The document discusses dual antiplatelet therapy (DAPT) with aspirin and a P2Y12 receptor inhibitor for patients receiving coronary stents. It addresses three questions on optimal DAPT duration: 1) Is shorter DAPT (3-6 months) as effective as 12 months for newer-generation drug-eluting stents? 2) Does longer DAPT (>12 months) reduce ischemic events more than 12 months of DAPT? 3) Does continued DAPT past 12 months benefit stable post-MI patients more than aspirin alone? The document summarizes several studies investigating these questions and guidelines on DAPT duration and choice of P2Y12 inhibitor.
1) For stable patients who undergo percutaneous coronary intervention (PCI) with stenting, dual antiplatelet therapy (DAPT) with aspirin and a P2Y12 receptor blocker is recommended for at least 12 months.
2) For those at high risk of bleeding, DAPT may be limited to less than 1 year, with a minimum of 1 month.
3) After 1 year of DAPT without complications, continuing therapy for an additional 18 months can be considered based on the DAPT score and patient preferences regarding risk of bleeding or death.
The document discusses dual antiplatelet therapy (DAPT) which refers to combination therapy with aspirin and a P2Y12 receptor inhibitor like clopidogrel, prasugrel, or ticagrelor. It addresses three questions on DAPT duration: 1) Is shorter DAPT (3-6 months) as effective as 12 months for newer generation drug-eluting stents? 2) Does longer DAPT (>12 months) reduce events more than 12 months? 3) Does continued DAPT reduce events in stable post-MI patients compared to aspirin alone? Studies of shorter DAPT found no increased risk of stent thrombosis. Extended DAPT was found to reduce stent thrombosis
Antiplatelet therapy is an important part of treatment for acute coronary syndrome. There are four main classes of antiplatelet agents: aspirin, P2Y12 receptor antagonists like clopidogrel and prasugrel, GP IIb/IIIa inhibitors like abciximab, and PAR-1 receptor antagonists like vorapaxar. Aspirin is recommended for all patients, and dual antiplatelet therapy with aspirin and a P2Y12 receptor antagonist is recommended for at least 1 year following ACS depending on the treatment strategy and patient risk factors.
This document discusses antiplatelet therapies and summarizes several studies on their use. It provides guidelines for antiplatelet treatment in different clinical scenarios, such as acute coronary syndrome or stent placement. It also discusses controversies around restarting aspirin after intracerebral hemorrhage and managing dual antiplatelet therapy following a bleed. The document emphasizes the need to balance bleeding risks against risks of stent thrombosis.
The CAPRIE study found that clopidogrel therapy resulted in a relative risk reduction of 8.7% compared to aspirin therapy for preventing cardiovascular events in patients with atherosclerosis, with fewer gastrointestinal hemorrhages. The CURE trial found that in patients with acute coronary syndrome receiving aspirin, pretreatment with clopidogrel followed by long-term therapy reduced major cardiovascular events compared to placebo. The CLASSICS trial found that clopidogrel had superior safety and tolerability to ticlopidine for antiplatelet therapy after coronary stenting, with comparable efficacy.
This document discusses antiplatelet therapy and P2Y12 platelet inhibition. It notes that dual antiplatelet therapy with aspirin and a P2Y12 inhibitor such as clopidogrel, prasugrel, or ticagrelor is the standard treatment for patients with acute coronary syndrome. It reviews the mechanisms of action and pharmacological properties of different antiplatelet drugs. It also summarizes key trials that have evaluated antiplatelet therapies and provides recommendations from guidelines on treatment selection and duration based on a patient's risk of bleeding and thrombosis.
This document summarizes a study comparing long-term outcomes of clopidogrel versus aspirin monotherapy after percutaneous coronary intervention (PCI). The study included over 5,400 patients who received dual antiplatelet therapy for 6-18 months after PCI. Patients were then randomized to clopidogrel or aspirin monotherapy. After a median follow up of 5.8 years, the primary endpoint occurred in 12.8% of clopidogrel patients and 16.9% of aspirin patients, showing clopidogrel reduced risk. Secondary endpoints including thrombosis and bleeding were also lower with clopidogrel. The study concludes clopidogrel provides significant relative risk reduction compared to aspirin for long-term
The document discusses dual antiplatelet therapy (DAPT) with aspirin and a P2Y12 receptor inhibitor for patients receiving coronary stents. It addresses three questions on optimal DAPT duration: 1) Is shorter DAPT (3-6 months) as effective as 12 months for newer-generation drug-eluting stents? 2) Does longer DAPT (>12 months) reduce ischemic events more than 12 months of DAPT? 3) Does continued DAPT past 12 months benefit stable post-MI patients more than aspirin alone? The document summarizes several studies investigating these questions and guidelines on DAPT duration and choice of P2Y12 inhibitor.
1) For stable patients who undergo percutaneous coronary intervention (PCI) with stenting, dual antiplatelet therapy (DAPT) with aspirin and a P2Y12 receptor blocker is recommended for at least 12 months.
2) For those at high risk of bleeding, DAPT may be limited to less than 1 year, with a minimum of 1 month.
3) After 1 year of DAPT without complications, continuing therapy for an additional 18 months can be considered based on the DAPT score and patient preferences regarding risk of bleeding or death.
