[真实临床实践中动脉高血压和伴随疾病患者的抗高血压治疗(根据国家动脉高血压登记处,2019-2022 年)】。]

Pub Date : 2024-10-10 DOI:10.26442/00403660.2024.09.202848
A V Aksenova, E V Oschepkova, I E Chazova
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引用次数: 0

摘要

背景:动脉高血压(AH)仍然是与心血管疾病(CVD)、脑血管疾病和慢性肾脏疾病相关的主要风险因素。在接受单一疗法的动脉高血压患者中,约有 70% 的患者无法达到血压(BP)目标,因此,最近所有动脉高血压管理指南都建议处方联合疗法(PCT)。在实际临床实践(RCP)中,尽管抗高血压药物(AHD)种类繁多,而且有建议指出在不同临床情况下应采取循序渐进的方式对特定类别的抗高血压药物进行组合处方,但治疗的有效性和合理性仍存在很大的不确定性。目的:分析实际正在进行的抗高血压治疗,包括 PCT;RCP 中药物的国际非专利名称及其剂量;治疗是否符合临床建议;PCT 的变化趋势:对 AH 登记数据、不同临床组患者的治疗依从性以及 2019-2022 年样本(n=5012)中血压和低密度脂蛋白胆固醇目标的实现情况进行了分析。AHD的处方和目标值的实现情况是根据目前AH和高胆固醇血症管理的临床指南进行评估的。对2010年(n=7782)和2020年(n=3061)的数据进行了分析,以评估单一疗法和PCT处方的动态变化:结果显示:高血压合并冠心病、心力衰竭和心房颤动患者的 AHD 数量增幅最大。在一小部分无其他心血管疾病的高血压患者中,没有处方推荐的抗高血压药物组合,而是优先选择了血管紧张素转换酶抑制剂、血管紧张素受体阻滞剂和β-肾上腺素受体阻滞剂(β-AB)。PCT 与推荐组合的主要区别在于更广泛地使用了 β-AB 组药物。高血压合并冠状动脉疾病患者的 PCT 值最高,超过 90%;高血压合并心力衰竭患者的 PCT 值最高,达到 56.2%;高血压合并心房颤动患者的 PCT 值最高,达到 33.3%;高血压合并慢性肾病患者的 PCT 值最高,达到 19.6%。在所有被分析的群体中,血压和低密度脂蛋白胆固醇的目标都没有达到。在国际非专有药名中,最常用的处方药如下:比索洛尔、美托洛尔、利辛普利、培哚普利、洛沙坦、螺内酯、氨氯地平、托拉塞米、吲哒帕胺、次氯噻嗪、莫索尼定。处方的每日剂量更接近最初推荐的剂量。到 2020 年,PCT 与 β-AB 的处方和各种组合的处方将更加统一,而 2010 年的 PCT 处方特点是存在一到两个领先组合:结论:所描述的 AHD 处方特点部分再现了 AH 治疗的临床建议。RCP中提供的治疗差异可能与试图加强对合并其他心血管疾病的高血压患者的治疗有关。同时,对处方药组合和剂量的分析表明,存在进一步升级治疗的广泛机会。所提供的数据可以让人们深入了解目前 RCP 患者的降压治疗处方模式,并为优化不同类别高血压患者的治疗奠定基础。
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[Antihypertensive therapy in patients with arterial hypertension and concomitant diseases in real clinical practice (according to the National Registry of Arterial Hypertension, 2019-2022)].

Background: Arterial hypertension (AH) remains the leading risk factor associated with cardiovascular diseases (CVDs), cerebrovascular disease and chronic kidney disease. About 70% of patients with AH who are on monotherapy cannot achieve blood pressure (BP) targets, and therefore all quidelines for the management of AH have recently recommended prescribing combination therapy (PCT). In real clinical practice (RCP), there remains significant uncertainty in the effectiveness and rationality of therapy, despite the wide availability of antihypertensive drugs (AHD) and the presence of recommendations for a stepwise approach to prescribing combinations of specific groups of AHD in different clinical situations.

Aim: Analyze the real ongoing antihypertensive therapy, including the PCT; international nonproprietary names of drugs and their dosages in RCP; compliance of therapy with clinical recommendations; changing trends in the PCT.

Materials and methods: An analysis was carried out of the data from the register of AH, the compliance of treatment in different clinical groups of patients and the achievement of BP and low-density lipoprotein cholesterol targets in the sample of 2019-2022 (n=5012). The prescription of AHD and achievement of targets values were assessed in accordance with current clinical guidelines for the management of AH and hypercholesterolemia. Data from 2010 (n=7782) and 2020 (n=3061) were analyzed to assess the dynamics of prescription of monotherapy and PCT.

Results: The greatest increase in the number of AHD was observed in patients with hypertension in combination with coronary heart disease, heart failure, and atrial fibrillation. In a small group of patients with hypertension without other CVDs, the recommended combinations of AHD were not prescribed; preference was given to angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, and β-adrenoblocker (β-AB). PCT mainly differed from the recommended combinations by the wider use of drugs from the β-AB group. The PCT of recommended drugs was highest in patients with hypertension and coronary artery disease - more than 90%, hypertension and heart failure in 56.2%, hypertension and atrial fibrillation - 33.3%, hypertension and chronic kidney desease - 19.6%. Achievement of BP and low-density lipoprotein cholesterol targets was insufficient in all analyzed groups. Among the international nonproprietary names of drugs, the most frequently prescribed are the following: bisoprolol, metoprolol, lisinopril, perindopril, losartan, spironolactone, amlodipine, torasemide, indapamide, hypochlorothiazide, moxonidine. The prescribed daily dosages were closer to the initial recommended ones. By 2020, the prescription of PCT with β-AB and a more uniform prescription of various combinations will come to the fore, while PCT in 2010 is characterized by the presence of one or two leaders combinations.

Conclusion: The described features of prescribing AHD partially reproduce clinical recommendations for the management of AH. Differences in therapy provided in RCP may be associated with an attempt to intensify the treatment of hypertension in patients with other concomitant CVDs. At the same time, analysis of combinations and dosages of prescribed drugs suggests the presence of wide opportunities for further escalation of therapy. The presented data can provide insight into current patterns of antihypertensive therapy prescription in patients in RCP and lay the foundation for optimizing therapy in different categories hypertensive patients.

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