The Pediatric Clinician’s Approach to Adolescent Reproductive Health in Females with Sickle Cell Disease

Eugenia Vicky Asare, William Kwesi Ghunney, Samuel Antwi Oppong

Research output: Contribution to journalReview articlepeer-review

Abstract

With improvements in health care, most females with sickle cell disease (SCD) are surviving into adolescence and adulthood. Delayed onset menarche, increased risk of acute vaso-occlusive pain associated with menstruation and dysmenorrhea, and increased odds of pregnancy-related complications are prevalent in females with SCD. Significant knowledge gaps exist in the management of reproductive health issues in adolescent females with SCD. This article highlights the pediatric clinicians’ approach to essential reproductive health issues such as menarche, acute vaso-occlusive pain temporarily associated with menstruation and dysmenorrhea, and pregnancy in adolescent females with SCD.

Original languageEnglish
JournalPediatric Clinics of North America
DOIs
Publication statusAccepted/In press - 2025

Keywords

  • Acute vaso-occlusive pain temporarily associated with menstruation (acute VOPAM)
  • Adolescent care in sickle cell disease
  • Dysmenorrhea in sickle cell disease
  • Menarche in sickle cell disease
  • Pregnancy in adolescents with sickle cell disease

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