The document discusses dual antiplatelet therapy (DAPT) which refers to combination therapy with aspirin and a P2Y12 receptor inhibitor like clopidogrel, prasugrel, or ticagrelor. It addresses three questions on DAPT duration: 1) Is shorter DAPT (3-6 months) as effective as 12 months for newer generation drug-eluting stents? 2) Does longer DAPT (>12 months) reduce events more than 12 months? 3) Does continued DAPT reduce events in stable post-MI patients compared to aspirin alone? Studies of shorter DAPT found no increased risk of stent thrombosis. Extended DAPT was found to reduce stent thrombosis
Antiplatelet therapy is an important part of treatment for acute coronary syndrome. There are four main classes of antiplatelet agents: aspirin, P2Y12 receptor antagonists like clopidogrel and prasugrel, GP IIb/IIIa inhibitors like abciximab, and PAR-1 receptor antagonists like vorapaxar. Aspirin is recommended for all patients, and dual antiplatelet therapy with aspirin and a P2Y12 receptor antagonist is recommended for at least 1 year following ACS depending on the treatment strategy and patient risk factors.
This document discusses antiplatelet therapies and summarizes several studies on their use. It provides guidelines for antiplatelet treatment in different clinical scenarios, such as acute coronary syndrome or stent placement. It also discusses controversies around restarting aspirin after intracerebral hemorrhage and managing dual antiplatelet therapy following a bleed. The document emphasizes the need to balance bleeding risks against risks of stent thrombosis.
The CAPRIE study found that clopidogrel therapy resulted in a relative risk reduction of 8.7% compared to aspirin therapy for preventing cardiovascular events in patients with atherosclerosis, with fewer gastrointestinal hemorrhages. The CURE trial found that in patients with acute coronary syndrome receiving aspirin, pretreatment with clopidogrel followed by long-term therapy reduced major cardiovascular events compared to placebo. The CLASSICS trial found that clopidogrel had superior safety and tolerability to ticlopidine for antiplatelet therapy after coronary stenting, with comparable efficacy.
This document discusses antiplatelet therapy and P2Y12 platelet inhibition. It notes that dual antiplatelet therapy with aspirin and a P2Y12 inhibitor such as clopidogrel, prasugrel, or ticagrelor is the standard treatment for patients with acute coronary syndrome. It reviews the mechanisms of action and pharmacological properties of different antiplatelet drugs. It also summarizes key trials that have evaluated antiplatelet therapies and provides recommendations from guidelines on treatment selection and duration based on a patient's risk of bleeding and thrombosis.
This document summarizes a study comparing long-term outcomes of clopidogrel versus aspirin monotherapy after percutaneous coronary intervention (PCI). The study included over 5,400 patients who received dual antiplatelet therapy for 6-18 months after PCI. Patients were then randomized to clopidogrel or aspirin monotherapy. After a median follow up of 5.8 years, the primary endpoint occurred in 12.8% of clopidogrel patients and 16.9% of aspirin patients, showing clopidogrel reduced risk. Secondary endpoints including thrombosis and bleeding were also lower with clopidogrel. The study concludes clopidogrel provides significant relative risk reduction compared to aspirin for long-term
Choosing antiplatelet therapy before during and after hosp for acscardiositeindia
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- The document discusses guidelines for antiplatelet therapy before, during, and after hospitalization for acute coronary syndrome (ACS).
- It recommends aspirin for all patients without contraindications, and ticagrelor over clopidogrel or prasugrel due to its greater effectiveness in reducing ischemic events, stent thrombosis, and death for up to one year.
- For patients undergoing percutaneous coronary intervention (PCI), pretreatment with a P2Y12 inhibitor such as clopidogrel is recommended to reduce complications, with higher loading doses for those who have not received previous treatment.
This document discusses anti-platelet drugs used to treat arterial thrombi, specifically newer P2Y12 receptor antagonists. It provides details on Clopidogrel, Prasugrel, and Ticagrelor which are widely used due to being more potent than Aspirin. Clinical trials including TRITON-TIMI 38, TRILOGY-ACS and PLATO compared the drugs and found Ticagrelor and Prasugrel superior to Clopidogrel in reducing ischemic events without increasing major bleeding risk. The document concludes the drugs have differences in efficacy against stent thrombosis and risk of bleeding.
The document provides guidance from the 2016 ACC/AHA on the duration of dual antiplatelet therapy (DAPT) in patients with coronary artery disease. It aims to update several previous guidelines. Key recommendations include:
- For patients with stable ischemic heart disease treated with PCI, DAPT including clopidogrel should be given for at least 1 month after bare-metal stent placement and at least 6 months after drug-eluting stent placement.
- For patients with acute coronary syndrome treated with PCI, DAPT including clopidogrel, prasugrel or ticagrelor should be given for at least 12 months. Ticagrelor and prasugrel may be preferred over clopid
Coronary artery disease remains the leading cause of death in the US. Acute coronary syndromes are caused by a sudden reduction in coronary blood flow due to atherosclerosis. There are three presentations of ACS: unstable angina, NSTEMI, and STEMI. Treatment involves stabilizing the patient, risk stratification, and determining reperfusion strategy which may involve fibrinolysis, PCI, or CABG. Long term management focuses on preventative therapies including antiplatelets, statins, beta blockers, ACE inhibitors, and other secondary prevention medications.
