4.5 Review

Central nervous system tuberculosis

Journal

CURRENT OPINION IN NEUROLOGY
Volume 34, Issue 3, Pages 396-402

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/WCO.0000000000000920

Keywords

central nervous system; granuloma; treatment optimization; tuberculosis; Xpert/Rif

Funding

  1. National Institute of Health [R01AI145781]
  2. Medical Research Council UK, High Dose Oral Rifampicin to Improve Survival from Adult TB Meningitis -(HARVEST) Trial [MR/S004963/1]

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Recent studies in the field of CNS-TB have focused largely on TB meningitis. The outcome may improve by optimizing treatment dosing, but this needs to be confirmed in clinical trials. Due to the important role of inflammation, these trials should be used as the platform to study the inflammatory and metabolomic responses, which could improve understanding of the biology of this disease and improve patient outlook by enabling individualized host-directed therapy.
Purpose of review Central nervous system (CNS) tuberculosis is the most devastating form of tuberculosis (TB), with mortality and or neurological sequelae in over half of individuals. We reviewed original research and systematic reviews published since 1 January 2019 for new developments in CNS TB pathophysiology, diagnosis, management and prognosis. Recent findings Insight in the pathophysiology is increasing steadily since the landmark studies in 1933, focussing on granuloma type classification, the relevance of the M. tuberculosis bacterial burden and the wide range of immunological responses. Although Xpert/RIF has been recommended by the WHO for extrapulmonary TB diagnosis, culture is still needed to increase the sensitivity of TB meningitis diagnosis. Sequential MRIs can improve understanding of neurological deficits at baseline and during treatment. Pharmacokinetic/pharmacodynamic modelling suggests that higher doses of rifampicin and isoniazid in TB meningitis could improve survival. Summary Recent studies in the field of CNS-TB have largely focussed on TB meningitis. The outcome may improve by optimizing treatment dosing. This needs to be confirmed in clinical trials. Due to the important role of inflammation, these trials should be used as the platform to study the inflammatory and metabolomic responses. This could improve understanding of the biology of this disease and improve patient outlook by enabling individualised host-directed therapy.

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