Aim. To describe a 2-stage treatment pathway for managing neuropathic forefoot ulcers and the safety and efficacy of percutaneous tendo-Achilles lengthening (TAL) in out-patient clinics. Methods. Forefoot ulcers in patients with diabetic neuropathy are a result of factors that result in increased forefoot plantar pressure. Plantar flexed metatarsal heads secondary to progressive claw toe deformity and hindfoot equinus from changes within the gastrocnemius-soleus-tendo-Achilles complex, with additional contraction of tibialis posterior and peroneal longus, secondary to motor neuropathy results in progressive increase in forefoot plantar pressures. Consecutive patients, who presented to our Diabetic Foot clinic since February 2019 with forefoot ulcers or recurrent forefoot callosity were treated with TAL in the first instance, and in patients with recurrent or non-healing ulcers, by proximal dorsal closing wedge osteotomy; a 2-stage treatment pathway. Patients were followed up at 3, 6, and 12 months to assess ulcer healing and recurrence. Results. One hundred and twelve patients (146 feet) underwent TAL by 3 consultants in the out-patient clinics. Of these, 96 feet were followed for a minimum of 12 months (range 12–36 months). None had infection or wound related problems at the tenotomy sites; complete transection of the tendon was noted in 4 patients (4%) and one-patient developed heel callosity suggestive of over-lengthening. In 92 feet (96%), the ulcers healed within 10 weeks (± 4 weeks). Additional z-lengthening of peroneal longus and tibialis posterior tendons helped in patients with big-toe and 5. th. metatarsal head ulcers. In 12 feet (10%), the ulcer failed to heal or recurred, the MRI scan in these patients showed plantar flexed metatarsals secondary to progressive claw toe deformity. The ulcer in this group healed after surgical offloading with proximal dorsal closing wedge osteotomy. In patients with osteomyelitis, the intramedullary canal was curetted and filled with local antibiotic eluting agents such as Cerament G. ®. The osteotomy site was stabilised with a percutaneous 1.6mm k-wire. Conclusion. The described 2-stage treatment pathway results in long-term healing of neuropathic forefoot ulcers, and in 96% of patients, the ulcer healed after out-patient percutaneous TAL alone. TAL is a safe and effective initial out-patient procedure with improved patient outcomes

To evaluate the results of the reconstructive surgical treatment of complicated forms of infected osteoarthropathy with diabetic foot syndrome (DFS). The analysis of the results of the treatment of 58 patients with infectious complications of osteoarthropathy with the neuropathic form of the DFS, the average age 57.7+1.2 years. In 5 patients with Type I according to the Sanders & Frykberg classification, grade C according to the Roger classification of with neuropathic ulcers caused by deformation of the bones we employed corrective mini-osteotomy. In 32 patients with Type I, grade D with the infected ulcers associated with destruction of the metatarsal bones and the metatarsophalangeal joints, we performed the resection of the affected bones, subsequently filling the defects with antibiotic impregnated collagen sponge (AICS*), and then we closed the wound with primary suture. In 15 patients with Type II, grade D we performed the resection of the affected bones and stabilize the mid-foot using compressive screws and AICS. In 4 patients with Type III, grade D we perfomed the following resection of the affected bones we used AICS and the extrafocal corrective osteosynthesis using the Ilizarov's method. In 2 patients with Type IV+V, grade D we did an amputation using the Syme's technique and osteosynthesis using the Ilizarov's method. There was one case of septic instability of the compressive screw after more than one month: the screw was then removed; and there was one case of an unstable bone fragment: its removal was necessary. No recurrence of the trophic ulcers or osteomyelitis of the foot bones was observed during a 6 – 24 mounth follow-up in any other treated patients. The described methods are promising in the treatment of patients with DFS; their effectiveness can be evaluated after randomized trials will be completed

Background. This study was conducted to assess the clinical and radiologic results of total knee arthroplasty (TKA) with an allogenic bone graft using varus-valgus constrained (VVC) prostheses in knees with severe bone defects and unstable neuropathy. Methods. This study included 20 knees of 16 patients who underwent TKA between August 2001 and January 2006 due to unstable knees with severe bone destruction resulting from neuropathic arthritis. At the time of surgery, the mean age of the patients was 56 years. The mean length of the follow-up period was 10.7 years. A VVC condylar prosthesis was used with an allogenic femoral head graft to reconstruct large bony defects. Clinical results were evaluated using the Hospital for Special Surgery (HSS), Knee Society (KS) function, and Western Ontario and McMaster Universities Osteoarthritis (WOMAC) scores. Three-dimensional computed tomography (3D-CT) was used to evaluate the radiological parameters, which included the tibiofemoral angle, loosening or osteolysis of components, and incorporation of the bone graft. Results. The preoperative mean HSS, KS function, and WOMAC scores were 40.5, 43.2, and 78.3, respectively, and these scores improved to 86.0, 64.6, and 33.8 at the final follow-up. The mean postoperative alignment was 6.1° of valgus angulation. One knee had instability, another knee had partial bony absorption, which was confirmed using 3D-CT, and the other 18 cases (90%) had satisfactory results. No cases experienced radiolucency, fracture, or infection. Conclusions. TKA with an allogenic bone graft using a VVC prosthesis provides a viable option for the treatment of severe bone defects with soft tissue insufficiency in neuropathic knee arthropathy. Level of Study: Level IV, therapeutic study

