The Challenge of Obtaining Qualitative Bacterial Cultures in Non-expectorating Cystic Fibrosis Patients
- Conditions
- Cystic Fibrosis
- Interventions
- Procedure: Nasal swabProcedure: Cough swabProcedure: Spontaneous expectorated sputumProcedure: Induced sputumProcedure: Bronchoalveolar lavageOther: Questionnaire
- Registration Number
- NCT02363764
- Lead Sponsor
- Universitair Ziekenhuis Brussel
- Brief Summary
Accurate identification of lower respiratory tract pathogens is standard of care in the management of CF patients and it is therefore recommended to perform regular bacterial cultures, at least once a year, but some even recommend monthly cultures. This can be done through different methods, of which sputum and bronchoalveolar lavage (BAL) are the gold standard. However, BAL is an invasive method, not designated to repeat monthly. Therefore, the diagnosis of lower respiratory tract infections can be challenging in the non-expectorating CF patient. Other methods, such as induced sputum (IS), cough swabs and nasal swabs, have been developed to obtain bacterial cultures in these patients. Studies have investigated the reliability of these different sampling methods, however, with controversial conclusions.
- Detailed Description
I. Protocol design:
The current protocol is designed to compare:
* Group 1: nasal swab, cough swab and spontaneous expectorated sputum in expectorating CF patients
* Group 2: nasal swab, cough swab and induced sputum in non-expectorating CF patients
* Group 3: nasal swab, cough swab, induced sputum and BAL in both expectorating and non-expectorating CF patients requiring clinically indicated bronchoscopy
II. Flow chart:
1. Nasal swab obtained by the physiotherapyst (PT)
2. Patient rinses his mouth with water, followed by autogenic drainage
3. Cough swab obtained by the PT
4. Obtainment of 3rd (4th) sample:
* Group 1: Sputum sample voluntary expectorated by the patient
* Group 2 and 3: Induced sputum sample --\> voluntary coughed up and expectorated by the patient after inhalation of 4ml of HS OR
* Group 3: BAL --\>obtained by the pulmonologist during bronchoscopy
5. Filling out questionnaire on acceptability of the different sampling methods by patients \>6 years of age (not in Group 3)
III. Analysis of the samples:
(Induced) Sputum samples, cough and nasal swabs are aseptically collected in the appropriate disposable and are immediately sent to the Laboratory for Microbiology and Infection Control of the Universitair Ziekenhuis Brussel, where analyses are carried out within 24h post-sampling.
These analyses include:
* Culture and identification of respiratory pathogens on selective and non-selective media
* Each type of colony will be identified by MALDI-TOF mass spectrometry, completed by other identification tests if needed
* When appropriate, susceptibility tests will be performed on the isolated bacteria
IV. Statistical analysis:
* Determination of sensitivity, specificity, positive predicted value, negative predicted value of the different sampling methods
* Preference for one method over another: crosstabs, Chi-square test
* Pain experienced with any method (Yes/No): Student's t-test
* VAS-scale pain per method: ANOVA
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 175
- Both expectorating and non-expectorating CF patients with confirmed diagnosis (sweat test / genotyping)
- All ages
- Attending the UZ Brussel CF Clinic
- Written informed consent from each participant and/or his parents or legal guardian
- CF patients who underwent lung transplantation
- Denial of participation to the study
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Non-expectorating CF patients Nasal swab (=unable to expectorate sputum spontaneously) 1. Nasal swab 2. Cough swab 3. Induced sputum after inhalation of hypertonic saline (NaCl 6%) 4. Questionnaire Expectorating CF patients Cough swab (=able to expectorate sputum spontaneously) 1. Nasal swab 2. Cough swab 3. Spontaneous expectorated sputum 4. Questionnaire Expectorating CF patients Nasal swab (=able to expectorate sputum spontaneously) 1. Nasal swab 2. Cough swab 3. Spontaneous expectorated sputum 4. Questionnaire Expectorating CF patients Spontaneous expectorated sputum (=able to expectorate sputum spontaneously) 1. Nasal swab 2. Cough swab 3. Spontaneous expectorated sputum 4. Questionnaire Bronchoscopy CF patients Bronchoalveolar lavage (=undergoing clinically indicated bronchoscopy) 1. Nasal swab 2. Cough swab 3. Induced sputum after inhalation of hypertonic saline (NaCl 6%) 4. Bronchoalveolar lavage (BAL) Expectorating CF patients Questionnaire (=able to expectorate sputum spontaneously) 1. Nasal swab 2. Cough swab 3. Spontaneous expectorated sputum 4. Questionnaire Bronchoscopy CF patients Nasal swab (=undergoing clinically indicated bronchoscopy) 1. Nasal swab 2. Cough swab 3. Induced sputum after inhalation of hypertonic saline (NaCl 6%) 4. Bronchoalveolar lavage (BAL) Non-expectorating CF patients Questionnaire (=unable to expectorate sputum spontaneously) 1. Nasal swab 2. Cough swab 3. Induced sputum after inhalation of hypertonic saline (NaCl 6%) 4. Questionnaire Bronchoscopy CF patients Cough swab (=undergoing clinically indicated bronchoscopy) 1. Nasal swab 2. Cough swab 3. Induced sputum after inhalation of hypertonic saline (NaCl 6%) 4. Bronchoalveolar lavage (BAL) Non-expectorating CF patients Cough swab (=unable to expectorate sputum spontaneously) 1. Nasal swab 2. Cough swab 3. Induced sputum after inhalation of hypertonic saline (NaCl 6%) 4. Questionnaire Non-expectorating CF patients Induced sputum (=unable to expectorate sputum spontaneously) 1. Nasal swab 2. Cough swab 3. Induced sputum after inhalation of hypertonic saline (NaCl 6%) 4. Questionnaire Bronchoscopy CF patients Induced sputum (=undergoing clinically indicated bronchoscopy) 1. Nasal swab 2. Cough swab 3. Induced sputum after inhalation of hypertonic saline (NaCl 6%) 4. Bronchoalveolar lavage (BAL)
- Primary Outcome Measures
Name Time Method Sensitivity, specificity, positive and negative predicted value 2 years Sensitivity, specificity, positive and negative predicted value of different sampling methods
- Secondary Outcome Measures
Name Time Method Preference of method Questionnaire: day of sampling, Analysis: 2 years If no differences are observed between sampling methods, which method would be preferred by the patient?
Pain experienced with any method Questionnaire: day of sampling, Analysis: 2 years Is there any pain experienced? If so, how much? --\> VAS