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Reduced treatment delays for people with drug-resistant TB and HIV co-infection through decentralised care and rapid Xpert MTB/RIF test
Lesley Odendal, 2014-07-23 17:30:00

Decentralisation of drug-resistant tuberculosis (DR-TB) management and use of the Xpert MTB/RIF test improves the time from clinic presentation to treatment from 50 days to 7 days in a population with a high burden of HIV and TB co-infection, according to a study from Khayelitsha, South Africa, presented at the 20th International AIDS Conference (AIDS 2014) on Monday.

Xpert MTB/RIF is a rapid test for identification of TB and rifampicin-resistance. The test is being rolled out as a new diagnostic for TB management in countries with a high burden of TB and HIV co-infection, but there is limited evidence on the impact of the test in improving access to care.

Reducing the time between identification of symptoms that suggest TB and the start of treatment is critically important. A long delay between seeking health care and starting treatment increases the risk of death from TB. People with TB may be lost from care and in the meantime pass on TB to their close contacts.

The South African study found that the decentralisation of treatment for drug-resistant TB reduced the time from diagnosis to treatment initiation from nine weeks to less than four weeks. Xpert MTB/RIF further reduced the time to treatment initiation to a median of seven days, with more than 90% of people living with HIV who had rifampicin-resistant TB starting treatment.

More than 14,000 people are diagnosed with drug-resistant TB in South Africa every year, with 65% estimated to be living with HIV (often referred to as HIV and TB co-infection). While case detection of drug-resistant TB is high, only 50% of people identified start second-line TB treatment, with delays often up to several months. This leads to high mortality, particularly for people living with HIV, and ongoing transmission.

Khayelitsha is a large township 40km outside Cape Town with a population of approximately 400,000 people. The antenatal HIV prevalence is 37% and there are currently 26,000 people on antiretroviral therapy (ART).  Approximately 5100 TB cases are registered each year, with approximately 200 rifampicin-resistant cases per year, 75% of both are in people living with HIV.

Between 2007 and 2013, decentralised management of drug-resistant TB was implemented progressively. Simultaneously, over 2007-2008, first-line drug susceptibility testing (DST) moved from culture-based DST to line probe assay (LPA).

The decentralised programme diagnosed 1368 people with drug-resistant TB (rifampicin-resistance), of whom 51% were female and 72% were living with HIV. Prior to decentralisation (2003-2006), the median time to treatment was 71 days, using culture DST (IQR 22-120 days), declining to 50 (IQR 12-88) with LPA and some decentralisation during 2007-08 (p< 0.0001). Further decentralisation in 2009, 2010 and 2011 reduced the median delay to 39 days (IQR: 11-67), 32 (IQR 12-52), and 27 (IQR: 12-42) days respectively using LPA (p< 0.0001 for trend).

Xpert MTB/RIF was introduced in late 2011. This resulted in median delays of 13 (IQR: 7-19) and 7 (IQR: 3-11) days for 2012 and 2013 (p< 0.0001 when compared to the use of LPA). While HIV infection was associated with longer delays across 2009 to 2011 using LPA (p = 0.02), this significant difference disappeared in 2012-13 once Xpert MTB/RIF was being used. Across 2009 to 2011, 94% of HIV-negative patients initiated treatment, compared to 86% among people living with HIV (p = 0.001). Corresponding figures for 2012-13 using Xpert MTB/RIF were 100% and 89% respectively (p = 0.001).

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