Percutaneous flexor tenotomy involves cutting the flexor digitorum tendons to correct claw toe deformity to treat apical pressure areas and prevent subsequent infection in patients with peripheral neuropathy. Performing this under ultrasound guidance provides reassurance of complete release of the tendon and increases procedural safety.

This study is a retrospective case series evaluating the effectiveness, safety, and patient satisfaction of performing percutaneous ultrasound-guided flexor tenotomy in an outpatient setting. People with loss of protective sensation, a digital flexion deformity, and an apical toe ulcer or pre-ulcerative lesion who presented to our institution between December 2019 and June 2022 were included in this study. Participants were followed-up at a minimum of 3 months. Time to ulcer healing, re-ulceration rate, patient satisfaction, and complications were recorded. An Australian cost analysis was performed comparing this procedure performed in rooms versus theatres.

There were 28 ulcers and 41 pre-ulcerative lesions. A total of 69 tenotomy procedures were performed on 38 patients across 52 episodes of care. The mean time to ulcer healing was 22.5 +/- 6.4 days. There were 2 cases of re-ulceration. 1 patient sustained a transfer lesion. There were four toes that went onto require amputation, all in the setting of pre-existing osteomyelitis. 94% of patients strongly agreed that they were satisfied with the outcome of the procedure. Costs saved were estimated to be $1426.

Flexor tenotomy is a minimally invasive procedure that can be performed in the outpatient setting, and therefore without delay to treatment, reducing risk of ulcer progression and need for subsequent amputation. This is the first study to report on flexor tenotomy under ultrasound-guidance.

Ultrasound-guided percutaneous flexor tenotomy is safe and effective, with high patient satisfaction and low recurrence rates. This performance in the outpatient setting ensures significant time and cost savings for both the practitioner and patient.

Introduction. Pain after trauma has received relatively little research attention compared with surgical techniques and functional outcomes, but is important to patients. We aimed to describe nerve dysfunction and pain characteristics using tibial fractures as a model. We hypothesized that early nerve dysfunction was associated with neuropathic and chronic pain. Materials and Methods. Adult patients with isolated open or closed tibial diaphyseal fractures were prospectively observed for 1-year in 5 Major Trauma Centres. Nerve dysfunction was assessed using Semmes-Weinstein monofilaments, acute pain with the visual numerical rating scale (VNRS), neuropathic pain with the doleur neuropathique-4 score and quality of life (QOL) using the EQ-5D score. Results. Of 77 included patients, twenty-six (33.8%) had Gustilo-Anderson grade II or worse injuries. Forty-six (63.0%) had operative repair; 0 operation notes reported nerve injury. Mean VNRS pain scores one week post-injury were 4.6/10 (SD 2.4). Seventeen patients (23.3%) presented with impaired sensation, persisting in 11 (15.1%) at 3-months. Neuropathic pain affected 16 (20.8%) patients one week post-injury; a further 20 (26.0%) had >2 symptoms of nerve pain. Only four (11.1%) received anti-neuropathic drugs. At 6-months, twenty-three (31.5%) reported mobility problems, 21 (28.8%) difficulty completing normal activities, 25 (34.2%) pain and 15 (20.5%) anxiety and depression. Conclusions. Nerve dysfunction and neuropathic pain are common early features in patients with tibial fractures, but are poorly recognised and inadequately treated. Pain has long-term effects on patients’ QOL. Future work should aim to improve identification and management of neuropathic pain

