Thromb Haemost 1987; 58(04): 1068-1072
DOI: 10.1055/s-0038-1646058
Original Article
Schattauer GmbH Stuttgart

Circulating Activities During Constant Infusion of Heparin or a Low Molecular Weight Derivative (Enoxaparine): Failure to Demonstrate any Circadian Variations

P Toulon
1   The Centre de Recherche Claude-Bernard sur les maladies vasculaires périphériques et Laboratoire d’hémostase, Hôspital Broussais, France
,
J F Vitoux
1   The Centre de Recherche Claude-Bernard sur les maladies vasculaires périphériques et Laboratoire d’hémostase, Hôspital Broussais, France
,
C Leroy
1   The Centre de Recherche Claude-Bernard sur les maladies vasculaires périphériques et Laboratoire d’hémostase, Hôspital Broussais, France
,
T Lecomte
1   The Centre de Recherche Claude-Bernard sur les maladies vasculaires périphériques et Laboratoire d’hémostase, Hôspital Broussais, France
,
M Roncato
1   The Centre de Recherche Claude-Bernard sur les maladies vasculaires périphériques et Laboratoire d’hémostase, Hôspital Broussais, France
,
Y Motobashi
2   The Laboratoire de Physiologie (Pr Reinberg), Fondation Rothschild, Paris, France
,
M Aiach
1   The Centre de Recherche Claude-Bernard sur les maladies vasculaires périphériques et Laboratoire d’hémostase, Hôspital Broussais, France
,
J N Fiessinger
1   The Centre de Recherche Claude-Bernard sur les maladies vasculaires périphériques et Laboratoire d’hémostase, Hôspital Broussais, France
› Author Affiliations
Further Information

Publication History

Received 16 April 1987

Accepted after revision 08 September 1987

Publication Date:
29 June 2018 (online)

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Summary

We compared in six patients successively treated with an unfractionated heparin (UFH) and a low molecular weight heparin (LMWH) the variations in plasma anti-Xa activity, measured in a chromogenic assay, during a 36 h constant infusion. The values varied in a wider range during UHF infusion, but remained in the therapeutic range except once in one patient. No circadian rhythm could be demonstrated in our six patients. LMWH infusion yielded very constant anti-Xa circulating activities. In both cases, there were no significant modifications of three proteins with high heparin affinity (antithrombin III, heparin cofactor II, histidine-rich glycoprotein).

Our results suggest that the circadian rhythm of the biological activities previously observed in patients treated with constant heparin infusion using clotting method is due to other factors than heparin itself.