Slower response to treatment of iron-deficiency anaemia in pregnant women infected with HIV: a prospective cohort study.


Journal

BJOG : an international journal of obstetrics and gynaecology
ISSN: 1471-0528
Titre abrégé: BJOG
Pays: England
ID NLM: 100935741

Informations de publication

Date de publication:
Sep 2021
Historique:
accepted: 30 01 2021
pubmed: 16 2 2021
medline: 1 9 2021
entrez: 15 2 2021
Statut: ppublish

Résumé

Antenatal anaemia is associated with increased peripartum transfusion requirement in South Africa. We studied whether HIV was associated with the response to treatment of iron-deficiency anaemia. Prospective cohort study. Hospital-based antenatal anaemia clinic in South Africa. Equal-sized cohorts of pregnant women testing positive for HIV (HIV+) and testing negative for HIV (HIV-) with iron-deficiency anaemia. Haemoglobin trajectories of women with confirmed iron-deficiency anaemia (ferritin < 50 ng/ml) were estimated from the initiation of iron supplementation using mixed-effects modelling, adjusted for baseline HIV status, ferritin level, maternal and gestational ages and time-varying iron supplementation. Haemoglobin trajectories. Of 469 women enrolled, 51% were HIV+, 90% of whom were on antiretroviral therapy (with a mean CD4+ lymphocyte count of 403 cells/mm Compared with women who were HIV-, women who were HIV+ with iron-deficiency anaemia had slower but successful haemoglobin recovery with iron therapy. Earlier effective management of iron deficiency could reduce the incidence of peripartum blood transfusion. Among pregnant women with iron-deficiency anaemia in South Africa, HIV slows haemoglobin recovery in response to oral iron therapy.

Identifiants

pubmed: 33587784
doi: 10.1111/1471-0528.16671
pmc: PMC8364561
mid: NIHMS1674983
doi:

Substances chimiques

Iron E1UOL152H7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1674-1681

Subventions

Organisme : National Heart, Lung and Blood Institute (NHLBI) of the National Institutes of Health for the Recipient Epidemiology and Donor Evaluation Study-III International program
ID : HHSN2682011-00001I
Organisme : WHI NIH HHS
ID : HHSN268201100002C
Pays : United States
Organisme : NHLBI NIH HHS
ID : HHSN268201100009C
Pays : United States
Organisme : NHLBI NIH HHS
ID : HHSN268201100002I
Pays : United States
Organisme : WHI NIH HHS
ID : HHSN268201100001C
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL151826
Pays : United States
Organisme : NHLBI NIH HHS
ID : HHSN268201100001I
Pays : United States
Organisme : NHLBI NIH HHS
ID : HHSN268201100009I
Pays : United States
Organisme : FIC NIH HHS
ID : D43 TW010345
Pays : United States
Organisme : National Heart, Lung and Blood Institute (NHLBI) of the National Institutes of Health for the Recipient Epidemiology and Donor Evaluation Study-III International program
ID : K23-HL151826

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 John Wiley & Sons Ltd.

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Auteurs

J C Hull (JC)

Chris Hani Baragwanath Academic Hospital, Soweto, South Africa.
University of the Witwatersrand, Johannesburg, South Africa.

E M Bloch (EM)

Johns Hopkins University School of Medicine, Baltimore, MA, USA.

C Ingram (C)

National Bone Marrow Registry, Cape Town, South Africa.

R Crookes (R)

Cryo-Save Inc., Johannesburg, South Africa.

J Vaughan (J)

National Health Laboratory Services, CH Baragwanath Hospital, Soweto, South Africa.
Department of Molecular Medicine and Haematology, University of the Witwatersrand, Johannesburg, South Africa.

L Courtney (L)

RTI International, Rockville, MA, USA.

A Jauregui (A)

Stanford University School of Medicine, Stanford, CA, USA.

J F Hilton (JF)

University of California San Francisco (UCSF), San Francisco, CA, USA.

E L Murphy (EL)

University of California San Francisco (UCSF), San Francisco, CA, USA.
Vitalant Research Institute (VRI), San Francisco, CA, USA.

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Classifications MeSH