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 in | Ophthalmology (Rochester, Minn.) Vol. 120; no. 7; pp. 1476 - 1481 |
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Language | English |
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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. |
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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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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23511116$$D View this record in MEDLINE/PubMed |
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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 |
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