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Published online before print August 9, 2007
Eur Respir J 2007, doi:10.1183/09031936.00077307
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RAPID COMMUNICATION

Clinical and operational value of the XDR-TB definition

G.B. Migliori 1*, G. Besozzi 2, E. Girardi 3, K. Kliiman 4, C. Lange 5, O.S. Toungoussova 6, G. Ferrara 7, D.M. Cirillo 8, A. Gori 9, A. Matteelli 10, A. Spanevello 6, L.R. Codecasa 11, M.C. Raviglione 12, SMIRA/TBNET Study Group

1 WHO Collaborating Centre for TB and Lung Diseases, Fondazione S. Maugeri, Care and Research Institute, Tradate, Italy
2 E. Morelli Hospital, Reference Hospital for MDR and HIV TB, Sondalo, Italy
3 National Institute for Infectious Diseases (INMI) L. Spallanzani, Rome, Italy
4 University of Tartu, Tartu, Estonia
5 Division of Clinical Infectious Diseases, Medical Clinic, Research Centre Borstel, Borstel, Germany
6 Fondazione S. Maugeri, Care and Research Institute, Cassano delle Murge, Italy
7 University of Perugia, Internal Medicine, Section of Respiratory Diseases, Perugia, Italy
8 Supranational Reference Laboratory, S. Raffaele Institute, Milano, Italy
9 San Paolo Hospital, University of Milan, Milano, Italy
10 University of Brescia, Brescia, Italy
11 TB Reference Centre, Villa Marelli Institute, Niguarda Hospital, Milano, Italy
12 Stop TB Dept, World Health Organization, Geneva, Switzerland

* To whom correspondence should be addressed. E-mail: gbmigliori{at}fsm.it.


   Abstract

No information is available on the effect of resistance/susceptibility to first-line drugs different from isoniazid and rifampicin in determining the outcome of extensively drug-resistant tuberculosis (XDR-TB) patients, and if being XDR-TB is a more accurate indicator of poor clinical outcome than being resistant to all first-line anti-TB drugs.

To investigate this issue large series of multidrug-resistant (MDR-) and XDR-TB cases diagnosed in Estonia, Germany, Italy and Russian Federation (Archangels Oblast) in the period 1999–2006 were analyzed.

Drug susceptibility testing for first- and second-line anti-TB drugs, quality assurance and treatment delivery was performed according to WHO recommendations in all study sites.

Out of 4,583 culture-positive TB cases analyzed, 361 (7.9%) were MDR and 64 (1.4%) XDR.

XDR-TB cases had a relative risk of 1.58 to have an unfavourable outcome compared with "MDR-TB cases resistant to all first-line drugs" (isoniazid, rifampicin ethambutol, streptomycin and, when tested, pyrazinamide) and a RR of 2.61 compared with "other" MDR-TB cases (those susceptible to at least one first-line anti-TB drug among ethambutol, pyrazinamide and streptomycin, regardless to resistance to the second-line drugs not defining XDR-TB).

The emergence of XDR-TB confirms that problems in TB management are still present in Europe. While waiting for new tools which will facilitate management of XDR-TB, accessibility to quality diagnostic and treatment services should be urgently ensured and adequate public health policies should be rapidly implemented to prevent further development of drug resistance.

Keywords:  Clinical value, drug resistance, extensively drug-resistant tuberculosis, multidrug-resistant tuberculosis, tuberculosis




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