Analysis of the first therapeutic-target-achieving time of warfarin therapy and associated factors in patients with pulmonary embolism
- PMID: 27698722
- PMCID: PMC5038483
- DOI: 10.3892/etm.2016.3610
Analysis of the first therapeutic-target-achieving time of warfarin therapy and associated factors in patients with pulmonary embolism
Abstract
The present study aimed to investigate the factors affecting the first therapeutic-target-achieving (TTA) time of warfarin therapy in patients with acute pulmonary embolism (PTE). Between January 2008 and June 2013, patients with PTE confirmed by transpulmonary arterial enhanced computed tomographic pulmonary angiography or pulmonary ventilation perfusion scanning were included in the present study. Data collected included demographic information, history of tobacco and alcohol intake, basic diseases (stable and unstable hypertension, diabetes, heart failure, cancer/cerebral infarction, old myocardial infarction and atrial fibrillation), liver and kidney function, the haemoglobin and platelet count of the blood, international normalized ratio monitoring, warfarin dosage adjustment and medication combinations. Dynamic changes in international normalized ratio, anticoagulant efficacy, and adverse events within 90 days were monitored and analyzed. Univariate analysis demonstrated that the following factors affect the first TTA time: Initial dose, body mass index (BMI), liver function, heart failure, and the administration of levofloxacin, cephalosporins, and blood circulation-activating drugs. Logistic regression analysis revealed that the following were independent factors of the first TTA time: Initial dose, BMI, liver function, heart failure and levofloxacin. Therefore, the results of the present study demonstrated that various factors may affect the first TTA time of warfarin therapy, including the initial dose, BMI, liver function, heart function and concomitant medication.
Keywords: first therapeutic-target-achieving time; influencing factors; international normalized ratio; pulmonary embolism; warfarin.
Figures

Similar articles
-
A new regimen for starting warfarin therapy in out-patients.Br J Clin Pharmacol. 1998 Aug;46(2):157-61. doi: 10.1046/j.1365-2125.1998.00755.x. Br J Clin Pharmacol. 1998. PMID: 9723825 Free PMC article. Clinical Trial.
-
Anticoagulation Control in Warfarin-Treated Patients Undergoing Cardioversion of Atrial Fibrillation (from the Edoxaban Versus Enoxaparin-Warfarin in Patients Undergoing Cardioversion of Atrial Fibrillation Trial).Am J Cardiol. 2017 Sep 1;120(5):792-796. doi: 10.1016/j.amjcard.2017.06.005. Epub 2017 Jun 15. Am J Cardiol. 2017. PMID: 28709650 Clinical Trial.
-
Outcomes of discontinuing rivaroxaban compared with warfarin in patients with nonvalvular atrial fibrillation: analysis from the ROCKET AF trial (Rivaroxaban Once-Daily, Oral, Direct Factor Xa Inhibition Compared With Vitamin K Antagonism for Prevention of Stroke and Embolism Trial in Atrial Fibrillation).J Am Coll Cardiol. 2013 Feb 12;61(6):651-8. doi: 10.1016/j.jacc.2012.09.057. J Am Coll Cardiol. 2013. PMID: 23391196 Clinical Trial.
-
Dabigatran and atrial fibrillation: the alternative to warfarin for selected patients.Prescrire Int. 2012 Feb;21(124):33-6. Prescrire Int. 2012. PMID: 22413715 Review.
-
Oral anticoagulant therapy.Curr Opin Hematol. 1996 Sep;3(5):361-4. doi: 10.1097/00062752-199603050-00005. Curr Opin Hematol. 1996. PMID: 9372102 Review.
Cited by
-
Impact of genetic and clinical factors on warfarin therapy in patients early after heart valve replacement surgery.Eur J Clin Pharmacol. 2019 Dec;75(12):1685-1693. doi: 10.1007/s00228-019-02747-5. Epub 2019 Aug 23. Eur J Clin Pharmacol. 2019. PMID: 31444512
-
Ultrasound-triggered herceptin liposomes for breast cancer therapy.Sci Rep. 2021 Apr 6;11(1):7545. doi: 10.1038/s41598-021-86860-5. Sci Rep. 2021. PMID: 33824356 Free PMC article.
References
LinkOut - more resources
Full Text Sources
Other Literature Sources