Progress Analysis of Personalized Antiplatelet Therapy in Patients with Coronary Heart Disease Undergoing

Ji-Tong Yang1, Qiu-Juan Zhang2, Hua Li3

  • 1Department of Clinical Medicine, Kunming Medical University, 651106 Kunming, Yunnan, China.

PubMed

Insights

Coronary heart disease (CHD) treatment involves stent implantation and dual antiplatelet therapy (DAPT). Personalized antiplatelet therapy is crucial due to high on-treatment platelet reactivity (HTPR) in some patients.

Area of Science:

  • Cardiology
  • Pharmacology
  • Vascular Medicine

Background:

  • Coronary atherosclerosis (coronary heart disease, CHD) is a prevalent cardiovascular disease with significant health impacts.
  • Percutaneous coronary stent implantation is a primary treatment for severe CHD, often accompanied by dual antiplatelet therapy (DAPT) to prevent thrombosis.
  • High on-treatment platelet reactivity (HTPR), or antiplatelet resistance, occurs in some patients despite DAPT, posing a risk for stent thrombosis.

Purpose of the Study:

  • To review the mechanisms of action of current antiplatelet drugs.
  • To discuss the rationale for personalized antiplatelet therapy in CHD patients.
  • To explore methods for screening antiplatelet reactions and the development of novel antiplatelet agents.

Main Methods:

  • Review of existing literature on antiplatelet drug mechanisms.
  • Analysis of clinical studies on high on-treatment platelet reactivity (HTPR).
  • Discussion of screening methods and emerging antiplatelet therapies.

Main Results:

  • Current antiplatelet drugs like aspirin and clopidogrel have unclear mechanisms, leading to variable patient responses.
  • High on-treatment platelet reactivity (HTPR) is a recognized clinical challenge in patients undergoing DAPT after stenting.
  • Ticagrelor, indobufen, and rivaroxaban are identified as common, safe, and promising antiplatelet options.

Conclusions:

  • Personalized antiplatelet therapy is essential for managing CHD and preventing stent thrombosis.
  • Screening for high on-treatment platelet reactivity (HTPR) is necessary for optimizing treatment.
  • Further research into novel antiplatelet drugs is warranted to improve patient outcomes.

Related Concept Videos

Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors01:20

Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors

Antiplatelet drugs emerge as frontline defenders against the insidious threat of thromboembolic diseases, where abnormal clots obstruct vital blood vessels. These drugs stand as bulwarks, inhibiting platelet aggregation and clot formation, thereby mitigating the risk of life-threatening conditions like myocardial infarction, coronary artery disease, and thrombotic strokes.
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
384
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists01:23

Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists

Prostacyclin receptor agonists are a class of therapeutic agents integral to managing pulmonary arterial hypertension (PAH). These drugs operate by mimicking the action of prostaglandin I2, or PGI2, a naturally occurring compound in the body.
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...
97
Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers01:26

Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers

Receptor tyrosine kinase inhibitors (TKIs) and calcium channel blockers (CCBs) are two critical categories of drugs employed in the treatment of pulmonary artery hypertension (PAH). PAH is a disease that causes high blood pressure in the pulmonary arteries, resulting in chest pain, fatigue, and shortness of breath.
TKIs, such as imatinib (Gleevec), are particularly effective in tackling the growth and mitogenic factors that become upregulated in PAH patients. These factors contribute to the...
89
Antianginal Drugs: Calcium Channel Blockers and Ranolazine01:25

Antianginal Drugs: Calcium Channel Blockers and Ranolazine

Angina pectoris, a primary symptom of ischemic heart disease, requires careful pharmacological interventions. In this context, calcium channel blockers (CCBs) and ranolazine have emerged as crucial pharmacotherapeutic agents, providing deep insights into the complexities of angina management.
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...
382