Evidence map›Paper›PMID 42015888›Full record

ArticlePain medicine (Malden, Mass.)2026

Real world treatment patterns among patients with painful diabetic peripheral neuropathy in the United States.

Nathaniel M Schuster, Sushanth Jeyakumar, Ann M Menzie, Moeen Panni, Nicole Princic, Meghan Moynihan, Charles E Argoff

Abstract read
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Article in Pain medicine (Malden, Mass.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Nathaniel M SchusterUC San Diego Health, San Diego, CA, United States.
Sushanth JeyakumarVertex Pharmaceuticals Incorporated, Boston, MA, United States.
Ann M MenzieVertex Pharmaceuticals Incorporated, Boston, MA, United States.ORCID 0000-0002-6394-2914
Moeen PanniVertex Pharmaceuticals Incorporated, Boston, MA, United States.
Nicole PrincicMarketScan by Merative, Ann Arbor, MI, United States.
Meghan MoynihanMarketScan by Merative, Ann Arbor, MI, United States.
Charles E ArgoffAlbany Medical College, Albany, NY, United States.

Funding

Vertex Pharmaceuticals Incorporated
6 · The paper itself

Abstract

objectiveThis study analyzes real-world treatment patterns among patients newly initiating treatment for painful diabetic peripheral neuropathy using a contemporary dataset in the United States.

methodsA retrospective study using the MarketScan database (January 1, 2016, to June 30, 2023) identified adults newly prescribed pain medication(s) used to treat neuropathic pain within 60 days of a diabetic peripheral neuropathy diagnosis. Patients with prior medication, conditions with similar treatment indications, cancer, or major surgery were excluded. Treatment patterns over a 12-month period and variable-length follow-up (four sequential treatment episodes) were captured, including treatment type, dosage, adherence, discontinuation (≥90-day gap), and switching.

resultsAmong 22 955 patients identified, 98.5% initiated monotherapy treatment for painful diabetic peripheral neuropathy. The majority initiated treatment with gabapentinoids (gabapentin 59.0%; pregabalin 5.3%), followed by opioids (tramadol 15.1%, oxycodone 7.0%), and antidepressants (duloxetine 5.2%). Among patients initiating gabapentin, pregabalin, or duloxetine, most were prescribed daily doses below recommended levels (79% gabapentin, 91% pregabalin, 61% duloxetine), and the majority (81%-96%) did not increase their dose. Adherence was low. Over 50% discontinued their initial treatment within 3 months, and approximately 75% discontinued in the 12-month follow-up period, with fewer than 25% switching to another medication. When evaluating treatment patterns across sequential treatment episodes, almost 65% discontinued all pain medications and did not receive subsequent treatment by the fourth treatment episode.

conclusionsHigh rates of treatment discontinuation and suboptimal adherence likely indicate challenges with tolerability and insufficient pain relief associated with current therapies for painful diabetic neuropathy. These findings emphasize the limitations of existing treatment options and highlight the unmet need for more effective and better-tolerated treatments for these patients.

Indexed as

AnalgesicsDiabetic NeuropathiesNeuralgiaPractice Patterns, Physicians'AdultAgedAnalgesics, OpioidDuloxetine HydrochlorideFemaleGabapentinHumansMaleMiddle AgedPregabalinRetrospective StudiesUnited StatesAnalgesicsAnalgesics, OpioidDuloxetine HydrochlorideGabapentinPregabalindiabetic neuropathydrug therapyhealthcare administrative claimsmedication adherenceneuropathic pain

Identifiers

PMID42015888
PMCPMC13537738

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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.