Databases assessed for eligible studies included EMBASE, MEDLINE, Scopus, Web of Science Core Collection, Cochrane Central Register of Controlled Trials, Cumulative Index to Nursing and Allied Health Literature, and ClinicalTrials. gov. Searches occurred until September 26, 2022.
Eligibility assessment was performed by 2 independent reviewers, with disagreements resolved by consensus or a third reviewer. Data extraction was performed using a Microsoft Excel data extraction tool by one reviewer and independently by a second reviewer from the investigation team.1
Relevant data included location and year of study, duration of study, bias assessment, inclusion and exclusion criteria, methodology, number of participants and dropouts, demographic data, iron formulations, fatigue scored, Hb and ferritin concentrations, anemia symptoms, breastfeeding rates, adverse drug effects, depression scores, and other quality-of-life outcomes.
Fatigue was reported as the primary outcome of the analysis and was determined by any dichotomous patient reporting. Secondary outcomes included Hb, ferritin, adverse effects, breastfeeding, anemia symptoms, psychological well-being, and other quality-of-life measures.
There were 20 studies included in the final analysis, including 4196 women. Fifteen of the studies reported postpartum Hb concentration as the primary outcome. Baseline Hb ranged from 7 g/dL or less to 10.1 g/dL or more.1
Half of the studies with IV-iron intervention had IV ferric sucrose as the formation, vs IV ferric carboxymaltose in 7 and IV-iron isomaltoside in 2. Fixed IV-iron doses were reported in 5 studies, 400 mg IV-iron sucrose in 5, 600 mg IV-iron sucrose in 1, 1000 mg in 1, 1200 mg of IV-iron Isomaltoside in 1, and 1500 mg of IV-iron Isomaltoside in 1.
For oral iron, 13 studies assessed ferrous sulfate, 2 assessed ferrous ascorbate, and 1 assessed ferrous fumarate.RBC-T was assessed in 3 trials, with 1 determining RBC-T units by baseline Hb, the second randomizing women to receive a single or multiple units, and a third providing at least 1 unit to participants in the treatment arm.
When comparing fatigue between IV-iron and RBC-T, a significantly higher mean fatigue score based on the Multidimensional Fatigue Inventory was reported in women without intervention, with a mean difference (MD) of 1.06 at week 1. However, physical fatigue scores at week 12 did not significantly differ between IV-iron and RBC-T at week 12, with an MD of -0.63.1
There were also no differences in median general fatigue scores at weeks 4 through 9 between interventions in the trial comparing single and multiple units of RBC-T. Additionally, fatigue scores were similar between IV-iron and oral-iron at 14 and 42 days.
For secondary outcomes, IV-iron was associated with significantly higher Hb and overall higher ferritin concentration. When compared to oral iron, IV-iron had a significantly decreased prevalence of adverse effects. Breastfeeding outcomes did not differ between treatment modalities.1
While IV-iron led to significantly increased depression outcomes compared to oral iron, differences were not observed between IV-iron and RBC-T. Most other quality of life outcomes did not differ based on treatment, but physical function was significantly improved by RBC-T vs no intervention.
These results indicated high heterogeneity between treatment outcomes for PPA. However, evidence on RBC-T remains limited, indicating a need for future research based on the review.1
References
- Calije E, Groom KM, Dixon L, et al. Intravenous iron versus blood transfusion for postpartum anemia: a systematic review and meta-analysis. Systematic Reviews. 2024;13(9). doi:10.1186/s13643-023-02400-4
- Krewosn C. The impact of postpartum anemia and effective management strategies. Contemporary OB/GYN. June 3, 2024. Accessed July 8, 2024. https://www.contemporaryobgyn.net/view/the-impact-of-postpartum-anemia-and-effective-management-strategies