Reduced calf muscle pump function is a risk factor for venous thromboembolism: a population-based cohort study.


Journal

Blood
ISSN: 1528-0020
Titre abrégé: Blood
Pays: United States
ID NLM: 7603509

Informations de publication

Date de publication:
10 06 2021
Historique:
received: 03 12 2020
accepted: 29 01 2021
pubmed: 4 3 2021
medline: 15 12 2021
entrez: 3 3 2021
Statut: ppublish

Résumé

The calf muscle pump is a major determinate of venous return in the legs but has not been studied as a risk factor for venous thromboembolism (VTE). A population-based cohort study of Olmsted County, Minnesota residents was performed using calf pump function (CPF) measurements from venous plethysmography studies from 1998 to 2015. Patients with a history of VTE were excluded. Nursing validated VTE outcomes from the Rochester Epidemiology Project were identified after the index study date, and patients with reduced CPF (rCPF) were compared with patients with normal CPF. A total of 1532 patients with recorded CPF (28% air and 72% strain gauge plethysmography) were included; 591 (38.5%) had normal CPF, 353 (23.0%) had unilateral rCPF, and 588 (38.3%) had bilateral rCPF. Any VTE occurred in 87 patients (5.7%) after a median follow-up of 11.7 years (range, 0-22.0 years). Comparing patients with bilateral reduced to bilateral normal CPF, the unadjusted hazard ratio (HR) for incident VTE was 2.0 (95% confidence interval [CI], 1.2-3.4) and after adjusting for age, BMI, and Charlson Comorbidity Index, the HR was 1.68 (95% CI, 0.98-2.89). The adjusted HR for ipsilateral deep vein thrombosis was evaluated in 3064 legs comparing legs with reduced to normal CPF and was 1.71 (95% CI, 1.03-2.84). Mortality was significantly higher in both the bilateral (P < .001) and unilateral (P < .001) rCPF groups compared with normal CPF. Our results demonstrate that CPF is a risk factor for VTE in an otherwise low-risk ambulatory population and might be a useful component in risk stratification models.

Identifiants

pubmed: 33657212
pii: S0006-4971(21)00517-6
doi: 10.1182/blood.2020010231
pmc: PMC8351902
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

3284-3290

Subventions

Organisme : NIA NIH HHS
ID : R01 AG034676
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL066216
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 by The American Society of Hematology.

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Auteurs

Damon E Houghton (DE)

Division of Vascular Medicine, Department of Cardiovascular Diseases.
Division of Hematology/Oncology, Department of Internal Medicine.
Gonda Vascular Center, and.

Aneel Ashrani (A)

Division of Hematology/Oncology, Department of Internal Medicine.

David Liedl (D)

Gonda Vascular Center, and.

Ramila A Mehta (RA)

Division of Biomedical Statistics and Informatics, Department of Health Science Research, Mayo Clinic, Rochester, MN; and.

David O Hodge (DO)

Department of Health Sciences Research, Mayo Clinic, Jacksonville, FL.

Thom Rooke (T)

Division of Vascular Medicine, Department of Cardiovascular Diseases.
Gonda Vascular Center, and.

Paul Wennberg (P)

Division of Vascular Medicine, Department of Cardiovascular Diseases.
Gonda Vascular Center, and.

Waldemar Wysokinski (W)

Division of Vascular Medicine, Department of Cardiovascular Diseases.
Gonda Vascular Center, and.

Robert McBane (R)

Division of Vascular Medicine, Department of Cardiovascular Diseases.
Gonda Vascular Center, and.

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Classifications MeSH