Aims

Liposomal bupivacaine (LB) as part of a periarticular injection protocol continues to be a highly debated topic in total knee arthroplasty (TKA). We evaluated the effect of discontinuing the use of LB in a periarticular protocol on immediate postoperative pain scores, opioid consumption, and objective functional outcomes.

Aims. This study aims to report the outcomes in the treatment of unstable proximal third scaphoid nonunions with arthroscopic curettage, non-vascularized bone grafting, and percutaneous fixation. Methods. This was a retrospective analysis of 20 patients. All cases were delayed presentations (n = 15) or failed nonoperatively managed scaphoid fractures (n = 5). Surgery was performed at a mean duration of 27 months (7 to 120) following injury with arthroscopic debridement and arthroscopic iliac crest autograft. Fracture fixation was performed percutaneously with Kirschner (K)-wires in 12 wrists, a headless screw in six, and a combination of a headless screw and single K-wire in two. Clinical outcomes were assessed using grip strength, patient-reported outcome measures, and wrist range of motion (ROM) measurements. Results. Intraoperatively, established avascular necrosis of the proximal fragment was identified in ten scaphoids. All fractures united within 16 weeks, confirmed by CT. At a mean follow-up of 31 months (12 to 64), there were significant improvements in the Patient-Rated Wrist Evaluation, Mayo Wrist Score, abbreviated Disabilities of the Arm, Shoulder and Hand score, wrist ROM, grip strength, and the patients’ subjective pain score. No peri- or postoperative complications were encountered. Conclusion. Our data indicate that arthroscopic bone grafting and fixation with cancellous autograft is a viable method in the treatment of proximal third scaphoid nonunions, regardless of the vascularity of the proximal fragment. Cite this article: Bone Joint J 2022;104-B(8):946–952

Introduction. The use of intraoperative liposomal bupivacaine (LB) peri-articular injection has been highly debated for total knee arthroplasty (TKA). We evaluated the effect of an institutional-wide discontinuation of intraoperative LB on immediate postoperative pain scores, opioid consumption, and objective functional outcomes. Material and Methods. Between July 1, 2019 and November 30, 2019, an institutional policy discontinued use of intraoperative LB, while the volume of non-LB with epinephrine was increased from 40-ml to 60-ml. A historical cohort was derived from patients undergoing TKA between January 1, 2019 and June 30, 2019. All patients received the same opioid sparing protocol, minimizing variability in prescribing habits. No adductor canal blocks/pumps were utilized. Nursing documented verbal rating scale (VRS) pain scores were collected from our electronic data warehouse and averaged per patient per 12-hour interval. Opiate administration events were derived as Morphine Milligram Equivalences (MMEs) per patient per 24-hour interval. To assess immediate postoperative functional status, the validated Activity Measure for Post-Acute Care (AM-PAC) tool was utilized. All time events were calculated relative to TKA completion instant. Results. 789 primary TKAs did not receive intraoperative LB, while 888 patients acted as controls. Age was significantly greater in patients that did not receive intraoperative liposomal bupivacaine (66.80±8.97 vs 65.57±9.46; p<.01). Gender, BMI, ASA physical status score, race, smoking status, marital status, surgical time, length of stay and discharge disposition were similar between the two groups (p>.05). Compared to historical controls, discontinuation of LB demonstrated no significant difference in postoperative inpatient VRS pain scores up to 72 hours (p>.05), opioid administration up to 96 hours (p>.05), or AM-PAC scores within the first 24 hours (p>.05). Discussion. Subjective pain scores, opioid consumption, and functional scores were unchanged in the early postoperative period following the discontinuation of intraoperative liposomal delivery of bupivacaine in TKA

