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Biliary gastritis: modern methods of diagnosis and therapy 胆道性胃炎:现代诊断与治疗方法
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-5-244-251
M. Livzan, O. Gaus, S. Mozgovoi
According to the prevalence, chronic biliary gastritis is among the most common etiological variants of chronic gastritis along with Helicobacter pylori associated gastritis and NSAID gastropathy. This review has been prepared to systematize data on the causes, pathogenetic mechanisms and methods of the diagnosis and therapy of chronic biliary gastritis. The widespread prevalance of biliary gastritis in clinical practice with insufficient understanding of the pathogenesis, the lack of diagnostic standards and unified treatment methods make the coverage of this problem very relevant. The review also systematizes known information about risk factors and pathogenetic mechanisms of biliary gastritis, discusses methods of the diagnosis and treatment of this disease, in particular, the use of ursodeoxycholic acid and cytoprotectors as pathogenetic therapy. The authors note that the treatment of biliary gastritis should be comprehensive and aimed not only at relieving dyspeptic symptoms and improving the life quality of patients, but also at preventing and inhibiting atrophic changes in the gastric mucosa. KEYWORDS: biliary gastritis, duodenogastric reflux, reactive gastritis, bile reflux gastropathy, reactive gastropathy, ursodeoxycholic acid, cytoprotectors. FOR CITATION: Livzan M.A., Gaus O.V., Mozgovoi S.I., Telyatnikova L.I. Biliary gastritis: modern methods of diagnosis and therapy. Russian Medical Inquiry. 2022;6(5):244–251 (in Russ.). DOI: 10.32364/2587-6821-2022-6-5-244-251.
根据患病率,慢性胆道性胃炎与幽门螺杆菌相关的胃炎和非甾体抗炎药胃病是慢性胃炎最常见的病因变体之一。本文对慢性胆道性胃炎的病因、发病机制、诊断和治疗方法进行了系统的综述。胆道性胃炎在临床上普遍存在,对其发病机制认识不足,缺乏诊断标准和统一的治疗方法,使得对这一问题的报道非常有意义。本文还对胆道性胃炎的危险因素和发病机制进行了系统整理,讨论了该病的诊断和治疗方法,特别是熊去氧胆酸和细胞保护剂作为发病治疗的应用。胆道性胃炎的治疗应全面,不仅要缓解消化不良症状,提高患者的生活质量,而且要预防和抑制胃粘膜的萎缩变化。关键词:胆道性胃炎,十二指肠胃反流,反应性胃炎,胆汁反流性胃病,反应性胃病,熊去氧胆酸,细胞保护剂。引用本文:Livzan m.a., Gaus o.v., Mozgovoi s.i., Telyatnikova L.I.胆道性胃炎:现代诊断和治疗方法。俄罗斯医学调查。2022;6(5):244-251(俄文)。DOI: 10.32364 / 2587-6821-2022-6-5-244-251。
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引用次数: 0
POEMS-syndrome with the disease onset in the form of сhronic dysimmune neuropathy 以慢性免疫功能障碍神经病为发病形式的poems综合征
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-10-589-595
V. Korotaeva, Y. Kushnir, O. Kudyasheva, A. Polushin, V. Krasnov
POEMS syndrome (Polyneuropathy, Organomegaly, Endocrinopathy, M-protein, Skin changes) is a rare paraneoplastic disease associated with plasma cell dyscrasias, the pathogenesis of which is currently not fully understood. The diagnosis of POEMS syndrome is commonly confirmed after an extended period of time from the disease onset, since the syndrome is rare and can be mistaken for other neurological diseases, for instance, chronic inflammatory demyelinating polyneuropathy (CIDP). The article describes a clinical case of the disease in a young male patient with the onset of neurological disorders in the form of the CIDP clinical phenotype, refractory to first-line therapy, and further systemic clinical and laboratory comorbidities of POEMS syndrome. The necessary laboratory and radiological studies were performed to confirm the diagnosis. The diagnosis was established based on the presence of 2 major, 1 additional major and 4 minor criteria of POEMS syndrome in the patient. Then the patient was discharged for further observation of hematologists to initiate basic therapy of POEMS syndrome. Early detection of the POEMS syndrome "red flags" in patients with the CIDP allows for timely treatment initiation, prevention of further disease progression and the development of persistent disabling disorders. KEYWORDS: POEMS-syndrome, chronic inflammatory demyelinating polyneuropathy, paraprotein, monoclonal gammopathy of undetermined significance. FOR CITATION: Korotaeva V.V., Kushnir Ya.B., Kudyasheva O.V. et al. POEMS-syndrome with the disease onset in the form of сhronic dysimmune neuropathy. Russian Medical Inquiry. 2022;6(10):589–595 (in Russ.). DOI: 10.32364/2587-6821-2022-6-10-589-595.
