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1.
Acta Orthop Traumatol Turc ; 51(2): 104-109, 2017 Mar.
Article de Anglais | MEDLINE | ID: mdl-28314555

RÉSUMÉ

OBJECTIVE: The aim of this study was to compared the effectiveness of intraarticular levobupivacain with levobupivacain and magnesium sulfate. METHODS: In this prospective randomized double blinded study, 96 patients (67 male, 29 female; age range: 18-65 years) with ASA (American Society of Anesthesiologist) score I and II, who had undergone arthroscopic meniscectomy operation, were divided to 3 groups that had postoperative analgesia with intra-articular saline injection (control group), levobupivacain injection (L group) or levobupivacain and magnesium sulfate injection (LM group). Patients were compared with postoperative VAS (Visual Analog Score) score during rest and activity, opioid analgesic need, non-opioid analgesic need and other medication needs. RESULTS: Postoperative VAS scores during rest and activation at early postoperative period were significantly lower at LM group when compared with L group and lower than control group at all time periods. Opioid analgesic need, non-opioid analgesic need and other medication needs for non-pain symptoms were lower at LM group when compared with L and control groups at all time periods. CONCLUSION: Intraarticular magnesium sulfate plus Levobupivacain injection is a safe and effective method for post operative pain management after arthroscopic meniscectomy.


Sujet(s)
Analgésie/méthodes , Arthroscopie , Bupivacaïne/analogues et dérivés , Sulfate de magnésium/administration et posologie , Méniscectomie/méthodes , Mesure de la douleur/méthodes , Douleur postopératoire/traitement médicamenteux , Adolescent , Adulte , Sujet âgé , Analgésiques/administration et posologie , Anti-inflammatoires non stéroïdiens/usage thérapeutique , Bupivacaïne/administration et posologie , Méthode en double aveugle , Association de médicaments , Femelle , Humains , Injections articulaires , Lévobupivacaïne , Mâle , Adulte d'âge moyen , Douleur postopératoire/diagnostic , Études prospectives , Résultat thérapeutique , Jeune adulte
2.
Acta Orthop Traumatol Turc ; 49(3): 255-9, 2015.
Article de Anglais | MEDLINE | ID: mdl-26200403

RÉSUMÉ

OBJECTIVE: Prevention of deep venous thrombosis (DVT) and associated pulmonary embolism following major orthopedic surgeries is challenging, and there is an increased interest in developing new treatment strategies. We compared 2 switch-therapy modalities-enoxaparin to rivaroxaban and enoxaparin to dabigatran-and enoxaparin monotherapy for preventing DVT after total knee arthroplasty (TKA) and total hip arthroplasty (THA). METHODS: This was a prospective, non-blinded, randomized controlled study. We selected 180 eligible patients out of 247 patients undergoing TKA or THA. During the preoperative checkup, patients were randomized to receive either enoxaparin (enoxaparin group) or switch-therapy regimens, comprising enoxaparin during hospitalization and rivaroxaban (rivaroxaban group) or dabigatran (dabigatran group) during the outpatient period. All patients were evaluated for DVT using Doppler ultrasonography (USG) 6 weeks postoperatively. The primary efficacy outcome was the prevention of symptomatic or Doppler ultrasonography (USG)-proven DVT, whereas the primary safety outcome was the incidence of bleeding during the DVT-prophylaxis period. RESULTS: Doppler USG at 6 weeks after surgery revealed no signs of DVT in any patient. During the hospitalization period, only 2 major bleeding events were reported (1 [1.6%] in the enoxaparin group and 1 [1.6%] in the dabigatran group). No major bleeding events were reported during the outpatient follow-up period in any group. Differences among the 3 groups regarding bleeding events were not statistically significant (p>0.05). CONCLUSION: When using switch-therapy modalities, clinicians can take advantage of the safety of enoxaparin during the hospitalization period and ease of use of new oral anticoagulant drugs during the outpatient period.


