Medical Faculty Hasanuddin University 2021 INTRODUCTION WHO : about half million people suffer from multidrug (MDR-) or rifampicin-resistant (RR-) tuberculosis (TB) in 2019 38% accessed treatment and 57% were successfully treated.
Bedaquiline (group A) and Delamanid (group C) have been recently licensed
to manage MDR- and XDR-TB into a new WHO drug classification.
Many evidence is becoming available from experimental and observational
studies on the efficacy and effectiveness of new drugs, but their effectiveness is still incomplete worldwide.
The aim of the study is to prospectively evaluate the effectiveness of
bedaquiline and/or delamanid containing regimens in a cohort of consecutive TB patients treated globally. METHODS Study design is observational, prospective and based on the collection twice a year and analysis of data provided by GTN (Global Tuberculosis Network) centres.
All consecutive patients (including children and adolescents) treated with
bedaquiline and/or delamanid were enrolled either from the beginning of the study or from the time the drugs under study were introduced in the respective country centre (e.g. in Mexico, Nepal, Paraguay, Spain, Slovakia and Sudan) and data collected up to the 31st January 2021.
The information collected (from the clinical files of the participating
centres) included patient’s demographic data, bacteriological, radiological and clinical status at diagnosis, and details on bacteriological conversion and final treatment outcomes. RESULTS RESULTS DISCUSSION The aim of the present study was to prospectively evaluate the outcome of a global cohort of patients treated with new anti-TB drugs first global study prospectively reporting detailed information on treatment outcomes.