Aim. The aim of this paper is to analyse the cause of neuropathic diabetic foot ulcers and discuss their preventive measures. Methods. Review of patients with foot ulcers managed in our diabetic MDT clinics since Feb 2018 were analysed. Based on this observation and review of pertinent literature, following observations were made. Results. Forefoot. Progressive hindfoot equinus from contraction of gastroc-soleus-tendo-Achilles complex, with additional contraction of tibialis posterior and peroneal longus muscles and, progressive plantar flexed metatarsal heads secondary to claw toe deformity results in increased forefoot plantar pressures. In patients with insensate feet, this result in ulcer formation under the metatarsal heads from shear stress when walking. Callosity under the metatarsal heads is the earliest clinical sign. Most patients by this time have fixed tightness of the muscle groups as assessed by negative Silfverskiold test. Percutaneous tendo-Achilles lengthening (TAL) has shown to reduce the mid-forefoot plantar pressures by 32% and ulcer healing in 96% of patients within 10 weeks (± 4 weeks). Additional z-lengthening of peroneal longus and tibialis posterior tendons helped in patients with big-toe and 5. th. metatarsal head ulcers. Proximal metatarsal osteotomies further reduce the forefoot pressures to near normality. Midfoot. Midfoot ulcers are secondary to rocker-bottom deformity a consequence of Charcot neuroarthropathy (CN). Hindfoot equinus as described and relative osteopenia from neurally mediated increased blood flow (neurovascular theory) and repeated micro-trauma (neurotraumatic theory) result in failure of medial column osseo-ligamentous structures. As the disease progress to the lateral column, the cuboid height drops resulting in a progressive rocker bottom deformity. The skin under this deformity gradually breaks down to ulceration. In the pre-ulcerative stages of midfoot CN, TAL has shown to stabilise the disease progression and in some patents’ regression of the disease process was noted. The lump can excised electively and the foot accommodated in surgical shoes. Hindfoot. These develop commonly at the pressure areas and bony exostosis in non-ambulatory patients. In ambulatory patients, the most common cause are factors that result in over lengthening of tendo-Achilles such as after TAL, spontaneous tears, or tongue-type fractures. Conclusions. Early identification of factors that result in plantar skin callosity and treating the deforming forces prevent progression to ulceration. Total contact cast without treatment of these deforming forces results in progression of these callosities to ulceration while in the cast or soon after completion of cast treatment

Pain is a common presenting symptom of patients with shoulder conditions, yet there has been little work done to accurately describe its distribution and nature. We studied all patients attending the Royal Devon and Exeter Hospital shoulder clinic from August 2012 – 2013. Patients completed a questionnaire detailing their Oxford Shoulder Score and a validated neuropathic pain questionnaire. Patients were given diagrams to draw on their perceived location of pain or abnormal sensation. We analysed all patients with frozen shoulder (48), osteoarthritis (37) and rotator cuff arthropathy (17). We found that neuropathic pain is common in patients with shoulder conditions identified in 39% of OA patients, 42% with rotator cuff arthropathy and 57% with frozen shoulder. Pain outside the shoulder was reported in over 50% of patients, commonly the forearm, hand, neck and chest. Frozen shoulder was especially associated with pain outside of the shoulder with 39% describing symptoms in the neck or chest, 21% into the forearm and 18% into the hand. Interestingly, neuropathic pain radiating down the arm was not described in the rotator cuff arthropathy group. The high prevalence of neuropathic symptoms and pain felt outside the shoulder aids diagnosis and more accurately identifies these conditions

Introduction. Genu recurvatum deformities are unusual before total knee arthroplasty (TKA), occurring in less than 1% of patients. The purpose of this study is to evaluate the clinical and radiographic results of primary TKA in patients that had recurvatum deformities before surgery. Patients and Methods. The inclusion criteria was to have recurvatum deformity over 10 degrees on lateral standing X-ray view. We retrospectively reviewed 22 knees with pre-operative recurvatum deformities, and the incident was 1.0% of all TKAs at our hospital. The etiology of the arthritis was osteoarthritis in 21 knees, of which 3 knees were neuropathic disease, and rheumatoid arthritis in 1 knee. There were 6 men and 16 women, and the average age was 73.3 years (range, 53 to 83 years) at the time of operation. The average follow-up period was 15 months (range, 3 to 81 months). We performed to use medial parapatellar approach and bone cutting was done by measured resection technique. The surgical knacks were resection of less distal femur and proximal tibia bone to make extension gap tightly, additionally decrease the tibial posterior slope. Posterior-stabilizer (PS) implants (NexGen LPS: Zimmer, Bisurface KU4+: JMM) were used in 20 knees and constrained implants (NexGen RH knee: Zimmer, Endo-Model Hinge Knee: Link) were in 2 knees with neuropathic joints. Results. The averaged Knee Society Knee and Function score improved from 33.1 points to 94.1 points, and 28.0 points to 60.5 points at the time of the last follow-up. The femorotibial angle changed from averaged 183.4 degrees (range, 162 to 195 degrees) preoperatively to averaged 173.3 degrees (range, 170 to 177 degrees). Preoperative hyperextension was averaged 18.2 degrees (range, 10 to 40 degrees). Intraoperatively, the hyperextension deformity was corrected in all cases. The tibial posterior slope was averaged 1.7 degrees (range, −2.7 to 6 degrees). The final hyperextension improved averaged 6.9 degrees (range, −1.7 to 26.6 degrees), all but one knee were corrected. One case treated with a standard PS type, who was associated with neuropathic disease, had a recurrence of recurvatum deformity and required revision surgery. Discussion. Recurvatum may be associated with a severe osseous deformity, capsular or ligamentous laxity, and neuromuscular disease. Surgical solutions may be to use a standard PS prosthesis with a slight underresection of the bone edge, and decrease tibial posterior slope. An alternative solution is to use a rotating-hinge prosthesis with less than antigravity quadriceps strength for neuromuscular disease

