To assess the prevalence of nocturnal enuresis in children and adolescents
with sickle cell disease (SCD) and associated factors, structured telephone
interviews were conducted with primary caregivers of 217 children and adol
escents with SCD aged 5 years or older. Prevalence, perceived causes, inter
ventions undertaken, and emotional impact were assessed. Nocturnal enuresis
was significantly higher for males (28.2% of males) than for females (11%
of females), p = .002, and compared with cited population prevalence rates,
nocturnal enuresis was significantly higher for children with SCD, p < .01
. SCD was the most common reason given by primary caregivers for enuresis.
Primary caregivers used a wide range of interventions for nocturnal enuresi
s, but few used empirically supported treatments for enuresis or spoke with
their health care team about the enuresis. These data suggest that systema
tic assessment and intervention for nocturnal enuresis must be implemented
in the follow-up care of children and adolescents with SCD.