Diagnostic Accuracy of Urine Lipoarabinomannan Testing in Early Morning Urine versus Spot Urine for Diagnosis of Tuberculosis among People with HIV.


Journal

Microbiology spectrum
ISSN: 2165-0497
Titre abrégé: Microbiol Spectr
Pays: United States
ID NLM: 101634614

Informations de publication

Date de publication:
27 04 2022
Historique:
pubmed: 1 4 2022
medline: 30 4 2022
entrez: 31 3 2022
Statut: ppublish

Résumé

The Fujifilm SILVAMP TB LAM (FujiLAM) assay offers improved sensitivity compared to Determine TB LAM Ag (AlereLAM) for detecting tuberculosis (TB) among people with HIV. Here, we examined the diagnostic value of FujiLAM testing on early morning urine versus spot urine and the added value of a two-sample strategy. We assessed the diagnostic accuracy of FujiLAM on cryopreserved urine samples collected and stored as part of a prospective cohort of adults with HIV presenting for antiretroviral treatment in Ghana. We compared FujiLAM sensitivity and specificity in spontaneously voided urine samples collected at inclusion (spot urine) versus in the first voided early morning urine (morning urine) and for a one (spot urine) versus two samples (spot and morning urine) strategy. Diagnostic accuracy was determined against both microbiological (using sputum culture and Xpert MTB/RIF testing of sputum and urine to confirm TB) and composite reference standards (including microbiologically confirmed and probable TB cases). Paired urine samples of spot and morning urine were available for 389 patients. Patients had a median CD4 cell count of 176 cells/μL (interquartile range [IQR], 52 to 361). Forty-three (11.0%) had confirmed TB, and 19 (4.9%) had probable TB. Overall agreement for spot versus morning urine test results was 94.6% (kappa, 0.81). Compared to a microbiological reference standard, the FujiLAM sensitivity (95% confidence interval [CI]) was 67.4% (51.5 to 80.9) for spot and 69.8% (53.9 to 82.8) for morning urine, an absolute difference (95% CI) of 2.4% (-10.2 to 14.8). Specificity was 90.2% (86.5 to 93.1) versus 89.0% (85.2 to 92.1) for spot and morning urine, respectively, a difference of 1.2% (-3.7 to 1.4). A two-sample strategy increased FujiLAM sensitivity from 67.4% (51.5 to 80.9) to 74.4% (58.8 to 86.5), a difference of 7.0% (-3.0 to 16.9), while specificity decreased from 90.2% (86.5 to 93.1) to 87.3% (83.3 to 90.6), a difference of -2.9% (-4.9 to -0.8). This study indicates that FujiLAM testing performs equivalently on spot and early morning urine samples. Sensitivity could be increased with a two-sample strategy but at the risk of lower specificity. These data can inform future guidelines and clinical practice.

Identifiants

pubmed: 35357206
doi: 10.1128/spectrum.00208-22
pmc: PMC9045128
doi:

Substances chimiques

Lipopolysaccharides 0
lipoarabinomannan 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0020822

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Auteurs

Stephanie Bjerrum (S)

University of Southern Denmark, Research Unit for Infectious Diseases, Odense, Denmark.
Odense University Hospitalgrid.7143.1, Department of Infectious Diseases, Mycobacterial Centre for Research Southern Denmark MyCRESD, Odense, Denmark.

Johanna Åhsberg (J)

University of Southern Denmark, Research Unit for Infectious Diseases, Odense, Denmark.
Odense University Hospitalgrid.7143.1, Department of Infectious Diseases, Mycobacterial Centre for Research Southern Denmark MyCRESD, Odense, Denmark.

Rita Szekely (R)

FIND, Geneva, Switzerland.

Japheth Opintan (J)

Department of Medical Microbiology, University of Ghana Medical School, Accra, Ghana.

Margaret Lartey (M)

Department of Medicine & Therapeutics, University of Ghana Medical School, Accra, Ghana.

Maunank Shah (M)

Department of Medicine, Division of Infectious Diseases, Johns Hopkins Universitygrid.21107.35, John Hopkins University School of Medicine, Baltimore, Maryland, USA.

Satoshi Mitarai (S)

Department of Mycobacterium Reference and Research, Research Institute of Tuberculosis, Japan Anti-Tuberculosis Association, Tokyo, Japan.

Tobias Broger (T)

FIND, Geneva, Switzerland.
Division of Tropical Medicine, Center for Infectious Diseases, Heidelberg University Hospital, Heidelberg, Germany.

Isik Somuncu Johansen (IS)

University of Southern Denmark, Research Unit for Infectious Diseases, Odense, Denmark.
Odense University Hospitalgrid.7143.1, Department of Infectious Diseases, Mycobacterial Centre for Research Southern Denmark MyCRESD, Odense, Denmark.

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