Zhong-Shu Kuang 1 , Yi-Lin Yang 1 , Wei Wei 1 , Jian-Li Wang 1 , Xiang-Yu Long 1 , Ke-Yong Li 2 , Chao-Yang Tong 1 , Zhan Sun 1 , Zhen-Ju Song 1 . Show Affiliations »
Abstract
BACKGROUND: Community-acquired pneumonia (CAP) in autoimmune diseases (AID)-induced immunocompromised host (ICH) had a high incidence and poor prognosis. However, only a few studies had determined the clinical characteristics of these patients. Our study was to explore the characteristics and predictors of mortality in CAP patients accompanied with AID-induced ICH. METHODS: From 2013 to 2018, a total of 94 CAP patients accompanied with AID-induced ICH, admitted to Emergency Department of Zhongshan Hospital, Fudan University, were enrolled in this study. Clinical data and the risk regression estimates of repeated predictors were evaluated by generalized estimating equations (GEEs) analysis. An open-cohort approach was used to classify patient's outcomes into the survival or non-survival group. RESULTS: The hospital mortality of patients with CAP occurring in AID-induced ICH was 60.64%. No significant differences were found with respect to clinical symptoms and lung images between survival and non-survival groups, while renal insufficiency and dysfunction of coagulation had higher proportions in non-survival patients (P<0.05). Both noninvasive ventilation (NIV) and invasive mechanical ventilation (IMV) were performed more frequently in non-survival group (P< 0.05). By the multivariate GEEs analysis, the repeated measured longitudinal indices of neutrophil-to-lymphocyte ratio (NLR) (odds ratio [OR]=1.055, 95% confidence interval [95%CI] 1.025-1.086), lactate dehydrogenase (LDH) (OR=1.004, 95%CI 1.002-1.006) and serum creatinine (sCr) (OR=1.018, 95%CI 1.008-1.028), were associated with a higher risk of mortality. CONCLUSION: The CAP patients in AID-induced ICH had a high mortality. A significant relationship was demonstrated between the factors of NLR, LDH, sCr and mortality risk in these patients. Copyright: © World Journal of Emergency Medicine.
BACKGROUND: Community-acquired pneumonia (CAP) in autoimmune diseases (AID)-induced immunocompromised host (ICH ) had a high incidence and poor prognosis. However, only a few studies had determined the clinical characteristics of these patients . Our study was to explore the characteristics and predictors of mortality in CAP patients accompanied with AID-induced ICH . METHODS: From 2013 to 2018, a total of 94 CAP patients accompanied with AID-induced ICH , admitted to Emergency Department of Zhongshan Hospital, Fudan University, were enrolled in this study. Clinical data and the risk regression estimates of repeated predictors were evaluated by generalized estimating equations (GEEs) analysis. An open-cohort approach was used to classify patient 's outcomes into the survival or non-survival group. RESULTS: The hospital mortality of patients with CAP occurring in AID-induced ICH was 60.64%. No significant differences were found with respect to clinical symptoms and lung images between survival and non-survival groups, while renal insufficiency and dysfunction of coagulation had higher proportions in non-survival patients (P<0.05). Both noninvasive ventilation (NIV) and invasive mechanical ventilation (IMV) were performed more frequently in non-survival group (P< 0.05). By the multivariate GEEs analysis, the repeated measured longitudinal indices of neutrophil-to-lymphocyte ratio (NLR) (odds ratio [OR]=1.055, 95% confidence interval [95%CI] 1.025-1.086), lactate dehydrogenase (LDH) (OR=1.004, 95%CI 1.002-1.006) and serum creatinine (sCr) (OR=1.018, 95%CI 1.008-1.028), were associated with a higher risk of mortality . CONCLUSION: The CAP patients in AID-induced ICH had a high mortality . A significant relationship was demonstrated between the factors of NLR, LDH, sCr and mortality risk in these patients . Copyright: © World Journal of Emergency Medicine.
Entities: Chemical
Disease
Species
Keywords:
Autoimmune disease; Community-acquired pneumonia; Immunocompromised hosts; Prognostic marker
Year: 2020
PMID: 32351646 PMCID: PMC7183923 DOI: 10.5847/wjem.j.1920-8642.2020.03.003
Source DB: PubMed Journal: World J Emerg Med ISSN: 1920-8642