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1.
Medicina (Kaunas) ; 59(9)2023 Sep 06.
Artigo em Inglês | MEDLINE | ID: mdl-37763727

RESUMO

Background: Revision hip arthroplasty presents a surgical challenge, necessitating meticulous preoperative planning to avert complications like periprosthetic fractures and aseptic loosening. Historically, assessment of the accuracy of three-dimensional (3D) versus two-dimensional (2D) templating has focused exclusively on primary hip arthroplasty. Materials and Methods: In this retrospective study, we examined the accuracy of 3D templating for acetabular revision cups in 30 patients who underwent revision hip arthroplasty. Utilizing computed tomography scans of the patients' pelvis and 3D templates of the implants (Aesculap Plasmafit, B. Braun; Aesculap Plasmafit Revision, B. Braun; Avantage Acetabular System, Zimmerbiomet, EcoFit 2M, Implantcast; Tritanium Revision, Stryker), we performed 3D templating and positioned the acetabular cup implants accordingly. To evaluate accuracy, we compared the planned sizes of the acetabular cups in 2D and 3D with the sizes implanted during surgery. Results: An analysis was performed to examine potential influences on templating accuracy, specifically considering factors such as gender and body mass index (BMI). Significant statistical differences (p < 0.001) in the accuracy of size prediction were observed between 3D and 2D templating. Personalized 3D templating exhibited an accuracy rate of 66.7% for the correct prediction of the size of the acetabular cup, while 2D templating achieved an exact size prediction in only 26.7% of cases. There were no statistically significant differences between the 2D and 3D templating methods regarding gender or BMI. Conclusion: This study demonstrates that 3D templating improves the accuracy of predicting acetabular cup sizes in revision arthroplasty when compared to 2D templating. However, it should be noted that the predicted implant size generated through 3D templating tended to overestimate the implanted implant size by an average of 1.3 sizes.


Assuntos
Artroplastia de Quadril , Humanos , Estudos Retrospectivos , Acetábulo/diagnóstico por imagem , Acetábulo/cirurgia , Índice de Massa Corporal , Pelve
2.
Orthopadie (Heidelb) ; 52(7): 532-538, 2023 Jul.
Artigo em Alemão | MEDLINE | ID: mdl-37286621

RESUMO

BACKGROUND: For the preparation of surgical procedures in orthopedics and trauma surgery, precise knowledge of imaging and the three-dimensional imagination of the surgeon are of outstanding importance. Image-based, preoperative two-dimensional planning is the gold standard in arthroplasty today. In complex cases, further imaging such as computed tomography (CT) or magnetic resonance imaging is also performed, generating a three-dimensional model of the body region and helping the surgeon in the planning of the surgical treatment. Four-dimensional, dynamic CT studies have also been reported and are available as a complementary tool. DIGITAL AIDS: Furthermore, digital aids should generate an improved representation of the pathology to be treated and optimize the surgeon's imagination. The finite element method allows patient-specific and implant-specific parameters to be taken into account in preoperative surgical planning. Intraoperatively, relevant information can be provided by augmented reality without significantly influencing the surgical workflow.


Assuntos
Síndrome da Imunodeficiência Adquirida , Realidade Aumentada , Cirurgia Assistida por Computador , Humanos , Cirurgia Assistida por Computador/métodos , Imageamento por Ressonância Magnética , Tomografia Computadorizada Quadridimensional
3.
J Pers Med ; 13(3)2023 Mar 12.
Artigo em Inglês | MEDLINE | ID: mdl-36983692

RESUMO

INTRODUCTION: Revision hip arthroplasty is a challenging surgical procedure, especially in cases of advanced acetabular bone loss. Accurate preoperative planning can prevent complications such as periprosthetic fractures or aseptic loosening. To date, the accuracy of three-dimensional (3D) versus two-dimensional (2D) templating has been evaluated only in primary hip and knee arthroplasty. METHODS: We retrospectively investigated the accuracy of 3D personalized planning of reinforcement cages (Burch Schneider) in 27 patients who underwent revision hip arthroplasty. Personalized 3D modeling and positioning of the reinforcement cages were performed using computed tomography (CT) of the pelvis of each patient and 3D templates of the implant. To evaluate accuracy, the sizes of the reinforcement cages planned in 2D and 3D were compared with the sizes of the finally implanted cages. Factors that may potentially influence planning accuracy such as gender and body mass index (BMI) were analyzed. RESULTS: There was a significant difference (p = 0.003) in the accuracy of correct size prediction between personalized 3D templating and 2D templating. Personalized 3D templating predicted the exact size of the reinforcement cage in 96.3% of the patients, while the exact size was predicted in only 55.6% by 2D templating. Regarding gender and BMI, no statistically significant differences in planning accuracy either for 2D or 3D templating were observed. CONCLUSION: Personalized 3D planning of revision hip arthroplasty using Burch Schneider reinforcement cages leads to greater accuracy in the prediction of the required size of implants than conventional 2D templating.

