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[Experience in the application of ultrasound indices for assessing the activity of inflammatory bowel diseases]. 【超声指标在炎性肠病活动性评价中的应用体会】。
IF 0.3 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-28 DOI: 10.26442/00403660.2025.08.203303
D D Mukhametova, I M Minnemullin, O E Akchurina, A K Odintsova, D I Abdulganieva

Aim: To evaluate the diagnostic value of ultrasound (US) parameters and indices for assessing the active inflammatory bowel diseases (IBD).

Materials and methods: The study included 115 patients with IBD, 41 (36%) patients were with ulcerative colitis (UC) and 74 (64%) - with Crohn's disease (CD). Transabdominal US examination of the intestine was performed on Sonoscape S2N, with a bowel wall thickness (BWT) of 3 mm considered the norm. To assess activity in UC, the Milan Ultrasound Criteria (MUC) score was used, and in CD - International Bowel Ultrasound Segmental Activity Score (IBUS-SAS).

Results: In active UC BWT (5.91 [4.87; 6.95] mm) was greater than in remission (2.9 [2.6; 3.1] mm; p = 0.003). For active UC diagnosis BWT greater than 3 mm had sensitivity (Se) of 90.5% and specificity (Sp) of 70.6%. The MUC in exacerbation (9 [7.88; 11.8]) was higher than in remission (4.2 [3.64; 4.9]; p < 0.001). In 31 (89%) patients in exacerbation, the MUC was higher than 6.2 (Se 88.9%, Sp 87.5%), and in 34 (97%) at a threshold of 5.18 (Se 96.3%, Sp 87.5%). In active CD, BWT (4.9 [3.8; 6.6] mm) was greater than in remission (3.18 [2.6; 3.5]; p = 0.0001), with Se 87.0%, Sp 71.4%. The IBUS-SAS in active CD (46.8 [27; 71.5]) was higher than the remission (12.6 [11.2; 30.2]; p = 0.001). At a threshold of 37.5, the IBUS-SAS had Se 92.6%, Sp 61.5%, and at 45.2, Se 92.6%, Sp 87.2%.

Conclusion: US imaging is a useful and effective tool for assessing IBD activity; a threshold value of the MUC score of 5.18 and IBUS-SAS of 45.2 suggests better diagnostic value for differentiating between exacerbation and remission.

目的:探讨超声参数及指标对活动性炎症性肠病(IBD)的诊断价值。材料和方法:本研究纳入115例IBD患者,41例(36%)溃疡性结肠炎(UC)患者和74例(64%)克罗恩病(CD)患者。在S2N超声显像上对肠道进行经腹超声检查,肠壁厚度(BWT)为3mm。为了评估UC的活动,使用米兰超声标准(MUC)评分,并使用CD -国际肠超声节段活动评分(IBUS-SAS)。结果:活动期UC患者BWT (5.91 [4.87; 6.95] mm)大于缓解期患者(2.9 [2.6;3.1]mm; p = 0.003)。对于活动性UC诊断,BWT大于3 mm的敏感性(Se)为90.5%,特异性(Sp)为70.6%。加重期MUC(9[7.88; 11.8])高于缓解期MUC (4.2 [3.64; 4.9]; p < 0.001)。在31例(89%)急性加重患者中,MUC高于6.2 (Se 88.9%, Sp 87.5%), 34例(97%)的阈值高于5.18 (Se 96.3%, Sp 87.5%)。活动性CD患者BWT (4.9 [3.8; 6.6] mm)大于缓解期患者(3.18 [2.6;3.5];p = 0.0001), Se为87.0%,Sp为71.4%。活动性CD患者IBUS-SAS评分46.8[27;71.5]高于缓解期患者(12.6 [11.2;30.2];p = 0.001)。当阈值为37.5时,IBUS-SAS的Se值为92.6%,Sp值为61.5%;当阈值为45.2时,Se值为92.6%,Sp值为87.2%。结论:超声显像是评估IBD活动性的有效工具;MUC评分的阈值为5.18,IBUS-SAS评分的阈值为45.2,表明对区分加重和缓解有更好的诊断价值。
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引用次数: 0
[The high-dose dual therapy for eradication of Helicobacter pylori: efficacy and safety]. 【大剂量双重治疗根除幽门螺杆菌的疗效与安全性】。
IF 0.3 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-28 DOI: 10.26442/00403660.2025.08.203300
N V Bakulina, V A Ponomarenko, A S Kerimova, T Thai Hien, A S Shikhmagomedova, A M Veliev, I V Savilova

Background: The article presents the results of a prospective open-label comparative interventional study of the efficacy and safety of high-dose dual therapy (HDDT) for eradicating Helicobacter pylori infection.

Aim: To evaluate the efficacy and safety of HDDT of the H. pylori eradication regimen, as well as the possible increase in the efficacy of this regimen with the addition of rebamipide.

Materials and methods: All patients with verified H. pylori infection were randomized into three groups depending on the treatment regimen. The Era-AmIPP group (n = 24) received HDDT (esomeprazole 120 mg/day and amoxicillin 3000 mg/day) for 14 days. The Era-RebAmIPP group (n = 121) received HDDT with rebamipide 300 mg/day for 14 days. The comparison group (n = 101) received conventional triple eradication therapy enhanced with bismuth tripotassium dicitrate for 14 days. The effectiveness of eradication was evaluated at 4-6 weeks after the end of therapy. Particular attention was paid to assessing the safety of therapy, the incidence of adverse events, and treatment adherence.

Results: The study included 246 patients. Low efficacy (87.5% [95% confidence interval [CI] 69.0-95.7]) of HDDT was shown. Adding rebamipide 300 mg/day to HDDT increased the eradication rate to 96.3% (95% CI 90.9-98.6). The efficacy of the Era-RebAmIPP regimen in patients previously treated with conventional eradication regimens was 91.7% (95% CI 64.6-98.5). Adverse events were reported in 37.5% (95% CI 21.2-57.3) patients in the Era-AmIPP group, 19.8% (95% CI 13.7-27.8) in the Era-RebAmIPP group, and 31.3% (95% CI 22.9-41.1) in the comparison group (p = 0.07).

