Postoperative bleeding complications in patients with hemophilia undergoing major orthopedic surgery: A prospective multicenter observational study.


Journal

Journal of thrombosis and haemostasis : JTH
ISSN: 1538-7836
Titre abrégé: J Thromb Haemost
Pays: England
ID NLM: 101170508

Informations de publication

Date de publication:
04 2022
Historique:
revised: 18 01 2022
received: 25 08 2021
accepted: 19 01 2022
pubmed: 27 1 2022
medline: 23 4 2022
entrez: 26 1 2022
Statut: ppublish

Résumé

Persons with hemophilia (PWH) are at risk for chronic hemophilic arthropathy (HA). Joint replacement surgery may be used to relieve intractable pain and/or restore joint function. This multicenter, prospective, observational cohort study evaluated the rate of bleeding during the postoperative period after total hip (THA) or knee arthroplasty (TKA). We included PWH of any severity ≥18 years of age who were undergoing THA or TKA. Clinical decisions were made at the discretion of the treating physician according to local standards of care. Clinical data were prospectively recorded. Major bleeding was defined as bleeding in a critical site, bleeding that resulted in either a 2 g/dl or greater decrease in hemoglobin during any 24-h period, or transfusion of two or more units of packed red blood cells. One hundred thirty-one procedures (98 TKA and 33 THA) were performed, 39 (29.8%) of which were complicated by major bleeding, including 46% of THA and 25% of TKA. The risk of major bleeding was increased in THA compared to TKA (OR 2.50, p = .05), and by the presence of an inhibitor (OR 4.29, p = .04), increased BMI (OR 4.49 and 6.09 for overweight and obese, respectively, compared to normal BMI, each p < .01), and non-use of an antifibrinolytic medication (OR 3.00, p = .03). Neither continuous clotting factor infusion (versus bolus infusion) nor pharmacologic thromboprophylaxis were associated with bleeding risk. The bleeding risk remains substantial after THA and TKA in PWH, despite factor replacement. Use of antifibrinolytic medications is associated with decreased risk.

Sections du résumé

BACKGROUND
Persons with hemophilia (PWH) are at risk for chronic hemophilic arthropathy (HA). Joint replacement surgery may be used to relieve intractable pain and/or restore joint function.
OBJECTIVES
This multicenter, prospective, observational cohort study evaluated the rate of bleeding during the postoperative period after total hip (THA) or knee arthroplasty (TKA).
PATIENTS/METHODS
We included PWH of any severity ≥18 years of age who were undergoing THA or TKA. Clinical decisions were made at the discretion of the treating physician according to local standards of care. Clinical data were prospectively recorded. Major bleeding was defined as bleeding in a critical site, bleeding that resulted in either a 2 g/dl or greater decrease in hemoglobin during any 24-h period, or transfusion of two or more units of packed red blood cells.
RESULTS
One hundred thirty-one procedures (98 TKA and 33 THA) were performed, 39 (29.8%) of which were complicated by major bleeding, including 46% of THA and 25% of TKA. The risk of major bleeding was increased in THA compared to TKA (OR 2.50, p = .05), and by the presence of an inhibitor (OR 4.29, p = .04), increased BMI (OR 4.49 and 6.09 for overweight and obese, respectively, compared to normal BMI, each p < .01), and non-use of an antifibrinolytic medication (OR 3.00, p = .03). Neither continuous clotting factor infusion (versus bolus infusion) nor pharmacologic thromboprophylaxis were associated with bleeding risk.
CONCLUSIONS
The bleeding risk remains substantial after THA and TKA in PWH, despite factor replacement. Use of antifibrinolytic medications is associated with decreased risk.

Identifiants

pubmed: 35080347
doi: 10.1111/jth.15654
pmc: PMC8940712
mid: NIHMS1775358
pii: S1538-7836(22)00145-3
doi:

Substances chimiques

Anticoagulants 0
Antifibrinolytic Agents 0

Types de publication

Journal Article Multicenter Study Observational Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

857-865

Subventions

Organisme : NHLBI NIH HHS
ID : T32 HL007149
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002489
Pays : United States

Informations de copyright

© 2022 International Society on Thrombosis and Haemostasis.

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Auteurs

Brendan Kleiboer (B)

Department of Medicine and UNC Blood Research Center, University of North Carolina, Chapel Hill, North Carolina, USA.

Marcus A Layer (MA)

Department of Medicine and UNC Blood Research Center, University of North Carolina, Chapel Hill, North Carolina, USA.

Lorraine A Cafuir (LA)

Emory University School of Medicine, Atlanta, Georgia, USA.

Adam Cuker (A)

Department of Medicine and Department of Pathology & Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Miguel Escobar (M)

McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.

M Elaine Eyster (ME)

Penn State Hershey Medical Center, Hershey, Pennsylvania, USA.

Eric Kraut (E)

The Ohio State University Hemostasis and Thrombosis Center, Columbus, Ohio, USA.

Andrew D Leavitt (AD)

Department of Laboratory Medicine and Department of Internal Medicine, University of California San Francisco, San Francisco, California, USA.

Steven R Lentz (SR)

Department of Internal Medicine, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA.

Doris Quon (D)

Orthopaedic Hemophilia Treatment Center, Orthopaedic Institute for Children, Los Angeles, California, USA.

Margaret V Ragni (MV)

Department of Medicine and Clinical and Translational Science, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.

Dianne Thornhill (D)

University of Colorado School of Medicine, Aurora, Colorado, USA.

Michael Wang (M)

University of Colorado School of Medicine, Aurora, Colorado, USA.

Nigel S Key (NS)

Department of Medicine and UNC Blood Research Center, University of North Carolina, Chapel Hill, North Carolina, USA.

Tyler W Buckner (TW)

University of Colorado School of Medicine, Aurora, Colorado, USA.

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Classifications MeSH