How are we doing with the treatment of essential tremor (ET)?: Persistence of patients with ET on medication: data from 528 patients in three settings. Academic Article uri icon

Overview

abstract

  • BACKGROUND: The pharmacological treatment of essential tremor (ET) is not optimal. There are only two first-line medications and troublesome side effects are common. It is not uncommon for patients to simply stop taking medication. Yet, no published data substantiate or quantify this anecdotal impression. OBJECTIVES: To determine, amongst patients with ET who were prescribed medication for tremor, what proportion are still taking medication and what proportion have stopped? METHODS: Five hundred and twenty-eight patients with ET from three distinct study settings (clinical, brain donors, population) were interviewed. RESULTS: A clear pattern that emerged across settings was that the proportion of patients with ET who had stopped medication was sizable and consistently similar (nearly one-third): 31.4% (clinical), 24.3% (brain donors), 30.0% (population), 29.8% (overall). A similarly high proportion of cases with severe tremor had stopped their medication: 31.9% (clinical), 36.4% (brain donors). For the four most commonly used medications (propranolol, primidone, diazepam, topiramate), one-half or more of the treated patients had stopped the medication; amongst the less commonly used medications, the proportion who stopped was even higher. CONCLUSIONS: Nearly one of every three patients with ET who had been prescribed medication for tremor had discontinued pharmacotherapy. Even more revealing was that a similar proportion of cases with severe tremor had stopped medication. These data make tangibly evident that there is a sizable population of patients with ET who are untreated and disabled, and underscore the inadequacy of current pharmacotherapeutic options for this common neurological disease.

publication date

  • January 7, 2010

Research

keywords

  • Essential Tremor
  • Medication Adherence

Identity

PubMed Central ID

  • PMC2889923

Scopus Document Identifier

  • 77952501959

Digital Object Identifier (DOI)

  • 10.1111/j.1468-1331.2009.02926.x

PubMed ID

  • 20067514

Additional Document Info

volume

  • 17

issue

  • 6