4.
J Med Case Rep ; 6: 363, 2012 Oct 25.
Artigo em Inglês | MEDLINE | ID: mdl-23098161

RESUMO

INTRODUCTION: Although palsy of the long thoracic nerve is the classical pathogenesis of winging scapula, it may also be caused by osteochondroma. This rare etiopathology has previously been described in pediatric patients, but it is seldom observed in adults. CASE PRESENTATION: We describe three cases of static scapular winging with pain on movement.Case 1 is a Caucasian woman aged 35 years with a wing-like prominence of the medial margin of her right scapula due to an osteochondroma originating from the ventral omoplate. Histopathological evaluation after surgical resection confirmed the diagnosis. The postoperative course was unremarkable without signs of recurrence on examination at 2 years.Case 2 is a Caucasian woman aged 39 years with painful scapula alata and neuralgic pain projected along the left ribcage caused by an osteochondroma of the left scapula with contact to the 2nd and 3rd rib. Following surgical resection, the neuropathic pain continued, demanding neurolysis of the 3rd and 4th intercostal nerve after 8 months. The patient was free of symptoms 2 years after neurolysis.Case 3 is a Caucasian woman aged 48 years with scapular winging due to a large exostosis of the left ventral scapular surface with a broad cartilaginous cap and a large pseudobursa. Following exclusion of malignancy by an incisional biopsy, exostosis and pseudobursa were resected. The patient had an unremarkable postoperative course without signs of recurrence 1 year postoperatively.Based on these cases, we developed an algorithm for the diagnostic evaluation and therapeutic management of scapula alata due to osteochondroma. CONCLUSIONS: Orthopedic surgeons should be aware of this uncommon condition in the differential diagnosis of winged scapula not only in children, but also in adult patients.

5.
Spine (Phila Pa 1976) ; 33(22): 2379-86, 2008 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-18923312

RESUMO

STUDY DESIGN: Prospective, double-blind, randomized, placebo-controlled study. OBJECTIVE: To assess the efficacy and safety of 0.4 mg intrathecal morphine for postoperative pain control after posterior lumbar interbody fusion (PLIF) surgery. SUMMARY OF BACKGROUND DATA: Multiple studies have established the technique of intrathecal morphine analgesia in a wide variety of clinical settings. Several trials were conducted in patients undergoing spine surgery, generally supporting the efficacy for this type of surgery. Many exhibit methodologic problems with dosing regimes or study design. METHODS: After the institutional review board-approval and written informed consent, 52 patients scheduled for PLIF-surgery were enrolled, of whom 46 could be analyzed. Patients were randomized to receive 0.4 mg morphine (M-group) or normal saline (P-group) intrathecally under direct vision before the end of surgery. Additionally, all patients received a piritramide patient-controlled-analgesia for individual pain control. Measures included visual analog scale-scores and blood-gas analysis over 20 hours after surgery. Morphine associated side effects and complications were recorded. RESULTS: Visual analog scale-scores at rest and when the patients bent their legs were comparable between groups throughout the observation period, only being significantly lower in the M-group at rest 4 and 8 hours after surgery. Cumulative piritramide patient-controlled-analgesia requirements were significantly lower in the M-group throughout the observed 20 hours after surgery. Patients of the M-group were experiencing mild respiratory depression 4 hours after surgery not demanding any intervention, though. With respect to other morphine associated side effects or complications, there was no difference between the study groups. CONCLUSION: We demonstrated the efficacy of 0.4 mg intrathecal morphine after PLIF-surgery as indicated by a significantly lower cumulative piritramide requirement without any serious increase of opioid associated side effects. Therefore, morphine in a dose of 0.4 mg administered intrathecally seems to be a viable alternative therapeutic option to provide postoperative analgesia with PLIF-surgery.


