Anemia Defisiensi Besi pada Kehamilan
Published on September 5, 2026
Risk Factors
Multigravida, short interpregnancy interval, adolescent pregnancy, poor dietary intake (low iron, folate, B12), helminth infection (hookworm), malaria-endemic regions, thalassemia trait, heavy menstrual history before pregnancy
Etiology
Most commonly iron deficiency anemia (IDA); also folate deficiency, B12 deficiency, chronic infection (TB, malaria, helminthiasis), thalassemia, and physiologic hemodilution of pregnancy
Presentation
Fatigue, weakness, pallor, dyspnea on exertion, dizziness, palpitations; often asymptomatic in mild cases (the "5L" mnemonic from Indonesian practice: Lesu, Letih, Lemah, Lelah, Lalai)
Classic Exam
Conjunctival pallor, pale nail beds, tachycardia, koilonychia (spoon nails) in severe IDA, glossitis, angular cheilitis; in severe anemia: flow murmur, signs of high-output cardiac failure
Diagnostics
Hb < 11 g/dL (WHO/Kemenkes threshold for pregnant women); low MCV and MCH in IDA; low serum ferritin (most useful single test for iron stores); elevated TIBC; peripheral smear showing microcytic hypochromic red cells
Management
Iron supplementation: 60 mg elemental iron + 400 mcg folic acid daily throughout pregnancy (Kemenkes standard TTD); dietary counseling emphasizing heme-iron sources and vitamin C; treat underlying infections; parenteral iron or transfusion for severe/refractory cases
Keywords
"Hb < 11 g/dL in pregnancy," "microcytic hypochromic," "iron deficiency," "TTD" (Tablet Tambah Darah), "blanket approach," "pallor + fatigue + pregnant," "koilonychia," "pica/pagophagia"
01Pathophysiology
Pregnancy induces a state of physiologic hemodilution. Plasma volume expands by approximately 40 to 50 percent, while red blood cell mass increases by only about 20 to 30 percent. This disproportionate expansion causes a relative drop in hemoglobin concentration, even in well-nourished women. The nadir of this physiologic dilution typically occurs around 28 to 34 weeks of gestation. This is why a mildly low Hb in the second trimester does not always indicate pathology, but values falling below 11 g/dL at any point during pregnancy are classified as anemia per WHO and Kemenkes criteria.
Buku Saku Pencegahan Anemia Kemenkes 2023 notes that during pregnancy, the body undergoes enlargement of several organs including the breasts, uterus, and placenta, along with an increase in total blood volume. Combined with fetal growth that accelerates over time, these changes markedly increase the demand for iron, folate, and other nutrients. If dietary intake cannot keep pace, the mother develops a true nutrient-deficit anemia on top of the physiologic dilution.
Iron deficiency is by far the most common cause, accounting for roughly 50 percent of anemia in pregnancy globally and an even higher proportion in developing countries. Iron is needed to synthesize hemoglobin, and during pregnancy the total iron requirement rises to approximately 1,000 mg over the entire gestational period (300 mg for the fetus and placenta, 500 mg for the expanded maternal red cell mass, and 200 mg for basal losses). Because most women begin pregnancy with suboptimal iron stores, supplementation is given as a blanket approach without checking anemia status first, as the Buku Saku Pencegahan Anemia Kemenkes 2023 explicitly recommends. The rationale cited is that with a 48.9% prevalence of anemia in Indonesian pregnant women, and an even larger proportion having depleted iron stores without overt anemia, universal supplementation is both safe and cost-effective.
At the cellular level, iron deficiency impairs hemoglobin production in developing erythroblasts, yielding smaller, paler red blood cells (microcytic, hypochromic). With fewer oxygen-carrying molecules per cell, oxygen delivery to tissues falls. The body compensates through increased cardiac output (hence palpitations and tachycardia), redistribution of blood flow (hence pallor in less critical vascular beds), and upregulation of 2,3-DPG to shift the oxygen-hemoglobin dissociation curve rightward. When these compensatory mechanisms are overwhelmed, symptoms of tissue hypoxia emerge: fatigue in muscles, poor concentration in the brain, and dyspnea reflecting increased ventilatory drive.
