2016
DOI: 10.5603/cj.a2015.0054
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The use of anticoagulants in morbidly obese patients

Abstract: (Cardiol J 2016; 23, 1: 12-16)

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Cited by 10 publications
(7 citation statements)
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“…NOACs have short half-lives and if patients miss 2 doses they will be unprotected. A recent review has shown that morbid adiposity may reduce the efficacy of NOACs [19]. NOACs have fewer pharmacokinetic/-dynamic interactions than VKAs but they have important interactions with inhibitors of the P-glycoprotein transporter and with several drugs used in cardiology [15][16][17][20][21][22].…”
Section: Risks Of Oral Anticoagulationmentioning
confidence: 99%
“…NOACs have short half-lives and if patients miss 2 doses they will be unprotected. A recent review has shown that morbid adiposity may reduce the efficacy of NOACs [19]. NOACs have fewer pharmacokinetic/-dynamic interactions than VKAs but they have important interactions with inhibitors of the P-glycoprotein transporter and with several drugs used in cardiology [15][16][17][20][21][22].…”
Section: Risks Of Oral Anticoagulationmentioning
confidence: 99%
“…Prothrombin time is an assay evaluating the extrinsic pathway of coagulation. The international normalized ratio (INR) is used to standardize the prothrombin time and the optimal intensity of anticoagulant therapy corresponds to a target INR of 2.5 (range, 2.0 to 3.0) [ 12 ].…”
Section: Introductionmentioning
confidence: 99%
“…Both prophylaxis and treatment of VTE and pulmonary embolism (PE) with anticoagulants are associated with significant risks of major and fatal hemorrhage. Both anticoagulant treatment and lifestyle changes should be individualized to prevent further complications [ 9 , 12 ].…”
Section: Introductionmentioning
confidence: 99%
“…ey are also deemed safe for use as prophylaxis for venous thromboembolism (VTE) in patients undergoing knee or hip replacement surgery. ese newer agents have shown equal efficacy as low-molecular weight heparin (LMWH) and VKAs [6,7]. In addition, studies have shown no differences in efficacy to VKAs or LMWH in overweight and obese patients [8][9][10][11][12][13].…”
Section: Introductionmentioning
confidence: 99%
“…Drug exposures were found to be decreased along with reduced concentrations and shortened half-lives (time to steady state) in patients with BMI >40 kg/m 2 . Other smaller studies and case reports have demonstrated stable pharmacokinetics and pharmacodynamics in obese patients for both rivaroxaban and apixaban [7,19,20]. To date, there exists no strong evidence of clinical efficacy and safety in obese patients on therapeutic DOACs.…”
Section: Introductionmentioning
confidence: 99%