Evidence map›Paper›PMID 31931842›Full record

ArticleJournal of cardiothoracic surgery2020

Adult ALCAPA: from histological picture to clinical features.

Hiroshi Kubota, Hidehito Endo, Hikaru Ishii, Hiroshi Tsuchiya, Yusuke Inaba, Katsunari Terakawa, Yu Takahashi, Mio Noma, Kazuya Takemoto, Seiichi Taniai and 12 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of cardiothoracic surgery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

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  10. Clinical manifestations and computed tomography angiography features of anomalous left coronary artery from the pulmonary artery syndrome.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2023
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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

22 authors at 7 institutions in 1 country.

Hiroshi KubotaDepartment of Cardiovascular Surgery, Kyorin University, 6-20-2, Shinkawa, Mitaka, Tokyo, 181-8611, Japan. kub@ks.kyorin-u.ac.jp.ORCID http://orcid.org/0000-0002-0036-2226
Hidehito EndoDepartment of Cardiovascular Surgery, Kyorin University, 6-20-2, Shinkawa, Mitaka, Tokyo, 181-8611, Japan.
Hikaru IshiiDepartment of Cardiovascular Surgery, Kyorin University, 6-20-2, Shinkawa, Mitaka, Tokyo, 181-8611, Japan.
Hiroshi TsuchiyaDepartment of Cardiovascular Surgery, Kyorin University, 6-20-2, Shinkawa, Mitaka, Tokyo, 181-8611, Japan.
Yusuke InabaDepartment of Cardiovascular Surgery, Kyorin University, 6-20-2, Shinkawa, Mitaka, Tokyo, 181-8611, Japan.
Katsunari TerakawaDepartment of Cardiac Surgery, University of Tokyo, Tokyo, Japan.
Yu TakahashiDepartment of Cardiovascular Surgery, National Disaster Medical Center, Tachikawa, Japan.
Mio NomaDepartment of Cardiovascular Surgery, Tokyo Metropolitan Children's Medical Center, Fuchu, Japan.
Kazuya TakemotoDepartment of Internal Medicine, Jyukoukai Hospital, Miyoshi, Japan.
Seiichi TaniaiDepartment of Cardiology, Kyorin University, Mitaka, Japan.
Konomi SakataDepartment of Cardiology, Kyorin University, Mitaka, Japan.
Kyoko SoejimaDepartment of Cardiology, Kyorin University, Mitaka, Japan.
Hiroaki ShimoyamadaDepartment of Pathology, Kyorin University, Mitaka, Japan.
Hiroshi KammaDepartment of Pathology, Kyorin University, Mitaka, Japan.
Hayato KawakamiDepartment of Anatomy, Kyorin University, Mitaka, Japan.
Yukihiro KanekoDepartment of Cardiovascular Surgery, National Center for Child Health and Development, Tokyo, Japan.
Satoru HironoDepartment of Cardiovascular Biology and Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Daisuke IzumiDepartment of Cardiovascular Biology and Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Kazuyuki OzakiDepartment of Cardiovascular Biology and Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Tohru MinaminoDepartment of Cardiovascular Biology and Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Hideaki YoshinoJiseikai Nomura Hospital, Mitaka, Japan.
Kenichi SudoJiseikai Nomura Hospital, Mitaka, Japan.
Kyorin University · JPNiigata University · JPKawamura Hospital · JPNational Center For Child Health and Development · JPNational Disaster Medical Center · JPThe University of Tokyo · JPTokyo Metropolitan Children's Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAnomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital coronary anomaly that results in high mortality if left untreated. Our aim was to extend our knowledge of the histological, angiographic, and clinical characteristics of ALCAPA in order to deepen our understanding of this rare entity. CASE PRESENTATION: We were involved in the assessment, treatment, and pathological evaluation of two adult ALCAPA patients who were rescued from ventricular fibrillation and then surgically treated to establish a dual coronary artery system. Histological studies indicated various chronic ischemic changes in the myocardium, patchy fibrosis, and severely thickened arteriolar walls in both ventricles. The first patient is alive and well 11.5 years after surgical correction without any implantable cardioverter defibrillator (ICD) activations. The second patient required re-do surgery 9 months after the initial operation but subsequently died. Histologically, chronic ischemic alteration of the myocardium and thickened arteriolar walls persisted even after surgical correction, and coronary angiography (CAG) showed an extremely slow flow phenomenon even after surgical correction in both patients. The average postoperative opacification rate in the first case was 7.36 + 1.12 (n = 2) in the RCA, 3.81 + 0.51 (n = 3) in the left anterior descending (LAD) artery, and 4.08 + 0.27 (n = 4) in the left circumflex (LCx) artery. The slow flow phenomenon may represent persistent high arteriolar resistance in both ventricles.

conclusionsSeldom reported or new findings in adult ALCAPA were identified in two cases. More frequent diagnosis of adult ALCAPA can be expected because of the widespread availability of resuscitation and more advanced diagnostic modalities. Accumulation of pathological and clinical findings and confirmation of the long-term follow-up results after treatment may contribute to expanding our knowledge of this rare entity and establishing optimal treatment.

Indexed as

Anomalous Left Coronary ArteryBland White Garland SyndromeAdultCardiac Surgical ProceduresCoronary Vessel AnomaliesHumansMaleMiddle AgedPulmonary ArteryALCAPABWG syndromeCardiac pathologyCongenital heart diseaseCoronary angiographyICD implantationSlow flow phenomenonSudden deathVentricular arterioleVentricular fibrillation

Identifiers

PMID31931842
PMCPMC6958604
OpenAlexW3005234937

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.