Sujet(s)
Arthroplastie prothétique de hanche/effets indésirables , Arthroplastie prothétique de genou/effets indésirables , Dabigatran/usage thérapeutique , Énoxaparine/usage thérapeutique , Rivaroxaban/usage thérapeutique , Thrombose veineuse/prévention et contrôle , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Anticoagulants/usage thérapeutique , Femelle , Hémorragie/étiologie , Humains , Mâle , Adulte d'âge moyen , Complications postopératoires/prévention et contrôle , Études prospectives , Échographie-doppler
3.
Acta Orthop Traumatol Turc ; 48(3): 249-52, 2014.
Article de Anglais | MEDLINE | ID: mdl-24901912

RÉSUMÉ

OBJECTIVE: The aim of this study was to evaluate the injury mechanism and clinical and radiological results of the patients with isolated posterior malleolar fracture. METHODS: Seven patients (5 male, 2 female; mean age: 32 years; range: 23-40) with a missed isolated posterior malleolar fracture were included in the study. All patients had initially been examined for an ankle sprain in the emergency room, where the initial plain radiographs did not show any abnormality. Due to the long lasting symptoms all patients underwent an MRI scan by the 3rd week which revealed a posterior malleolar fracture. Patients were treated with an ankle brace for 3 weeks. All patients were followed up for 1 year. Bone healing and degenerative changes were evaluated with plain Radiographs, including a 50° external rotation lateral. Clinical outcome was evaluated with American Orthopedic Foot and Ankle Society ankle hindfoot scale. RESULTS: Fracture healing was seen in 6 of the 7 patients by the 6th week. There was no radiographic healing by 6th month in the remaining patient. Mean AOFAS ankle hindfoot scores at the beginning of the treatment and at 3rd month were 20 (11-31) and 86 (43-96), respectively. There was no instability or degenerative changes at one-year follow-up. CONCLUSION: Isolated posterior malleolar fracture should be kept in mind in patients who present with pain at the posterior part of the ankle following a forced plantar flexion and/or axial compression injury. A 50° external rotation lateral radiograph can be useful in detecting the fracture.


Sujet(s)
Orthèses de maintien , Fractures osseuses/thérapie , Os du tarse/traumatismes , Adulte , Retard de diagnostic , Femelle , Études de suivi , Consolidation de fracture , Fractures osseuses/diagnostic , Humains , Mâle , Adulte d'âge moyen , Radiographie , Études rétrospectives , Os du tarse/imagerie diagnostique , Os du tarse/anatomopathologie , Résultat thérapeutique
4.
Mol Imaging Radionucl Ther ; 23(1): 39-42, 2014 Feb.
Article de Anglais | MEDLINE | ID: mdl-24653936

RÉSUMÉ

UNLABELLED: Positron Emission Tomography with 2-deoxy-[F-18]-fluoro-D-glucose (FDG-PET) has become a reliable diagnostic tool in clinical practice similar to Magnetic Resonance (MR) imaging and Computed Tomography (CT). FDG-PET has especially been used to differentiate malignant from benign lesions, and for staging and follow- up malignant tumors. However, FDG-PET has some pitfalls in cancer screening and FDG tracer accumulates at sites of infection and inflammation. Bone tuberculosis may be confused with malignant tumors of bone and its metastases, and can accumulate focally increased FDG in active period. We present a 60-year-old woman with lytic bone lesions and mediastinal hypermetabolic foci, initially suspected to be malignant by means of FDG-PET and the other imaging modalities; however, bone biopsy confirmed the diagnosis of bone tuberculosis. CONFLICT OF INTEREST: None declared.

5.
Plast Reconstr Surg Glob Open ; 2(12): e263, 2014 Dec.
Article de Anglais | MEDLINE | ID: mdl-25587497

RÉSUMÉ

SUMMARY: Streptococcus mitis is a commensal organism of the human oropharynx that rarely causes infection in healthy individuals. Herein, we describe a previously healthy 35-year-old woman who presented with acute pyogenic flexor tenosynovitis of the left index finger due to S. mitis infection. The patient's infection was treated successfully via surgical and medical interventions, and during follow-up, it was determined that she was complement component C3 deficient. Tenosynovitis is an emergent clinical syndrome that can result in permanent disability or amputation. To the best of our knowledge, this case report is the first to describe tenosynovitis due to S. mitis; in addition, it highlights the importance of initiating therapy with antibiotics that are effective against this rare pathogen.

