AHA GUIDELINES Bundle (free trial)

2017 Update Incorporated - Valvular Heart Disease

AHA GUIDELINES Apps brought to you courtesy of Guideline Central. All of these titles are available for purchase on our website, GuidelineCentral.com. Enjoy!

Issue link: https://eguideline.guidelinecentral.com/i/362033

Contents of this Issue

Navigation

Page 40 of 63

41 Prosthetic Valves Table 26. Diagnosis and Anticoagulation for Prosthetic Valves Recommendations COR LOE Diagnosis An initial TTE study is recommended in patients aer prosthetic valve implantation for evaluation of valve hemodynamics. I B Repeat TTE is recommended in patients with prosthetic heart valves if there is a change in clinical symptoms or signs suggesting valve dysfunction. I C TEE is recommended when clinical symptoms or signs suggest prosthetic valve dysfunction. I C Annual TTE is reasonable in patients with a bioprosthetic valve aer the first 10 years, even in the absence of a change in clinical status. IIa C Antithrombotic erapy Anticoagulation with a VKA and International Normalized Ratio (INR) monitoring is recommended in patients with a mechanical prosthetic valve. I A Anticoagulation with a VKA to achieve an INR of 2.5 is recommended in patients with a mechanical AVR (bileaflet or current-generation single tilting disc) and no risk factors for thromboembolism. I B Anticoagulation with a VKA is indicated to achieve an INR of 3.0 in patients with a mechanical AVR and additional risk factors for thromboembolic events (AF, previous thromboembolism, LV dysfunction, or hypercoagulable conditions) or an older-generation mechanical AVR (such as ball-in-cage). I B Anticoagulation with a VKA is indicated to achieve an INR of 3.0 in patients with a mechanical MVR. I B ASA 75–100 mg daily is recommended in addition to anticoagulation with a VKA in patients with a mechanical valve prosthesis. I A ASA 75–100 mg daily is reasonable in all patients with a bioprosthetic aortic or MV. IIa B Anticoagulation with a VKA to achieve an INR of 2.5 is reasonable for at least 3 months and for as long as 6 months aer surgical bioprosthetic MVR or AVR in patients at low risk of bleeding. (Modified recommendation for 2017) IIa B-NR

Articles in this issue

Archives of this issue

view archives of AHA GUIDELINES Bundle (free trial) - 2017 Update Incorporated - Valvular Heart Disease