Peripheral nerve injuries (PNI) occur in 10% of combat casualties. In the immediate field-hospital setting, an insensate limb can affect the surgeon's assessment of limb viability and in the long-term PNI remain a source of considerable morbidity. Therefore the aims of this study are to document the recovery of combat PNI, as well as report on the effect of current medical management in improving functional outcome. In this study, we present the largest series of combat related PNI in Coalition troops since World War II. From May 2007 – May 2010, 100 consecutive patients (261 nerve injuries) were prospectively reviewed in a specialist PNI clinic. The functional recovery of each PNI was determined using the MRC grading classification (good, fair and poor). In addition, the incidence of neuropathic pain, the results of nerve grafting procedures, the return of plantar sensation, and the patients' current military occupational grading was recorded. At mean follow up 26.7 months, 175(65%) of nerve injuries had a good recovery, 57(21%) had a fair recovery and 39(14%) had a poor functional recovery. Neuropathic pain was noted in 33 patients, with Causalgia present in 5 cases. In 27(83%) patients, pain was resolved by medication, neurolysis or nerve grafting. In 35 cases, nerve repair was attempted at median 6 days from injury. Of these 62%(22) gained a good or fair recovery with 37%(13) having a poor functional result. Forty-two patients (47 limbs) initially presented with an insensate foot. At final follow up (mean 25.4 months), 89%(42 limbs) had a return of protective plantar sensation. Overall, 9 patients were able to return to full military duty (P2), with 45 deemed unfit for military service (P0 or P8). This study demonstrates that the majority of combat PNI will show some functional recovery. Adherence to the principles of war surgery to ensure that the wound is clear of infection and associated vascular and skeletal injuries are promptly treated will provide the optimal environment for nerve recovery. Although neuropathic pain affects a significant proportion of casualties, pharmacological and surgical intervention can alleviate the majority of symptoms. Finally, the presence of an insensate limb at initial surgery, should not be used as a marker of limb viability. The key to recovery of the PNI patient lies in a multi-disciplinary approach. Essential to this is regular surgical review to assess progress and to initiate prompt surgical intervention when needed. This approach allows early determination of prognosis, which is of huge value to the rehabilitating patient psychologically, and to the whole rehabilitation team

Persistent post-surgical pain remains a problem after knee replacement with some studies reporting up to 20% incidence. Pain is usually felt by those who do not operate to be a monolithic entity. All orthopaedic surgeons know that this is not the case. At its most basic level, pain can be divided into two categories, mechanical and non-mechanical. Mechanical pain is like the pain of a fresh fracture. If the patient does not move, the pain is less. This type of pain is relieved by opiates. Mechanical pain is seen following knee replacement, but is fortunately becoming less frequent. It is caused by a combination of malrotations and maltranslations, often minor, which on their own would not produce problems. The combination of them, however, may produce a knee in which there is overload of the extensor mechanism or of the medial stabilizing structures. If these minor mechanical problems can be identified, then corrective surgery will help. Non-mechanical pain is present on a constant basis. It is not significantly worsened by activities. Opiates may make the patient feel better, but they do not change the essential nature of the pain. Non-mechanical pain falls into three broad groups, infection, neuropathic and perceived pain. Infection pain is usually relieved by opiates. Since some of this pain is probably due to pressure, its inclusion in the non-mechanical pain group is questionable, but it is better left there so that the surgeon always considers it. Low grade chronic infection can be extremely difficult to diagnose. Loosening of noncemented knee components is so rare that when it is noted radiologically, infection should be very high on the list of suspicions. The name neuropathic pain suggests that we know much more about it than we do in reality. Causalgia or CRPS-type two is rare following knee replacement. CRPS type one or reflex sympathetic dystrophy probably does exist, but it is probably over-diagnosed especially by the author of this abstract. The optimum treatment I have found is lumbar sympathetic blocks. Perceived pain is the largest group. It does not matter what you tell the patient, some believe a new knee should be like a new car, i.e. you step into it and drive away. The fact that they have to work to make it work is horrifying. Some of this pain is actually mechanical, especially in those with no benefits such as hairstylists. Perceived pain is widespread. The classic treatise on this is Dr. Ian McNabb's book “Backache”. It should be studied by all orthopaedic surgeons, who wish to understand pain complaints. Any experienced knee surgeon will have his list of red flags or caveats. These are often politically incorrect and this information is transferred to young surgeons, usually in dim bars late at night. I will list only a few. If the patient comes in with a form asking for a disability pension on the first visit. If the patient's mother answers the questions. If the patient comes in taking massive doses of opiates. If the patient is referred to you by a surgeon, who does more knee replacements than you do. There is also the recently described Fern Silverman's syndrome

