{"title":"显微镜下多血管炎合并弥漫性肺泡出血和间质性肺疾病的特点及预后","authors":"Yu Gu, Ting Zhang, Min Peng, Juhong Shi","doi":"10.24920/004067","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>To evaluate the clinical characteristics and prognostic predictors of patients with diffuse alveolar hemorrhage (DAH) and/or interstitial lung disease (ILD) secondary to microscopic polyangiitis (MPA) in a Chinese general hospital.</p></div><div><h3>Methods</h3><p>We retrospectively reviewed the medical records of MPA patients admitted to internal medicine departments between the year 2002 and 2012. The patients were divided into the ILD, DAH, DAH combined with ILD (DAHILD), and no pulmonary involvement (NPI) groups according to pulmonary involvement patterns. The clinical characteristics at diagnosis were analyzed. The risk factors associated with short-term death and long-term death were identified with Logistic regression and Cox analysis.</p></div><div><h3>Results</h3><p>Of 193 newly diagnosed MPA patients, 181 patients were enrolled in the research, of which 19 had DAH alone, 96 had ILD alone, 18 had DAH and DAH concurrently, and 48 had NPI. The median of serum creatine level in the DAH group was 449 µmol/L, significantly higher than that in the ILD group (123 µmol/L, <em>Nemenyi</em> = -35.215, P = 0.045) and DAHILD group (359 µmol/L, <em>Nemenji</em> = -43.609, <em>P</em> = 0.007). The median follow-up time was 67 (range: 1-199) months. Patients in the ILD group were older than those in the DAH group (median: 69 years <em>vs.</em> 57 years, <em>Nemenji</em> = 43.853, <em>P</em> = 0.005). The patients with both DAH and ILD had combined features of the two subtypes, and the highest mortality (72.2% at the end of follow-up). The elevated white blood cell count was a risk factor for short-term death (<em>OR</em> = 1.103, 95%<em>CI</em>: 1.008-1.207, <em>P</em> = 0.032 for one month; <em>OR</em> = 1.103, 95%<em>CI</em>: 1.026-1.186, <em>P</em> = 0.008 for one year). Old age (<em>HR</em> = 1.044, 95%C7: 1.023-1.066, <em>P</em> < 0.001), cardiovascular system involvement (<em>HR</em> = 2.093, 95%<em>CI</em>: 1.195-3.665, <em>P</em> = 0.010), poor renal function (<em>HR</em> = 1.001, 95%<em>CI</em>: 1.000-1.002, <em>P</em> = 0.032) were risk factors for long-term death. Pulmonary infections (38/54) were the leading causes of death, especially for the patients with ILD. Besides, 49 patients suffered from pulmonary infections in the first year after diagnosis.</p></div><div><h3>Conclusions</h3><p>MPA patients who presented with different pulmonary involvement patterns have completely different clinical features. These subtypes probably have different pathogenesis and should be studied separately.</p></div>","PeriodicalId":35615,"journal":{"name":"Chinese Medical Sciences Journal","volume":"37 4","pages":"Pages 293-302"},"PeriodicalIF":0.0000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Characteristics and Prognosis of Microscopic Polyangiitis Patients with Diffuse Alveolar Hemorrhage and Interstitial Lung Disease\",\"authors\":\"Yu Gu, Ting Zhang, Min Peng, Juhong Shi\",\"doi\":\"10.24920/004067\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><p>To evaluate the clinical characteristics and prognostic predictors of patients with diffuse alveolar hemorrhage (DAH) and/or interstitial lung disease (ILD) secondary to microscopic polyangiitis (MPA) in a Chinese general hospital.</p></div><div><h3>Methods</h3><p>We retrospectively reviewed the medical records of MPA patients admitted to internal medicine departments between the year 2002 and 2012. The patients were divided into the ILD, DAH, DAH combined with ILD (DAHILD), and no pulmonary involvement (NPI) groups according to pulmonary involvement patterns. The clinical characteristics at diagnosis were analyzed. The risk factors associated with short-term death and long-term death were identified with Logistic regression and Cox analysis.</p></div><div><h3>Results</h3><p>Of 193 newly diagnosed MPA patients, 181 patients were enrolled in the research, of which 19 had DAH alone, 96 had ILD alone, 18 had DAH and DAH concurrently, and 48 had NPI. The median of serum creatine level in the DAH group was 449 µmol/L, significantly higher than that in the ILD group (123 µmol/L, <em>Nemenyi</em> = -35.215, P = 0.045) and DAHILD group (359 µmol/L, <em>Nemenji</em> = -43.609, <em>P</em> = 0.007). The median follow-up time was 67 (range: 1-199) months. Patients in the ILD group were older than those in the DAH group (median: 69 years <em>vs.