Asthma
Conditions
Keywords
Asthma, Acute asthma exacerbation, Pediatric, Azithromycin, Macrolide, Length of Stay, Hospital Medicine
Brief summary
Asthma is a chronic lung condition in children, and often requires hospitalization for acute exacerbations. Azithromycin has been used successfully in other chronic lung diseases, including cystic fibrosis. Despite limited clinical evidence, some pediatricians use azithromycin in children hospitalized with asthma, citing either treatment of atypical pathogens or its proposed anti-inflammatory properties. This study proposes a clinical trial to determine if azithromycin will shorten length of stay in children hospitalized with acute asthma exacerbations.
Detailed description
Asthma is a chronic lung condition that accounts for over 130,000 pediatric hospitalizations nationally at a cost of almost 1.4 billion dollars. Atypical pathogens have been implicated both in initiating asthma and triggering acute asthma exacerbations. Azithromycin, a macrolide antibiotic, is known to have antibacterial activity against atypical pathogens and gram positive bacteria. More recently, macrolides have been increasingly used and effective against gram negative bacteria and inflammation in the lungs of patients with chronic respiratory illnesses. This effect may be secondary to the immunomodulatory effects macrolides possess, in addition to their anti-bacterial effects. In long-term therapy with macrolides, patients with asthma have shown improved bronchiolar hyperreactivity, spirometry, symptoms, and quality of life. However, studies of short-term treatment in the acute setting and in children are limited. Some practitioners use azithromycin in the treatment of acute asthma, despite limited data. The investigators propose a double-blind, randomized, placebo-controlled trial of azithromycin in children aged 4-12 years with persistent asthma hospitalized with acute asthma exacerbations. Children will be enrolled within 12 hours of admission and will be randomized to receive three days of either azithromycin or placebo suspension (10mg/kg/dose, max of 500mg). The primary outcome measure will be length of stay (LOS). Secondary outcome measures will include: days of school/work missed, readmission rates, return to medical care rates, recurrence of symptoms, and steroid courses. In the future, patients may also be approached to enroll in the Mechanism Subset Study a separate pilot and feasibility study which will require two blood samples and two nasal aspirate samples and will test for atypical pathogens, interleukin-8 levels, and neutrophil/eosinophil counts. The average length of stay for patients in this age range with asthma in 2011 at our institution was 3.0 days. The investigators will enroll to achieve a power of 80%, with an alpha of 0.05, which will require 107 patients in each group to detect a 16 hour (0.67 day) difference in the primary outcome, LOS. This study hypothesizes that azithromycin treatment in children hospitalized with acute asthma will decrease LOS.
Interventions
Azithromycin suspension (200mg/5mL)
Sponsors
Study design
Eligibility
Inclusion criteria
* 4-12 years of age * Admission diagnosis of asthma at the Children's Hospital at Montefiore * History of persistent asthma (as defined by National Heart, Lung, and Blood Institute)
Exclusion criteria
* Concurrent bacterial infection requiring antibiotics * Antibiotics received within previous 2 weeks * Contraindication to azithromycin (including allergy to macrolides) * Chronic lung disease other than asthma (including bronchopulmonary dysplasia, cystic fibrosis, bronchiectasis) or home oxygen requirement * Immunodeficiency (primary or acquired) * Chronic systemic steroid use * Invasive or non-invasive mechanical ventilation required acutely as result of current asthma admission * Significant cardiac co-morbidity (including hemodynamically significant cardiac disease or arrhythmia) * Liver disease (hepatitis) * Pregnancy * Seizure disorder, currently on anti-epileptic medication) * Receiving albuterol every 4 hours (q4h) at the time of enrollment * Previous enrollment in study
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Length of Stay | Admission time to discharge time (average LOS is 3 days) | Hospital length of stay |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| School Missed | One month after discharge | Days of school missed by patient at telephone follow-up phone calls at 1-week and 1-month interval after discharge |
| Readmission Rate | One month after discharge | Number of hospital readmissions for asthma at telephone follow-up phone calls at 1-week and 1-month interval after discharge |
| Work Missed | One month after discharge | Days of work missed by parent/guardian at telephone follow-up phone calls at 1-week and 1-month interval after discharge |
| Physician Office Visits | One month after discharge | Number of physician office visits for asthma symptoms since discharge at telephone follow-up phone calls at 1-week and 1-month interval after discharge |
| Recurrence of Asthma Symptoms | One month after discharge | Number of recurrences of asthma symptoms since discharge at telephone follow-up phone calls at 1-week and 1-month interval after discharge |
| Steroid Courses | One month after discharge | Number of courses of oral steroids since discharge at telephone follow-up phone call 1-month after discharge |
