Suppr超能文献

符合确诊和疑似人类粒细胞无形体病标准的患者的临床和实验室特征比较。

Comparison of clinical and laboratory characteristics of patients fulfilling criteria for proven and probable human granulocytic anaplasmosis.

作者信息

Lotrič-Furlan Stanka, Rojko Tereza, Jelovšek Mateja, Petrovec Miroslav, Avšič-Županc Tatjana, Lusa Lara, Strle Franc

机构信息

Department of Infectious Diseases, University Medical Center Ljubljana, Slovenia.

Department of Infectious Diseases, University Medical Center Ljubljana, Slovenia.

出版信息

Microbes Infect. 2015 Nov-Dec;17(11-12):829-33. doi: 10.1016/j.micinf.2015.09.017. Epub 2015 Sep 30.

Abstract

To assess the value of clinical definitions for human granulocytic anaplasmosis (HGA) epidemiological, clinical and laboratory findings in 50 adult patients with proven HGA (Anaplasma phagocytophilum isolated from blood, and/or positive PCR result, and/or seroconversion or ≥4-fold change in serum IFA antibody titres to A. phagocytophilum) and 46 patients with probable HGA (demonstration of serum antibodies to A. phagocytophilum in titres ≥1:256) were compared. Patients with proven HGA were older (55 versus 43.5 years; p = 0.001), were more often treated with doxycycline (31/50, 62% versus 11/46, 23.9%; p < 0.001), more frequently reported chills (40/50, 80% versus 17/46, 36.9%; p < 0.001), myalgia (37/50, 74% versus 21/46, 45.7%; p = 0.005) and cough (10/50, 20% versus 2/46, 4.4%; p = 0.02), and had more often abnormal laboratory findings such as thrombocytopenia (45/50, 90% versus 22/46, 47.8%; p < 0.001), abnormal liver function test results (45/50, 87% versus 22/46, 47.8%; p < 0.001), leukopenia (38/50, 76% versus 21/46, 45.7%; p = 0.002) and elevated serum CRP concentration (48/50, 96% versus 31/46, 67.4%; p < 0.001). The dissimilarities imply that in some patients fulfilling criteria for probable HGA the signs and symptoms most likely are not the result of a recent infection with A. phagocytophilum and indicate that clinical definitions used in the present study have a distinctive value.

摘要

为评估人类粒细胞无形体病(HGA)临床定义的价值,对50例确诊为HGA的成年患者(从血液中分离出嗜吞噬细胞无形体,和/或PCR结果呈阳性,和/或血清间接荧光抗体试验(IFA)针对嗜吞噬细胞无形体的抗体滴度出现血清学转换或≥4倍变化)与46例疑似HGA患者(血清中针对嗜吞噬细胞无形体的抗体滴度≥1:256)的流行病学、临床和实验室检查结果进行了比较。确诊为HGA的患者年龄更大(55岁对43.5岁;p = 0.001),更常接受强力霉素治疗(31/50,62%对11/46,23.9%;p < 0.001),更频繁报告寒战(40/50,80%对17/46,36.9%;p < 0.001)、肌痛(37/50,74%对21/46,45.7%;p = 0.005)和咳嗽(10/50,20%对2/46,4.4%;p = 0.02),并且更常出现异常实验室检查结果,如血小板减少(45/50,90%对22/46,47.8%;p < 0.001)、肝功能检查结果异常(45/50,87%对22/46,47.8%;p < 0.001)、白细胞减少(38/50,76%对21/46,45.7%;p = 0.002)以及血清CRP浓度升高(48/50,96%对31/46,67.4%;p < 0.001)。这些差异表明,在一些符合疑似HGA标准的患者中,其体征和症状很可能并非近期嗜吞噬细胞无形体感染的结果,这表明本研究中使用的临床定义具有独特价值。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验