Intravenous nitroglycerin-induced heparin resistance: A qualitative antithrombin III abnormality
American Heart Journal, ISSN: 0002-8703, Vol: 119, Issue: 6, Page: 1254-1261
1990
- 78Citations
- 12Captures
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Metrics Details
- Citations78
- Citation Indexes74
- 74
- CrossRef64
- Clinical Citations4
- PubMed Guidelines4
- Captures12
- Readers12
- 12
Article Description
An ability of intravenous nitroglycerin to interfere with the anticoagulant properties of intravenous heparin would have profound clinical implications. To investigate nitroglycerin-heparin interactions, the following pilot study was performed. Patients ( N =18) admitted to the coronary care unit with a diagnosis of either acute myocardial infarction or unstable angina were divided into four treatment groups: (1) intravenous nitroglycerin and intravenous heparin; (2) intravenous nitroglycerin alone; (3) intravenous heparin alone; or (4) neither intravenous nitroglycerin nor intravenous heparin. Serial determinations of activated partial thromboplastin time (APTT), serum heparin concentration, antithrombin III (ATIII) antigen (ATA), and ATIII activity (ATC) were obtained over a 72-hour period. Overall, patients receiving intravenous nitroglycerin did not differ significantly from other patients in APTT, heparin dose, heparin concentration, ATA, ATC, or ATA/ATC ratio (ATR). However, patients receiving intravenous nitroglycerin at a rate exceeding 350 μg per minute had a lower APTT ( p <0.05), lower ATC ( p =0.02), higher ATR ( p =0.004), and a larger heparin dose requirement than patients receiving lower infusion rates. ATR correlated directly ( r =0.91; p <0.05) and ATC inversely ( r =−0.78; p <0.05) with the intravenous nitroglycerin dose. Serum heparin concentration did not correlate with the intravenous nitroglycerin dose. Intravenous nitroglycerin-induced heparin resistance occurs at a critical nitroglycerin dose. A nitroglycerin-induced qualitative ATIII abnormality may be the underlying mechanism.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0002870305801723; http://dx.doi.org/10.1016/s0002-8703(05)80172-3; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0025308891&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/2112878; https://linkinghub.elsevier.com/retrieve/pii/S0002870305801723; http://linkinghub.elsevier.com/retrieve/pii/S0002870305801723; http://api.elsevier.com/content/article/PII:S0002870305801723?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:S0002870305801723?httpAccept=text/plain; http://dx.doi.org/10.1016/s0002-8703%2805%2980172-3; https://dx.doi.org/10.1016/s0002-8703%2805%2980172-3
Elsevier BV
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