Conclusion: The efficacy of the Era-RebAmIPP regimen is comparable to conventional triple therapy with bismuth. To assess the effectiveness of this regimen, larger-scale studies are required in various regions of our country.

背景:本文介绍了一项关于高剂量双重治疗(HDDT)根除幽门螺杆菌感染的疗效和安全性的前瞻性开放标签比较介入研究的结果。目的:评价HDDT在幽门螺杆菌根除方案中的有效性和安全性,以及加入利巴米胺后可能提高该方案的有效性。材料与方法:所有确诊幽门螺旋杆菌感染的患者根据治疗方案随机分为三组。Era-AmIPP组(n = 24)给予HDDT(埃索美拉唑120 mg/天,阿莫西林3000 mg/天)治疗14天。Era-RebAmIPP组(n = 121)使用HDDT和rebamipide 300 mg/天,持续14天。对照组(101例)接受常规三联根除治疗,外加三硝酸铋,疗程14天。在治疗结束后4-6周评估根除的有效性。特别关注的是评估治疗的安全性、不良事件的发生率和治疗依从性。结果:纳入246例患者。HDDT的疗效较低(87.5%[95%可信区间[CI] 69.0 ~ 95.7])。在HDDT中加入300 mg/天的瑞巴米胺可将根除率提高到96.3% (95% CI 90.9-98.6)。Era-RebAmIPP方案对先前接受常规根除方案治疗的患者的疗效为91.7% (95% CI 64.6-98.5)。Era-AmIPP组不良事件发生率为37.5% (95% CI 21.2-57.3), Era-RebAmIPP组为19.8% (95% CI 13.7-27.8),对照组为31.3% (95% CI 22.9-41.1) (p = 0.07)。结论:Era-RebAmIPP方案的疗效与传统的铋三联疗法相当。为了评估该方案的有效性,需要在我国不同地区进行更大规模的研究。
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引用次数: 0
[Clinical and morphological features and functional parameters in patients with gastroesophageal reflux disease and Barrett's esophagus]. 胃食管反流病与Barrett食管患者的临床、形态学特征及功能参数。
IF 0.3 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-28 DOI: 10.26442/00403660.2025.08.203299
A S Trukhmanov, A V Paraskevova, O A Storonova, A B Ponomarev, A A Makushina, V T Ivashkin

Aim: To develop a treatment strategy based on the analysis of clinical manifestations and the results of morphofunctional diagnostics for patients with gastroesophageal reflux disease (GERD) aimed at preventing the development and progression of intestinal metaplasia (IM) of the esophageal epithelium.

Materials and methods: The study included 50 subjects diagnosed with GERD. After esophagogastroduodenoscopy with biopsy and subsequent morphological examination of the esophageal mucosa, two groups were formed: patients with GERD complicated by IM, also known as Barrett's esophagus (n = 19), patients with GERD without IM (n = 31). All participants underwent high-resolution esophageal manometry and 24-hour impedance pH monitoring.

Results: The study found that in patients with GERD complicated by IM, complaints of intense heartburn and difficulty swallowing occurred more often than in patients with GERD without IM. According to manometry, the resting pressure of the lower esophageal sphincter in patients with GERD and IM (15.1 [1.3; 36.4] mmHg) was lower than in patients with GERD without IM (20.3 [5.5; 42.1] mmHg). This difference was statistically significant (p = 0.002). In patients with GERD and IM, esophageal motility is less effective; this was translated in a decrease in the distal contractile integral of the esophagus to 276.5 [0.2; 567.7] mmHg × s × cm, while in patients with GERD without IM, it was much higher: 942.5 [47.3; 3759.7] mmHg × s × cm. Difficulties in swallowing were associated with a reduced effectiveness of esophageal motility. In patients with GERD complicated by IM, more acid gastroesophageal refluxes were observed compared to patients without IM (72.5 [53.5; 91.5] vs 54.2 [29.9; 78.3]; p = 0.036). They also have a greater percentage of time with pH < 4.0 in the esophagus (14.5 [9.7; 19.3] vs 10.3 [5.6; 14.9]; p = 0.028) and higher DeMeester index values (35.4 [1.9; 114.5] vs 15.1 [0.2; 47.7]; p = 0.004).

Conclusion: GERD is a multifactorial disease with a primary impairment of the motor function of the upper gastrointestinal tract. The acidic reflux may affect the development of the intestinal type of epithelial metaplasia.

目的:通过分析胃食管反流病(GERD)患者的临床表现和形态功能诊断结果,探讨预防食管上皮肠上皮化生(IM)发生发展的治疗策略。材料和方法:本研究纳入50例诊断为胃食管反流的受试者。经食管胃十二指肠镜活检及随后食管黏膜形态学检查后,分为两组:胃食管反流合并IM (Barrett食管)患者(n = 19)和无IM的胃食管反流患者(n = 31)。所有参与者都进行了高分辨率食管测压和24小时阻抗pH监测。结果:研究发现,与没有IM的GERD患者相比,合并IM的GERD患者出现强烈烧心和吞咽困难的主诉更为频繁。测压结果显示,胃食管反流合并IM患者食管下括约肌静息压(15.1 [1.3;36.4]mmHg)低于无IM的胃食管反流患者(20.3 [5.5;42.1]mmHg)。差异有统计学意义(p = 0.002)。在胃食管反流和IM患者中,食管运动效果较差;这意味着食管远端可收缩积分减少到276.5 [0.2;无IM的胃食管反流患者则高得多:942.5 [47.3];3759.7] mmHg × s × cm。吞咽困难与食管运动功能降低有关。在合并IM的胃食管反流患者中,与未合并IM的患者相比,胃酸倒流发生率更高(72.5例[53.5;91.5]vs 54.2例[29.9;78.3];p = 0.036)。食管pH < 4.0的时间比例更高(14.5 [9.7;19.3]vs 10.3 [5.6; 14.9]; p = 0.028), DeMeester指数值更高(35.4 [1.9;114.5]vs 15.1 [0.2; 47.7]; p = 0.004)。结论:胃食管反流是一种多因素疾病,以上消化道运动功能受损为主要病因。酸性反流可能影响肠型上皮化生的发生。
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引用次数: 0
[Personalised treatment of patients with immune thrombotic thrombocytopenic purpura]. [免疫性血栓性血小板减少性紫癜患者的个性化治疗]。
IF 0.3 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-28 DOI: 10.26442/00403660.2025.08.203326
G M Galstyan, E E Klebanova, S Y Mamleeva, P V Avdonin, Z T Fidarova, M Y Drokov, E N Parovichnikova

Background: Treatment of immune thrombotic thrombocytopenic purpura (iTTP) includes plasma exchange (PEX) and immunosuppression (glucocorticoids and rituximab). The addition of caplacizumab to therapy has improved treatment outcomes in iTTP. However, the available therapies focus on the duration of drug administration and clinical response rather than ADAMTS13 activity.

