HIV-positive patients presenting with peripheral blood cytopenias: is bone marrow assessment a priority?
Journal
Hematology, transfusion and cell therapy
ISSN: 2531-1387
Titre abrégé: Hematol Transfus Cell Ther
Pays: Brazil
ID NLM: 101725732
Informations de publication
Date de publication:
Historique:
received:
06
11
2020
revised:
21
01
2021
accepted:
18
02
2021
pubmed:
28
7
2021
medline:
28
7
2021
entrez:
27
7
2021
Statut:
ppublish
Résumé
Hematologic abnormalities are frequent among persons living with HIV (PLWH). The bone marrow aspirate (BMA) and biopsy (BMB) are commonly performed in the diagnostic approach of patients with unexplained cytopenias. Changes in antiretrovirals, supportive therapy and increased life expectancy have modified the distribution and etiology of cytopenias, questioning their use. Our aim was to analyze the diagnostic yield of BMA, BMB and marrow cultures for the evaluation of cytopenias in PLWH. This was a retrospective cohort of ≥ 18-year-old PLWH undergoing bone marrow assessment (MA) for the evaluation of cytopenias between January 2002 and December 2015. A total of 236 cytopenic events were analyzed, 47.9% being PLWH who had a longstanding diagnosis (≥ 1 year). Adherence to antiretrovirals was 63.5%. Anemia was seen in 91.9% and pancytopenia in 39%. Common presentations included fever (52.1%), weight loss (42.8%) and adenopathies (28.8%). Median days from detection to MA was 5 (0 - 63 days). Most common etiologies were non-HIV infectious diseases (31.4%) and benign/malignant hematologic diseases (26.3%). The diagnostic yield was 16.1% for BMA, 20.3% for BMB, 30.5% for both and 35.6% when cultures were added. Patients most likely to have conclusive MA were those with moderate/severe thrombocytopenia (p = 0.007). Fever, splenomegaly, and low CD4+ counts were associated with infectious etiologies, while hematologic diagnoses were related to the presence of adenopathies. As a minimally invasive intervention, the MA has a high yield for identifying the etiology of cytopenic events in PLWH, being conclusive in one in three patients. Early performance could lead to prompt diagnosis and timely therapy initiation.
Identifiants
pubmed: 34312113
pii: S2531-1379(21)00049-3
doi: 10.1016/j.htct.2021.02.008
pmc: PMC9605914
pii:
doi:
Types de publication
Journal Article
Langues
eng
Pagination
542-548Informations de copyright
Copyright © 2021 Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular. Published by Elsevier España, S.L.U. All rights reserved.
Références
J Infect Public Health. 2010;3(3):124-9
pubmed: 20869673
AIDS. 2003 Jan 3;17(1):81-7
pubmed: 12478072
J Infect. 2007 Apr;54(4):362-6
pubmed: 16875738
Baillieres Best Pract Res Clin Haematol. 2000 Jun;13(2):215-30
pubmed: 10942622
Am J Med. 2004 Apr 5;116 Suppl 7A:27S-43S
pubmed: 15050884
Am J Med. 2001 Dec 15;111(9):704-11
pubmed: 11747850
Biosci Trends. 2015 Apr;9(2):91-6
pubmed: 26173294
J Clin Pathol. 2015 Mar;68(3):241-5
pubmed: 25589792
Am J Clin Pathol. 2013 Jan;139(1):9-29
pubmed: 23270895
Int J Lab Hematol. 2011 Jun;33(3):258-66
pubmed: 21118385
South Afr J HIV Med. 2019 Sep 30;20(1):974
pubmed: 31616572
Br J Haematol. 2015 Dec;171(5):695-709
pubmed: 26452169
Ann Intern Med. 1982 Jun;96(6 Pt 1):714-7
pubmed: 6178333
BMC Infect Dis. 2014 Sep 10;14:496
pubmed: 25209550
Genitourin Med. 1997 Apr;73(2):117-21
pubmed: 9215093
J Clin Diagn Res. 2014 Nov;8(11):FC11-5
pubmed: 25584228
Clin Infect Dis. 2004 May 15;38(10):1454-63
pubmed: 15156485