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dc.contributor.authorMtafya, Bariki Anyamkisye
dc.contributor.authorSabi, Issa
dc.contributor.authorJohn, Joseph
dc.contributor.authorSichone, Emanuel
dc.contributor.authorOlomi, Wilyhelmina
dc.contributor.authorGillespie, Stephen Henry
dc.contributor.authorNtinginya, Nyanda E.
dc.contributor.authorSabiiti, Wilber
dc.date.accessioned2022-10-31T10:30:16Z
dc.date.available2022-10-31T10:30:16Z
dc.date.issued2022-10-28
dc.identifier281526072
dc.identifierac7693f8-7ba3-4993-945f-2f0e0d2a8bd2
dc.identifier85142266069
dc.identifier000888313000001
dc.identifier.citationMtafya , B A , Sabi , I , John , J , Sichone , E , Olomi , W , Gillespie , S H , Ntinginya , N E & Sabiiti , W 2022 , ' Systematic assessment of clinical and bacteriological markers for tuberculosis reveals discordance and inaccuracy of symptom-based diagnosis for treatment response monitoring ' , Frontiers in Medicine , vol. 9 , 992451 . https://doi.org/10.3389/fmed.2022.992451en
dc.identifier.issn2296-858X
dc.identifier.otherORCID: /0000-0001-6537-7712/work/122216271
dc.identifier.otherORCID: /0000-0002-4742-2791/work/122216707
dc.identifier.urihttps://hdl.handle.net/10023/26273
dc.descriptionFunding: This work was supported by Commonwealth PhD studentship award to Dr Bariki Mtafya (Award number: TZS-2016-718) at University of St Andrews and European and Developing Countries Clinical Trials Partnership through TWENDE project (grant number; TWENDE-EDCTP-CSA-2014-283) and PanACEA II (grant number; 97118-PanACEA-TRIA.2015.1102) awarded to Professor Stephen Gillespie and Dr Wilber Sabiiti at the University of St Andrews, UK.en
dc.description.abstractBackground : Clinical symptoms are the benchmark of tuberculosis (TB) diagnosis and monitoring of treatment response but is not clear how they relate to TB bacteriology, particularly the novel tuberculosis Molecular Bacterial Load Assay (TB-MBLA). Methods : Presumptive cases were bacteriologically confirmed for TB and assessed for symptom and bacteriological resolution using smear microscopy (SM), culture and TB-MBLA over 6-month treatment course. Kaplan Meier and Kappa statistics were used to test relationship between symptom- and bacteriological-positivity. Results : A cohort of 46 bacteriologically confirmed TB cases were analysed for treatment response over a six-month treatment course. Pre-treatment symptom and bacteriological positivity concurred in over 70% of the cases. This agreement was lost in over 50% of cases whose chest pain, night sweat, and loss of appetite had resolved by week 2 of treatment. Cough resolved at a 3.2% rate weekly and was 0.3% slower than the combined bacteriological (average of MGIT and TB-MBLA positivity) resolution rate, 3.5% per week. Drop in TB-MBLA positivity reflected fall in bacillary load, 5.7±1.3- at baseline to 0.30±1.0- log10 eCFU/mL at month 6, and closer to cough resolution than other bacteriological measures, accounting for the only one bacteriologically positive case out of seven still coughing at month 6. Low baseline bacillary load patients were more likely to be bacteriologically negative, HR 5.6, p=0.003 and, HR 3.2, p=0.014 by month-2 and 6 of treatment respectively. Conclusion : The probability of clinical symptoms reflecting bacteriological positivity weakens as patient progresses on anti-TB therapy, making symptom-based diagnosis a less reliable marker of treatment response.
dc.format.extent11
dc.format.extent1925967
dc.language.isoeng
dc.relation.ispartofFrontiers in Medicineen
dc.subjectTB-MBLAen
dc.subjectDiagnosisen
dc.subjectMonitoringen
dc.subjectSymptomsen
dc.subjectBacteriological testsen
dc.subjectQR Microbiologyen
dc.subjectNDASen
dc.subjectSDG 3 - Good Health and Well-beingen
dc.subjectMCCen
dc.subject.lccQRen
dc.titleSystematic assessment of clinical and bacteriological markers for tuberculosis reveals discordance and inaccuracy of symptom-based diagnosis for treatment response monitoringen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Medicineen
dc.contributor.institutionUniversity of St Andrews. Sir James Mackenzie Institute for Early Diagnosisen
dc.contributor.institutionUniversity of St Andrews. Centre for Biophotonicsen
dc.contributor.institutionUniversity of St Andrews. Infection and Global Health Divisionen
dc.contributor.institutionUniversity of St Andrews. Global Health Implementation Groupen
dc.contributor.institutionUniversity of St Andrews. Gillespie Groupen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.identifier.doi10.3389/fmed.2022.992451
dc.description.statusPeer revieweden


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