Toxic and infectious lung injury differential diagnosis specifics in oncohematological patients

Q4 Medicine
V. R. Yanbukhtina, I. Zyuzgin, T. Shneyder, P. K. Khorosheva, A. A. Zver’kova, I. A. Borovichkov, G. Kuchma, E. A. Kulagin, L. Stel'makh, A. Smirnova, Y. Vlasova, E. Morozova, Y. Rabik, I. Moiseev, V. Trofimov
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引用次数: 0

Abstract

Background. Assessment of lung injury in oncohematological patients is a relevant problem, since the spectrum of pathological changes is wide and includes pulmonary infections, tumor cell infiltration, cardiogenic and non-cardiogenic pulmonary edema, bronchiolitis obliterans, interstitial pneumonitis, post-radiation and post-inflammatory pneumofibrosis, pulmonary vasculopathy and pleural effusion. At the moment there are no approved recommendations with criteria of differential diagnosis for these conditions, in particular, with differences between the most common therapy complication represented by pulmonary infections and poorly explored drug-induced toxic lesions.Aim. Identification of criteria for pneumotoxicity, allowing for differential diagnosis with pulmonary infections developing during chemotherapy, according to data routinely obtained in real clinical practice.Materials and methods. The study group included 38 patients with cytotoxic and autoimmune lung injury caused by specific therapy (group 1); the comparison group included 38 patients with infectious lesions receiving the same antitumor drugs (group 2). The data of the anamnesis, clinical course, instrumental studies and standard laboratory tests was studied retrospectively. For statistical analysis, the Mann–Whitney, χ2, Kruskal–Wallis tests were used. ROC analysis was performed to assess the sensitivity and specificity of various factors in relation to toxic damage.Results. Patients with lymphomas predominated in group of toxic lung injury (63 %). In patients who underwent allogeneic hematopoietic stem cells transplantation, toxic complications developed in the period from 35 to 1289 days, infectious – from 4 to 43 days. Statistically significant differences were obtained in the presence of a concomitant state of an altered immune response: 32 % of patients in the toxic lesion group versus 5 % in the infectious group had a history of allergy, and, in contrast to the infectious lesion group, in the toxic lesion group autoimmune diseases were detected. The main symptom in patients of the first group was shortness of breath, which was observed in 68 % of cases, of the second – an increased body temperature, observed in 92 % of cases; cough was also a common symptom – in 19 % and 13 % of patients respectively. In 58 % of patients of the second group, concomitant mucositis was detected, while in the first group this complication did not occur in any of them. The most common radiological pattern (71 % of cases in each group) was ground-glass opacities, in patients of the second group often combined with infiltrative changes and thickening of the bronchial walls (in 53 and 42 % of cases respectively). Among laboratory results, the largest differences between groups were observed in the leukocyte levels (with an average level of 2.5 . 109 / L in the infectious group versus 6 . 109 / L in the toxic group), eosinophils (with an average of 3.6 % in the toxic group versus 1.75 % in the infectious group), C-reactive protein (with an average level of 146.7 mg / L in the infectious group versus 52.4 mg / L in the toxic group), and creatinine (with an average of 0.085 mmol / L in the toxic group versus 0.071 mmol / L in the infectious group).Conclusion. The data obtained in this research indicates the value of taking an anamnesis and the importance of performing additional studies in patients with suspected drug-induced lung injury, as well as identifies risk groups. Based on the revealed differences, a scale for the differential diagnosis of drug-induced toxic and infectious lung damage, which includes the results of publicly available research methods, with high sensitivity and specificity, was proposed. Further research for more specific, but, at the same time, universal for various drugs, criteria for toxic lung damage is relevant.
血液肿瘤患者中毒性和感染性肺损伤的鉴别诊断特点
背景。肿瘤血液学患者肺损伤的评估是一个相关的问题,因为病理改变的范围很广,包括肺部感染、肿瘤细胞浸润、心源性和非心源性肺水肿、闭塞性细支气管炎、间质性肺炎、放疗后和炎症后肺纤维化、肺血管病变和胸腔积液。目前,这些疾病的鉴别诊断标准还没有得到批准的建议,特别是以肺部感染为代表的最常见的治疗并发症与药物引起的毒性病变之间存在差异。确定肺毒性的标准,根据实际临床实践中常规获得的数据,对化疗期间发生的肺部感染进行鉴别诊断。材料和方法。研究组纳入特异性治疗所致细胞毒性和自身免疫性肺损伤患者38例(1组);对照组为38例接受相同抗肿瘤药物治疗的感染性病变患者(第二组)。回顾性分析患者的记忆、临床病程、仪器检查和标准实验室检查资料。统计分析采用Mann-Whitney、χ2、Kruskal-Wallis检验。采用ROC分析评估与毒性损害相关的各种因素的敏感性和特异性。中毒性肺损伤组以淋巴瘤为主(63%)。在接受同种异体造血干细胞移植的患者中,毒性并发症的发生时间为35 - 1289天,感染性并发症的发生时间为4 - 43天。在同时存在免疫反应改变的情况下,统计学上存在显著差异:毒性病变组中32%的患者有过敏史,而感染性病变组中5%的患者有过敏史,与感染性病变组相比,毒性病变组中检测到自身免疫性疾病。第一组患者的主要症状是呼吸短促,占68%;第二组患者的主要症状是体温升高,占92%;咳嗽也是一种常见症状,分别占19%和13%的患者。在第二组中,58%的患者发现了伴随性粘膜炎,而在第一组中,没有任何患者出现这种并发症。最常见的影像学表现(两组各占71%)为毛玻璃样混浊,第二组患者常伴有浸润性改变和支气管壁增厚(分别占53%和42%)。在实验室结果中,各组之间最大的差异是白细胞水平(平均为2.5)。感染组为109 / L,感染组为6 / L。嗜酸性粒细胞(中毒组平均3.6%,感染组平均1.75%)、c反应蛋白(感染组平均146.7 mg / L,中毒组平均52.4 mg / L)、肌酐(中毒组平均0.085 mmol / L,感染组平均0.071 mmol / L)。本研究获得的数据表明,对疑似药物性肺损伤的患者进行记忆的价值和进行额外研究的重要性,以及确定危险人群。基于所揭示的差异,我们提出了一个包含公开研究方法结果的药物致毒性和感染性肺损伤鉴别诊断量表,该量表具有较高的敏感性和特异性。进一步的研究需要更具体,但同时,对于各种药物通用,中毒性肺损伤的标准是相关的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
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