Asthma is a problem that affects many children and affects their physical health in addition to having a social and financial burden on individuals, families and healthcare systems. In our pediatric emergency department, nebulizers are still used for the management of asthma and, with the poor resources of families, they have no option of treatment at home. In this study, the investigators will compare the effectiveness of treatment through nebulizer versus metered dose inhaler and spacer in children with an acute asthmatic attack seeking medical care at the Pediatric Emergency Department of Suez Canal University Hospital.

Brief Title

Salbutamol Administration by Nebulizer Versus Metered Dose Inhaler With Spacer in Asthma in Children

Official Title

Effectiveness of Salbutamol Administration by Nebulizer Versus Metered Dose Inhaler With Spacer in Acute Asthma in Children in Suez Canal University Hospital Emergency Department: A Randomized Control Trial

Brief Summary

Asthma is a problem that affects many children and affects their physical health in addition<br /> to having a social and financial burden on individuals, families and healthcare systems. In<br /> our pediatric emergency department, nebulizers are still used for the management of asthma<br /> and, with the poor resources of families, they have no option of treatment at home. In this<br /> study, the investigators will compare the effectiveness of treatment through nebulizer versus<br /> metered dose inhaler and spacer in children with an acute asthmatic attack seeking medical<br /> care at the Pediatric Emergency Department of Suez Canal University Hospital.

Detailed Description

Primary Objective:

To determine whether the administration of a B2 agonist by metered dose inhaler with spacer
is as effective as the administration of B2 agonist by nebulizer for the treatment of an
acute asthmatic episode in children seeking medical care in the Pediatric Emergency
Department of Suez Canal University Hospital.

Secondary Objectives:

1. Comparison of patients' visit duration in the ER room between the two groups.

2. Comparison of hospitalization rate between the two groups.

3. Comparison of parent/patient satisfaction between the two groups. Study design
Single-blinded randomized control trial.

Study location This study will be conducted in the Pediatric Emergency Department in Suez
Canal University Hospital.

Study population This study will include patients presenting with an acute exacerbation of
asthma at the Pediatric Emergency Department in Suez Canal University Hospital starting July
2017 until our sample size is fulfilled.

Inclusion criteria:

Children ranging from 2 - 14 years old. Both genders will be included. Patients with an acute
exacerbation of asthma.

Exclusion criteria:

Patients with arrhythmia and cardiac diseases. Patients with thyroid diseases. Patients with
bronchiolitis, pneumonia. Patients with status asthmaticus requiring immediate pediatric
intensive care unit hospitalization.

Sampling All children fulfilling the inclusion criteria will be included consecutively until
the calculated sample size has been reached.

Sample size

The sample size will be calculated using the following formula:

(Dawson & Trapp, 2004)

Where:

n= sample size Zα/2 = 1.96 (The critical value that divides the central 95% of the Z
distribution from the 5% in the tail) Zβ = 0.84 (The critical value that separates the lower
20% of the Z distribution from the upper 80%) σ = the estimate of the standard deviation =
1.5 (Rubilar et al., 2000) µ1 = mean in the nebulizer group = 4.4 (Rubilar et al., 2000) µ2 =
mean in the metered-dose inhaler group = 3.3 (Rubilar et al., 2000) So, by calculation, the
sample size will be equal to 30 cases per group, giving a total sample size of 60 cases.

Methods of data collection

Infants and children known to have asthma coming to the Pediatric Emergency Department of
Suez Canal University Hospital and fulfilling the inclusion criteria will be assessed
according to the following clinical respiratory score:

(Mild 0-3 moderate 4-7 severe 8-12)17

The target population is patients who presented with moderate to severe wheezing (score
4-12).

Randomization will take place through an online program for randomization of clinical trials.
The patients will be divided into two groups, one of them treated by the available nebulizer
and the other by MDI with spacer. The investigators cannot blind patients to the treatment as
there is an obvious difference between the two modalities.

However, the assessment of the respiratory score before and after the treatment will be
performed by an independent physician who will not be involved in the decision-making and
randomization of treatment. This physician will be asked to assess initially and then
reassess after the equipment has been removed to avoid any bias.

Dosage and administration:

The nebulizer group will receive salbutamol aerosol solution (0.25 mg/kg weight, up to a
maximum of 5 mg in 3.5 mL of normal saline solution. Aerosols will be generated by jet
nebulizers powered by oxygen and delivered via a face mask for 7 min every 20 min during the
first hour (a total of three nebulizations/hr.). A flow rate of 7 L/min will be used.

The metered dose inhaler with spacer group will receive two puffs of salbutamol (100
mcg/puff) every 10 min 5 times over 1 hr. (a total of 10 puffs/hr.), using a spacer device
with a face mask. Following each puff, the children will take breaths for a full minute from
the spacer device held in place.

Assessment:

Patients will be reassessed after one hour and score <4 is considered a success while score>4
is failure of therapy.

Patients of same degree of severity of the attack will be compared together according to the
following characteristics: duration of treatment preparation and delivery, clinical outcome,
patient satisfaction after use and hospitalization rate.

Each patient will have a form: Page 1 will be an informed consent to be signed before
randomization of treatment. Page 2 will include the following items

1. personal data (name, age, address, telephone number to be in contact with the patient
and know if there were repeated visits after this attack within the same week). In
addition, the researcher's phone number will be accessible to the patients.

2. Medical history (other illnesses, medications, degree of asthma either intermittent or
persistent)

3. Clinical assessment (clinical respiratory score before and after treatment)

4. Patient satisfaction with given modality on a Likert scale from 1-5. This will be asked
by the blinded assessor and will include questions regarding:

- Comfort with modality used

- Duration of modality used

- Ease of administration

- Confidence in repeating treatment on their own at home if required

Outcome Measures

Outcome measures are the tests that investigators perform to prove whether or not a treatment being tested in a clinical trial is having any effect.