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The standard
All pregnant women in areas of high prevalence of malnutrition should
routinely receive iron and folate supplements, together with appropriate
dietary advice, to prevent anaemia. Where the prevalence of anaemia in
pregnant women is high (40% or more), supplementation should continue
for three months in the postpartum period.
Aim
ȱȱȱȱȱę¢ȱȱȱ ȱȱ¢ȱȱ
in the postpartum period in order to improve maternal and perinatal health.
Requirements
A national policy and locally adapted guidelines on iron and folate supplementation are
in place and are correctly implemented.
Health care providers of maternal and neonatal care are competent in: the importance of
iron supplementation during pregnancy and the postpartum period; the correct dosage
and duration of supplementation for the prevention and treatment of anaemia; anaemia
detection in pregnant women; and when to refer women for further diagnosis and
treatment.
Iron and folate supplements are available at all levels of care.
There is a functioning referral system that ensures timely referral of pregnant women
for monitoring and treatment, especially in the case of severe anaemia.
A mechanism is in place for recording cases and care of anaemia.
Health education activities are carried out to increase awareness among women and in
the community of the importance of iron and folate supplementation in pregnancy.
ȱǰȱȱȱȱĴǰȱĴȱ ȱȱȱȱ
postpartum visits must:
Give all pregnant women a standard dose of 60 mg iron + 400 μg folic acid daily for 6
months or, if 6 months of treatment cannot be achieved during the pregnancy, either
continue supplementation during the postpartum period or increase the dosage to 120
mg iron during pregnancy.
Where the prevalence of anaemia in pregnancy is over 40%, advise the woman to
continue the prophylaxis for three months in the postpartum period.
2006
Treat anaemia with doses of 120 mg iron daily for three months.
Follow up in two weeks to check clinical progress, test results and compliance and again four
weeks later all women with severe anaemia that have been treated with iron and folate.
Refer women with severe anaemia to a higher level of care if they are in the last month of
pregnancy, have signs of respiratory distress or cardiac abnormalities such as oedema, or when
ȱȱȱȱȱȱ ȱĞȱȱ ȱȱȦȱ¢ǯȱ
ȱ ȱȱȱȱȱȱȬȱȱȱȱǯ
Record test results and the treatment provided in the woman’s card.
Audit
ȱ
ȱ ȱȱȱ¢ȱȱȱȱȱȱȱȱę¢ȱȱȱ
available in health facilities.
Iron/folate supplements are available and are properly managed.
ȱ ěȱȱȱȱȱȱǻǼȱȱȱȱǻǼȱȱǰȱȱȱ
administer iron/folate supplements.
ȱȱȱ
ȱ ȱȱȱ ȱ¢ȱȱȦȱȱȱȱȱǯ
ȱ ȱȱȱ ȱȱ¢ȱȱȱȱȱǯ
The proportion of women with severe anaemia referred.
ȱ
Maternal mortality associated with severe anaemia.
Maternal complications associated with severe anaemia.
Perinatal mortality associated with severe anaemia in pregnancy.
Incidence of low birth weight associated with anaemia in pregnancy.
Rationale
ȱȱě
Ȭę¢ȱȱȱȱȱȱ ȱǰȱȱę¢ȱȱ¢ȱȱ
ȱę¢ȱȱȱ ǰȱ most common cause (1).
ěȱȱȱ ȱȱȱ
globally (1). It contributes to low birth weight, ȱȱȱȱȱę¢ȱ
lowered resistance to infection, poor cognitive anaemia by the year 2000 was among the
development and reduced work capacity (1). most important nutritional goals adopted by
Pregnant and postpartum women and children ȱęȱȱȱȱȱǻŗşşŖǼǰȱ
ȱ¢ȱȱȱȱȱ
aged 6–24 months are usually the most
ȱǻŗşşŘǼȱ(1).
