Evidence map›Paper›PMID 32495116›Full record

ArticleJournal of medical toxicology : official journal of the American College of Medical Toxicology2020

Effect of Methylene Blue on a Porcine Model of Amlodipine Toxicity.

Jenna M LeRoy, Sean P Boley, Justin N Corcoran, Kristin M Engebretsen, Samuel J Stellpflug

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of medical toxicology : official journal of the American College of Medical Toxicology, 2020. 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
0.7field-weighted citation impact, top 28% 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, 9 citations in OpenAlex.

  1. Use of Methylene Blue to Treat Hypotension in Poisoned Patients in the Toxicology Investigators Consortium (ToxIC) Core Registry: 2016-2023.Journal of medical toxicology : official journal of the American College of Medical Toxicology · 2026
    Article
  2. A Case of Angiotensin II Utilization for Refractory Shock in a Polysubstance Overdose.Journal of medical toxicology : official journal of the American College of Medical Toxicology · 2025
    Article
  3. Methylene Blue-Induced Serotonin Toxicity: Case Files of the Medical Toxicology Fellowship at the New York City Poison Control Center.Journal of medical toxicology : official journal of the American College of Medical Toxicology · 2024
    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

5 authors at 2 institutions in 1 country.

Jenna M LeRoyDepartment of Emergency Medicine, Regions Hospital, Saint Paul, MN, USA. jennaleroy3@gmail.com.ORCID http://orcid.org/0000-0003-0634-0287
Sean P BoleyDepartment of Emergency Medicine, United Hospital, Saint Paul, MN, USA.
Justin N CorcoranDepartment of Emergency Medicine, Regions Hospital, Saint Paul, MN, USA.
Kristin M EngebretsenDepartment of Emergency Medicine, Regions Hospital, Saint Paul, MN, USA.
Samuel J StellpflugDepartment of Emergency Medicine, Regions Hospital, Saint Paul, MN, USA.
Regions Hospital · USUnited Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCalcium channel blocker (CCB) overdoses cause significant morbidity and mortality. Dihydropyridine CCBs cause peripheral vascular dilation and at high doses cardiac dysfunction. Amlodipine, a dihydropyridine, causes peripheral vasodilation from release of nitric oxide (NO) in addition to calcium channel blockade; NO scavenging is a potential treatment. Methylene blue (MB) inhibits NO directly and inhibits NO production. We compared the effects of MB versus norepinephrine (NE), with time to death as the primary outcome, in a porcine amlodipine toxicity model.

methodsAnimals were anesthetized and instrumented, and an amlodipine infusion was administered to mimic oral overdose. After 70 minutes, each group was resuscitated with normal saline. Animals in each group were then randomized to receive either MB or NE. Hemodynamic parameters, including mean arterial pressure and cardiac output, were recorded every 10 minutes. The primary outcome was survival time (Kaplan-Meier analysis and log-rank test).

resultsInterim analysis after 15 animals (7 MB, 8 NE) revealed that MB was clearly not superior to NE. Overall, 1 of 7 animals in the MB group survived to 300 minutes compared with 2 of 8 animals in the NE group. The median survival time was 100 minutes for the MB group and 177 minutes for the NE group. Survival time did not differ by group (log-rank test p = 0.29).

conclusionIn this porcine model of amlodipine toxicity, methylene blue did not improve survival time compared with norepinephrine. Whether methylene blue is beneficial in combatting distributive shock in amlodipine toxicity remains unclear and requires further study.

Indexed as

AmlodipineAnimalsAntidotesCardiotoxicityCardiovascular DiseasesCardiovascular SystemDisease Models, AnimalHemodynamicsMethylene BlueNorepinephrineSus scrofaTime FactorsAmlodipineAntidotesMethylene BlueNorepinephrineAmlodipineCardiovascular toxinMethylene blueOverdosePig

Identifiers

PMID32495116
PMCPMC7554284
OpenAlexW3029952120

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.