Objective. To examine the outcome and risk factors for renal sequelae in an
unselected population of adults with Henoch-Schonlein Purpura (HSP).
Methods. Retrospective study of adult patients (>20 years) with biopsy prov
ed cutaneous vasculitis diagnosed as having HSP seen at a single center bet
ween 1984 and 1998. Patients were classified as having HSP according to pro
posed criteria. Only those patients with a followup of at least 1 year wen
included in this study of renal sequelae.
Results, Twenty-eight patients with a mean followup of 5.5 years fulfilled
the inclusion criteria. When the study was concluded, 10 patients (36%) had
renal sequelae and 2 (7%) had renal insufficiency. Men outnumbered women,
However, neither a previous history of drugs, gender, nor age at disease on
set was associated with a higher risk of permanent renal involvement. Patie
nts with hematuria at disease onset or renal involvement during the course
of the disease more commonly developed renal sequelae (p < 0.001). The pres
ence of anemia (p = 0.05) at the time of diagnosis and the onset in summer
(p < 0.05) were also more common in those with permanent renal involvement
(renal sequelae). Patients with relapses had also a higher trend to develop
renal sequelae (p = 0.07). All patients who fulfilled more than 2 of these
5 risk factors developed permanent renal involvement. With this model we w
ere able to predict renal sequelae in 8 of the 10 patients who had this com
plication. The Goodman-Kruskal gamma test value was 0.92 (95% CI 0.78-1.00)
.
Conclusion. In unselected adults with HSP, permanent renal involvement (ren
al sequelae) is not uncommon, Hematuria at disease onset and persistence of
renal manifestations during the course of the disease are significant indi
cators of possible development of renal sequelae, These manifestations plus
other features such as onset in summer, anemia at disease onset, or relaps
es of the disease may predict the development of renal sequelae in most pat
ients.