Diagnostic accuracy of the Xpert MTB/Rif Ultra for tuberculosis adenitis.


Journal

BMC infectious diseases
ISSN: 1471-2334
Titre abrégé: BMC Infect Dis
Pays: England
ID NLM: 100968551

Informations de publication

Date de publication:
13 Jan 2020
Historique:
received: 05 08 2019
accepted: 28 12 2019
entrez: 15 1 2020
pubmed: 15 1 2020
medline: 9 4 2020
Statut: epublish

Résumé

The WHO recently recommended the new Xpert MTB/RIF Ultra assay (Ultra) instead of the Xpert MTB/RIF assay because Ultra has improved sensitivity. We report the diagnostic accuracy of Ultra for tuberculous adenitis in a tuberculosis and HIV endemic setting. We obtained fine-needle aspirates (FNA) and lymph node tissue by core-needle biopsy in adult patients with peripheral lymphadenopathy of >20 mm. Ultra and mycobacterial culture were performed on FNA and tissue specimens, with histological examination of tissue specimens. We assessed the diagnostic accuracy of Ultra against a composite reference standard of 'definite tuberculosis' (microbiological criteria) or 'probable tuberculosis' (histological and clinical criteria). We prospectively evaluated 99 participants of whom 50 were HIV positive: 21 had 'definite tuberculosis', 15 'probable tuberculosis' and 63 did not have tuberculosis (of whom 38% had lymphoma and 19% disseminated malignancy). Using the composite reference standard the Ultra sensitivity on FNA was 70% (95% CI 51-85; 21 of 30), and on tissue was 67% (45-84; 16/24) these were far superior to the detection of acid-fast bacilli on an FNA (26%; 7/27); AFB on tissue (33%; 8/24); or tissue culture (39%; 9/23). The detection of granulomas on histology had high senstivity (83%) but the lowest specficity. When compared with culture the Ultra on FNA had a sensitvity of 78% (40-97; 7/9) and tissue 90% (55-100; 9/10). Ultra performed on FNA or tissue of a lymph node had good sensitivity and high specificity. Ultra had a higher yield than culture and has the advantage of being a rapid test. Ultra on FNA would be an appropriate initial investigation for lymphadenopathy in tuberculosis endemic areas followed by a core biopsy for histopathology with a repeat Ultra on tissue if granulomas are present.

Sections du résumé

BACKGROUND BACKGROUND
The WHO recently recommended the new Xpert MTB/RIF Ultra assay (Ultra) instead of the Xpert MTB/RIF assay because Ultra has improved sensitivity. We report the diagnostic accuracy of Ultra for tuberculous adenitis in a tuberculosis and HIV endemic setting.
METHODS METHODS
We obtained fine-needle aspirates (FNA) and lymph node tissue by core-needle biopsy in adult patients with peripheral lymphadenopathy of >20 mm. Ultra and mycobacterial culture were performed on FNA and tissue specimens, with histological examination of tissue specimens. We assessed the diagnostic accuracy of Ultra against a composite reference standard of 'definite tuberculosis' (microbiological criteria) or 'probable tuberculosis' (histological and clinical criteria).
RESULTS RESULTS
We prospectively evaluated 99 participants of whom 50 were HIV positive: 21 had 'definite tuberculosis', 15 'probable tuberculosis' and 63 did not have tuberculosis (of whom 38% had lymphoma and 19% disseminated malignancy). Using the composite reference standard the Ultra sensitivity on FNA was 70% (95% CI 51-85; 21 of 30), and on tissue was 67% (45-84; 16/24) these were far superior to the detection of acid-fast bacilli on an FNA (26%; 7/27); AFB on tissue (33%; 8/24); or tissue culture (39%; 9/23). The detection of granulomas on histology had high senstivity (83%) but the lowest specficity. When compared with culture the Ultra on FNA had a sensitvity of 78% (40-97; 7/9) and tissue 90% (55-100; 9/10).
CONCLUSIONS CONCLUSIONS
Ultra performed on FNA or tissue of a lymph node had good sensitivity and high specificity. Ultra had a higher yield than culture and has the advantage of being a rapid test. Ultra on FNA would be an appropriate initial investigation for lymphadenopathy in tuberculosis endemic areas followed by a core biopsy for histopathology with a repeat Ultra on tissue if granulomas are present.

Identifiants

pubmed: 31931736
doi: 10.1186/s12879-019-4749-x
pii: 10.1186/s12879-019-4749-x
pmc: PMC6958753
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

33

Subventions

Organisme : FIC NIH HHS
ID : D43 TW010543
Pays : United States
Organisme : National Research Foundation
ID : 119078
Organisme : FIC NIH HHS
ID : D43 TW010345
Pays : United States
Organisme : Foundation for the National Institutes of Health
ID : D43-TW010345
Organisme : NIH HHS
ID : D43-TW010543]
Pays : United States

Commentaires et corrections

Type : ErratumIn

Références

Cochrane Database Syst Rev. 2018 Aug 27;8:CD012768
pubmed: 30148542
Am J Clin Oncol. 1982 Dec;5(6):649-55
pubmed: 7165009
Clin Infect Dis. 2011 Sep;53(6):555-62
pubmed: 21865192
Acta Cytol. 1999 Mar-Apr;43(2):153-7
pubmed: 10097702
PLoS One. 2018 Aug 13;13(8):e0201934
pubmed: 30102737
AIDS. 1993 Sep;7(9):1221-5
pubmed: 8216979
Medicine (Baltimore). 2005 Nov;84(6):350-62
pubmed: 16267410
N Engl J Med. 2017 Sep 14;377(11):1043-1054
pubmed: 28902596
J Clin Pathol. 2000 May;53(5):355-61
pubmed: 10889817
Lancet Infect Dis. 2018 Jan;18(1):76-84
pubmed: 29198911
BMJ Open. 2016 Nov 14;6(11):e012799
pubmed: 28137831
Lancet Infect Dis. 2018 Jan;18(1):68-75
pubmed: 28919338
Eur Respir J. 2014 Aug;44(2):435-46
pubmed: 24696113
Int J Tuberc Lung Dis. 2010 Jan;14(1):93-8
pubmed: 20003701
Int J Tuberc Lung Dis. 2005 Feb;9(2):220-2
pubmed: 15732745
Acad Emerg Med. 1996 Sep;3(9):895-900
pubmed: 8870764
Indian J Med Res. 2004 Oct;120(4):316-53
pubmed: 15520485
Int J Tuberc Lung Dis. 1999 Feb;3(2):162-5
pubmed: 10091884
Int J Tuberc Lung Dis. 2009 Nov;13(11):1373-9
pubmed: 19861009

Auteurs

Katherine Antel (K)

Division of Haematology, Department of Medicine, University of Cape Town, Anzio Rd, Observatory, Cape Town, 7925, South Africa. katherineantel@gmail.com.

Jenna Oosthuizen (J)

Division of Haematology, Department of Medicine, University of Cape Town, Anzio Rd, Observatory, Cape Town, 7925, South Africa.

Francois Malherbe (F)

Department of Surgery, University of Cape Town, Cape Town, South Africa.

Vernon J Louw (VJ)

Division of Haematology, Department of Medicine, University of Cape Town, Anzio Rd, Observatory, Cape Town, 7925, South Africa.

Mark P Nicol (MP)

Division of Medical Microbiology, University of Cape Town, Cape Town, South Africa.

Gary Maartens (G)

Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.

Estelle Verburgh (E)

Division of Haematology, Department of Medicine, University of Cape Town, Anzio Rd, Observatory, Cape Town, 7925, South Africa.

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Classifications MeSH