Department of Emergency Medicine, Indiana University School of Medicine, Indianapolis.
Department of Emergency Medicine, Parma Medical Center, University Hospitals, Parma, Ohio.
JAMA Neurol. 2022 Sep 1;79(9):846-855. doi: 10.1001/jamaneurol.2022.1858.
Acute vertigo can be disabling. Antihistamines and benzodiazepines are frequently prescribed as "vestibular suppressants," but their efficacy is unclear.
To assess the efficacy of antihistamines and benzodiazepines in the treatment of acute vertigo from any underlying cause.
We searched the PubMed, CENTRAL, EMBASE, CINAHL, Scopus, and ClinicalTrials.gov databases from inception to January 14, 2019, without language restrictions. Bibliographies of the included studies and relevant reviews were also screened.
We included randomized clinical trials (RCTs) comparing antihistamine or benzodiazepine use with another comparator, placebo, or no intervention for patients with a duration of acute vertigo for 2 weeks or less. Studies of healthy volunteers, prophylactic treatment, or induced vertigo were excluded, as were studies that compared 2 medications from the same class.
Following Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines, data were extracted and risk of bias was assessed by 2 authors independently for each study. Data were pooled using a random-effects model.
The predefined primary outcome was change in 10- or 100-point vertigo or dizziness visual analog scale (VAS) scores at 2 hours after treatment. Secondary outcomes included change in nausea VAS scores at 2 hours, use of rescue medication at 2 hours, and improvement or resolution of vertigo at 1 week or 1 month.
Of the 27 trials identified in the systematic review, 17 contributed to the quantitative meta-analysis and involved a total of 1586 participants. Seven trials with a total of 802 participants evaluated the primary outcome of interest: single-dose antihistamines resulted in significantly more improvement on 100-point VAS scores compared with benzodiazepines (difference, 16.1 [95% CI, 7.2 to 25.0]) but not compared with other active comparators (difference, 2.7 [95% CI, -6.1 to 11.5]). At 1 week and 1 month, neither daily benzodiazepines nor antihistamines were reported to be superior to placebo. RCTs comparing the immediate effects of medications (at 2 hours) after a single dose generally had a low risk of bias, but those evaluating 1-week and 1-month outcomes had a high risk of bias.
Moderately strong evidence suggests that single-dose antihistamines provide greater vertigo relief at 2 hours than single-dose benzodiazepines. Furthermore, the available evidence did not support an association of benzodiazepine use with improvement in any outcomes for acute vertigo. Other evidence suggested that daily antihistamine use may not benefit patients with acute vertigo. Larger randomized trials comparing both antihistamines and benzodiazepines with placebo could better clarify the relative efficacy of these medications.
急性眩晕可能使人丧失能力。抗组胺药和苯二氮䓬类药物经常被用作“前庭抑制剂”,但其疗效尚不清楚。
评估抗组胺药和苯二氮䓬类药物治疗任何潜在病因引起的急性眩晕的疗效。
我们从建库到 2019 年 1 月 14 日在 PubMed、CENTRAL、EMBASE、CINAHL、Scopus 和 ClinicalTrials.gov 数据库中进行了无语言限制的检索。还对纳入研究的参考文献和相关综述进行了筛选。
我们纳入了比较抗组胺药或苯二氮䓬类药物与其他对照物、安慰剂或无干预治疗急性眩晕持续时间不超过 2 周的患者的随机临床试验(RCT)。健康志愿者、预防性治疗或诱导性眩晕的研究,以及比较同一类别的两种药物的研究被排除在外。
根据系统评价和荟萃分析的首选报告项目(PRISMA)指南,两位作者独立提取数据,并对每项研究的偏倚风险进行评估。使用随机效应模型进行数据合并。
预设的主要结局是治疗后 2 小时 10 点或 100 点眩晕或头晕视觉模拟量表(VAS)评分的变化。次要结局包括治疗后 2 小时恶心 VAS 评分的变化、2 小时内使用急救药物的情况以及治疗后 1 周或 1 个月时眩晕的改善或缓解情况。
在系统评价中确定的 27 项试验中,有 17 项试验有助于定量荟萃分析,共涉及 1586 名参与者。7 项涉及 802 名参与者的试验评估了我们感兴趣的主要结局:与苯二氮䓬类药物相比,单剂量抗组胺药可显著改善 100 点 VAS 评分(差异为 16.1 [95%CI,7.2 至 25.0]),但与其他活性对照物相比无差异(差异为 2.7 [95%CI,-6.1 至 11.5])。在 1 周和 1 个月时,每日苯二氮䓬类药物和抗组胺药均未被报告优于安慰剂。一般来说,比较单次剂量药物(治疗后 2 小时)即时效果的 RCT 偏倚风险较低,但评估 1 周和 1 个月结局的 RCT 偏倚风险较高。
有中等强度的证据表明,与单剂量苯二氮䓬类药物相比,单剂量抗组胺药可在 2 小时内提供更大的眩晕缓解。此外,现有证据不支持苯二氮䓬类药物治疗与急性眩晕任何结局的改善有关。其他证据表明,每日抗组胺药治疗可能对急性眩晕患者无益。比较抗组胺药和苯二氮䓬类药物与安慰剂的更大规模随机试验可能更好地阐明这些药物的相对疗效。