DIURNAL CHANGES IN HEPARIN EFFECT DURING CONTINUOUS CONSTANT-RATE INFUSION - A STUDY IN 9 PATIENTS WITH VENOUS THROMBOEMBOLISM

Citation
Jwm. Krulder et al., DIURNAL CHANGES IN HEPARIN EFFECT DURING CONTINUOUS CONSTANT-RATE INFUSION - A STUDY IN 9 PATIENTS WITH VENOUS THROMBOEMBOLISM, Journal of internal medicine, 235(5), 1994, pp. 411-417
Citations number
17
Categorie Soggetti
Medicine, General & Internal
ISSN journal
09546820
Volume
235
Issue
5
Year of publication
1994
Pages
411 - 417
Database
ISI
SICI code
0954-6820(1994)235:5<411:DCIHED>2.0.ZU;2-N
Abstract
Objective, To evaluate the importance of diurnal variations in the eff ect of a continuous infusion of unfractionated heparin. Design. Twenty -four-hour follow-up. Setting. Tertiary referral centre. Subjects. Pat ients (five male, four female) with acute venous thromboembolic diseas es. Main outcome measures. Two-hourly measurement of anti-IIa activity , anti-Xa activity, APTT (Cephotest and automated APTT), antithrombin III and cortisol for 24 h. Results, The maximum anticoagulant effect w as found at 04.00-06.00 hours, and the minimum effect at 12.00 hours. The difference was 0.40 U ml(-1) for anti-IIa activity (95% confidence interval (CI) 0.03-0.78; P < 0.05), 0.36 U ml(-1) for anti-Xa activit y (95% CI-0.05-0.72; not significant [NS]), 15.1 s for Cephotest APTT (95% CI 3.3-26.9; P < 0.03), and 112.9 s for automated APTT (95% CI 7. 8-218.0; P < 0.05). Antithrombin III decreased from 97.9% at the start to 82.6% 24 h later (P = 0.001). Cortisol showed a typical diurnal rh ythm. Expressed as a percentage of the individual 24-h mean, a maximum was found at 04.00 hours (anti-IIa activity), 06.00 hours (both APTTs ), and 08.00 hours (anti-Xa activity) and a minimum at 12.00 hours (al l variables). The difference was 26% for anti-IIa activity (P < 0.05) and anti-Xa activity (NS), 22% for APTT (Cephotest; P < 0.03), and 44% for APTT (automated APTT; P < 0.05). Conclusions. A continuous intrav enous infusion of unfractionated heparin has a maximum anticoagulant e ffect between 04.00 and 8.00 hours and a minimum effect at noon. For i ndividual patients the moment of minimum and maximum effect varies wid ely. Because the most impressive changes occur between 06.00 and 08.00 hours, laboratory control can best be performed at fixed times, e.g. at 10.00 and at 22.00 hours.