Introduction: We hereby present results of controlled randomized trial of use of popliteal block for pain relief in ankle and hind foot surgery. Materials and Methods: We have studied 47 patients over period of 9 months in 2007–08. Patients who needed ankle or hind foot procedure were selected for trial. Patients were explained about the trial and popliteal block along with leaflets at preoperative clinics. Patients were randomized on the day of surgery. A sealed envelop stating whether patient will go to block group (A) or no block group (B) was opened in the anaesthetic room before the patient was anaesthetized. Patients were evaluated for subjective pain scores at 30 min, 6hrs, 12 hrs and 24 hrs after surgery. Amount of anaelgesic required and time to first dose was documented. Popliteal blocks were given by one foot and ankle consultant and one trained fellow. The block was administered in lateral position at 0.8 mamp stimulus to detect the nerve. The data was compared statistically between group A and B. Results: Average subjective pain scores in group A were reported to be 1.2 at 30 min, 1.23 at 6 hrs, 2.1 at 12 and 3 at 24 hrs. Where as in group B it was 1.2, 7.2, 8.1 and 4 at 30 min, 6 hrs, 12 hrs and 24 hrs respectively. There was statistically significant difference in pain scores at 6 and 12 hrs. There was no statistically significant difference in pain scores at 30 min and 24 hrs. Conclusion: Popliteal block offers an effective way of pain relief in ankle and hind foot surgery. We believe that it may reduce amount of anaesthetic or anaelgesic drug requirement as well

Purpose: To assess moderate-term outcomes of silastic joint replacements of the first metatarsophalangeal joint. Method: The thirty-two patients (37 feet) that had silastic implants inserted were reviewed at an average of 2 years and 4 months (ranging 7 months to 5 years and 4 months). The mean patient age was 63 years. These patients answered a subjective questionnaire, had their feet examined clinically and radiographically and a pre-operative and post-operative AOFAS score was calculated for each. Results: The follow-up assessment revealed that every patient described that their pain had decreased after surgery and 17 feet (46%) were completely pain free. There was a significant improvement in patients’ subjective pain scores after surgery (t value = < 0.0001). Pre-operatively, the mean pain score for all 37 feet was 8.14, whereas post-operative the mean pain score was 1.32. The mean AOFAS score before surgery was 39.97. This increased to a mean score of 87.40 after surgery (P = < 0.0001). This again is a significant improvement. No patient was dissatisfied with the outcome with their surgery. Conclusion: These moderate term results are encouraging, with good subjective and objective results. However, long-term follow-up will be required to assess the longevity of this implant

Aims

Spinal anaesthesia has seen increased use in contemporary primary total knee arthroplasties (TKAs). However, controversy exists about the benefits of spinal in comparison to general anaesthesia in primary TKAs. This study aimed to investigate the pain control, length of stay (LOS), and complications associated with spinal versus general anaesthesia in primary TKAs from a single, high-volume academic centre.

Introduction. We hereby present results of controlled randomized trial of use of popliteal block for pain relief in ankle and hind foot surgery. Materials and methods. We have studied 63 patients over period of 9 months. Patients who needed ankle or hind foot procedure were selected for trial. Patients were explained about the trial and popliteal block along with leaflets at preoperative clinics. Patients were randomized on the day of surgery. A sealed envelop stating whether patient will go to block group (A) or no block group (B) was opened in the anaesthetic room before the patient was anaesthetized. Patients were evaluated for subjective pain scores at 30 min, 6 hrs, 12 hrs and 24 hrs after surgery. Amount of anaelgesic required and time to first dose was documented. Popliteal blocks were given by one foot and ankle consultant and one trained fellow. The block was administered in lateral position at 0.8 mA stimulus to detect the nerve. The data was compared statistically between group A and B. Results. The average pain scores in Group A (33 pts) were 0.72, 1.60, 1.51 and 1.03 at 30 min, 6 hrs, 12 hrs and 24 hrs respectively. While in Group B (30 pts) it was 2.73, 5.5, 6.03 and 3.33 at 30 min, 6 hrs, 12 hrs and 24 hrs respectively. There was statistically significant difference in pain scores at 6 and 12 hrs. There was no statistically significant difference in pain scores at 30 min and 24 hrs. Time to the request for first analgesic was statistically longer in Group A. Conclusion. Popliteal block offers an effective way of pain relief in ankle and hind foot surgery. We believe that it may reduce amount of anaesthetic or anaelgesic drug requirement as well

