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代谢综合征和/或2型糖尿病患者的高血压治疗:门诊研究中的治疗有效性和治疗惰性分析

Hypertension Treatment in Patients with Metabolic Syndrome and/or Type 2 Diabetes Mellitus: Analysis of the Therapy Effectivity and the Therapeutic Inertia in Outpatient Study.

作者信息

Farský Štefan, Strišková Andrea, Borčin Marián

机构信息

House of the Heart (Dom Srdca), Slovak League against Hypertension, Martin, Slovakia.

出版信息

Cardiol Res Pract. 2018 Apr 1;2018:8387613. doi: 10.1155/2018/8387613. eCollection 2018.

Abstract

We have analysed the database of 1,595 consecutive patients visiting our department of cardiology and internal medicine clinic in 2005-2014. The analysis included 13,990 visit records, and the average number of visits per patient was 8.5 ± 7.0. Our goals were to evaluate the effectivity of hypertension treatment as for drug choice, decrease of sBP and dBP associated with a certain drug, a drug combination, and therapeutic inertia in patients with metabolic syndrome and/or diabetes mellitus. The final number of patients for analysis who fulfilled the inclusion criteria for interpenetration of both diagnostic circles was 570. . 15% of patients were treated using hypertension monotherapy, 70% of patients were treated using 2- to 4-drug combination therapy, and 15% of patients were treated using 5- to 6-drug combination. The drugs used most frequently were perindopril (perin), nitrendipine (nitre), amlodipine (amlo), telmisartan (telmi), hydrochlorothiazide (hydro), rilmenidine, and nebivolol (used in >100 patients). The most significant decrease of sBP was associated with treatment by nitre, hydro, telmi, and urapidil (>19 mmHg). The most significant decrease of dBP was associated with treatment by nitre, hydro, telmi, and verapamil (>10 mmHg). The most significant decrease of both sBP and dBP was associated with treatment using 3-drug combination of telmi + hydro + spironolactone (41 and 16 mmHg, resp.), telmi + hydro + nitre (34 and 15 mmHg, resp.), and telmi + hydro + urapidil (34 and 15 mmHg, resp.). At the last visit, 281 out of 413 patients at the first visit had sBP >140 mmHg (68%); that is, sBP control was 32%. At the last visit, 76 patients out of 217 at the first visit had dBP >90 mmHg (35%); that is, dBP control was 65%. Therapeutic inertia was calculated by evaluating the proportion of visits at which sBP was above the target for eligible visits minus the proportion of visits where the change was made in antihypertensive treatment (AHT), either medication type or dose, over the number of eligible visits, with the resultant value multiplied by the mean of the difference between the actual sBP and the target value at clinic visits. TIQ was counted at first 200 consecutive patients, and the average value was 57.30 ± 147.20. . The study presents the real-life data concerning the difficulties in hypertension treatment in patients with concomitant metabolic syndrome and/or type 2 diabetes mellitus. sBP was controlled at 32% patients only. The study results allow evaluating the effectivity of hypertension treatment as for drug choice, decrease of sBP and dBP associated with a certain drug, a drug combination, and therapeutic inertia in these patients.

摘要

我们分析了2005年至2014年期间连续就诊于我们心内科和内科门诊的1595例患者的数据库。该分析包括13990条就诊记录,每位患者的平均就诊次数为8.5±7.0次。我们的目标是评估高血压治疗在药物选择、与某种药物、药物组合相关的收缩压和舒张压降低以及代谢综合征和/或糖尿病患者的治疗惰性方面的有效性。符合两个诊断圈相互渗透纳入标准的最终分析患者数量为570例。15%的患者采用高血压单一疗法治疗,70%的患者采用2至4种药物联合疗法治疗,15%的患者采用5至6种药物联合治疗。最常用的药物是培哚普利(perin)、尼群地平(nitre)、氨氯地平(amlo)、替米沙坦(telmi)、氢氯噻嗪(hydro)、利美尼定和奈必洛尔(使用患者超过100例)。收缩压下降最显著与使用nitre、hydro、telmi和乌拉地尔治疗相关(>19 mmHg)。舒张压下降最显著与使用nitre、hydro、telmi和维拉帕米治疗相关(>10 mmHg)。收缩压和舒张压下降最显著与使用telmi + hydro + 螺内酯三联药物治疗相关(分别为41和16 mmHg)、telmi + hydro + nitre(分别为34和15 mmHg)以及telmi + hydro + 乌拉地尔(分别为34和15 mmHg)。在最后一次就诊时,首次就诊的413例患者中有281例收缩压>140 mmHg(68%);即收缩压控制率为32%。在最后一次就诊时,首次就诊的217例患者中有76例舒张压>90 mmHg(35%);即舒张压控制率为65%。治疗惰性通过评估符合条件就诊时收缩压高于目标值的就诊比例减去在抗高血压治疗(AHT)中进行了药物类型或剂量改变的就诊比例,再除以符合条件就诊次数,所得值乘以门诊就诊时实际收缩压与目标值之差的平均值来计算。对前200例连续患者计算治疗惰性商数(TIQ),平均值为57.30±147.20。该研究呈现了合并代谢综合征和/或2型糖尿病患者高血压治疗困难的真实生活数据。仅32%的患者收缩压得到控制。研究结果有助于评估高血压治疗在药物选择、与某种药物、药物组合相关的收缩压和舒张压降低以及这些患者治疗惰性方面的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/934f/5901812/64bdb238b099/CRP2018-8387613.001.jpg

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