Persistent post-surgical pain (PPSP) remains a problem after knee replacement with some studies reporting up to 20% incidence. Pain is usually felt by those who do not operate to be a monolithic entity. All orthopaedic surgeons know that this is not the case. At its most basic level, pain can be divided into two categories, mechanical and non-mechanical. Mechanical pain is like the pain of a fresh fracture. If the patient does not move, the pain is less. This type of pain is relieved by opiates. Mechanical pain is seen following knee replacement, but is becoming less frequent. It is caused by a combination of malrotations and maltranslations, often minor, which on their own would not produce problems. The combination of them, however, may produce a knee in which there is overload of the extensor mechanism or of the medial stabilizing structures. If these minor mechanical problems can be identified, then corrective surgery will help. Non-mechanical pain is present on a constant basis. It is not significantly worsened by activities. Opiates may make the patient feel better, but they do not change the essential nature of the pain. Non-mechanical pain falls into three broad groups, infection, neuropathic and perceived pain. Infection pain is usually relieved by opiates. Since some of this pain is probably due to pressure, its inclusion in the non-mechanical pain group is questionable, but it is better left there so that the surgeon always considers it. Low grade chronic infection can be extremely difficult to diagnose. Loosening of noncemented knee components is so rare that when it is noted radiologically, infection should be very high on the list of suspicions. The name neuropathic pain suggests that we know much more about it than we do in reality. Causalgia or CRPS-type two is rare following knee replacement. CRPS-type one or reflex sympathetic dystrophy probably does exist, but it is probably over-diagnosed. The optimum treatment I have found is lumbar sympathetic blocks. Lyrica, Gabapentin and Cymbalta may also help. Perceived pain is the largest group. It does not matter what you tell the patient, some believe a new knee should be like a new car, i.e. you step into it and drive away. The fact that they have to work to make it work is horrifying. Perceived pain is widespread. The classic treatise, Dr. Ian McNabb's book “Backache”, should be studied by all who wish to understand pain complaints. Any experienced knee surgeon will have his list of red flags or caveats. I will list only a few. If the patient comes in with a form asking for a disability pension on the first visit. If the patient's mother answers the questions. If the patient comes in taking massive doses of opiates. If the patient is referred to you by a surgeon who does more knee replacements than you do. There are other issues such as good old fibromyalgia, which appears to have gone the way of the dodo. It has been replaced by something equally silly called central sensitization. The theory of central sensitization is that if one has pain somewhere or other for three months or six months or whatever, there are going to be changes in the brain and spinal cord. It then does not matter what happens to the original pain, i.e. whether or not it goes away, the pain will persist because of the changes in the brain, hence, the title of the pain in the brain syndrome. If this theory was correct, we might as well all go home because we have all been wasting our time for the last 30 years because none of our patients would get any better. After all, all of our patients have had pain for a lot longer than three months, many of them have been involved in trauma and sometimes, compensation is at issue. The pain in the brain theory, therefore, sounds about as realistic as the flat earth society or the treatment of Galileo

Aim. To compare outcomes and incidence of adverse events (AE) of colistin versus tigecycline for treatment of patients with carbapenem-resistant Acinetobacter baumannii (CRAB) osteomyelitis. Method. Retrospective study. Records of 111 patients with microbiologically confirmed CRAB osteomyelitis were analyzed. Colistin (34 cases) and tigecycline (31 cases) were the main drugs used for treatment of extremely-drug resistant (XDR) isolates. Patients who received these two antimicrobials were compared according to baseline features (sex, age, length of hospital stay, Charlson index, presence of comorbidities or immunosuppression, previous renal disease, smoking, alcoholism or use of illicit drugs, previous orthopedic surgery on affected limb, topography of infection, classification of osteomyelitis, ASA score, infection related to pressure ulcer or neuropathic foot, presence of implant, need for soft tissue repair or negative pressure therapy and previous antimicrobial use), clinical outcome after 12 months of treatment (remission of infection was considered the favorable outcome; recurrence of infection, amputation and death were considered unfavorable outcomes; loss of follow-up was analyzed separately) and AE during treatment (impaired renal function; liver abnormalities; nausea; skin rash; neurological abnormalities and other events in general). Quantitative variables were described using summary measures and compared using Student's t or Mann-Whitney tests. Qualitative characteristics were described with absolute and relative frequencies and compared using chi-square or exact tests (Fisher's exact or likelihood ratio test). Results. Regarding baseline characteristics, proportion of male patients was higher in the group treated with colistin (p = 0.028). In the group treated with tigecycline, there was a significant predominance of smokers (p = 0.021) and patients with chronic osteomyelitis (p = 0.036). Regarding clinical outcomes after 12 months of treatment, there was no difference between groups. Overall incidence of AE was significantly higher among patients treated with colistin (p=0,047), as well as renal impairment (p = 0.003). Incidence of nausea was higher in patients treated with tigecycline (p = 0.046), but there was no difference between groups in relation to altered liver enzymes and other events. Conclusions. In this retrospective analysis, there was no significant difference between clinical outcomes of patients with CRAB osteomyelitis treated with colistin compared to tigecycline. Although the occurrence of nausea was greater in the group receiving tigecycline, this antimicrobial appeared to have a better safety profile for treatment of osteomyelitis related to XDR A. baumannii