Introduction: We present the results of a controlled randomized trial of the use of a popliteal block for pain relief in ankle and hindfoot surgery. Materials and methods: We studied 47 patients over period of nine months in 2007 to 2008. Patients undergoing an ankle or hindfoot procedure were included in the trial. The trial was explained to the patients. Written information leaflets were also used in the preoperative clinics. Patients were randomized on the day of surgery. A sealed envelope randomizing the patient to block (A), or no block (B) was opened in the anaesthetic room before the patient was anaesthetised. Patients were subjective pain scores were recorded at 30 min, 6, 12 and 24 hours after surgery. The amount of analgesia required and time to first dose was documented. One foot and ankle consultant and one trained fellow gave the popliteal blocks. The block was administered in the lateral position at 0.8 mAmp stimulus to detect the nerve. Group A and B data was compared statistically. Results: The average pain scores in group A were reported to be 1.2 at 30min, 1.23 at 6, 2.1 at 12 and 3 at 24 hours. In group B it was 1.2 at 30min, 7.2, 8.1 and 4 at 6, 12 and 24 hours. There was a statistical significant difference in the pain scores at 6 and 12 hours. There was no statistical significant difference in the pain scores at 30 min and 24 hours. Conclusion: Popliteal block gives effective pain relief in ankle and hindfoot surgery. We believe that it may reduce anaesthetic and analgesic drug requirement as well

Aims

The aim of this study was to report patient and clinical outcomes following robotic-assisted total knee arthroplasty (RA-TKA) at multiple institutions with a minimum two-year follow-up.

Aims: To study clinical outcome of patients treated with a new design of the patellar tendon-tibial tubercle graft, which has reliable stability for transfer in recurrent dislocation of patella. Methods: 22 dislocations in 19 patients (3 bilateral) operated by this new technique were reviewed. There were 14 female and 5 male patients. Indications for surgery included functional disability due to repeated dislocations and failure of conservative management. Average age of the patient: 26 years (15–39 years). Duration of follow-up: 12–88months. Demographic data was collected by reviewing the case notes. Postoperative evaluation based on subjective pain evaluation score and Lysholm knee score. Surgical approach: limited infrapatellar midline incision, no internal fixation in any of the cases. Results: 75% of the patients had excellent to good result. There was no recurrence of instability/dislocation in any of the cases. Fair & poor (25%) results were graded based on stiffness and pain Conclusions: Multiple surgical procedures have been described for the management of recurrent dislocation of patella ranging from soft tissue realignment to bony procedures with internal fixation. Our results showed good functional improvement in the majority of the patients. This procedure is less extensive compared to the original procedure. Also there is the added advantage of no internal fixation and hence a second surgery for the removal of the implant can be avoided

Introduction: The nonunion rate is higher and loss of reduction is common after reduction and fusion for the higher grades of spondylolisthesis. This is due to fusion bone base deficiency and lack of anterior column support, and can be addressed by supplementing the posterolateral fusion with a posterior lumbar interbody fusion (PLIF). Materials: All patients had a single disc level degenerative or spondylolytic slip exceeding 25%. Laminectomy and instrumented reduction (VSP or TSRH) was performed. 86 patients underwent posterolateral fusion and 82 underwent the same procedure plus a PLIF (done by tightly impacting bone chips into the disc cavity after a very aggressive discectomy). No fusion cages were used. Results: Presented as No-PLIF vs. PLIF. Age: 56 vs. 52 years. Male/Female: 14:72 vs. 15:67. Cases with pars fx: 44% vs. 56%. Level of slip (L3-4, L4-5, L5-S1): 9, 59, 18 vs. 4, 60, 18. Iatrogenic neurological injury: none vs. none. Deep infection: 1 vs. none. Nonunion: 9.3% vs. 2.4%. Broken screws: 6 vs. 2. Degree of slip (pre-op to post-op to 2 years): 34% to 11% to 20% vs. 38% to 4% to 8%. Patients that lost reduction: 67% vs. 18%. Disc height gained at 2 years: −0.2 mm vs. 2.3 mm. Subjective back pain score: 3.5 vs. 2.0. Greenough LBOS score: 54 vs. 62. Patients very satisfied: 43% vs. 60%. Cases with adjacent level slip: 4 vs. 4. Discussion: Spondylolisthesis is commonly treated with a spinal fusion. The goal of surgery is to eliminate motion between the unstable segments, and mechanically it is preferable that the vertebrae fuse in as near anatomic position as possible. It has been shown that the fusion rate decreases with higher degrees of slip, with the spondylolytic types, and with severely degenerated discs. Pedicle screw instrumentation can increase the fusion rate. Reduction of the slip can often be achieved, but it is common to lose the reduction over the course of 1–2 years if only posterolateral fusion is done. Adding an interbody fusion cage can help restore the disc height and widen the intervertebral foramen, but increases complexity, cost, and may actually decrease bone contact area and compression forces. We have found that in grade II and worse slips, pedicle screw fixation alone is not strong enough to maintain reduction of either vertebral alignment or disc height. Adding a chip PLIF appears safe and effective in increasing the union rate and the disc height, and in maintaining reduction in grade II spondylolisthesis. Clinical results are better, the infection rate is not higher. In our hands, there have been no neurological injuries. This study also raises questions about the role and need for interbody fusion cages

