Possible local anesthetic resistance in Emery–Dreifuss muscular dystrophy during regional anesthesia
نویسندگان
چکیده
31-year-old man with Emery–Dreifuss muscular dystrophy (EDMD) presenting for bilateral Achilles lengthening and equinoplanovalgus deformity correction. We performed bilateral popliteal sciatic and femoral nerve blockade, using ultrasound guidance and nerve stimulator confirmation, mainly to avoid some potential pitfalls of general anesthesia and airway instrumentation. However, the patient appeared resistant to the effects of local anesthetic. The few published reports of anesthesia management for such patients describe general and neuraxial techniques [1,2]. To our knowledge, this is the first written description of regional anesthesia in this rare patient population. EDMD is a rare X-linked condition that primarily affects skeletal muscle, leading to joint contractures with progressive weakness, and cardiac muscle, leading to malignant arrhythmias and cardiomyopathy [3]. EDMD presents unique challenges to the anesthetist, including arrhythmias (i.e., atrioventricular heart block), cardiomyopathy, possible compromised airway mechanics leading to difficult intubation (i.e., cervical paraspinal contractures and hypoplasia of the third to fifth cervical vertebral bodies that can influence neck flexion and extension), potential for difficult neuraxial access due to paraspinal muscle contractures, and concern for adverse medication reactions (i.e., succinylcholine exaggerated hyperkalemic response or risk of rhabdomyolysis [3] and negative volatile anesthetic reactions [1]). Considering the challenges of anesthetic management in this patient, it seemed reasonable that bilateral sciatic and femoral nerve blockade could avoid airway instrumentation and general anesthesia. Notably, however, the patient commented preoperatively that “...every time I received a local anesthetic injection at the dentist’s office, I required multiple injections in order to feel any effect.” A popliteal approach nerve block of the sciatic nerves was performed bilaterally with ultrasound, visualizing the circumferential perineural spread of ropivacaine at the junction of the tibial and common peroneal nerves. Bilateral perineural catheters were then placed. Then, a single-shot block of the femoral nerves at the inguinal crease was performed bilaterally with ultrasound, visualizing the circumferential perineural spread of ropivacaine. Despite nerve stimulation confirmation (Stimuplex HNS12, B. Braun Medical, Bethlehem, PA, USA) with less than 0.5 milliamperes and ultrasound imaging of perineural local anesthetic spread at all block sites (Fig. 1), the patient reported intact sensation to temperature (alcohol pad testing) and nociception (blunt needle prick) within all affected nerve distributions. Both sciatic catheters were then bolused with lidocaine, yet the patient reported achieving only a minimal degree of temperature sensation change. Owing to inadequate surgical anesthesia with the regional technique, we decided to administer total intravenous anesthesia (TIVA) using a laryngeal mask airway, thereby avoiding endotracheal intubation, muscle relaxation, and volatile anesthetics. The surgical procedure was completed within 2 hours with evidence of stable hemodynamics with TIVA using a propofol infusion and intermittent boluses of Letter to the Editor
منابع مشابه
Emery-Dreifuss Muscular Dystrophy: a Report of a Large Family with 11 Affected Individuals
No abstract is needed for letter to the editor
متن کاملAnaesthetic management of a patient with Emery-Dreifuss muscular dystrophy.
Emery-Dreifuss muscular dystrophy is a rare form of muscular dystrophy associated with cardiac implications such as cardiomyopathy and arrhythmias leading to sudden death. We describe the anesthetic management of a patient with Emery-Dreifuss muscular dystrophy who presented for orthopaedic surgery and discuss the disorder and its potential anaesthetic implications.
متن کاملIn Vitro Contracture Test Results and Anaesthetic Management of a Patient with Emery-Dreifuss Muscular Dystrophy for Cardiac Transplantation
Emery-Dreifuss muscular dystrophy (EDMD) is a hereditary neuromuscular disorder characterized by slowly progressive muscle weakness, early contractures, and dilated cardiomyopathy. We reported an uneventful general anaesthesia using total intravenous anaesthesia (TIVA) for cardiac transplantation in a 19-year-old woman suffering from EDMD. In vitro contracture test results of two pectoralis maj...
متن کاملEmery dreifuss muscular dystrophy: a clinico-pathological study.
Emery-Dreifuss muscular dystrophy (EDMD) is a rare and genetically heterogeneous disorder. We report two patients with emerin deficient X-linked EDMD and two probable patients with EDMD with typical early contractures, progressive muscle weakness and cardiac involvement. Family history was noted in one case. Muscle biopsy revealed features of dystrophy in all.
متن کاملIncreased Apolipoprotein E ~4 in Epilepsy with Senile Plaques
Dubowics V. Muscle biopsy: a practical approach. 2nd ed. London: Bailliere Tindall, 1985:340-343 Consalez GG, Thomas NST, Stayton CL, et al. Assignment of Emery-Dreifuss muscular dystrophy to the distal region of Xq28: the results of a collaborative study. Am J Hum Genet 199 1 ;48:468 -480 Yates JRW, Warner JP, Smith JA, et al. Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq2...
متن کامل