The authors obtained the patient's consent and consulted the Institutional Ethics Review Board (IRB) for approval (not deemed necessary by the IRB) for publishing in this journal. A 18 year old man, weight 50 kg, height 173 cm, was admitted in our center, with tibia and fibula fractures and undiagnosed severe congenital AS, he presented in CHF with functional capacity II (New York Heart Association Functional Classification). Preoperative examination attained findings revealed his valvular heart disease. He had palpitations and a fainting history, but had not receive any medical therapy before the present admission. An electrocardiogram (ECG) showed left ventricular hypertrophy (LVH) and strain pattern. Echocardiography revealed a bicuspid aortic valve, thickened leaflets, aortic valve area of 0.75 cm2, pressure gradient across aortic valve (peak) of 100 mm Hg, concentric LVH, and ejection fraction of 60%. Cardiologic consult reported high risk surgery for this patient, but because of a partially good functional capacity and preserved EF, they did not recommend AVR before orthopedic surgery. On the second day of admission, acute signs and symptoms of FES were observed in the patient. He had hypoxemia (SPO2 = 83%), tachypnea (34/min), tachycardia (120-140 beats/min), acute mental status deterioration, petechiae over the chest and in conjunctiva, thrombocytopenia, and anemia (Hb: 8.1 g/dL). Blood gas (ABG) analysis showed hypoxemia (PaO2 of 57.6 mm Hg), and metabolic acidosis (PH 7.27, base excess of -5.8). The patient was intubated and transferred to the intensive care unit (ICU). Mechanical ventilation with FIO2 of 1.0, IV methyl-prednisolone (125 mg/qid), infusion of heparin (18 units/kg/h), and delay in orthopedic surgery until symptoms recovery, were administrated. Fortunately he recovered after about 13 hours and was extubated by himself on the 3rd day of admission. After two units of packed RBC transfusion, his Hb rose to 10.8 g/dL, he was then sent to the operating room on the morning of the 4th day. The patient received all cardiac medications, oxazepam (10 mg) and ranitidine (50 mg), one hour before surgery, and anticoagulation was on hold for 6 hours before surgery. In the operation room, he had stable vital signs and his ABG analysis was normal. The last chest X-ray showed cardiomegaly, and an ECG revealed sinus rhythm and LVH. He received 2 mg midazolam, 100 µg fentanyl for premedication, and he was then put on monitoring (ECG, noninvasive blood pressure, pulse oximetry and urine output) and oxygen therapy with a mask. For management of the anesthesia, after informed consent was obtained, a sciatic and femoral nerve block (SFB), with ultrasound and nerve stimulator guided method (double guidance), was selected. SFB was performed, using a nerve stimulator (Temena, Felsberg-Gensungen, Germany) delivering 0.5 mA impulse for femoral nerve and 1 mA for sciatic nerve (0.1 ms) at 1 Hz and a SonoSite S-Nerve ultrasound platform.
An 8 to 15 MHz linear transducer (SonoSite, Bothell, Washington) was used for femoral nerve block only. Femoral nerve block was done by a 22 gauge, 50 mm short beveled, Teflon-coated needle (Locoplex, Vygon, Ecouen, France), with a 20 mL lidocaine 1% and bupivacaine 0.25% combination, and when nerve stimulation was led to a contraction of the quadriceps muscle and anterior movement of the patella, 20 cc of local anesthetic was injected. T sciatic nerve block was done by an anterior approach, with a 22 gauge, 150-mm short beveled, Teflon-coated needle (Locoplex, Vygon, Ecouen, France) needle and and when nerve stimulation was led to any foot movement, 25 mL of the previously mentioned local anesthetic drug combination. In case of failure in our regional techniques, our rescue method was general anesthesia (GA) with appropriate drugs (etomidate, cisatracuriom plus opioids and nitrose oxide) which may be anesthesiologists preferred choice for patients suffering from serious cardiac complications, including severe AS, or if their peripheral nerve block fails before or during surgery.
Surgery was started after twenty minutes, during which the patient was comfortable and did not sense any pain; furthermore, there were no hemodynamic complications during the next 150 minutes of operation time. Further course of recovery was uneventful, and the patient was discharged from the hospital in a satisfactory condition on the 6th day of admission. After six months, follow up was performed by phone and no orthopedic or general condition complications were reported.