{"title":"Effect of amphetamines on blood pressure.","authors":"Magnus Chan, Jocelyn Joy Chan, James M Wright","doi":"10.1002/14651858.CD007896.pub4","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Daily ingestion of amphetamines is common, as they are widely prescribed for attention-deficit hyperactivity disorder (ADHD) and other diagnoses. People also use amphetamines recreationally or in an attempt to boost cognitive or athletic performance. Amphetamines have the potential to increase blood pressure, and we do not know if the long-term benefits of daily amphetamine use outweigh the potential harms.</p><p><strong>Objectives: </strong>Primary: to quantify the changes in systolic and diastolic blood pressure in children and adults taking amphetamines, compared to placebo. Secondary: to quantify the changes in heart rate in children and adults taking amphetamines, compared to placebo; to quantify the number of withdrawals due to adverse effects of amphetamine, compared to placebo.</p><p><strong>Search methods: </strong>We used the Cochrane Hypertension Specialized Register, CENTRAL, MEDLINE, Embase and two clinical trial registers, together with reference checking and contact with study authors to identify the studies included in the review. We imposed no restrictions on language, publication year or publication status. The latest search date was March 2023.</p><p><strong>Selection criteria: </strong>Randomized controlled trials (RCTs) that compared the effects of daily oral amphetamines versus placebo on blood pressure. There were no restrictions on participants' age or gender.</p><p><strong>Data collection and analysis: </strong>We used standard methods expected by Cochrane. Primary outcomes were change in systolic and diastolic blood pressure (measured in millimeters of mercury (mmHg) above atmospheric pressure; continuous outcomes). Secondary outcomes were heart rate (measured as beats per minute; continuous outcome) and withdrawals due to adverse effects (dichotomous outcome). We calculated continuous outcomes as mean differences (MD) with 95% confidence intervals (CI). We expressed withdrawals due to adverse effects as a risk ratio with 95% CI. We used a fixed-effect model to pool effect sizes from all studies.</p><p><strong>Main results: </strong>We included 56 RCTs with a total of 10,583 participants, both adults and children. Most studies were conducted in North America (mainly the USA), followed by Europe. A few studies took place in Asia (Japan) and Australia. The studies tested racemic amphetamine, dextroamphetamine, mixed amphetamine salts, lisdexamfetamine dimesylate, methylenedioxymethamphetamine (MDMA) and methylphenidate. The amphetamines were prescribed for ADHD, weight loss and other indications. In 48 RCTs, blood pressure was measured within 24 hours of the last dose. Based on data from all included studies, amphetamines increased systolic blood pressure (SBP) by 1.93 mmHg (95% CI 1.54 to 2.31) and diastolic blood pressure (DBP) by 1.84 mmHg (95% CI 1.51 to 2.16) (56 studies, 10,583 participants; high-certainty evidence for both). Amphetamines increased heart rate by 3.71 beats per minute (95% CI 3.27 to 4.14; 47 studies, 10,075 participants; high-certainty evidence). In a subgroup analysis limited to studies that gave participants amphetamines for at least eight weeks, the effects were similar, suggesting that these are sustained effects. These findings suggest that people taking daily oral amphetamines are at increased risk of adverse cardiovascular events. Participants in the amphetamine group were also more likely to withdraw from the study due to adverse effects compared to those given placebo (risk ratio 2.69, 95% CI 2.13 to 3.40; absolute risk increase of 4.3% over an average duration of 1 month; 42 studies, 8952 participants; high-certainty evidence). In general, the studies were well-executed, and the methodology was sound. We judged most studies to have a low risk of bias across most domains. Selection bias (random sequence generation and allocation concealment) was the domain most often rated as at unclear risk of bias, because the methods used were not reported. We judged 13 studies (23%) to have a high risk of bias in at least one of the seven domains, primarily due to high dropout rates, leading to a high risk of attrition bias.</p><p><strong>Authors' conclusions: </strong>Daily oral amphetamines increase blood pressure, heart rate, and withdrawals due to adverse effects, with these effects observed across all time points, including shorter (≤ four weeks) and longer durations (> four weeks to < eight weeks; ≥ eight weeks) of use. Future trials should measure blood pressure using 24-hour ambulatory monitoring and assess the effect of long-term use.</p>","PeriodicalId":10473,"journal":{"name":"Cochrane Database of Systematic Reviews","volume":"3 ","pages":"CD007896"},"PeriodicalIF":8.8000,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11951410/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cochrane Database of Systematic Reviews","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/14651858.CD007896.pub4","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Daily ingestion of amphetamines is common, as they are widely prescribed for attention-deficit hyperactivity disorder (ADHD) and other diagnoses. People also use amphetamines recreationally or in an attempt to boost cognitive or athletic performance. Amphetamines have the potential to increase blood pressure, and we do not know if the long-term benefits of daily amphetamine use outweigh the potential harms.