Anti thrombotic therapy in difficult clinical conditionsDrArpan Chouhan
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This document discusses anti-thrombotic therapy in difficult clinical conditions. It summarizes various antiplatelet and anticoagulant drugs, difficult situations for their use including high ischemic or bleeding risk, and strategies for balancing thrombotic and hemorrhagic risks. Certain drugs like prasugrel and ticagrelor are preferred for high ischemic burden due to more potent platelet inhibition, while dose adjustments and shorter durations are recommended for high bleeding risk. Careful management is needed in situations like surgery, renal dysfunction, and pregnancy to minimize risks.
"Decoding Antithrombotics in Acute Ischemic Events with Dr. Ganesh"
🌟 Greetings, everyone! I'm Dr. Ganesh, and today we're diving into a critical topic: Antithrombotics in Acute Ischemic Events. Whether you're a healthcare professional, a patient, or just someone keen on understanding the complexities of cardiovascular health, this discussion is for you.
This document summarizes a randomized controlled trial that compared clopidogrel to ticagrelor or prasugrel in 1002 patients aged 70 years or older with non-ST-elevation acute coronary syndrome. Patients were randomly assigned to receive clopidogrel or ticagrelor/prasugrel. The primary outcome was major or minor bleeding, while the co-primary outcome included mortality, myocardial infarction, stroke, and bleeding. The results found clopidogrel was associated with fewer bleeding events compared to ticagrelor/prasugrel without increasing the risk of the combined clinical outcome. The conclusion is that clopidogrel could be an alternative P2Y12 inhibitor, especially for elderly patients
This document summarizes recent studies on the duration of dual antiplatelet therapy (DAPT) following percutaneous coronary intervention (PCI) with drug-eluting stents (DES). The 2016 ACC/AHA guidelines recommend 6-12 months of DAPT depending on patient risk factors. Newer studies show shorter DAPT durations of 1-3 months followed by antiplatelet monotherapy may be noninferior or superior to 12 months of DAPT in reducing bleeding risks, especially for patients at high bleeding risk. Emerging data suggests a P2Y12 inhibitor alone may be preferable to aspirin monotherapy after DAPT. While shorter DAPT durations show promise, the 2016 guidelines should still be
This document summarizes different antiplatelet medications used to prevent blood clots, including aspirin, clopidogrel, prasugrel, ticagrelor, and others. Aspirin works by irreversibly inhibiting the COX-1 enzyme and blocking thromboxane A2 production. Clopidogrel and prasugrel are prodrugs that require metabolic conversion to irreversibly inhibit the P2Y12 receptor. Ticagrelor is a reversible P2Y12 inhibitor with a faster onset than clopidogrel. Clinical trials such as PLATO found ticagrelor reduced cardiovascular events compared to clopidogrel in ACS patients.
This document summarizes various trials that have evaluated antiplatelet drugs like aspirin, clopidogrel, prasugrel, ticagrelor, as well as oral anticoagulants in patients with acute coronary syndromes or those undergoing percutaneous coronary intervention. It discusses major trials such as ISIS-2, CURE, TRITON, PLATO and others that helped establish the efficacy and safety of these antiplatelet and anticoagulant drugs. It also summarizes recent trials that have evaluated shorter durations of dual antiplatelet therapy compared to longer durations.
This document provides guidelines for the evaluation and treatment of patients presenting with chest pain and suspected ST-elevation myocardial infarction (STEMI). It recommends administering aspirin and nitroglycerin in the prehospital setting. Upon arrival, an ECG should be obtained without delaying reperfusion therapy. For early presenters (<3 hours), fibrinolysis is preferred if an invasive strategy is not available within 90 minutes. Otherwise, an invasive strategy involving percutaneous coronary intervention is preferred if it can be performed within 90 minutes. Guidelines are provided for pain control, anticoagulation, antiplatelet therapy, and other medications in the management of STEMI.
The TWILIGHT trial compared ticagrelor monotherapy to ticagrelor plus aspirin in patients at high risk of bleeding and ischemic events after PCI. Over 7,000 patients received ticagrelor and aspirin for 3 months after PCI. Then patients were randomized to ticagrelor alone or with aspirin for 12 more months. The study found ticagrelor monotherapy was associated with a 44% lower risk of bleeding over 1 year without increasing ischemic events, suggesting it may be a safer option for high risk patients after a brief initial period of dual antiplatelet therapy.
This document outlines guidelines for secondary stroke prevention through lifestyle modifications, medication management of risk factors like hypertension, diabetes, and dyslipidemia, use of antiplatelet and anticoagulant medications, and surgical or endovascular interventions if needed. Key recommendations include maintaining a Mediterranean diet, regular exercise, smoking cessation, controlling blood pressure to 130/80 mmHg or lower, managing diabetes to an A1C of 7% or lower, using high intensity statins to target an LDL of 70 mg/dL or lower, and prescribing antiplatelet or anticoagulant medications depending on individual risk factors. Surgical procedures may be considered for severe carotid stenosis, atrial fibrillation with contraindications to ant
This document discusses antiplatelet therapy for acute coronary syndromes. It provides information on dual antiplatelet therapy using aspirin and P2Y12 inhibitors like clopidogrel, prasugrel, and ticagrelor. It summarizes trials comparing these drugs and outlines treatment strategies and duration of dual antiplatelet therapy based on a patient's risk level. Factors influencing response to clopidogrel and the potential additional mechanisms of action of ticagrelor are also reviewed.