Buku Saku Pencegahan Anemia Kemenkes 2023 emphasizes that anemia develops gradually, allowing the body to adapt so that symptoms are often not noticed until the condition is already moderate or severe. This insidious onset is the reason screening is built into routine antenatal care rather than relying on symptomatic presentation.
Folate deficiency produces a different picture: impaired DNA synthesis leads to megaloblastic erythropoiesis with large, oval macrocytes and hypersegmented neutrophils. Neural tube defects in the fetus are the feared consequence, which is why folic acid (400 mcg) is combined with iron in the standard TTD formulation.
02Classification and Clinical Manifestation
By Severity (WHO)
Mild
Hemoglobin Level
10 to 10.9 g/dL
Typical Clinical Features
Usually asymptomatic or vague fatigue; the "5L" symptoms (Lesu, Letih, Lemah, Lelah, Lalai) may be dismissed as normal pregnancy tiredness
Moderate
Hemoglobin Level
7 to 9.9 g/dL
Typical Clinical Features
Noticeable pallor, palpitations with ordinary activities, dyspnea on exertion, exercise intolerance
Severe
Hemoglobin Level
< 7 g/dL
Typical Clinical Features
Pronounced pallor, persistent tachycardia, resting dyspnea, chest pain, signs of high-output heart failure, risk of hemodynamic instability during delivery
Severity | Hemoglobin Level | Typical Clinical Features |
|---|---|---|
Mild | 10 to 10.9 g/dL | Usually asymptomatic or vague fatigue; the "5L" symptoms (Lesu, Letih, Lemah, Lelah, Lalai) may be dismissed as normal pregnancy tiredness |
Moderate | 7 to 9.9 g/dL | Noticeable pallor, palpitations with ordinary activities, dyspnea on exertion, exercise intolerance |
Severe | < 7 g/dL | Pronounced pallor, persistent tachycardia, resting dyspnea, chest pain, signs of high-output heart failure, risk of hemodynamic instability during delivery |
By Morphology (MCV-Based)
Microcytic (MCV < 80 fL)
MCV Range
Low
Common Causes in Pregnancy
Iron deficiency (most common), thalassemia trait, anemia of chronic disease (less common in pregnancy)
Normocytic (MCV 80 to 100 fL)
MCV Range
Normal
Common Causes in Pregnancy
Acute blood loss, physiologic hemodilution, anemia of chronic disease, early iron deficiency, mixed deficiency
Macrocytic (MCV > 100 fL)
MCV Range
High
Common Causes in Pregnancy
Folate deficiency, B12 deficiency, hypothyroidism, medications (e.g., anticonvulsants)
Morphologic Type | MCV Range | Common Causes in Pregnancy |
|---|---|---|
Microcytic (MCV < 80 fL) | Low | Iron deficiency (most common), thalassemia trait, anemia of chronic disease (less common in pregnancy) |
Normocytic (MCV 80 to 100 fL) | Normal | Acute blood loss, physiologic hemodilution, anemia of chronic disease, early iron deficiency, mixed deficiency |
Macrocytic (MCV > 100 fL) | High | Folate deficiency, B12 deficiency, hypothyroidism, medications (e.g., anticonvulsants) |
Maternal and Fetal Complications
Affected Party | Complication |
|---|---|
Mother | Increased risk of hemorrhagic complications and maternal mortality; decreased immune function leading to susceptibility to infection; miscarriage/abortion |
Fetus/Neonate | Preterm birth (< 37 weeks); low birth weight / BBLR (< 2500 g); short birth length / PBLR (< 48 cm); neonatal anemia with low iron stores manifesting from age 6 months; stillbirth risk in severe maternal anemia |
Long-term offspring | Increased risk of stunting (within the 1000 HPK window), reduced cognitive development, and intergenerational cycle of non-communicable diseases (hypertension, diabetes, cardiovascular disease) |
