Antimicrobial-Induced Cytopenia and Bone Marrow Hypocellularity in Patients with Cirrhosis.

Bone Marrow Research Pub Date : 2018-05-14 eCollection Date: 2018-01-01 DOI:10.1155/2018/4029648
Anupama Patil, Vikas Khillan, Monika Thakur, Pratibha Kale, Chhagan Bihari
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引用次数: 2

Abstract

There is great variation in cytopenias in cirrhotic patients with same severity and hypersplenism and their causative factors are not clear. Recent studies have highlighted the role of gut microbiome in regulation of constant and emergency hematopoiesis. Broad-spectrum antibiotics can disrupt the homeostatic or adaptive microbiota in cirrhosis, leading to impaired hematopoiesis and a higher susceptibility to infections. We studied all patients with cirrhosis with cytopenia (anemia, leucopenia, and/or thrombocytopenia), admitted in the Institute of Liver & Biliary Sciences, between January 2016 and July 2017, who underwent a bone marrow examination. The effect of the different antimicrobial agents on peripheral blood counts and bone marrow cellularity was assessed. A total of 196 patients' data was analyzed for this study. Patients on antimicrobials (n = 115) had significantly lower hemoglobin (p < 0.001), total leucocyte count (p = 0.048), and platelet count (p = 0.043) compared to patients not on antimicrobials. On unadjusted analysis, significant association with thrombocytopenia existed in beta-lactams (OR = 1.56, 95% CI = 1.06-2.40), quinolones (OR = 1.66, 95% CI = 1.11-2.61), and antifungals (OR = 2.24, 95% CI = 1.96-4.34). Cephalosporins were found to be significantly associated with anemia (OR = 1.91, 95% CI = 1.07-3.41). Patients who received antimicrobials had hypocellular marrow (p < 0.001) as compared to nonrecipients of antibiotics. The adjusted analysis showed that quinolones and beta-lactam antibiotics are the drug classes having significant association with thrombocytopenia and alternative class of drug should be explored in these patients to avoid severe thrombocytopenia.

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肝硬化患者抗菌剂诱导的细胞减少和骨髓细胞减少。
相同严重程度的肝硬化患者和脾功能亢进患者的血小板减少有很大差异,其病因尚不清楚。最近的研究强调了肠道微生物组在持续和紧急造血中的调节作用。广谱抗生素可破坏肝硬化的内稳态或适应性微生物群,导致造血功能受损和对感染的易感性增加。我们研究了2016年1月至2017年7月期间在肝脏和胆道科学研究所接受骨髓检查的所有肝硬化伴细胞减少(贫血、白细胞减少和/或血小板减少)患者。评估不同抗菌药物对外周血计数和骨髓细胞的影响。本研究共分析了196例患者的数据。与未使用抗菌素的患者相比,使用抗菌素的患者(n = 115)的血红蛋白(p < 0.001)、总白细胞计数(p = 0.048)和血小板计数(p = 0.043)显著降低。在未经校正的分析中,β -内酰胺类药物(OR = 1.56, 95% CI = 1.06-2.40)、喹诺酮类药物(OR = 1.66, 95% CI = 1.11-2.61)和抗真菌药物(OR = 2.24, 95% CI = 1.96-4.34)与血小板减少症存在显著关联。头孢菌素与贫血显著相关(OR = 1.91, 95% CI = 1.07-3.41)。与未接受抗生素治疗的患者相比,接受抗菌素治疗的患者骨髓细胞减少(p < 0.001)。调整后的分析显示,喹诺酮类和β -内酰胺类抗生素是与血小板减少有显著相关性的药物类别,这类患者应探索替代药物类别,以避免严重的血小板减少。
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