacy of air exchange and wheezing-on a 3-point scale. A higher score indicates worsening respiratory status.
Time Frame
baseline until transfer from PICU
Title
tolerability
Description
Number of hours patient able to wear the NPPV mask will be recorded in 2 hour segments.
Time Frame
baseline until transfer from PICU
Title
patient care costs
Description
Actual costs accrued during PICU stay.
Time Frame
baseline until transfer from PICU
Title
safety
Description
measure of clinical monitoring parameters: Respiratory rate pH PaCO2
Time Frame
baseline until transfer from PICU

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1-18 years old Known H/O asthma With status asthmaticus CAS score 2-8 after one dose of systemic steroid, 1 hour of continuous albuterol and 3 doses of ipratropium bromide. Exclusion Criteria: No previous history of asthma. Absence of airway protective reflexes. Absence of respiratory drive. Problems with clearing oral secretions. Need for emergent intubation as determined by the attending physician. Facial or airway anomaly or injury precluding the use of tight fitting mask. Discretion of the attending physician depending on the severity of illness
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sangita Basnet, MD
Organizational Affiliation
Southern Illinois University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Southern Illinois University School of Medicine
City
Springfield
State/Province
Illinois
ZIP/Postal Code
62702
Country
United States

12. IPD Sharing Statement

Links:
URL
http://www.siumed.edu/
Description
Southern Illinois University School of Medicine website
URL
http://www.st-johns.org/childrensHospital/main/default.asp
Description
St. John's Children's Hospital
URL
http://www.lungusa.org/lung-disease/asthma/
Description
American Lung Association - asthma webpage

Learn more about this trial

Non Invasive Positive Pressure Ventilation in Status Asthmaticus

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