Evidence map›Paper›PMID 39175543›Full record

ArticleFrontiers in pharmacology2024

Long-term efficacy and reduced side-effects of buprenorphine in patients with moderate and severe chronic pain.

Alfonso Papa, Anna Maria Salzano, Maria Teresa Di Dato, Vincenzo Desiderio, Pietro Buonavolontà, Pietro Mango, Elisabetta Saracco, Dario Tammaro, Livio Luongo, Sabatino Maione

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Article in Frontiers in pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

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

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Alfonso PapaDepartment of Pain Management-AO "Ospedale dei Colli"-Monaldi Hospital, Napoli, Italy.
Anna Maria SalzanoDepartment of Pain Management-AO "Ospedale dei Colli"-Monaldi Hospital, Napoli, Italy.
Maria Teresa Di DatoDepartment of Pain Management-AO "Ospedale dei Colli"-Monaldi Hospital, Napoli, Italy.
Vincenzo DesiderioDepartment of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Pietro BuonavolontàDepartment of Pain Management-AO "Ospedale dei Colli"-Monaldi Hospital, Napoli, Italy.
Pietro MangoDepartment of Pain Management-AO "Ospedale dei Colli"-Monaldi Hospital, Napoli, Italy.
Elisabetta SaraccoDepartment of Pain Management-AO "Ospedale dei Colli"-Monaldi Hospital, Napoli, Italy.
Dario TammaroDepartment of Pain Management-AO "Ospedale dei Colli"-Monaldi Hospital, Napoli, Italy.
Livio Luongo *Department of Experimental Medicine, Division of Pharmacology, University of Campania "Luigi Vanvitelli", Naples, Italy.
Sabatino Maione *Department of Experimental Medicine, Division of Pharmacology, University of Campania "Luigi Vanvitelli", Naples, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chronic pain significantly impacts quality of life and poses substantial public health challenges. Buprenorphine, a synthetic analog of thebaine, is recognized for its potential in managing moderate to severe chronic pain with fewer side effects and a lower incidence of tolerance compared to traditional opioids. Objective: This retrospective study aimed to assess the long-term efficacy and safety of buprenorphine transdermal patches in patients with moderate and severe chronic pain, with a focus on pain relief sustainability and tolerance development. Methods: This retrospective observational study involved 246 patients prescribed buprenorphine transdermal patches. We evaluated changes in pain intensity using the Numeric Rating Scale (NRS), assessed opioid tolerance based on FDA guidelines for morphine-equivalent doses, and measured patient-reported outcomes through the Patients' Global Impression of Change (PGIC). Any adverse events were also recorded. Results: Over the 36-month period, there was a significant reduction in NRS scores for both moderate and severe pain patients, demonstrating buprenorphine's sustained analgesic effect. Tolerance measurement indicated that no patients required increases in morphine-equivalent doses that would meet or exceed the FDA's threshold for opioid tolerance (60 mg/day of morphine or equivalent). Additionally, patient satisfaction was high, with the PGIC reflecting significant improvements in pain management and overall wellbeing. The side effects were minimal, with skin reactions and nausea being the most commonly reported but manageable adverse events. Conclusion: The study findings validate the long-term use of buprenorphine transdermal patches as an effective and safe option for chronic pain management, maintaining efficacy without significant tolerance development. These results support the continued and expanded use of buprenorphine in clinical settings, emphasizing its role in reducing the burdens of chronic pain and opioid-related side effects. Further research is encouraged to refine pain management protocols and explore buprenorphine's full potential in diverse patient populations.

Indexed as

chronic painopioid crisisopioidspain relieftolerancetransdermal patches

Identifiers

PMID39175543
PMCPMC11338866

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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.