1992
DOI: 10.1016/0049-3848(92)90213-t
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Correlation between anti-Xa and occurrence of thrombosis and haemorrhage in post-surgical patients treated with either logiparin® (LMWH) or unfractionated heparin

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Cited by 55 publications
(37 citation statements)
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“…Levine et al [24] reported a highly significant association between anti-Xa levels and rates of venographically confirmed deep vein thrombosis and wound hematomas with LMWH prophylaxis following total hip arthroplasty. Other investigators have noted weaker associations between anti-Xa levels and deep vein thrombosis rates with LMWH prophylaxis following general surgery [19,22], but not for major orthopedic procedures [16,21,23,26].…”
Section: Discussionmentioning
confidence: 99%
“…Levine et al [24] reported a highly significant association between anti-Xa levels and rates of venographically confirmed deep vein thrombosis and wound hematomas with LMWH prophylaxis following total hip arthroplasty. Other investigators have noted weaker associations between anti-Xa levels and deep vein thrombosis rates with LMWH prophylaxis following general surgery [19,22], but not for major orthopedic procedures [16,21,23,26].…”
Section: Discussionmentioning
confidence: 99%
“…In addition, the relevance of anti-factor Xa levels is unclear; several studies have failed to show a relationship between the anti-Xa levels and bleeding. [158][159][160] For patients treated with LMWH, the risk of bleeding was generally higher in patients with a creatinine clearance , 30 mL/min compared with patients with a creatinine clearance . 30 mL/min (5.0% vs 2.4%; OR, 2.25; 95% CI, 1.19-4.27; P 5 .013).…”
Section: Should the Therapeutic Dose Of Lmwh Be Modifi Ed For Decreasmentioning
confidence: 99%
“…In this context it needs to be born in mind that target ranges are different for different LMWHs, and that it is still unknown if targets derived from pharmacological studies in healthy volunteers are indeed applicable to the critically ill population with major, heterogeneous and unpredictable modifications in pharmacokinetics and pharmacodynamics, as well as changes in haemostatic competence. Another problem is the only weak relationship between anti-Xa activity and clinical occurrence of symptomatic and asymptomatic VTE [18][19][20]. However, determination of anti-Xa activity is recommended if renal elimination of LMWH is impaired [2].…”
Section: Discussionmentioning
confidence: 99%