Venous thromboembolism in orthopaedic oncology.


Journal

The bone & joint journal
ISSN: 2049-4408
Titre abrégé: Bone Joint J
Pays: England
ID NLM: 101599229

Informations de publication

Date de publication:
Dec 2020
Historique:
entrez: 30 11 2020
pubmed: 1 12 2020
medline: 15 12 2020
Statut: ppublish

Résumé

Malignancy and surgery are risk factors for venous thromboembolism (VTE). We undertook a systematic review of the literature concerning the prophylactic management of VTE in orthopaedic oncology patients. MEDLINE (PubMed), EMBASE (Ovid), Cochrane, and CINAHL databases were searched focusing on VTE, deep vein thrombosis (DVT), pulmonary embolism (PE), bleeding, or wound complication rates. In all, 17 studies published from 1998 to 2018 met the inclusion criteria for the systematic review. The mean incidence of all VTE events in orthopaedic oncology patients was 10.7% (1.1% to 27.7%). The rate of PE was 2.4% (0.1% to 10.6%) while the rate of lethal PE was 0.6% (0.0% to 4.3%). The overall rate of DVT was 8.8% (1.1% to 22.3%) and the rate of symptomatic DVT was 2.9% (0.0% to 6.2%). From the studies that screened all patients prior to hospital discharge, the rate of asymptomatic DVT was 10.9% (2.0% to 20.2%). The most common risk factors identified for VTE were endoprosthetic replacements, hip and pelvic resections, presence of metastases, surgical procedures taking longer than three hours, and patients having chemotherapy. Mean incidence of VTE with and without chemical prophylaxis was 7.9% (1.1% to 21.8%) and 8.7% (2.0% to 23.4%; p = 0.11), respectively. No difference in the incidence of bleeding or wound complications between prophylaxis groups was reported. Current evidence is limited to guide clinicians. It is our consensus opinion, based upon logic and deduction, that all patients be considered for both mechanical and chemical VTE prophylaxis, particularly in high-risk patients (pelvic or hip resections, prosthetic reconstruction, malignant diagnosis, presence of metastases, or surgical procedures longer than three hours). Additionally, the surgeon must determine, in each patient, if the risk of haemorrhage outweighs the risk of VTE. No individual pharmacological agent has been identified as being superior in the prevention of VTE events. Cite this article:

Identifiants

pubmed: 33249908
doi: 10.1302/0301-620X.102B12.BJJ-2019-1136.R3
doi:

Substances chimiques

Anticoagulants 0
Fibrinolytic Agents 0
Hematologic Agents 0

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1743-1751

Auteurs

Johnathan R Lex (JR)

Division of Orthopaedic Surgery, University of Toronto, Toronto, Canada.
Oncology Department, Royal Orthopaedic Hospital NHS Foundation Trust, Birmingham, UK.

Scott Evans (S)

Oncology Department, Royal Orthopaedic Hospital NHS Foundation Trust, Birmingham, UK.

Paul Cool (P)

Robert Jones and Agnes Hunt Orthopaedic Hospital, Oswestry, UK.
Medical School, Keele University, Keele, UK.

Jonathan Gregory (J)

Oncology Department, Royal Orthopaedic Hospital NHS Foundation Trust, Birmingham, UK.

Robert U Ashford (RU)

Joint Reconstruction and Oncology, University Hospitals of Leicester NHS Trust, Leicester, UK.
Leicester Cancer Research Centre, University of Leicester, Leicester, UK.

Kenneth S Rankin (KS)

Translational and Clinical Sciences Institute, Newcastle University, Newcastle, UK.
North of England Bone and Soft Tissue Tumour Service, Newcastle upon Tyne University Hospitals NHS Foundation Trust, Newcastle, UK.

Tom Cosker (T)

Orthopaedic Oncology, University of Oxford Nuffield Department of Orthopaedics Rheumatology and Musculoskeletal Sciences, Oxford, UK.

Amit Kumar (A)

Orthopaedics Department, Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK.

Craig Gerrand (C)

Royal National Orthopaedic Hospital NHS Trust, Stanmore, UK.

Jonathan Stevenson (J)

Oncology Department, Royal Orthopaedic Hospital NHS Foundation Trust, Birmingham, UK.
Medical School, Aston University, Birmingham, UK.

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