Evidence map›Paper›PMID 37233171›Full record

ArticleJournal of cardiovascular development and disease2023

Feasibility of Short-Term Aggressive Lipid-Lowering Therapy with the PCSK9 Antibody in Acute Coronary Syndrome.

Satoshi Yamashita, Atsushi Sakamoto, Satoshi Shoji, Yoshitaka Kawaguchi, Yasushi Wakabayashi, Masaki Matsunaga, Kiyohisa Suguro, Yuji Matsumoto, Hiroyuki Takase, Tomoya Onodera and 13 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cardiovascular development and disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 3 pooled it
1.6field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 3 syntheses or guidelines pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Review
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

23 authors at 12 institutions in 1 country.

Satoshi YamashitaDivision of Cardiology, Internal Medicine III, Hamamatsu University School of Medicine, Hamamatsu 4313192, Japan.
Atsushi SakamotoDivision of Cardiology, Internal Medicine III, Hamamatsu University School of Medicine, Hamamatsu 4313192, Japan.
Satoshi ShojiDepartment of Cardiology, Hino Municipal Hospital, Hino 1910062, Japan.ORCID 0000-0002-2223-7215
Yoshitaka KawaguchiDepartment of Cardiology, Seirei Mikatahara Hospital, Hamamatsu 4338558, Japan.
Yasushi WakabayashiDepartment of Cardiology, Seirei Mikatahara Hospital, Hamamatsu 4338558, Japan.
Masaki MatsunagaDepartment of Cardiology, Iwata City Hospital, Iwata 4388550, Japan.
Kiyohisa SuguroDepartment of Cardiology, Fujinomiya City Hospital, Fujinomiya 4180076, Japan.
Yuji MatsumotoDepartment of Cardiology, Kikugawa City Hospital, Kikugawa 4390022, Japan.
Hiroyuki TakaseDepartment of Internal Medicine, Enshu Hospital, Hamamatsu 4300929, Japan.
Tomoya OnoderaDepartment of Cardiology, Shizuoka City Shizuoka Hospital, Shizuoka 4208630, Japan.
Kei TawaraharaDepartment of Cardiology, Hamamatsu Red Cross Hospital, Hamamatsu 4348533, Japan.
Masahiro MutoDepartment of Cardiology, Hamamatsu Medical Center, Hamamatsu 4328580, Japan.
Yasutaka ShirasakiShirasaki Clinic, Kuki 3460031, Japan.
Hideki KatohDepartment of Cardiology, Kosai General Hospital, Kosai 4310431, Japan.
Makoto SanoDivision of Cardiology, Internal Medicine III, Hamamatsu University School of Medicine, Hamamatsu 4313192, Japan.
Kenichiro SuwaDivision of Cardiology, Internal Medicine III, Hamamatsu University School of Medicine, Hamamatsu 4313192, Japan.ORCID 0000-0001-6934-7932
Yoshihisa NaruseDivision of Cardiology, Internal Medicine III, Hamamatsu University School of Medicine, Hamamatsu 4313192, Japan.ORCID 0000-0001-9630-951X
Hayato OhtaniDivision of Cardiology, Internal Medicine III, Hamamatsu University School of Medicine, Hamamatsu 4313192, Japan.
Masao SaotomeDivision of Cardiology, Internal Medicine III, Hamamatsu University School of Medicine, Hamamatsu 4313192, Japan.ORCID 0000-0001-6197-1669
Tsuyoshi UrushidaDivision of Cardiology, Internal Medicine III, Hamamatsu University School of Medicine, Hamamatsu 4313192, Japan.
Shun KohsakaDepartment of Cardiology, Keio University School of Medicine, Tokyo 1608582, Japan.ORCID 0000-0003-3779-2972
Eisaku OkadaDepartment of Faculty of Social Policy and Administration, Hosei University, Tokyo 1028160, Japan.
Yuichiro MaekawaDivision of Cardiology, Internal Medicine III, Hamamatsu University School of Medicine, Hamamatsu 4313192, Japan.
Hamamatsu University School of Medicine · JPHamamatsu Medical Center · JPHosei University · JPIwata City Hospital · JPJA Shizuoka Koseiren ENSHU hospital · JPKansai Electric Power (Japan) · JPKeio University · JPMorinomiya Hospital · JPNagano Municipal Hospital · JPSasaki Institute · JPShizuoka City Hospital · JPTakamatsu Red Cross Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe guideline-recommended low-density lipoprotein cholesterol target level of <70 mg/dL may not be achieved with statin administration in some patients with acute coronary syndrome (ACS). Therefore, the proprotein convertase subtilisin-kexin type 9 (PCSK9) antibody can be added to high-risk patients with ACS. Nevertheless, the optimal duration of PCSK9 antibody administration remains unclear. METHODS AND

resultsPatients were randomized to receive either 3 months of lipid lowering therapy (LLT) with the PCSK9 antibody followed by conventional LLT (with-PCSK9-antibody group) or 12 months of conventional LLT alone (without-PCSK9-antibody group). The primary endpoint was the composite of all-cause death, myocardial infarction, stroke, unstable angina, and ischemia-driven revascularization. A total of 124 patients treated with percutaneous coronary intervention (PCI) were randomly assigned to the two groups (n = 62 in each). The primary composite outcome occurred in 9.7% and 14.5% of the patients in the with- and without-PCSK9-antibody groups, respectively (hazard ratio: 0.70; 95% confidence interval: 0.25 to 1.97;

conclusionsIn ACS patients who underwent PCI, short-term PCSK9 antibody therapy with conventional LLT was feasible in this pilot clinical trial. Long-term follow-up in a larger scale clinical trial is warranted.

Indexed as

acute coronary syndromelipid-lowering therapylow-density lipoprotein cholesterolPCSK9 antibody

Identifiers

PMID37233171
PMCPMC10219227
OpenAlexW4376115119

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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.