Prediction of anemia at delivery

Sci Rep. 2021 Mar 18;11(1):6309. doi: 10.1038/s41598-021-85622-7.

Abstract

We aimed to assess risk factors for anemia at delivery by conducting a secondary analysis of a prospective cohort study database including 1527 women who delivered vaginally ≥ 36 gestational weeks. Anemia (Hemoglobin (Hb) < 10.5 g/dL) was assessed at delivery. A complete blood count results during pregnancy as well as maternal and obstetrical characteristics were collected. The primary endpoint was to determine the Hb cutoff between 24 and 30 gestational weeks that is predictive of anemia at delivery by using the area under the curve (AUC) of the receiver operating characteristic curve. Independent risk factors for anemia at delivery were assessed using stepwise multivariable logistic regression. Hb and infrequent iron supplement treatment were independent risk factors for anemia at delivery (OR 0.3 95%CI [0.2-0.4] and OR 2.4 95%CI [1.2-4.8], respectively; C statistics 83%). Hb 10.6 g/dL was an accurate cutoff to predict anemia at delivery (AUC 80% 95%CI 75-84%; sensitivity 75% and specificity 74%). Iron supplement was beneficial to prevent anemia regardless of Hb value. Altogether, Hb should be routinely tested between 24 and 30 gestational weeks to screen for anemia. A flow chart for anemia screening and treatment during pregnancy is proposed in the manuscript.Trial registration: ClinicalTrials.gov Identifier: NCT02434653.

Publication types

  • Clinical Trial

MeSH terms

  • Adult
  • Anemia / blood*
  • Anemia / genetics
  • Anemia / metabolism
  • Anemia / pathology
  • Anemia, Iron-Deficiency / blood*
  • Anemia, Iron-Deficiency / genetics
  • Anemia, Iron-Deficiency / metabolism
  • Anemia, Iron-Deficiency / pathology
  • Area Under Curve
  • Blood Cell Count
  • Delivery, Obstetric
  • Female
  • Hemoglobins / genetics*
  • Hemoglobins / isolation & purification
  • Hemoglobins / metabolism
  • Humans
  • Iron / metabolism*
  • Pregnancy
  • Risk Factors

Substances

  • Hemoglobins
  • Iron

Associated data

  • ClinicalTrials.gov/NCT02434653