Evidence map›Paper›PMID 37867585›Full record

ArticleResearch and practice in thrombosis and haemostasis2023

Surgery in rare bleeding disorders: the prospective MARACHI study.

Florence Rousseau, Benoit Guillet, Thibault Mura, Alexandra Fournel, Fabienne Volot, Hervé Chambost, Pierre Suchon, Brigit Frotscher, Christine Biron-Andréani, Raphaël Marlu and 17 more

Open access · goldAbstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
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

27 authors at 19 institutions in 1 country.

Florence RousseauDépartement d'hématologie biologique, CHU Montpellier, France.
Benoit GuilletHaemophilia Treatment Center, University Hospital, Rennes, France and Univ Rennes, CHU Rennes, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail) - UMR_S 1085, F-35000 Rennes, France.
Thibault MuraDépartement d'informatique médicale, CHU Montpellier, CHU Nîmes, Université de Montpellier FR 34090, France.
Alexandra FournelHaemophilia Treatment Centre, University Hospital of Besançon, Besançon, France.
Fabienne VolotCRC-MHC Dijon, CHU Dijon, France.
Hervé ChambostAP-HM Marseille, France.
Pierre SuchonAix Marseille University, Inserm, Inrae, C2VN, Marseille, France.
Brigit FrotscherHaemophilia Treatment Centre, University Hospital of Nancy, France.
Christine Biron-AndréaniCRC-MHC, CHU Montpellier, France.
Raphaël MarluHemostasis Unit, CHU Grenoble Alpes, Université Grenoble Alpes, France.
Nathalie HezardLaboratoire d'hématologie, CHU Reims, France.
Ségolène ClayssensCRC-MHC, CHU Toulouse, France.
Elodie BoissierLaboratoire d'hématologie, CHU Nantes, France.
Florence Blanc-JouvanLaboratoire d'hématologie, CH Annecy Genevois, France.
Pierre ChamouniHTC, University Hospital, Rouen, France.
Nathalie TieulieService de Rhumatologie, CHU Nice, France.
Lucia RugeriUnité Hémostase Clinique, Hospices Civils de Lyon, France.
Annie Borel-DerlonCRC-MHC, CHU Caen, France.
Emmanuelle de RaucourtService d'hématologie Biologique Hôpital Beaujon, HUPNVS, AP-HP, France.
Isabelle Martin-ToutainCRC-MHC, Service d'hématologie clinique, Hôpital Mignot Le Chesnay, France.
Sabine CastetCRC-MHC, CHU Bordeaux, France.
Aurélien LebretonLaboratoire d'hématologie, CHU Clermont Ferrand, Unité de Nutrition Humaine UMR1019, INRAE / Université Clermont Auvergne, Clermont-Ferrand, France.
Stéphane GiraultConsultation d'hémostase, CHU Limoges, France.
Dominique Helley-RussickLaboratoire d'hématologie, Hôpital Georges Pompidou, AP-HP, France.
Roseline D'OironCentre de référence de l'hémophilie et des maladies hémorragiques constitutionnelles, Hôpital Bicêtre, APHP and Hith, UMR_S1176, INSERM, Université Paris Saclay, Le Kremlin Bicêtre, France.
Jean-François SchvedDépartement d'hématologie biologique, CHU Montpellier, France.
Muriel Giansily-BlaizotDépartement d'hématologie biologique, CHU Montpellier, France.
Assistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Universitaire de Montpellier · FRAssistance Publique Hôpitaux de Marseille · FRCentre de Recherche en Nutrition Humaine d'Auvergne · FRCentre Hospitalier Annecy Genevois · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier Universitaire de Besançon · FRCentre Hospitalier Universitaire de Limoges · FRCentre Hospitalier Universitaire de Reims · FRDépartement d'Informatique · FRÉcole des Hautes Études en Santé Publique · FRHôpital André Mignot · FRHospices Civils de Lyon · FRInserm · FRUniversité de Caen Normandie · FRUniversité de Montpellier · FRUniversité de Rouen Normandie · FRUniversité Grenoble Alpes · FRUniversité Paris-Saclay · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Despite the wide use of bleeding scores and the reliability of clotting factor level measurement, bleeding risk stratification before surgery remains challenging in patients with rare inherited bleeding disorders. Objectives: This multicenter observational prospective study assessed in patients with rare coagulation factor deficiency, the perioperative hemostatic management choices by hemostasis experts and the bleeding outcomes after surgery. Methods: One hundred seventy-eight patients with low coagulation activity level (factor [F] II, FV, combined FV-FVIII, FVII, FX, or FXI <50%) underwent 207 surgical procedures. The bleeding outcome, Tosetto's bleeding score, and perioperative hemostatic protocols were collected. Results: Among the 81 procedures performed in patients with severe factor deficiency (level ≤10%), 27 were done without factor replacement (including 6 in patients at high bleeding risk), without any bleeding event. Factor replacement therapy was used mainly for orthopedic procedures. In patients with mild deficiency, 100/126 surgical procedures were carried out without perioperative hemostatic treatment. In patients with FVII or FXI deficiency, factor replacement therapy was in function of the procedure, bleeding risk, and to a lesser extent previous bleeding history. Tranexamic acid was used in almost half of the procedures, particularly in case of surgery in tissues with high fibrinolytic activity (76.8%). Conclusions: The current perioperative hemostatic management of patients with rare bleeding disorders appears to be adapted. Among the 207 procedures, only 6 were associated with excessive bleeding. Our findings suggest that rather than the bleeding score, factor level and surgery type are the most relevant criteria for perioperative factor replacement therapy.

Indexed as

bleeding scorehemorrhagic disordersrare bleeding disorderreplacement therapysurgerytranexamic acid

Identifiers

PMID37867585
PMCPMC10585326
OpenAlexW4386484931

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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.