Diagnostic value of the urine lipoarabinomannan assay in HIV-positive, ambulatory patients with CD4 below 200 cells/μl in 2 low-resource settings: A prospective observational study.


Journal

PLoS medicine
ISSN: 1549-1676
Titre abrégé: PLoS Med
Pays: United States
ID NLM: 101231360

Informations de publication

Date de publication:
04 2019
Historique:
received: 09 11 2018
accepted: 28 03 2019
entrez: 1 5 2019
pubmed: 1 5 2019
medline: 28 11 2019
Statut: epublish

Résumé

Current guidelines recommend the use of the lateral flow urine lipoarabinomannan assay (LAM) in HIV-positive, ambulatory patients with signs and symptoms of tuberculosis (TB) only if they are seriously ill or have CD4 count ≤ 100 cells/μl. We assessed the diagnostic yield of including LAM in TB diagnostic algorithms in HIV-positive, ambulatory patients with CD4 < 200 cells/μl, as well as the risk of mortality in LAM-positive patients who were not diagnosed using other diagnostic tools and not treated for TB. We conducted a prospective observational study including HIV-positive adult patients with signs and symptoms of TB and CD4 < 200 cells/μl attending 6 health facilities in Malawi and Mozambique. Patients were included consecutively from 18 September 2015 to 27 October 2016 in Malawi and from 3 December 2014 to 22 August 2016 in Mozambique. All patients had a clinical exam and LAM, chest X-ray, sputum microscopy, and Xpert MTB/RIF assay (Xpert) requested. Culture in sputum was done for a subset of patients. The diagnostic yield was defined as the proportion of patients with a positive assay result among those with laboratory-confirmed TB. For the 456 patients included in the study, the median age was 36 years (IQR 31-43) and the median CD4 count was 50 cells/μl (IQR 21-108). Forty-five percent (205/456) of the patients had laboratory-confirmed TB. The diagnostic yields of LAM, microscopy, and Xpert were 82.4% (169/205), 33.7% (69/205), and 40.0% (84/205), respectively. In total, 50.2% (103/205) of the patients with laboratory-confirmed TB were diagnosed only through LAM. Overall, the use of LAM in diagnostic algorithms increased the yield of algorithms with microscopy and with Xpert by 38.0% (78/205) and 34.6% (71/205), respectively, and, specifically among patients with CD4 100-199 cells/μl, by 27.5% (14/51) and 29.4% (15/51), respectively. LAM-positive patients not diagnosed through other tools and not treated for TB had a significantly higher risk of mortality than LAM-positive patients who received treatment (adjusted risk ratio 2.57, 95% CI 1.27-5.19, p = 0.009). Although the TB diagnostic conditions in the study sites were similar to those in other resource-limited settings, the added value of LAM may depend on the availability of microscopy or Xpert results. LAM has diagnostic value for identifying TB in HIV-positive patients with signs and symptoms of TB and advanced immunodeficiency, including those with a CD4 count of 100-199 cells/μl. In this study, the use of LAM enabled the diagnosis of TB in half of the patients with confirmed TB disease; without LAM, these patients would have been missed. The rapid identification and treatment of TB enabled by LAM may decrease overall mortality risk for these patients.

Sections du résumé

BACKGROUND
Current guidelines recommend the use of the lateral flow urine lipoarabinomannan assay (LAM) in HIV-positive, ambulatory patients with signs and symptoms of tuberculosis (TB) only if they are seriously ill or have CD4 count ≤ 100 cells/μl. We assessed the diagnostic yield of including LAM in TB diagnostic algorithms in HIV-positive, ambulatory patients with CD4 < 200 cells/μl, as well as the risk of mortality in LAM-positive patients who were not diagnosed using other diagnostic tools and not treated for TB.
METHODS AND FINDINGS
We conducted a prospective observational study including HIV-positive adult patients with signs and symptoms of TB and CD4 < 200 cells/μl attending 6 health facilities in Malawi and Mozambique. Patients were included consecutively from 18 September 2015 to 27 October 2016 in Malawi and from 3 December 2014 to 22 August 2016 in Mozambique. All patients had a clinical exam and LAM, chest X-ray, sputum microscopy, and Xpert MTB/RIF assay (Xpert) requested. Culture in sputum was done for a subset of patients. The diagnostic yield was defined as the proportion of patients with a positive assay result among those with laboratory-confirmed TB. For the 456 patients included in the study, the median age was 36 years (IQR 31-43) and the median CD4 count was 50 cells/μl (IQR 21-108). Forty-five percent (205/456) of the patients had laboratory-confirmed TB. The diagnostic yields of LAM, microscopy, and Xpert were 82.4% (169/205), 33.7% (69/205), and 40.0% (84/205), respectively. In total, 50.2% (103/205) of the patients with laboratory-confirmed TB were diagnosed only through LAM. Overall, the use of LAM in diagnostic algorithms increased the yield of algorithms with microscopy and with Xpert by 38.0% (78/205) and 34.6% (71/205), respectively, and, specifically among patients with CD4 100-199 cells/μl, by 27.5% (14/51) and 29.4% (15/51), respectively. LAM-positive patients not diagnosed through other tools and not treated for TB had a significantly higher risk of mortality than LAM-positive patients who received treatment (adjusted risk ratio 2.57, 95% CI 1.27-5.19, p = 0.009). Although the TB diagnostic conditions in the study sites were similar to those in other resource-limited settings, the added value of LAM may depend on the availability of microscopy or Xpert results.
CONCLUSIONS
LAM has diagnostic value for identifying TB in HIV-positive patients with signs and symptoms of TB and advanced immunodeficiency, including those with a CD4 count of 100-199 cells/μl. In this study, the use of LAM enabled the diagnosis of TB in half of the patients with confirmed TB disease; without LAM, these patients would have been missed. The rapid identification and treatment of TB enabled by LAM may decrease overall mortality risk for these patients.

