Body | Year | Title | Recommendations in the antenatal period (evidence level) |
---|---|---|---|
British Committee for Standards in Haematology [5] | 2012 | UK guidelines on the management of iron deficiency in pregnancy | • Women with Hb <110 g/l or <105 g/l in the second and third trimesters, should have a trial of oral iron as the first line diagnostic test for microcytic or normocytic anaemia; an increased Hb after two weeks of therapy is taken to be confirmatory (1B). |
• Refer to secondary care for further investigation for other causes of anaemia if Hb does not improve after 2 weeks, severe <70 g/l, significant symptoms or late gestation (>34 weeks) (2B). | |||
• Routine ferritin testing in non-anaemic pregnant women is not recommended unless they are ‘at risk’ of iron deficiency (2B). | |||
• Treatment is suggested where ferritin is <30 mcg/l with rapid review and follow up of results (2A) | |||
Women at risk include: 1. anaemic women where estimation of iron stores is necessary, e.g. women with haemogloblinopathies or prior to parenteral iron replacement | |||
2. those who are not anaemic but at risk of iron depletion (previous anaemia, multiparity > 3, consecutive pregnancy, vegetarians, teenage pregnancies, recent history of bleeding) | |||
3. Non-anaemic women where estimation of iron stores is necessary as significant blood loss may occur (high bleeding risk, Jehovah witnesses). | |||
• Consider IV iron from the 2nd trimester onwards if absolute non-compliance or intolerance to oral iron or proven malabsorption (1A) | |||
• All women should receive dietary counselling detailing iron rich foods, inhibitory factors reinforced by provision of an information leaflet (1A) | |||
• Evidence level AHCPR methodology | |||
National Institute for Health and Care Excellence Clinical [4] | 2008 | Antenatal Care: routine care for the healthy pregnant woman. Guideline 62. | • Hb should be checked at booking and 28 weeks when other blood screening tests are being carried out (B) |
• nutritional information should be offered to all pregnant women (A) | |||
• Hb <110 g/l 1st trimester and 105 g/l at 28 weeks should be investigated and iron supplementation considered in indicated (A) | |||
• iron supplementation should not be offered routinely as there are unpleasant maternal side effects with no clearly demonstrated maternal and infant benefits (A) | |||
• Evidence level GRADE methodology | |||
Royal College of Obstetricians and Gynaecologists [6] | 2007 | Blood Transfusions in Obstetrics Green-top 47 | • Anaemia should be treated to reduce probability of transfusion requirement (GPP). |
• If Hb <105 g/l in the antenatal period, consider haematinic deficiency (GPP). | |||
• Once haemoglobinopathies have been excluded, oral iron should be the first-line treatment for iron deficiency (GPP). | |||
• Parenteral iron is indicated when oral iron is not tolerated, absorbed or patient compliance is in doubt (GPP). | |||
• Evidence level AHCPR methodology + GPP (clinical good practice point where evidence lacking) |