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All issues Volume 8 (2022) SICOT-J, 8 (2022) 28 Full HTML
Open Access
Issue
SICOT-J
Volume 8, 2022
Article Number 28
Number of page(s) 6
Section Lower Limb
DOI https://doi.org/10.1051/sicotj/2022029
Published online 28 June 2022

© The Authors, published by EDP Sciences, 2022

Licence Creative CommonsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Introduction

The venous thromboembolism rate post total hip arthroplasty (THA) and total knee arthroplasty (TKA) is higher than most other orthopaedic surgery, as well as other surgical disciplines [1]. It has been noted that in the absence of thromboprophylaxis, the Deep Venous Thrombosis (DVT) rate for THA is as high as 40–60% and in TKA is 40–85% [2]. This can be reduced to 1–10% with routine thromboprophylaxis agents [2, 3]. Furthermore, the pulmonary embolism rates after THA are 0.9–28% and after TKA is 1.5–25%, with a mortality rate of up to 15% [4–6]. The current health service executive (HSE) guideline recommends mechanical prophylaxis with 72 h of 40 mg enoxaparin, initiated 6–12 h after surgery, and a further 4 weeks of aspirin therapy for patients who received a THA or TKA [7]. This practice is based on recent publications from the American College of Chest Physicians (ACCP) 2012 and the American Academy of Orthopaedic Surgeons (AAOS) 2011 [8, 9]. In our department, we initiate patients on enoxaparin 6–12 h after THA and TKA; we then continue enoxaparin for their hospital stay and discharge patients for a further 4 weeks of 150 mg once daily aspirin therapy. Aspirin, known as acetylsalicylic acid, is a non-steroidal anti-inflammatory drug with anticoagulation effects due to its irreversible inhibition of platelet cyclo-oxygenase and selective inhibition of thromboxane A2 inhibition [10].

But is this practice still relevant with more recent guidelines suggesting that aspirin is not recommended as a single pharmacological agent [11, 12]. The National Institute of Clinical Excellence (NICE) 2021 guidelines for THA recommends either low molecular weight heparin (LMWH) for 10 days followed by 4 weeks of aspirin, or 4 weeks of LMWH, or one of the newer oral anticoagulants (NOAC) [11]. Whereas the Scottish Intercollegiate Guidelines Network (SIGN) 2014 clearly states that aspirin is not recommended as a sole pharmacological agent but recommends LMWH, fondaparinux, rivaroxaban or dabigatran [12]. The question that therefore arises is whether aspirin can be considered an optimal agent for venous thromboembolism (VTE) prophylaxis, in light of these more recent guidelines.

Materials and methods

This study selected all the patients who received an elective total hip arthroplasty or total knee arthroplasty, in a single center, between January 2016 and May 2021 retrospectively. Letterkenny University Hospital serves the population of Donegal with a catchment area of about 159,000 people [13]. All patients who had already been on Warfarin, Rivaroxaban, Dabigatran, or Fondaparinux prior to surgery were excluded from the study, which included 56 patients as they would continue with their regular anticoagulation therapy instead of receiving aspirin prophylaxis therapy. A total of 1178 patients who received aspirin for VTE prophylaxis were included, of which 721 underwent THA, and 457 received a TKA. This study assessed the rate of VTE as well as mortality for these patients over the first 3 months post-surgery, which was then compared to other similar studies to determine whether our VTE rate is comparable to other studies where a variety of different pharmacological prophylactic agents was used. If this is the case, it will support our statement that aspirin is still relevant as a sole pharmacological agent even with more recent guidelines contradicting this [11, 12].

One thousand one hundred and seventy-eighth patients who underwent a THA and TKA received 40 mg of enoxaparin within 12 h post-surgery and continued with a once-daily dose until they were discharged on aspirin for another 4 weeks [7]. The mean age for THA and TKA arthroplasty was 69.35 (SD ± 9.77) and 70.47 (SD ± 8.79), respectively. The female to male ratio was 1:1.1. The average length of hospital stay was 5.19 (SD ± 7.48) days for THA and 5.09 (SD ± 5.68) days for TKA. They also received mechanical prophylaxis with graduated compression stockings up to 6 weeks post the index procedure. The compression stockings were not used if any specific contra-indications were present (peripheral vascular disease, severe congestive cardiac failure, local skin problems). Patients receiving surgery in the morning were mobilized the same day by physiotherapy, and those receiving surgery in the afternoon were mobilized the following day.

The patients with signs and symptoms suggestive of symptomatic VTE would be identified either as an in-patient prior to discharge or presenting to the accident and emergency department after discharge from the hospital. If there is any suspicion of deep venous thrombosis (DVT), patients will undergo a Doppler Compression B-mode Ultrasound scan [14]. All patients with suspected PE received a Computerized Tomographic Pulmonary Arteriogram (CTPA) as this is the imaging of choice with high sensitivity and specificity demonstrated by the PIOPED II trial [15].