03Diagnostic Workup
Complete Blood Count (CBC)
Role
Best initial test
Key Findings in IDA
Hb < 11 g/dL, low MCV (< 80 fL), low MCH, elevated RDW
Peripheral Blood Smear
Role
Morphologic confirmation
Key Findings in IDA
Microcytic hypochromic RBCs, pencil cells (elliptocytes), occasional target cells
Serum Ferritin
Role
Most useful single marker for iron stores
Key Findings in IDA
< 30 ng/mL confirms depleted stores (< 15 ng/mL is definitive); note that ferritin is an acute phase reactant and can be falsely normal in concurrent infection
Serum Iron / TIBC / Transferrin Saturation
Role
Supportive
Key Findings in IDA
Low serum iron, elevated TIBC, transferrin saturation < 16%
Reticulocyte Count
Role
Assess marrow response
Key Findings in IDA
Low or inappropriately normal in IDA; rises after iron supplementation (reticulocyte response expected within 5 to 7 days)
Hemoglobin Electrophoresis
Role
Rule out thalassemia
Key Findings in IDA
Elevated HbA2 in beta-thalassemia trait; essential when microcytosis persists despite iron supplementation
Stool Examination
Role
Rule out helminthiasis
Key Findings in IDA
Ova and parasites; Buku Saku Pencegahan Anemia Kemenkes 2023 highlights hookworm as a cause of chronic GI blood loss contributing to anemia
Test | Role | Key Findings in IDA |
|---|---|---|
Complete Blood Count (CBC) | Best initial test | Hb < 11 g/dL, low MCV (< 80 fL), low MCH, elevated RDW |
Peripheral Blood Smear | Morphologic confirmation | Microcytic hypochromic RBCs, pencil cells (elliptocytes), occasional target cells |
Serum Ferritin | Most useful single marker for iron stores | < 30 ng/mL confirms depleted stores (< 15 ng/mL is definitive); note that ferritin is an acute phase reactant and can be falsely normal in concurrent infection |
Serum Iron / TIBC / Transferrin Saturation | Supportive | Low serum iron, elevated TIBC, transferrin saturation < 16% |
Reticulocyte Count | Assess marrow response | Low or inappropriately normal in IDA; rises after iron supplementation (reticulocyte response expected within 5 to 7 days) |
Hemoglobin Electrophoresis | Rule out thalassemia | Elevated HbA2 in beta-thalassemia trait; essential when microcytosis persists despite iron supplementation |
Stool Examination | Rule out helminthiasis | Ova and parasites; Buku Saku Pencegahan Anemia Kemenkes 2023 highlights hookworm as a cause of chronic GI blood loss contributing to anemia |
Buku Saku Pencegahan Anemia Kemenkes 2023 stipulates that hemoglobin should be checked at least twice during pregnancy: once in the first trimester and once in the third trimester, integrated into standard ANC visits. This dual-timepoint strategy captures women who enter pregnancy already anemic as well as those who develop anemia as fetal demands peak in the third trimester.
The best initial test is a CBC. In a licensing exam vignette, you will be given a pregnant woman with fatigue and pallor, and the first thing to confirm is the hemoglobin level. A value below 11 g/dL establishes the diagnosis of anemia in pregnancy.
Once anemia is identified, the next step is to characterize it by MCV. A low MCV points toward iron deficiency or thalassemia trait. To distinguish between these two, order a serum ferritin: if ferritin is low, the diagnosis is iron deficiency. If ferritin is normal or high despite a low MCV, consider thalassemia and order hemoglobin electrophoresis. A practical discriminator often tested: in iron deficiency the RDW is elevated (anisocytosis) whereas in thalassemia trait the RDW is typically normal.