This study compared ticagrelor pretreatment versus prasugrel at time of PCI in NSTE-ACS patients undergoing PCI. The primary outcome was rate of periprocedural myonecrosis within 24 hours of PCI. Results showed ticagrelor pretreatment significantly reduced myonecrosis compared to prasugrel at PCI (16.9% vs. 35.8%, p=0.003), due to faster onset of platelet inhibition. Secondary outcomes including MACE at 1 month were similar. This pilot study supports ticagrelor pretreatment to improve outcomes in intermediate-high risk NSTE-ACS undergoing PCI.
0900 0920 Antiplatelet and Anticoaulation Therapy Aleti FINAL(1).pptxAdelSALLAM4
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This document provides guidelines for antiplatelet and anticoagulation therapy. It discusses:
1) Current practice guidelines for managing antiplatelet therapy in CAD patients, including the selection of different antiplatelet medications and optimal durations of dual antiplatelet therapy.
2) Evidence for aspirin, clopidogrel, prasugrel, and ticagrelor in primary and secondary prevention. It finds prasugrel and ticagrelor reduce ischemic events compared to clopidogrel but with potential for higher bleeding risks.
3) Guidelines for dual antiplatelet therapy duration after stent implantation, recommending at least 1 year for most patients but shorter durations for those at high bleeding risk
This document discusses the classification, presentation, diagnosis, and treatment of acute coronary syndrome (ACS). ACS results from an imbalance between myocardial oxygen supply and demand due to a thrombotic coronary artery. It is classified as ST-elevation myocardial infarction (STEMI), non-ST-elevation myocardial infarction (NSTEMI), or unstable angina (UA) based on electrocardiogram findings and cardiac biomarker levels. Initial treatment involves oxygen, nitroglycerin, aspirin, a P2Y12 inhibitor, and anticoagulation. STEMI patients should receive reperfusion via primary percutaneous coronary intervention or fibrinolysis if primary PCI cannot be performed in a timely manner.
Among patients with or at high risk of CVD, use of an FDC strategy for blood pressure, cholesterol, and platelet control vs usual care resulted in significantly improved medication adherence.Polypill therapy significantly improved adherence, SBP and LDL-cholesterol in high risk patients compared with usual care, especially among those who were under-treated at baseline.
1) The study investigated the effects of prolonged dual antiplatelet therapy (DAPT) beyond 12 months after drug-eluting stent implantation for coronary bifurcation lesions.
2) Among 2082 patients event-free at 12 months post-procedure, those receiving DAPT for ≥12 months (n=1776) had lower rates of all-cause death, myocardial infarction, and stent thrombosis at 4 years compared to those on DAPT <12 months (n=306).
3) Prolonged DAPT ≥12 months was associated with reduced long-term risks for bifurcation lesions, including left main lesions, compared to shorter DAPT.
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Choosing antiplatelet therapy before during and after hosp for acscardiositeindia
Â
- The document discusses guidelines for antiplatelet therapy before, during, and after hospitalization for acute coronary syndrome (ACS).
- It recommends aspirin for all patients without contraindications, and ticagrelor over clopidogrel or prasugrel due to its greater effectiveness in reducing ischemic events, stent thrombosis, and death for up to one year.
- For patients undergoing percutaneous coronary intervention (PCI), pretreatment with a P2Y12 inhibitor such as clopidogrel is recommended to reduce complications, with higher loading doses for those who have not received previous treatment.
This document discusses anti-platelet drugs used to treat arterial thrombi, specifically newer P2Y12 receptor antagonists. It provides details on Clopidogrel, Prasugrel, and Ticagrelor which are widely used due to being more potent than Aspirin. Clinical trials including TRITON-TIMI 38, TRILOGY-ACS and PLATO compared the drugs and found Ticagrelor and Prasugrel superior to Clopidogrel in reducing ischemic events without increasing major bleeding risk. The document concludes the drugs have differences in efficacy against stent thrombosis and risk of bleeding.
The document provides guidance from the 2016 ACC/AHA on the duration of dual antiplatelet therapy (DAPT) in patients with coronary artery disease. It aims to update several previous guidelines. Key recommendations include:
- For patients with stable ischemic heart disease treated with PCI, DAPT including clopidogrel should be given for at least 1 month after bare-metal stent placement and at least 6 months after drug-eluting stent placement.
- For patients with acute coronary syndrome treated with PCI, DAPT including clopidogrel, prasugrel or ticagrelor should be given for at least 12 months. Ticagrelor and prasugrel may be preferred over clopid
Coronary artery disease remains the leading cause of death in the US. Acute coronary syndromes are caused by a sudden reduction in coronary blood flow due to atherosclerosis. There are three presentations of ACS: unstable angina, NSTEMI, and STEMI. Treatment involves stabilizing the patient, risk stratification, and determining reperfusion strategy which may involve fibrinolysis, PCI, or CABG. Long term management focuses on preventative therapies including antiplatelets, statins, beta blockers, ACE inhibitors, and other secondary prevention medications.