Assuntos
Analgésicos Opioides/administração & dosagem , Vértebras Lombares/cirurgia , Morfina/administração & dosagem , Dor Pós-Operatória/prevenção & controle , Fusão Vertebral , Idoso , Analgesia Controlada pelo Paciente , Analgésicos Opioides/efeitos adversos , Método Duplo-Cego , Feminino , Humanos , Injeções Espinhais , Masculino , Pessoa de Meia-Idade , Morfina/efeitos adversos , Medição da Dor , Dor Pós-Operatória/etiologia , Pirinitramida/administração & dosagem , Cuidados Pós-Operatórios , Estudos Prospectivos , Fatores de Tempo , Resultado do Tratamento
6.
Spine (Phila Pa 1976) ; 28(15): 1693-9, 2003 Aug 01.
Artigo em Inglês | MEDLINE | ID: mdl-12897494

RESUMO

STUDY DESIGN: Retrospective radiographic evaluation of the sagittal alignment of the lumbar spine in patients undergoing short-segment instrumented posterior lumbar interbody fusion with cage systems of different shape. OBJECTIVES: To determine whether rectangular and wedge-shaped cages have a different influence on the sagittal alignment of the lumbar spine in patients undergoing short-segment instrumented posterior lumbar interbody fusion. SUMMARY OF BACKGROUND DATA: Previous studies of sagittal alignment after posterior lumbar interbody fusion have focused on the impact of intraoperative patient, hip, and knee positioning, as well as instrumentation characteristics on sagittal posture. The influence of the cage shape on indexes of total and segmental sagittal alignment of the lumbar spine is yet unknown. METHODS: Forty-two patients having undergone instrumented short-segment posterior lumbar interbody fusion were reviewed retrospectively. Twenty-two patients (12 women and 10 men, 38-78 years of age) had posterior lumbar interbody fusion with rectangular cages. The fused segments were: 4 at L3-L4, 16 at L4-L5, 11 at L5-S1. Thirteen patients had single- and nine patients double-level fusion. Twenty patients (8 women and 12 men, 34-81 years of age) had posterior lumbar interbody fusion with wedge-shaped cages. The fused segments were: 4 at L3-L4, 15 at L4-L5, 11 at L5-S1. Ten patients had single- and 10 patients double-level fusion. Cages were packed with cancellous bone from the posterior iliac crest and/or bone fragments harvested by laminectomy. All patients had additional pedicle screw fixation. Pre- and postoperative standing lateral radiographs were assessed for segmental and lumbar lordosis as well lumbar and sacral tilt. Data were analyzed with repeated measures analysis of variance. RESULTS The mean follow-up period was 18 months with a minimum follow-up period of 14 months. Mean segmental lordosis of the fused segments showed significant changes between the two implant groups (P < 0.05). Segmental lordosis decreased in the rectangular cage group from 10 degrees to 2 degrees at L3-L4, from 10 degrees to 5 degrees at L4-L5, and from 9 degrees before to 6 degrees after fusion surgery at L5-S1. In the wedge-shaped cage group, segmental lordosis increased from 4 degrees to 7 degrees at L3-L4, from 2 degrees to 8 degrees at L4-L5, and from 9 degrees to 17 degrees at L5-S1. Analysis of changes in lumbar lordosis and lumbar and sacral tilt did not show significant differences though opposite trends: lumbar lordosis decreased from 55 degrees to 48 degrees in the rectangular cage group and increased from 45 degrees to 53 degrees in the wedge-shaped cage group. Lumbar tilt measured 98 degrees before and 102 degrees after surgery in the rectangular cage group and 97 degrees before and 94 degrees after surgery. Sacral tilt measured 44 degrees before and 40 degrees after surgery in the rectangular cage group and measured 42 degrees before and 45 degrees after surgery in the wedge-shaped cage group. CONCLUSIONS: The cage geometry has a significant impact on the alignment of the lumbar spine after instrumented posterior lumbar interbody fusion. With rectangular cages, lumbar lordosis and segmental lordosis of the segments fused decrease; sagittal balance is maintained by compensatory changes of the sacral tilt. Wedge-shaped cages significantly increase segmental lordosis, enhance lumbar lordosis, and therefore should be preferred for restoring sagittal alignment in instrumented posterior lumbar interbody fusion procedures.


