Tubulointerstitial Nephritis and Uveitis Syndrome in Children: A Prospective Multicenter Study

Purpose To evaluate the occurrence and characteristics of uveitis related to tubulointerstitial nephritis (TIN) in children. Design Prospective, observational, multicenter, partly placebo-controlled treatment trial. Participants Nineteen children with a biopsy-proven TIN. Methods Patients were treat...

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Published inOphthalmology (Rochester, Minn.) Vol. 120; no. 7; pp. 1476 - 1481
Main Authors Saarela, Ville, MD, PhD, Nuutinen, Matti, MD, PhD, Ala-Houhala, Marja, MD, PhD, Arikoski, Pekka, MD, PhD, Rönnholm, Kai, MD, PhD, Jahnukainen, Timo, MD, PhD
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Published United States Elsevier Inc 01.07.2013
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Abstract Purpose To evaluate the occurrence and characteristics of uveitis related to tubulointerstitial nephritis (TIN) in children. Design Prospective, observational, multicenter, partly placebo-controlled treatment trial. Participants Nineteen children with a biopsy-proven TIN. Methods Patients were treated with prednisone or followed without treatment. In addition to the nephrologic evaluations, the prospective follow-up included structured ophthalmological examinations at the onset of TIN and at 3 and 6 months after the diagnosis. Main Outcome Measures Occurrence, clinical features, and outcome of uveitis. Results Some 84% (16/19) of the patients had uveitis, 83% (5/6) in the nontreatment group and 82% (9/11) in the prednisone-treated group. The remaining 2 patients, originally in the nontreatment group, were switched to the prednisone group after 2 weeks. Both of them developed uveitis. Altogether, 3 patients developed uveitis during prednisone treatment and 2 patients showed worsening of uveitis despite the systemic corticosteroid. Some 50% (8/16) of the patients with uveitis presented with no ocular symptoms; 88% (14/16) of the patients had a chronic course of uveitis. Two patients were diagnosed with uveitis before nephritis; nephritis and uveitis were diagnosed within 1 week from each other in 7 patients, and uveitis developed 1 to 6 months after the diagnosis of TIN in 7 patients. Conclusions There was no statistically significant difference in the occurrence of uveitis in patients with TIN in the prednisone and nontreatment groups. In this study, the occurrence of uveitis associated with TIN was considerably higher than previously reported. Uveitis related to TIN may develop late and is often asymptomatic. The ophthalmological follow-up of all patients with TIN is warranted for at least 12 months starting with 3-month intervals. Financial Disclosure(s) The authors have no proprietary or commercial interest in any material discussed in this article.
AbstractList To evaluate the occurrence and characteristics of uveitis related to tubulointerstitial nephritis (TIN) in children. Prospective, observational, multicenter, partly placebo-controlled treatment trial. Nineteen children with a biopsy-proven TIN. Patients were treated with prednisone or followed without treatment. In addition to the nephrologic evaluations, the prospective follow-up included structured ophthalmological examinations at the onset of TIN and at 3 and 6 months after the diagnosis. Occurrence, clinical features, and outcome of uveitis. Some 84% (16/19) of the patients had uveitis, 83% (5/6) in the nontreatment group and 82% (9/11) in the prednisone-treated group. The remaining 2 patients, originally in the nontreatment group, were switched to the prednisone group after 2 weeks. Both of them developed uveitis. Altogether, 3 patients developed uveitis during prednisone treatment and 2 patients showed worsening of uveitis despite the systemic corticosteroid. Some 50% (8/16) of the patients with uveitis presented with no ocular symptoms; 88% (14/16) of the patients had a chronic course of uveitis. Two patients were diagnosed with uveitis before nephritis; nephritis and uveitis were diagnosed within 1 week from each other in 7 patients, and uveitis developed 1 to 6 months after the diagnosis of TIN in 7 patients. There was no statistically significant difference in the occurrence of uveitis in patients with TIN in the prednisone and nontreatment groups. In this study, the occurrence of uveitis associated with TIN was considerably higher than previously reported. Uveitis related to TIN may develop late and is often asymptomatic. The ophthalmological follow-up of all patients with TIN is warranted for at least 12 months starting with 3-month intervals. The authors have no proprietary or commercial interest in any material discussed in this article.