Anti thrombotic therapy in difficult clinical conditionsDrArpan Chouhan
Â
This document discusses anti-thrombotic therapy in difficult clinical conditions. It summarizes various antiplatelet and anticoagulant drugs, difficult situations for their use including high ischemic or bleeding risk, and strategies for balancing thrombotic and hemorrhagic risks. Certain drugs like prasugrel and ticagrelor are preferred for high ischemic burden due to more potent platelet inhibition, while dose adjustments and shorter durations are recommended for high bleeding risk. Careful management is needed in situations like surgery, renal dysfunction, and pregnancy to minimize risks.
"Decoding Antithrombotics in Acute Ischemic Events with Dr. Ganesh"
🌟 Greetings, everyone! I'm Dr. Ganesh, and today we're diving into a critical topic: Antithrombotics in Acute Ischemic Events. Whether you're a healthcare professional, a patient, or just someone keen on understanding the complexities of cardiovascular health, this discussion is for you.
This document summarizes a randomized controlled trial that compared clopidogrel to ticagrelor or prasugrel in 1002 patients aged 70 years or older with non-ST-elevation acute coronary syndrome. Patients were randomly assigned to receive clopidogrel or ticagrelor/prasugrel. The primary outcome was major or minor bleeding, while the co-primary outcome included mortality, myocardial infarction, stroke, and bleeding. The results found clopidogrel was associated with fewer bleeding events compared to ticagrelor/prasugrel without increasing the risk of the combined clinical outcome. The conclusion is that clopidogrel could be an alternative P2Y12 inhibitor, especially for elderly patients
This document summarizes recent studies on the duration of dual antiplatelet therapy (DAPT) following percutaneous coronary intervention (PCI) with drug-eluting stents (DES). The 2016 ACC/AHA guidelines recommend 6-12 months of DAPT depending on patient risk factors. Newer studies show shorter DAPT durations of 1-3 months followed by antiplatelet monotherapy may be noninferior or superior to 12 months of DAPT in reducing bleeding risks, especially for patients at high bleeding risk. Emerging data suggests a P2Y12 inhibitor alone may be preferable to aspirin monotherapy after DAPT. While shorter DAPT durations show promise, the 2016 guidelines should still be
This document summarizes different antiplatelet medications used to prevent blood clots, including aspirin, clopidogrel, prasugrel, ticagrelor, and others. Aspirin works by irreversibly inhibiting the COX-1 enzyme and blocking thromboxane A2 production. Clopidogrel and prasugrel are prodrugs that require metabolic conversion to irreversibly inhibit the P2Y12 receptor. Ticagrelor is a reversible P2Y12 inhibitor with a faster onset than clopidogrel. Clinical trials such as PLATO found ticagrelor reduced cardiovascular events compared to clopidogrel in ACS patients.
This document summarizes various trials that have evaluated antiplatelet drugs like aspirin, clopidogrel, prasugrel, ticagrelor, as well as oral anticoagulants in patients with acute coronary syndromes or those undergoing percutaneous coronary intervention. It discusses major trials such as ISIS-2, CURE, TRITON, PLATO and others that helped establish the efficacy and safety of these antiplatelet and anticoagulant drugs. It also summarizes recent trials that have evaluated shorter durations of dual antiplatelet therapy compared to longer durations.
This document provides guidelines for the evaluation and treatment of patients presenting with chest pain and suspected ST-elevation myocardial infarction (STEMI). It recommends administering aspirin and nitroglycerin in the prehospital setting. Upon arrival, an ECG should be obtained without delaying reperfusion therapy. For early presenters (<3 hours), fibrinolysis is preferred if an invasive strategy is not available within 90 minutes. Otherwise, an invasive strategy involving percutaneous coronary intervention is preferred if it can be performed within 90 minutes. Guidelines are provided for pain control, anticoagulation, antiplatelet therapy, and other medications in the management of STEMI.
The TWILIGHT trial compared ticagrelor monotherapy to ticagrelor plus aspirin in patients at high risk of bleeding and ischemic events after PCI. Over 7,000 patients received ticagrelor and aspirin for 3 months after PCI. Then patients were randomized to ticagrelor alone or with aspirin for 12 more months. The study found ticagrelor monotherapy was associated with a 44% lower risk of bleeding over 1 year without increasing ischemic events, suggesting it may be a safer option for high risk patients after a brief initial period of dual antiplatelet therapy.
This document outlines guidelines for secondary stroke prevention through lifestyle modifications, medication management of risk factors like hypertension, diabetes, and dyslipidemia, use of antiplatelet and anticoagulant medications, and surgical or endovascular interventions if needed. Key recommendations include maintaining a Mediterranean diet, regular exercise, smoking cessation, controlling blood pressure to 130/80 mmHg or lower, managing diabetes to an A1C of 7% or lower, using high intensity statins to target an LDL of 70 mg/dL or lower, and prescribing antiplatelet or anticoagulant medications depending on individual risk factors. Surgical procedures may be considered for severe carotid stenosis, atrial fibrillation with contraindications to ant
This document discusses antiplatelet therapy for acute coronary syndromes. It provides information on dual antiplatelet therapy using aspirin and P2Y12 inhibitors like clopidogrel, prasugrel, and ticagrelor. It summarizes trials comparing these drugs and outlines treatment strategies and duration of dual antiplatelet therapy based on a patient's risk level. Factors influencing response to clopidogrel and the potential additional mechanisms of action of ticagrelor are also reviewed.
