Abstract | OBJECTIVE: DESIGN: An observational study of pregnant women in Norway. SETTING: Delivery and haematological departments in Norway. POPULATION: METHODS: Patients were treated with dalteparin from diagnosis until delivery. Treatment was monitored with anti-activated factor Xa (anti-Xa) activity, and the dose was adjusted to achieve target 0.5-1.0 U/mL 2-3 hours post-injection. MAIN OUTCOME MEASURES: Anti-Xa activity and side effects. RESULT: None of the patients suffered recurrent venous thromboembolism or major bleeding complications. In 9 of 13 women starting with conventional dose of dalteparin (100 iu/kg bd), dose escalation was necessary to reach target anti-Xa activity. None of the six women who started with 105-118 iu/kg bd required dose escalation. One woman who started with 133 iu/kg bd required dose reduction. Bioaccumulation of dalteparin was not observed. CONCLUSION: Our study suggests that dalteparin may be used for the treatment of acute venous thromboembolism in pregnancy. Approximately 10-20% higher doses of dalteparin may be needed as compared with non-pregnant individuals.
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Authors | Anne Flem Jacobsen, Erik Qvigstad, Per Morten Sandset |
Journal | BJOG : an international journal of obstetrics and gynaecology
(BJOG)
Vol. 110
Issue 2
Pg. 139-44
(Feb 2003)
ISSN: 1470-0328 [Print] England |
PMID | 12618157
(Publication Type: Evaluation Study, Journal Article, Multicenter Study)
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Chemical References |
- Anticoagulants
- Factor Xa
- Dalteparin
|
Topics |
- Acute Disease
- Adult
- Anticoagulants
(administration & dosage)
- Dalteparin
(administration & dosage)
- Factor Xa
(metabolism)
- Female
- Humans
- Norway
- Pregnancy
- Pregnancy Complications, Cardiovascular
(drug therapy)
- Pregnancy Outcome
- Thromboembolism
(drug therapy)
- Treatment Outcome
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