Preoperative Drug Monitoring in Management of Patients with Hip Fracture on Treatment with Direct Oral Anticoagulants

Carlo Rostagno1,2, Giulio Maria Mannarino2, Alessandro Cartei2

  • 1Dipartimento Medicina sperimentale e clinica, Università di Firenze, Firenze, Italy.

Insights

Monitoring direct oral anticoagulant (DOAC) levels helps optimize surgery timing for hip fracture patients. Assaying DOAC levels can reduce delays, especially for those needing neuraxial anesthesia, improving patient management.

Area of Science:

  • Anesthesiology
  • Orthopedic Surgery
  • Pharmacology

Background:

  • Hip fracture patients on direct oral anticoagulants (DOACs) present management challenges for timely surgical intervention.
  • Current guidelines for managing DOACs before surgery may lead to prolonged waiting times.

Purpose of the Study:

  • To evaluate if monitoring DOAC levels improves surgical management in hip fracture patients.
  • To determine the impact of DOAC level monitoring on time to surgery (TTS) and hospitalization length.

Main Methods:

  • A study compared 147 hip fracture patients on DOACs (Group A) with 206 controls (Group B).
  • Group A was divided into A1 (guideline-based timing) and A2 (DOAC level-guided timing).
  • Specific DOAC level thresholds were used to guide anesthesia choices (neuraxial vs. general).

Main Results:

  • Surgery within 48 hours was more frequent in controls (80.6%) than DOAC patients (51%).
  • DOAC level-guided timing (A2) resulted in surgery within 48 hours for 56% of patients, compared to 45.1% in A1.
  • DOAC assay led to an average 1-day reduction in TTS and hospitalization.
  • 89% of patients with DOAC levels <50 ng/mL had surgery within 48 hours, with successful neuraxial anesthesia in 26 patients.

Conclusions:

  • DOAC level monitoring aids in defining optimal time to surgery for hip fracture patients.
  • This approach is particularly beneficial for patients requiring neuraxial anesthesia, potentially shortening delays by over 24 hours compared to standard guidelines.
Abstract

Related Concept Videos

Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants01:18

Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants

Oral anticoagulants are vital tools in preventing and treating blood clotting disorders. This diverse class of medications can be categorized as vitamin K antagonists, exemplified by warfarin, and direct thrombin inhibitors (DTIs), such as dabigatran, as well as factor Xa inhibitors, including rivaroxaban.
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
1.2K
Anticoagulant Drugs: Low-Molecular-Weight Heparins01:30

Anticoagulant Drugs: Low-Molecular-Weight Heparins

Hemostasis is a crucial process that prevents excessive blood loss from damaged blood vessels. It involves various mechanisms such as vasoconstriction, platelet adhesion and activation, and fibrin formation. The importance of each mechanism depends on the type of vessel injury. In contrast, thrombosis is the abnormal formation of a blood clot within the blood vessels, leading to potential complications if the clot obstructs blood flow. Thrombosis can be caused by increased coagulability of the...
686
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...
521
Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers01:22

Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers

Class I antiarrhythmic drugs are used to treat various types of arrhythmias or irregular heart rhythms. These drugs block the sodium (Na+) channels in the cardiac cells, thereby affecting the movement of electrical impulses across the heart. Class I antiarrhythmic drugs are divided into three subgroups: Class IA, Class IB, and Class IC, each with distinct mechanisms of action and effects on the heart.
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...
1.4K
Antihypertensive Drugs: Direct Renin Inhibitors01:25

Antihypertensive Drugs: Direct Renin Inhibitors

The renin-angiotensin-aldosterone system (RAAS) is an intricate physiological pathway involving numerous enzymes and hormones, including renin, angiotensin-converting enzyme (ACE), angiotensin I and II, and aldosterone. Imbalances within this system increase the production of angiotensin II and aldosterone. Increased angiotensin II levels promote vasoconstriction and blood pressure elevation. Concurrently, higher aldosterone levels stimulate sodium and water reabsorption in the kidneys,...
601
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...
167