Objectives: Primary: to quantify the changes in systolic and diastolic blood pressure in children and adults taking amphetamines, compared to placebo. Secondary: to quantify the changes in heart rate in children and adults taking amphetamines, compared to placebo; to quantify the number of withdrawals due to adverse effects of amphetamine, compared to placebo.
Search methods: We used the Cochrane Hypertension Specialized Register, CENTRAL, MEDLINE, Embase and two clinical trial registers, together with reference checking and contact with study authors to identify the studies included in the review. We imposed no restrictions on language, publication year or publication status. The latest search date was March 2023.
Selection criteria: Randomized controlled trials (RCTs) that compared the effects of daily oral amphetamines versus placebo on blood pressure. There were no restrictions on participants' age or gender.
Data collection and analysis: We used standard methods expected by Cochrane. Primary outcomes were change in systolic and diastolic blood pressure (measured in millimeters of mercury (mmHg) above atmospheric pressure; continuous outcomes). Secondary outcomes were heart rate (measured as beats per minute; continuous outcome) and withdrawals due to adverse effects (dichotomous outcome). We calculated continuous outcomes as mean differences (MD) with 95% confidence intervals (CI). We expressed withdrawals due to adverse effects as a risk ratio with 95% CI. We used a fixed-effect model to pool effect sizes from all studies.
Main results: We included 56 RCTs with a total of 10,583 participants, both adults and children. Most studies were conducted in North America (mainly the USA), followed by Europe. A few studies took place in Asia (Japan) and Australia. The studies tested racemic amphetamine, dextroamphetamine, mixed amphetamine salts, lisdexamfetamine dimesylate, methylenedioxymethamphetamine (MDMA) and methylphenidate. The amphetamines were prescribed for ADHD, weight loss and other indications. In 48 RCTs, blood pressure was measured within 24 hours of the last dose. Based on data from all included studies, amphetamines increased systolic blood pressure (SBP) by 1.93 mmHg (95% CI 1.54 to 2.31) and diastolic blood pressure (DBP) by 1.84 mmHg (95% CI 1.51 to 2.16) (56 studies, 10,583 participants; high-certainty evidence for both). Amphetamines increased heart rate by 3.71 beats per minute (95% CI 3.27 to 4.14; 47 studies, 10,075 participants; high-certainty evidence). In a subgroup analysis limited to studies that gave participants amphetamines for at least eight weeks, the effects were similar, suggesting that these are sustained effects. These findings suggest that people taking daily oral amphetamines are at increased risk of adverse cardiovascular events. Participants in the amphetamine group were also more likely to withdraw from the study due to adverse effects compared to those given placebo (risk ratio 2.69, 95% CI 2.13 to 3.40; absolute risk increase of 4.3% over an average duration of 1 month; 42 studies, 8952 participants; high-certainty evidence). In general, the studies were well-executed, and the methodology was sound. We judged most studies to have a low risk of bias across most domains. Selection bias (random sequence generation and allocation concealment) was the domain most often rated as at unclear risk of bias, because the methods used were not reported. We judged 13 studies (23%) to have a high risk of bias in at least one of the seven domains, primarily due to high dropout rates, leading to a high risk of attrition bias.
Authors' conclusions: Daily oral amphetamines increase blood pressure, heart rate, and withdrawals due to adverse effects, with these effects observed across all time points, including shorter (≤ four weeks) and longer durations (> four weeks to < eight weeks; ≥ eight weeks) of use. Future trials should measure blood pressure using 24-hour ambulatory monitoring and assess the effect of long-term use.