Aim. Our study aimed to analyze 1) the prevalence of peripheral arterial disease (PAD) and infection in diabetic patients with and without Charcot foot (CF), 2) the characteristics of PAD in these 2 groups, 3) the prognosis of patients with CF and PAD and/or infection. Method. We retrospectively reviewed the medical and radiological records of 172 hospitalized patients in our diabetic foot unit between 2010 and 2014. These patients were identified using the ICD-9-CM. The CF group and the diabetic foot (DF) group included 56 and 116 patients, respectively. All statistical analyses were performed using SPSS 25.0.01. A p <0.05 was considered as statistically significant. Results. In the CF group, the prevalence of PAD and infection reached 66.1% and 67.9%, respectively. Diabetic foot ulcers (DFUs) were neuroischemic, infected or both in 69.5%, 80% and 57.7% of cases, respectively. No significant difference was found with the DF group. PAD in the CF group affected the infrapopliteal arteries alone more often (59.4% vs 26.7%, p 0.005) and neuroischemic DFUs needed less often revascularization (34.4% vs 78.7%, p <0.001). Endovascular revascularization was feasible in 77.8% of cases in the CF group, without significant difference with the DF group. Independent predictors of PAD in CF were DFUs (OR 24.5, CI 1.8–334.4, p 0.016) and coronary artery disease (OR 17.1, CI 1.7–167.4, p 0.016). Both patients' survival and limb salvage were not affected by PAD, neuroischemic DFUs and infected neuroischemic DFUs in the CF group. Conclusions. In agreement with current literature, our study showed that infection is often associated with DFUs, both in DF and CF. However, our study demonstrated that beside infection, PAD is associated with CF more often than previously thought. As a consequence, DFUs in CF are most often neuroischemic. However, our study did not show worse outcomes in patients with CF and PAD or neuroischemic DFUs. This probably results from a less severe PAD in CF, a high rate of successful revascularization as well as a low rate of deaths and major amputations in our study. In conclusion, clinicians should no longer consider the CF as a purely neuropathic foot, especially in the presence of a DFU. Moreover, PAD in CF should be evaluated systematically before any surgical procedure as recommended in DF

It is unusual to require the use of a total knee implant with more constraint than a posterior-stabilised post in primary knee arthroplasty. The most common indication is a knee with a severe deformity, usually fixed valgus with an incompetent medial collateral ligament, and an inability to correctly balance the knee in both flexion and extension. The pre-operative deformity is usually greater than 15–20 degrees fixed valgus and may be associated with a severe flexion contracture. This is usually seen in an elderly female patient with advanced osteoarthritis. Those pre-operative diagnoses more likely to require a constrained design include advanced rheumatoid arthritis, true neuropathic joint, and the “Charcot-like” joint due to bone loss or crystalline arthritis. Rarely, patients with periarticular knee Paget's disease of bone may require more constraint following correction of a severe deformity through the knee joint. Beware those patients with a staple or screw at the medial epicondyle or those with severe heterotopic ossification at the medial joint line, as this may signify a serious prior injury to the medial collateral ligament. Finally, there is a possibility of inadvertent division of the medial collateral ligament intra-operatively. Although this situation may be treated with suture repair and bracing, my choice is to switch to more constraint and early unbraced motion. There are over 20 designs of varus-valgus constrained components, with a variety of tibial post designs with specific rotary and angular biomechanics, and many have the option of adding modular stems. Our experience with constrained, non-linked designs has been favorable with both the use of nonmodular and modular stem extensions. Longer-term survival analysis has shown a 96% survival at 10 years with these constrained components. However, the older designs frequently required a lateral retinacular release for proper patella tracking, and there were patella complications (fracture and osteonecrosis) in 16%. With a more modern design, over the past 12 years, the need for a lateral retinacular release and patella complications have been notably decreased. Varus-valgus constrained components have a small but important role in primary total knee arthroplasty for patients with severe deformity or an incompetent medial collateral ligament

