Evidence map›Paper›PMID 37244209›Full record

SynthesisJournal of critical care2023

Optimal dosing of heparin for prophylactic anticoagulation in critically ill COVID-19 patients a systematic review and meta-analysis of randomized controlled trials.

Luana C M G Bonfim, Isadora S Guerini, Marjorie G Zambon, Gabriela B Pires, Amanda C F Silva, André L N Gobatto, Marcela A Lopes, Shari B Brosnahan

Open access · greenAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Journal of critical care, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 6 institutions in 2 countries.

Luana C M G BonfimDepartment of Medicine, University of South Santa Catarina, Florianópolis, SC, Brazil. Electronic address: luanacarolinemgb@gmail.com.
Isadora S GueriniDepartment of Medicine, State University of Western Paraná, Francisco Beltrão, PR, Brazil.
Marjorie G ZambonDepartment of Medicine, Mackenzie Evangelical University Hospital, Curitiba, PR, Brazil.
Gabriela B PiresDepartment of Medicine, School of Medicine Souza Marques, Rio de Janeiro, RJ, Brazil.
Amanda C F SilvaDepartment of Medicine, Federal University of Santa Catarina, Florianópolis, SC, Brazil.
André L N GobattoDepartment of Critical Care, São Rafael Hospital, Salvador, Bahia, Brazil; Department of Critical Care, Hospital da Cidade, Salvador, Bahia, Brazil.
Marcela A LopesDepartment of Critical Care, Hospital da Cidade, Salvador, Bahia, Brazil.
Shari B BrosnahanDepartment of Pulmonary and Critical Care, New York University School of Medicine, New York, NY, USA.
Fundação Técnico Educacional Souza Marques · BRHospital São Rafael · BRHospital Universitário Evangélico de Curitiba · BRNew York University · USUniversidade do Sul de Santa Catarina · BRUniversidade Federal de Santa Catarina · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe optimal amount of anticoagulation for critically ill COVID-19 patients is controversial. Therefore, we aimed to evaluate the efficacy and safety of escalated doses of anticoagulation in critically ill patients with severe COVID-19. MATERIALS AND

methodsWe conducted a systematic search of three major databases, including PubMed, Cochrane Library, and Embase, from inception to May 2022. Randomized controlled trials (RCTs) were included comparing therapeutic or intermediate doses to standard prophylactic doses of anticoagulants in critically ill COVID-19 patients, with heparins as the only anticoagulation therapy considered.

resultsOut of the six RCTs, 2130 patients were administered escalated dose anticoagulation (50.2%) and standard thromboprophylaxis therapy (49.8%). The escalated dose showed no significant impact on mortality (RR, 1.01; 95% CI, 0.90-1.13). Although there was no significant difference in DVT (RR, 0.81; 95% CI, 0.61-1.08), the risk of PE was significantly reduced in patients receiving escalated dose anticoagulation (RR, 0.35; 95% CI, 0.21-0.60), with an increased risk of bleeding events (RR, 1.65; 95% CI, 1.08-2.53).

conclusionThis systematic review and meta-analysis fail to support escalated anticoagulation doses to reduce mortality in critically ill COVID-19 patients. However, higher doses of anticoagulants appear to reduce thrombotic events while increasing the risk of bleeding effectively.

Indexed as

COVID-19NeoplasmsVenous ThromboembolismAnticoagulantsCritical IllnessHemorrhageHeparinHeparin, Low-Molecular-WeightHumansRandomized Controlled Trials as TopicAnticoagulantsHeparinHeparin, Low-Molecular-WeightAnticoagulantsBleedingCOVID-19Critical careHeparinHypercoagulabilityIntensive care unitmeta-analysisMortalitySafetySARS-CoV2Venous thromboembolism

Identifiers

PMID37244209
PMCPMC10211463
OpenAlexW4378189828

What OpenQuestion holds

Textmetadata
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.