Update on Medical Treatments for Essential Tremor: An International Parkinson and Movement Disorder Society Evidence-Based Medicine Review.
Abstract
[BACKGROUND] The first International Parkinson and Movement Disorder Society Evidence-Based Medicine (MDS-EBM) review for essential tremor (ET) was published in 2019; since then, the modified Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) methodology was adopted by MDS, and new evidence exists.
[OBJECTIVE] The objective of this study was to update EBM conclusions for medical treatments of ET with a focus on longer follow-up periods.
[METHODS] A systematic literature search was conducted for randomized controlled trials (RCTs) investigating medical interventions for ET with a minimum 1-month follow-up, with subsequent appraisal of data using an MDS-EBM framework.
[RESULTS] Thirty-one RCTs were included evaluating 16 interventions against placebo. Nine interventions were evaluated by more than one RCT: alprazolam, botulinum toxin type A (BtA), levetiracetam, phenobarbitone, pregabalin, primidone, propranolol, topiramate, and trazodone. The remainder were studied in a single RCT (acetazolamide, flunarizine, gabapentin, mirtazapine, perampanel, progabide, and zonisamide). Trial sample size ranged from 5 to 117 participants, and study duration ranged from 4 to 28 weeks. More than one RCT documented improvement in tremor severity for propranolol, primidone, topiramate, and BtA. Using the modified GRADE framework, we found significant methodological shortcomings in the studies, resulting in insufficient evidence for all interventions. Concerns about risk of bias and imprecision commonly limited the ability to make stronger recommendations for these interventions.
[CONCLUSIONS] Current evidence from RCTs with at least 1 month of follow-up is insufficient to confidently support the efficacy of available medical treatments for ET. There is a need for longer, higher-quality clinical trials to improve treatment recommendations and guide decision-making for clinicians and patients with ET. © 2026 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. © 2026 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
[OBJECTIVE] The objective of this study was to update EBM conclusions for medical treatments of ET with a focus on longer follow-up periods.
[METHODS] A systematic literature search was conducted for randomized controlled trials (RCTs) investigating medical interventions for ET with a minimum 1-month follow-up, with subsequent appraisal of data using an MDS-EBM framework.
[RESULTS] Thirty-one RCTs were included evaluating 16 interventions against placebo. Nine interventions were evaluated by more than one RCT: alprazolam, botulinum toxin type A (BtA), levetiracetam, phenobarbitone, pregabalin, primidone, propranolol, topiramate, and trazodone. The remainder were studied in a single RCT (acetazolamide, flunarizine, gabapentin, mirtazapine, perampanel, progabide, and zonisamide). Trial sample size ranged from 5 to 117 participants, and study duration ranged from 4 to 28 weeks. More than one RCT documented improvement in tremor severity for propranolol, primidone, topiramate, and BtA. Using the modified GRADE framework, we found significant methodological shortcomings in the studies, resulting in insufficient evidence for all interventions. Concerns about risk of bias and imprecision commonly limited the ability to make stronger recommendations for these interventions.
[CONCLUSIONS] Current evidence from RCTs with at least 1 month of follow-up is insufficient to confidently support the efficacy of available medical treatments for ET. There is a need for longer, higher-quality clinical trials to improve treatment recommendations and guide decision-making for clinicians and patients with ET. © 2026 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. © 2026 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
추출된 의학 개체 (NER)
| 유형 | 영어 표현 | 한국어 / 풀이 | UMLS CUI | 출처 | 등장 |
|---|---|---|---|---|---|
| 시술 | botulinum toxin
|
보툴리눔독소 주사 | dict | 1 | |
| 약물 | alprazolam
|
C0002333
alprazolam
|
scispacy | 1 | |
| 약물 | BtA
→ botulinum toxin type A
|
C0006050
botulinum toxin type A
|
scispacy | 1 | |
| 약물 | levetiracetam
|
C0377265
levetiracetam
|
scispacy | 1 | |
| 약물 | phenobarbitone
|
C0031412
phenobarbital
|
scispacy | 1 | |
| 약물 | pregabalin
|
C0657912
pregabalin
|
scispacy | 1 | |
| 약물 | primidone
|
C0033148
primidone
|
scispacy | 1 | |
| 약물 | propranolol
|
C0033497
propranolol
|
scispacy | 1 | |
| 약물 | topiramate
|
C0076829
topiramate
|
scispacy | 1 | |
| 약물 | trazodone
|
C0040805
trazodone
|
scispacy | 1 | |
| 약물 | acetazolamide
|
C0000981
acetazolamide
|
scispacy | 1 | |
| 약물 | flunarizine
|
C0016295
flunarizine
|
scispacy | 1 | |
| 약물 | gabapentin
|
C0060926
gabapentin
|
scispacy | 1 | |
| 약물 | mirtazapine
|
C0049506
mirtazapine
|
scispacy | 1 | |
| 약물 | perampanel
|
C2698764
perampanel
|
scispacy | 1 | |
| 약물 | progabide
|
C0072076
progabide
|
scispacy | 1 | |
| 약물 | zonisamide
|
C0078844
zonisamide
|
scispacy | 1 | |
| 약물 | [BACKGROUND]
|
scispacy | 1 | ||
| 약물 | [OBJECTIVE]
|
scispacy | 1 | ||
| 약물 | [CONCLUSIONS]
|
scispacy | 1 | ||
| 질환 | Tremor
|
C0040822
Tremor
|
scispacy | 1 | |
| 질환 | Parkinson
|
scispacy | 1 | ||
| 질환 | Parkinson and Movement Disorder
|
scispacy | 1 | ||
| 질환 | MDS-EBM
→ Movement Disorder Society Evidence-Based Medicine
|
scispacy | 1 | ||
| 기타 | MDS-EBM
→ Movement Disorder Society Evidence-Based Medicine
|
scispacy | 1 | ||
| 기타 | botulinum toxin type A
|
scispacy | 1 | ||
| 기타 | patients
|
scispacy | 1 | ||
| 기타 | Wiley Periodicals
|
scispacy | 1 |
MeSH Terms
Humans; Essential Tremor; Evidence-Based Medicine; Randomized Controlled Trials as Topic; Societies, Medical; Anticonvulsants
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