| Literature DB >> 29806961 |
C Lange1,2,3,4, W A Alghamdi5, M H Al-Shaer5, S Brighenti6, A H Diacon7,8, A R DiNardo9, H P Grobbel1,2,3, M I Gröschel10,11, F von Groote-Bidlingmaier7, M Hauptmann2,12, J Heyckendorf1,2,3, N Köhler1,2,3, T A Kohl11, M Merker11, S Niemann2,11, C A Peloquin5, M Reimann1,2,3, U E Schaible2,12,13,14, D Schaub1,2,3, V Schleusener11, T Thye15, T Schön16,17.
Abstract
According to the World Health Organization (WHO), tuberculosis is the leading cause of death attributed to a single microbial pathogen worldwide. In addition to the large number of patients affected by tuberculosis, the emergence of Mycobacterium tuberculosis drug-resistance is complicating tuberculosis control in many high-burden countries. During the past 5 years, the global number of patients identified with multidrug-resistant tuberculosis (MDR-TB), defined as bacillary resistance at least against rifampicin and isoniazid, the two most active drugs in a treatment regimen, has increased by more than 20% annually. Today we experience a historical peak in the number of patients affected by MDR-TB. The management of MDR-TB is characterized by delayed diagnosis, uncertainty of the extent of bacillary drug-resistance, imprecise standardized drug regimens and dosages, very long duration of therapy and high frequency of adverse events which all translate into a poor prognosis for many of the affected patients. Major scientific and technological advances in recent years provide new perspectives through treatment regimens tailor-made to individual needs. Where available, such personalized treatment has major implications on the treatment outcomes of patients with MDR-TB. The challenge now is to bring these adances to those patients that need them most.Entities:
Keywords: MDR-TB; XDR-TB; individualized medicine; personalized medicine
Year: 2018 PMID: 29806961 DOI: 10.1111/joim.12780
Source DB: PubMed Journal: J Intern Med ISSN: 0954-6820 Impact factor: 8.989