# Gynecologic and Reproductive Health in Patients with Sickle Cell Disease: Underrecognized Challenges and Care Management Opportunities

## TL;DR

This paper reviews reproductive health challenges in sickle cell disease patients and highlights care strategies to support their reproductive goals.

## Contribution

The paper emphasizes overlooked reproductive health issues and provides guidance for healthcare providers in managing these challenges.

## Key findings

- Sickle cell disease patients face reproductive challenges like diminished ovarian reserve and infertility.
- Obstetric and perinatal risks are heightened in these patients.
- Improved counseling and care strategies can help patients achieve reproductive goals.

## Abstract

Sickle cell disease is an autosomal recessive hemoglobin disorder affecting about 100,000 people in the United States, predominantly those of African descent. A point mutation in the β-globin gene in red blood cells causes these cells to sickle under hypoxemic conditions, reducing blood flow and oxygen delivery to tissues. This manifests in the form of painful vaso-occlusive episodes, acute chest syndrome, and acute infarction of various organs, including the spleen, bone, and lung. While sickle cell disease complications such as hemolytic anemia, tissue hypoxia, and chronic organ damage are well studied, attention to the unique reproductive challenges faced by patients with sickle cell disease remains underrecognized and underappreciated. This review aims to explore key reproductive health issues in patients with sickle cell disease, including diminished ovarian reserve, infertility, and obstetric and perinatal risk. Secondly, this review aims to identify key counseling and care opportunities for providers to support patients with sickle cell disease in meeting their reproductive goals.