AORD: Antibiotic Observatory for Respiratory Diseases, Apart From Tuberculosis and Reportable Diseases

Sponsor
University of Monastir (Other)
Overall Status
Completed
CT.gov ID
NCT04482231
Collaborator
(none)
9,944
1
7.9
1255.9

Study Details

Study Description

Brief Summary

the study aimed to determine the distribution of respiratory infections in Tunisian population and evaluate the frequency of antibiotics prescribed according to current international recommendations.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    It is an observational, cross-sectional, multicenter, national clinical study . The study was carried out from January 2018 to August 2018 in Tunisian population involving 57 primary care outpatient centers and 6 emergency departments from the 24 departments of the country .

    We included all patients with lower and upper respiratory tract infections (RTIs) who have recieved antibiotic treatment.

    Lower respiratory tract infection (LRTI) include pneumonia and acute bronchitis.

    Acute upper respiratory tract infection (URTIs) include rhinitis, pharyngitis/tonsillitis, and laryngitis. Rhinitis, also known as coryza, is irritation and inflammation of the mucous membrane inside the nose.

    The protocol of our study includes the demographic characteristics and the history of the sample as well as the symptomatology at inclusion. The data from the clinical examination were reported by the investigating doctor. After the diagnosis retained by the doctor is noted with the management of the patient which includes additional explorations if they have been requested. Finally, the investigating doctor specifies the antibiotic therapy prescribed.Appropriateness of antibiotic prescription was assessed in patients managed in the EDs . We used the MAI score (medication appropriateness index) wich includes 10 criteria. For each criterion, the evaluator rates whether the medication is appropriate, marginally appropriate, or inappropriate. Support is provided through explicit definitions and instructions.The MAI has been used in observational and interventional studies.Its feasibility, content validity, predictive validity, and reliability have been demonstrated in ambulatory settings. The maximum score is 20 which translates into maximum inappropriateness. If a patient is on multiple drugs, this test can be repeated for each drug in order to determine a total MAI score.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Actual Enrollment :
    9944 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    Antibiotic Observatory for Respiratory Diseases, Apart From Tuberculosis and Reportable Diseases
    Actual Study Start Date :
    Jan 2, 2018
    Actual Primary Completion Date :
    Aug 31, 2018
    Actual Study Completion Date :
    Aug 31, 2018

    Outcome Measures

    Primary Outcome Measures

    1. Appropriateness of antibiotic prescription [1 day]

      dichotomous (yes / no) criterion that characterizes appropriate or inappropriate use of antibiotics based on respiratory indication and patient profile

    Secondary Outcome Measures

    1. inappropriatness of antibiotic prescription [1 day]

      number of inappropriate antibiotic prescriptions by clinical indication

    2. international recommendations [1 day]

      description of therapeutic strategies inconsistent with international recommendations

    3. patients profile with inappropriate antibiotic therapy [1 day]

      profile of patients with inappropriate antibiotic therapy

    4. patients profile with infectious disease [1 day]

      profile of patients with infectious disease

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 90 Years
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • patients with lower and upper RTIs who recieved antibiotic treatment.
    Exclusion Criteria:
    • not obtained informed consent, specific respiratory infection such as tuberculosis, life-threatening emergency necessitating hospitalization or non-probabilistic antibiotic therapy and contraindication to antibiotic use

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Emergency department of fattouma bourguiba university hospital Monastir Tunisia 5020

    Sponsors and Collaborators

    • University of Monastir

    Investigators

    • Principal Investigator: nouira semir, MD, University of Monastir

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Pr. Semir Nouira, professor semir nouira, University of Monastir
    ClinicalTrials.gov Identifier:
    NCT04482231
    Other Study ID Numbers:
    • BAROMETRE
    First Posted:
    Jul 22, 2020
    Last Update Posted:
    Jul 22, 2020
    Last Verified:
    Jul 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Pr. Semir Nouira, professor semir nouira, University of Monastir
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 22, 2020