Identifiants

pubmed: 31039161
doi: 10.1371/journal.pmed.1002792
pii: PMEDICINE-D-18-03873
pmc: PMC6490904
doi:

Substances chimiques

Lipopolysaccharides 0
lipoarabinomannan 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1002792

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Références

Lancet. 2018 Jul 28;392(10144):292-301
pubmed: 30032978
Lancet. 2016 Mar 19;387(10024):1187-97
pubmed: 26970721
BMC Med. 2016 Mar 23;14:53
pubmed: 27007773
Open Forum Infect Dis. 2017 Aug 14;4(3):ofx167
pubmed: 28979922
BMC Med. 2017 Mar 21;15(1):67
pubmed: 28320384
Trans R Soc Trop Med Hyg. 2016 Mar;110(3):180-5
pubmed: 26884498
BMC Med. 2017 Aug 4;15(1):145
pubmed: 28774293
Int J Tuberc Lung Dis. 2012 Aug;16(8):1108-12
pubmed: 22710609
PLoS One. 2015 Apr 21;10(4):e0123323
pubmed: 25897661
BMC Infect Dis. 2015 Oct 01;15:407
pubmed: 26427365
J Acquir Immune Defic Syndr. 2014 Jul 1;66(3):270-9
pubmed: 24675585
BMJ Open. 2015 Apr 15;5(4):e006833
pubmed: 25877271
J Acquir Immune Defic Syndr. 2015 Aug 1;69(4):e144-6
pubmed: 25961395
AIDS. 2014 Jun 1;28(9):1307-14
pubmed: 24637544
Sci Rep. 2016 Feb 11;6:19992
pubmed: 26865526
PLoS One. 2017 Jan 26;12(1):e0170976
pubmed: 28125693
Int J Infect Dis. 2017 Jun;59:96-102
pubmed: 28457751
Int J Tuberc Lung Dis. 2013 Apr;17(4):552-8
pubmed: 23485389
PLoS One. 2015 Jul 29;10(7):e0133756
pubmed: 26222142
BMC Infect Dis. 2015 Jul 09;15:262
pubmed: 26156025
Scand J Infect Dis. 2014 Feb;46(2):144-8
pubmed: 24274710
Clin Infect Dis. 2017 Oct 1;65(7):1226-1228
pubmed: 28575238
Cochrane Database Syst Rev. 2016 May 10;(5):CD011420
pubmed: 27163343
AIDS. 2013 Nov 28;27(18):2883-92
pubmed: 25119690
BMC Infect Dis. 2012 Apr 26;12:103
pubmed: 22536883

Auteurs

Sekai Chenai Mathabire Rucker (SC)

Epicentre, Paris, France.
Médecins Sans Frontières, Lilongwe, Malawi.

Loide Cossa (L)

Médecins Sans Frontières, Maputo, Mozambique.

Isabel Amoros (I)

Médecins Sans Frontières, Lilongwe, Malawi.

Ivan Manhiça (I)

Ministry of Health, Maputo, Mozambique.

Kuzani Mbendera (K)

Ministry of Health, Lilongwe, Malawi.

Alex Telnov (A)

Médecins Sans Frontières, Geneva, Switzerland.

Elisabeth Szumilin (E)

Médecins Sans Frontières, Paris, France.

Elisabeth Sanchez-Padilla (E)

Epicentre, Paris, France.

Lucas Molfino (L)

Médecins Sans Frontières, Maputo, Mozambique.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH