Anticoagulation After Shoulder Arthroplasty
Routine pharmacologic anticoagulation beyond low-dose aspirin is not necessary for most patients undergoing shoulder arthroplasty, but mechanical prophylaxis should be used universally, with risk-stratified chemical prophylaxis reserved for high-risk patients. 1
Standard Prophylaxis Approach
For Average-Risk Patients
Mechanical prophylaxis (sequential compression devices) should be used intraoperatively and during the immediate postoperative period for all shoulder arthroplasty patients. 1
Low-dose aspirin (81 mg daily) for 6 weeks postoperatively is the preferred chemical prophylaxis for standard-risk patients, with a demonstrated VTE rate of only 0.56% and minimal bleeding complications (0.19%). 2
The American Academy of Orthopaedic Surgeons consensus recommendation supports routine use of mechanical and/or chemical prophylaxis despite limited evidence, acknowledging that shoulder arthroplasty carries lower VTE risk than lower extremity procedures. 1
Rationale for Conservative Approach
The overall VTE incidence after shoulder arthroplasty is substantially lower than lower extremity arthroplasty: 0.53% versus 1.2% in Medicare populations, with some studies reporting ranges from 0.2% to 0.63%. 2, 3, 4
Shoulder arthroplasty demonstrates a VTE rate approximately 3-5 times lower than hip arthroplasty (5.0 per 1000 vs 15.7 per 1000) and approximately 5 times lower than knee arthroplasty (5.0 per 1000 vs 26.9 per 1000). 4
The bleeding risk must be weighed against the lower baseline VTE risk, as wound hematoma rates are similar between shoulder and lower extremity procedures despite lower VTE rates. 3
High-Risk Patient Identification and Management
Patients Requiring Enhanced Prophylaxis
Chemical prophylaxis beyond aspirin should be considered for patients with specific high-risk features, including: 2, 3, 4
- History of prior VTE (most significant risk factor)
- Active malignancy or metastatic disease
- Known thrombophilia or hypercoagulable state
- Cardiac arrhythmia
- Congestive heart failure
- Coagulopathy
- Obesity
- Fracture as primary indication (hemiarthroplasty for fracture carries higher risk than elective total shoulder arthroplasty)
- Advanced age with multiple comorbidities
- Prolonged immobility or bed confinement expected postoperatively
Enhanced Prophylaxis Options for High-Risk Patients
For patients with demonstrated VTE risk factors, consider therapeutic anticoagulation with agents beyond aspirin, such as low-molecular-weight heparin or novel oral anticoagulants, after careful assessment of bleeding risk. 3
Each high-risk patient should undergo individualized risk stratification weighing their specific thrombotic risk against bleeding potential, as medically high-risk patients demonstrate significantly higher VTE rates (P = 0.018). 2
Special Considerations for Patients with History of Thromboembolic Events
Patients on Chronic Anticoagulation
For patients on chronic warfarin therapy who require shoulder arthroplasty, warfarin should be discontinued 4 days before the procedure. 1
Postoperative intravenous heparin should be considered only for patients with recent arterial or venous thromboembolism (within 1 month), continuing until therapeutic anticoagulation is re-established with warfarin. 1
The decision to bridge with heparin depends on the timing of the prior thromboembolic event and the patient's ongoing thrombotic risk versus surgical bleeding risk. 1
Patients with Mechanical Heart Valves or Atrial Fibrillation
Shoulder arthroplasty is classified as a procedure with low-to-moderate bleeding risk (2-day major bleeding risk 0-2%), which influences perioperative anticoagulation management decisions. 1
For patients with high thrombotic risk (e.g., mechanical mitral valve, recent stroke, CHADS₂ score ≥5), bridging anticoagulation may be warranted despite the surgical bleeding risk. 1
For patients with lower thrombotic risk (e.g., bileaflet aortic valve without atrial fibrillation, CHADS₂ score 0-2), temporary interruption of anticoagulation without bridging is generally acceptable. 1
Clinical Presentation and Diagnosis
VTE Characteristics After Shoulder Arthroplasty
A notably high proportion of VTE events after shoulder arthroplasty present as pulmonary embolism (4 of 6 patients in one series, representing 67%), which is a higher percentage than seen with lower extremity arthroplasty. 5, 4
Deep vein thromboses occur in both upper extremity (ipsilateral to surgery) and lower extremity locations, requiring comprehensive evaluation when VTE is suspected. 5
The typical presentation occurs within the first 90 days postoperatively, with diagnosis confirmed by duplex ultrasound for DVT and chest CT for PE. 2, 6, 5
Critical Pitfalls to Avoid
Do not routinely use the same aggressive anticoagulation protocols employed for lower extremity arthroplasty, as the VTE risk profile is substantially different and bleeding complications may outweigh benefits. 3
Do not overlook preoperative risk stratification, as failure to identify high-risk patients (particularly those with prior VTE, malignancy, or cardiac disease) leads to inadequate prophylaxis in those who need it most. 2, 3
Do not dismiss subtle postoperative symptoms such as unexplained dyspnea or ipsilateral arm swelling, as the high proportion of pulmonary embolisms requires vigilant surveillance. 5, 4
Do not assume all patients require the same prophylaxis regimen—the evidence supports risk-stratified approaches rather than universal aggressive anticoagulation. 1, 2, 3