6.
Acta Orthop Traumatol Turc ; 47(5): 330-3, 2013.
Article de Anglais | MEDLINE | ID: mdl-24164942

RÉSUMÉ

OBJECTIVE: We aimed to find out the distribution of etiological factors in patients who had total hip replacement for coxarthrosis. METHODS: The medical records of the 965 hips of 886 patients operated with total hip replacement between 2001 and 2012 in two separate arthroplasty clinics were analyzed by two separate senior surgeons. Each patient's pre- and postoperative X-rays and demographic data such as gender, age, side and probable etiologic factors were noted. RESULTS: Six hundred and eighty-four patients were women and 202 were men. The mean age were 62.7±14.3 (range: 16 to 91) in women, 58.8±17.1 (range: 25 to 91) in men. 52.1% of the surgeries were performed on the right side, 39% on the left, and 8.9% bilaterally. In women 36.2% of the cases were primary coxarthrosis, while the etiology was developmental dysplasia of the hip (DDH) in 43.5% of the cases, avascular necrosis in 10%, romatoid diseases in 7%, slipped capital femoral epiphysis in 5%, posttraumatic coxarthrosis in 3.9%, pathologic coxarthrosis in 1.9%, and Perthes sequel in 1.7%. In men, 24.4% of the cases were primary coxarthrosis, while the etiology was avascular necrosis in 21% of the cases, DDH in 17.6%, posttraumatic coxarthrosis in 16.8%, romatoid diseases in 10.9%, Perthes sequel in 4.2%, slipped capital femoral epiphysis in 2.5%, and pathologic coxarthrosis in 2.5%. The most common etiologic factor was DDH with a rate of 37.1%. CONCLUSION: Despite the heterogeneity of our study population, our results may reflect the distribution of coxarthrosis etiologies in Turkey. Developmental dysplasia of the hip appears to be the most frequent cause of coxarthrosis among the patients undergoing total hip replacement.


Sujet(s)
Arthroplastie prothétique de hanche/effets indésirables , Luxation de la hanche/chirurgie , Coxarthrose/étiologie , Adolescent , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Femelle , Études de suivi , Humains , Mâle , Adulte d'âge moyen , Coxarthrose/diagnostic , Complications postopératoires , Études rétrospectives , Jeune adulte
7.
J Am Podiatr Med Assoc ; 103(2): 145-8, 2013.
Article de Anglais | MEDLINE | ID: mdl-23536506

RÉSUMÉ

The incidence and life-threatening complications of thromboembolic disease after major orthopedic surgical procedures have been extensively defined in the medical literature. However, there are few studies concerning the incidence of thromboembolic disease after foot and ankle surgery. We describe a 57-year-old female patient who underwent surgery for bilateral hallux valgus deformities and was diagnosed as having deep venous thrombosis and pulmonary embolism after the surgery despite early mobilization and mechanical prohylaxis. Her preoperative physical examination revealed varicose veins in both cruris. She was treated for pulmonary embolism with low-molecular-weight heparin and an oral anticoagulant in the postoperative period. Although venous thromboembolism is more commonly described after proximal lower-extremity procedures, it can occur after foot and ankle surgery, particularly if the patient has certain risk factors. Therefore, in addition to mechanical prophylaxis, pharmacologic prophylaxis should be kept in mind in such patients.


Sujet(s)
Hallux valgus/chirurgie , Procédures orthopédiques/effets indésirables , Complications postopératoires/diagnostic , Embolie pulmonaire/étiologie , Thrombose veineuse/étiologie , Femelle , Humains , Incidence , Adulte d'âge moyen , Embolie pulmonaire/diagnostic , Facteurs de risque , Thrombose veineuse/diagnostic
8.
Eklem Hastalik Cerrahisi ; 23(3): 168-72, 2012.
Article de Turc | MEDLINE | ID: mdl-23145762

RÉSUMÉ

OBJECTIVES: This study aims to investigate whether the usage of fondaparinux sodium may result in major hemorrhages following major orthopedic surgery. PATIENTS AND METHODS: Forty-three patients (30 females and 13 males; mean age 66 years; range 34 to 94 years) at the age of >18 years who were scheduled for major orthopedic surgery were included. Total hip arthroplasty, total knee arthroplasty and proximal femur fracture surgeries were defined as the major orthopedic surgeries. Prophylaxis was administered with 2.5 mg fondaparinux sodium once daily subcutaneously. Prophylaxis was initiated at 6-8 hours after the closure of incision. During the prophylaxis period (31±3 days), the patients were monitored for symptomatic deep venous thrombosis. Serum creatinine, platelet and hemoglobin levels were measured at the baseline and in the first week and at one month postoperatively. Wound healing time, healing complications, and major/minor hemorrhages seen during the prophylaxis period were recorded. RESULTS: During the follow-up, none of the patients had symptomatic deep vein thrombosis or symptomatic pulmonary embolism. Two patients (4.6%) had delayed wound healing, while four (9.3%) had minor ecchymosis. No major hemorrhages were observed in any patients. CONCLUSION: With the long-term use of fondaparinux, we did not observe any major hemorrhagic complications. However, further large-scale studies including control groups are required to establish the effects of long-term use of fondaparinux.


