From January 2019 to February 2020, forty adults with DRF undergoing open reduction and plating surgery at a standard operation theater of a university-affiliated hospital were recruited. This prospective observational study was approved by the Institutional Review Board of Kaohsiung Medical University Hospital (KMUHIRB-F(I)-20180116). The mean age of the patient was 61 ± 14 years old. Eleven patients had diabetes mellitus, 13 patients had hypertension, three patients had history of cerebral vascular accident, two patients had chronic kidney disease and one patient had chronic heart failure, and two patients had evidence of vascular calcification in wrist and hand vessels. Regarding the anesthetic risk of the included patients, 25 patients were classified as American Society of Anesthesiologists physical status (ASA) 2, 14 patients were classified as ASA 3, and one patient was classified as ASA 4. Patients with multiple injuries, an open fracture, or a pathological fracture were excluded. The indication for undergoing WALANT or general GA depended on the patients’ preference. Patients in group A underwent surgery using the WALANT technique, and all surgical procedures and administration of local anesthetics were performed by the same surgeon.
In group A (WALANT), 1% lidocaine with 1:100,000 epinephrine was used. Patients’ forearms were placed in a supine position. Local anesthetic injection began with employing the Henry approach to make an incision at the proximal end with a 26-G needle. After 2–3 mL had been injected into the subcutaneous fat, the 26-G needle was exchanged with a 22-G long needle, and the local anesthetic was slowly injected along the volar incision wound from the same entry point. Typically, 15 mL is enough to cover all the volar surface of the subcutaneous area for Henry approach incisions. A 24 G needle was then used through the pronator quadratus and touched the volar surface of the radius; 10 mL of local anesthetic was injected into the fracture site and along the distal radius volar periosteum. Patients pronated their forearm, and 10 mL of local anesthetic was injected along the dorsal periosteum. Finally, 2–3 mL was injected over the radial styloid to prepare for preliminary K-wire fixation. The local anesthetic injection procedure generally took 5–10 minutes to perform. We prepped after the injection of local anesthetic. Surgery was performed 20 minutes after local anesthetic injection, once the haemostatic effect of epinephrine was observed.
In group B (GA), patients underwent surgery using GA with ultrasound-guided brachial plexus block (BPB) at the supraclavicular level. GA was induced with 1 mcg/kg fentanyl and 2 mg/kg propofol and maintained with 2–4% sevoflurane. The anesthesiologist identified the ultrasound image of brachial plexus at the supraclavicular level. Under real-time ultrasound guidance, the anesthesiologist performed supraclavicular block with 25 mL of 0.25% bupivacaine. Thereafter, a tourniquet was applied to the patient’s upper arm. After exsanguinating the forearm blood with an Esmach bandage, the tourniquet was set up at 250 mmHg and the surgery for DRF was performed.
GA was induced by two experienced anesthesiologists, and the surgical procedure was performed by three surgeons. All surgeons performing the surgical procedures were classified as having level 3 expertise 11. Different volar locking plates (ACU-LOC plate, ACUMED, LLC., USA; Anatomic Volar Plate System, Depuy Synthes, Johnson & Johnson Co., USA; Distal R.A.F. Locking plate, APLUS Co., Taiwan) were used for internal fixation in all cases. A standard volar approach was used to expose the fractured side. The fracture was approached from the radial side of the flexor carpi radialis, and the quadrate pronator muscle was incised to reduce the fracture.
In group A, MAP, HR, and NRS were measured by nursing staff in the operation theatre seven times perioperatively, namely before surgery (T0) and at the time of injection of local anesthesia (T1), skin incision (T2), fracture reduction (T3), plating and screwing (T4), skin closure (T5), surgery completion (T6). In group B, the anesthesia team continuously monitored patients’ intraoperative physiological status. MAP and HR in group B were marked after induction (T1) and at the other six same time points as in group A.
We recorded the operative time of each group, from skin incision to wound closure. The blood loss was record in each group. In GA group, the blood loss was recorded after wound closure and before tourniquet deflation. The radiographic parameters to examining the preoperative and postoperative quality of reduction and plating including radial height, radial inclination, volar tilt, ulnar variance and articular step-offs were compared between each group. Anesthesia-related (and surgery-related) risk within 30 days of surgery was also recorded.
The data in this study were examined by an independent operator using descriptive statistics. Continuous variables were expressed as the mean and standard deviation, and categorical variables were expressed as the total number of events. Fisher’s exact test was used to analyse the categorical data. After assessing normal distribution, repeated measures ANOVA were used for comparing MAP and HR within and between treatment groups, and the means of absolute changes in MAP and HR among treatment groups. Paired t-tests were used to compare radial inclination, radial height, and ulnar variance. to Depending on the nonnormal distribution, the Wilcoxon singed-rank test was used for comparing NRS from T1 to T6 and T0. The Mann-Whitney U test was used to comparing the articular step-offs. A two-tailed p < 0.05 or an adjusted p-value (false discover rate) < 0.05 after accounting for multiple testing was considered statistically significant.