In this study the NIMIS system was used, which is a picture archive and communication system (PACS), to achieve our primary outcome in identifying how many patients received a workup (Doppler or CTPA) for potential symptomatic VTE within 90 days and who had a confirmed diagnosis on imaging. This is used as the cut-off by most similar studies as observational data suggests that the incidence of VTE after TKA and THA returns to the presurgical risk level at about 3 months post-surgery [16]. The NIMIS system is widely incorporated throughout Ireland hospital systems and is active in 70 hospitals across Ireland [17]. This meant that we could collect symptomatic VTE data from across the country for the patients who received their index arthroplasty surgery at Letterkenny University Hospital. Our secondary outcome assessed if any patients suffered from a fatal pulmonary embolism or any other cause of mortality within 3 months post-surgery. To establish this, we used the ICM system, which is used by our hospital, through which we could identify if and when a patient has passed away.

Results

Of the 1178 patients included in the study, a total of 124 (10.53%) patients received a workup for potential symptomatic VTE (Table 1). This would include patients with signs and symptoms suggestive of either a deep venous thrombosis or pulmonary embolism. Patients mainly complained of leg pain, swelling and discomfort or shortness of breath, and chest pain, respectively. Doppler ultrasound was performed on 94 patients with DVT symptoms, and 30 patients received a CTPA. Only 7 of 1178 (0.59%) patients had a confirmed DVT, and 7 patients (0.59%) had a confirmed Pulmonary Embolism (Table 1). There was an overall VTE rate of 14 of 1178 (1.19%) for all arthroplasties performed (Table 1).

Table 1

A summary of total number of surgeries performed and how many patients received a workup with a confirmed diagnosis of PE or DVT.

Table 2

Summary of key studies included in the study.

The overall VTE, PE, and DVT rate for THA was 1.8%, 0.97%, and 0.83% (13, 7, and 6 out of 721), respectively, whereas the overall VTE, PE, and DVT rate for TKA patients was 0.22%, 0%, and 0.22% (1, 0, and 1 out of 457), respectively (Table 1).

The mean time to presentation was 44.43 days (SD ± 32.59) for the symptomatic DVT patients and 24.57 days (SD ± 13.43) for the symptomatic PE patients.

No patients suffered a fatal pulmonary embolism within 90 days of index surgery nor any other cause of mortality.

Discussion

It is well-established that some of the major causes of readmission post THA and TKA are patients developing symptomatic DVT and PE [18]. For this reason, it is imperative that we, as orthopedic surgeons have an in-depth knowledge of pathophysiology and potential treatment modalities to prevent this. Many retrospective and prospective studies have been performed to identify the ideal pharmacological agent for VTE prophylaxis but there continues to be controversy regarding the optimal agent after joint arthroplasty [19]. A number of national guidelines are available and attempt to give guidance to orthopedic surgeons as to which agent is most effective [7, 11, 12]. The HSE guidelines advise prolonged low-dose aspirin therapy, which is not advised as a single pharmacological agent by the NICE and SIGN guidelines, but rather LMWH, Fondaparinux, Rivaroxaban, Apixaban, or Dabigatran [11, 12]. SIGN argues that there is sufficient data available to support the fact that aspirin is inferior to other anticoagulants [12]. A pharmacological agent can be considered an optimal treatment modality if it meets the following criteria: high efficacy in VTE prevention, low risk of bleeding, easily administered, cost-effective, and decreased postoperative complications [20].

Aspirin is easily administered, readily available and the most inexpensive of the comparative agents. Aspirin is an effective agent in preventing ischaemic cardiovascular and cerebrovascular disease, however, there remains controversy about whether aspirin is an effective drug for VTE prophylaxis post arthroplasty surgery [21]. We aimed to add data to support that aspirin is in fact a suitable agent.

Our local overall VTE rate for a 90-day follow-up period for 1178 arthroplasties performed was 1.19%. This is comparable to other large retrospective databases [22–25]. One of the largest databases was the American College of Surgeons National Surgical Quality Improvement Program (NSQIP) database which identified 363,530 patients who received a TKA or THA from 2008 to 2016. The overall VTE rate for THA and TKA was 0.6% and 1.4% respectively within 30 days post-surgery [22]. The numbers will likely be higher if a 90-day follow-up period was used as our mean time to presentation for symptomatic DVT was 44 days. A large Danish Hip Arthroplasty registry between 1997 and 2011 found a VTE rate of 1.3% for THA and 1.5% for TKA [26]. In Japan an administrative database of patients from 2008 to 2013 had an overall VTE rate of 1.4% [25]. The UK National Joint Registry (NJR) reports of 2010 and 2007 showed 90-day PE rates of 0.68% and 0.6%, respectively, post-THA and 0.6% post-TKA in the 2007 report [23, 24]. In our study, the overall PE rates post THA and TKA was 0.59% which is comparable to the UK NJR.

