Suica Zorica, Behrendt Frank, Ziller Carina, Gäumann Szabina, Schädler Stefan, Hilfiker Roger, Parmar Katrin, Gerth Hans Ulrich, Bonati Leo H, Schuster-Amft Corina
Research Department, Reha Rheinfelden, Rheinfelden, Switzerland.
School of Engineering and Computer Science, Bern University of Applied Sciences, Burgdorf, Switzerland.
Front Neurol. 2024 Jul 12;15:1426566. doi: 10.3389/fneur.2024.1426566. eCollection 2024.
The patho-psychological mechanisms of persistent postural-perceptual dizziness (PPPD) appear to be very complex, and a multimodal, multidisciplinary approach is suggested for treating patients with PPPD. The aim of this review was to provide a comprehensive overview of non-pharmacological treatments and their comparative effectiveness in patients with PPPD.
Scopus, Web of Science, PsycINFO, Medline, Embase, CINAHL, Cochrane Library and ClinicalTrials.gov were searched in April 2022 with a search update in August 2023. Only randomized controlled trials (RCTs) were included. There was no restrictions regarding publication date. Two reviewers independently identified eligible trials, extracted data, double-checked all extracted information from the included articles and assessed the risk of bias using the Cochrane risk of bias tool. A qualitative synthesis was performed, considering methodological heterogeneity between trials. Finally, an effect size analysis was performed for each treatment comparison. The standardized mean differences (SMD) and their corresponding 95% confidence intervals (95%CI) were calculated for each trial using Review Manager 5.4.
Thirteen RCTs (618 patients with moderate or mild dizziness) out of 1,362 references describing seven different non-pharmacological comparisons were selected. Nine trials included patients with PPPD, and four trials included patients with functional dizziness. The trials used different interventions that were classified as: (1) psychotherapeutic interventions (cognitive behavioral therapy, patient education), (2) physiotherapeutic interventions/training (vestibular rehabilitation, optokinetic stimulation), (3) stimulation procedures (vagus nerve stimulation, transcranial direct current stimulation) and (4) device application (visual desensitization using personalized glasses). However, most of the trials investigated the effects of single interventions, rather than multimodal interdisciplinary treatment of patients with PPPD. The SMD for dizziness handicap and severity was between 0.04 and 0.52 in most trials. In one trial using visual desensitization, the SMD was 1.09 (strong effect on the severity of dizziness) and 1.05 (strong effect on dizziness handicap).
Several individual interventions have shown benefits in the treatment of patients with PPPD with small to moderate effects. However, the multimodal treatment or a combination of vestibular rehabilitation with visual desensitization, cognitive behavioral therapy including patient education, and medication support should be further investigated. Future trials should include a large sample size with severe dizziness, and provide a longer follow-up period.
PROSPERO CRD42022320344.
持续性姿势-感知性头晕(PPPD)的病理心理机制似乎非常复杂,建议采用多模式、多学科方法治疗PPPD患者。本综述的目的是全面概述非药物治疗及其在PPPD患者中的相对疗效。
于2022年4月检索了Scopus、Web of Science、PsycINFO、Medline、Embase、CINAHL、Cochrane图书馆和ClinicalTrials.gov,并于2023年8月进行了检索更新。仅纳入随机对照试验(RCT)。对发表日期无限制。两名 reviewers 独立识别符合条件的试验,提取数据,对纳入文章中所有提取的信息进行二次核对,并使用Cochrane偏倚风险工具评估偏倚风险。考虑到试验之间的方法学异质性,进行了定性综合分析。最后,对每种治疗比较进行效应量分析。使用Review Manager 5.4为每个试验计算标准化均数差(SMD)及其相应的95%置信区间(95%CI)。
从1362篇描述七种不同非药物比较的参考文献中,选择了13项RCT(618例中度或轻度头晕患者)。9项试验纳入了PPPD患者,4项试验纳入了功能性头晕患者。试验采用了不同的干预措施,分为:(1)心理治疗干预(认知行为疗法、患者教育),(2)物理治疗干预/训练(前庭康复、视动刺激),(3)刺激程序(迷走神经刺激、经颅直流电刺激)和(4)设备应用(使用个性化眼镜进行视觉脱敏)。然而,大多数试验研究的是单一干预措施的效果,而不是对PPPD患者进行多模式跨学科治疗。在大多数试验中,头晕障碍和严重程度的SMD在0.04至0.52之间。在一项使用视觉脱敏的试验中,SMD为1.09(对头晕严重程度有强烈影响)和1.05(对头晕障碍有强烈影响)。
几种单独的干预措施已显示出对PPPD患者治疗有益,效果从小到中等。然而,多模式治疗或前庭康复与视觉脱敏、包括患者教育的认知行为疗法以及药物支持的联合应用应进一步研究。未来的试验应纳入大样本的重度头晕患者,并提供更长的随访期。
PROSPERO CRD42022320344。