ěȱȱ(1,2). It is highly prevalent in
less developed countries, where, in addition
to poor nutrition, parasitic and bacterial Ĝ¢ȱȱě
infections can contribute to depletion of iron Anaemia prophylaxis
reserves (1–4). Where the prevalence of anaemia in pregnant
women is <40%, a dose of 60 mg iron and 400
ȱȱ¢ȱȱęȱȱ μg folic acid daily for 6 months is considered
haemoglobin <11g/dl or haematocrit <33% (1). to meet the physiological requirements
ȱȱȱěȱȱȱȱȱ for iron in pregnancy. If the duration of
and infections at childbirth, and is associated supplementation is shorter, a higher dose
with increased maternal and perinatal (120 mg) is recommended. However, the
mortality and morbidity (3,4). Where anaemia majority of the systematic reviews on this
Standards 1.8 Iron and folate supplementation 3
topic refer to a dose of around 100 mg iron proportion of severe morbidity and mortality
and 350–500 μg folic acid daily for 16 weeks ȱȱȱę¢ǯȱȱȱ
or more during pregnancy (5–7). In areas and timely treatment or referral of women
with a higher prevalence of anaemia, it is with severe anaemia are therefore important
recommended that supplementation continue at the primary care level. With proper training,
for three months postpartum. and using a multiple-site assessment (inferior
conjunctiva, palm and nail bed) (10), health
Based on the possible association between workers can assess extreme pallor or very
maternal anaemia and negative perinatal low haemoglobin levels with reasonable
outcome (8)ǰȱȱȱȱȱěȱȬȱ ¢ȱȱȱę¢ȱ(10–12). Further
supplementing programmes where anaemia ȱȱȱ¢ȱȱę¢ȱ
is prevalent may reduce the incidence of of the clinical assessment could be achieved
low birth weight and perinatal mortality, as by adding a few anamnestic symptoms to
well as maternal mortality and obstetrical the pallor assessment and using a simple
complications associated to severe anaemia. colorimetric scale (12).
According to currently available reviews,
however, while there is clear evidence of a ȱȱěȱȱȱȱ
ȱěȱȱȱȱȱ supplementation is hindered by many
during pregnancy in preventing low factors, including supply problems and poor
haemoglobin at delivery or at six weeks adherence to regimens owing to the frequency
postpartum (5,6), there is no evidence of ȱȬěȱ(5,13,14), a variety of other
¢ȱěǰȱęȱȱǰȱȱȱ
interventions have been proposed to prevent
outcomes for the mother and the baby (5,6).
ȱȱȬę¢ȱǰȱȱ
ȱȱȱȱȱěȱȱȱȱȱ
ȱęǰȱ¢ȱ¢ȱȱ
the small sample size in the studies that tried
ȱȱǯȱȱěȱ
to assess those clinical aspects. The results of
of these interventions is still unclear. Dietary
the largest trial included in one review suggest
improvements (15)ȱȱęȱȱ ȱ
that routine iron supplementation may reduce
(16) and foods (17) are not supported by
the need for postpartum blood transfusions
ȱȱȱěǰȱ ȱȱ
(5). This result must be interpreted with
of parasitic (helminth and plasmodium)
caution since, as noted by the authors of the
review, the trial was not blind in respect of infections seems to enhance iron prophylaxis
treatment allocation and therapeutic decisions ȱȱĜ¢ȱȱ¢ȱ(14,18). More
could thus have been biased. Nevertheless, if research is needed in communities where iron-
ęǰȱȱȱȱȱȱ ę¢ȱȱȱȱȱȱȱ
in HIV-prevalent areas. most appropriate strategies.
The table below summarizes the evidence from the most relevant studies. The level of evidence is
ȱȱȱȱ¢ȱ ȱȱȱȱȱŗȱǻȱǼȱȱŚȱǻ ȱǼǯȱȱȱȱ
For details, see also the Introduction to the Standards for Maternal and Neonatal Care and the Process
to develop the Standards for Maternal and Neonatal CareȱȱĴDZȦȦ ǯ ǯȦȏ¢ȏ
safer/publications/en. For an overview of a comprehensive list of evidence, please refer to the
reference section of the standard.