Aim: To evaluate the efficacy of therapy for iTTP targeting ADAMTS13 activity.

Materials and methods: Treatment of patients with iTTP was started with PEX, prednisolone (1 mg/kg) and caplacizumab (10 mg/day). PEX was discontinued after an increase of platelet count > 150×109/L. Only after PEX cessation treatment with rituximab (375 mg/m2 weekly) was started. Caplacizumab was discontinued when partial remission (ADAMTS13 > 20%) was achieved. Rituximab and glucocorticoids were discontinued when complete remission (ADAMTS13 > 40%) was achieved. Platelet count, schistocyte count, haemoglobin, haptoglobin, lactate dehydrogenase activity, ADAMTS13, ADAMTS13 inhibitor titre, number of PEX, plasma volume replaced, time to increase platelet count > 150×109/L, achievement of partial and complete remission were analyzed. Data are presented as median and interquartile range.

Results: From 2021 to 2025, the diagnosis of TTP was confirmed in 102 patients. 35 patients were included in the study. Platelet counts > 150×109/L were achieved after 4 (3-5) PEX procedures in 4 (3-4.5) days. In total, 11 395 (7241-16 343) ml of plasma were exchanged. Partial remission was achieved in 100% of patients, the duration of caplacizumab therapy was 23 (12-30) days. Rituximab was administered from 4 to 8 times (median 4), complete remission was achieved in 33 out of 35 patients, 2 patients achieved only partial remission, they were treated with bortezomib and 1 with anti-CD38 monoclonal antibody. The probability of complete remission was 97.1%.

Conclusion: The duration of therapy with caplacizumab, rituximab and glucocorticoids in patients with iTTP should be determined by the achievement of target ADAMTS13 activity.

背景:免疫性血栓性血小板减少性紫癜(iTTP)的治疗包括血浆置换(PEX)和免疫抑制(糖皮质激素和利妥昔单抗)。在治疗中加入卡普拉珠单抗改善了iTTP的治疗结果。然而,现有的治疗方法侧重于给药时间和临床反应,而不是ADAMTS13活性。目的:评价针对ADAMTS13活性的iTTP治疗的疗效。材料和方法:iTTP患者开始使用PEX、强的松龙(1mg /kg)和卡普拉珠单抗(10mg /天)治疗。血小板计数升高> 150×109/L后停用PEX。只有在PEX停止后,才开始用利妥昔单抗(每周375 mg/m2)治疗。当达到部分缓解(ADAMTS13 bb0 20%)时停用卡普拉珠单抗。当达到完全缓解(ADAMTS13 bb0 40%)时,停用利妥昔单抗和糖皮质激素。分析血小板计数、血吸虫细胞计数、血红蛋白、接触珠蛋白、乳酸脱氢酶活性、ADAMTS13、ADAMTS13抑制剂滴度、PEX次数、血浆置换量、血小板计数增加时间> 150×109/L、部分缓解和完全缓解情况。数据以中位数和四分位数范围表示。结果:从2021年到2025年,102例患者被确诊为TTP。研究纳入了35名患者。在4(3-4.5)天内进行4(3-5)次PEX手术后,血小板计数达到> 150×109/L。总共交换了11 395 (7241-16 343)ml血浆。100%的患者部分缓解,卡普拉珠单抗治疗持续时间为23(12-30)天。利妥昔单抗给药4 ~ 8次(中位4次),35例患者中有33例完全缓解,2例仅部分缓解,他们接受硼替佐米治疗,1例接受抗cd38单克隆抗体治疗。完全缓解的概率为97.1%。结论:iTTP患者卡普拉珠单抗、利妥昔单抗和糖皮质激素治疗的持续时间应由目标ADAMTS13活性的实现来确定。
{"title":"[Personalised treatment of patients with immune thrombotic thrombocytopenic purpura].","authors":"G M Galstyan, E E Klebanova, S Y Mamleeva, P V Avdonin, Z T Fidarova, M Y Drokov, E N Parovichnikova","doi":"10.26442/00403660.2025.08.203326","DOIUrl":"https://doi.org/10.26442/00403660.2025.08.203326","url":null,"abstract":"<p><strong>Background: </strong>Treatment of immune thrombotic thrombocytopenic purpura (iTTP) includes plasma exchange (PEX) and immunosuppression (glucocorticoids and rituximab). The addition of caplacizumab to therapy has improved treatment outcomes in iTTP. However, the available therapies focus on the duration of drug administration and clinical response rather than ADAMTS13 activity.</p><p><strong>Aim: </strong>To evaluate the efficacy of therapy for iTTP targeting ADAMTS13 activity.</p><p><strong>Materials and methods: </strong>Treatment of patients with iTTP was started with PEX, prednisolone (1 mg/kg) and caplacizumab (10 mg/day). PEX was discontinued after an increase of platelet count > 150×10<sup>9</sup>/L. Only after PEX cessation treatment with rituximab (375 mg/m<sup>2</sup> weekly) was started. Caplacizumab was discontinued when partial remission (ADAMTS13 > 20%) was achieved. Rituximab and glucocorticoids were discontinued when complete remission (ADAMTS13 > 40%) was achieved. Platelet count, schistocyte count, haemoglobin, haptoglobin, lactate dehydrogenase activity, ADAMTS13, ADAMTS13 inhibitor titre, number of PEX, plasma volume replaced, time to increase platelet count > 150×10<sup>9</sup>/L, achievement of partial and complete remission were analyzed. Data are presented as median and interquartile range.</p><p><strong>Results: </strong>From 2021 to 2025, the diagnosis of TTP was confirmed in 102 patients. 35 patients were included in the study. Platelet counts > 150×10<sup>9</sup>/L were achieved after 4 (3-5) PEX procedures in 4 (3-4.5) days. In total, 11 395 (7241-16 343) ml of plasma were exchanged. Partial remission was achieved in 100% of patients, the duration of caplacizumab therapy was 23 (12-30) days. Rituximab was administered from 4 to 8 times (median 4), complete remission was achieved in 33 out of 35 patients, 2 patients achieved only partial remission, they were treated with bortezomib and 1 with anti-CD38 monoclonal antibody. The probability of complete remission was 97.1%.</p><p><strong>Conclusion: </strong>The duration of therapy with caplacizumab, rituximab and glucocorticoids in patients with iTTP should be determined by the achievement of target ADAMTS13 activity.</p>","PeriodicalId":22209,"journal":{"name":"Terapevticheskii Arkhiv","volume":"97 8","pages":"711-718"},"PeriodicalIF":0.3,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144969898","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Impact of atrial functional mitral regurgitation on clinical outcomes in patients with HFpEF and atrial fibrillation during optimal drug therapy]. [心房功能性二尖瓣反流对HFpEF合并心房颤动患者最佳药物治疗期间临床结局的影响]。
IF 0.3 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-28 DOI: 10.26442/00403660.2025.08.203337
A F Safarova, Z D Kobalava, S B Adam, T M Timofeeva

