Evidence map›Paper›PMID 40182387›Full record

ReviewCureus2025

Efficacy of Thromboprophylaxis in Preventing Thrombotic Events in Pediatric Patients With COVID-19 or Multisystem Inflammatory Syndrome: A Systematic Review.

Jaqueline L Castillo, Andrea Medel Sánchez, Danna M Miranda Lugo, Natalia Núñez Muratalla, Cristina P Agredano Chávez, Juan M Cervantes Carrillo, Gabriela V Martínez Sánchez, Mildred Rios Torres, Karina Aguilar García, Lilia Rubio Alfaro and 2 more

Abstract readReview
In one paragraph

Review in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. 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

12 authors.

Jaqueline L CastilloGeneral Medicine, Universidad Autónoma de Guadalajara, Guadalajara, MEX.
Andrea Medel SánchezGeneral Practice, Universidad de Guanajuato, León, MEX.
Danna M Miranda LugoGeneral Practice, Universidad Nacional Autónoma de México, Mexico City, MEX.
Natalia Núñez MuratallaGeneral Medicine, Universidad Autónoma de Guadalajara, Guadalajara, MEX.
Cristina P Agredano ChávezGeneral Medicine, Universidad de Colima, Colima, MEX.
Juan M Cervantes CarrilloGeneral Medicine, Universidad Autónoma de Guadalajara, Guadalajara, MEX.
Gabriela V Martínez SánchezGeneral Medicine, Universidad Autónoma de Guadalajara, Guadalajara, MEX.
Mildred Rios TorresGeneral Practice, Benemérita Universidad Autónoma de Puebla, Puebla, MEX.
Karina Aguilar GarcíaGeneral Medicine, Tecnológico de Monterrey, Mexico City, MEX.
Lilia Rubio AlfaroGeneral Medicine, Universidad Autónoma de Chihuahua, Chihuahua, MEX.
Mauricio Montelongo QuevedoGeneral Medicine, Universidad Autónoma de Guadalajara, Guadalajara, MEX.
Jose R Flores ValdésGeneral Practice, Oncology Consultants PA, Houston, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The COVID-19 pandemic has been associated with a broad spectrum of clinical manifestations, including multisystem inflammatory syndrome in children (MIS-C), a rare but serious condition characterized by a proinflammatory and hypercoagulable state. MIS-C has been linked to an elevated risk of venous thromboembolism (VTE), necessitating a focus on thromboprophylaxis to prevent potentially fatal complications in pediatric patients. This systematic review aims to evaluate the association between COVID-19/MIS-C and thromboembolism and to assess the efficacy of thromboprophylaxis protocols in reducing thrombotic events and mortality in children. A systematic review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 guidelines. Literature searches were performed in PubMed, Cochrane, and Science Direct databases. Randomized controlled trials, cohort studies, and case-control studies reporting on thromboprophylaxis, thrombotic events, and associated outcomes in pediatric patients (<21 years) with COVID-19 and/or MIS-C were included. The Newcastle-Ottawa Scale was used to assess the quality of included studies. Primary outcomes were the incidence of thrombotic events and mortality, while secondary outcomes included bleeding events, clinical recovery, and changes in coagulation markers. Of the 375 articles identified, three studies (n=771 patients) met the inclusion criteria. Thromboprophylaxis protocols primarily included low molecular weight heparin (LMWH) such as enoxaparin and antiplatelet agents such as aspirin, with varied doses and treatment durations. Thrombotic events were reported in 3.3% of patients, with a higher incidence in MIS-C cases compared to COVID-19 alone. Prophylactic anticoagulation was effective in preventing thrombotic events in high-risk patients without increasing the risk of major bleeding. The studies emphasized individualized treatment approaches based on risk factors such as elevated D-dimer levels, obesity, prolonged immobilization, and central venous catheter presence. All studies reported a low mortality rate, ranging from 0% to 2.2%, highlighting the potential benefit of thromboprophylaxis in this population. Pediatric patients with MIS-C or severe COVID-19 are at an increased risk of thrombotic complications due to their heightened proinflammatory and hypercoagulable states. Thromboprophylaxis using enoxaparin and aspirin appears effective in reducing thrombotic events and mortality in these patients. Individualized protocols based on clinical risk factors and D-dimer levels are critical to optimizing outcomes while minimizing bleeding risks. Standardized, evidence-based guidelines are needed to refine thromboprophylaxis strategies and determine the optimal duration of therapy in this vulnerable population. Further research is essential to better understand the role of coagulation markers in guiding treatment cessation and improving outcomes.

Indexed as

covid-19mis-cpediatricthromboprophylaxisthrombosis

Identifiers

PMID40182387
PMCPMC11966085

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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.