There have also been multiple direct comparative studies of aspirin versus Rivaroxaban and LMWH, suggesting that aspirin is as effective in preventing VTE post arthroplasty surgery [27, 28]. The EPCAT I trial (Extended Prophylaxis Comparing Low-Molecular-Weight Heparin to Aspirin in Total Hip Arthroplasty) suggested that the extended course of aspirin is non-inferior to extended LMWH [28]. The EPCAT II trial, which enrolled 3424 patients, also confirmed no statistically significant difference in outcome comparing Aspirin versus Rivaroxaban [27].

It has already been well established that the bleeding and wound complication risk of aspirin is comparable to or even better than most other anticoagulants used for VTE prophylaxis. Zou et al. stated that rivaroxaban had increased postoperative hidden blood loss, and postoperative wound complications [29]. This was also the case in the EPCAT I trial where aspirin was found to have a better bleeding risk rate than LMWH [28]. Multiple studies have cited a low risk of bleeding among patients receiving aspirin post total joint arthroplasty [20, 30–32].

The HSE guidelines suggest 150 mg of aspirin once daily for 4 weeks [7]. The importance of prolonged anticoagulation therapy was underlined in a retrospective study performed by Wells et al. that indicated a much higher VTE rate in patients receiving anticoagulation therapy for less than 14 days (3.9%) compared to more than 14 days (1.4%) [33]. Similarly, a systematic review comparing low dose (<162 mg/day) to high-dose (>162 mg/day) aspirin in patients post total joint arthroplasty found no statistically significant difference in terms of DVT, PE, 90-day mortality, and major bleeding [34]. Two large retrospective reviews performed recently supported this finding that low dose of aspirin (81 mg) had a similar outcome to a high dose of aspirin (325 mg) in THA and TKA patients [35, 36].

Graduated compression stockings are also provided to the patients as per the HSE guidelines, and their benefits have been undeniably supported by a study performed by Agu et al. which showed a 57% reduction of DVT post-THA [37].

The results of this study support the fact that low dose, prolonged duration aspirin with appropriate mechanical prophylaxis is comparable to the other anticoagulation therapy advised by the NICE and SIGN guidelines [11, 12].

But one of the limitations to this study is that our hospital technically uses combined pharmacological treatment, with enoxaparin given as an in-patient and then changed to aspirin therapy on discharge. The use of combined pharmacological therapy was supported by the EPCAT II trial, which showed that no statistically significant difference in VTE risk after TKA and THA if aspirin was given after an initial 5 days of rivaroxaban [27]. A recent review of the use of aspirin after joint arthroplasty concluded that for appropriately selected low-risk patients, aspirin is effective following initial rivaroxaban therapy [38]. The EPCAT III trial is an ongoing trial that will focus on comparing aspirin as a solo pharmacological agent to a combined regimen which will give us better clarity if the VTE rate would still be comparable without the initial transition phase. As stated by Fontalis et al., it is essential to accurately risk stratify patients into low-intermediate-high individuals as this will allow us to adjust our prophylaxis strategy accordingly [39] and therefore improve our overall VTE rates.

Conclusion

Aspirin is not only still relevant but can be considered one of the most optimal pharmacological agents in preventing VTE after THA and TKA. Aspirin has an efficacy comparable to the other anticoagulation drugs, has a low bleeding and wound complication risk, is easily administered, and is cost-effective.

Importance of article

There is a major risk of developing VTE post total knee and hip arthroplasty. There is still ongoing controversy regarding the optimal prophylactic agent to be used. Aspirin is an inexpensive, readily available agent used for a long time by orthopedic surgeons for VTE prophylaxis. But confidence in aspirin has been waning recently, with national guidelines like NICE and SIGN suggesting that it should not be used as a single pharmacological agent. The Irish HSE guideline still suggests the use of aspirin therapy – as is the case in our hospital. Our review of 1178 patients who underwent a THA and TKA suggests that aspirin is still relevant for use in VTE prophylaxis and can even be considered one of the most optimal agents.

Conflict of interest

The authors declare that they have no conflicting interests.

Funding

There is no funding source.

Ethical approval

Ethical approval was not required.

Informed consent

This article does not contain any studies involving human subjects.

Authors’ contributions

JP: Study design, data analyzing, original writing of the manuscript, editing manuscript. NN: Data Collection, Literature review, Formal analysis. IA: Data Collection, Literature review. AS: Supervision, Editing manuscript. SN: Project administration, Validation. YH: Conceptualization, Project administration.

Acknowledgments

We thank the HIPE (hospital in-patient enquire) department for assisting us in acquiring the patient lists and relevant demographics.

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Cite this article as: Pretorius J, Nemat N, Azeem I, Shaju T, Nadeem S & Hammad Y (2022) Is aspirin still relevant as a single pharmacological agent for venous thromboembolism prophylaxis post hip and knee arthroplasty surgery: A retrospective review. SICOT-J 8, 28

All Tables

Table 1

A summary of total number of surgeries performed and how many patients received a workup with a confirmed diagnosis of PE or DVT.

In the text
Table 2

Summary of key studies included in the study.

In the text

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