Aim: To evaluate the clinical and prognostic significance of atrial functional mitral regurgitation (AFMR) in patients with heart failure with preserved ejection fraction (HFpEF) and atrial fibrillation (AF) on the background of optimal drug therapy.

Materials and methods: The retrospective study included 150 patients (age 75.5 ± 9.9 years, 54% men) with HFpEF with AF and AFMR on the background of optimal drug therapy. Clinical and demographic characteristics (including the scale of assessment of the clinical condition), laboratory and instrumental diagnostic results, and drug therapy were evaluated. MR was assessed as minor, moderate, or severe using a multiparametric approach, including an assessment of the effective area of the regurgitation hole and the MR fraction. The effect of AFMR on rehospitalization for HF, combined endpoint (CE) was studied [cardiovascular death (CVD) and rehospitalization] during the follow-up period of 589 (217-1039) days.

Results: Eighty (53.3%) patients had moderate AFMR, and 23 (15.3%) had severe AFMR. These patients had lower SBP and DBP values (p = 0.014), and permanent AF was more common among them (p = 0.025) compared with patients with minor MR. Independent predictors of moderate/severe AFMR were the constant form of AF (OR 3.3 [1.4-8.0]; p = 0.007), end-systolic left ventricular distance (OR 3.0 [1.4-6.5]; p = 0.006), taking antiplatelet agents (OR 0.11 [0.02-0.70]; p = 0.020). The frequency of outcomes in the general group was 46.7% for CE, 34.0% for rehospitalization for HF, and 14.0% for CVD. The predictors of CE were moderate/severe FMR (HR 2.6 [1.4-4.9]; p = 0.002), scores on the scale of assessment of the clinical condition (HR 1.14 [1.04-1.25]; p = 0.003); severe FMR (HR 4.1 [1.7-10.2]; p = 0.002), moderate FMR (HR 2.7 [1.2-5.8]; p = 0.013), creatinine level (HR 0.990 [0.980-1,000]; p = 0.040).

Conclusion: Despite the limitations, the importance of AFMR as a factor influencing clinical outcomes in patients with HFpEF and AF has been demonstrated. The present study highlights the need for further investigation of this condition and the development of personalized patient management strategies.