</em> 57 years, <em>Nemenji</em> = 43.853, <em>P</em> = 0.005). The patients with both DAH and ILD had combined features of the two subtypes, and the highest mortality (72.2% at the end of follow-up). The elevated white blood cell count was a risk factor for short-term death (<em>OR</em> = 1.103, 95%<em>CI</em>: 1.008-1.207, <em>P</em> = 0.032 for one month; <em>OR</em> = 1.103, 95%<em>CI</em>: 1.026-1.186, <em>P</em> = 0.008 for one year). Old age (<em>HR</em> = 1.044, 95%C7: 1.023-1.066, <em>P</em> < 0.001), cardiovascular system involvement (<em>HR</em> = 2.093, 95%<em>CI</em>: 1.195-3.665, <em>P</em> = 0.010), poor renal function (<em>HR</em> = 1.001, 95%<em>CI</em>: 1.000-1.002, <em>P</em> = 0.032) were risk factors for long-term death. Pulmonary infections (38/54) were the leading causes of death, especially for the patients with ILD. Besides, 49 patients suffered from pulmonary infections in the first year after diagnosis.</p></div><div><h3>Conclusions</h3><p>MPA patients who presented with different pulmonary involvement patterns have completely different clinical features. These subtypes probably have different pathogenesis and should be studied separately.</p></div>\",\"PeriodicalId\":35615,\"journal\":{\"name\":\"Chinese Medical Sciences Journal\",\"volume\":\"37 4\",\"pages\":\"Pages 293-302\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Medical Sciences Journal\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1001929423000032\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Medical Sciences Journal","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1001929423000032","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 2
摘要
目的探讨某综合医院弥漫性肺泡出血(DAH)和/或间质性肺疾病(ILD)继发于显微多血管炎(MPA)的临床特点及预后预测因素。方法回顾性分析2002 ~ 2012年内科收治的MPA患者的病历资料。根据肺受累情况将患者分为ILD组、DAH组、DAH合并ILD组(DAHILD)和无肺受累组(NPI)。分析诊断时的临床特点。通过Logistic回归和Cox分析确定与短期死亡和长期死亡相关的危险因素。结果193例新诊断的MPA患者中,181例纳入研究,其中单独DAH 19例,单独ILD 96例,DAH合并DAH 18例,NPI 48例。DAH组血清肌酸水平中位数为449µmol/L,显著高于ILD组(123µmol/L, Nemenyi = -35.215, P = 0.045)和DAHILD组(359µmol/L, Nemenyi = -43.609, P = 0.007)。中位随访时间为67个月(范围:1-199个月)。ILD组患者年龄大于DAH组(中位数:69岁vs. 57岁,Nemenji = 43.853, P = 0.005)。DAH和ILD患者具有两种亚型的综合特征,死亡率最高(随访结束时为72.2%)。白细胞计数升高是短期死亡的危险因素(OR = 1.103, 95%CI: 1.008-1.207, P = 0.032);OR = 1.103, 95%CI: 1.026-1.186, 1年P = 0.008)。老年组(HR = 1.044, 95%C7: 1.023-1.066, P <0.001)、心血管系统受累(HR = 2.093, 95%CI: 1.195 ~ 3.665, P = 0.010)、肾功能不佳(HR = 1.001, 95%CI: 1.000 ~ 1.002, P = 0.032)是长期死亡的危险因素。肺部感染(38/54)是主要死亡原因,尤其是ILD患者。49例患者在确诊后一年内出现肺部感染。结论不同肺部受累类型的smpa患者具有完全不同的临床特征。这些亚型可能有不同的发病机制,应分别研究。
Characteristics and Prognosis of Microscopic Polyangiitis Patients with Diffuse Alveolar Hemorrhage and Interstitial Lung Disease
Objective
To evaluate the clinical characteristics and prognostic predictors of patients with diffuse alveolar hemorrhage (DAH) and/or interstitial lung disease (ILD) secondary to microscopic polyangiitis (MPA) in a Chinese general hospital.
Methods
We retrospectively reviewed the medical records of MPA patients admitted to internal medicine departments between the year 2002 and 2012. The patients were divided into the ILD, DAH, DAH combined with ILD (DAHILD), and no pulmonary involvement (NPI) groups according to pulmonary involvement patterns. The clinical characteristics at diagnosis were analyzed. The risk factors associated with short-term death and long-term death were identified with Logistic regression and Cox analysis.
Results
Of 193 newly diagnosed MPA patients, 181 patients were enrolled in the research, of which 19 had DAH alone, 96 had ILD alone, 18 had DAH and DAH concurrently, and 48 had NPI. The median of serum creatine level in the DAH group was 449 µmol/L, significantly higher than that in the ILD group (123 µmol/L, Nemenyi = -35.215, P = 0.045) and DAHILD group (359 µmol/L, Nemenji = -43.609, P = 0.007). The median follow-up time was 67 (range: 1-199) months. Patients in the ILD group were older than those in the DAH group (median: 69 years vs. 57 years, Nemenji = 43.853, P = 0.005). The patients with both DAH and ILD had combined features of the two subtypes, and the highest mortality (72.2% at the end of follow-up). The elevated white blood cell count was a risk factor for short-term death (OR = 1.103, 95%CI: 1.008-1.207, P = 0.032 for one month; OR = 1.103, 95%CI: 1.026-1.186, P = 0.008 for one year). Old age (HR = 1.044, 95%C7: 1.023-1.066, P < 0.001), cardiovascular system involvement (HR = 2.093, 95%CI: 1.195-3.665, P = 0.010), poor renal function (HR = 1.001, 95%CI: 1.000-1.002, P = 0.032) were risk factors for long-term death. Pulmonary infections (38/54) were the leading causes of death, especially for the patients with ILD. Besides, 49 patients suffered from pulmonary infections in the first year after diagnosis.
Conclusions
MPA patients who presented with different pulmonary involvement patterns have completely different clinical features. These subtypes probably have different pathogenesis and should be studied separately.