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Evaluation of the duration of thromboembolic prophylaxis after high-risk orthopaedic surgery: the ETHOS observational study

dc.contributor.authorBergqvist, D
dc.contributor.authorArcelus, J
dc.contributor.authorFelicíssimo, P
dc.contributor.authorETHOS investigators
dc.date.accessioned2013-03-12T12:41:09Z
dc.date.available2013-03-12T12:41:09Z
dc.date.issued2012
dc.description.abstractReal-life data on post-discharge venous thromboembolism (VTE) prophylaxis practices and treatments are lacking. We assessed post-operative VTE prophylaxis prescribed and received in a prospective registry, compared with the 2004 American College of Chest Physicians (ACCP) guidelines in high-risk orthopaedic surgery patients. Consecutive patients undergoing total hip arthroplasty (THA), hip fracture surgery (HFS), or knee arthroplasty (KA) were enrolled at discharge from 161 centres in 17 European countries if they had received in-hospital VTE prophylaxis that was considered in accordance with the ACCP guidelines by the treating physician. Data on prescribed and actual prophylaxis were obtained from hospital charts and patient post-discharge diaries. Post-operative prophylaxis prescribed and actual prophylaxis received were considered adherent or adequate, respectively, if recommended therapies were used for ≥28 days (HFS and THA) or ≥10 days (KA). Among 4,388 patients, 69.9% were prescribed ACCP-adherent VTE prophylaxis (THA: 1,411/2,217 [63.6%]; HFS: 701/1,112 [63.0%]; KA: 955/1,059 [90.2%]). Actual prophylaxis received was described in 3,939 patients with an available diary after discharge (non-evaluability rate of 10%). Mean actual durations of pharmacological prophylaxis from surgery were: 28.4 ± 13.7 (THA), 29.3 ± 13.9 (HFS), and 28.7 ± 14.1 days (KA). ACCP-adequate VTE prophylaxis was received by 66.5% of patients (60.9% THA, 55.4% HFS, and 88.7% KA). Prophylaxis inadequacies were mainly due to inadequate prescription, non-recommended prophylaxis prescription at discharge, or too short prophylaxis prescribed. In high-risk orthopaedic surgery patients with hospital-initiated prophylaxis, there is a gap between ACCP recommendations, prescribed and actual prophylaxis received, mainly due to inadequate prescription at discharge.por
dc.identifier.citationThromb Haemost. 2012 Feb;107(2):270-9por
dc.identifier.issn0340-6245
dc.identifier.urihttp://hdl.handle.net/10400.10/880
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherSchattauerpor
dc.subjectVenous thromboembolismpor
dc.subjectPostoperative complicationspor
dc.subjectAnticoagulantspor
dc.subjectOrthopaedic surgerypor
dc.subjectPatient dischargepor
dc.subjectETHOS registrypor
dc.subjectTromboembolia venosapor
dc.titleEvaluation of the duration of thromboembolic prophylaxis after high-risk orthopaedic surgery: the ETHOS observational studypor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceStuttgartpor
oaire.citation.endPage279por
oaire.citation.startPage270por
oaire.citation.titleThrombosis and Haemostasispor
oaire.citation.volume107por
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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