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Updated: May 16, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Understanding and treating menstruation associated sickle cell pain
Halimat Olaniyan1, Bria Carrithers2, Layla Van Doren3
1Department of Clinical Pathology and Laboratory Medicine, School of Medicine, Indiana University, Bloomington, USA.
Hormonal therapies, particularly progestin-only options, can effectively manage menstruation-associated pain in sickle cell disease (SCD). These treatments reduce blood loss and acute pain episodes, while combined hormonal contraceptives should be used cautiously due to thrombotic risks.
Area of Science:
- Hematology
- Gynecology
- Vascular Biology
Background:
- Sickle cell disease (SCD) is a chronic inflammatory condition causing vaso-occlusion and organ damage.
- Menstruation exacerbates SCD pain due to blood loss and inflammation.
- The interplay between SCD vascular stress and menstruation increases acute pain episodes.
Purpose of the Study:
- To explore the intersection of SCD and menstruation.
- To emphasize hormonal therapy's role in managing menstruation-associated acute SCD pain.
Main Methods:
- Review of existing data on hormonal therapies for SCD and menstruation.
- Analysis of progestin-only therapies (DMPA, LNG-IUDs) for menstrual blood loss.
- Evaluation of risks associated with combined hormonal contraceptives (CHCs) in SCD.
Main Results:
- Progestin-only therapies effectively reduce menstrual blood loss.
- Depot medroxyprogesterone acetate (DMPA) may mitigate acute SCD pain with low thrombotic risk.
- Combined hormonal contraceptives (CHCs) may increase hypercoagulable state risks in SCD patients.
Conclusions:
- Progestin-only hormonal therapies are beneficial for managing menstruation-associated pain in SCD.
- Careful consideration of thrombotic risks is crucial when selecting contraceptives for SCD patients.
- Collaboration between gynecologists and hematologists is vital for optimal patient care.
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