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Use of intravenous iron polymaltose in the management of iron deficiency in pregnancy: A retrospective cohort study
Author(s) -
Qassim Alaa,
Gergis Rosina G.,
Jeffries Bill,
Grivell Rosalie M.,
Grzeskowiak Luke E.
Publication year - 2018
Publication title -
australian and new zealand journal of obstetrics and gynaecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.734
H-Index - 65
eISSN - 1479-828X
pISSN - 0004-8666
DOI - 10.1111/ajo.12645
Subject(s) - medicine , intravenous iron , pregnancy , iron deficiency , retrospective cohort study , cohort , adverse effect , pediatrics , guideline , anemia , obstetrics , pathology , genetics , biology
Background Intravenous iron polymaltose ( IPM ) is commonly utilised in pregnancy when oral treatment is not tolerated or where rapid replenishment of iron stores is required, but data on use in pregnancy is scarce. Aim To examine the use, safety and efficacy of intravenous IPM in pregnancy. Methods Retrospective cohort study of pregnant women administered intravenous IPM between January 2014 and January 2016 at a Tertiary teaching hospital in Adelaide, Australia. Data on maternal characteristics, intravenous iron infusion details, and haematological parameters were collected from case notes and electronic records. Main outcome measures included indication for intravenous iron infusion, prevalence of infusion reactions, change in haemoglobin and correction of anaemia prior to delivery. Results Intravenous IPM was administered in 213 pregnancies, 62.0% of women with iron deficiency anaemia ( IDA ) and the remainder (38.0%) with non‐anaemic iron deficiency. Adverse drug reactions ( ADR s) occurred in 24% of women, of which 32% required infusion cessation. Anaemia was still present at delivery among 7%, and 17% of women with mild, and moderate/severe anaemia respectively. Approximately one in five anaemic women received an intravenous IPM dose below that recommended by the local guideline, particularly in women with a body mass index ≥ 25 kg/m 2 compared with <25 kg/m 2 (30.9% vs 6.3%; P < 0.001). Doses ‘at recommended’ resulted in a greater increase in haemoglobin from treatment until delivery than doses ‘below recommended’ (adjusted beta coefficient 8.4 g/L; 95% CI 2.7–14.1 g/L). Conclusion Intravenous IPM is effective in treating IDA in pregnancy but is associated with a high prevalence of ADR s and treatment cessation.