Infection control, genetic assessment of drug resistance and drug susceptibility testing in the current management of multidrug/extensively-resistant tuberculosis (M/XDR-TB) in Europe: A tuberculosis network European Trialsgroup (TBNET) study
Europe has the highest documented caseload and greatest increase in multidrug and extensively drug-resistant tuberculosis (M/XDR-TB) of all World Health Organization (WHO) regions. This survey examines how recommendations for M/XDR-TB management are being implemented. TBNET is a pan-European clinica...
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| Veröffentlicht in: | Respiratory medicine Jg. 132; S. 68 - 75 |
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| Format: | Journal Article |
| Sprache: | Englisch |
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England
Elsevier Ltd
01.11.2017
Elsevier Limited |
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| ISSN: | 0954-6111, 1532-3064, 1532-3064 |
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| Abstract | Europe has the highest documented caseload and greatest increase in multidrug and extensively drug-resistant tuberculosis (M/XDR-TB) of all World Health Organization (WHO) regions. This survey examines how recommendations for M/XDR-TB management are being implemented.
TBNET is a pan-European clinical research collaboration for tuberculosis. An email survey of TBNET members collected data in relation to infection control, access to molecular tests and basic microbiology with drug sensitivity testing.
68/105 responses gave valid information and were from countries within the WHO European Region. Inpatient beds matched demand, but single rooms with negative pressure were only available in low incidence countries; ultraviolet decontamination was used in 5 sites, all with >10 patients with M/XDR-TB per year. Molecular tests for mutations associated with rifampicin resistance were widely available (88%), even in lower income and especially in high incidence countries. Molecular tests for other first line and second line drugs were less accessible (76 and 52% respectively). A third of physicians considered that drug susceptibility results were delayed by > 2 months.
Infection control for inpatients with M/XDR-TB remains a problem in high incidence countries. Rifampicin resistance is readily detected, but tests to plan regimens tailored to the drug susceptibilities of the strain of Mycobacterium tuberculosis are significantly delayed, allowing for further drug resistance to develop.
•M/XDR-TB poses a serious threat to TB control in Europe.•Isolation rooms are insufficient for safe diagnosis.•Drug susceptibility testing results are frequently delayed.•A positive test for rifampicin resistance should lead automatically to tests for other first- and second-line drug resistance. |
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| AbstractList | Europe has the highest documented caseload and greatest increase in multidrug and extensively drug-resistant tuberculosis (M/XDR-TB) of all World Health Organization (WHO) regions. This survey examines how recommendations for M/XDR-TB management are being implemented.AIMEurope has the highest documented caseload and greatest increase in multidrug and extensively drug-resistant tuberculosis (M/XDR-TB) of all World Health Organization (WHO) regions. This survey examines how recommendations for M/XDR-TB management are being implemented.TBNET is a pan-European clinical research collaboration for tuberculosis. An email survey of TBNET members collected data in relation to infection control, access to molecular tests and basic microbiology with drug sensitivity testing.METHODSTBNET is a pan-European clinical research collaboration for tuberculosis. An email survey of TBNET members collected data in relation to infection control, access to molecular tests and basic microbiology with drug sensitivity testing.68/105 responses gave valid information and were from countries within the WHO European Region. Inpatient beds matched demand, but single rooms with negative pressure were only available in low incidence countries; ultraviolet decontamination was used in 5 sites, all with >10 patients with M/XDR-TB per year. Molecular tests for mutations associated with rifampicin resistance were widely available (88%), even in lower income and especially in high incidence countries. Molecular tests for other first line and second line drugs were less accessible (76 and 52% respectively). A third of physicians considered that drug susceptibility results were delayed by > 2 months.RESULTS68/105 responses gave valid information and were from countries within the WHO European Region. Inpatient beds matched demand, but single rooms with negative pressure were only available in low incidence countries; ultraviolet decontamination was used in 5 sites, all with >10 patients with M/XDR-TB per year. Molecular tests for mutations associated with rifampicin resistance were widely available (88%), even in lower income and especially in high incidence countries. Molecular tests for other first line and second line drugs were less accessible (76 and 52% respectively). A third of physicians considered that drug susceptibility results were delayed by > 2 months.Infection control for inpatients with M/XDR-TB remains a problem in high incidence countries. Rifampicin resistance is readily detected, but tests to plan regimens tailored to the drug susceptibilities of the strain of Mycobacterium tuberculosis are significantly delayed, allowing for further drug resistance to develop.CONCLUSIONInfection control for inpatients with M/XDR-TB remains a problem in high incidence countries. Rifampicin resistance is readily detected, but tests to plan regimens tailored to the drug susceptibilities of the strain of Mycobacterium tuberculosis are significantly delayed, allowing for further drug resistance to develop. Europe has the highest documented caseload and greatest increase in multidrug and extensively drug-resistant tuberculosis (M/XDR-TB) of all World Health Organization (WHO) regions. This survey examines how recommendations for M/XDR-TB management are being implemented. TBNET is a pan-European clinical research collaboration for tuberculosis. An email survey of TBNET members collected data in relation to infection control, access to molecular tests and basic microbiology with drug sensitivity testing. 68/105 responses gave valid information and were from countries within the WHO European Region. Inpatient beds matched demand, but single rooms with negative pressure were only available in low incidence countries; ultraviolet decontamination was used in 5 sites, all with >10 patients with M/XDR-TB per year. Molecular tests for mutations associated with rifampicin resistance were widely available (88%), even in lower income and especially in high incidence countries. Molecular tests for other first line and second line drugs were less accessible (76 and 52% respectively). A third of physicians considered that drug susceptibility results were delayed by > 2 months. Infection control for inpatients with M/XDR-TB remains a problem in high incidence countries. Rifampicin resistance is readily detected, but tests to plan regimens tailored to the drug susceptibilities of the strain of Mycobacterium tuberculosis are significantly delayed, allowing for further drug resistance to develop. Europe has the highest documented caseload and greatest increase in multidrug and extensively drug-resistant tuberculosis (M/XDR-TB) of all World Health Organization (WHO) regions. This survey examines how recommendations for M/XDR-TB management are being implemented. TBNET is a pan-European clinical research collaboration for tuberculosis. An email survey of TBNET members collected data in relation to infection control, access to molecular tests and basic microbiology with drug sensitivity testing. 68/105 responses gave valid information and were from countries within the WHO European Region. Inpatient beds matched demand, but single rooms with negative pressure were only available in low incidence countries; ultraviolet decontamination was used in 5 sites, all with >10 patients with M/XDR-TB per year. Molecular tests for mutations associated with rifampicin resistance were widely available (88%), even in lower income and especially in high incidence countries. Molecular tests for other first line and second line drugs were less accessible (76 and 52% respectively). A third of physicians considered that drug susceptibility results were delayed by > 2 months. Infection control for inpatients with M/XDR-TB remains a problem in high incidence countries. Rifampicin resistance is readily detected, but tests to plan regimens tailored to the drug susceptibilities of the strain of Mycobacterium tuberculosis are significantly delayed, allowing for further drug resistance to develop. •M/XDR-TB poses a serious threat to TB control in Europe.•Isolation rooms are insufficient for safe diagnosis.•Drug susceptibility testing results are frequently delayed.