If the MCV is high (macrocytic), check folate and B12 levels. The peripheral smear showing hypersegmented neutrophils (five or more lobes) is the classic finding of megaloblastic anemia.
Buku Saku Pencegahan Anemia Kemenkes 2023 adopts a blanket supplementation policy and does not mandate Hb testing before starting TTD, because prevalence is high enough that the population-level benefit outweighs the cost of universal screening. However, for clinical management and exam purposes, Hb measurement remains the cornerstone of diagnosis and monitoring.
04Management and Treatment
Prevention (all pregnant women)
Intervention
Oral iron + folic acid (TTD)
Details
60 mg elemental iron + 400 mcg folic acid, 1 tablet daily throughout pregnancy (Kemenkes blanket approach)
Prevention (adolescent girls)
Intervention
Weekly TTD
Details
1 tablet per week year-round, given through the school-based Aksi Bergizi program
Mild to moderate IDA
Intervention
Therapeutic oral iron
Details
Increase to 120 mg elemental iron daily in divided doses + continued folic acid; reassess Hb in 4 weeks
Severe anemia (Hb < 7 g/dL) or intolerance
Intervention
IV iron (ferric carboxymaltose or iron sucrose)
Details
When oral iron fails, is not tolerated, or rapid correction is needed (e.g., third trimester with upcoming delivery)
Life-threatening / hemorrhagic
Intervention
Packed RBC transfusion
Details
Indicated for hemodynamic instability, Hb < 5 g/dL, or active hemorrhage
Adjunctive dietary counseling
Intervention
Balanced nutrition rich in heme iron
Details
Heme-iron sources (liver, shellfish, red meat, fish) and vitamin C-rich foods (citrus, guava, tomato) to enhance non-heme iron absorption; avoid tea, coffee, milk, and calcium supplements within 2 hours of taking TTD (per Kemenkes)
Treat underlying cause
Intervention
Deworming, antimalarials, TB treatment
Details
Buku Saku Pencegahan Anemia Kemenkes 2023 names kecacingan, malaria, and TB as comorbid infections that must be treated alongside iron supplementation
Setting | Intervention | Details |
|---|---|---|
Prevention (all pregnant women) | Oral iron + folic acid (TTD) | 60 mg elemental iron + 400 mcg folic acid, 1 tablet daily throughout pregnancy (Kemenkes blanket approach) |
Prevention (adolescent girls) | Weekly TTD | 1 tablet per week year-round, given through the school-based Aksi Bergizi program |
Mild to moderate IDA | Therapeutic oral iron | Increase to 120 mg elemental iron daily in divided doses + continued folic acid; reassess Hb in 4 weeks |
Severe anemia (Hb < 7 g/dL) or intolerance | IV iron (ferric carboxymaltose or iron sucrose) | When oral iron fails, is not tolerated, or rapid correction is needed (e.g., third trimester with upcoming delivery) |
Life-threatening / hemorrhagic | Packed RBC transfusion | Indicated for hemodynamic instability, Hb < 5 g/dL, or active hemorrhage |
Adjunctive dietary counseling | Balanced nutrition rich in heme iron | Heme-iron sources (liver, shellfish, red meat, fish) and vitamin C-rich foods (citrus, guava, tomato) to enhance non-heme iron absorption; avoid tea, coffee, milk, and calcium supplements within 2 hours of taking TTD (per Kemenkes) |
Treat underlying cause | Deworming, antimalarials, TB treatment | Buku Saku Pencegahan Anemia Kemenkes 2023 names kecacingan, malaria, and TB as comorbid infections that must be treated alongside iron supplementation |
All pregnant women in Indonesia receive TTD containing 60 mg of elemental iron and 400 mcg folic acid, one tablet daily, starting as early as possible in pregnancy. Buku Saku Pencegahan Anemia Kemenkes 2023 stresses that this is equivalent to 300 mg of ferrous sulfate heptahydrate, or 180 mg of ferrous fumarate, or 500 mg of ferrous gluconate. This distinction matters because many commercial multivitamins list iron in salt weight rather than elemental weight, leading to underdosing. For example, a tablet containing "60 mg ferrous fumarate" provides only about 10 mg of elemental iron, far below the recommended 60 mg.