POEMS综合征(多神经病变、器官肿大、内分泌病变、m蛋白、皮肤改变)是一种罕见的与浆细胞异常相关的副肿瘤疾病,其发病机制目前尚不完全清楚。POEMS综合征的诊断通常在发病后较长一段时间后才得到证实,因为该综合征罕见,可被误认为是其他神经系统疾病,例如慢性炎症性脱髓鞘性多神经病变(CIDP)。本文描述了一名年轻男性患者的临床病例,该患者以CIDP临床表型的形式出现神经系统疾病,对一线治疗难治,并进一步出现POEMS综合征的系统性临床和实验室合并症。进行了必要的实验室和放射学检查以确认诊断。根据患者POEMS综合征的2项主要标准、1项附加主要标准和4项次要标准进行诊断。出院后接受血液科医生进一步观察,开始POEMS综合征的基础治疗。在CIDP患者中早期发现POEMS综合征的“危险信号”,可以及时开始治疗,预防进一步的疾病进展和持续致残障碍的发展。关键词:poems综合征,慢性炎症性脱髓鞘性多神经病变,副蛋白,意义不明的单克隆γ病。引文:Korotaeva v.v., Kushnir Ya.B。Kudyasheva O.V.等。以慢性免疫功能障碍神经病为发病形式的poems综合征。俄罗斯医学调查。2022;6(10):589-595(俄文)。DOI: 10.32364 / 2587-6821-2022-6-10-589-595。
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引用次数: 1
Clinical study of the URSosan Forte in patients with non-alcoholic fatty liver disease and cholelithiasis (KURS study) URSosan Forte治疗非酒精性脂肪肝合并胆石症的临床研究(KURS研究)
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-5-213-220
I. Pirogova, I.V. Ufimtseva
Aim: to evaluate the effect of ursodeoxycholic acid (UDCA) on hepatic fibrosis and steatosis, dyslipidemia, carbohydrate metabolism, and litholysis of cholesterol gallstones in patients with a combination of non-alcoholic fatty liver disease (NAFLD) and gallstone disease (GD). Patients and Methods: a prospective monocenter study was conducted, which included patients with NAFLD and GD at the age of 19 to 65 years. The diagnosis was established on the basis of clinical, laboratory, ultrasound and radiological data. The nature and incidence of comorbid pathology were assessed. The degree of hepatic fibrosis and steatosis was determined according to the abdominal MSCT and serum tests of liver fibrosis (FIB 4, APRI) and hepatic steatosis (FLI), as well as liver elastography. All patients received UDCA at a dose of 15 mg/kg for 6 months. Results: 85 patients were included in the study, 59 (70%) of them were female, the mean age was 49.3±9 years. Gallstones of low density (up to 75 HU) were detected in 45 (52%) patients who made up the group 1, of high density (75–120 HU) — in 40 (48%) patients included in the group 2. 42 (49%) patients had comorbidity. In group 2, comorbid pathology was significantly more common and the degree of hepatic steatosis and fibrosis was higher. During treatment with UDCA, the positive trend in group 1 was expressed in a significant decrease in the gallstone density and size, normalization of liver density, cytolysis and cholestasis indicators, improvement of carbohydrate metabolism, and regression of hepatic steatosis according to MSCT and elastography. In group 2, there was a decrease in bile density and gallstone size according to MSCT, as well as a positive trend of lipidogram, HOMA-IR index, hepatic density and steatosis according to MSCT and elastography.Conclusion: the use of UDCA in patients with NAFLD and GD as pathogenetic therapy has a positive effect on hepatic fibrosis and steatosis, dyslipidemia, carbohydrate metabolism, and provides litholysis of cholesterol stones, mainly with a density of less than 75 HU. KEYWORDS: comorbidity, non-alcoholic fatty liver disease, cholelithiasis, cholesterol stones, litholysis, hepatic steatosis. FOR CITATION: Pirogova I.Yu., Ufimtseva I.V. Clinical study of the URSosan Forte in patients with non-alcoholic fatty liver disease and cholelithiasis (KURS study). Russian Medical Inquiry. 2022;6(5):213–220 (in Russ.). DOI: 10.32364/2587-6821-2022-6-5-213-220.
