Abstract
Introduction
Patients who undergo total joint arthroplasty (TJA) are at a high risk for the development of thromboembolic complications. The rate at which venous thromboembolism occurs following TJA has been reported to be between 1.3–9.4%. As a result, the utilization of prophylactic therapies is considered standard of care in this patient population. The primary purpose of the current study was to 1) evaluate patient satisfaction with the use of intermittent compression devices 2) evaluate the risk of self-reported falls secondary to the use of these devices following TJA.
Methods
This is a single institution, prospective study on patients who underwent TJA at an urban, academic orthopedic specialty hospital. Patients were surveyed using an electronic patient rehabilitation application regarding their use and satisfaction with their home intermittent compression devices with a battery and power cord attachment that the patient must wear while using the devices. They were also asked if any falls or near-falls they may have experienced. Surveys were administered on postoperative Day 14, and patients were given 10 days to submit their responses. Using our institutions data warehouse, patient demographics were also collected (Table 1).
Results
Survey responses were collected from 479 patients who underwent TJA between August 2018 and October 2018. Of the respondents, 278 were female and 201 were male. Approximately 79% of patients in the cohort were satisfied with their use of their compression devices compared to 21% of patients who were unsatisfied. During this time, 16% of patients (75 pts) also reported at least one tripping episode at home and 11 patients (2.3%) had at least one fall at home.
Conclusion
These results suggest that patients are generally satisfied with their home intermittent compression devices. There are a significant number of trips or falls after surgery and further study examining the potential role of these devices and their cords in these falls is needed.
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