Evidence mapPaperPMID 41210669Full record

ReviewThe International journal of angiology : official publication of the International College of Angiology, Inc2025

Medical Management of Coronary Artery Disease: An Update.

Darshan Hullon, Mohammad Bilal, Nicolas W Shammas

Abstract readReview
In one paragraph

Review in The International journal of angiology : official publication of the International College of Angiology, Inc, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  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

3 authors.

Darshan HullonDepartment of Internal Medicine, MercyOne Clinton Medical Center, Clinton, Iowa.
Mohammad BilalDepartment of Internal Medicine, Tower Health Phoenixville, Phoenixville, Pennsylvania.
Nicolas W ShammasMidwest Cardiovascular Research Foundation, Davenport, Iowa.ORCID 0000-0001-8279-0111

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic coronary artery disease (CAD) remains a leading cause of global morbidity and mortality, necessitating a nuanced approach to long-term management. While revascularization strategies play a crucial role in select high-risk patients, optimal medical therapy (OMT) is the foundation of care for most individuals with stable disease. This review critically appraises contemporary pharmacological strategies for CAD, integrating the latest information from randomized trials and guideline-directed recommendations. Antihypertensive therapy, particularly renin-angiotensin system inhibitors and beta-blockers, remains central to reducing myocardial workload and preventing adverse cardiovascular events. Lipid-lowering agents, including high-intensity statins, ezetimibe, PCSK9 inhibitors, and inclisiran, have redefined risk stratification by demonstrating incremental reductions in low-density lipoprotein and atherosclerotic progression and event recurrence. The emergence of novel antidiabetic agents-SGLT2 inhibitors and GLP-1 receptor agonists-has expanded the therapeutic landscape, offering cardioprotective benefits independent of glycemic control. Additionally, the growing recognition of inflammation as a driver of CAD progression has led to the exploration of anti-inflammatory agents such as colchicine and interleukin-1 beta inhibitors. Landmark trials, including COURAGE, ISCHEMIA, and FREEDOM, reaffirm the noninferiority of OMT to revascularization in stable CAD, underscoring the need for an individualized approach. Future directions encompass precision medicine, artificial intelligence-driven risk stratification, and gene-based interventions, which may redefine therapeutic paradigms in CAD management.

Indexed as

cardiovascular riskchronic coronary artery diseaseinflammationlipid-lowering therapymedical managementprecision medicine

Identifiers

PMID41210669
PMCPMC12591713

What Socratic 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 Socratic graph.