European Society of Mycobacteriology - Instituto Nacional de Saúde ...
European Society of Mycobacteriology - Instituto Nacional de Saúde ...
European Society of Mycobacteriology - Instituto Nacional de Saúde ...
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PP-105<br />
Implementation <strong>of</strong> liquid culture for tuberculosis<br />
diagnosis in a remote setting: lessons learned<br />
Pamela Hepple 1 , Jonathan Novoa-Cain 2 , Chris Cheruiyot 2 , Elvira Richter 3 , Koert Ritmeijer 4<br />
1 - Manson Unit, Mé<strong>de</strong>cins sans Frontières, London, UK<br />
2 - Mé<strong>de</strong>cins sans Frontières OCA South Sudan, Lokichoggio, Kenya<br />
3 - Forschungszentrum Borstel, Nationales Referenzzentrum für Mykobakterien, D-23845 Borstel, Germany<br />
4 - Mé<strong>de</strong>cins sans Frontières OCA, Amsterdam, the Netherlands<br />
Issues<br />
The diagnosis <strong>of</strong> tuberculosis (TB) in Mé<strong>de</strong>cins sans Frontières (MSF) projects is based on sputum smear microscopy,<br />
which has low sensitivity. Following WHO recommendations, MSF established a TB liquid culture laboratory in<br />
Lokichoggio, Kenya, processing samples from 4 South Sudan projects, for diagnosis <strong>of</strong> smear-negative and extra-pulmonary<br />
(EP) TB and follow-up <strong>of</strong> patients.<br />
Description<br />
The manual MGIT (mycobacterial growth indicator tube, Becton Dickinson) system was used with Lowenstein-Jensen<br />
media. One positive culture per patient was sent to Borstel Supranational Reference Laboratory, Germany for speciation<br />
using the Hain Genotype Mycobacteria series and sequencing techniques.<br />
From March 2007 to December 2008, sputum culture was performed for 64 diagnostic and 24 follow-up patients. Ten<br />
EP samples were also cultured.<br />
For diagnostic patients, <strong>of</strong> two smear-positives, one was culture-positive for both Mycobacterium tuberculosis (MTB) and<br />
M. fortuitum, and one for M. fortuitum.<br />
Eight <strong>of</strong> 62 (13%) smear-negatives were culture-positive for MTB complex (3 for MTB and 5 for MTBC) with nine (14%)<br />
culture-positive for other i<strong>de</strong>ntified mycobacteria; six (9%) grew unknown, not validly-<strong>de</strong>scribed mycobacteria, and 39<br />
(61%) were culture negative.<br />
For follow-up patients, <strong>of</strong> seven smear-positives, one was culture-positive for MTB, one for M. intracellulare and one for<br />
M. fortuitum complex, and four (57%) were culture-negative. Among the smear-negatives, eight <strong>of</strong> 17 (47%) were culturepositive,<br />
four <strong>of</strong> which were unknown mycobacterial species, and four non-tuberculous mycobacteria (NTM). Nine (53%)<br />
were culture-negative.<br />
Samples from three EP patients <strong>of</strong> 10 grew mycobacteria, species uni<strong>de</strong>ntifiable.<br />
In total, only 10 <strong>of</strong> 36 (28%) culture-positive patients grew mycobacteria from sputum which could be i<strong>de</strong>ntified as MTB or MTBC.<br />
Lessons learned<br />
Due to the long turn-around time between sample production and species i<strong>de</strong>ntification due to shipment issues (approximately<br />
4-6 weeks), clinicians <strong>of</strong>ten did not wait for results before initiating or adjusting therapy. The high proportion<br />
<strong>of</strong> NTM was difficult to interpret. The culture results had little clinical impact, and culture lab activities were suspen<strong>de</strong>d<br />
in February 2009.<br />
Recommendations<br />
Future TB culture programmes require facilities for on-site speciation <strong>of</strong> mycobacteria or, if working with reference labs,<br />
should minimize turn-around time to results by ensuring timely shipment <strong>of</strong> samples.<br />
<strong>European</strong> <strong>Society</strong> <strong>of</strong> <strong>Mycobacteriology</strong> | 30 th Annual Congress | July 2009 | Porto - Portugal<br />
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