Patients should be counseled to take TTD after meals (not on an empty stomach) or at bedtime to minimize gastrointestinal side effects such as nausea, epigastric discomfort, constipation, or diarrhea. Buku Saku Pencegahan Anemia Kemenkes 2023 also recommends taking TTD with plain water and consuming vitamin C-rich foods to enhance absorption. Within two hours before or after taking TTD, patients should avoid tea, coffee, milk, calcium tablets, and antacids, all of which impair iron absorption through chelation or mucosal coating.
Black stools are a normal and expected effect of oral iron supplementation and should not be mistaken for melena. Patients should be reassured about this.
If oral iron is not tolerated or if Hb fails to rise by at least 1 g/dL after 4 weeks of adequate oral therapy, consider parenteral iron. IV iron formulations such as ferric carboxymaltose allow large single-dose infusions and are safe in the second and third trimesters. Parenteral iron is also preferred when there is documented malabsorption or when delivery is imminent and time for oral correction is insufficient.
Blood transfusion is reserved for severe symptomatic anemia or hemodynamic compromise. The threshold is generally Hb < 5 g/dL or clinical instability regardless of Hb level.
Buku Saku Pencegahan Anemia Kemenkes 2023 explicitly addresses several myths that can undermine adherence: that TTD is a "medicine" only for sick people (it is also a supplement for prevention), that TTD raises blood pressure (it does not; iron and folic acid do not affect sodium balance), that TTD causes heavier menstruation (menstrual volume is governed by hormones, not iron), and that TTD makes the baby too large (macrosomia is related to gestational diabetes, not iron supplementation).
05Differential Diagnosis and Distractors
Physiologic anemia of pregnancy (hemodilution)
Why It Looks Similar
Hb drops in mid-pregnancy in all women; fatigue is common
Key Discriminator
Hb typically stays above 10 g/dL; MCV remains normal; ferritin is normal; no treatment needed beyond routine supplementation
Thalassemia trait (alpha or beta)
Why It Looks Similar
Microcytic anemia with low MCV, may coexist with pregnancy
Key Discriminator
MCV is disproportionately low for the degree of anemia; RDW is normal (uniform microcytosis); ferritin is normal or elevated; Hb electrophoresis shows elevated HbA2 (beta-thal trait) or is normal (alpha-thal trait, requiring genetic testing)
Folate deficiency
Why It Looks Similar
Fatigue and pallor in pregnancy, overlapping risk factors (poor diet)
Key Discriminator
MCV is elevated (macrocytic), not low; hypersegmented neutrophils on smear; low serum folate; associated neural tube defect risk
B12 deficiency
Why It Looks Similar
Macrocytic anemia, neurologic symptoms possible
Key Discriminator
Elevated MCV; low serum B12; neurologic findings (paresthesias, proprioception loss) that do not occur in folate or iron deficiency
Anemia of chronic disease (ACD)
Why It Looks Similar
Can present as microcytic or normocytic; common in women with TB or chronic infections
Key Discriminator
Ferritin is normal or elevated (key distinguisher from IDA); low TIBC (opposite of IDA); low serum iron but for different reasons (iron sequestration, not depletion)
Sickle cell disease
Why It Looks Similar
Chronic anemia, fatigue, may worsen during pregnancy
Key Discriminator
Normocytic; sickle cells and target cells on smear; Hb electrophoresis shows HbS; history of vaso-occlusive crises
Hemorrhagic anemia (placenta previa, abruption)
Why It Looks Similar
Acute drop in Hb during pregnancy
Key Discriminator
Acute onset with vaginal bleeding; normocytic anemia; hemodynamic instability; diagnosis is clinical + ultrasound for placental location
Differential | Why It Looks Similar | Key Discriminator |
|---|---|---|
