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Drug-induced acute interstitial nephritis: A clinicopathological study and comparative trial of steroid regimens

Steroids are used in the management of drug-induced acute interstitial nephritis (AIN). The present study was undertaken to compare the efficacy of pulse methyl prednisolone with oral prednisolone in the treatment of drug-induced AIN. Patients with biopsy-proven AIN with a history of drug intake wer...

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Autores principales: Ramachandran, R., Kumar, K., Nada, R., Jha, V., Gupta, K. L., Kohli, H. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588323/
https://www.ncbi.nlm.nih.gov/pubmed/26628793
http://dx.doi.org/10.4103/0971-4065.147766
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author Ramachandran, R.
Kumar, K.
Nada, R.
Jha, V.
Gupta, K. L.
Kohli, H. S.
author_facet Ramachandran, R.
Kumar, K.
Nada, R.
Jha, V.
Gupta, K. L.
Kohli, H. S.
author_sort Ramachandran, R.
collection PubMed
description Steroids are used in the management of drug-induced acute interstitial nephritis (AIN). The present study was undertaken to compare the efficacy of pulse methyl prednisolone with oral prednisolone in the treatment of drug-induced AIN. Patients with biopsy-proven AIN with a history of drug intake were randomized to oral prednisolone (Group 1) 1 mg/kg for 3 weeks or a pulse methyl prednisolone (Group II) 30 mg/kg for 3 days followed by oral prednisolone 1 mg/kg for 2 weeks, tapered over 3 weeks. Kidney biopsy scoring was done for interstitial edema, infiltration and tubular damage. The response was reported as complete remission (CR) (improvement in estimated glomerular filtration rate [eGFR] to ≥60 ml/min/1.73 m(2)), partial remission (PR) (improvement but eGFR <60 ml/min/1.73 m(2)) or resistance (no CR/PR). A total of 29 patients, Group I: 16 and Group II: 13 were studied. Offending drugs included nonsteroidal anti-inflammatory drugs, herbal drugs, antibiotics, diuretic, rifampicin and omeprazole. There was no difference in the baseline parameters between the two groups. The biopsy score in Groups I and II was 5.9 ± 1.1 and 5.1 ± 1.2, respectively. At 3 months in Group I, eight patients each (50%) achieved CR and PR. In Group II, 8 (61%) achieved CR and 5 (39%) PR. This was not significantly different. Percentage fall in serum creatinine at 1 week (56%) was higher in CR as compared to (42%) those with PR. (P = 0.14). Patients with neutrophil infiltration had higher CR compared to patients with no neutrophil infiltration (P = 0.01). Early steroid therapy, both oral and pulse steroid, is equally effective in achieving remission in drug-induced AIN.
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spelling pubmed-45883232015-12-01 Drug-induced acute interstitial nephritis: A clinicopathological study and comparative trial of steroid regimens Ramachandran, R. Kumar, K. Nada, R. Jha, V. Gupta, K. L. Kohli, H. S. Indian J Nephrol Original Article Steroids are used in the management of drug-induced acute interstitial nephritis (AIN). The present study was undertaken to compare the efficacy of pulse methyl prednisolone with oral prednisolone in the treatment of drug-induced AIN. Patients with biopsy-proven AIN with a history of drug intake were randomized to oral prednisolone (Group 1) 1 mg/kg for 3 weeks or a pulse methyl prednisolone (Group II) 30 mg/kg for 3 days followed by oral prednisolone 1 mg/kg for 2 weeks, tapered over 3 weeks. Kidney biopsy scoring was done for interstitial edema, infiltration and tubular damage. The response was reported as complete remission (CR) (improvement in estimated glomerular filtration rate [eGFR] to ≥60 ml/min/1.73 m(2)), partial remission (PR) (improvement but eGFR <60 ml/min/1.73 m(2)) or resistance (no CR/PR). A total of 29 patients, Group I: 16 and Group II: 13 were studied. Offending drugs included nonsteroidal anti-inflammatory drugs, herbal drugs, antibiotics, diuretic, rifampicin and omeprazole. There was no difference in the baseline parameters between the two groups. The biopsy score in Groups I and II was 5.9 ± 1.1 and 5.1 ± 1.2, respectively. At 3 months in Group I, eight patients each (50%) achieved CR and PR. In Group II, 8 (61%) achieved CR and 5 (39%) PR. This was not significantly different. Percentage fall in serum creatinine at 1 week (56%) was higher in CR as compared to (42%) those with PR. (P = 0.14). Patients with neutrophil infiltration had higher CR compared to patients with no neutrophil infiltration (P = 0.01). Early steroid therapy, both oral and pulse steroid, is equally effective in achieving remission in drug-induced AIN. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4588323/ /pubmed/26628793 http://dx.doi.org/10.4103/0971-4065.147766 Text en Copyright: © Indian Journal of Nephrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Ramachandran, R.
Kumar, K.
Nada, R.
Jha, V.
Gupta, K. L.
Kohli, H. S.
Drug-induced acute interstitial nephritis: A clinicopathological study and comparative trial of steroid regimens
title Drug-induced acute interstitial nephritis: A clinicopathological study and comparative trial of steroid regimens
title_full Drug-induced acute interstitial nephritis: A clinicopathological study and comparative trial of steroid regimens
title_fullStr Drug-induced acute interstitial nephritis: A clinicopathological study and comparative trial of steroid regimens
title_full_unstemmed Drug-induced acute interstitial nephritis: A clinicopathological study and comparative trial of steroid regimens
title_short Drug-induced acute interstitial nephritis: A clinicopathological study and comparative trial of steroid regimens
title_sort drug-induced acute interstitial nephritis: a clinicopathological study and comparative trial of steroid regimens
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588323/
https://www.ncbi.nlm.nih.gov/pubmed/26628793
http://dx.doi.org/10.4103/0971-4065.147766
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