Study
Population & ȱǭȱ ȱȱ
ǻ¢ȱǭȱȱ Results Comments
Ĵ to the Standard
ȱǼ
5. Mahomed 20 trials; pregnant To assess the Low pre-delivery Iron vs no iron
2004 women prior to 28 ěȱȱȱ haemoglobin (<10 min. NNT a 13 (12–14)
weeks’ gestation supplementation g/dl) max. NNT 2 (2–3)
Most recent and with normal on haematological 12 studies, 1802 women
substantive haemoglobin levels and biochemical
amendment, (>10 g/dl) (number parameters and on Low haemoglobin 6 ǯȱȱŗśȱǻŗřȮŗşǼȱ
ȱŗşşŝ of enrolled women pregnancy outcomes weeks postpartum ¡ǯȱȱŝȱǻŜȮŗŖǼȱȱȱȱȱȱȱ
ȱęǼ 2 studies, 1482 women
Intervention: 100
Europe, North mg elemental iron Selective vs routine
¢ȱ iron
ȱ America, Australia, orally compared
Gambia, India, with placebo or no ȱ NNH bȱŚŘȱǻŘŖȮřŜşǼȱȱȱȱȱȱȱȱȱȱ ȱȱȱ
1++ Myanmar, Niger treatment authors: increase in
Mother: blood
ȱŝśȱǻřŗȮŗŖŗŗǼȱ
Baseline risk In one study: iron caesarean sections and
transfusion needed
Low pre-delivery given routinely blood transfusions
haemoglobin level vs iron given Ȧȱ ȱŘŖŖȱǻŗśŖȮŗřȱŚśşǼȱ in the selective iron
ȮȱȱşƖȱ selectively to death supplementation
– maximum 56% women with group possibly due to
Ȭěȱȱ ȱŗŗȱǻşȮŗřǼȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱ fear of midwife and
Low post-delivery haemoglobin <10 treatment avoided ŗȱ¢ǰȱŘŜşŚȱ
haemoglobin level g/dl doctors (not blind to
ȮȱȱşǯŝƖ treatment)
6. Mahomed 8 trials involving To assess the Iron & folic acid vs Results of relevant
2004 śŚŚşȱȱ ěȱȱȱ placebo clinical outcomes are
women prior to 28 iron and folate based on a very small
Most recent weeks’ gestation supplementation Low pre-delivery ǯȱȱşȱǻşȮŗŖǼȱ single study (low
substantive and with normal on haematological haemoglobin (<10 max. NNT 3 (2–3) birth weight, stillbirth,
amendment, haemoglobin levels and biochemical g/dl) ŜȱǰȱŗŖşşȱ preterm delivery)
ȱŗşşŝ (>10g/dl) including parameters and on Low haemoglobin 6 min. NNT 11 (11–12)
adolescent women pregnancy outcomes weeks postpartum max. NNT 5 (5–6)
Myanmar, Nigeria, Intervention: 100 ŘȱǰȱŘŞşŜȱ
¢ȱ
United Kingdom, mg elemental iron ȱ ǯȱȱŗŚȱǻŗŘȮŜşǼȱ
plus 350 μg folic ¡ǯȱȱŗŗȱǻşȮśśǼȱȱȱȱȱ
1++ Baseline risk acid taken daily by 2 studies, 104 women
Low pre-delivery mouth compared
haemoglobin level with placebo or no Low birth weight ȱc
– minimum 14% treatment 1 study, 48 women
– maximum 56% 1 study, 48 women
Ȧȱ
Low post-delivery death
haemoglobin level
– minimum 10%
– maximum 20%
ȱȱ
ȮȱȱşƖȱ
– maximum 11%
a
ȱȱȱȱȱǯȱǻşśƖȱęȱǼ
b
ȱȱȱȱǯȱǻşśƖȱęȱǼ
c
ȱȱȬę
ŗǯȱ £ȱǰȱ¢ȱǯȱGuidelines for the use of iron supplements to prevent and treat iron
ę¢ȱǯȱǰȱǰȱȱǰȱŗşşŞȱǻĴDZȦȦǯǯȦęȦŘȏ
Ş
ǯ
ǰȱȱŝȱ¢ȱŘŖŖśǼǯ
2. Ȯ¢ȱDZȱȱȱȱȱǯ Geneva, World Health
£ǰȱŗşşŜȱǻȱ
Ȧ
ȦȦȱşŚǯŗŗǼȱǻĴDZȦȦ ǯ ǯȦȬ
ȦȦȏşŚȏŗŗȦȏşŚȏŗŗȏȏȏǯǯǰȱȱŗřȱ
December 2004).
