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Total dose iron dextran infusion versus oral iron for treating iron deficiency anemia in pregnant women: a randomized controlled trial.
Darwish, A M; Khalifa, E E; Rashad, E; Farghally, E.
Afiliação
  • Darwish AM; a Department of Obstetrics and Gynecology , Woman's Health University Hospital , Faculty of Medicine , Assiut University , Assiut , Egypt.
  • Khalifa EE; a Department of Obstetrics and Gynecology , Woman's Health University Hospital , Faculty of Medicine , Assiut University , Assiut , Egypt.
  • Rashad E; a Department of Obstetrics and Gynecology , Woman's Health University Hospital , Faculty of Medicine , Assiut University , Assiut , Egypt.
  • Farghally E; a Department of Obstetrics and Gynecology , Woman's Health University Hospital , Faculty of Medicine , Assiut University , Assiut , Egypt.
J Matern Fetal Neonatal Med ; 32(3): 398-403, 2019 Feb.
Article em En | MEDLINE | ID: mdl-28901214
ABSTRACT
STUDY

OBJECTIVE:

To test safety, efficacy, and cost-effectiveness of total dose infusion (TDI) of low molecular weight (LMW) iron dextran for treatment of iron deficiency anemia (IDA) during pregnancy in comparison to oral ferrous fumarate.

DESIGN:

Prospective interventional randomized controlled trial (RCT). Design classification. Canadian Task Force II3.

SETTING:

Antenatal clinic and causality unit of a tertiary care referral facility and University Hospital. PATIENTS A total 66 anemic pregnant women (hemoglobin level between 7-10 g/dl). INTERVENTION Administration of a LMW iron dextran as a TDI (group A) or Oral iron ferrous fumarate 60 mg elemental iron three times daily (group B) followed by remeasurement of hemoglobin after 4 weeks. MEASURES AND MAIN

RESULTS:

The main outcome measure was clinical and laboratory improvement of anemia after 4 weeks of starting the therapy. Both groups showed a significant clinical improvement of anemia 4 weeks post-therapy. However, the first improvement of symptoms was significantly faster in group A. Complete blood count (CBC) as well as all iron indices were improved in both groups after 4 weeks of therapy, but were significantly better in group A than B. Side effects in group B were mainly gastrointestinal (GIT) while one case of mild hypersensitivity to TDI and another one case of local reaction at the site of injection were reported in group A.

CONCLUSIONS:

It is concluded that despite being equally effective in improving both clinical and laboratory evidence of IDA, TDI allows iron restoration with a single dose faster than oral iron therapy with a reasonable safety profile. It is a good example of office one-stop therapy. Nevertheless, noninvasive selfusage at home is a clear advantage of the cheaper oral iron therapy which makes it the first choice for treating IDA in the second and third trimesters of pregnancy in tolerable cases.
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Texto completo: 1 Coleções: 01-internacional Temas: Agentes_cancerigenos Base de dados: MEDLINE Assunto principal: Complicações Hematológicas na Gravidez / Anemia Ferropriva / Ferro / Complexo Ferro-Dextran Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: J Matern Fetal Neonatal Med Assunto da revista: OBSTETRICIA / PERINATOLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Egito

Texto completo: 1 Coleções: 01-internacional Temas: Agentes_cancerigenos Base de dados: MEDLINE Assunto principal: Complicações Hematológicas na Gravidez / Anemia Ferropriva / Ferro / Complexo Ferro-Dextran Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: J Matern Fetal Neonatal Med Assunto da revista: OBSTETRICIA / PERINATOLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Egito