Sujet(s)
Anticoagulants/administration et posologie , Procédures orthopédiques , Polyosides/administration et posologie , Complications postopératoires/prévention et contrôle , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Femelle , Fondaparinux , Humains , Injections sous-cutanées , Mâle , Adulte d'âge moyen , Embolie pulmonaire/prévention et contrôle , Résultat thérapeutique , Thrombose veineuse/prévention et contrôle
9.
Acta Orthop Traumatol Turc ; 46(4): 237-42, 2012.
Article de Anglais | MEDLINE | ID: mdl-22951753

RÉSUMÉ

OBJECTIVE: We aimed to evaluate the results and complications of open reduction and internal fixation by locked anatomic plates in adult midshaft clavicular fractures. METHODS: Sixteen patients (11 males, 5 females; mean age: 39.6 years) who underwent open reduction and internal fixation with locked anatomic plate for displaced-comminuted midshaft clavicular fractures and were followed-up for at least one year were reviewed retrospectively. Complications in the early and late postoperative periods and functional scores according to the Constant and DASH scoring systems from the latest follow-up were evaluated. RESULTS: Mean follow-up period was 24.6 (range: 12 to 52) months and mean union time was 13.3 (range: 10 to 23) weeks. None of the patients had superficial and/or deep infections in the early postoperative period or neurovascular complications. Two (12.5%) patients had implant irritation. In two (12.5%) patients, implant failure was detected in the late postoperative period. Delayed union was suspected in these patients and they were operated with longer plate and grafting in the 4th month. At the final follow-up, none of the patients had nonunion or malunion and the mean Constant and DASH scores were 85.5 and 12.8, respectively. Constant scores in patients with complications (p=0.007) and DASH scores in patients with no complications (p=0.001) were significantly lower. CONCLUSION: Fixation with locked anatomic plates in displaced midshaft clavicular fractures has lower complication rates. Possible postoperative complications are generally associated with implant irritation and failure. These problems can be avoided with the development in implant technology and new implant designs.


Sujet(s)
Plaques orthopédiques , Clavicule/traumatismes , Ostéosynthèse interne/méthodes , Fractures osseuses/chirurgie , Adulte , Clavicule/chirurgie , Femelle , Études de suivi , Humains , Mâle , Conception de prothèse , Amplitude articulaire , Études rétrospectives , Articulation glénohumérale/physiopathologie , Résultat thérapeutique
10.
Geriatr Orthop Surg Rehabil ; 3(4): 150-6, 2012 Dec.
Article de Anglais | MEDLINE | ID: mdl-23569709

RÉSUMÉ

OBJECTIVE: We aimed to evaluate possible risk factors associated with acute kidney injury (AKI) after hip fracture surgery in the elderly individuals. DESIGN: Level II diagnostic study, evidence obtained from prospective cohort study from 1 center with level 2, and 3 patients. PATIENTS: A total of 165 patients (>65 years) with femoral neck fracture were enrolled in this prospective study between 2007 and 2010. Two patients were dropped for inadequate laboratory follow-up data. Patients with kidney failure or renal replacement therapy (RRT) history or AKI at admission were excluded. INTERVENTION: Nephrology consultation was obtained from all patients at admission. All patients had undergone bipolar cemented hip arthroplasty that was performed by the same surgical team in all patients within 24 hours of fracture and admission under the same protocol. MAIN OUTCOME MEASUREMENTS: Serum creatinine (SCr), urine output, and complete blood counts were evaluated at baseline and daily basis thereafter. The AKI was defined based on Acute Kidney Injury Network classification. Hospital charges were converted from Turkish Liras to US dollars and rounded. RESULTS: Among 163 patients, AKI occurred in 25 (15.3%) patients, all within the first 48 postoperative hours. Three (1.8%) patients required RRT. Baseline SCr levels were restored within 4.84 ± 1.34 days on average (3-8 days). No patient required RRT after discharge. The mean hospital stay was 3 days (2-6 days) longer and the hospital charge was 2500 US$ higher for the patients with AKI. After multivariable adjustment, only lower estimated glomerular filtration rate levels (odds ratio 0.945, 95%confidence interval 0.92-0.96) emerged as an independent predictor for AKI. CONCLUSION: The AKI represents a frequent complication after hip fracture surgery associated with longer hospital stay and higher treatment costs with increased morbidity. Our results show baseline renal function is an independent predictor of AKI.

