Evidence map›Paper›PMID 35642281›Full record

Trial reportThrombosis and haemostasis2022

Continuous Infusion of Factor VIII and von Willebrand Factor in Surgery: Trials with pdFVIII LFB or pdVWF LFB in Patients with Bleeding Disorders.

Jerzy Windyga, Benoît Guillet, Lucia Rugeri, Alexandra Fournel, Ewa Stefanska-Windyga, Valérie Chamouard, Sonia Pujol, Céline Henriet, Françoise Bridey, Claude Négrier

Open access · hybridAbstract readClinical Trial, Phase III
In one paragraph

Trial report in Thrombosis and haemostasis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 5 institutions in 2 countries.

Jerzy WindygaDepartment of Hemostasis Disorders and Internal Medicine, Laboratory of Hemostasis and Metabolic Diseases, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.
Benoît GuilletDepartment of Hemophilia Treatment, CHU Rennes, University of Rennes, Inserm, EHESP, IRSET (Institut de recherche en santé, environnement et travail) - UMR_S 1085, F-35000 Rennes, France.
Lucia RugeriHematology Division, Hemophilia Comprehensive Care Center, Hôpital Louis Pradel, Hospices Civils de Lyon, Bron, Université Claude Bernard, Lyon, France.ORCID 0000-0002-3103-1737
Alexandra FournelHematology Department, CHRU Besançon, France.
Ewa Stefanska-WindygaDepartment of Hemostasis Disorders and Internal Medicine, Laboratory of Hemostasis and Metabolic Diseases, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.
Valérie ChamouardHematology Division, Hemophilia Comprehensive Care Center, Hôpital Louis Pradel, Hospices Civils de Lyon, Bron, Université Claude Bernard, Lyon, France.
Sonia PujolClinical Development, Laboratoire français du Fractionnement et des Biotechnologies (LFB), Les Ulis, France.
Céline HenrietClinical Development, Laboratoire français du Fractionnement et des Biotechnologies (LFB), Les Ulis, France.ORCID 0000-0002-7796-1569
Françoise BrideyFormerly Clinical Development, LFB, Les Ulis, France.
Claude NégrierHematology Division, Hemophilia Comprehensive Care Center, Hôpital Louis Pradel, Hospices Civils de Lyon, Bron, Université Claude Bernard, Lyon, France.
LFB (France) · FRUniversité Claude Bernard Lyon 1 · FRInstytut Hematologii i Transfuzjologi · PLCentre Hospitalier Universitaire de Besançon · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA plasma-derived factor VIII product (pdFVIII; Factane 100 or 200 IU/mL) and a plasma-derived von Willebrand factor product (pdVWF; Wilfactin 100 IU/mL) are approved for replacement therapy by intravenous bolus injections in hemophilia A (HA) and von Willebrand disease (VWD), respectively. However, in situations requiring intensive treatment, continuous infusion (CI) may be desirable to better control target plasma factor levels.

aimTo evaluate the perioperative hemostatic efficacy and safety of these concentrates administered by CI.

methodsThree phase III trials were conducted. Adults with HA (FVIII:C < 1%) (studies 1 and 2) or VWD (VWF:RCo < 20%) (Study 3) received a preoperative bolus followed by CI of undiluted concentrate for at least 6 days. Bolus doses and CI rates were based on individual recovery and clearance, respectively. The initial infusion rate had to be higher for 48 hours for HA and 24 hours for VWD patients to anticipate potential fluctuations of factor concentrations during major surgery. Target levels of FVIII:C in HA and VWF:RCo in VWD were 80 and 70 IU/dL, respectively. Efficacy was assessed using a global hemostatic efficacy score.

resultsStudies 1, 2, and 3 included 12, 4, and 6 patients, respectively. Efficacy outcomes were excellent/good in all 22 major surgeries including 18 orthopedic procedures. Most daily measured FVIII and VWF levels (92%) were on target. No safety concerns, thrombotic events, or inhibitors were identified.

conclusionpdFVIII and pdVWF administered by CI represent an effective and safe alternative to bolus injections in patients with severe HA or VWD undergoing surgery.

Indexed as

Hemophilia AHemostaticsvon Willebrand DiseasesAdultFactor VIIIHumansvon Willebrand FactorFactor VIIIHemostaticsvon Willebrand Factor

Identifiers

PMID35642281
PMCPMC9393085
OpenAlexW4281663342

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.