•A positive test for rifampicin resistance should lead automatically to tests for other first- and second-line drug resistance. AimEurope has the highest documented caseload and greatest increase in multidrug and extensively drug-resistant tuberculosis (M/XDR-TB) of all World Health Organization (WHO) regions. This survey examines how recommendations for M/XDR-TB management are being implemented.MethodsTBNET is a pan-European clinical research collaboration for tuberculosis. An email survey of TBNET members collected data in relation to infection control, access to molecular tests and basic microbiology with drug sensitivity testing.Results68/105 responses gave valid information and were from countries within the WHO European Region. Inpatient beds matched demand, but single rooms with negative pressure were only available in low incidence countries; ultraviolet decontamination was used in 5 sites, all with >10 patients with M/XDR-TB per year. Molecular tests for mutations associated with rifampicin resistance were widely available (88%), even in lower income and especially in high incidence countries. Molecular tests for other first line and second line drugs were less accessible (76 and 52% respectively). A third of physicians considered that drug susceptibility results were delayed by > 2 months.ConclusionInfection control for inpatients with M/XDR-TB remains a problem in high incidence countries. Rifampicin resistance is readily detected, but tests to plan regimens tailored to the drug susceptibilities of the strain ofMycobacterium tuberculosisare significantly delayed, allowing for further drug resistance to develop. |
| Author | Wagner, Dirk Balasanyants, Goar Holmoka, Jiri Avsar, Korkut Soriano-Arandes, Antoni Skrahina, Alena Selmeryd, Ingrid Duarte, Raquel Ladeira, Inês Kuksa, Liga Tiberi, Simon Lange, Christoph Ravn, Pernille Kaluzhenina, Anna Jachym, Mathilde Fréchet Bruchfeld, Judith Solovic, Ivan Volchenkov, Grigory Joan-Pau, Millet Bogyi, Matthias Gomez-Pastrana, David Gyorfy, Zsuzsanna Andersen, Aase Bengaard Kruczak, Katarzyna Giacomet, Vania Kulcitkaia, Stela Esteban, Jaime Anibarro, Luis García-García, José-María Muylle, Inge Confalonieri, Marco Thouvenin, Guillaume Pontali, Emanuele Belton, Moerida van Ingen, Jakko Lillebæk, Troels Manika, Katerina Luiza de Souza Galvao, Maria Chesov, Dumitru García, Cristina Berastegui Dyrhol-Riise, Anne Ma Magis-Escurra, Cecile Dudnyk, Andrii Dedicoat, Martin Fløe, Andreas Konstantynovska, Olha Polanova, Monika Janssens, Jean-Paul Eisenhut, Michael Sánchez-Montalvá, Adrian Gomez, Neus Altet van der Werf, Tjip Jonsson, Jerker Albrecht, Dirk Palmieri, Fabrizio Chiappini, Elena Schoch, Otto Pesut, Dragica Vicente, Diego Cam |
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29229108$$D View this record in MEDLINE/PubMed http://kipublications.ki.se/Default.aspx?queryparsed=id:137327789$$DView record from Swedish Publication Index (Karolinska Institutet) |
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| CitedBy_id | crossref_primary_10_1164_rccm_201909_1874ST crossref_primary_10_1111_resp_13311 crossref_primary_10_1136_bmjgh_2020_004735 crossref_primary_10_4103_ijmy_ijmy_187_22 crossref_primary_10_1183_13993003_02089_2018 |
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| ContentType | Journal Article |
| Contributor | Wagner, Dirk Balasanyants, Goar Holmoka, Jiri Avsar, Korkut Soriano-Arandes, Antoni Skrahina, Alena Selmeryd, Ingrid Duarte, Raquel Ladeira, Inês Kuksa, Liga Tiberi, Simon Ravn, Pernille Kaluzhenina, Anna Jachym, Mathilde Fréchet Bruchfeld, Judith Solovic, Ivan Volchenkov, Grigory Joan-Pau, Millet Bogyi, Matthias Gomez-Pastrana, David Gyorfy, Zsuzsanna Andersen, Aase Bengaard Kruczak, Katarzyna Giacomet, Vania Kulcitkaia, Stela Esteban, Jaime Anibarro, Luis García-García, José-María Muylle, Inge Confalonieri, Marco Thouvenin, Guillaume Pontali, Emanuele Belton, Moerida van Ingen, Jakko Lillebæk, Troels Manika, Katerina Luiza de Souza Galvao, Maria Chesov, Dumitru García, Cristina Berastegui Dyrhol-Riise, Anne Ma Magis-Escurra, Cecile Dudnyk, Andrii Dedicoat, Martin Fløe, Andreas Konstantynovska, Olha Polanova, Monika Janssens, Jean-Paul Eisenhut, Michael Sánchez-Montalvá, Adrian Gomez, Neus Altet van der Werf, Tjip Jonsson, Jerker Albrecht, Dirk Palmieri, Fabrizio Chiappini, Elena Schoch, Otto Pesut, Dragica Vicente, Diego Caminero, Jose Popa, |