目的:评价熊去氧胆酸(UDCA)对合并非酒精性脂肪性肝病(NAFLD)和胆结石病(GD)患者肝纤维化和脂肪变性、血脂异常、碳水化合物代谢和胆固醇结石溶解的影响。患者和方法:进行了一项前瞻性单中心研究,纳入了年龄在19至65岁的NAFLD和GD患者。诊断依据临床、实验室、超声和放射学资料。评估共病病理的性质和发生率。根据腹部MSCT、血清肝纤维化(FIB 4、APRI)、肝脂肪变性(FLI)及肝弹性图确定肝纤维化和脂肪变性程度。所有患者均以15mg /kg的剂量接受UDCA治疗,疗程6个月。结果:85例患者纳入研究,其中女性59例(70%),平均年龄49.3±9岁。1组45例(52%)患者检测到低密度(75 HU)胆结石,2组40例(48%)患者检测到高密度(75 - 120 HU)胆结石。42例(49%)患者有合并症。2组共病病理更常见,肝脂肪变性和纤维化程度更高。在UDCA治疗期间,MSCT和弹性成像显示,1组患者的阳性趋势表现为胆结石密度和大小明显下降,肝密度、细胞溶解和胆汁淤积指标正常化,碳水化合物代谢改善,肝脂肪变性消退。2组MSCT显示胆密度和胆结石大小下降,MSCT和弹性图显示脂质图、HOMA-IR指数、肝脏密度和脂肪变性呈阳性趋势。结论:UDCA用于NAFLD和GD患者的病理治疗对肝纤维化和脂肪变性、血脂异常、碳水化合物代谢有积极作用,并提供胆固醇结石的溶解,主要以密度小于75 HU的结石为主。关键词:合并症、非酒精性脂肪性肝病、胆石症、胆固醇结石、溶石、肝脂肪变性。引证:Pirogova I.Yu。URSosan Forte在非酒精性脂肪肝合并胆石症患者中的临床研究(KURS研究)。俄罗斯医学调查。2022;6(5):213-220(俄文)。DOI: 10.32364 / 2587-6821-2022-6-5-213-220。
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引用次数: 0
Interferon profile of the mucosal immunity in women with papillomavirus infection 乳头瘤病毒感染妇女粘膜免疫的干扰素谱分析
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-2-67-71
E. Markelova, M. S. Tulupova, T. Nevezhkina, L. S. Matyushkina, M. Chernikova, S. Knysh
Papillomaviruses are a group of DNA viruses belonging to the Papillomavirida family. These viruses provoke pathological conditions manifesting with inflammation, exophytic masses, carcinogenesis, reproductive and perinatal disorders. Immune status is an essential factor de-termining the severity and duration of inflammatory diseases, the course of latent viral infections, including papillomavirus infection (PVI). The human immune system prevents the persistence, reactivation, and development of PVI clinical presentations. The cellular immune response is realized under the control of interferons (IFNs). Today, no complex studies on type 1, 2, or 3 IFNs in the cervical mucus of women with PVI associated with herpesvirus and chlamydia infec-tions are available. Aim: to compare IFN profile of mucosal immunity in women with PVI associated with herpesvirus and chlamydia infections. Patients and Methods: this study enrolled 149 women aged 25–44. Women were divided into four groups. Group 1 included women with PVI only (n=21). Group 2 included women with PVI and herpesvirus infection (n=47). Group 3 included women with PVI and chlamydia infec-tions (n=39). Group 4 included controls (n=30). Complex outpatient clinical laboratory examina-tion included clinical functional, biochemical, and immunological tests to detail pathophysiolog-ical mechanisms of urogenital PVIs. IFN (IFN-β, IFN-γ, IFN-λ1/IL-29, IFN-λ3/IL-28B) levels in the cervical mucus were measured by ELISA. Results: in all groups, IFN-λ3 and IFN-γ deficiencies were detected. In PVI, IFN-γ deficiency prevailed. In PVI associated with herpesvirus infection, IFN-λ3 deficiency prevailed. In PVI associated with chlamydia infection, a severe IFN-β deficiency was revealed. Conclusion: these patterns demonstrate a relevant role of the interferon arm of the im-mune response in the pathogenesis of isolated PVI and PVI associated with herpesvirus and chlamydia infections. These alterations in mucosal immunity support the prescription of immu-notherapy for these infections. KEYWORDS: human papillomavirus, herpesvirus infection, chlamydia infection, interferons, immune system, cervical mucus, mucosal immunity. FOR CITATION: Markelova E.V., Tulupova M.S., Nevezhkina T.A. et al. Interferon profile of the mucosal immunity in women with papillomavirus infection. Russian Medical Inquiry. 2022;6(2):67–71 (in Russ.). DOI: 10.32364/2587-6821-2022-6-2-67-71.
