Open Access
CC BY 4.0 · Handchir Mikrochir Plast Chir
DOI: 10.1055/a-2739-3810
Fallbericht

Late-Onset Digital Ischaemia after WALANT: Successful Reversal with Off-Label Urapidil

Verzögert auftretende digitale Ischämie nach WALANT: Erfolgreiche Behandlung mit Off-Label Einsatz von Urapidil

Authors

  • Andrea Frey

    1   Hand Surgery, Kantonsspital Basel, Basel, Switzerland
  • Lukas Mathys

    1   Hand Surgery, Kantonsspital Basel, Basel, Switzerland
  • Christine Kammerhofer

    1   Hand Surgery, Kantonsspital Basel, Basel, Switzerland
 

Abstract

Background

WALANT (Wide Awake Local Anaesthesia No Tourniquet) has revolutionised hand surgery by enabling procedures with a combination of lidocaine and epinephrine, thereby eliminating the need for sedation or a tourniquet. Although epinephrine is now considered safe in low concentrations, rare ischaemic complications may still occur.

Case Report

This report concerns a 74-year-old woman who developed delayed-onset digital ischaemia after WALANT-assisted excision of a Dupuytren’s nodule. Phentolamine, the standard reversal agent, was unavailable. Local infiltration with urapidil (12.5 mg), a selective α₁-adrenergic antagonist, rapidly restored perfusion and sensation. The patient recovered fully without sequelae.

Conclusion

This case highlights a rare but critical complication of WALANT. Urapidil may represent a safe and effective alternative to phentolamine in the management of epinephrine-induced vasospasm.


Zusammenfassung

Hintergrund

WALANT (Wide Awake Local Anesthesia No Tourniquet) hat die Handchirurgie durch die Kombination von Lidocain und Adrenalin ohne Sedierung und Blutleere wesentlich verändert. Obwohl niedrig dosiertes Adrenalin heute als sicher gilt, können in seltenen Fällen ischämische Komplikationen auftreten.

Fallbericht

Wir berichten über eine 74-jährige Patientin, die nach der WALANT-gestützten Exzision eines Dupuytren-Knotens eine verspätet einsetzende digitale Ischämie entwickelte. Da Phentolamin – das Standardantidot – nicht verfügbar war, erfolgte die Infiltration mit Urapidil (12,5 mg), einem selektiven α₁-Blocker. Darunter kam es rasch zur Reperfusion und vollständigen Sensibilitätsrückkehr. Die Patientin erholte sich ohne bleibende Schäden.

Schlussfolgerung

Dieser Fall verdeutlicht eine seltene, aber kritische Komplikation der WALANT-Technik. Urapidil könnte eine sichere und wirksame Alternative zu Phentolamin darstellen, wenn dieses nicht verfügbar ist.


Introduction

The WALANT (Wide Awake Local Anesthesia No Tourniquet) technique, first described by Lalonde [1], has fundamentally changed modern hand surgery practice. By combining lidocaine with low-dose epinephrine (typically 1:100,000), surgeons achieve both effective anesthesia and hemostasis without the need for sedation or tourniquet use. The technique allows patients to remain awake and cooperative, enabling real-time intraoperative assessment of active motion, which is particularly useful for tendon and nerve procedures. WALANT has been increasingly adopted worldwide due to its cost-effectiveness, reduced perioperative morbidity, and the ability to perform procedures in minor procedure rooms outside traditional operating theaters [2], [3].

Epinephrine serves a dual role within the WALANT protocol. Its vasoconstrictive effect significantly reduces intraoperative bleeding, providing a clear surgical field and potentially shortening operative time. Moreover, by decreasing local blood flow, epinephrine slows systemic absorption of lidocaine, thereby prolonging its anesthetic effect and enhancing patient comfort throughout the procedure. The anesthetic duration typically ranges from 4 to 6 hours, depending on tissue characteristics and injection technique. The maximal vasoconstrictive effect generally occurs 20 to 30 minutes after infiltration, underscoring the importance of adequate waiting time before incision to achieve optimal hemostasis [3].