目的:探讨保留射血分数(HFpEF)合并心房颤动(AF)心力衰竭患者心房功能性二尖瓣反流(AFMR)在最佳药物治疗背景下的临床及预后意义。材料与方法:在最佳药物治疗背景下,对150例HFpEF合并AF和AFMR患者(年龄75.5±9.9岁,男性占54%)进行回顾性研究。评估临床和人口学特征(包括临床状况评估量表)、实验室和仪器诊断结果以及药物治疗。使用多参数方法评估MR为轻度、中度或重度,包括评估回流孔的有效面积和MR分数。在589(217-1039)天的随访期间,研究了AFMR对HF再住院的影响,联合终点(CE)[心血管死亡(CVD)和再住院]。结果:中度AFMR 80例(53.3%),重度AFMR 23例(15.3%)。这些患者的收缩压和舒张压值较低(p = 0.014),与轻度mr患者相比,永久性房颤在这些患者中更为常见(p = 0.025),中/重度AFMR的独立预测因素是房颤的恒定形式(OR 3.3 [1.4-8.0]; p = 0.007),收缩期末左心室距离(OR 3.0 [1.4-6.5]; p = 0.006),服用抗血小板药物(OR 0.11 [0.02-0.70]; p = 0.020)。在普通组中,CE的发生率为46.7%,HF的发生率为34.0%,CVD的发生率为14.0%。CE的预测因子为中度/重度FMR(风险比2.6 [1.4-4.9],p = 0.002)、临床状况评估量表得分(风险比1.14 [1.04-1.25],p = 0.003);重度FMR (HR 4.1 [1.7-10.2], p = 0.002)、中度FMR (HR 2.7 [1.2-5.8], p = 0.013)、肌酐水平(HR 0.990 [0.980- 1000], p = 0.040)。结论:尽管存在局限性,但AFMR作为影响HFpEF和AF患者临床结局的重要因素已得到证实。目前的研究强调需要进一步调查这种情况和个性化的病人管理策略的发展。
{"title":"[Impact of atrial functional mitral regurgitation on clinical outcomes in patients with HFpEF and atrial fibrillation during optimal drug therapy].","authors":"A F Safarova, Z D Kobalava, S B Adam, T M Timofeeva","doi":"10.26442/00403660.2025.08.203337","DOIUrl":"https://doi.org/10.26442/00403660.2025.08.203337","url":null,"abstract":"<p><strong>Aim: </strong>To evaluate the clinical and prognostic significance of atrial functional mitral regurgitation (AFMR) in patients with heart failure with preserved ejection fraction (HFpEF) and atrial fibrillation (AF) on the background of optimal drug therapy.</p><p><strong>Materials and methods: </strong>The retrospective study included 150 patients (age 75.5 ± 9.9 years, 54% men) with HFpEF with AF and AFMR on the background of optimal drug therapy. Clinical and demographic characteristics (including the scale of assessment of the clinical condition), laboratory and instrumental diagnostic results, and drug therapy were evaluated. MR was assessed as minor, moderate, or severe using a multiparametric approach, including an assessment of the effective area of the regurgitation hole and the MR fraction. The effect of AFMR on rehospitalization for HF, combined endpoint (CE) was studied [cardiovascular death (CVD) and rehospitalization] during the follow-up period of 589 (217-1039) days.</p><p><strong>Results: </strong>Eighty (53.3%) patients had moderate AFMR, and 23 (15.3%) had severe AFMR. These patients had lower SBP and DBP values (<i>p</i> = 0.014), and permanent AF was more common among them (<i>p</i> = 0.025) compared with patients with minor MR. Independent predictors of moderate/severe AFMR were the constant form of AF (OR 3.3 [1.4-8.0]; <i>p</i> = 0.007), end-systolic left ventricular distance (OR 3.0 [1.4-6.5]; <i>p</i> = 0.006), taking antiplatelet agents (OR 0.11 [0.02-0.70]; <i>p</i> = 0.020). The frequency of outcomes in the general group was 46.7% for CE, 34.0% for rehospitalization for HF, and 14.0% for CVD. The predictors of CE were moderate/severe FMR (HR 2.6 [1.4-4.9]; <i>p</i> = 0.002), scores on the scale of assessment of the clinical condition (HR 1.14 [1.04-1.25]; <i>p</i> = 0.003); severe FMR (HR 4.1 [1.7-10.2]; <i>p</i> = 0.002), moderate FMR (HR 2.7 [1.2-5.8]; <i>p</i> = 0.013), creatinine level (HR 0.990 [0.980-1,000]; <i>p</i> = 0.040).</p><p><strong>Conclusion: </strong>Despite the limitations, the importance of AFMR as a factor influencing clinical outcomes in patients with HFpEF and AF has been demonstrated. The present study highlights the need for further investigation of this condition and the development of personalized patient management strategies.</p>","PeriodicalId":22209,"journal":{"name":"Terapevticheskii Arkhiv","volume":"97 8","pages":"618-626"},"PeriodicalIF":0.3,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144969870","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Structural and functional parameters of erythrocytes as predictors of unfavorable outcome in patients with colorectal cancer]. [红细胞结构和功能参数作为结直肠癌患者不良预后的预测指标]。
IF 0.3 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-28 DOI: 10.26442/00403660.2025.08.203336
M V Kruchinina, M F Osipenko, A A Gromov, A V Starikov
<p><strong>Aim: </strong>Identification the characteristics of fatty acids (FAs) in erythrocyte membranes and in blood serum, as well as the electrical and viscoelastic parameters of erythrocytes to assess their ability to be predictors of an unfavorable outcome in patients with colorectal cancer (CRC).</p><p><strong>Materials and methods: </strong>112 people with an average age of 63.1 ± 9.5 years (62 men, 50 women) with CRC of stages I-IV were examined. The patients were divided into 2 groups depending on the outcome of the disease after 6 years of follow-up: group 1 - with stabilization of the disease (<i>n</i> = 55), group 2 (<i>n</i> = 57) - with an unfavorable outcome. The FA composition of erythrocyte membranes and blood serum was studied using gas chromatography/mass spectrometry, a system based on three Agilent 7000B quadrupoles (USA). The electrical and viscoelastic parameters of erythrocytes were studied using the method of dielectrophoresis.</p><p><strong>Results: </strong>An unfavorable outcome in patients with CRC is associated with elevated levels of docosapentaenoic acid (C22:5n-3) (<i>p</i> = 0.0003), docosahexaenoic acid (C22:6n-3) (<i>p</i> = 0.001), docosathetraenoic acid (C22:4n-6) (<i>p</i> = 0.004), and total omega-3 polyunsaturated fatty acids (PUFA) (<i>p</i> = 0.0004) in erythrocyte membranes, eicosadienoic acid (C20:2 n-6) in erythrocyte membranes (<i>p</i> = 0.03) and blood serum (<i>p</i> = 0.01), and, conversely, reduced levels of ratios saturated fatty acids (SFA)/PUFA (<i>p</i> = 0.004), SFA / unsaturated fatty acids (USFA) (<i>p</i> = 0.01) and concentrations of myristic FA (C14:0) (<i>p</i> = 0.03) in erythrocyte membranes, as well as with a number of changes in electrical, viscoelastic parameters of red blood cells: with increased hemolysis of red blood cells at high frequencies (10<sup>6 </sup>Hz - <i>p</i> = 0.0006 and 5 × 10<sup>5 </sup>Hz - <i>p</i> = 0.046), increased aggregation indices at low frequencies (10<sup>5 </sup>Hz - <i>p</i> = 0.04 and 5 × 10<sup>4 </sup>Hz - <i>p</i> = 0.047), as well as a shift in the crossover frequency to the high frequency range (<i>p</i> = 0.036). In patients with stages 1-2 of CRC, omega-6 PUFAs, eicosadienoic acid C20:2n-6 (<i>p</i> = 0.006), docosatetraenoic acid C22:4n-6 (<i>p</i> = 0.012), were of the greatest importance for differentiating disease outcomes, while total content omega-3 PUFAs in erythrocyte membranes (<i>p</i> = 0.0129), docosahexaenoic acid C22:6 n-3 (<i>p</i> = 0.0169), total content (C20:5n-3+C22:6n-3) in erythrocyte membranes (<i>p</i> = 0.0198), docosapentaenoic acid C22:5 n-3 (<i>p</i> = 0.022) were slightly less important. As in the general group of patients with CRC, the degree of hemolysis at a frequency of 10<sup>6 </sup>Hz was a predictor of an unfavorable outcome in people with early stages of the oncological process. ROC analysis revealed a high potential of palmitic acid in erythrocyte membranes to predict an unfavorable CRC outcome (AUC 0
目的:鉴定红细胞膜和血清中脂肪酸(FAs)的特征,以及红细胞的电和粘弹性参数,以评估它们作为结直肠癌(CRC)患者不良结局预测因子的能力。材料与方法:112例平均年龄63.1±9.5岁(男62例,女50例)的I-IV期结直肠癌患者。根据6年随访后的疾病结果将患者分为两组:1组(55例)病情稳定,2组(57例)预后不佳。采用气相色谱/质谱法研究红细胞膜和血清的FA组成,该系统基于三台安捷伦7000B四极杆(美国)。用介质电泳法研究了红细胞的电学参数和粘弹性参数。结果:CRC患者不利结果与高浓度的docosapentaenoic酸(C22:5n-3) (p = 0.0003),二十二碳六烯酸(C22:6n-3) (p = 0.001), docosathetraenoic酸(C22:4n-6) (p = 0.004),和总ω- 3多不饱和脂肪酸(PUFA) (p = 0.0004)红细胞细胞膜,eicosadienoic酸(C20:2 n-6)在红血球膜(p = 0.03)和血清(p = 0.01),相反,水平的比率减少饱和脂肪酸(SFA) / PUFA (p = 0.004),红细胞膜中SFA /不饱和脂肪酸(USFA) (p = 0.01)和肉豆蔻FA浓度(C14:0) (p = 0.03),以及红细胞电、粘弹性参数的一些变化:高频(106 Hz - p = 0.0006和5 × 105 Hz - p = 0.046)时红细胞溶血增加,低频(105 Hz - p = 0.04和5 × 104 Hz - p = 0.047)时聚集指数增加,以及交叉频率向高频范围转移(p = 0.036)。在结直肠癌1-2期患者中,omega-6 PUFAs、二十碳二烯酸C20:2n-6 (p = 0.006)、二十二碳四烯酸C22:4n-6 (p = 0.012)是鉴别疾病结局的最重要指标,而红细胞膜中omega-3 PUFAs总含量(p = 0.0129)、二十二碳六烯酸C22:6n-3 (p = 0.0169)、红细胞膜中总含量(C20:5n-3+C22:6n-3) (p = 0.0198)、二十二碳五烯酸C22:5 n-3 (p = 0.022)的重要性略低。与一般的结直肠癌患者组一样,106 Hz频率下的溶血程度是早期肿瘤患者不良预后的预测因子。ROC分析显示,红细胞膜中棕榈酸预测CRC不良结局的可能性很高(AUC 0.786, 95%可信区间0.638-0.901,敏感性84.4%,特异性68.2%)。该诊断模型包括5个参数——红细胞水平C16:0、SFA/PUFA比率、总USFA、总PUFA和血清水平C20:2n-6, AUC为0.663(95%可信区间0.483-0.801),最高敏感性为85.2%,但预测CRC不良结局的特异性不高,为60.1%。结论:红细胞膜脂肪酸、血清、红细胞电性和粘弹性参数应被视为有希望的CRC患者生物标志物预测指标,需要进一步研究。
{"title":"[Structural and functional parameters of erythrocytes as predictors of unfavorable outcome in patients with colorectal cancer].","authors":"M V Kruchinina, M F Osipenko, A A Gromov, A V Starikov","doi":"10.26442/00403660.2025.08.203336","DOIUrl":"https://doi.org/10.26442/00403660.2025.08.203336","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Aim: &lt;/strong&gt;Identification the characteristics of fatty acids (FAs) in erythrocyte membranes and in blood serum, as well as the electrical and viscoelastic parameters of erythrocytes to assess their ability to be predictors of an unfavorable outcome in patients with colorectal cancer (CRC).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Materials and methods: &lt;/strong&gt;112 people with an average age of 63.1 ± 9.5 years (62 men, 50 women) with CRC of stages I-IV were examined. The patients were divided into 2 groups depending on the outcome of the disease after 6 years of follow-up: group 1 - with stabilization of the disease (&lt;i&gt;n&lt;/i&gt; = 55), group 2 (&lt;i&gt;n&lt;/i&gt; = 57) - with an unfavorable outcome. The FA composition of erythrocyte membranes and blood serum was studied using gas chromatography/mass spectrometry, a system based on three Agilent 7000B quadrupoles (USA). The electrical and viscoelastic parameters of erythrocytes were studied using the method of dielectrophoresis.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;An unfavorable outcome in patients with CRC is associated with elevated levels of docosapentaenoic acid (C22:5n-3) (&lt;i&gt;p&lt;/i&gt; = 0.0003), docosahexaenoic acid (C22:6n-3) (&lt;i&gt;p&lt;/i&gt; = 0.001), docosathetraenoic acid (C22:4n-6) (&lt;i&gt;p&lt;/i&gt; = 0.004), and total omega-3 polyunsaturated fatty acids (PUFA) (&lt;i&gt;p&lt;/i&gt; = 0.0004) in erythrocyte membranes, eicosadienoic acid (C20:2 n-6) in erythrocyte membranes (&lt;i&gt;p&lt;/i&gt; = 0.03) and blood serum (&lt;i&gt;p&lt;/i&gt; = 0.01), and, conversely, reduced levels of ratios saturated fatty acids (SFA)/PUFA (&lt;i&gt;p&lt;/i&gt; = 0.004), SFA / unsaturated fatty acids (USFA) (&lt;i&gt;p&lt;/i&gt; = 0.01) and concentrations of myristic FA (C14:0) (&lt;i&gt;p&lt;/i&gt; = 0.03) in erythrocyte membranes, as well as with a number of changes in electrical, viscoelastic parameters of red blood cells: with increased hemolysis of red blood cells at high frequencies (10&lt;sup&gt;6 &lt;/sup&gt;Hz - &lt;i&gt;p&lt;/i&gt; = 0.0006 and 5 × 10&lt;sup&gt;5 &lt;/sup&gt;Hz - &lt;i&gt;p&lt;/i&gt; = 0.046), increased aggregation indices at low frequencies (10&lt;sup&gt;5 &lt;/sup&gt;Hz - &lt;i&gt;p&lt;/i&gt; = 0.04 and 5 × 10&lt;sup&gt;4 &lt;/sup&gt;Hz - &lt;i&gt;p&lt;/i&gt; = 0.047), as well as a shift in the crossover frequency to the high frequency range (&lt;i&gt;p&lt;/i&gt; = 0.036). In patients with stages 1-2 of CRC, omega-6 PUFAs, eicosadienoic acid C20:2n-6 (&lt;i&gt;p&lt;/i&gt; = 0.006), docosatetraenoic acid C22:4n-6 (&lt;i&gt;p&lt;/i&gt; = 0.012), were of the greatest importance for differentiating disease outcomes, while total content omega-3 PUFAs in erythrocyte membranes (&lt;i&gt;p&lt;/i&gt; = 0.0129), docosahexaenoic acid C22:6 n-3 (&lt;i&gt;p&lt;/i&gt; = 0.0169), total content (C20:5n-3+C22:6n-3) in erythrocyte membranes (&lt;i&gt;p&lt;/i&gt; = 0.0198), docosapentaenoic acid C22:5 n-3 (&lt;i&gt;p&lt;/i&gt; = 0.022) were slightly less important. As in the general group of patients with CRC, the degree of hemolysis at a frequency of 10&lt;sup&gt;6 &lt;/sup&gt;Hz was a predictor of an unfavorable outcome in people with early stages of the oncological process. ROC analysis revealed a high potential of palmitic acid in erythrocyte membranes to predict an unfavorable CRC outcome (AUC 0","PeriodicalId":22209,"journal":{"name":"Terapevticheskii Arkhiv","volume":"97 8","pages":"668-679"},"PeriodicalIF":0.3,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144969879","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Fixed-dose combinations of hypoglycemic drugs: potential of alogliptin/pioglitazone in type 2 diabetes mellitus: a review]. [固定剂量联合降糖药:阿格列汀/吡格列酮治疗2型糖尿病的潜力:综述]。
IF 0.3 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-28 DOI: 10.26442/00403660.2025.08.203345
O I Butranova, S K Zyryanov, A R Melnikova, A E Matsepuro

Type 2 diabetes mellitus is one of the most common chronic diseases, which is a risk factor for a wide range of complications. The introduction of an approach consisting of early administration of combination hypoglycemic therapy into clinical practice makes it relevant to study available fixed-dose combinations of hypoglycemic drugs. Alogliptin and pioglitazone are of interest in terms of their complex effect on the patient's organism. The purpose of this review is to assess the advantages of the combination of alogliptin and pioglitazone based on an analysis of published data on the pharmacodynamics, pharmacokinetics, efficacy and safety of these drugs.

2型糖尿病是最常见的慢性疾病之一,是多种并发症的危险因素。在临床实践中引入早期联合降糖治疗的方法,使得研究可用的固定剂量降糖药物组合具有重要意义。阿格列汀和吡格列酮对患者机体的复杂作用引起了人们的兴趣。本综述的目的是基于对阿格列汀和吡格列酮的药效学、药代动力学、疗效和安全性的已发表数据的分析,评估阿格列汀和吡格列酮联合使用的优势。
{"title":"[Fixed-dose combinations of hypoglycemic drugs: potential of alogliptin/pioglitazone in type 2 diabetes mellitus: a review].","authors":"O I Butranova, S K Zyryanov, A R Melnikova, A E Matsepuro","doi":"10.26442/00403660.2025.08.203345","DOIUrl":"https://doi.org/10.26442/00403660.2025.08.203345","url":null,"abstract":"<p><p>Type 2 diabetes mellitus is one of the most common chronic diseases, which is a risk factor for a wide range of complications. The introduction of an approach consisting of early administration of combination hypoglycemic therapy into clinical practice makes it relevant to study available fixed-dose combinations of hypoglycemic drugs. Alogliptin and pioglitazone are of interest in terms of their complex effect on the patient's organism. The purpose of this review is to assess the advantages of the combination of alogliptin and pioglitazone based on an analysis of published data on the pharmacodynamics, pharmacokinetics, efficacy and safety of these drugs.</p>","PeriodicalId":22209,"journal":{"name":"Terapevticheskii Arkhiv","volume":"97 8","pages":"735-749"},"PeriodicalIF":0.3,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144969888","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[The introduction into clinical practice of an algorithm for the diagnosis of liver steatosis in patients with viral pneumonia]. 一种病毒性肺炎肝脂肪变性诊断算法的临床应用
IF 0.3 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-28 DOI: 10.26442/00403660.2025.08.203365
T A Turankova, A Y Brazhnikov, N G Moroz, A V Mudrova, D L Varganova, C S Pavlov

Aim: To study the ability and significance of detecting liver steatosis during chest computed tomography (CT) in patients with viral pneumonia.

Materials and methods: A prospective cohort study included 100 patients over the age of 18 who were hospitalized with an established diagnosis of viral pneumonia. To CT detection significant liver steatosis (more than 33%), several approaches were used: liver density less than 40 HU; decrease in liver density by at least 10 HU less than the spleen; the ratio of decrease in liver density to the spleen is less than 0.9.

Results: According to CT data 2 groups were identified: 25 patients with existing liver steatosis and metabolically associated fatty liver disease, and 74 patients of the control group without signs of significant steatosis, оne patient was excluded due to alcohol abuse. There was a significant difference in the study of liver density (31.68 ± 10.67 and 54.44 ± 5.95; p < 0.001), the ratio of decrease in liver density to spleen density (0.66 ± 0.22 and 1.16 ± 0.13; p < 0.001), as well as a decrease in liver density relative to the spleen (16.30 ± 10.38 and -7.26 ± 6.10; p < 0.001). In the steatosis group, a more severe course of pneumonia was noted (p = 0.041). The incidence of deterioration according to CT was comparable in both groups: 19 (76%) and 45 (60.8%); p = 0.169, although its severity was higher in the group with steatosis (p = 0.012). Patients from the steatosis group were significantly more often prescribed biological (88.0 and 39.19%; p < 0.001) and antibacterial therapy (68.0 and 40.54%; p = 0.017).

Conclusion: The use of assessment of liver steatosis according to CT data simultaneously with the study of the underlying disease can become an important diagnostic step determining the prognosis of the course of the disease, as well as a tool for risk stratification in patients with metabolically associated fatty liver disease.

目的:探讨病毒性肺炎患者胸部CT检查肝脏脂肪变性的能力及意义。材料和方法:一项前瞻性队列研究包括100名年龄在18岁以上的确诊为病毒性肺炎的住院患者。对于明显的肝脂肪变性(大于33%),采用以下几种方法:肝密度小于40 HU;肝脏密度比脾脏降低至少10 HU;肝脏密度与脾脏密度的比值小于0.9。结果:根据CT资料确定2组:存在肝脏脂肪变性及代谢性脂肪性肝病患者25例,对照组无明显脂肪变性体征74例,因酗酒排除1例。肝密度(31.68±10.67)和54.44±5.95,p < 0.001)、肝密度与脾密度的比值(0.66±0.22,1.16±0.13,p < 0.001)、肝密度与脾密度的比值(16.30±10.38,-7.26±6.10,p < 0.001)均有统计学差异。脂肪变性组出现了更严重的肺炎病程(p = 0.041)。CT显示两组的恶化发生率相当:19例(76%)和45例(60.8%);P = 0.169,但脂肪变性组的严重程度更高(P = 0.012)。脂肪变性组患者接受生物治疗(88.0和39.19%,p < 0.001)和抗菌治疗(68.0和40.54%,p = 0.017)的频率显著高于对照组。结论:结合基础疾病的研究,利用CT资料评估肝脏脂肪变性,可成为判断病程预后的重要诊断步骤,也是代谢性脂肪肝患者危险分层的工具。
{"title":"[The introduction into clinical practice of an algorithm for the diagnosis of liver steatosis in patients with viral pneumonia].","authors":"T A Turankova, A Y Brazhnikov, N G Moroz, A V Mudrova, D L Varganova, C S Pavlov","doi":"10.26442/00403660.2025.08.203365","DOIUrl":"https://doi.org/10.26442/00403660.2025.08.203365","url":null,"abstract":"<p><strong>Aim: </strong>To study the ability and significance of detecting liver steatosis during chest computed tomography (CT) in patients with viral pneumonia.</p><p><strong>Materials and methods: </strong>A prospective cohort study included 100 patients over the age of 18 who were hospitalized with an established diagnosis of viral pneumonia. To CT detection significant liver steatosis (more than 33%), several approaches were used: liver density less than 40 HU; decrease in liver density by at least 10 HU less than the spleen; the ratio of decrease in liver density to the spleen is less than 0.9.</p><p><strong>Results: </strong>According to CT data 2 groups were identified: 25 patients with existing liver steatosis and metabolically associated fatty liver disease, and 74 patients of the control group without signs of significant steatosis, оne patient was excluded due to alcohol abuse. There was a significant difference in the study of liver density (31.68 ± 10.67 and 54.44 ± 5.95; <i>p</i> < 0.001), the ratio of decrease in liver density to spleen density (0.66 ± 0.22 and 1.16 ± 0.13; <i>p</i> < 0.001), as well as a decrease in liver density relative to the spleen (16.30 ± 10.38 and -7.26 ± 6.10; <i>p</i> < 0.001). In the steatosis group, a more severe course of pneumonia was noted (<i>p</i> = 0.041). The incidence of deterioration according to CT was comparable in both groups: 19 (76%) and 45 (60.8%); <i>p</i> = 0.169, although its severity was higher in the group with steatosis (<i>p</i> = 0.012). Patients from the steatosis group were significantly more often prescribed biological (88.0 and 39.19%; <i>p</i> < 0.001) and antibacterial therapy (68.0 and 40.54%; <i>p</i> = 0.017).</p><p><strong>Conclusion: </strong>The use of assessment of liver steatosis according to CT data simultaneously with the study of the underlying disease can become an important diagnostic step determining the prognosis of the course of the disease, as well as a tool for risk stratification in patients with metabolically associated fatty liver disease.</p>","PeriodicalId":22209,"journal":{"name":"Terapevticheskii Arkhiv","volume":"97 8","pages":"704-710"},"PeriodicalIF":0.3,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144969910","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Medicine during the Great Patriotic War of 1941-1945]. [1941-1945年卫国战争时期的医学]。
IF 0.3 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-28 DOI: 10.26442/00403660.2025.08.203354
K A Pashkov

The article highlights the main events, discoveries and principles of organizing medical care at the front and in the rear during the Great Patriotic War of 1941-1945. The main aspects of the battlefield medical doctrine, the system of stepwise casualty care, the complex of anti-epidemic measures, the care of motherhood and childhood, the role of outstanding scientists and health care organizers in the victory over fascism are considered.

本文着重介绍了1941-1945年卫国战争期间前线和后方医疗工作的主要事件、发现和组织原则。讨论了战场医学学说的主要方面,阶梯式伤病员护理制度,复杂的防疫措施,母亲和儿童的照顾,杰出的科学家和卫生保健组织者在战胜法西斯主义中的作用。
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引用次数: 0
[Side effects and ineffectiveness of standard therapy for idiopathic recurrent pericarditis: status of the problem and description of clinical cases. Case report]. 特发性复发性心包炎标准治疗的副作用及无效:问题现状及临床病例描述。病例报告)。
IF 0.3 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-08-28 DOI: 10.26442/00403660.2025.08.203342
A A Petrukhina, A А Safiullina, Y F Osmolovskaya, I V Zhirov, O V Stukalova, V N Shitov, S N Tereshchenko

Idiopathic recurrent pericarditis is a rare pathology characterised by recurrent inflammation in the cardiac cavity. Treatment of recurrent pericarditis is empirical and based on the use of drugs with anti-inflammatory properties. First-line drugs are non-steroidal anti-inflammatory drugs and colchicine, second-line drugs are glucocorticosteroids. This is associated with the development of undesirable side effects, which makes it impossible to continue therapy in a number of patients. This article presents two clinical cases, describes the course of the disease and the development of complications at different stages. This article demonstrates the complexity of selecting the optimal therapy in real clinical practice.

特发性复发性心包炎是一种罕见的病理特征,其特征是在心脏腔内反复发生炎症。治疗复发性心包炎是经验性的,基于使用具有抗炎特性的药物。一线药物是非甾体抗炎药和秋水仙碱,二线药物是糖皮质激素。这与不良副作用的发展有关,这使得许多患者无法继续治疗。本文介绍两例临床病例,描述了不同阶段的病程和并发症的发展。本文展示了在实际临床实践中选择最佳治疗方法的复杂性。
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Terapevticheskii Arkhiv
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