| Emergency Room Visits | One month after discharge | Number of emergency room visits for asthma symptoms since discharge at telephone follow-up phone calls at 1-week and 1-month interval after discharge |
Other
| Measure | Time frame | Description |
|---|---|---|
| Routine Clinical Results and Symptoms | One week after discharge | Respiratory viral panel or rapid viral testing results (if obtained as part of medical care), chest x-ray results/lab results (if obtained as part of medical care), vital signs, medications received during admission, medication side effects (diarrhea, abdominal pain, vomiting, flatulence), transfer to intensive care unit, time of wean of beta-agonists (q3h and q4h), and asthma severity (PASS score) at time of enrollment. |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Azithromycin Suspension Azithromycin suspension at 10mg/kg/dose (max 500mg)
Once daily for 3 days
Azithromycin: Azithromycin suspension (200mg/5mL) | 80 |
| Placebo Suspension Same volume as active drug
Once daily for 3 days
Placebo | 79 |
| Total | 159 |
Baseline characteristics
| Characteristic | Azithromycin Suspension | Placebo Suspension | Total |
|---|---|---|---|
| Age, Continuous | 7.5 years | 7.1 years | 7.3 years |
| Ethnicity (NIH/OMB) Hispanic or Latino | 55 Participants | 56 Participants | 111 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 25 Participants | 23 Participants | 48 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| PASS Score on enrollment | 2.35 Score on a scale STANDARD_DEVIATION 1.25 | 2.71 Score on a scale STANDARD_DEVIATION 1.29 | 2.53 Score on a scale STANDARD_DEVIATION 1.28 |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 40 Participants | 33 Participants | 73 Participants |
| Race (NIH/OMB) More than one race | 29 Participants | 32 Participants | 61 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 11 Participants | 14 Participants | 25 Participants |
| Sex: Female, Male Female | 29 Participants | 26 Participants | 55 Participants |
| Sex: Female, Male Male | 51 Participants | 53 Participants | 104 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 80 | 0 / 79 |
| other Total, other adverse events | 2 / 80 | 7 / 79 |
| serious Total, serious adverse events | 0 / 80 | 1 / 79 |
Outcome results
Length of Stay
Hospital length of stay
Time frame: Admission time to discharge time (average LOS is 3 days)
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Azithromycin Suspension | Length of Stay | 1.69 days |
| Placebo Suspension | Length of Stay | 1.86 days |
Emergency Room Visits
Number of emergency room visits for asthma symptoms since discharge at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Time frame: One month after discharge
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Azithromycin Suspension | Emergency Room Visits | 6 Participants |
| Placebo Suspension | Emergency Room Visits | 7 Participants |
Physician Office Visits
Number of physician office visits for asthma symptoms since discharge at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Time frame: One month after discharge
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Azithromycin Suspension | Physician Office Visits | 7 Participants |
| Placebo Suspension | Physician Office Visits | 5 Participants |
Readmission Rate
Number of hospital readmissions for asthma at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Time frame: One month after discharge
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Azithromycin Suspension | Readmission Rate | 1 Participants |
| Placebo Suspension | Readmission Rate | 1 Participants |
Recurrence of Asthma Symptoms
Number of recurrences of asthma symptoms since discharge at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Time frame: One month after discharge
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Azithromycin Suspension | Recurrence of Asthma Symptoms | 18 Participants |
| Placebo Suspension | Recurrence of Asthma Symptoms | 23 Participants |
School Missed
Days of school missed by patient at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Time frame: One month after discharge
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Azithromycin Suspension | School Missed | 0 Participants |
| Placebo Suspension | School Missed | 0 Participants |
Steroid Courses
Number of courses of oral steroids since discharge at telephone follow-up phone call 1-month after discharge
Time frame: One month after discharge
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Azithromycin Suspension | Steroid Courses | 8 Participants |
| Placebo Suspension | Steroid Courses | 11 Participants |
Work Missed
Days of work missed by parent/guardian at telephone follow-up phone calls at 1-week and 1-month interval after discharge
Time frame: One month after discharge
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Azithromycin Suspension | Work Missed | 0 Participants |
| Placebo Suspension | Work Missed | 0 Participants |
Routine Clinical Results and Symptoms
Respiratory viral panel or rapid viral testing results (if obtained as part of medical care), chest x-ray results/lab results (if obtained as part of medical care), vital signs, medications received during admission, medication side effects (diarrhea, abdominal pain, vomiting, flatulence), transfer to intensive care unit, time of wean of beta-agonists (q3h and q4h), and asthma severity (PASS score) at time of enrollment.
Time frame: One week after discharge