In primary TKA, non- or semi-constrained TKA implants might have their limitations in the absence of collateral ligaments, severe deformity, large osseous defects and gross flexion-extension instability. Although most primary TKA indications can be solved with modular, non-hinged implants, an adequate balancing might require a relevant soft tissue release. This consequently adds complexity and operative time with less predictable results in the elderly patient. The current literature reporting on short- to mid-term results of rotating hinged implants in primary osteoarthritis shows some quite diverse results and consequently different interpretations of this implant type in primary knee arthroplasty. Although some authors were able to show good and excellent clinical results in 91% of patients and consequent survival rates of a rotating hinge implant after 15 years up to 96% in primary indications, others found high complication rates of up to 25% of all operated patients, which remains unclear for us and is inconsistent with our clinical results in primary and revision TKA in over 30 years of experience with the ENDO-Model rotating hinge implant. Our potential indications in the elderly for a rotating or pure hinged implant in primary TKA include: Complete MCL instability; Severe varus or valgus deformity (>20 degrees) with necessary relevant soft tissue release; Relevant bone loss including insertions of collaterals; Gross flexion-extension gap imbalance; Ankylosis; One staged implantation with specific antibiotics after PJI. Due to general limited soft tissues or hyperlaxity, patients with neuropathic joints, or lack of extensor mechanism should be considered for a complete hinged implant. The ENDO-model hinge has only been minimally adapted since its development in the 70´s, including fully cemented long stems, in modular and non-modular versions. We strictly reserve a rotational hinge in primary indications for patients >70 years with a combined varus alignment, whereas in severe valgus deformities, a complete hinged implant version should be used for our implant design

Osteoid osteoma is a benign bone-forming lesion, characterized by its small size, its clearly demarcated outline and by the usual presence of a surrounding zone of reactive bone formation. It often poses a diagnostic challenge due to its ambiguous presentation. The aetiology of osteoid osteoma is poorly understood. The previous suggestion that osteoid osteoma was not associated with trauma or infection has been challenged by more recent literature raising the possibility that it could be a reactive or healing response or a phenomenon associated with the revascularisation process. This case report describes an unusual presentation of a post-traumatic osteoid osteoma. Two years following a diaphyseal, spiral tibial fracture treated nonoperatively, the patient developed new pain at the previous fracture site. The pain was constant, relieved by non-steroidal analgesia and not associated with systemic upset. It was initially attributed to other more likely diagnoses such as osteomyelitis and neuropathic pain. Multiple investigations and interventions were undertaken prior to the definitive diagnosis being obtained by surgical excision of the lesion and histological studies five years after the injury and three years following the initiation of the discomfort. In both English and foreign language literature there are only seven case reports that document osteoid osteoma following fracture, these are predominantly in the lower limb with no predominance to operative or nonoperative management. This case report should raise the index of clinical suspicion of osteoid osteoma occurring post fracture

In primary TKA, non- or semi-constraint TKA implants might have their limitations in the absence of collateral ligaments, severe deformity, large osseous defects and gross flexion - extension instability. Although most primary TKA indications can be solved with modular, non-hinged implants, an adequate balancing might require a relevant soft tissue release. This consequently adds complexity and operative time with less predictable results in the elderly patient. The current literature reporting on short to mid-term results of rotating hinged implants in primary osteoarthritis shows some quite diverse results and consequently different interpretations of this implant type in primary knee arthroplasty. Although some authors were able to show good and excellent clinical results in 91% of patients and consequent survival rates of a rotating hinge implant after 15 years up to 96% in primary indications, others found high complication rates of up to 25% of all operated patients, which remains unclear for us and is inconsistent with our clinical results in primary and revision TKA in over 30 years of experience with the Endo-Model rotating hinge implant. Our potential indications in the elderly for a rotating- or pure-hinged implant in primary TKA include: Complete MCL instability, Severe varus or valgus deformity (>20 degrees) with necessary relevant soft tissue release, Relevant bone loss including insertions of collaterals, Gross flexion-extension gap imbalance, Ankylosis, One staged implantation with specific antibiotics after PJI. Due to general limited soft tissues or hyper laxity, patients with neuropathic joints, or lack of extensor mechanism should be considered to a complete hinged implant. The ENDO-model hinge has only been minimal adapted since its development in the 70's, including fully cemented long stems, in modular and non-modular versions. We strictly reserve a rotational hinge in primary indications for patients >70 years with a combined varus alignment, whereas in severe valgus deformities, a complete hinged implant version should be used for our implant design