PURPOSETo evaluate the occurrence and characteristics of uveitis related to tubulointerstitial nephritis (TIN) in children.DESIGNProspective, observational, multicenter, partly placebo-controlled treatment trial.PARTICIPANTSNineteen children with a biopsy-proven TIN.METHODSPatients were treated with prednisone or followed without treatment. In addition to the nephrologic evaluations, the prospective follow-up included structured ophthalmological examinations at the onset of TIN and at 3 and 6 months after the diagnosis.MAIN OUTCOME MEASURESOccurrence, clinical features, and outcome of uveitis.RESULTSSome 84% (16/19) of the patients had uveitis, 83% (5/6) in the nontreatment group and 82% (9/11) in the prednisone-treated group. The remaining 2 patients, originally in the nontreatment group, were switched to the prednisone group after 2 weeks. Both of them developed uveitis. Altogether, 3 patients developed uveitis during prednisone treatment and 2 patients showed worsening of uveitis despite the systemic corticosteroid. Some 50% (8/16) of the patients with uveitis presented with no ocular symptoms; 88% (14/16) of the patients had a chronic course of uveitis. Two patients were diagnosed with uveitis before nephritis; nephritis and uveitis were diagnosed within 1 week from each other in 7 patients, and uveitis developed 1 to 6 months after the diagnosis of TIN in 7 patients.CONCLUSIONSThere was no statistically significant difference in the occurrence of uveitis in patients with TIN in the prednisone and nontreatment groups. In this study, the occurrence of uveitis associated with TIN was considerably higher than previously reported. Uveitis related to TIN may develop late and is often asymptomatic. The ophthalmological follow-up of all patients with TIN is warranted for at least 12 months starting with 3-month intervals.FINANCIAL DISCLOSURE(S)The authors have no proprietary or commercial interest in any material discussed in this article.
Purpose To evaluate the occurrence and characteristics of uveitis related to tubulointerstitial nephritis (TIN) in children. Design Prospective, observational, multicenter, partly placebo-controlled treatment trial. Participants Nineteen children with a biopsy-proven TIN. Methods Patients were treated with prednisone or followed without treatment. In addition to the nephrologic evaluations, the prospective follow-up included structured ophthalmological examinations at the onset of TIN and at 3 and 6 months after the diagnosis. Main Outcome Measures Occurrence, clinical features, and outcome of uveitis. Results Some 84% (16/19) of the patients had uveitis, 83% (5/6) in the nontreatment group and 82% (9/11) in the prednisone-treated group. The remaining 2 patients, originally in the nontreatment group, were switched to the prednisone group after 2 weeks. Both of them developed uveitis. Altogether, 3 patients developed uveitis during prednisone treatment and 2 patients showed worsening of uveitis despite the systemic corticosteroid. Some 50% (8/16) of the patients with uveitis presented with no ocular symptoms; 88% (14/16) of the patients had a chronic course of uveitis. Two patients were diagnosed with uveitis before nephritis; nephritis and uveitis were diagnosed within 1 week from each other in 7 patients, and uveitis developed 1 to 6 months after the diagnosis of TIN in 7 patients. Conclusions There was no statistically significant difference in the occurrence of uveitis in patients with TIN in the prednisone and nontreatment groups. In this study, the occurrence of uveitis associated with TIN was considerably higher than previously reported. Uveitis related to TIN may develop late and is often asymptomatic. The ophthalmological follow-up of all patients with TIN is warranted for at least 12 months starting with 3-month intervals. Financial Disclosure(s) The authors have no proprietary or commercial interest in any material discussed in this article.
Author Rönnholm, Kai, MD, PhD
Saarela, Ville, MD, PhD
Nuutinen, Matti, MD, PhD
Jahnukainen, Timo, MD, PhD
Arikoski, Pekka, MD, PhD
Ala-Houhala, Marja, MD, PhD
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Snippet Purpose To evaluate the occurrence and characteristics of uveitis related to tubulointerstitial nephritis (TIN) in children. Design Prospective, observational,...
To evaluate the occurrence and characteristics of uveitis related to tubulointerstitial nephritis (TIN) in children. Prospective, observational, multicenter,...
PURPOSETo evaluate the occurrence and characteristics of uveitis related to tubulointerstitial nephritis (TIN) in children.DESIGNProspective, observational,...
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SubjectTerms Adolescent
Age of Onset
Biopsy
Child
Child, Preschool
Double-Blind Method
Female
Glucocorticoids - therapeutic use
Humans
Male
Nephritis, Interstitial - complications
Nephritis, Interstitial - diagnosis
Nephritis, Interstitial - drug therapy
Ophthalmology
Prednisone - therapeutic use
Prospective Studies
Syndrome
Treatment Outcome
Uveitis - complications
Uveitis - diagnosis
Uveitis - drug therapy
Title Tubulointerstitial Nephritis and Uveitis Syndrome in Children: A Prospective Multicenter Study
URI https://www.clinicalkey.es/playcontent/1-s2.0-S0161642012012614
https://dx.doi.org/10.1016/j.ophtha.2012.12.039
https://www.ncbi.nlm.nih.gov/pubmed/23511116
https://search.proquest.com/docview/1398424452
Volume 120
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