This study compared ticagrelor pretreatment versus prasugrel at time of PCI in NSTE-ACS patients undergoing PCI. The primary outcome was rate of periprocedural myonecrosis within 24 hours of PCI. Results showed ticagrelor pretreatment significantly reduced myonecrosis compared to prasugrel at PCI (16.9% vs. 35.8%, p=0.003), due to faster onset of platelet inhibition. Secondary outcomes including MACE at 1 month were similar. This pilot study supports ticagrelor pretreatment to improve outcomes in intermediate-high risk NSTE-ACS undergoing PCI.
0900 0920 Antiplatelet and Anticoaulation Therapy Aleti FINAL(1).pptxAdelSALLAM4
Â
This document provides guidelines for antiplatelet and anticoagulation therapy. It discusses:
1) Current practice guidelines for managing antiplatelet therapy in CAD patients, including the selection of different antiplatelet medications and optimal durations of dual antiplatelet therapy.
2) Evidence for aspirin, clopidogrel, prasugrel, and ticagrelor in primary and secondary prevention. It finds prasugrel and ticagrelor reduce ischemic events compared to clopidogrel but with potential for higher bleeding risks.
3) Guidelines for dual antiplatelet therapy duration after stent implantation, recommending at least 1 year for most patients but shorter durations for those at high bleeding risk
This document discusses the classification, presentation, diagnosis, and treatment of acute coronary syndrome (ACS). ACS results from an imbalance between myocardial oxygen supply and demand due to a thrombotic coronary artery. It is classified as ST-elevation myocardial infarction (STEMI), non-ST-elevation myocardial infarction (NSTEMI), or unstable angina (UA) based on electrocardiogram findings and cardiac biomarker levels. Initial treatment involves oxygen, nitroglycerin, aspirin, a P2Y12 inhibitor, and anticoagulation. STEMI patients should receive reperfusion via primary percutaneous coronary intervention or fibrinolysis if primary PCI cannot be performed in a timely manner.
Among patients with or at high risk of CVD, use of an FDC strategy for blood pressure, cholesterol, and platelet control vs usual care resulted in significantly improved medication adherence.Polypill therapy significantly improved adherence, SBP and LDL-cholesterol in high risk patients compared with usual care, especially among those who were under-treated at baseline.
1) The study investigated the effects of prolonged dual antiplatelet therapy (DAPT) beyond 12 months after drug-eluting stent implantation for coronary bifurcation lesions.
2) Among 2082 patients event-free at 12 months post-procedure, those receiving DAPT for ≥12 months (n=1776) had lower rates of all-cause death, myocardial infarction, and stent thrombosis at 4 years compared to those on DAPT <12 months (n=306).
3) Prolonged DAPT ≥12 months was associated with reduced long-term risks for bifurcation lesions, including left main lesions, compared to shorter DAPT.
Similar to Antiplatelets in IHD, Dose Duration, DAPT vs SAPT (20)
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Promoting Wellbeing - Applied Social Psychology - Psychology SuperNotesPsychoTech Services
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A proprietary approach developed by bringing together the best of learning theories from Psychology, design principles from the world of visualization, and pedagogical methods from over a decade of training experience, that enables you to: Learn better, faster!
Histololgy of Female Reproductive System.pptxAyeshaZaid1
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Dive into an in-depth exploration of the histological structure of female reproductive system with this comprehensive lecture. Presented by Dr. Ayesha Irfan, Assistant Professor of Anatomy, this presentation covers the Gross anatomy and functional histology of the female reproductive organs. Ideal for students, educators, and anyone interested in medical science, this lecture provides clear explanations, detailed diagrams, and valuable insights into female reproductive system. Enhance your knowledge and understanding of this essential aspect of human biology.
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The UK is currently facing a Adhd Medication Shortage Uk, which has left many patients and their families grappling with uncertainty and frustration. ADHD, or Attention Deficit Hyperactivity Disorder, is a chronic condition that requires consistent medication to manage effectively. This shortage has highlighted the critical role these medications play in the daily lives of those affected by ADHD. Contact : +1 (747) 209 – 3649 E-mail : sales@trinexpharmacy.com
- Video recording of this lecture in English language: https://youtu.be/Pt1nA32sdHQ
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These lecture slides, by Dr Sidra Arshad, offer a simplified look into the mechanisms involved in the regulation of respiration:
Learning objectives:
1. Describe the organisation of respiratory center
2. Describe the nervous control of inspiration and respiratory rhythm
3. Describe the functions of the dorsal and respiratory groups of neurons
4. Describe the influences of the Pneumotaxic and Apneustic centers
5. Explain the role of Hering-Breur inflation reflex in regulation of inspiration
6. Explain the role of central chemoreceptors in regulation of respiration
7. Explain the role of peripheral chemoreceptors in regulation of respiration
8. Explain the regulation of respiration during exercise
9. Integrate the respiratory regulatory mechanisms
10. Describe the Cheyne-Stokes breathing
Study Resources:
1. Chapter 42, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 36, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 13, Human Physiology by Lauralee Sherwood, 9th edition
10 Benefits an EPCR Software should Bring to EMS Organizations Traumasoft LLC
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The benefits of an ePCR solution should extend to the whole EMS organization, not just certain groups of people or certain departments. It should provide more than just a form for entering and a database for storing information. It should also include a workflow of how information is communicated, used and stored across the entire organization.
