TY - JOUR
T1 - Optimising molecular diagnostic capacity for effective control of tuberculosis in high-burden settings
AU - Sabiiti, Wilber
AU - Mtafya, Bariki
AU - Kuchaka, Davis
AU - Azam, Khalide
AU - Viegas, Sofia
AU - Mdolo, Aaron
AU - Farmer, Eoghan
AU - Khonga, Margaret
AU - Evangelopoulos, Dimitrios
AU - Honeyborne, Isobella
AU - Rachow, Andrea
AU - Heinrich, Norbert
AU - Ntinginya, Nyanda Elias
AU - Bhatt, Nilesh
AU - Davies, Gerry R
AU - Jani, Ilesh V
AU - McHugh, Timothy D
AU - Kibiki, Gibson
AU - Hoelscher, Michael
AU - Gillespie, Stephen Henry
AU - PANBIOME (Pan-African Biomarker Expansion Programme) consortium
PY - 2016/8/1
Y1 - 2016/8/1
N2 - The World Health Organization's 2035 vision is to reduce tuberculosis (TB) associated mortality by 95%. While low-burden, well-equipped industrialised economies can expect to see this goal achieved, it is challenging in the low- and middle-income countries that bear the highest burden of TB. Inadequate diagnosis leads to inappropriate treatment and poor clinical outcomes. The roll-out of the Xpert® MTB/RIF assay has demonstrated that molecular diagnostics can produce rapid diagnosis and treatment initiation. Strong molecular services are still limited to regional or national centres. The delay in implementation is due partly to resources, and partly to the suggestion that such techniques are too challenging for widespread implementation. We have successfully implemented a molecular tool for rapid monitoring of patient treatment response to anti-tuberculosis treatment in three high TB burden countries in Africa. We discuss here the challenges facing TB diagnosis and treatment monitoring, and draw from our experience in establishing molecular treatment monitoring platforms to provide practical insights into successful optimisation of molecular diagnostic capacity in resource-constrained, high TB burden settings. We recommend a holistic health system-wide approach for molecular diagnostic capacity development, addressing human resource training, institutional capacity development, streamlined procurement systems, and engagement with the public, policy makers and implementers of TB control programmes.
AB - The World Health Organization's 2035 vision is to reduce tuberculosis (TB) associated mortality by 95%. While low-burden, well-equipped industrialised economies can expect to see this goal achieved, it is challenging in the low- and middle-income countries that bear the highest burden of TB. Inadequate diagnosis leads to inappropriate treatment and poor clinical outcomes. The roll-out of the Xpert® MTB/RIF assay has demonstrated that molecular diagnostics can produce rapid diagnosis and treatment initiation. Strong molecular services are still limited to regional or national centres. The delay in implementation is due partly to resources, and partly to the suggestion that such techniques are too challenging for widespread implementation. We have successfully implemented a molecular tool for rapid monitoring of patient treatment response to anti-tuberculosis treatment in three high TB burden countries in Africa. We discuss here the challenges facing TB diagnosis and treatment monitoring, and draw from our experience in establishing molecular treatment monitoring platforms to provide practical insights into successful optimisation of molecular diagnostic capacity in resource-constrained, high TB burden settings. We recommend a holistic health system-wide approach for molecular diagnostic capacity development, addressing human resource training, institutional capacity development, streamlined procurement systems, and engagement with the public, policy makers and implementers of TB control programmes.
KW - Tuberculosis
KW - Diagnostics
KW - Health systems
KW - Policy
KW - Disease control
U2 - 10.5588/ijtld.15.0951
DO - 10.5588/ijtld.15.0951
M3 - Article
SN - 1027-3719
VL - 20
SP - 1004
EP - 1009
JO - International Journal of Tuberculosis and Lung Disease
JF - International Journal of Tuberculosis and Lung Disease
IS - 8
ER -