Historically, concerns existed regarding the risk of digital necrosis when epinephrine was used in the fingers or toes, largely due to reports involving high-concentration solutions or unbuffered preparations [4], [5]. However, numerous studies in the last two decades have confirmed the safety of appropriately buffered, low-concentration epinephrine in digital blocks, demonstrating extremely low rates of ischemic complications (<0.1%) even in elderly patients or those with mild vascular comorbidities [3], [6].

Despite its overall safety, WALANT requires careful patient selection. Contraindications include known peripheral vascular disease, Raynaud’s phenomenon, Buerger’s disease, prior digital replantation, severe arteriosclerosis, uncontrolled hypertension, and systemic conditions that may compromise microvascular circulation [5], [7]. Age-related endothelial dysfunction and reduced microvascular reserve may increase susceptibility to vasospastic events even in patients without overt vascular disease. Preoperative assessment should include a detailed vascular history and consideration of alternative anesthetic strategies in high-risk patients.

While phentolamine, a non-selective α-adrenergic antagonist, remains the standard reversal agent for epinephrine-induced digital ischemia, access may be limited in some institutions. Alternative pharmacologic approaches, including selective α₁-blockers such as urapidil, are worth considering. Understanding the mechanisms of vasospasm, the pharmacology of reversal agents, and the risk factors for ischemia is critical to ensuring patient safety during WALANT procedures [7], [8].


Case Report

A 74-year-old right-handed woman presented with a Dupuytren’s nodule at the base of her right middle finger. Past medical history included well-controlled hypertension. She had no history of Raynaud’s phenomenon, peripheral vascular disease, diabetes, or smoking.

Preoperative planning included discussion of observation, collagenase injection, and surgical excision. The patient complained of progressive discomfort due to the nodule, experiencing pain particularly when applying pressure on the hand against a flat surface or when gripping and holding objects. Given the increasing symptoms and functional limitation affecting daily activities, the patient elected to proceed with surgical excision under WALANT. Written informed consent was obtained after comprehensive counseling regarding the nature of the procedure, potential risks, benefits, and alternative treatment options.

On the day of surgery, 9 mL of 1% lidocaine with epinephrine (1:100,000) was infiltrated using a field block technique. One mL of sodium bicarbonate was added to buffer the solution. A dwell time of 40 minutes ensured optimal vasoconstriction and anesthesia [3].

Surgery was performed via a Bruner incision, excising the Dupuytren’s nodule. Tenosynovitis was observed in both the deep and superficial flexor tendons, and a prophylactic A1 pulley release was performed to facilitate improved tendon gliding. Intraoperative perfusion appeared normal. The patient experienced an uneventful postoperative recovery and was subsequently discharged from the hospital.

Four hours postoperatively, the patient noticed increasing coldness and numbness of the digit, leading to urgent consultation in our emergency department. Examination revealed cyanosis distal to the proximal interphalangeal joint, absent capillary refill, and complete sensory loss, consistent with digital ischemia [6], [9].

Phentolamine was unavailable in our institution; 2.5 mL of urapidil (12.5 mg) was injected locally near the A1 pulley. Urapidil is accessible within our anesthesia service for use in the treatment of hypertensive emergencies. Within minutes, reperfusion was evident, with restoration of warmth, normal color, and sensation [7], [8]. Systemic hemodynamics remained stable. The patient was monitored overnight; recovery was uneventful.

At two-week follow-up, the finger was well-perfused with normal motion and sensation. At six weeks, wound healing was complete, and the patient reported full satisfaction.


Discussion

This case highlights several important considerations in the management of rare delayed-onset digital ischemia following WALANT. First, even in patients without evident vascular disease, advanced age and microvascular changes may increase susceptibility to prolonged vasospasm. Clinicians should be aware that ischemic complications can present hours after surgery, necessitating patient education regarding early warning signs, including persistent coldness, discoloration, or sensory loss [6], [9].