乳头瘤病毒是一组属于乳头瘤病毒科的DNA病毒。这些病毒引起的病理状况表现为炎症、外生性肿块、致癌、生殖和围产期疾病。免疫状态是决定炎症性疾病的严重程度和持续时间,潜伏病毒感染的过程,包括乳头瘤病毒感染(PVI)的重要因素。人体免疫系统阻止PVI临床表现的持续、再激活和发展。细胞免疫应答是在干扰素(ifn)的控制下实现的。目前,对于与疱疹病毒和衣原体感染相关的PVI患者宫颈粘液中1型、2型或3型ifn的复杂研究尚无。目的:比较与疱疹病毒和衣原体感染相关的PVI妇女粘膜免疫的IFN谱。患者和方法:本研究招募了149名年龄在25-44岁之间的女性。女性被分成四组。第1组仅包括患有PVI的女性(n=21)。第2组包括伴有PVI和疱疹病毒感染的女性(n=47)。第3组包括合并PVI和衣原体感染的女性(n=39)。第4组包括对照组(n=30)。复杂的门诊临床实验室检查包括临床功能、生化和免疫学检查,以详细了解泌尿生殖器PVIs的病理生理机制。ELISA法检测宫颈黏液中IFN (IFN-β、IFN-γ、IFN-λ1/IL-29、IFN-λ3/IL-28B)水平。结果:各组均检测到IFN-λ3和IFN-γ缺乏。在PVI中,IFN-γ缺乏普遍存在。在与疱疹病毒感染相关的PVI中,IFN-λ3缺乏普遍存在。在衣原体感染相关的PVI中,发现严重的IFN-β缺乏。结论:这些模式表明免疫-免疫反应的干扰素臂在分离的PVI和与疱疹病毒和衣原体感染相关的PVI发病机制中的相关作用。这些粘膜免疫的改变支持了针对这些感染的免疫治疗处方。关键词:人乳头瘤病毒,疱疹病毒感染,衣原体感染,干扰素,免疫系统,宫颈粘液,粘膜免疫。引用本文:Markelova e.v., Tulupova m.s., Nevezhkina T.A.等。乳头瘤病毒感染妇女粘膜免疫的干扰素谱分析。俄罗斯医学调查。2022;6(2):67-71(俄文)。DOI: 10.32364 / 2587-6821-2022-6-2-67-71。
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引用次数: 0
Postcovid syndrome: risk factors, pathogenesis, diagnosis and treatment of patients with respiratory damage after COVID-19 (overview) COVID-19后综合征:COVID-19后呼吸损伤患者的危险因素、发病机制、诊断和治疗(综述)
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-7-367-375
T. Bilichenko
In COVID-19 of moderate to severe degree, there are significant inflammatory changes in the lungs and other organs involved in the pathological process with corresponding symptoms and functional disorders lasting longer than 12 weeks. They are designated as postcovid syndrome (PCS) and require further treatment. The article presents the pathogenetic mechanism of PCS, in which organ damage has the systemic nature. Special attention is paid to the changes in the organs of the respiratory system (atelectasis in the alveoli within the lungs, remodeling of the bronchial epithelium, hyaluronan deposition in the lumen of alveoli, bronchi and perialveolar interstitial with the formation of connective tissue), which in the long term lead to fibrous changes, especially in patients with severe COVID-19 and concomitant respiratory diseases. This, in turn, makes oxygen and carbon dioxide to pass through the alveoli wall with difficulties, decreases exercise tolerance and life quality, and increases mortality in elderly patients. The article also outlines the main directions of pathogenetically conditioned therapy of patients with respiratory disorder in the outpatient settings, providing a decrease in rehabilitation period and improving the patients condition. KEYWORDS: postcovid syndrome, alveolar epithelium, atelectasis, comorbidity, rehabilitation. FOR CITATION: Bilichenko T.N. Postcovid syndrome: risk factors, pathogenesis, diagnosis and treatment of patients with respiratory damage after COVID-19 (overview). Russian Medical Inquiry. 2022;6(7):367–375 (in Russ.). DOI: 10.32364/2587-6821-2022-6-7-367-375.
中重度COVID-19患者,肺部及其他参与病理过程的器官出现明显的炎症改变,相应的症状和功能障碍持续时间超过12周。他们被指定为covid后综合征(PCS),需要进一步治疗。本文介绍了PCS的发病机制,其中器官损害具有全身性。特别关注呼吸系统器官的变化(肺内肺泡不张、支气管上皮重塑、肺泡腔、支气管和肺泡周围间质中透明质酸沉积以及结缔组织的形成),这些变化长期导致纤维改变,特别是在严重的COVID-19和伴随呼吸道疾病的患者中。这反过来又使氧气和二氧化碳难以通过肺泡壁,降低运动耐量和生活质量,并增加老年患者的死亡率。本文还概述了呼吸系统疾病患者病理条件治疗在门诊的主要方向,缩短康复时间,改善患者病情。关键词:covid后综合征,肺泡上皮,肺不张,合并症,康复。引用本文:Bilichenko T.N. COVID-19后综合征:COVID-19后呼吸损伤患者的危险因素、发病机制、诊断和治疗(概述)。俄罗斯医学调查。2022;6(7):367-375(俄文)。DOI: 10.32364 / 2587-6821-2022-6-7-367-375。
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引用次数: 2
Pulmonary surfactant in the complex treatment of severe pneumonia associated with COVID-19. Efficacy markers 肺表面活性物质在新冠肺炎合并重症肺炎综合治疗中的作用疗效指标
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-7-352-359
E. Volchkova, Y. Alexandrovich, O. Titova, N. Kuzubova, V. Volchkov, D. Piskunov, M. N. Bakholdina, F. Bitakova
