This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Take the CME quiz:
Vol. 14 No. 6, December 2005
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow E-mail this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to My File Cabinet
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Aldous, M. B.
Right arrow Articles by Friedman, A. L.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Aldous, M. B.
Right arrow Articles by Friedman, A. L.
Related Collections
Right arrow Epidemiology
Right arrow Nephrology

AAP Grand Rounds 14:65 (2005)
© 2005 American Academy of Pediatrics

NEPHROLOGY AND EPIDEMIOLOGY

HSP: Risk of Renal Damage & Follow-Up Recommendations

Source: Narchi H. Risk of long term renal impairment and duration of followup recommended for Henoch-Schönlein purpura (HSP) with normal or minimal urinary findings: a systems review. Arch Dis Child. 2005;90:916–920.[Abstract/Free Full Text]

The first 20% of the full text of this article appears below.

Using the Cochrane Library, Medline, and EMBASE, the author analyzed the literature to determine the duration of follow-up needed to assess long-term risk of renal impairment after Henoch-Schönlein purpura (HSP). Of the 34 studies retrieved, only 12 met the criteria for use (previously normal renal function, timed follow-up, presence/absence of renal involvement). The 12 reports were from Europe, the United States, East Asia, the subcontinent of Asia, and the Middle East and included 1,133 children. Across the studies, follow-up ranged from 6 weeks to 36 years. Nearly 66% of the children had normal urinalysis throughout the follow- up period, while 34% had hematuria and/or proteinuria (H/P). Among the children with H/P, 80% had only isolated hematuria or proteinuria, and 20% demonstrated evidence of nephritis (hematuria with 1 or more of the following: elevated serum urea or creatinine, hypertension, or oliguria) or nephrotic syndrome (nephrotic range proteinuria >40µ/m2/hour or 50µ/kg/24 hours . . . [Full Text of this Article]

Michael B. Aldous, MD, MPH, FAAP1
1 Pediatrics, University of Arizona, Tucson, AZ

 
Aaron L. Friedman, MD, FAAP2
2 Pediatrics, Brown Medical School, Providence, RI

 



This article has been cited by other articles:


Home page
AAP Grand RoundsHome page
S. C. Li
Risk Factors for the Development of Nephritis in Henoch-Schonlein Purpura
AAP Grand Rounds, August 1, 2006; 16(2): 14 - 15.
[Full Text] [PDF]