11.
Foot (Edinb) ; 19(2): 93-7, 2009 Jun.
Article de Anglais | MEDLINE | ID: mdl-20307456

RÉSUMÉ

Intraosseous lipoma is among rare benign tumors of the bone. The aim of the present study was to evaluate the long-term surgical results of calcaneal lipomas, representing a relatively rare localization for this type of tumors. The present study included 21 calcaneal lipoma cases (22 feet) referred to our podiatry clinic between 1991 and 2001 with complaints of foot and heel pain resistant to conservative treatment for the last 3-6 months. In all cases, the diagnosis of calcaneal intraosseous lipoma was first confirmed radiologically, then histologically. The mean age was 39 years (range 16-62), 15 were females (71%) and 6 were males (29%). One patient had bilateral disease, whereas 11 and 9 patients had right and left calcaneal involvement, respectively. None of the patients have a palpable mass in their foot. For pre-operative differential diagnosis, 3 patients had computerized tomography examination (CT scan) and 8 patients underwent magnetic resonance imaging (MRI). All lesions were totally curetted out with angled curettes. The defect was filled with cancellous autografts taken from the ipsilateral iliac crest. In only four patients, the amount of autograft was not sufficient, so a combination of cancellous allograft and autograft was used. No drain was used. An elastic bandage was wrapped around the foot and ankle, and cold packs were applied to the surgical site. The mean duration of follow up was 94 (45-143) months. Pain improved in 17 feet at 4 months, in an additional 4 feet at 8 months and in the remaining one foot at 12 months. The mean time to the graft consolidation was 5 months (range 3-7 months). There were no recurrences or pathological fractures during the follow up. No wound infection or necrosis was seen at the surgical sites. There were no neurovascular complications. Five cases experienced pain in the iliac bone for 1 month, due to grafting procedures. Although calcaneal intraosseous lipoma accounts for a small portion of cases in the huge differential diagnosis chart for foot pain, it should be kept in mind as a possible diagnosis in unresolved cases. Most of the patients would benefit from non-surgical treatments. But if this is not the case, surgical treatment is indicated. In conclusion, curettage and autogenous bone grafting is an easy and effective method for the surgical treatment of calcaneal intraosseous lipomas.


Sujet(s)
Tumeurs osseuses/chirurgie , Calcanéus , Lipome/chirurgie , Adolescent , Adulte , Tumeurs osseuses/imagerie diagnostique , Transplantation osseuse , Calcanéus/imagerie diagnostique , Femelle , Humains , Lipome/imagerie diagnostique , Imagerie par résonance magnétique , Mâle , Adulte d'âge moyen , Tomodensitométrie , Jeune adulte
12.
Acta Orthop Traumatol Turc ; 41(5): 337-42, 2007.
Article de Turc | MEDLINE | ID: mdl-18180567

RÉSUMÉ

OBJECTIVES: We investigated the effectiveness of arthroscopic debridement followed by viscosupplementation using different hyaluronic acid (HA) products in selected patients with knee osteoarthritis. METHODS: The study included 77 women (mean age 50+/-5 years; range 40 to 60 years) who had mild knee osteoarthritis according to the modified ARA (American Rheumatism Association) criteria and Ahlback classification. All the patients had degenerative meniscal tears. After three weeks from arthroscopic treatment (partial meniscectomy and debridement), the patients were randomly assigned to intra-articular injections of Na-hyaluronate (Orthovisc, n=38), streptococcal HA (Adant, n=21), and Hylan G-F 20 (Synvisc, n=18) given once a week for three weeks. Evaluations were made preoperatively, before and three weeks after injections using a patient satisfaction questionnaire, visual analog scale (VAS), and the WOMAC (Western Ontario and McMaster Universities) osteoarthritis index. RESULTS: All patients had significant improvement following both arthroscopic treatment and viscosupplementation (p<0.0001). Following injections, patient satisfaction (p<0.01), WOMAC and VAS (p<0.0001) scores were significantly improved in the Na-hyaluronate and Hylan G-F 20 groups, whereas the only significant change was in VAS scores in the streptococcal HA group. However, comparison of the three groups did not yield any significant difference with respect to patient satisfaction, WOMAC, and VAS scores (p>0.05). CONCLUSION: Our results suggest that arthroscopic debridement combined with viscosupplementation is an effective treatment option for selected patients with knee osteoarthritis.


Sujet(s)
Débridement , Acide hyaluronique/analogues et dérivés , Gonarthrose/thérapie , Adulte , Arthroscopie/méthodes , Femelle , Humains , Acide hyaluronique/administration et posologie , Injections articulaires , Adulte d'âge moyen , Gonarthrose/imagerie diagnostique , Gonarthrose/anatomopathologie , Mesure de la douleur , Radiographie , Indice de gravité de la maladie , Enquêtes et questionnaires , Résultat thérapeutique
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