Epinephrine-induced vasoconstriction occurs through stimulation of α₁-adrenergic receptors in the vascular smooth muscle, resulting in decreased perfusion distal to the injection site. Normally, this effect is transient, and perfusion recovers spontaneously as the epinephrine is metabolized. However, in rare cases, vasospasm may persist or be exacerbated by patient-specific factors such as endothelial dysfunction, microvascular disease, or local tissue characteristics [2], [3].

Phentolamine is the traditionally recommended reversal agent due to its rapid α-adrenergic blockade and ability to restore digital perfusion effectively. Several case reports have demonstrated successful reversal of delayed ischemia even up to 14 hours post-injection [10]. In the absence of phentolamine, urapidil—a selective peripheral α₁-adrenergic antagonist with central sympatholytic effects–offers a useful alternative. Its advantages include potent peripheral vasodilation, minimal reflex tachycardia, and a favorable safety profile in elderly patients [7], [8]. In our case, local infiltration of urapidil rapidly restored perfusion, suggesting that it may serve as an effective off-label rescue therapy in settings where phentolamine is unavailable.

From a practical standpoint, urapidil is generally more accessible in European hospitals than phentolamine. Marketed as Ebrantil or Urapidil Stragen, it is widely used for perioperative blood pressure control and hypertensive emergencies, as well as in patients requiring stable hemodynamic management without excessive cardiac workload or reflex tachycardia [11]. In Switzerland and other European countries, a pack of five 50 mg/10 mL ampoules typically costs between CHF 75–150 (€ 70–140), corresponding to approximately CHF 15–30 (€ 14–28) per ampoule, depending on supplier and regional availability [12]. In contrast, phentolamine (Regitine) is less frequently available and often requires special ordering, as it is no longer routinely marketed in several European countries. Where obtainable, its cost is typically higher–often CHF 40–60 (€ 38–56) per ampoule–and supply limitations further restrict its use in acute settings. Consequently, urapidil may represent not only a pharmacologically suitable but also a more practical and cost-effective alternative for the reversal of epinephrine-induced digital ischemia in the clinical environment.

From a clinical perspective, this case emphasizes several preventive and management strategies: preoperative screening for vascular risk factors, careful use of epinephrine in elderly or patients with vascular disease, standardized monitoring protocols post-WALANT procedures, patient education regarding ischemic symptoms, and ensuring immediate access to reversal agents. Additionally, the successful use of urapidil in this case warrants further investigation in prospective studies or animal models to determine optimal dosing, safety, and comparative efficacy with phentolamine.

Finally, while WALANT is generally safe and transformative in hand surgery, awareness of rare but potentially severe complications is critical. Expanding the repertoire of available reversal agents, including off-label options like urapidil, may enhance patient safety and provide clinicians with effective tools for managing digital ischemia.


Conclusion

WALANT is a safe and transformative technique in hand surgery. Rare ischemic complications require vigilance and preparedness. Urapidil may serve as an effective alternative to phentolamine for epinephrine-induced digital ischemia. Early recognition and intervention are essential to ensure complete recovery [3], [7].


Patient Consent Statement

Written informed consent was obtained from the patient for publication of this case report, including all clinical information and associated images. Confidentiality and anonymity were maintained.



Dr. med. univ. Andrea Frey

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is a specialist in orthopedics and traumatology of the musculoskeletal system and prospective specialist of hand surgery (FMH, EBHS). After several years of clinical work in various university and cantonal centers in Switzerland, including Zurich, Basel, and Solothurn, she is currently employed as a senior physician in the Hand Surgery Clinic at the Cantonal Hospital Baselland.

Conflict of Interest

The authors declare that they have no conflict of interest.


Correspondence

Dr. Andrea Frey
Kantonsspital Basel, Hand Surgery
Gemeindeholzweg
4101 Basel
Switzerland   

Publication History

Received: 01 September 2025

Accepted: 20 October 2025

Article published online:
11 December 2025

© 2025. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/).

Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany


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