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Predictive factors of mortality in granulomatosis with polyangiitis: A single-center study
OBJECTIVES: The aim of this study was to identify predictors of mortality in granulomatosis with polyangiitis (GPA) patients and to seek the ways of improving survival in GPA patients. PATIENTS AND METHODS: Between January 2005 and June 2020, a total of 60 patients (26 males, 34 females; median age:...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Turkish League Against Rheumatism
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612489/ https://www.ncbi.nlm.nih.gov/pubmed/34870176 http://dx.doi.org/10.46497/ArchRheumatol.2021.8594 |
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author | Aydın Tufan, Müge Tekkarışmaz, Nihan |
author_facet | Aydın Tufan, Müge Tekkarışmaz, Nihan |
author_sort | Aydın Tufan, Müge |
collection | PubMed |
description | OBJECTIVES: The aim of this study was to identify predictors of mortality in granulomatosis with polyangiitis (GPA) patients and to seek the ways of improving survival in GPA patients. PATIENTS AND METHODS: Between January 2005 and June 2020, a total of 60 patients (26 males, 34 females; median age: 49 years; range, 19 to 75 years) who were diagnosed with GPA were retrospectively analyzed. Demographic, clinical, laboratory, and radiological findings of all patients were recorded. Survival rates were analyzed using the Kaplan-Meier plot. RESULTS: The median follow-up was 36 months, and 10 (16.7%) patients died during the study period. Univariate analysis showed that the prognostic values were attributed to high serum creatinine levels (>2.1 mg/dL; p=0.01), proteinuria (p=0.01), dialysis-requiring renal damage at the time of diagnosis (p=0.01) or at any time during follow-up (p=0.01), low lymphocyte levels (p=0.01), hypoalbuminemia (p=0.04), absence of upper respiratory tract involvement (p=0.01), presence of lung involvement with cavitary lesions (p=0.01), high Birmingham Vascular Activity Score (p=0.02), and history of serious infection (p=0.01). In the multivariate analysis, the presence of renal damage requiring dialysis at any time during follow-up (relative risk [95% confidence interval]: 21 [4.1-18.3]; p=0.01) was found to be an independent predictor of mortality. Immunosuppressive drugs exerted no effect on mortality, and the most common causes of death were infections (50%). CONCLUSION: The presence of dialysis-requiring renal damage is the most important risk factor for mortality in GPA patients. These patients should be followed more closely and carefully to improve survival. |
format | Online Article Text |
id | pubmed-8612489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Turkish League Against Rheumatism |
record_format | MEDLINE/PubMed |
spelling | pubmed-86124892021-12-03 Predictive factors of mortality in granulomatosis with polyangiitis: A single-center study Aydın Tufan, Müge Tekkarışmaz, Nihan Arch Rheumatol Original Article OBJECTIVES: The aim of this study was to identify predictors of mortality in granulomatosis with polyangiitis (GPA) patients and to seek the ways of improving survival in GPA patients. PATIENTS AND METHODS: Between January 2005 and June 2020, a total of 60 patients (26 males, 34 females; median age: 49 years; range, 19 to 75 years) who were diagnosed with GPA were retrospectively analyzed. Demographic, clinical, laboratory, and radiological findings of all patients were recorded. Survival rates were analyzed using the Kaplan-Meier plot. RESULTS: The median follow-up was 36 months, and 10 (16.7%) patients died during the study period. Univariate analysis showed that the prognostic values were attributed to high serum creatinine levels (>2.1 mg/dL; p=0.01), proteinuria (p=0.01), dialysis-requiring renal damage at the time of diagnosis (p=0.01) or at any time during follow-up (p=0.01), low lymphocyte levels (p=0.01), hypoalbuminemia (p=0.04), absence of upper respiratory tract involvement (p=0.01), presence of lung involvement with cavitary lesions (p=0.01), high Birmingham Vascular Activity Score (p=0.02), and history of serious infection (p=0.01). In the multivariate analysis, the presence of renal damage requiring dialysis at any time during follow-up (relative risk [95% confidence interval]: 21 [4.1-18.3]; p=0.01) was found to be an independent predictor of mortality. Immunosuppressive drugs exerted no effect on mortality, and the most common causes of death were infections (50%). CONCLUSION: The presence of dialysis-requiring renal damage is the most important risk factor for mortality in GPA patients. These patients should be followed more closely and carefully to improve survival. Turkish League Against Rheumatism 2021-02-08 /pmc/articles/PMC8612489/ /pubmed/34870176 http://dx.doi.org/10.46497/ArchRheumatol.2021.8594 Text en Copyright © 2021, Turkish League Against Rheumatism https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Article Aydın Tufan, Müge Tekkarışmaz, Nihan Predictive factors of mortality in granulomatosis with polyangiitis: A single-center study |
title | Predictive factors of mortality in granulomatosis with polyangiitis: A single-center study |
title_full | Predictive factors of mortality in granulomatosis with polyangiitis: A single-center study |
title_fullStr | Predictive factors of mortality in granulomatosis with polyangiitis: A single-center study |
title_full_unstemmed | Predictive factors of mortality in granulomatosis with polyangiitis: A single-center study |
title_short | Predictive factors of mortality in granulomatosis with polyangiitis: A single-center study |
title_sort | predictive factors of mortality in granulomatosis with polyangiitis: a single-center study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612489/ https://www.ncbi.nlm.nih.gov/pubmed/34870176 http://dx.doi.org/10.46497/ArchRheumatol.2021.8594 |
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