New options for replenishing the iron stores in patients with abnormal uterine bleeding

Author:

Kononova I. N.1ORCID,Dobrokhotova Ju. E.2ORCID,Kareva E. N.3,Stebenyaeva E. V.4ORCID,Shmakova N. A.5ORCID,Graban I. V.6,Krasnoshchok E. V.3,Kochina N. A.2ORCID,Orlova S. V.7ORCID,Narimanova M. R.2ORCID

Affiliation:

1. Pirogov Russian National Research Medical University; Interregional Center for Continuing Professional Education

2. Pirogov Russian National Research Medical University

3. Pirogov Russian National Research Medical University; Sechenov First Moscow State Medical University (Sechenov University)

4. Medical Center “SMARTLAB”

5. Medical Center “Angioline”

6. Medical Center “Edelweiss”

7. Peoples’ Friendship University of Russia named after Patrice Lumumba

Abstract

Introduction. The high incidence of abnormal uterine bleeding (AUB) (over 30%) among patients of reproductive age is accompanied by the development of iron deficiency anaemia (IDA), which, in turn, is a social problem among global burden diseases throughout the world.Aim. To evaluate the clinical efficacy and compliance with the Vojea complex regimen to prevent IDA in women with abnormal uterine bleeding.Materials and methods. A multicentre clinical observational study was conducted in 6 health care facilities and women’s health clinics in Yekaterinburg and Moscow. The study included 52 patients with latent iron deficiency (serum ferritin level < 15 ng/ml) who were diagnosed with abnormal uterine bleeding (AUB) due to ovulatory dysfunction. All patients received Vojea complex at a dose of 1 tablet QD for 3 months while taking pharmaceutical therapy for AUB. The clinical and laboratory efficacy and medication compliance were assessed at 30, 60 and 90 days after initiation of treatment.Results. Starting from the 1st month of treatment with the study complex, positive trends in clinical and laboratory findings were observed in both groups. After the three-month therapy with Vojea, ferritin levels increased 5.4 times (a clinically significant growth was reported after the two-month intake), plasma folate levels increased 4.9 times and red blood cell folate concentrations increased by 45%. The complex therapy helped reach and maintain the average red blood cell folate concentration >400 ng/ml (906 nmol/l). Side effects included isolated events of gastrointestinal dyspepsia and individual intolerance. All patients reported good and excellent tolerance of the complex, which ensured high compliance with the drug regimen (92%).Conclusion. The three-month therapy with Vojea complex as part of the combination approach to the treatment of AUB in women with latent iron deficiency showed high clinical and laboratory efficacy, as well as good compliance with the drug regimen.

Publisher

Remedium, Ltd.

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