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Clinical characteristics and prognosis in 269 patients with antineutrophil cytoplasimc antibody associated vasculitis. / 269例抗中性粒细胞胞浆抗体相关性血管炎患者的临床病理特征及预后.
Wu, Ting; Zhong, Yong; Zhou, Ya'ou; Chen, Jinbiao; Yang, Yingqiang; Tang, Rong; Meng, Ting; Xiao, Zhou; Xiao, Xiangcheng; Zhou, Qiaoling; Xiao, Ping.
Afiliação
  • Wu T; Department of Nephrology, Xiangya Hospital, Central South University, Changsha 410008. m15274820431@163.com.
  • Zhong Y; Department of Nephrology, Xiangya Hospital, Central South University, Changsha 410008. zhongyong121@163.com.
  • Zhou Y; Department of Rheumatology and Immunology, Xiangya Hospital, Central South University, Changsha 410008.
  • Chen J; Department of Medical Records & Information, Xiangya Hospital, Central South University, Changsha 410008, China.
  • Yang Y; Department of Nephrology, Xiangya Hospital, Central South University, Changsha 410008.
  • Tang R; Department of Nephrology, Xiangya Hospital, Central South University, Changsha 410008.
  • Meng T; Department of Nephrology, Xiangya Hospital, Central South University, Changsha 410008.
  • Xiao Z; Department of Nephrology, Xiangya Hospital, Central South University, Changsha 410008.
  • Xiao X; Department of Nephrology, Xiangya Hospital, Central South University, Changsha 410008.
  • Zhou Q; Department of Nephrology, Xiangya Hospital, Central South University, Changsha 410008.
  • Xiao P; Department of Nephrology, Xiangya Hospital, Central South University, Changsha 410008. xiaoping.x@163.com.
Zhong Nan Da Xue Xue Bao Yi Xue Ban ; 45(8): 916-922, 2020 Aug 28.
Article em En, Zh | MEDLINE | ID: mdl-33053532
ABSTRACT

OBJECTIVES:

To investigate the clinic-pathological characteristics, prognosis and its risk factors for antineutrophil cytoplasimc antibody (ANCA)-associated vasculitis (AAV).

METHODS:

The basic information and clinic-pathological characteristics of AAV patients, who was diagnosed from January 2010 to January 2018 in Xiangya Hospital, Central South University, were retrospectively collected. The renal survival and patient survival were regular followed up, and their clinical pathological, prognosis data and risk factors for renal were analyzed.

RESULTS:

Among 269 AAV patients, 225 patients (83.64%) were microscopic polyangiitis (MPA), 33 patients (12.27%) were granulomatosis with polyangiitis (GPA), and 11 patients (4.09%) were eosinophilic granulomatosis with polyangiitis (EGPA). Male-to-female ratio was almost 1∶1 for MPA (147/122), but GPA and EGPA was more frequent among man. The medium time from disease onset to diagnosis was 64.0 (32.5, 148.5) days, 65 patients (24.16%) were diagnosed within 30 days. A total of 94.67% patients had kidney involvement in MPA patients, which was significantly higher than that in patients with GPA (63.63%), but ear, nose, and throat manifestations were more frequent in GPA patients. The 1-year kidney survival rates of GPA and MPA patients in this study were 75% and 59.3%, respectively. The 1-year death rates were 16.7% and 16.9%, respectively. The multivariable logistic regression analysis revealed that the low platelet level, low globulin level, low immunoglobin G, and high serum creatinine level were independent risk factors for the 1-year renal survival rate in AAV patients. Multiple factor logistic regression analysis showed that the serum creatinine level was an independent risk factor for all-cause mortality.

CONCLUSIONS:

MPA is the priority in the AAV patients. The proportion of patients with advanced end-stage renal disease and mortality is still high, and the early diagnosis and treatment in time is crucial for the improvement of prognosis for AAV.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Churg-Strauss / Granulomatose com Poliangiite Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Female / Humans / Male Idioma: En / Zh Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Churg-Strauss / Granulomatose com Poliangiite Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Female / Humans / Male Idioma: En / Zh Ano de publicação: 2020 Tipo de documento: Article