Treatment status of iron medications for anemia in patients visiting gynecological or obstetric facilities: analyses using Japanese claims data
4 affiliations
- 1Department of Obstetrics and Gynecology, Juntendo University Faculty of Medicine, Tokyo, Japan
- 2Milliman, Inc, Tokyo, Japan
- 3Medical Planning Dept, Nippon Shinyaku Co.,Ltd, Kyoto, Japan
- 4Department of Obstetrics and Gynecology, Reproductive Medicine Graduate School of Medicine Chiba University, Chiba, Japan
Abstract
Background: Anemia is highly prevalent among women of reproductive age and can have negative health effects. Thus, appropriate and effective treatment is essential to mitigate these effects. This study assessed the current treatment status of iron-deficiency anemia in this population.
Methods: Data from women aged 20–49 years who visited gynecological or obstetric facilities were analyzed using a Japanese health insurance claims database (June 2018–August 2022) provided by DeSC Healthcare, Inc.; the database included health checkup data. Patients were identified based on diagnoses of gynecological or obstetric disorders, diagnoses of obstetric supervision, or family identification based on a newborn baby. The duration of oral iron administration, the amount of iron replenished by intravenous (IV) iron infusions (saccharated ferric oxide [SFO] or ferric carboxymaltose [FCM]), and the status of oral iron medication prescriptions following IV iron infusions were analyzed.
Results: The median treatment durations with oral iron were 4.1 weeks for all patients, 4.4 weeks for those with Hb levels of 8–10 g/dL, and 8.7 weeks for those with Hb levels < 8 g/dL. The doses of IV iron preparations, particularly SFO, were often lower than the required doses calculated based on Hb levels and body weight. The required dose was achieved in 0.7% of the total administration episodes for SFO and in 46.4% of those for FCM. Oral iron medications were prescribed within 4 weeks after IV infusion for 37.5% of the SFO administration episodes and 20.8% of the FCM administration episodes. The iron dose administered per episode via oral medications exceeded that administered via IV infusions with SFO.
Conclusions: Treatment duration of approximately 1 month with oral iron appears insufficient to fully replenish iron reserves. IV iron therapy doses were often lower than required. Despite recommendations against following IV iron therapy with oral iron treatment, frequent use of oral iron medications was observed shortly after IV infusion. Considering the potential negative effects of anemia, women of reproductive age should receive appropriate and effective treatment for iron-deficiency anemia, regardless of the presence of subjective symptoms.
Supplementary Information: The online version contains supplementary material available at https://doi.org/10.1186/s12905-026-04769-5.
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BibTeX
@article{takeda2026treatment,
title = {{Treatment status of iron medications for anemia in patients visiting gynecological or obstetric facilities: analyses using Japanese claims data}},
author = {Jun Takeda and Tomomi Takeshima and Kosuke Iwasaki and Yohei Sonoyama and Natsumi Honda and Hiromichi Niida and Kaori Koga},
journal = {BMC Women's Health},
year = {2026},
month = aug,
doi = {10.1186/s12905-026-04769-5},
url = {https://doi.org/10.1186/s12905-026-04769-5},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Treatment status of iron medications for anemia in patients visiting gynecological or obstetric facilities: analyses using Japanese claims data
AU - Jun Takeda
AU - Tomomi Takeshima
AU - Kosuke Iwasaki
AU - Yohei Sonoyama
AU - Natsumi Honda
AU - Hiromichi Niida
AU - Kaori Koga
PY - 2026
DA - 2026/08/08
JO - BMC Women's Health
DO - 10.1186/s12905-026-04769-5
UR - https://doi.org/10.1186/s12905-026-04769-5
AB - Background: Anemia is highly prevalent among women of reproductive age and can have negative health effects. Thus, appropriate and effective treatment is essential to mitigate these effects. This study assessed the current treatment status of iron-deficiency anemia in this population. Methods: Data from women aged 20–49 years who visited gynecological or obstetric facilities were analyzed using a Japanese health insurance claims database (June 2018–August 2022) provided by DeSC Healthcare, Inc.; the database included health checkup data. Patients were identified based on diagnoses of gynecological or obstetric disorders, diagnoses of obstetric supervision, or family identification based on a newborn baby. The duration of oral iron administration, the amount of iron replenished by intravenous (IV) iron infusions (saccharated ferric oxide [SFO] or ferric carboxymaltose [FCM]), and the status of oral iron medication prescriptions following IV iron infusions were analyzed. Results: The median treatment durations with oral iron were 4.1 weeks for all patients, 4.4 weeks for those with Hb levels of 8–10 g/dL, and 8.7 weeks for those with Hb levels < 8 g/dL. The doses of IV iron preparations, particularly SFO, were often lower than the required doses calculated based on Hb levels and body weight. The required dose was achieved in 0.7% of the total administration episodes for SFO and in 46.4% of those for FCM. Oral iron medications were prescribed within 4 weeks after IV infusion for 37.5% of the SFO administration episodes and 20.8% of the FCM administration episodes. The iron dose administered per episode via oral medications exceeded that administered via IV infusions with SFO. Conclusions: Treatment duration of approximately 1 month with oral iron appears insufficient to fully replenish iron reserves. IV iron therapy doses were often lower than required. Despite recommendations against following IV iron therapy with oral iron treatment, frequent use of oral iron medications was observed shortly after IV infusion. Considering the potential negative effects of anemia, women of reproductive age should receive appropriate and effective treatment for iron-deficiency anemia, regardless of the presence of subjective symptoms. Supplementary Information: The online version contains supplementary material available at https://doi.org/10.1186/s12905-026-04769-5.
SN - 1472-6874
ER -