Introduction. Review of the literature indicates variable results for ankle arthrodesis with many complications. With improved prothesis and technique for total ankle arthroplasty and an increase in severe ankle deformities such as Charcot's joint and the neuropathic diabetic foot we are faced with the need to decrease the variables in ankle arthrodesis in primary and salvage arthrodesis. We will review current methods for ankle arthrodesis and critic how they deal with primary and revision ankle arthrodesis surgery. Materials and methods. A customised plate or modified synthes proximal tibial plate and technique for salvage of complex pathology utilising a anterior approach and application of a contoured ustomised plate with co-axial screw fixation. Anterior incision was performed with removal of the lateral malleolus, for bone grafting in revision cases only. Thirteen arthrodeses were performed; four of these were pan-talar. All patients underwent objective and subjective assessments including overall patient satisfaction. The American Orthopaedic Foot and Ankle Society ankle/hind foot scoring system was used. The aim of this study is to identify the time taken to achieve radiologic arthrodesis, complications encountered, the required post-operative recovery for arthrodesis to be achieved and the overall patient satisfaction of results in the early to midterm post-operative period have been followed up for three years. Conclusion. The technique offers considerable flexibility allowing the calcaneus to be incorporated in the proposed arthrodesis where necessary. With multiple points for fixation and coaxial screw entry points the contoured customised plate provides a rigid fixation for arthrodesis stabilisation with added compression being the major advantage of this technique

Background:. Potential systemic toxicity of metal ions from metal-on-metal hip arthroplasties (MoMHA) is concerning. High blood cobalt (Co) levels have been associated with neurological, cardiac and thyroid dysfunctions. Questions/purposes:. The aim of this research was to investigate the prevalence of systemic Co toxicity in a MoMHA population, to identify confounding factors, and to indicate a Co level above which there is a high risk for systemic toxicity. Patients and Methods:. We conducted a cross-sectional study of patients with a MoMHA, using questionnaires validated to detect cobaltism in cobalt industry workers. We retrospectively identified 161 patients with Co levels >4 μg/L and 337 patients with Co levels <4 μg/L and collected 385 completed questionnaires. There were 207 men and 178 women with a mean age of 60 years (24–86). Mean follow-up was 5.7 years (1 to 13). Co levels were subdivided into <4 μg/L, 4–10 μg/L, 10–20 μg/L and >20 μg/L groups. Results:. There were significant correlations (p ≤ 0.003) between increasing Co levels and prevalence of sleeping disorders, cognitive problems, equilibrium disturbances, neuropathic symptoms, fatigue, somatic disorders and mood changes. More frequent and severe symptoms were found with Co > 20 μg/L (p = 0.017). Several years post-revision, some patients still complained of chronic symptoms possibly associated with longer exposure. Female gender and age ≤50 years were confounding factors. Conclusions:. We demonstrated a correlation between increasing Co levels and toxicity symptoms (p ≤ 0.003). As in the published case reports of MoMHA related cobaltism, the highest incidence of symptoms was found with Co > 20 μg/L. Patients with repeated Co measurements >20 μg/L are at risk for systemic toxicity

Introduction. Taylor Spatial Frame (TSF) has been designed to treat complex tibial, foot and ankle deformities using computer software. We have performed various osteotomies in combination with different soft tissue procedures, with the use of TSF. Material and Methods. A retrospective study of 20 consecutive patients operated by, senior author SSM, from 2004 onwards who underwent surgical correction of tibia, ankle, midfoot and hind foot including lateral column lengthening, calcaneal and midfoot osteotomies. Demographic details, diagnosis, procedures (including previous operations), length of follow-up, outcome and complications were recorded. Of the 20 patients, 13 were men and 7 women. The mean age was 39 years (range 18 to 70). 5 patients had TSF for malunion or non-union of ankle fractures, malunion of tibia (5), congenital talipes equino-varus(3), acute fracture of ankle (2), one patient each for spina bifida, Poliomyelitis, Charcot-Marie-Tooth disease, equino-varus due to periventricular leuco-encephalopathy and avascular necrosis of the talus. Bilateral TSF for torsional malalignment of tibia (1). Results. Follow up 6 to 54 months (mean 19.4). Patient based foot and ankle outcome criteria were used. Of the 20 patients, 16 had no pain and satisfactory range of movement and function at the last follow up. Post-operative complications included pin site infection(2) and frame hardware malfunction (2)patients, residual deformity requiring surgical correction at 22 months, (1) delayed union, neuropathic pain in (1), residual equinus deformity requiring Botox injections(1) and osteomyelitis requiring debridement(1). Conclusion. We present this series of complex congenital and acquired conditions of the foot and ankle treated with corrective osteotomies and Taylor Spatial Frame with good results