背景:每天服用安非他明是很常见的,因为它们被广泛用于治疗注意力缺陷多动障碍(ADHD)和其他诊断。人们也使用安非他明娱乐或试图提高认知或运动表现。安非他明有可能升高血压,我们不知道每天服用安非他明的长期益处是否大于潜在的危害。目的:主要:量化服用安非他明的儿童和成人与安慰剂相比收缩压和舒张压的变化。其次:量化服用安非他明的儿童和成人与安慰剂相比心率的变化;量化因安非他明的不良反应而退出的次数,与安慰剂相比。检索方法:我们使用Cochrane高血压专科登记处、CENTRAL、MEDLINE、Embase和两个临床试验登记处,结合参考资料检查和与研究作者的联系来确定纳入本综述的研究。我们对语言、出版年份和出版状态没有限制。最近一次搜索日期是2023年3月。选择标准:比较每日口服安非他明与安慰剂对血压影响的随机对照试验(rct)。对参与者的年龄和性别没有限制。资料收集和分析:我们采用Cochrane期望的标准方法。主要结局是收缩压和舒张压的变化(测量单位为大气压以上毫米汞柱;连续的结果)。次要结局是心率(以每分钟心跳数计;连续结果)和因不良反应而停药(二分类结果)。我们以95%置信区间(CI)的均值差(MD)计算连续结果。我们用95% CI表示因不良反应而停药的风险比。我们使用固定效应模型来汇总所有研究的效应大小。主要结果:我们纳入56项随机对照试验,共10,583名参与者,包括成人和儿童。大多数研究是在北美(主要是美国)进行的,其次是欧洲。在亚洲(日本)和澳大利亚进行了一些研究。这些研究测试了外消旋苯丙胺、右苯丙胺、混合苯丙胺盐、利地安非他明二烷基酯、甲基烯二氧基甲基苯丙胺(MDMA)和哌醋甲酯。安非他明是用来治疗多动症、减肥和其他症状的。在48项随机对照试验中,在最后一次给药后24小时内测量血压。根据所有纳入研究的数据,安非他明使收缩压(SBP)增加1.93 mmHg (95% CI 1.54至2.31),舒张压(DBP)增加1.84 mmHg (95% CI 1.51至2.16)(56项研究,10,583名参与者;两者都有高确定性的证据)。安非他明使心率每分钟增加3.71次(95%可信区间3.27至4.14;47项研究,10075名参与者;高确定性的证据)。在一项仅限于给参与者服用安非他明至少8周的研究的亚组分析中,效果是相似的,这表明这些效果是持续的。这些发现表明,每天口服安非他明的人发生不良心血管事件的风险增加。与安慰剂组相比,安非他明组的参与者也更有可能因不良反应而退出研究(风险比2.69,95% CI 2.13至3.40;平均1个月的绝对风险增加4.3%;42项研究,8952名受试者;高确定性的证据)。总的来说,这些研究执行得很好,方法也很合理。我们判断大多数研究在大多数领域具有低偏倚风险。选择偏倚(随机序列生成和分配隐藏)是最常被评为具有不明确偏倚风险的领域,因为所使用的方法未被报道。我们判断13项研究(23%)在七个领域中至少有一个具有高偏倚风险,主要是由于高辍学率,导致高损耗偏倚风险。作者的结论是:每日口服安非他明会增加血压、心率和不良反应引起的停药,这些影响在所有时间点都可以观察到,包括较短(≤四周)和较长的持续时间(从4周到< 8周;≥8周)。未来的试验应该使用24小时动态监测来测量血压,并评估长期使用的效果。
期刊介绍:
The Cochrane Database of Systematic Reviews (CDSR) stands as the premier database for systematic reviews in healthcare. It comprises Cochrane Reviews, along with protocols for these reviews, editorials, and supplements. Owned and operated by Cochrane, a worldwide independent network of healthcare stakeholders, the CDSR (ISSN 1469-493X) encompasses a broad spectrum of health-related topics, including health services.