Aim: to evaluate the effect of pulmonary surfactant therapy in the complex treatment of severe community-acquired pneumonia caused by the SARS-CoV-2 on the disease course and outcome and to determine the possibility of using the level of surfactant protein D (surfactant protein D, SP-D) in blood serum as a criterion for the treatment efficacy. Patients and Methods: a prospective randomized study included 60 patients. Inclusion criteria confirmed SARS-CoV-2; bilateral pneumonia with at least grade 3 of lesion according to CT; SpO2 less than 92%. Patients were divided into two groups: group 1 (n=30) received surfactant therapy in addition to standard therapy, group 2 (n=30) received only standard therapy. Surfactant was administered by inhalation at a dose of 150–300 mg/day. The duration of surfactant therapy was 10 days. Arterial blood gas values, clinical parameters and SP-D levels were analyzed before and after treatment. Results: 48 hours after the therapy start, a statistically significant increase in SpO2 was registered in patients from group 1 versus an increase in patients from group 2 (p=0.048). On the 10th day of treatment, group 1 versus group 2 showed a statistically significant increase in the oxygenation index (PaO2/FiO2) (266.82±10.5 mmHg vs. 199.67±11.7 mmHg, respectively, p=0.001), a decrease in the frequency of artificial lung ventilation (ALV) (27% vs. 67%, respectively, p=0.002), length of hospital stay (21.0 (15;25) days vs. 27.0 (15;35) days, respectively, p=0.05). The fatal outcome was registered in 8 (27%) patients from group 1 and 18 (60%) patients from group 2 (p=0.001). Among patients from group 1 who had a favorable disease outcome, in 84% of cases surfactant therapy was prescribed in a shorter period from the disease onset versus patients whose treatment was ineffective (3±1.5 days vs. 7±2.0 days). A stable, reliable correlation was established between SP-D and PaO2 (r= 420, p=0.001), between SP-D and PaO2/FiO2 (r=460, p=0.001). Conclusion: the major effects of surfactant therapy are a faster recovery of the arterial blood gas, a decrease in the frequency of ALV, the length of hospital stay, and mortality. The success of surfactant therapy is associated with its early prescription. Surfactant therapy can be considered as an additional pathogenetically justified component in the complex treatment of severe pneumonia caused by the SARS-CoV-2. Significantly higher levels of SP-D were observed in patients with severe pneumonia associated with COVID-19, with the disease progression and adverse outcome. KEYWORDS: SARS-CoV-2, COVID-19, pneumonia, surfactant, artificial lung ventilation, respiratory failure, surfactant protein D, SP-D. FOR CITATION: Volchkova E.V., Alexandrovich Yu.S., Titova O.N. et al. Pulmonary surfactant in the complex treatment of severe pneumonia associated with COVID-19. Efficacy markers. Russian Medical Inquiry. 2022;6(7):352–359 (in Russ.). DOI: 10.32364/2587-6821-2022-6-7-352-359.
目的:评价复合治疗SARS-CoV-2所致重症社区获得性肺炎中肺表面活性物质治疗对病程和转转率的影响,探讨以血清表面活性物质蛋白D (SP-D)水平作为治疗疗效指标的可能性。患者和方法:一项前瞻性随机研究包括60例患者。纳入标准确诊为SARS-CoV-2;双侧肺炎,CT显示病变3级以上;SpO2小于92%。将患者分为两组:组1 (n=30)在标准治疗的基础上给予表面活性剂治疗,组2 (n=30)只给予标准治疗。表面活性剂吸入给药,剂量为150-300 mg/天。表面活性剂治疗10 d。分析治疗前后动脉血气值、临床参数及SP-D水平。结果:治疗开始48小时后,1组患者SpO2升高,与2组患者相比有统计学意义(p=0.048)。治疗第10天,1组与2组相比,氧合指数(PaO2/FiO2)升高(分别为266.82±10.5 mmHg和199.67±11.7 mmHg, p=0.001),人工肺通气(ALV)频率降低(分别为27%和67%,p=0.002),住院时间分别为21.0(15;25)天和27.0(15;35)天,p=0.05)。1组有8例(27%)患者死亡,2组有18例(60%)患者死亡(p=0.001)。在疾病预后良好的第1组患者中,与治疗无效的患者相比,84%的病例在发病后较短的时间内给予表面活性剂治疗(3±1.5天对7±2.0天)。SP-D与PaO2 (r= 420, p=0.001)、SP-D与PaO2/FiO2 (r=460, p=0.001)存在稳定、可靠的相关性。结论:表面活性剂治疗的主要作用是动脉血气恢复较快,ALV发作次数减少,住院时间延长,死亡率降低。表面活性剂治疗的成功与其早期处方有关。表面活性剂治疗可以被认为是SARS-CoV-2引起的严重肺炎复杂治疗中一个额外的病理合理的组成部分。在与COVID-19相关的严重肺炎患者中,随着疾病进展和不良结局的发生,SP-D水平显著升高。关键词:SARS-CoV-2、COVID-19、肺炎、表面活性剂、人工肺通气、呼吸衰竭、表面活性剂蛋白D、SP-D引文:Volchkova e.v., Alexandrovich yus。, Titova O.N.等。肺表面活性物质在新冠肺炎合并重症肺炎综合治疗中的作用功效标记。俄罗斯医学调查。2022;6(7):352-359(俄文)。DOI: 10.32364 / 2587-6821-2022-6-7-352-359。
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引用次数: 2
