Evidence map›Paper›PMID 21674518›Full record

ArticleMuscle & nerve2011

An interactive voice response diary for patients with non-dystrophic myotonia.

Jeffrey M Statland, Yunxia Wang, Rachel Richesson, Brian Bundy, Laura Herbelin, Joe Gomes, Jaya Trivedi, Shannon Venance, Anthony Amato, Michael Hanna and 3 more

Open access · greenAbstract readComparative StudyMulticenter Study
In one paragraph

Article in Muscle & nerve, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
1.1field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 29 citations in OpenAlex.

  1. Drug treatment for myotonia.The Cochrane database of systematic reviews · 2025
    Pooled it
  2. Pooled it
  3. Mexiletine in spinal and bulbar muscular atrophy: a randomized controlled trial.Annals of clinical and translational neurology · 2022
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  8. Article
  9. Preclinical study of the antimyotonic efficacy of safinamide in the myotonic mouse model.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2024
    Article
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  11. Article
  12. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 7 institutions in 3 countries.

Jeffrey M StatlandDepartment of Neurology, University of Rochester Medical Center, Rochester, New York, USA.
Yunxia Wang
Rachel Richesson
Brian Bundy
Laura Herbelin
Joe Gomes
Jaya Trivedi
Shannon Venance
Anthony Amato
Michael Hanna
Robert Griggs
Richard J Barohn
Cinch Consortium
University of Kansas Medical Center · USUniversity of South Florida · USUniversity of Rochester Medical Center · USHarvard University · USLondon Health Sciences Centre · CAThe University of Texas Southwestern Medical Center · USUniversity College London · GB

Funding

UNIVERSITY OF ROCHESTER'S RESEARCH ASSOCIATE ORGANIZATIONUL1RR024160 · NCRR · UNIVERSITY OF ROCHESTER · PI PEARSON, THOMAS ARTHUR · 2006 to 2011
$38.7M
RARE DISEASES DATA AND TECHNOLOGY COORDINATING CENTERU54RR019259 · NCRR · UNIVERSITY OF SOUTH FLORIDA · PI KRISCHER, JEFFREY P · 2003 to 2008
$14.4M
The University of Rochester's Clinical and Translational Science InstituteUL1TR000042 · NCATS · UNIVERSITY OF ROCHESTER · PI BENNETT, NANCY M, KIEBURTZ, KARL D. · 2012 to 2015
$14.4M
WRITING AND WT LOSS MAINTENANCEM01RR023940 · NCRR · UNIVERSITY OF KANSAS MEDICAL CENTER · PI BURNS, JEFFREY MURRAY · 2007 to 2009
$6.6M
NERVOUS SYSTEM CHANNELOPATHIES: PATHOGENESIS &TREATMENTU54RR019482 · NCRR · UNIVERSITY OF ROCHESTER · PI GRIGGS, ROBERT C · 2003 to 2005
$3.7M
Medical Research Council G0601943NCATS NIH HHS UL1 TR000042NCRR NIH HHS M01 RR 023940NCRR NIH HHS M01 RR023940NCRR NIH HHS RR019259NCRR NIH HHS U54 RR019259NCRR NIH HHS U54 RR019482NCRR NIH HHS U54RR019482NCRR NIH HHS UL1 RR 024160NCRR NIH HHS UL1 RR024160
6 · The paper itself

Abstract

introductionNon-dystrophic myotonia (NDM) is caused by mutations in muscle chloride and sodium channels. Currently, there is no standardized instrument for documenting symptom frequency and severity in NDM.

methodsSubjects used an automated, interactive, telephone-based voice response diary (IVR) to record frequency and severity of stiffness, weakness, pain, and tiredness once a week for 8 weeks, after their baseline visits.

resultsWe describe the IVR and report data on 76 subjects for a total of 385 person-weeks. Overall there were 5.1 calls per subject. Forty-eight subjects called in 5 or more times, and 14 called in 8 times. Stiffness was both the most frequent and severe symptom. Warm-up and handgrip myotonia were associated with higher severity scores for stiffness.

conclusionsIVR is a convenient technology to allow patient reporting of repeated and real-time symptom frequency and severity, and it is presently being used in a trial of mexiletine in NDM.

Indexed as

Medical RecordsMyotoniaSeverity of Illness IndexTelephoneVoiceAdolescentAdultAgedChildFemaleHumansLongitudinal StudiesMaleMiddle AgedYoung Adult

Identifiers

PMID21674518
PMCPMC3233757
OpenAlexW2002362182

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.