Abstract | BACKGROUND: METHODS: RESULTS: Thirteen patients (59%) achieved remission (complete in 31.8% and partial in 27.2%) and 12 patients showed stable or improved renal function over an average follow-up of 2.9 years (range: 0.5-7 years). There was no significant difference in response rate between African American and Caucasian patients. None of the patients had significant side-effect to tacrolimus and none of the repeat biopsies showed an increase in interstitial fibrosis compared to baseline. The best renal outcome was for patients who achieved complete remission. Partially responsive patients had improved renal function compared with resistant patients. CONCLUSION:
Tacrolimus is a viable option in the treatment of children with idiopathic steroid resistant FSGS.
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Authors | Mahmoud Kallash, Diego Aviles |
Journal | World journal of pediatrics : WJP
(World J Pediatr)
Vol. 10
Issue 2
Pg. 151-4
(May 2014)
ISSN: 1867-0687 [Electronic] Switzerland |
PMID | 24801235
(Publication Type: Journal Article)
|
Chemical References |
- Immunosuppressive Agents
- Steroids
- Tacrolimus
|
Topics |
- Adolescent
- Child
- Child, Preschool
- Female
- Glomerulosclerosis, Focal Segmental
(drug therapy)
- Humans
- Immunosuppressive Agents
(therapeutic use)
- Infant
- Male
- Proteinuria
(drug therapy)
- Retrospective Studies
- Steroids
(therapeutic use)
- Tacrolimus
(therapeutic use)
- Treatment Outcome
|