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