Satisfaction is increasingly employed as an outcome measure for a successful total knee replacement (TKR). Satisfaction as an outcome measure encompasses many different intrinsic and extrinsic factors related to a person’s experience before and after TKR. The Swedish Knee Arthroplasty Registry has previously demonstrated on a large population study that 17% of TKR recipients are not satisfied with their TKR outcome. This finding has been replicated in other countries. Similar significant factors emerged from these registry studies that are related to satisfaction. It would appear that satisfaction is better after more chronic diseases and whether the TKR results in pain relief or improved function. Importantly, unmet pre-operative expectations are a significant predictor for dissatisfaction following a TKR. It may be possible to improve rates by addressing the issues surrounding pain, function and expectation before embarking on surgery.

Cite this article: Bone Joint J 2013;95-B, Supple A:148–52.

The October 2012 Knee Roundup³⁶⁰ looks at: autologous chondrocytes and chondromalacia patellae; drilling the femoral tunnel at ACL reconstruction; whether we repair the radially torn lateral meniscus; factors associated with patellofemoral pain; mechanoreceptors and the allografted ACL; whether high tibial osteotomy can delay the need for knee replacement; return to sport after ACL reconstruction; tissue-engineered cartilage; and the benefits of yoga.

We analysed the outcome of the Coonrad-Morrey total elbow replacement used for fracture of the distal humerus in elderly patients with no evidence of inflammatory arthritis and compared the results for early versus delayed treatment. We studied a total of 32 patients with 15 in the early treatment group and 17 in the delayed treatment group. The mean follow-up was 56.1 months (18 to 88). The percentage of excellent to good results based on the Mayo elbow performance score was not significantly different, 84% in the early group and 79% in the delayed group. Subjective satisfaction was 92% in both the groups.

One patient in the early group developed chronic regional pain syndrome and another type 4 aseptic loosening. Two elbows in the early group also showed type 1 radiological loosening.

Two patients in the delayed group had an infection, two an ulnar nerve palsy, one developed heterotopic ossification and one type 4 aseptic loosening. Two elbows in this group also showed type 1 radiological loosening. The Kaplan-Meier survivorship analysis for the early and delayed treatment groups was 93% at 88 months and 76% at 84 months, respectively.

No significant difference was found between the two groups.

We performed a double-blind, randomised controlled trial to assess the effectiveness of a continuous-infusion brachial plexus block with levobupivacaine compared with that of a standard single injection for the management of post-operative pain after surgery on the shoulder.

Eight patients were randomised to receive a pre-operative brachial plexus block using 30 ml of levobupivacaine 0.5% with adrenaline 1:200 000 followed by insertion of a 20-gauge polyamide catheter. This was connected to a disposable elastometric pump, set immediately after surgery to administer a continuous flow of levobupivacaine 0.25% at a rate of 5 ml per hour. The other eight patients were randomised to receive only the initial injection of 30 ml. The study was double-blinded with the aid of sham catheters and clamped pumps.

All patients were given regular paracetamol and were prescribed morphine through a patient-controlled analgesia pump. Motor and sensory block assessments, visual analogue scale pain scores and consumption of morphine were recorded after the operation and then at 6, 12 and 24 hours after administration of the block.

Satisfactory motor and sensory block was achieved in all patients. The mean visual analogue scale pain score at 12 hours and consumption of morphine at 24 hours after injection were significantly lower (p < 0.05) in the continuous-infusion group. This group also took longer to request their first additional analgesia and reported a significantly higher overall level of satisfaction.

Our study has shown that continuous interscalene infusion of levobupivacaine is an effective method of post-operative analgesia after major surgery of the shoulder.