2013
DOI: 10.1007/s11239-013-0922-z
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Design and establishment of a biobank in a multicenter prospective cohort study of elderly patients with venous thromboembolism (SWITCO65+)

Abstract: In the field of thrombosis and haemostasis, many preanalytical variables influence the results of coagulation assays and measures to limit potential results variations should be taken. To our knowledge, no paper describing the development and maintenance of a haemostasis biobank has been previously published. Our description of the biobank of the Swiss cohort of elderly patients with venous thromboembolism (SWITCO65+) is intended to facilitate the set-up of other biobanks in the field of thrombosis and haemost… Show more

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Cited by 11 publications
(21 citation statements)
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“…The Swiss Venous Thromboembolism Cohort 65+ (SWITCO65+) is a prospective multicenter cohort study enrolling patients aged ≥ 65 years with acute, symptomatic VTE at nine Swiss university and non-university hospitals from 2009 to 2013 [ 15 , 16 ]. Patients with acute VTE were identified in the inpatient and outpatient services of the study sites.…”
Section: Methodsmentioning
confidence: 99%
“…The Swiss Venous Thromboembolism Cohort 65+ (SWITCO65+) is a prospective multicenter cohort study enrolling patients aged ≥ 65 years with acute, symptomatic VTE at nine Swiss university and non-university hospitals from 2009 to 2013 [ 15 , 16 ]. Patients with acute VTE were identified in the inpatient and outpatient services of the study sites.…”
Section: Methodsmentioning
confidence: 99%
“…Samples were immediately centrifuged, frozen and stored at– 80°C until analyses. Details regarding blood sampling/processing were described elsewhere [ 18 ].…”
Section: Methodsmentioning
confidence: 99%
“…A full description of the cohort methods, including eligibility criteria, definition of VTE, and follow-up procedures, has been published elsewhere. 17,18 Anticoagulant treatment (i.e., parenteral anticoagulant followed by vitamin K antagonists or parenteral anticoagulation alone) was left to the discretion of the managing hospital and primary care physicians. For this project, we excluded all patients who did not receive oral anticoagulation with vitamin K antagonists within 14 days of the index VTE event.…”
Section: Cohort Samplementioning
confidence: 99%