Concurrent surgeries in patients with varicose vein disease and ventral hernias 静脉曲张合并腹疝的并发手术治疗
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-4-164-170
A. Chernookov, M. R. Kuznetsov, S. Kandyba, A. Atayan, Yu. N. Lebedeva, A. A. Ramazanov
Aim: to substantiate the feasibility of concurrent surgeries in patients with varicose vein disease and anterior abdominal wall hernias (ventral hernias). Patients and Methods: the paper presents the treatment results of 82 patients with ventrial hernias and lower limb varicose vein disease. The method choice and the scope of surgical intervention were determined on the basis of clinical and instrumental examination data. Commonly, Lichtenstein tension-free hernia repair in combination with crossectomy, endovasal laser coagulation (EVLC), varicose veins radiofrequency ablation (VVRFA) were performed. The long-term results were analyzed 1–2 years after the use of concurrent surgeries. The life quality before surgery and a year after was determined by the SF-36 questionnaire. Results: the patients consisted of 45 (54.9%) men and 37 (45.1%) women aged 19 to 69 years. In 20 (24.4%) of the admitted patients, work was associated with physical activity, and 56 (68.3%) patients were at the most capable age: 19 to 50 years. Upon admission to the clinic, 78 patients had complaints. Commonly, they had a combination of varicose vein disease with inguinal or umbilical hernias. After the use of concurrent surgeries, no specific complications were observed in this patient cohort, as well as complications associated with both diseases concomitantly. In the long-term period, patients noted an improvement in their general health by 23.2%. In the preoperative period, the indicator of physical functioning was 41.27 points; after the operation, there was an increase in this indicator according to patients’ estimates by 1.6 times — to 67.32 points. After surgery, the greatest positive trend of vital activity (42.8%) and role limitations due to emotional state (57.3%) were observed. There was an increase in all indicators of life quality by 18.2–53.9% in patients who underwent concurrent surgeries. Conclusion: the obtained results demonstrated the safety and high efficacy of concurrent surgeries in patients with varicose vein disease and ventral hernias. Thus, the use of concurrent surgeries is considered to be an alternative to the staged treatment of patients with varicose vein disease and ventral hernias KEYWORDS: concurrent surgeries, varicose vein disease, ventral hernias, life quality, postoperative complications. FOR CITATION: Chernookov A.I., Kuznetsov M.R., Kandyba S.I. et al. Concurrent surgeries in patients with varicose vein disease and ventral hernias. Russian Medical Inquiry. 2022;6(4):164–170 (in Russ.). DOI: 10.32364/2587-6821-2022-6-4-164-1.
目的:探讨静脉曲张合并前腹壁疝(腹疝)并发手术的可行性。患者与方法:报告82例腹疝合并下肢静脉曲张病患者的治疗结果。根据临床和器械检查资料确定手术方法选择和手术干预范围。通常,利希滕斯坦无张力疝修补联合横切面切除术、血管内激光凝固(EVLC)、静脉曲张射频消融(VVRFA)。在采用并行手术后1-2年分析远期结果。术前及术后1年的生活质量采用SF-36量表进行评定。结果:男性45例(54.9%),女性37例(45.1%),年龄19 ~ 69岁。在20例(24.4%)住院患者中,工作与身体活动有关,56例(68.3%)患者处于最能运动的年龄:19至50岁。入院时,78名患者有抱怨。通常,他们有合并静脉曲张疾病与腹股沟或脐疝。在采用并行手术后,在该患者队列中未观察到特异性并发症,以及两种疾病合并的并发症。长期来看,患者的总体健康状况改善了23.2%。术前身体功能指标41.27分;手术后,该指标根据患者的估计增加了1.6倍,达到67.32分。术后生命活动的积极趋势最大(42.8%),情绪状态导致的角色限制最大(57.3%)。同时进行手术的患者生活质量各项指标均提高18.2-53.9%。结论:所获得的结果证明了并发手术治疗静脉曲张病变合并腹疝的安全性和有效性。关键词:并发手术,静脉曲张病变,腹侧疝,生活质量,术后并发症。引用本文:Chernookov a.i., Kuznetsov m.r., Kandyba S.I.等。静脉曲张合并腹疝的并发手术治疗。俄罗斯医学调查。2022;6(4):164-170(俄文)。DOI: 10.32364 / 2587-6821-2022-6-4-164-1。
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引用次数: 0
Rational approach to the treatment of otitis externa 外耳炎的合理治疗方法
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-7-404-410
A. V. Gurov, A. V. Muzhichkova
