Evidence map›Paper›PMID 39468095›Full record

ArticleScientific reports2024

Monitoring anti-factor Xa activity in patients with chronic thromboembolic pulmonary hypertension treated with factor Xa inhibitors.

Yoshihisa Nakano, Shiro Adachi, Miku Hirose, Takeshi Adachi, Itsumure Nishiyama, Kenichiro Yasuda, Masahiro Yoshida, Takahisa Kondo, Toyoaki Murohara

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

  1. Pooled it
  2. Review
  3. Expert Opinion on Implementing Oral Anticoagulation Reversal Protocols in US Hospitals.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    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

9 authors.

Yoshihisa NakanoDepartment of Advanced Medicine, Nagoya University Hospital, Nagoya, Japan.
Shiro AdachiDepartment of Cardiology, Nagoya University Hospital, 65 Tsurumai-cho, Shouwa-ku, Nagoya, 466-8560, Japan. adachi.shiro.b6@f.mail.nagoya-u.ac.jp.
Miku HiroseDepartment of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Takeshi AdachiDepartment of Cardiology, Nagoya University Hospital, 65 Tsurumai-cho, Shouwa-ku, Nagoya, 466-8560, Japan.
Itsumure NishiyamaDepartment of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Kenichiro YasudaDepartment of Cardiology, Nagoya University Hospital, 65 Tsurumai-cho, Shouwa-ku, Nagoya, 466-8560, Japan.
Masahiro YoshidaDepartment of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Takahisa KondoDepartment of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Toyoaki MuroharaDepartment of Cardiology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Direct oral anticoagulants (DOACs) have been used clinically in patients with chronic thromboembolic pulmonary hypertension (CTEPH) for secondary prevention after acute venous thromboembolism, although the data are limited. We evaluated the effects of DOACs-especially factor Xa (FXa) inhibitors-by measuring anti-factor Xa activity (AXA). Fifty consecutive CTEPH patients treated with rivaroxaban, apixaban, or edoxaban were enrolled. Heparin-calibrated AXA was measured at peak and trough. The median peak heparin-calibrated AXA across all 50 patients was 1.90 IU/mL and was comparable among the three FXa inhibitors. At trough, heparin-calibrated AXA was significantly higher in apixaban-treated patients (median 0.70 IU/mL) than in those given rivaroxaban (median 0.11 IU/mL) or edoxaban (median 0.11 IU/mL, p < 0.001). Peak heparin-calibrated AXA was significantly lower with reduced-dosage FXa inhibitor (edoxaban 30 mg/day) than with the reference dosage (edoxaban 60 mg/day, apixaban 10 mg/day, or rivaroxaban 15 mg/day, p = 0.01). The heparin-calibrated AXA of both rivaroxaban and apixaban was strongly significantly correlated with the plasma concentration of each drug. The cumulative rate of major and clinically relevant non-major bleeding was significantly higher in patients with peak heparin-calibrated AXA ≥ 2.09 IU/mL. Heparin-calibrated AXA could provide useful information for treating CTEPH patients with FXa inhibitors.

Indexed as

Factor Xa InhibitorsHypertension, PulmonaryPulmonary EmbolismPyrazolesPyridonesRivaroxabanAgedAged, 80 and overChronic DiseaseDrug MonitoringFactor XaFemaleHumansMaleMiddle AgedPyridinesapixabanedoxabanFactor XaFactor Xa InhibitorsPyrazolesPyridinesPyridonesRivaroxabanThiazolesChronic thromboembolic pulmonary hypertensionDirect-acting oral anticoagulant; pulmonary thromboembolismFactor XaPulmonary hypertension

Identifiers

PMID39468095
PMCPMC11519886

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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.