Evidence map›Paper›PMID 35585718›Full record

Trial reportMuscle & nerve2022

A secondary analysis of PAIN-CONTRoLS: Pain's impact on sleep, fatigue, and activities of daily living.

Salman F Bhai, Alexandra Brown, Byron Gajewski, Kim S Kimminau, Lemuel R Waitman, Mamatha Pasnoor, Richard J Barohn, PAIN-CONTRoLS Study Team

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Muscle & nerve, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Salman F BhaiDepartment of Neurology, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID 0000-0003-4702-9380
Alexandra BrownDepartment of Biostatistics and Data Science, The University of Kansas Medical Center, Kansas City, Kansas, USA.
Byron GajewskiDepartment of Biostatistics and Data Science, The University of Kansas Medical Center, Kansas City, Kansas, USA.
Kim S KimminauDepartment of Family and Community Medicine, The University of Missouri School of Medicine, Columbia, Missouri, USA.
Lemuel R WaitmanDepartment of Health Management and Informatics, The University of Missouri School of Medicine, Columbia, Missouri, USA.
Mamatha PasnoorDepartment of Neurology, The University of Kansas Medical Center, Kansas City, Kansas, USA.
Richard J BarohnDepartment of Neurology, The University of Missouri School of Medicine, Columbia, Missouri, USA.
PAIN-CONTRoLS Study Team
University of Kansas Medical Center · USUniversity of Missouri · USTexas Health Dallas · USUniversity of Missouri Health System · US

Funding

RADx-UP: Improving the Response of Local Urban and Rural Communities to Disparities in Covid-19 TestingUL1TR002366 · NCATS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Mario Castro, JAMES STEVEN LEEDER · 2017 to 2026
$44.3M
NCATS NIH HHS UL1 TR002366
6 · The paper itself

Abstract

INTRODUCTION/

aimsPeripheral neuropathies commonly affect quality of life of patients due to pain, sleep disturbances, and fatigue, although trials have not adequately explored these domains of care. The aim of this study was to assess the impact of nortriptyline, duloxetine, pregabalin, and mexiletine on pain, sleep, and fatigue in patients diagnosed with cryptogenic sensory polyneuropathy (CSPN).

methodsWe implemented a Bayesian adaptive design to perform a 12-wk multisite, randomized, prospective, open-label comparative effectiveness study in 402 CSPN patients. Participants received either nortriptyline (n = 134), duloxetine (n = 126), pregabalin (n = 73), or mexiletine (n = 69). At prespecified analysis timepoints, secondary outcomes, Patient Reported Outcomes Measurement Information System (PROMIS) surveys including Short Form (SF)-12, pain interference, fatigue, and sleep disturbance, were collected.

resultsMexiletine had the highest quit rate (58%) due to gastrointestinal side effects, while nortriptyline (38%) and duloxetine (38%) had the lowest quit rates. If tolerated for the full 12 wk of the study, mexiletine had the highest probability (>90%) of positive outcomes for improvements in pain interference and fatigue. There was no significant difference among the medications for sleep disturbance or SF-12 scores. Adverse events and lack of efficacy were the two most common reasons for cessation of therapy. DISCUSSION: Physicians caring for patients with CSPN should consider mexiletine to address pain and fatigue, although nortriptyline and duloxetine are better medications to trial first since they are better tolerated. Future research should compare other commonly used medications for CSPN to determine evidence-based treatment strategies.

Indexed as

Activities of Daily LivingDiabetic NeuropathiesBayes TheoremDouble-Blind MethodDuloxetine HydrochlorideFatigueHumansMexiletineNortriptylinePainPregabalinProspective StudiesQuality of LifeSleepTreatment OutcomeDuloxetine HydrochlorideMexiletineNortriptylinePregabalinfatiguepainrandomized control trialsensory neuropathysleep

Identifiers

PMID35585718
PMCPMC10629716
OpenAlexW4280491122

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.