Assuntos
Vértebras Lombares/diagnóstico por imagem , Vértebras Lombares/cirurgia , Próteses e Implantes/estatística & dados numéricos , Fusão Vertebral/instrumentação , Fusão Vertebral/estatística & dados numéricos , Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Seguimentos , Humanos , Lordose/diagnóstico por imagem , Região Lombossacral/diagnóstico por imagem , Masculino , Pessoa de Meia-Idade , Variações Dependentes do Observador , Postura , Próteses e Implantes/classificação , Radiografia , Estudos Retrospectivos , Sacro/diagnóstico por imagem , Doenças da Coluna Vertebral/cirurgia , Resultado do Tratamento
7.
Knee Surg Sports Traumatol Arthrosc ; 10(4): 233-40, 2002 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12172718

RESUMO

Aseptic osteonecrosis of the medial femoral condyle has recently been reported as a complication of arthroscopic surgery. The time interval between the onset of symptoms and pathognomonic MRI changes (diagnostic window) is not known for osteonecrosis of the knee. To determine the prevalence of early-stage spontaneous osteonecrosis of the knee (SONK) we prospectively examined 176 patients by MRI between May 1998 and December 1999. In six patients MRI revealed a bone marrow edema pattern and subtle subchondral bone changes in the medial condyle consistent with early-stage SONK (prevalence of 3.4%); in the 53 patients older than 65 years the prevalence was 9.4%. In 10 patients (5.7%) the bone and marrow changes on MRI imaging either resolved on follow-up MRI and were regarded as transient epiphyseal lesions or were considered to be reactive changes due to underlying degenerative articular disease. Including MRI in the preoperative diagnostic procedures could avoid missing the diagnosis of avascular necrosis before planning an operative treatment of suspected meniscal tears in elderly patients.


Assuntos
Fêmur/patologia , Osteonecrose/epidemiologia , Osteonecrose/patologia , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Estudos de Coortes , Diagnóstico Diferencial , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Meniscos Tibiais/patologia , Pessoa de Meia-Idade , Valor Preditivo dos Testes , Prevalência , Estudos Prospectivos , Lesões do Menisco Tibial , Fatores de Tempo
8.
Spine (Phila Pa 1976) ; 27(3): 269-74, 2002 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-11805690

RESUMO

STUDY DESIGN: The intervertebral stability of bony consolidated anteroposterior lumbosacral spondylodesis is evaluated by roentgen stereophotogrammetric analysis and direct surgical exploration before and after removal of the internal fixator. OBJECTIVES: To determine the remaining in vivo stability of spinal arthrodesis solely retained by a bony integrated carbon fiber cage. SUMMARY OF BACKGROUND DATA: Roentgen stereophotogrammetric analysis studies on posterolateral lumbar fusions demonstrate primary spinal stability after additional dorsal instrumentation, which is retained during bony fusion healing. Animal models show a persistent stabilizing effect of the fixator despite the presence of bony fusion. Although direct surgical inspection is the most reliable method to evaluate fused vertebrae, roentgen stereophotogrammetric analysis has also proven to be a highly accurate method to evaluate spinal stability. METHODS: In 10 patients lumbosacral fusion was performed using carbon interbody implants and an internal fixator. Ten months after initial surgery (range 7-15 months) the internal fixation was removed to reduce local soft tissue impingement as soon as bony fusion was achieved. Fusion site exploration in the course of instrumentation removal was performed by applying distraction, compression, and torque to the grafted area under fluoroscopic control. Any motion indicated a pseudarthrosis. Lumbosacral stability was evaluated by serial roentgen stereophotogrammetric analysis after fusion and after instrumentation removal. RESULTS: During instrumentation removal the mechanical stress test under fluoroscopic control did not indicate pseudarthrosis. After instrumentation removal, roentgen stereophotogrammetric analysis measurements revealed a nonsignificant increase in lumbosacral micromotions within the fused segment with 0.14, 0.31, and 0.44 mm in the transverse, vertical, and sagittal axes, respectively. CONCLUSIONS: The internal fixator could be removed without endangering the stability of the fusion. Direct surgical exploration confirmed the adequacy of roentgen stereophotogrammetric analysis as a reliable in vivo method to evaluate lumbosacral stability after anteroposterior fusion.


Assuntos
Fotogrametria , Próteses e Implantes , Fusão Vertebral/instrumentação , Coluna Vertebral/cirurgia , Espondilolistese/cirurgia , Adulto , Avaliação da Deficiência , Feminino , Seguimentos , Humanos , Imageamento Tridimensional/estatística & dados numéricos , Período Intraoperatório , Região Lombossacral/diagnóstico por imagem , Região Lombossacral/cirurgia , Masculino , Implantação de Prótese , Radiografia , Reoperação/efeitos adversos , Fusão Vertebral/métodos , Fusão Vertebral/estatística & dados numéricos , Coluna Vertebral/diagnóstico por imagem , Resultado do Tratamento
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