Integration of drug safety monitoring in tuberculosis treatment programmes: country experiences
- PMID: 31604816
- PMCID: PMC9488907
- DOI: 10.1183/16000617.0115-2018
Integration of drug safety monitoring in tuberculosis treatment programmes: country experiences
Abstract
New drugs and shorter treatments for drug-resistant tuberculosis (DR-TB) have become available in recent years and active pharmacovigilance (PV) is recommended by the World Health Organization (WHO) at least during the early phases of implementation, with active drug safety monitoring and management (aDSM) proposed for this. We conducted a literature review of papers reporting on aDSM. Up to 18 April, 2019, results have only been published from one national aDSM programme. Because aDSM is being introduced in many low- and middle-income countries, we also report experiences in introducing it into DR-TB treatment programmes, targeting the reporting of a restricted set of adverse events (AEs) as per WHO-recommended aDSM principles for the period 2014-2017. Early beneficial effects of active PV for TB patients include increased awareness about the occurrence, detection and management of AEs during TB treatment, and the increase of spontaneous reporting in some countries. However, because PV capacity is low in most countries and collaboration between national TB programmes and national PV centres remains weak, parallel and coordinated co-development of the capacities of both TB programmes and PV centres is needed.
Copyright ©ERS 2019.
Conflict of interest statement
Conflict of interest: E. Tiemersma reports grants from USAID under the Challenge TB Project, during the conduct of the study. Conflict of interest: S. van den Hof has nothing to disclose. Conflict of interest: G. Dravniece has nothing to disclose. Conflict of interest: F. Wares reports grants from USAID under the Challenge TB Project, during the conduct of the study. Conflict of interest: Y. Molla reports grants from the USAID under the Challenge TB Project, during the conduct of the study. Conflict of interest: Y. Permata has nothing to disclose. Conflict of interest: E. Lukitosari has nothing to disclose. Conflict of interest: M. Quelapio has nothing to disclose. Conflict of interest: S.T. Aung has nothing to disclose. Conflict of interest: K.M. Aung has nothing to disclose. Conflict of interest: H.T. Thuy has nothing to disclose. Conflict of interest: V.D. Hoa has nothing to disclose. Conflict of interest: M. Sulaimanova has nothing to disclose. Conflict of interest: S. Sagyndykova has nothing to disclose. Conflict of interest: M. Makhmudova has nothing to disclose. Conflict of interest: A. Soliev has nothing to disclose. Conflict of interest: M. Kimerling has nothing to disclose.
References
-
- Aung KJ, Van Deun A, Declercq E, et al. . Successful ‘9-month Bangladesh regimen’ for multidrug-resistant tuberculosis among over 500 consecutive patients. Int J Tuberc Lung Dis 2014; 18: 1180–1187. - PubMed
-
- Van Deun A, Maug AK, Salim MA, et al. . Short, highly effective, and inexpensive standardized treatment of multidrug-resistant tuberculosis. Am J Respir Crit Care Med 2010; 182: 684–692. - PubMed
-
- Kuaban C, Noeske J, Rieder HL, et al. . High effectiveness of a 12-month regimen for MDR-TB patients in Cameroon. Int J Tuberc Lung Dis 2015; 19: 517–524. - PubMed
-
- Piubello A, Harouna SH, Souleymane MB, et al. . High cure rate with standardised short-course multidrug-resistant tuberculosis treatment in Niger: no relapses. Int J Tuberc Lung Dis 2014; 18: 1188–1194. - PubMed
-
- Ahmad Khan F, Salim MAH, du Cros P, et al. . Effectiveness and safety of standardised shorter regimens for multidrug-resistant tuberculosis: individual patient data and aggregate data meta-analyses. Eur Respir J 2017; 50: 1700061. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous