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Comparison of the three liquid metered dose inhalers technique in patients with COPD and bronchial asthma 三种液体计量吸入器技术在慢性阻塞性肺病和支气管哮喘患者中的比较
Pub Date : 2023-05-21 DOI: 10.32756/0869-5490-2023-2-21-26
I. Vizel’, A. I. Rezyapova, A. Vizel’
In respiratory medicine, the correct inhaler technique determines the clinical efficacy of inhaled medications.
在呼吸医学中,正确的吸入器技术决定了吸入药物的临床疗效。
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引用次数: 0
Current diagnosis and treatment of arterial hypertension induced by antiangiogenic antitumour agents 抗血管生成抗肿瘤药物致动脉高血压的诊断与治疗现状
Pub Date : 2023-05-21 DOI: 10.32756/0869-5490-2023-2-32-36
E. Shavarova, E. Khachaturyan, I. Pokatayev, Z. Kobalava
The use of angiogenesis inhibitors (anti-VGEF antibodies and tyrosine kinase inhibitors) in oncology significantly increases both the tumor response to therapy and the risk of cardiovascular toxicity. Arterial hypertension is the main adverse effect of antiangiogenic therapy frequently limiting the doses of angiogenesis inhibitors, although it is also considered as a possible surrogate marker of the effectiveness of targeted therapy. In 2022, the recommendations of the European Society of Cardiology on the prevention and correction of cardiotoxicity of antitumor therapy were published. The article reviews the current diagnosis and treatment of arterial hypertension induced by antiangiogenic medicines.
在肿瘤学中使用血管生成抑制剂(抗vgef抗体和酪氨酸激酶抑制剂)显著增加了肿瘤对治疗的反应和心血管毒性的风险。动脉高血压是抗血管生成治疗的主要不良反应,经常限制血管生成抑制剂的剂量,尽管它也被认为是靶向治疗有效性的可能替代标志。2022年,欧洲心脏病学会关于预防和纠正抗肿瘤治疗心脏毒性的建议发表。本文就抗血管生成药物致动脉性高血压的诊断和治疗现状作一综述。
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引用次数: 0
Principles of effective management of neuropathic pain in primary care 初级保健中神经性疼痛的有效管理原则
Pub Date : 2023-05-21 DOI: 10.32756/0869-5490-2023-2-37-42
O. S. Davydov
Neuropathic pain caused by disease or damage affecting the somatosensory nervous system is a common problem in the primary care patients. Neuropathic pain can occur in postherpetic neuralgia, Guillain-Barré syndrome, neuroborreliosis, painful diabetic neuropathy, rheumatoid arthritis, systemic lupus erythematosus, psoriatic arthritis, Sjögren's syndrome, after trauma, due to cancer, stroke, etc. The treatment of neuropathic pain involves a comprehensive multimodal approach using pharmacotherapy with antidepressants and anticonvulsants, the most convenient of which is gabapentin, pathogenetic therapy of the underlying disease and non-pharmacological methods. Only integrated approach can provide effective therapy and improve the quality of life of patients with neuropathic pain.
由影响体感觉神经系统的疾病或损伤引起的神经性疼痛是初级保健患者的常见问题。神经性疼痛可发生在疱疹后神经痛、格林-巴罗综合征、神经螺旋体病、疼痛性糖尿病神经病、类风湿关节炎、系统性红斑狼疮、银屑病关节炎、Sjögren综合征、外伤后、因癌症、中风等。神经性疼痛的治疗包括使用抗抑郁药和抗惊厥药的综合多模式药物治疗,其中最方便的是加巴喷丁,基础疾病的病理治疗和非药物方法。只有综合治疗才能有效地改善神经性疼痛患者的生活质量。
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引用次数: 0
Efficacy of direct-acting antivirals in patients with HCV-associated cryoglobulinemia and monoclonal gammapathy 直接抗病毒药物治疗丙型肝炎相关冷球蛋白血症和单克隆γ病的疗效
Pub Date : 2023-05-21 DOI: 10.32756/0869-5490-2023-2-15-20
S. Gavrisheva, D. Abdurakhmanov, N. Bulanov, E. Tanaschuk, T. Rozina, E. Nikulkina, S. Milovanova, A. Filatova, T. Krasnova, E. Starostina, V. Avdeev, P. Novikov, S. Moiseev
To evaluate the efficacy of direct-acting antivirals (DAA) in patients with hepatitis C virus (HCV) associated cryoglobulinemia and monoclonal gammapathy (MG).
目的:评价直接作用抗病毒药物(DAA)治疗丙型肝炎病毒(HCV)相关冷球蛋白血症和单克隆γ病变(MG)的疗效。
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引用次数: 0
Pharmacoepidemiologic study of antipsychotics safety 抗精神病药物安全性的药物流行病学研究
Pub Date : 2023-05-21 DOI: 10.32756/0869-5490-2023-2-66-72
V. Skryabin, A. Masyakin, S. Nazimova, D. Sosin, A. Khannanova, V. Shipitsyn, M. Zastrozhin, D. Sychev
To analyse spontaneous reports (SRs) of adverse drug reactions (ADRs) related to antipsychotics in Russia.
目的分析俄罗斯抗精神病药物不良反应自发性报告(SRs)。
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引用次数: 0
Tumour necrosis factor receptor-associated periodic syndrome (TRAPS) 肿瘤坏死因子受体相关周期性综合征
Pub Date : 2023-05-21 DOI: 10.32756/0869-5490-2023-2-43-50
V. Rameev, L. Lysenko (Kozlovskaya), S. Salugina, N. Chebotareva, N. Bulanov, A. Novikov, M. Barsuk, S. Moiseev
Tumour necrosis factor receptor-associated periodic syndrome (TRAPS) belongs to a group of rare hereditary autoinflammatory diseases (familial periodic fevers). TRAPS is characterized by the periodic occurrence of fever, abdominal pain, maculopapular rash, arthralgia/myalgia and laboratory signs of inflammation that persisit for 5 days to 3 weeks. AAamyloidosis can complicate persisting autoinlammation in TRAPS. The authors report two cases of TRAPS and discuss its diagnosis and treatment.
肿瘤坏死因子受体相关周期性综合征(TRAPS)属于一组罕见的遗传性自身炎症性疾病(家族性周期性发热)。TRAPS的特点是周期性出现发烧、腹痛、黄斑丘疹、关节痛/肌痛和实验室炎症症状,持续5天至3周。AAamyloidosis可使trap患者持续的自身炎症复杂化。作者报告了2例trap,并对其诊断和治疗进行了讨论。
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引用次数: 0
Complement inhibition therapy in patients with atypical hemolytic uremic syndrome and secondary microangiopathies 补体抑制治疗在非典型溶血性尿毒症综合征和继发性微血管病变患者中的应用
Pub Date : 2023-05-21 DOI: 10.32756/0869-5490-2023-2-7-14
Y. Korotchaeva, N. Kozlovskaya, S. Moiseev
Atypical hemolytic uremic syndrome (aHUS) is a rare form of thrombotic microangiopathy (TMA) caused by uncontrolled complement activation and leading to thrombocytopenia, microangiopathic hemolysis and acute kidney injury. Eculizumab, a humanized monoclonal antibody that inhibits the cleavage of complement protein C5, effectively reverses laboratory evidence of TMA and improves kidney function in most patients with aHUS. Hereditary aHUS should be differentiated from the secondary HUS associated with drugs, autoimmune diseases (e.g. antiphospholipid syndrome), malignancies, infections, solid organ transplantation. Case reports and retrospective studies suggest that eculizumab may be effective in a proportion of patients with secondary TMA, although its efficacy and regimens of administration should be evaluated in additional studies.
非典型溶血性尿毒症综合征(aHUS)是一种罕见的血栓性微血管病(TMA),由补体激活失控引起,可导致血小板减少、微血管病性溶血和急性肾损伤。Eculizumab是一种抑制补体蛋白C5切割的人源化单克隆抗体,在大多数aHUS患者中有效逆转TMA的实验室证据并改善肾功能。遗传性溶血性尿毒综合征应与与药物、自身免疫性疾病(如抗磷脂综合征)、恶性肿瘤、感染、实体器官移植相关的继发性溶血性尿毒综合征相鉴别。病例报告和回顾性研究表明,eculizumab可能对一部分继发性TMA患者有效,尽管其疗效和给药方案应在其他研究中进行评估。
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引用次数: 0
Investigation of pharmacokinetics and drug-drug interactions of melatonin and memantine as components of the new original combination drug Miladean® 褪黑素和美金刚作为新组合药物Miladean®的药代动力学和药物相互作用的研究
Pub Date : 2023-05-21 DOI: 10.32756/0869-5490-2023-2-59-65
A. Goncharov, A. Grigoriev, A. Globenko, I. Goncharov, K. A. Muratov, A. Sidorova, A. A. Nikitin, A. Kapashin, O. Kovchan, A. I. Bashkatova, M. Pasko
To compare pharmacokinetics and evaluate drug-drug interactions of the studied drug Miladean® oral dispersible tablets 3 mg + 5 mg (JSC Valenta Pharm, Russia) and reference products Akatinol Memantine 10 mg film-coated tablets (Merz Pharma GmbH & Co. KGaA, Germany) and Melaxen 3 mg film-coated tablets (Unipharm Inc., USA).
比较研究药物Miladean®口服分散片3mg + 5mg(俄罗斯JSC Valenta Pharm)与参比产品Akatinol Memantine 10mg薄膜包衣片(德国Merz Pharma GmbH & Co. KGaA)和Melaxen 3mg薄膜包衣片(美国Unipharm Inc.)的药代动力学和药物相互作用。
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引用次数: 0
Targeted treatment challenges in patients with adult-onset Still’s disease 成人发病斯蒂尔氏病患者的靶向治疗挑战
Pub Date : 2023-05-21 DOI: 10.32756/0869-5490-2023-2-51-58
A. Zavrazhnova, E. Kuvardin, V. Myachikova, A. Khadgidis, N. Anokhina, M. Anriyanova, Y. Kozlova, A. Maslyanskiy
Adult-onset Still’s disease (AOSD) is a systemic autoinflammatory disease mediated by interleukin (IL)-1 production. There are no treatment guidelines for AOSD due to its rarity and heterogenous manifestations. Therefore, each case is challenging and requires a multidisciplinary approach. We report a case of AOSD occurring in pregnant patient who did not respond to standard treatment with glucocorticoids and developed skin reaction to IL-1 receptor antagonist. However, drug desensibilisation was effective and allowed to continue treatment with anakinra.
成人发病斯蒂尔氏病(AOSD)是一种由白细胞介素(IL)-1产生介导的全身性自身炎症性疾病。由于AOSD的罕见性和异质性,目前尚无治疗指南。因此,每个案例都具有挑战性,需要多学科的方法。我们报告一例AOSD发生在妊娠患者谁没有响应标准治疗糖皮质激素和发展皮肤反应对IL-1受体拮抗剂。然而,药物脱敏是有效的,并允许继续用阿那白治疗。
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引用次数: 0
Fabry disease in female patients: clinical features, outcomes and indications for enzyme replacement therapy 法布里病在女性患者:临床特点,结果和适应症的酶替代治疗
Pub Date : 2023-05-21 DOI: 10.32756/0869-5490-2023-2-27-31
S. Moiseev, N. Bulanov, A. Moiseev, E. Tao, V. Sholomova, D. Ismailova, E. Mershina
To evaluate clinical features and indications for enzyme replacement therapy (ERT) in female patients with Fabry disease (FD) in the Russian population.
目的评价俄罗斯人群中女性法布里病(FD)患者的临床特点和酶替代治疗(ERT)的适应症。
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引用次数: 0
期刊
Clinical pharmacology and therapy
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