Evidence map›Paper›PMID 38003878›Full record

ReviewJournal of personalized medicine2023

Anomalous Left Coronary Artery from the Pulmonary Artery: How to Diagnose and Treat.

Elaina A Blickenstaff, Sean D Smith, Frank Cetta, Heidi M Connolly, David S Majdalany

Open access · goldAbstract readReview
In one paragraph

Review in Journal of personalized medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

22 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Anomalous Left Coronary Artery From Pulmonary Artery Masquerading as Myocarditis in an Infant: A Case Report.Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc · 2025
    Article
  12. Article
  13. An Uncommon Cause of Angina.Diagnostics (Basel, Switzerland) · 2025
    Article
  14. A 39-year-old women with newly diagnosed ALCAPA syndrome during pregnancy.Clinical research in cardiology : official journal of the German Cardiac Society · 2025
    Article
  15. Article
  16. Article
  17. Article
  18. Article
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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 3 institutions in 1 country.

Elaina A BlickenstaffSchool of Science, Marshall University, Huntington, WV 25755, USA.ORCID 0009-0005-5679-5265
Sean D SmithDivision of Cardiology, Mayo Clinic, Scottsdale, AZ 85259, USA.ORCID 0000-0002-7796-4313
Frank CettaDivision of Cardiology, Mayo Clinic, Rochester, MN 55905, USA.
Heidi M ConnollyDivision of Cardiology, Mayo Clinic, Rochester, MN 55905, USA.
David S MajdalanyDivision of Cardiology, Mayo Clinic, Scottsdale, AZ 85259, USA.ORCID 0000-0002-5472-6689
Mayo Clinic · USMayo Clinic in Arizona · USMarshall University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare coronary anomaly that can present in childhood or adulthood with a multitude of symptoms depending on the age of presentation. It should be suspected in infants presenting with heart failure in the setting of left ventricular systolic dysfunction and associated mitral regurgitation from papillary muscle ischemia. Adults with ALCAPA may present with cardiac ischemic symptoms. Prompt diagnosis with echocardiography and cross-sectional chest imaging is important to guide surgical intervention and improve the patients' survival and prognosis. The goal of surgery is to establish a dual-coronary system with mid-term results revealing progressive recovery of left ventricular function and improvement in mitral regurgitation. Patients with ALCAPA should maintain life-long follow-up with a cardiologist with congenital heart disease expertise for surveillance of post-operative complications.

Indexed as

adult congenital heart diseaseanomalous coronary arteryanomalous left coronary artery from the pulmonary artery (ALCAPA)

Identifiers

PMID38003878
PMCPMC10672344
OpenAlexW4388048869

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.