Standards 1.8 Iron and folate supplementation 5
Study
Population & ȱǭȱ ȱȱȱ
ǻ¢ȱǭȱȱ Results Comments
Ĵ the standard
ȱǼ
ŗřǯȱǰȱ 23 randomized To review the Haemoglobin ŜŖȱDZȱƸȱŖǯŚŗȱǻƹŖǯŖŘŝǼȱȦ The authors
ȱǭȱ controlled trials, Ĝ¢ȱȱȱ increase by daily question the
ěȱŘŖŖŘȱ 15 of which supplementation dose of iron ŜŗȮşŖȱDZȱƸȱŖǯŞŜȱǻƹŖǯŖŗŞǼȱȦ opportunity of
conducted in on haemoglobin supplement şŗȮŗŘŖȱDZȱƸȱŗǯŞŝȱǻƹŖǯŖŘŝǼȱȦ recommending
developing level in pregnant large-scale,
¢ȱ countries; the women ǁŗŘŖȱDZȱƸȱŗǯŝŞȱǻƹŖǯŖŚŘǼȱȦ public health
majority set in ȱȱěȱȱȱ oral iron
Here results refer Haemoglobin
antenatal clinics; compared to iron alone (6 supplementation
1++ only to developing increase by
only 2 set in rural studies) programmes
country studies ȱěȱȱ
areas; around 1000 as a means
folate
pregnant women ȱ of reducing
dosages vary from Haemoglobin Only one small study: iron global maternal
<60 mg/day to increase by iron and + antimalarial is not more anaemia and
Average baseline >120 mg/day, the antimalarials ěȱȱȱ call for further
haemoglobin level ¢ȱȱǁşŖȱ alone studies to
<11 g/dl mg/day determine the
Haemoglobin In one study there is additive ěȱȱ
increase by iron and ě other approaches
vitamin A (prevention
The majority of the studies
reported it as a problem of hookworm
infection, food
Adherence to Only two studies quantify ęǰȱ
supplementation this aspect: 42% adherence prenatal
that increases (61%) with prophylactic
slow-release gastric delivery treatment of
system; low adherence is due falciparum
ȱȬěȱȱȱȱ malaria)
dose-dependent
ŗŖǯȱ£ȱȱ şŚśȱȱ To study the Pregnancy 3 months Multiple site
ǯȱŗşşş women and association postpartum assessment
ŝŘŖȱ ȱ between clinical is highly
Validation at 3 months pallor as detected řśǯŝƖȱ recommended
study Haemoglobin 10 g/dl 18.2%
postpartum from by health workers – sensitivity şŚǯŗƖ şŚǯřƖ (increase in
rural area opportunely Ȯȱę¢ sensitivity
trained and with just slight
Nepal haemoglobin decrease of
HaemoglobinȱşȱȦȱȱȱȱȱȱȱ 28% 51.5%
concentration – sensitivity şřǯŚƖ şŘǯŘƖ ę¢Ǽ
(sensitivity and Ȯȱę¢
ę¢Ǽ
Haemoglobin 8 g/dl 45.8% ŜŘǯŝƖȱȱȱȱȱȱ
ȱȱ – sensitivity ŞşǯŞƖ
şŘǯřƖ
assessed in three Ȯȱę¢
sites: inferior
conjunctiva, palm
ȱŝȱȦȱȱȱȱȱȱ ŜŝǯśƖȱȱȱȱȱ 81.0%
and nail bed – sensitivity şŗǯśƖ 88.1%
Ȯȱę¢
Two days of
training
ȱȱȱ
I. ȱę¢ȱȱǰȱȱȱǯȱȱȱȱȱ. Geneva,
World Health Organization, 2001 ( document WHO/NHD/10.3).
ǯȱ ȱȱȱǯȱȱȱȱȱȱȱȱȱȃȱȄȱǯȱIndian
Journal of PaediatricsǰȱŗşşŞǰȱŜśDZŞŚşȮŞśŜǯ
ǯȱ ȱǰȱȱǰȱȱ
ȱǯȱȱȱȱȱȱȱȱȱȱȱ-
mia. Public Health and Nutrition, 2000, 3:125–150.
ȱȱȱȱȱȱȱĴȱȱ
This document ȱȱȱȱȱȱ DZȱȱȱǰȱǰȱȱȱȱ
ȱȱDzȱȱȱȱȱȱȱȱȱȱȱȱ
is not a formal Standards for Maternal and Neonatal ȱĴǰȱ
ȱǰȱȱĴǰȱȱǰȱȱ
ȱȱȱȱȱ
publication of ǻȱȱȱ¢ȱǼǯ
ȱȱ¢ȱȱȱ
the World Health
ȱȱ¢ȱǰȱ
Organization ȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱȱ
World Health Organization.
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all rights are ȱĴȱȱ
ȱȱĜȱȱ ȱȱȱȱȱȱ
For further information please ǰȱŗŚȬŗŜȱȱŘŖŖŘǯȱȱȱȱȱȱȱȱěȱȱȱȬ
reserved by the
: ȱǻȱȱǰȱĴȱǰȱ ȱ ǰȱȱĴǰȱȱȱ
Organization.
Department of Making Pregnancy and Nicola Magrini) developed the table of evidence and provided additional insightful review of
The document
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may, however, be ęȱĞǰȱȱȱȱȱȱȱȱ ¢ȱȱȱ¢ǯ
World Health Organization (WHO)
freely reviewed,
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