Evidence map›Paper›PMID 30464403›Full record

ArticleDrug design, development and therapy2018

Efficacy evaluation of reteplase in a novel canine acute pulmonary thromboembolism model developed by minimally invasive surgery and digital subtraction angiography.

Yinbing Zhang, Haifeng Liu, Yingqian Zhang, Qiong Wu, Yanyan Zhang, Jie Zhang, Xiangshan Zhou, He Jiao, Feng Fan, Qi Xue and 2 more

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Animal models of right heart failure.Cardiovascular diagnosis and therapy · 2020
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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

12 authors at 4 institutions in 1 country.

Yinbing ZhangLaboratory of Nonhuman Primate Disease Modeling Research, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China, xin.wang@hcbiomed.com, zhongzhihui@scu.edu.cn.
Haifeng LiuAngde Biotech Pharmaceutical Co., Ltd., Liaocheng, China.
Yingqian ZhangDepartment of Physiology, Southwest Medical University, Luzhou, China.
Qiong WuLaboratory of Nonhuman Primate Disease Modeling Research, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China, xin.wang@hcbiomed.com, zhongzhihui@scu.edu.cn.
Yanyan ZhangLaboratory of Nonhuman Primate Disease Modeling Research, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China, xin.wang@hcbiomed.com, zhongzhihui@scu.edu.cn.
Jie ZhangLaboratory of Nonhuman Primate Disease Modeling Research, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China, xin.wang@hcbiomed.com, zhongzhihui@scu.edu.cn.
Xiangshan ZhouAngde Biotech Pharmaceutical Co., Ltd., Liaocheng, China.
He JiaoDepartment of Interventional therapy, West China Hospital, Sichuan University, Chengdu, China.
Feng FanDepartment of Neurointervention, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Qi XueFood and Drug Administration of Shibei District Government, Qingdao, China.
Xin WangLaboratory of Nonhuman Primate Disease Modeling Research, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China, xin.wang@hcbiomed.com, zhongzhihui@scu.edu.cn.
Zhihui ZhongLaboratory of Nonhuman Primate Disease Modeling Research, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China, xin.wang@hcbiomed.com, zhongzhihui@scu.edu.cn.
Sichuan University · CNSouthwest Medical University · CNState Key Laboratory of BiotherapyFirst Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIn order to evaluate the thrombolytic effects of reteplase in pulmonary thromboembolism (PTE), we developed a novel canine PTE model. The efficacy of reteplase against PTE in comparison to alteplase was clarified for the first time, and this PTE model could be further applied to studies of novel thrombolytic therapies. PATIENTS AND

methodsTwenty-four dogs were divided into four groups: sham operation, vehicle, alteplase, and reteplase. Autologous thrombi/saline were injected into the pulmonary artery, and thrombolytic agents were administrated. Thrombus formation and dissolution were monitored by real-time digital subtraction angiography (DSA), and pulmonary pressures were measured simultaneously. Blood coagulation, blood gas, hematology, and histopathologic examinations were used as subsidiary methods.

resultsThe canine PTE model was established with a significant decrease of blood flow and ~75% blocking area. Administration of reteplase (0.6 mg/kg) resulted in effective thrombus dissolution with a recovery of over 80% blood flow, as effective as alteplase (1.6 mg/kg). Correspondingly, the elevated pulmonary systolic, diastolic, and mean arterial pressures declined to the normal level. Blood coagulation was changed by reteplase, with a dramatic elongation of prothrombin time, activated partial thromboplastin time, and thrombin time, even longer than alteplase. In contrast to the vehicle group, no obvious pathological changes were found in the two thrombolytic groups. Hematological, blood biochemical, and blood gas results also indicated that reteplase had no adverse reactions in this PTE model.

conclusionReteplase proved to be an effective and safe therapy for PTE for the first time, and a small dosage of reteplase exerted an efficacy comparable to the routine dosage of alteplase. Our findings indicated the potential of reteplase as clinical treatment against PTE. This technically innovative, stability- and validity-proved canine PTE model developed by minimally invasive surgery and DSA resembled major clinical features. This may further facilitate our understanding of thrombotic disorders and development of prophylactic and therapeutic approaches.

Indexed as

Angiography, Digital SubtractionDisease Models, AnimalThrombolytic TherapyAnimalsDogsFemaleFibrinolytic AgentsInjections, IntravenousMalePulmonary EmbolismRecombinant ProteinsTissue Plasminogen ActivatorFibrinolytic AgentsRecombinant ProteinsreteplaseTissue Plasminogen Activatorcanine pulmonary thromboembolism modelreteplasethrombolytic therapy

Identifiers

PMID30464403
PMCPMC6219412
OpenAlexW2899375327

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.