Does Over-Masturbation Contribute to Chronic Prostatitis.pptxwalterHu5
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In some case, your chronic prostatitis may be related to over-masturbation. Generally, natural medicine Diuretic and Anti-inflammatory Pill can help mee get a cure.
Cell Therapy Expansion and Challenges in Autoimmune DiseaseHealth Advances
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There is increasing confidence that cell therapies will soon play a role in the treatment of autoimmune disorders, but the extent of this impact remains to be seen. Early readouts on autologous CAR-Ts in lupus are encouraging, but manufacturing and cost limitations are likely to restrict access to highly refractory patients. Allogeneic CAR-Ts have the potential to broaden access to earlier lines of treatment due to their inherent cost benefits, however they will need to demonstrate comparable or improved efficacy to established modalities.
In addition to infrastructure and capacity constraints, CAR-Ts face a very different risk-benefit dynamic in autoimmune compared to oncology, highlighting the need for tolerable therapies with low adverse event risk. CAR-NK and Treg-based therapies are also being developed in certain autoimmune disorders and may demonstrate favorable safety profiles. Several novel non-cell therapies such as bispecific antibodies, nanobodies, and RNAi drugs, may also offer future alternative competitive solutions with variable value propositions.
Widespread adoption of cell therapies will not only require strong efficacy and safety data, but also adapted pricing and access strategies. At oncology-based price points, CAR-Ts are unlikely to achieve broad market access in autoimmune disorders, with eligible patient populations that are potentially orders of magnitude greater than the number of currently addressable cancer patients. Developers have made strides towards reducing cell therapy COGS while improving manufacturing efficiency, but payors will inevitably restrict access until more sustainable pricing is achieved.
Despite these headwinds, industry leaders and investors remain confident that cell therapies are poised to address significant unmet need in patients suffering from autoimmune disorders. However, the extent of this impact on the treatment landscape remains to be seen, as the industry rapidly approaches an inflection point.
Mercurius is named after the roman god mercurius, the god of trade and science. The planet mercurius is named after the same god. Mercurius is sometimes called hydrargyrum, means ‘watery silver’. Its shine and colour are very similar to silver, but mercury is a fluid at room temperatures. The name quick silver is a translation of hydrargyrum, where the word quick describes its tendency to scatter away in all directions.
The droplets have a tendency to conglomerate to one big mass, but on being shaken they fall apart into countless little droplets again. It is used to ignite explosives, like mercury fulminate, the explosive character is one of its general themes.
2. Points to be covered
• Current antiplatelet drugs
• DAPT
• Antiplatelets in
1. stable angina with no intervention.
2. stable angina with intervention.
3. unstable angina.
4. ACS Treated With Medical Therapy Alone.
5. ST-elevation (STE)-ACS and receiving fibrinolytic therapy.
6. ACS and Primary PCI
7. CABG
4. DAPT
Aspirin (low dose) + P2Y12 inhibitor
• PLATO Trial - A significant reduction in mortality occurred with ticagrelor
compared to clopidogrel.
• TRITON study - Demonstrated no net benefit of prasugrel compared with
clopidogrel for patients with low body weight (<60 kg) or those ≥75 years of age .
Found net harm with prasugrel for patients with previous transient ischemic attack
or cerebrovascular accident.
• POPular AGE study - In patients aged 70 years or older presenting with NSTE-
ACS, clopidogrel is a favourable alternative to ticagrelor, because fewer bleeding
events were found without an increase in the combined endpoint of all-cause
death, myocardial infarction, stroke, and bleeding.
5. 1) Stable Angina no intervention
• In patients with stable angina low-dose aspirin is recommended to
reduce atherosclerotic events.
• Dose - 81 mg (75-100 mg)
• Routine combination of aspirin and a P2Y12 inhibitor is not
recommended due to an excessive risk of bleeding.
• European Society of Cardiology recommend daily use of low-dose
aspirin, and if allergic to aspirin then Clopidogrel can be used.
6. Aspirin monotherapy or Clopidogrel monotherapy?
• In Clopidogrel Versus Aspirin in Patients at Risk of Ischemic Events
(CAPRIE) trial interpreted that there was a relative increase (3.7%) in
risk of Myocardial infarction with clopidogrel only group.
• Clopidogrel reduced the rate of ischemic rehospitalizations compared
with aspirin when all 3 risk factors were taken into account -
Ischaemic stroke, myocardial infarction, or vascular death
7.
8. 2) Stable Angina with intervention
In patients with SIHD revascularized with
BMS - DAPT given for minimum of 1 month
DES - DAPT should be given for at least 6 month.
(DAPT – low dose aspirin (75-100) and P2Y12
Inhibitor
9.
10. Unstable Angina
• Aspirin (ASA) is the first choice and is administered as soon as
possible after presentation and continued indefinitely.
• clopidogrel should be administered to patients who are unable to take
ASA because of hypersensitivity or major gastrointestinal intolerance.
