Evidence map›Paper›PMID 33402927›Full record

ArticleAfrican health sciences2020

Comparative study of hypercoagulability change in steady state and during vaso-occlusive crisis among Sudanese patients living with sickle cell disease.

Elmigdad Abdelgadir Mohamed, Mamoud Mohamed Elgari, Asaad Mohammed Babker, Hisham Ali Waggiallah

Open access · diamondAbstract readComparative Study
In one paragraph

Article in African health sciences, 2020. 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
0.8field-weighted citation impact, top 29% 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, 8 citations in OpenAlex.

  1. Article
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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

4 authors at 4 institutions in 3 countries.

Elmigdad Abdelgadir MohamedAlghad International Colleges for Applied Medical Sciences, Educational and Academic Affairs.
Mamoud Mohamed ElgariTaibah university, college of Applied Medical science, Medical Laboratory Science.
Asaad Mohammed BabkerGulf Medical University, of Medical Laboratories Science.
Hisham Ali WaggiallahPrince Sattam Bin Abdulaziz University College of Applied Medical Sciences, Medical Laboratory Sciences.
Gulf Medical University · AEHodges University · USPrince Sattam Bin Abdulaziz University · SATaibah University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSickle cell disease (SCD) is an inherited blood disorder that affects red blood cells. (SCD) is characterized by recurrent vaso-occlusive crisis (VOC). MATERIAL AND

methodsThis was a descriptive cross sectional study conducted through the period from July 2015 to July 2017 in which a total of seventy two blood specimens were collected in 'EDTA' and citrated vacutainers from Sudanese patients with SCD attending "Fath Elrhman Albasheer" Centre. Both sexes' with different ages were included. Among these samples 49 (68.1%) were in steady state while the remained 23 (31.9%) were in VOC. All samples were tested for coagulation profile.

resultThere was increase in fibrinogen and D-dimer levels in most patients 67% and 71%, respectively. Significant increase in D-dimers was observed in patients with (VOC) compared with steady state (P. value = 0.006). Protein S was significantly increased in males in comparison with females P. value = 0.017. The results of prothrombin time (PT), international normalized ratio (INR) and thrombin time (TT) were within normal range.

conclusionSignificant increase in levels of D-dimer during VOC indicating abnormal coagulation and fibrinolysis activation. Reduced levels of natural anticoagulants proteins C and S can be consider as predictive markers indicate hepatic dysfunction in patients with SCD.

Indexed as

AdultAnemia, Sickle CellBiomarkersCross-Sectional StudiesFemaleFibrin Fibrinogen Degradation ProductsHumansMaleProtein SSudanThrombophiliaBiomarkersFibrin Fibrinogen Degradation Productsfibrin fragment DPROS1 protein, humanProtein ShypercoagulabilitySCDSudanese patientsVOC

Identifiers

PMID33402927
PMCPMC7750086
OpenAlexW3019662369

What OpenQuestion holds

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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.