Evidence map›Paper›PMID 31145103›Full record

ArticleBlood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis2019

Evolving paradigm in thrombophilia screening.

Noman Ashraf, Nathan Visweshwar, Michael Jaglal, Lubomir Sokol, Damian Laber

Open access · hybridAbstract read
In one paragraph

Article in Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Moringa Oleifera leaf extract induced pulmonary embolism-a case report.International journal of emergency medicine · 2022
    Article
  7. The procoagulant status. Hypercoagulability as a risk factor of primary and secondary infertility.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    Article
  8. Review
  9. Hereditary Antithrombin Deficiency in Pediatric Patients: Pathophysiology, Clinical Features, Diagnosis, and Antithrombin Replacement Therapy.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

5 authors at 3 institutions in 1 country.

Noman AshrafHematology/Oncology Section, Department of Hematology, James A. Haley Veterans' Hospital.
Nathan VisweshwarDepartment of Hematology, Morsani College of Medicine, University of South Florida, Tampa, Florida, USA.
Michael JaglalDepartments of Hematology/Medical Oncology, H. Lee Moffitt Cancer Center & Research Institute.
Lubomir SokolDepartments of Hematology/Medical Oncology, H. Lee Moffitt Cancer Center & Research Institute.
Damian LaberDepartments of Hematology/Medical Oncology, H. Lee Moffitt Cancer Center & Research Institute.
Moffitt Cancer Center · USJames A. Haley Veterans' Hospital · USUniversity of South Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

: The role of genetic thrombophilia screening for identifying a hypercoagulable state in the management of venous thromboembolism. We searched MEDLINE and EMBASE from 1995 to 2017, the websites of the professional bodies including American Society of Hematology, British Society of Hematology, International Society of Thrombosis and Hemostasis, College of American Pathologists, American College of Medical Genetics, and American Society of obstetrics and gynecology for their clinical practice guidelines. We used search strategy terms - venous thromboembolism, inherited, thrombophilia, and hypercoagulable state. Thrombophilia screening does not alter management in pregnancy, infertility, recurrent miscarriages, in primary occlusive arterial syndromes, and for primary prevention in relatives of venous thromboembolism patients considering hormonal manipulation including oral contraceptives. Routine thrombophilia screening for identifying a hypercoagulable state is not indicated in venous thromboembolism, as it is only useful in a select group of patients. There is no difference in the treatment of venous thromboembolism in patients with or without an inherited hypercoagulable state.

Indexed as

Disease ManagementFemaleGenetic TestingHumansPregnancyRisk FactorsThrombophiliaVenous Thromboembolism

Identifiers

PMID31145103
PMCPMC6687403
OpenAlexW2946895718

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.