Evidence map›Paper›PMID 37505425›Full record

ArticleCNS drugs2023

The Utilization of Low Dose Naltrexone for Chronic Pain.

Salomon Poliwoda, Bryant Noss, Gia Thinh D Truong, Zachary A Creech, Sarang S Koushik, Ivan Urits, Omar Viswanath

Abstract read
PubMed Publisher
In one paragraph

Article in CNS drugs, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
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

7 authors at 3 institutions in 1 country.

Salomon PoliwodaDepartment of Anesthesiology, Mount Sinai Medical Center, 4300 Alton Road, Miami Beach, FL, USA. Salomon.pb@gmail.com.
Bryant NossCreighton University School of Medicine Phoenix, Phoenix, AZ, USA.
Gia Thinh D TruongCreighton University School of Medicine Phoenix, Phoenix, AZ, USA.
Zachary A CreechCreighton University School of Medicine Phoenix, Phoenix, AZ, USA.
Sarang S KoushikDepartment of Anesthesiology and Pain Medicine, Valleywise Health Medical Center, Creighton University School of Medicine Phoenix, Phoenix, AZ, USA.
Ivan UritsDepartment of Anesthesiology, Louisiana State University Health Shreveport, Shreveport, LA, USA.
Omar ViswanathInnovative Pain and Wellness, Scottsdale, AZ, USA.ORCID 0000-0001-9273-9782
Creighton University · USLouisiana State University in Shreveport · USMount Sinai Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Naltrexone is a mu-opioid receptor antagonist with a long half-life compared with naloxone. Both of these drugs, along with others, were developed with the intention of reversing the effects of opioid abuse or toxicity. Evidence has also shown that naltrexone has a benefit in preventing relapse by reducing opioid cravings and reducing symptoms of opioid withdrawal. The benefits of this drug were not only shown with opioid abuse. In 1984 this drug was also approved for alcohol abuse. Naltrexone has been proven to decrease alcohol relapse by decreasing the craving. Apart from these approved indications for the use of naltrexone, with time, it has been seen that this drug has a benefit in treating chronic pain. A number of studies have shown the benefits of this drug with inflammatory bowel disease, fibromyalgia, multiple sclerosis, diabetic neuropathy, and complex regional pain syndrome, among others. More studies are needed to approve this medication for specific chronic pain conditions.

Indexed as

Chronic PainOpioid-Related DisordersAnalgesics, OpioidChronic DiseaseHumansNaltrexoneNarcotic AntagonistsRecurrenceAnalgesics, OpioidNaltrexoneNarcotic Antagonists

Identifiers

PMID37505425
OpenAlexW4385330807

What OpenQuestion holds

Textmetadata
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.