Sputum induction improves detection of pathogens in children with cystic fibrosis

Jordana E Hoppe1, Elinor Towler1, Brandie D Wagner2

  • 1Department of Pediatrics, Children's Hospital Colorado and the University of Colorado School of Medicine, Aurora, Colorado.

Pediatric Pulmonology
|January 8, 2015
PubMed

Insights

Sputum induction effectively diagnoses respiratory infections in children with cystic fibrosis (CF). This method improves pathogen detection compared to other sampling techniques, aiding in timely treatment adjustments for CF patients.

Area of Science:

  • Pediatric Pulmonology
  • Infectious Diseases
  • Clinical Microbiology

Background:

  • Sputum induction (IS) is a safe method for collecting lower airway secretions in children with cystic fibrosis (CF).
  • Its clinical utility in diagnosing outpatient infections requires further investigation.

Purpose of the Study:

  • To compare the success rate and microbiologic yield of induced sputum (IS) with oropharyngeal swabs (OP) and expectorated sputum (ES) in pediatric CF patients.
  • To determine if IS culture results influence antimicrobial treatment decisions.

Main Methods:

  • A prospective, longitudinal comparative study involving two cohorts of pediatric CF patients.
  • Simultaneous collection of OP, ES, and IS specimens in one cohort (n=17) over one year.
  • Comparison of IS culture results with the nearest respiratory culture within four months in the second cohort (n=35).

Main Results:

  • Sputum induction demonstrated a high success rate (94%) in outpatient pediatric CF encounters.
  • IS samples yielded a higher detection rate for polymicrobial infections, gram-negative organisms, Pseudomonas aeruginosa, and Stenotrophomonas maltophilia compared to OP swabs.
  • The microbiologic yield of serial IS samples remained stable over one year.

Conclusions:

  • Sputum induction is a feasible and effective method for pathogen detection in the outpatient setting for children with CF.
  • IS improves the identification of respiratory pathogens, potentially enhancing clinical management strategies.
Abstract

Related Concept Videos

Sputum Studies I: Gram Stain, cytology, and Acid-fast smear and culture01:26

Sputum Studies I: Gram Stain, cytology, and Acid-fast smear and culture

Sputum studies are a critical part of diagnosing and treating numerous respiratory conditions. These studies involve obtaining sputum samples for analysis to identify pathogenic organisms and assess the presence of abnormal cells indicative of malignant conditions. This lesson will delve into three fundamental sputum studies: Gram Stain, Cytology, and Acid-fast Smear and Culture.
Gram Stain
The Gram Stain is an integral part of sputum studies. It involves the staining of sputum, which permits...
1.2K
Sputum Studies II: Culture and Sensitivity01:20

Sputum Studies II: Culture and Sensitivity

Description
Sputum culture and sensitivity is a medical procedure used to diagnose bacterial infections in the respiratory tract and select the most appropriate antibiotics for treatment. This process involves analyzing sputum samples of thick and opaque secretions produced in the lungs and airways. These samples are collected from patients and then sent to the laboratory for analysis.
The test can identify various pathogens responsible for respiratory infections, including Streptococcus,...
1.9K
Cystic Fibrosis: Pathogenesis01:23

Cystic Fibrosis: Pathogenesis

Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
1.1K
Cystic Fibrosis: Management01:24

Cystic Fibrosis: Management

Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
Sinus disease and chronic...
656
Pulmonary Tuberculosis IV01:26

Pulmonary Tuberculosis IV

Tuberculosis, more commonly referred to as TB, is an infectious disease stemming from Mycobacterium tuberculosis. While it primarily impacts the lungs, TB can also affect other body areas. Given its severity and global impact, timely and accurate diagnosis is crucial for controlling its spread and improving patient outcomes.
Several diagnostic approaches are used to detect TB. The conventional method is the Tuberculin Skin Test (TST), also known as the Mantoux test. However, this method has...
758
Chronic Obstructive Pulmonary Disease-IV: Assessement and Diagnostic Studies01:27

Chronic Obstructive Pulmonary Disease-IV: Assessement and Diagnostic Studies

Assessing and diagnosing Chronic Obstructive Pulmonary Disease (COPD) involves a detailed approach that includes a comprehensive review of medical history, physical examination, and a variety of diagnostic tests. This thorough evaluation is essential to ensure an accurate diagnosis and guide effective management strategies.
Medical History
3.4K