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Oral thromboprophylaxis following total hip replacement: the issue of compliance.

Authors :
Lebel B
Malherbe M
Gouzy S
Parienti JJ
Dutheil JJ
Barrellier MT
Vielpeau C
Source :
Orthopaedics & traumatology, surgery & research : OTSR [Orthop Traumatol Surg Res] 2012 Apr; Vol. 98 (2), pp. 186-92. Date of Electronic Publication: 2012 Mar 03.
Publication Year :
2012

Abstract

Introduction: Thirty-five to 40 days' thromboprophylaxis is recommended following total hip replacement (THR). Low molecular weight heparin (LMWH) injected by a health professional ensures good compliance. Compliance with recent oral anticoagulants has not been precisely assessed. Oral self-administration, without coagulation monitoring tests, may be a worrying issue in the management of what is a potentially catastrophic adverse event, without prodromal symptoms alerting the patient to the need for regular intake throughout the prescription period.<br />Hypothesis: It was hypothesized that compliance with these new oral anticoagulants is good over the entire treatment period.<br />Patients and Method: The present cohort study prospectively assessed compliance with oral medication (two capsules of dabigatran etexilate [Pradaxa(®)] per day in a single dose at a set time) following THR. An electronic device continuously monitored the day and time of extraction of capsules from the package. All included patients underwent clinical and echo-Doppler examination at day 30±5 after the start of the study.<br />Results: Fifty-six patients were included at their discharge home. Overall compliance was 98.1% (3,188/3246 capsules correctly taken), falling off slightly over time but never below 97.1%. One patient was diagnosed with symptomatic thrombophlebitis 34 days postoperatively, associated with non-compliance at day 11. End of follow-up echo-Doppler found four cases of asymptomatic distal venous thrombosis. There were no hemorrhagic complications.<br />Discussion: The risk of thromboembolic complications diminishes over time, while oral anticoagulants have a wide therapeutic window and relatively long half-life (15-17 hrs). Efficacy was demonstrated, with improved patient comfort and cost-saving. Compliance in the present series was satisfactory. This, however, should not mean that patients not be appropriately informed, as in the present study, so as to improve compliance.<br />Level of Evidence: Level III, prospective diagnostic.<br /> (Copyright © 2012. Published by Elsevier Masson SAS.)

Details

Language :
English
ISSN :
1877-0568
Volume :
98
Issue :
2
Database :
MEDLINE
Journal :
Orthopaedics & traumatology, surgery & research : OTSR
Publication Type :
Academic Journal
Accession number :
22386648
Full Text :
https://doi.org/10.1016/j.otsr.2011.10.010