Physiologic anemia of pregnancy (hemodilution) | Hb drops in mid-pregnancy in all women; fatigue is common | Hb typically stays above 10 g/dL; MCV remains normal; ferritin is normal; no treatment needed beyond routine supplementation |
Thalassemia trait (alpha or beta) | Microcytic anemia with low MCV, may coexist with pregnancy | MCV is disproportionately low for the degree of anemia; RDW is normal (uniform microcytosis); ferritin is normal or elevated; Hb electrophoresis shows elevated HbA2 (beta-thal trait) or is normal (alpha-thal trait, requiring genetic testing) |
Folate deficiency | Fatigue and pallor in pregnancy, overlapping risk factors (poor diet) | MCV is elevated (macrocytic), not low; hypersegmented neutrophils on smear; low serum folate; associated neural tube defect risk |
B12 deficiency | Macrocytic anemia, neurologic symptoms possible | Elevated MCV; low serum B12; neurologic findings (paresthesias, proprioception loss) that do not occur in folate or iron deficiency |
Anemia of chronic disease (ACD) | Can present as microcytic or normocytic; common in women with TB or chronic infections | Ferritin is normal or elevated (key distinguisher from IDA); low TIBC (opposite of IDA); low serum iron but for different reasons (iron sequestration, not depletion) |
Sickle cell disease | Chronic anemia, fatigue, may worsen during pregnancy | Normocytic; sickle cells and target cells on smear; Hb electrophoresis shows HbS; history of vaso-occlusive crises |
Hemorrhagic anemia (placenta previa, abruption) | Acute drop in Hb during pregnancy | Acute onset with vaginal bleeding; normocytic anemia; hemodynamic instability; diagnosis is clinical + ultrasound for placental location |
06Traps and High-Yield Pearls
The most common trap with anemia in pregnancy is confusing physiologic hemodilution with pathologic anemia. A vignette describing a healthy-appearing woman at 28 weeks with an Hb of 10.5 g/dL, normal MCV, and normal ferritin does not require iron therapy beyond routine supplementation. The test-writer is checking whether you know that a modest Hb drop in the second trimester can be physiologic. Conversely, if that same patient has an Hb of 9.5 g/dL with a low MCV and low ferritin, the answer is iron deficiency anemia requiring therapeutic-dose iron.
Another frequent mistake is failing to distinguish iron deficiency from thalassemia trait when both present with microcytosis. The vignette clue is the Mentzer index or, more commonly on exams, the ferritin: low ferritin means iron deficiency, normal or high ferritin with microcytosis means thalassemia. Treating a thalassemia carrier with aggressive iron supplementation is ineffective and can lead to iron overload.
Watch for questions that test timing of supplementation and compliance barriers. Buku Saku Pencegahan Anemia Kemenkes 2023 dedicates an entire section to debunking myths (TTD raises blood pressure, TTD is only needed if you feel sick, TTD causes heavy periods). These appear as patient counseling questions where the correct answer involves reassuring the patient and emphasizing continued use.
Finally, remember the iron absorption interactions. A vignette describing a compliant patient whose Hb fails to improve despite daily iron should prompt you to ask about concurrent intake of tea, coffee, calcium supplements, or antacids, all of which inhibit absorption when taken close to the iron dose. The correct next step is counseling on proper timing (separate by at least 2 hours), not switching to parenteral iron.
The core competency being tested across all anemia-in-pregnancy questions is your ability to integrate epidemiologic context (who is at risk), laboratory interpretation (MCV, ferritin, and smear findings), and stepwise management (prevention, oral therapy, parenteral rescue, transfusion) into a coherent clinical decision.