| Contributor_xml | – sequence: 1 givenname: Dirk surname: Albrecht fullname: Albrecht, Dirk organization: Sunderby Sjukhus, 97180 Luleå, Sweden – sequence: 2 givenname: Luis surname: Anibarro fullname: Anibarro, Luis organization: Completo Hospitalario de Pontevedra, Spain – sequence: 3 givenname: Neus Altet surname: Gomez fullname: Gomez, Neus Altet organization: Unidad de Tratamiento Directamente Observado Serveis Clinics, Barcelona, Spain – sequence: 4 givenname: Aase Bengaard surname: Andersen fullname: Andersen, Aase Bengaard organization: Righospitalet, Copenhagen, Denmark – sequence: 5 givenname: Korkut surname: Avsar fullname: Avsar, Korkut organization: Asklepios Fachklinik, München-Gauting, Germany – sequence: 6 givenname: Goar surname: Balasanyants fullname: Balasanyants, Goar organization: Saint Petersburg Research Institute of Phthesiopulmonology, St. Petersburg, Russia – sequence: 7 givenname: Moerida surname: Belton fullname: Belton, Moerida organization: Lewisham and Greenwich NHS Trust, London UK – sequence: 8 givenname: Cristina Berastegui surname: García fullname: García, Cristina Berastegui organization: Servei Pneumologia, Hospital Universitari, Vall d'Hebron, Barcelona, Spain – sequence: 9 givenname: Matthias surname: Bogyi fullname: Bogyi, Matthias organization: Wilhelminspital, Wien, Austria – sequence: 10 givenname: Judith surname: Bruchfeld fullname: Bruchfeld, Judith organization: Karolinska University Hospital, Stockholm, Sweden – sequence: 11 givenname: Jose surname: Caminero fullname: Caminero, Jose organization: Hospital General Gran Canaria "Dr. Negrin", Las Palmas, Spain – sequence: 12 givenname: Dumitru surname: Chesov fullname: Chesov, Dumitru organization: USMPh Nicolae Testemitanu, Republic of Moldova – sequence: 13 givenname: Elena surname: Chiappini fullname: Chiappini, Elena organization: Meyer University Hospital, Florence, Italy – sequence: 14 givenname: Marco surname: Confalonieri fullname: Confalonieri, Marco organization: Pulmonology Department, University Hospital of Trieste, Italy – sequence: 15 givenname: Martin surname: Dedicoat fullname: Dedicoat, Martin organization: Heart of England NHS Foundation Trust, Birmingham, UK – sequence: 16 givenname: Maria surname: Luiza de Souza Galvao fullname: Luiza de Souza Galvao, Maria organization: Unitat de Tuberculosis, Vall d'Hebron-Drassanes, Spain – sequence: 17 givenname: Raquel surname: Duarte fullname: Duarte, Raquel organization: Pneumolgy Department, Centro Hospitalar Vila Nova de Gaia and ISPUP-EPIunit, Faculty of Medicine, University of Porto, Porto, Portugal – sequence: 18 givenname: Andrii surname: Dudnyk fullname: Dudnyk, Andrii organization: Tuberculosis and Immunology Department, National Pirogov Memorial University, Vinnytsia, 21037, Ukraine – sequence: 19 givenname: Anne Ma surname: Dyrhol-Riise fullname: Dyrhol-Riise, Anne Ma organization: Department of Infectious Disease, Oslo University Hospital, Oslo, Norway – sequence: 20 givenname: Michael surname: Eisenhut fullname: Eisenhut, Michael organization: Luton & Dunstable University Hospital, Luton, UK – sequence: 21 givenname: Jaime surname: Esteban fullname: Esteban, Jaime organization: Department of Clinical Microbiology, IIS-Fundacion Jiminez Diaz, Madrid, Spain – sequence: 22 givenname: Andreas surname: Fløe fullname: Fløe, Andreas organization: Aarhus University Hospital, Aarhus, Denmark – sequence: 23 givenname: José-María surname: García-García fullname: García-García, José-María organization: Hospital San Agustin, Avilés, Asturias, Spain – sequence: 24 givenname: Vania surname: Giacomet fullname: Giacomet, Vania organization: Clinic of Pediatrics, Luigi Sacco Hospital, Milan, Italy – sequence: 25 givenname: David surname: Gomez-Pastrana fullname: Gomez-Pastrana, David organization: Servicio de Pedatria, Hospital de Jerez, Jerez, Spain – sequence: 26 givenname: Zsuzsanna surname: Gyorfy fullname: Gyorfy, Zsuzsanna organization: Thomayer Hospital, 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Papanokolaou" Hospital, Exohi, Thessaloniki, Greece – sequence: 40 givenname: Millet surname: Joan-Pau fullname: Joan-Pau, Millet organization: Serveis Clinics SAU, Barcelona, Spain – sequence: 41 givenname: Inge surname: Muylle fullname: Muylle, Inge organization: UMC St. Pieter, Brussels, Belgium – sequence: 42 givenname: Fabrizio surname: Palmieri fullname: Palmieri, Fabrizio organization: National Institute for Infectious Diseases, L. 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| Title | Infection control, genetic assessment of drug resistance and drug susceptibility testing in the current management of multidrug/extensively-resistant tuberculosis (M/XDR-TB) in Europe: A tuberculosis network European Trialsgroup (TBNET) study |
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