Introduction

Carpal tunnel syndrome (CTS) is the most common compression neuropathy of the upper extremity [2]. For the treatment of CTS, conservative and surgical options are available. Conservative treatments include wrist splints and corticosteroid treatments [10, 12]. In more severe cases of CTS and when conservative treatment fails, surgical treatment is indicated. Surgery consists of dividing the transverse carpal ligament, reducing the pressure on the nerve [13]. The general consensus on open carpal tunnel release (OCTR) is confined to a 2 to 3 cm long incision in the palm of the hand [6]. All overlying structures and the transverse carpal ligament are divided. Alternatively, an endoscopic release has recently been developed, but among other alternatives has not resulted in improved overall outcome except for earlier return to work and daily activities in favor of endoscopic surgery with a mean difference of −6 days [17].

Antiplatelets (AP) and anticoagulants (AC) are commonly used for patients with cerebrovascular, cardiovascular and peripheral vascular problems to prevent future thromboembolic events. There is no clear consensus regarding the perioperative management of AP or AC treatment for a OCTR surgical procedure. Continuation of AP or AC treatment for small surgery has been proven safe for several indications in the field of cutaneous [1, 11], dental [14] and cataract surgery [7].

In order to evaluate the feasibility of a randomized controlled trial, we first wanted to investigate the magnitude of the problem and collect some data for the sample size calculation. Therefore, we performed this observational study.

Methods

Patients were referred because of an electrophysiological confirmed diagnosis of CTS. The data from all patients who were surgically treated for CTS from June 2008 till June 2009 were prospectively collected. They were advised to continue AP or AC treatments perioperatively. For AC therapy international normalized ratio (INR) values were kept within the therapeutic values. An OCTR with a 3 cm long incision in the palm of the hand was performed according to previously described surgical procedure [6]. Bleeding was stopped using bipolar coagulation. All patients received compression bandage for 24 h postoperatively, and postoperative instructions of care. Follow-up was performed by phone 3 weeks postoperatively, and patients with persisting symptoms or complaints were seen at our outpatient department at 6 weeks postoperatively. Complications of discontinuation of therapy were noted.

Results

A total of 364 patients underwent OCTR surgery. 45 patients continued ASA treatment perioperatively and seven patients continued ACM. Intraoperative bleeding was easily controlled and postoperative bleeding was recorded in one patient who used ASA. He complained of a subcutaneous hematoma, but additional treatment was not needed. In the ACM-group, postoperative bleeding did not occur. Patients without AC treatment did not suffer from postoperative bleeding.

Discussion

Discontinuation of AP or AC treatment for OCTR is not needed to avoid bleeding complications. In fact, it may increase the risk on ischemic problems in patients already at risk for thrombotic events [8, 18].

Although designed as an investigational study, one of the major flaws of this study is the observational design. However, we believe a randomized clinical trial (RCT) is not justified for three reasons.

The first reason is related to the ischemic events that may arise after discontinuation of AP or AC therapy. Patients who would discontinue AP or AC treatment, would be exposed to an increased risk of cardiovascular adverse events. The risk on thromboembolic complications depends on the etiology. The risk of recurrent venous thromboembolism in the 3 months after proximal deep-vein thrombosis is approximately 50% in the absence of anticoagulation; one month of AC therapy reduces this risk to about 10% and after 3 months of AC therapy the risk remains about 5% [8, 16]. In patients with nonvalvular atrial fibrillation anticoagulant therapy has proven to reduce this risk with 66 % [5]. Although the exact risks on thromboembolic adverse events after discontinuation of AP or AC therapy for surgery are unknown, it has been estimated that stopping anticoagulant treatment for major surgery may increase the risk of postoperative thromboembolism a 100-fold [8]. Even in smaller, laparoscopic surgery the risk is 10-fold increased [9]. In patients with a high risk on perioperative thromboembolic events, prophylactic inferior vena cava filter placement can be considered to reduce the risk of recurrent thromboembolic disease [19]. An alternative to AP or AC treatment can be the use of low-molecular weight heparin bridging the perioperative period [8, 15]. Unintended discontinuation of long-term oral anticoagulant use after overnight or ambulatory procedures has been present in up to 11.4 % of patients [3]. Future studies are necessary, to identify the exact risk of adverse events after discontinuation of AP or AC therapy. Until then a risk-based approach may be considered. As a result of the relatively low risk of perioperative hemorrhage in the field of cutaneous, dental and cataract surgery the surgical protocols have been changed in favor of perioperative continuation of anticoagulant therapy [1, 7, 11, 14]. The postoperative readjustment of the therapeutic values of INR can be troublesome after discontinuation of AC treatment. Patients need blood to be drawn regularly and may have to change the dose of anticoagulant treatment [8].

Clopidogrel is an antiplatelet agent with similar pharmacodynamics as ASA. It selectively alters the ADP receptor on the blood platelet resulting in lessened blood aggregation. Because of its selective blocking, the agent has a higher antiplatelet effect than ASA and is effective at a lower dose. In the field of cardiovascular disease it has shown to significantly reduce new ischemia in the acute state after myocardial infarction compared with ASA [4]. Although it is hard to compare AP agents with AC counterparts, the general consensus is that AC, which is directly involved in the coagulation cascade, has a stronger anticoagulatory effect than AP agents. Although, in our patient population no patients were on Clopidogrel, we hypothesize that it is also safe to continue Clopidogrel perioperatively, as we compare its effect on coagulation with ASA.

Secondly, in our series the magnitude of the clinical problem is minimal. Thirdly, a large number of patients are needed for a properly designed study. For example, to establish a difference of 2% in postoperative bleeding—with a α = 0.05 and a power of 80%—about 500 (inclusion of estimated lost to follow-up) patients are needed per group. As a result, around 1,000 patients would be needed for a RCT.

As a result of the large number of patients needed to study the effect of continuation of anticoagulant therapy perioperatively, as well as the risk of serious adverse events in discontinuation of anticoagulants, combined with the minor magnitude of the clinical problem a RCT is not feasible. Instead, because of the slight risk of hemorrhage and the absence of intervention as a result of it, we have changed our surgical protocol for OCTR. Patients with chronic anticoagulant treatment do not have to stop their anticoagulant therapy for carpal tunnel release surgery.