• A loading dose of non–enteric-coated aspirin 162 mg to 325 mg is the
initial antiplatelet therapy.
• Maintenance dose is 75 mg per day to 150 mg per day , lifelong.
11. CURE trial.
• Clopidogrel in Unstable Angina to Prevent Recurrent Ischemic Events
(CURE) trial.
• Among 12562 patients, the combination of clopidogrel and aspirin
lowered the composite of death, MI, or stroke by 21% at 30 days
compared with aspirin alone.
13. In patients with ST-elevation (STE)-ACS and
receiving fibrinolytic therapy
• With an initial non-invasive strategy, add a loading dose followed by
daily maintenance dose of clopidogrel or ticagrelor to aspirin (DAPT)
and anticoagulation as soon as possible after admission and up to 12
month
• Ticagrelor has rapid onset of action compared with clopidogrel, while
also allowing a higher level of platelet inhibition and more rapid
reversal compared with clopidogrel. (PLATO STUDY)
14.
15. Duration of DAPT in Patients With ACS Treated With
Medical Therapy Alone
• NO revascularization or fibrinolytic therapy – DAPT [Low dose
aspirin and P2Y12 inhibitor therapy (clopidogrel or ticagrelor)]
should be continued for at least 12 months(COR-1).
• In patients with NSTE–ACS who are managed with medical
therapy alone and treated with DAPT, it is reasonable to use
ticagrelor in preference to clopidogrel for maintenance P2Y12
inhibitor therapy.(COR-2A)
16. Duration of DAPT in Patients With STEMI Treated With Fibrinolytic Therapy
• In patients with STEMI treated with fibrinolytic therapy, DAPT
therapy should be continued for a minimum of 14 days and ideally
at least 12 months.(COR-1)
• And if they tolerate DAPT without bleeding complication and who
are not at high bleeding risk (e.g., prior bleeding on DAPT,
coagulopathy, oral anticoagulant use), continuation of DAPT for
longer than 12 months may be reasonable.(COR- 2B)
17.
18. In Patients with ACS and Primary PCI
• 2021 , Class I and IIa American College of Cardiology/American Heart
Association Guideline Recommendations for Antiplatelet Therapy in
Patients Receiving Primary PCI-
• Aspirin 162 to 325 mg load before procedure f/b 75-100mg daily
maintenance dose.
• Clopidogrel load: 600 mg as early as possible or at time of PCI. f/b 75mg
daily for 1 year.
• Prasugrel load: 60 mg as early as possible or at time of PCI f/b 10mg daily
for 1 year.
• Ticagrelor load: 180 mg as early as possible or at time of PCI f/b 90mg teice
a day for 1 year.
19. COR Recommendations
I
In patients withACS (NSTE-ACS or STEMI) treated with
DAPT after BMS or DES implantation, P2Y12 inhibitor therapy
(clopidogrel, prasugrel, or ticagrelor) should be
given for at least 12 months.
I
In patients treated with DAPT, a daily aspirin dose of 81 mg
(range, 75 mg to 100 mg) is recommended.
IIa
In patients withACS (NSTE-ACS or STEMI) treated with
DAPT after coronary stent implantation, it is reasonable to
use ticagrelor in preference to clopidogrel for maintenance P2Y12 inhibitor
therapy.
IIa
In patients withACS (NSTE-ACS or STEMI) treated with
DAPT after coronary stent implantation who are not at high risk for bleeding
complications and who do not have a history of stroke or TIA, it is reasonable
to choose prasugrel over clopidogrel for maintenance P2Y12 inhibitor therapy.
Duration of DAPT in Patients With ACS Treated With PCI
20. Duration of DAPT in Patients With ACS Treated With PCI
COR Recommendations
IIb
In patients with ACS (NSTE-ACS or STEMI) treated with coronary stent
implantation who have tolerated DAPT without a bleeding complication and who
are not at high bleeding risk (e.g., prior bleeding on DAPT, coagulopathy, oral
anticoagulant use), continuation of DAPT (clopidogrel, prasugrel, or ticagrelor) for
longer than 12 months may be reasonable .
IIb
In patients with ACS treated with DAPT after DES implantation who develop a high
risk of bleeding (e.g., treatment with oral anticoagulant therapy), are at high risk of
severe bleeding
complication (e.g., major intracranial surgery), or develop significant overt
bleeding, discontinuation of P2Y12 inhibitor therapy after 6 months may be
reasonable.
III:
Harm
Prasugrel should not be administered to patients with a prior history of stroke or
TIA.
21.
22. Recommendations for Duration of DAPT in
Patients Undergoing CABG
COR Recommendations
I
In patients treated with DAPT after coronary stent implantation who subsequently
undergo CABG, P2Y12 inhibitor therapy should be resumed postoperatively so that
DAPT continues until the recommended duration of therapy is completed.
I
In patients withACS (NSTE-ACS or STEMI) being treated with DAPT who
undergo CABG, P2Y12 inhibitor therapy should be resumed after CABG to
complete 12 months of DAPT therapy afterACS.
I
In patients treated with DAPT, a daily aspirin dose of 81 mg (range, 75 mg to 100
mg) is recommended.
IIb
In patients with SIHD, DAPT (with clopidogrel initiated early postoperatively) for
12 months after CABG may be reasonable to improve vein graft patency.