In recent years, there has been an increased number of calls to ENT specialists concerning otitis externa. These conditions are characterized by antibiotic resistance of key pathogens, as well as the presence of significant pain symptoms. In 60–98% of cases, inflammation in the external auditory canal has a bacterial etiology. Pseudomonas aeruginosa occupies a leading place in the microbial landscape — up to 78% on average, while Staphylococcus aureus is sown only in 9–27% of cases. Rational therapy of otitis externa is one of the urgent problems of otorhinolaryngology, despite the large variety of treatment methods. It is necessary to use complex therapy of external otitis, including a direct effect on the etiological factor, as well as pain relief. In the vast majority of cases, the frontline empirical therapy of otitis externa should be topical antimicrobial agents. The following combined drug is successfully used for the treatment of otitis externa: ear drops containing a combined antibiotic (aminoglycoside neomycin + cyclic polypeptide polymyxin B + topical anesthetic lidocaine). Early therapy of otitis externa with a combined antibiotic is the key to a fast and reliable clinical result. KEYWORDS: otitis externa, bacterial otitis, ear drops, combined antibiotic, aminoglycoside, cyclic polypeptide, topical anesthetics, neomycin, polymyxin B, lidocaine. FOR CITATION: Gurov A.V., Muzhichkova A.V. Rational approach to the treatment of otitis externa. Russian Medical Inquiry. 2022;6(7):404– 410 (in Russ.). DOI: 10.32364/2587-6821-2022-6-7-404-410.
近年来,有越来越多的电话呼叫耳鼻喉专科有关外耳炎。这些疾病的特点是主要病原体的抗生素耐药性,以及存在明显的疼痛症状。在60-98%的病例中,外耳道炎症是由细菌引起的。铜绿假单胞菌在微生物景观中占据主导地位-平均高达78%,而金黄色葡萄球菌仅在9-27%的病例中播种。尽管外耳炎的治疗方法多种多样,但合理治疗外耳炎仍是耳鼻喉科亟待解决的问题之一。外耳炎的综合治疗是必要的,包括对病因的直接影响,以及疼痛的缓解。在绝大多数情况下,外耳炎的一线经验性治疗应该是外用抗菌药物。以下联合药物成功用于治疗外耳炎:含联合抗生素(氨基糖苷新霉素+环多肽多粘菌素B +表面麻醉剂利多卡因)的滴耳液。早期联合应用抗生素治疗外耳炎是获得快速、可靠临床结果的关键。关键词:外耳炎、细菌性中耳炎、滴耳液、联合抗生素、氨基糖苷、环多肽、表面麻醉剂、新霉素、多粘菌素B、利多卡因。引用本文:Gurov A.V., Muzhichkova A.V.外耳炎的合理治疗方法。俄罗斯医学调查。2022;6(7):404 - 410(俄文)。DOI: 10.32364 / 2587-6821-2022-6-7-404-410。
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引用次数: 1
Endocrine adverse events in patients with malignant neoplasms receiving treatment with immune checkpoint inhibitors 恶性肿瘤患者接受免疫检查点抑制剂治疗的内分泌不良事件
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-9-528-533
K. Zherebchikova, Y. Sych, M. V. Amosova, M. Sekacheva, V. Fadeev, A.A. Vilensky
Immune checkpoint inhibitors are monoclonal antibodies directed against the molecules blocking immune response, such as cytotoxic T-lymphocyte- associated protein 4 (CTLA-4), programmed cell death protein-1 (PD1) and its ligand, which enhance anti-tumor immunity. Immune checkpoint inhibitors have demonstrated high efficacy in cancer treatment, including the most common types of cancer and helped to increase recurrence- free and overall survival of cancer patients. At the same time, the use of checkpoint inhibitors is associated with a high risk of immune-related adverse events (irAEs) — autoimmune conditions that occur in multiple organs and tissues, including endocrinopathies. Endocrine irAEs can affect the thyroid, pituitary gland, adrenal glands, and pancreas. These events are unique when compared with other irAEs because the manifestations are often irreversible. The awareness of clinicians of potential irAEs, including endocrinopathies caused by agents from the group of immune checkpoint inhibitors will improve their timely identification and treatment. Thus, it will promote the safe use of highly effective anti-tumor therapy. KEYWORDS: checkpoint inhibitors, CTLA-4, PD1, PDL1, immune-related adverse events, hypothyroidism, thyrotoxicosis, thyroiditis, hypophysitis, adrenal insufficiency. FOR CITATION: Zherebchikova K.Yu., Sych Yu.P., Amosova M.V. et al. Endocrine adverse events in patients with malignant neoplasms receiving treatment with immune checkpoint inhibitors. Russian Medical Inquiry. 2022;6(9):528–533 (in Russ.). DOI: 10.32364/2587-6821- 2022-6-9-528-533.
