Using dalteparin in quotidian and nocturnal hemodialysis patients: A prospective study
Autor: | Hanna Ke, Robert M. Lindsay, Karen Qi, Shih-Han S. Huang, Martha L Louzada, Norman Muirhead, Faisal Rehman |
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Rok vydání: | 2019 |
Předmět: |
Dalteparin
Male medicine.drug_class Fistula medicine.medical_treatment 030232 urology & nephrology Hemodialysis Home Low molecular weight heparin Pilot Projects 030204 cardiovascular system & hematology Nocturnal 03 medical and health sciences 0302 clinical medicine Bolus (medicine) Renal Dialysis medicine Humans Prospective Studies Prospective cohort study business.industry Home hemodialysis Anticoagulants Hematology Heparin Middle Aged medicine.disease Nephrology Anesthesia Kidney Failure Chronic Female Hemodialysis business medicine.drug |
Zdroj: | Hemodialysis International. 24:195-201 |
ISSN: | 1542-4758 1492-7535 |
DOI: | 10.1111/hdi.12805 |
Popis: | INTRODUCTION Low-molecular weight heparin, such as dalteparin, is an alternative anticoagulation method in conventional hemodialysis (HD). However, there are limited studies on its use in quotidian and nocturnal HD. We assessed the optimal dose, treatment efficacy, and patient safety of dalteparin in quotidian and nocturnal HD populations. METHODS This study included 10 quotidian (7 in-center and 3 home) and 8 nocturnal home HD patients. Dalteparin was initiated and titrated based on clotting score in these patients. Trough anti-Xa levels were measured. The dalteparin dose, the dialyzer and HD circuit clotting scores, and bleeding episodes were recorded at 4 weeks. Patients who continued dalteparin were followed to 12 months. FINDINGS For the 10 quotidian HD patients, the median dalteparin dose was 1875 units [1250, 2500] after 4 weeks. For nocturnal HD patients, five of the eight patients switched back to heparin due to high clotting scores while on dalteparin within 4 weeks. However, three patients continued on dalteparin at 4 weeks. After 12 months, one maintained on 5000 units and the other two maintained on 7500 units of dalteparin. All the clotting scores at month 12 were ≤2. One patient died due to an unrelated cause. For all patients who continued on dalteparin, only 9% of the HD treatments had circuit clotting score >2 after reaching stable dose. All trough anti-Xa levels were |
Databáze: | OpenAIRE |
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