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Management of pregnancy - VA/DoD Clinical Practice Guidelines ...

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<strong>VA</strong>/<strong>DoD</strong> <strong>Clinical</strong> <strong>Practice</strong> Guideline<br />

For Pregnancy <strong>Management</strong><br />

RECOMMENDATIONS<br />

1. All pregnant women should be screened for anemia during <strong>pregnancy</strong> with a hematocrit or hemoglobin<br />

measurement in the first and third trimester. [C]<br />

2. Pregnant women with anemia should be further evaluated to define the cause <strong>of</strong> the anemia and given nutrient<br />

supplementation if deficient (e.g. iron, B12 or Folate). [C]<br />

3.<br />

4.<br />

Red blood cell transfusion should be considered for pregnant women with severe anemia. [C]<br />

Iron sucrose transfusion should be considered for pregnant women with iron deficiency anemia who fail to<br />

respond to oral iron supplementation after eliminating modifiable causes <strong>of</strong> malabsorption. [C]<br />

EVIDENCE TABLE<br />

Recommendations Sources <strong>of</strong> Evidence LE QE SR<br />

1 All pregnant women should be<br />

screened for anemia during <strong>pregnancy</strong><br />

with a hematocrit or hemoglobin<br />

measurement in the first and third<br />

trimester<br />

2 Pregnant women with anemia should<br />

be further evaluated to define the cause<br />

<strong>of</strong> the anemia and given nutrient<br />

supplementation if deficient (e.g. iron,<br />

B12 or Folate)<br />

ACOG, 2008 #95<br />

CDC, 1998<br />

ACOG, 2008 #95<br />

Institute <strong>of</strong> Medicine, 1993<br />

Reveiz et al., 2007<br />

III Fair C<br />

II, III Fair C<br />

3 Red blood cell transfusion should be<br />

considered for pregnant women with<br />

severe anemia<br />

ACOG, 2008 #95 II Fair C<br />

4 Iron sucrose transfusion should be<br />

considered for pregnant women with<br />

iron deficiency anemia who fail to<br />

respond to oral iron supplementation<br />

after eliminating modifiable causes <strong>of</strong><br />

malabsorption<br />

ACOG, 2008 #95<br />

Faich & Strobos, 1999<br />

Bhandal & Russell, 2006<br />

III Fair C<br />

LE = Level <strong>of</strong> Evidence; QE = Quality <strong>of</strong> Evidence; SR = Strength <strong>of</strong> Recommendation (See Appendix A)<br />

I­ 19. Screening for Hemoglobinopathies: Weeks 6­8<br />

BACKGROUND<br />

The hemoglobinopathies are a heterogeneous group <strong>of</strong> single-gene disorders that includes the structural hemoglobin<br />

variants such as sickle cell disease and thalassemia. More than 270 million people worldwide are heterozygous<br />

carriers <strong>of</strong> hereditary disorders <strong>of</strong> hemoglobin, and at least 300,000 affected homozygotes or compound<br />

heterozygotes are born each year. Sickle cell disease and the thalassemias are discussed below.<br />

RECOMMENDATIONS<br />

1. Carrier screening should be <strong>of</strong>fered to individuals <strong>of</strong> African, Southeast Asian, and Mediterranean descent. [A]<br />

2. A complete blood count and hemoglobin electrophoresis are the recommended tests to screen for<br />

hemoglobinopathies. [B]<br />

Interventions Page - 46

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