In this case series, 58 patients who were scheduled for elective ORIF of hip fractures in a tertiary educational hospital from April 2013 to July 2013 were evaluated. The local Ethics Review Committee of Tehran University of medical sciences approved the study protocol. All participants signed written informed consent before participation.
Exclusion criteria were American Society of Anesthesiologists (ASA) class of more than III, injection site infection, coagulopathy, multiple fractures, substance abuse, and psychological disorder which disturb patient cooperation (
17). Among the 58 evaluated patients, 50 patients signed a written informed consent and accepted the procedure as the method of anesthesia after explanation of the risks and benefits of LPB. At least one day before the procedure time, all patients were interviewed by an anesthesiologist at the preoperative anesthesia clinic.
Before blocking procedure, all patients received intravenous midazolam of 0.15 to 0.3 mg/kg. Routine monitoring included electrocardiogram, pulse oximetry, noninvasive arterial blood pressure (BP), and side stream qualitative capnometry. Supplemental oxygen (4-6 L/min) through face mask was administered. Patients were positioned to lateral decubitus (operative site up). Preparation and draping of the relative lumbar region of the patient was done with 10% povidone iodine solution. After subcutaneous infiltration of entry point with 2 to 3 mL of 1% lidocaine, LPB was performed using an insulated 120-mm, 21-G, short (20° cutting) bevel needle (polymedic UPC, temena SAS, EU). The entry point was considered two to three patient's fingertip width (FTW) lateral to the midline, i.e. spinous process of lumbar vertebra, at the anterior superior iliac crest level (
Figure 1). The nerve stimulator (polystim II, polymedic, temena SAS, EU) was connected with the cathode to the insulated needle and with the anode to a solid-gel skin electrode at ipsilateral mid-thigh. Nerve stimulator was initially set at a current of 1.5 mA and 0.1 millisecond impulse duration at a 1 Hz frequency. The needle was advanced cautiously perpendicular to the skin, until the quadriceps femoris muscle twitches would be obtained or the transverse process of lumbar vertebrate was touched. In this situation, needle was redirected to pass above or below the transverse process and quadriceps twitches was elicited. Then the current was gradually lowered until motor response of quadriceps could be visible at a range of 0.3 to 0.5 mA. To avoid intraneural injection, contractions provoked by less than 0.3 mA were not accepted. thereafter, 30-mL mixture of 0.66% lidocaine hydrochloride (10-mL 2% lidocaine hydrochloride, Ferdows pharmacy, Tehran, Iran) and 0.166% Marcaine (10-mL 0.5% bupivacaine, Merk Generiques, Lyon, France), and 10-mL distilled water (
18,
19) was injected at that point after repeated negative aspirations. Injection against resistance was suspended and needle position was evaluated and adjusted properly. The interval between preparation and insulated needle extraction was considered as procedure time and was measured in minutes by an anesthesia nurse. The interval between completion of injection and painless abduction of Hansh joint was considered as establishment time and was recorded by the anesthetic nurse. Painful abduction of injured limb after about ten minutes was considered as block failure and another method of anesthesia would be planned. The patients were clinically sedated, i.e. fall asleep spontaneously in the absence of verbal, physical, or noxious stimuli while they were considered awaken and cooperating in the presence of each one) by a low infusion rate of anesthetic during surgery. An infusion of propofol (1% propofol MCT/LCT Fresenious, Fresenious Kabi, Austria, GmbH, Graz, Austria) in a rate of 20 to 30 µ/kg/min was started after transferring the patients to the surgery table and was gradually decreased by 50% after 20 to 30 minutes to the end of surgery and midazolam was repeated if needed. At the end of the operation, all the patients received 1-g intravenous acetaminophen, every 12 hours, which was started in the recovery room. Patients were mobilized after 24 hours of operation.
Block duration the interval between block establishment and first patient's opioids analgesic request (VAS > 3) up to 24 hours (off-bed time) were recorded in hours by an orthopedic resident who was blinded to the study. When the block was established, patient was transferred to the operation table. Surgery time was recorded in minutes by operating room staff and was defined as the time from patient transfer to the operation table to the time of transferring to the recovery room. At the end of operation, surgeon was asked to identify the degree of their satisfaction on immobilization and relaxation of operation site using numerical 11-point scale from zero (very unsatisfied) to 10 (very satisfied) (
20). Three to five minutes after premedication and before positioning, patients' BP and heart rate (HR) were recorded as BP1 and HR1. After patient settlement on the operation table, BP and HR were recorded as BP2 and HR2 by an anesthesia resident. Patients were asked to identify the degree of their pain using visual analogue pain scale (VAS) in which zero represented painless and ten was the worst experienced pain (
21). Partial effectiveness was considered as block failure and reported under failure cases. Any complication such as operation site sensitivity or mobility during surgery, hemodynamic changes, or patient irritability was reported. Any additional supplemental opioids were documented.