Trends in Sickle Cell Disease-related Priapism in U.S. Children's Hospitals

Hsin-Hsiao Scott Wang1, Katherine W Herbst2, Jennifer A Rothman3

  • 1Department of Surgery, Duke University Medical Center, Durham, NC.

Urology
|December 18, 2015
PubMed

Insights

Hospital admissions for priapism in males with sickle cell disease (SCD) decreased from 2004 to 2012. However, the overall number of patients diagnosed with SCD-related priapism remained stable, with wide variations in admission rates across hospitals.

Area of Science:

  • Hematology
  • Pediatric Urology

Background:

  • Sickle cell disease (SCD) is a genetic blood disorder.
  • Priapism, a prolonged erection, is a known complication of SCD.
  • Understanding diagnosis and admission patterns is crucial for managing SCD complications.

Purpose of the Study:

  • To determine the incidence of priapism diagnosis and inpatient admissions in males with SCD.
  • To analyze trends in priapism diagnosis and admissions over time.
  • To investigate variations in priapism admission rates among different hospitals.

Main Methods:

  • Retrospective review of the Pediatric Health Information System (PHIS) database.
  • Inclusion of males under 21 years old treated between 2004 and 2012.
  • Identification of SCD and priapism using ICD-9-CM codes; statistical analysis using logistic regression and GEE models.

Main Results:

  • 17,186 males with SCD were analyzed, with 748 priapism admissions (2.1%).
  • Priapism admissions significantly decreased from 0.81% in 2004 to 0.44% in 2012 (P < .001).
  • The number of patients diagnosed with SCD-related priapism showed no significant trend; older age correlated with higher admission likelihood.

Conclusions:

  • While priapism admissions for SCD decreased, the number of diagnosed patients did not change significantly.
  • Significant variability exists in priapism admission rates among hospitals.
  • Further research into hospital-specific management strategies for priapism in SCD patients is warranted.
Abstract

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