WHO updates policy for the use of lateral flow urine lipoarabinomannan assay (LF-LAM) for diagnosing active TB in people living with HIV
30 October 2019 | Geneva - The World Health Organization (WHO) has updated its guidance for the use of lateral flow urine lipoarabinomannan assay (LAM) in the diagnosis of tuberculosis (TB). Following new evidence, WHO now recommends a broader use of urinary LAM assays for diagnosis of TB in people living with HIV.
“As we accelerate efforts to reach 40 million people with
TB care by 2022 as per the UN high-level meeting political
declaration, we need to have more sensitive tools to diagnose TB
in all patients, including in those with smear-negative TB,
children and people living with HIV”, said Dr Tereza
Kasaeva, Director of the WHO Global TB Programme.
Tests based on the detection of mycobacterial LAM antigen in
urine have emerged as potential point-of-care tests for TB. The
WHO Global TB Programme recommended the use of LF-LAM for the
first time in 2015.
Urinary LAM assays have greater sensitivity when used for the
diagnosis of TB in people living with HIV. The sensitivity
increases significantly in patients with lower CD4 cell counts.
Following the new evidence, WHO is recommending LF-LAM use for
diagnosis in a broader group of patients, including in adults,
adolescents and children living with HIV with signs and symptoms
of TB and CD4 cell count under 200 in inpatient settings as well
as in adults, adolescents and children living with HIV with
signs and symptoms of TB irrespective of the CD4 cell count in
outpatient settings.
The WHO End TB Strategy prioritizes early diagnosis of TB. This
includes cases of smear-negative disease, which are often
associated with HIV coinfection and young age. An estimated 9%
(0.9 million ) of the 10.0 million people who developed TB
worldwide in 2018 were among people living with HIV. The vast
majority of them (71%) are in the WHO African Region.
Source:
WHO