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Dexamethasone- cyclophosphamide pulse in collagen vascular diseases: An observation

BACKGROUND: Treatment of collagen vascular diseases like systemic sclerosis, dermatomyositis, systemic lupus erythematosus (SLE) and even overlap syndromes has been difficult since long. Monumental success of dexamethasone-cyclophosphamide pulse (DCP) in pemphigus has prompted many a dermatologist t...

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Autores principales: Das, Sudip, Giri, Parag Prasun, Roy, Aloke Kr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3481802/
https://www.ncbi.nlm.nih.gov/pubmed/23130206
http://dx.doi.org/10.4103/2229-5178.79858
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author Das, Sudip
Giri, Parag Prasun
Roy, Aloke Kr
author_facet Das, Sudip
Giri, Parag Prasun
Roy, Aloke Kr
author_sort Das, Sudip
collection PubMed
description BACKGROUND: Treatment of collagen vascular diseases like systemic sclerosis, dermatomyositis, systemic lupus erythematosus (SLE) and even overlap syndromes has been difficult since long. Monumental success of dexamethasone-cyclophosphamide pulse (DCP) in pemphigus has prompted many a dermatologist to try it in other autoimmune diseases. MATERIALS AND METHODS: DCP was given as per standard regimen for six to nine pulses. Immunosuppressives were given for 12–18 months in dermatomyositis, SLE, and overlap syndrome, and for 12 months in systemic sclerosis. Daily dose of steroid was tapered off gradually. RESULTS: The treatment resulted in 90% improvement in skin binding in systemic sclerosis, 80% in exertional dyspnea, 40% in dysphagia, but minimum improvement was seen in Raynauds and digital tip ulcerations. No improvement in pigmentation was noted. In SLE, malar rash cleared in 70%, joint pain in 80%, oral ulcerations reduced in 80%, fever in 98%, and photosensitivity improved in one-third of patients. In dermatomyositis, improvement in muscle tenderness was seen in 100%, improvement in proximal myopathy and heliotrope rash in 80%, and improvement of shawl sign was observed in 80% of the patients. Some flattening of Gottron papules and plaques was noted in some patients. Both overlap patients improved significantly. Out of 24 patients, three were lost to follow-up, one resorted to homeopathic medicine and two expired (one dermatomyositis, one SLE). Side effects like hypertension, hyperglycemia, pyoderma, fungal infections, obesity, psychosis, etc. were seen in 25–30% of patients. CONCLUSIONS: We conclude that DCP is relatively safe, effective as well as cheap compared to methylprednisolone pulse. Side effects are also less compared to daily regimen of steroids. We also observed that patients who reported early and put on pulse early responded better.
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spelling pubmed-34818022012-11-05 Dexamethasone- cyclophosphamide pulse in collagen vascular diseases: An observation Das, Sudip Giri, Parag Prasun Roy, Aloke Kr Indian Dermatol Online J Original Article BACKGROUND: Treatment of collagen vascular diseases like systemic sclerosis, dermatomyositis, systemic lupus erythematosus (SLE) and even overlap syndromes has been difficult since long. Monumental success of dexamethasone-cyclophosphamide pulse (DCP) in pemphigus has prompted many a dermatologist to try it in other autoimmune diseases. MATERIALS AND METHODS: DCP was given as per standard regimen for six to nine pulses. Immunosuppressives were given for 12–18 months in dermatomyositis, SLE, and overlap syndrome, and for 12 months in systemic sclerosis. Daily dose of steroid was tapered off gradually. RESULTS: The treatment resulted in 90% improvement in skin binding in systemic sclerosis, 80% in exertional dyspnea, 40% in dysphagia, but minimum improvement was seen in Raynauds and digital tip ulcerations. No improvement in pigmentation was noted. In SLE, malar rash cleared in 70%, joint pain in 80%, oral ulcerations reduced in 80%, fever in 98%, and photosensitivity improved in one-third of patients. In dermatomyositis, improvement in muscle tenderness was seen in 100%, improvement in proximal myopathy and heliotrope rash in 80%, and improvement of shawl sign was observed in 80% of the patients. Some flattening of Gottron papules and plaques was noted in some patients. Both overlap patients improved significantly. Out of 24 patients, three were lost to follow-up, one resorted to homeopathic medicine and two expired (one dermatomyositis, one SLE). Side effects like hypertension, hyperglycemia, pyoderma, fungal infections, obesity, psychosis, etc. were seen in 25–30% of patients. CONCLUSIONS: We conclude that DCP is relatively safe, effective as well as cheap compared to methylprednisolone pulse. Side effects are also less compared to daily regimen of steroids. We also observed that patients who reported early and put on pulse early responded better. Medknow Publications Pvt Ltd 2011 /pmc/articles/PMC3481802/ /pubmed/23130206 http://dx.doi.org/10.4103/2229-5178.79858 Text en © Indian Dermatology Online Journal 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Das, Sudip
Giri, Parag Prasun
Roy, Aloke Kr
Dexamethasone- cyclophosphamide pulse in collagen vascular diseases: An observation
title Dexamethasone- cyclophosphamide pulse in collagen vascular diseases: An observation
title_full Dexamethasone- cyclophosphamide pulse in collagen vascular diseases: An observation
title_fullStr Dexamethasone- cyclophosphamide pulse in collagen vascular diseases: An observation
title_full_unstemmed Dexamethasone- cyclophosphamide pulse in collagen vascular diseases: An observation
title_short Dexamethasone- cyclophosphamide pulse in collagen vascular diseases: An observation
title_sort dexamethasone- cyclophosphamide pulse in collagen vascular diseases: an observation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3481802/
https://www.ncbi.nlm.nih.gov/pubmed/23130206
http://dx.doi.org/10.4103/2229-5178.79858
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