Airway Inflammation in Congenital Diaphragmatic Hernia Patients

The Hospital for Sick Children21 enrolled

Overview

We propose to examine Congenital Diaphragmatic Hernia (CDH) patients for evidence of airway inflammation as a first step to characterize the reported bronchodilator responsiveness. Airway biopsy studies are invasive and thus we propose to perform induced sputum studies to document the amount and type of inflammation present. Another ancillary non-invasive measure of airway inflammation that we will use is exhaled nitric oxide (NO). The primary objective of this study is to determine if CDH patients have any evidence of airway inflammation. The hypothesis of this study is that children with CDH do not have evidence of airway inflammation associated with bronchodilator responsiveness. Based on this information, treatment for CDH patients will hopefully be more accurate and appropriate for their specific needs.

Study Type

INTERVENTIONAL

Allocation

Purpose

DIAGNOSTIC

Masking

NONE

Enrollment

Conditions

Congenital Diaphragmatic Hernia

Interventions

Subject will inhale 5 mls of 3% hypertonic saline for 7 minutes by nebulizer. Sputum production (with cough) will be attempted post inhalation. A maximum of 3 hypertonic saline inhalations will be attempted if inhalation does not generate a productive cough. If sputum induction is not successful and the FEV1 falls \<10%, the concentration of inhaled hypertonic saline will increase from 3 to 4%. If 5 mls of 4% hypertonic saline inhaled for 7 minutes does not produce a productive cough we will proceed to 5%. If 5 mls of 5% hypertonic saline inhaled for 7 minutes does not produce a productive cough the test is complete and the sample is labelled 'no sputum collected'. If FEV1 falls \>10%, the previous step will be repeated.

Bronchodilator ResponseDRUG

A bronchodilator (Salbutamol 200 mcg or 2 puffs inhaled via spacer device) will be administered to all subjects in the pulmonary function laboratory. 15 minutes after administration of the bronchodilator spirometry will be repeated. This is performed routinely in CDH clinic and is not an additional test for this study.

Eligibility

Sex: ALLMin age: 6 YearsMax age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * 6 - 18 years of age at enrolment * Clinically stable at enrolment * Attending follow-up in the CDH Clinic at SickKids Exclusion Criteria: * Unable to perform pulmonary function testing * Clinically unstable at enrolment * Known hypersensitivity to salbutamol

Outcomes

Primary Outcomes

Number of Participants With Elevated Sputum Eosinophils

Number of participants with sputum eosinophils greater than 3% percent of cells in the sputum

Time frame: post sputum induction

Secondary Outcomes

Number of Participant With Elevated Sputum Neutrophils

Elevation is defined as sputum neutrophils \> or = 61% neutrophils = neutrophilic inflammation

Time frame: Baseline, +30 minutes

Number of Participant With Elevated Exhaled Nitric Oxide (NO) Level

exhaled NO measurements will be performed according to the American Thoracic Society and European Respiratory Society guidelines. These tests are performed routinely as part of the respiratory evaluation of these patients and are not additional tests added for this study. greater than 20 ppb was considered elevated

Time frame: 30 min

Number of Participant With Bronchodilator Response

defined as a = or \> 12% change in FEV1 post bronchodilator

Time frame: life time of child (age 6 to present age)