免疫检查点抑制剂是针对阻断免疫反应分子的单克隆抗体,如细胞毒性t淋巴细胞相关蛋白4 (CTLA-4)、程序性细胞死亡蛋白1 (PD1)及其配体,可增强抗肿瘤免疫。免疫检查点抑制剂在癌症治疗中已经证明了很高的疗效,包括最常见的癌症类型,并有助于增加癌症患者的无复发和总生存率。同时,检查点抑制剂的使用与免疫相关不良事件(irAEs)的高风险相关——包括内分泌疾病在内的多器官和组织中发生的自身免疫性疾病。内分泌干扰素可影响甲状腺、脑垂体、肾上腺和胰腺。与其他irae相比,这些事件是独特的,因为其表现往往是不可逆的。临床医生对潜在的irae,包括免疫检查点抑制剂组药物引起的内分泌病变的认识将提高其及时识别和治疗。从而促进高效抗肿瘤治疗的安全使用。关键词:检查点抑制剂、CTLA-4、PD1、PDL1、免疫相关不良事件、甲状腺功能减退、甲状腺毒症、甲状腺炎、垂体炎、肾上腺功能不全。引文:Zherebchikova K.Yu。, Sych。, Amosova M.V.等。恶性肿瘤患者接受免疫检查点抑制剂治疗的内分泌不良事件。俄罗斯医学调查。2022;6(9):528-533(俄文)。Doi: 10.32364/2587-6821- 2022-6-9-528-533。
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引用次数: 0
Alopecia areata in atopic dermatitis: coincidence or regularity? 特应性皮炎斑秃:偶然性还是规律性?
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-2-85-91
S. Petrova, V. Albanova
Extensive trials have identified a close relationship between atopic dermatitis (AD) and alopecia areata (AA). This review paper summarizes and analyzes available data on the immunological pattern of AD-associated AA. The analysis of scientific findings suggests that epidermal barrier dysfunction in AD promotes AA in the presence of target genes contributing to its development. Both pathological entities negatively affect each other. The results are the reduction in regulatory T cell (Treg) suppression activity and an increase in inflammatory and autoimmune activity of Th-17 cells. Hyperergic Th2 response affects AD-associated AA clinical presentations. The regression of bald patches after IL-4, IL-13, and histamine receptors blockage further establishes the association between AA and AD. The possibility of atopic alopecia requires both skin and hair care products in AD. Dry peeling skin vulnerable to infections should be treated to reduce the risk of autoimmunity in AA. The presence of two family lines of genetic predisposition (atopy and AA) results in severe combined manifestations of these disorders in progeny. Therefore, attention should be paid to early AD signs in children in these families to commence treatment timely. KEYWORDS: atopic dermatitis, аlopecia areata, genetics, autoimmunity, epidermal barrier, regulatory T cells, immune privilege, hair follicle, T helper 17 cells, mast cells. FOR CITATION: Petrova S.Yu., Albanova V.I. Alopecia areata in atopic dermatitis: coincidence or regularity? Russian Medical Inquiry. 2022;6(2):85–91 (in Russ.). DOI: 10.32364/2587-6821-2022-6-2-85-91.
广泛的试验已经确定了特应性皮炎(AD)和斑秃(AA)之间的密切关系。本文对ad相关AA的免疫学模式进行综述和分析。对科学发现的分析表明,AD的表皮屏障功能障碍在参与其发展的靶基因存在的情况下促进了AA的发生。两种病理实体相互负向影响。结果是调节性T细胞(Treg)抑制活性降低,Th-17细胞的炎症和自身免疫活性增加。超能Th2反应影响ad相关AA的临床表现。IL-4、IL-13和组胺受体阻断后秃斑的消退进一步证实了AA和AD之间的关联。特应性脱发的可能性需要皮肤和头发护理产品在AD。应治疗易受感染的干燥脱皮,以降低AA患者自身免疫的风险。遗传易感性的两个家族系(特应性和AA)的存在导致这些疾病在后代中严重的联合表现。因此,应重视这些家庭儿童的早期AD症状,及时开始治疗。关键词:特应性皮炎,斑秃,遗传学,自身免疫,表皮屏障,调节性T细胞,免疫特权,毛囊,辅助性T 17细胞,肥大细胞。引文:Petrova S.Yu。特应性皮炎的斑秃:偶然性还是规律性?俄罗斯医学调查。2022;6(2):85-91(俄文)。DOI: 10.32364 / 2587-6821-2022-6-2-85-91。
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引用次数: 0
期刊
Russian Medical Inquiry
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