Effectiveness of two-stage revision with commercial polymethylmethacrylate articulated hip spacer: similar outcomes against monomicrobial and polymicrobial hip periprosthetic joint infections.

Background: orthopaedic surgeons still struggle against a devastating complication - periprosthetic joint infection (PJI). A two-stage revision is considered the gold standard for chronic PJI for several authors, with success rates over 90 %. This strategy implies the remotion of the prosthesis and the implantation of an antibiotic-impregnated cement spacer in the joint. The primary objective of this study was to assess the effectiveness of a two-stage revision approach using a commercial prefabricated antibiotic-impregnated cement hip spacer for the treatment of hip PJI regarding monomicrobial and polymicrobial infections. Secondly, to assess risk factors for failure of two-stage revision. Material and methods: we conducted a retrospective study on patients that underwent revision of total hip arthroplasty (THA) between January 2002 and January 20218. We included adult patients with a diagnosis of chronic hip PJI that underwent two-stage revision using a prefabricated gentamicin-impregnated cement of polymethylmethacrylate (PMMA) hip spacer. We assessed whether it was monomicrobial or polymicrobial infections and comorbidities. Treatment success was defined when eradication of the infection was observed and no further procedures or mortality were registered after the second stage. Persistence or recurrence of infection was considered a failure of treatment. Results: the final series consisted of 84 patients treated with the same hip spacer: 60 (71.4 %) monomicrobial and 24 (28.6 %) polymicrobial joint infections with an overall follow-up of 59.0 (36.0-84.0) months. The overall success rate was 90.5 %. Eight (9.5 %) patients failed. Smoking and BMI greater than 30 m kg-2 were identified independent risk factors for failure in multivariate analysis. Conclusion: our study suggests that prefabricated gentamicin-impregnated PMMA spacer is an effective tool for the treatment of PJI, achieving similar outcomes whether it is monomicrobial or polymicrobial infections. Randomized prospective studies are needed to obtain more reliable conclusions.

Pre-fracture ambulation capacity, Charlson comorbidity index, and dementia as predictors of functional impairment after bipolar hemiarthroplasty for unstable intertrochanteric fracture. A retrospective analysis in 158 octogenarian patients.

Background: the primary purpose of this study was to assess the ambulatory capacity 12 months after surgery in patients that underwent bipolar hemiarthroplasty (BH) due to unstable intertrochanteric fractures (UITF). Secondly, to identify which preoperative variables influenced these modifications. Methods: We retrospectively analyzed a consecutive series of patients older than 80 years with UITF treated with BH between 2010 and 2019. Ambulatory capacity was assessed before surgery, at 3 and 12 months postoperatively, using Koval's classification and the modified Harris Hip Score (mHHS). The registered variables were: gender, age, osteoporosis, Charlson comorbidity index (CCI), ASA classification, body mass index (BMI), and dementia. The identification of variables that impaired postoperative functionality was performed by uni- and multivariate analysis. Results: 158 patients were included with a median age of 87 (range 80-102) years and a follow-up of 29.2 (range 12-56) months. The 1-year overall ambulatory capacity impairment was 28.5% and significantly affected pre-fracture community walkers (p = 0.001). A CCI >4 (OR 2.72; p = 0.044), dementia (OR 14.13; p = 0.0001), and a Koval 2-3 (OR 12.84; p = 0.001) were identified as risk factors for this impairment. Conclusion: Ambulation impairment at one year was 28.5%. The predictive characteristics found in this study help to identify patients with a greater risk of ambulation impairment and to focus rehabilitation plans to reduce this impact.

Culture-negative Peri-prosthetic Joint Infection after Total Hip Arthroplasty Treatment Protocol and Outcomes in Acute and Chronic Cases.

The treatment of culture-negative periprosthetic joint infections (CN PJI) of the hip represents complex entities. We, as a result of this, report on 12 cases. Irrigation and debridement (I&D) with implant retention were performed in acute cases and two-stage revisions in chronic infections. Combined antibiotic therapy was administered in all cases for 12 weeks. Infection control was achieved in all patients with an infection-free rate of 100% at 7.5 years of average follow-up.

Bipolar hemiarthroplasty in unstable intertrochanteric fractures in elderly patients. The predictive value of the Charlson Comorbidity Index in 1-year mortality.

BACKGROUND: Hip fractures have a significant impact on morbidity and mortality in the elderly. Aims: We retrospectively evaluated the predictive role of the Charlson Comorbidity Index (CCI) for 1-year mortality in elderly patients with unstable intertrochanteric hip fractures (ITHF) treated with bipolar hemiarthroplasty. The secondary objective was to identify other relationships, if any, between the variables recorded and mortality. METHODS: We included ≥75-year-old patients with unstable ITHF treated with bipolar hemiarthroplasty. We recorded patient gender, age, Body Mass Index, pre-fracture walking ability (Parker Mobility score, modified Harris Hip Score), America Society of Anesthesiologists (ASA) score, Charlson Comorbidity Index (CCI), time to surgery, time to mobilization, hospital stay, and postoperative complications. Uni- and multivariate logistic regression analysis were performed. Sensitivity and specificity were calculated using a ROC curve. RESULTS: A total of 135 patients with a mean age of 87.34 ± 5.5 years were included. The overall 1-year mortality rate was 18.5%. The CCI (OR 1.64 CI 95% 1.21-2.23; p 0.00821) and postoperative complications (OR 3.5 CI 95% 1.19-10.23 p 0.0202) were identified as independent predictors of 1-year mortality in the univariate regression and confirmed in the multivariate regression. CCI sensitivity to predict 1-year mortality was 80%. CONCLUSION: CCI has shown acceptable sensitivity in the prediction of 1-year mortality in elderly patients with unstable ITHF treated with bipolar hemiarthroplasty. It is of utmost importance to prevent postoperative complications due to their significant impact on 1-year mortality.

Genu valgo artrósico severo: Prótesis de estabilidad aumentada en artroplastia primaria / The severe valgus knee: Total knee arthroplasty with a constrained prosthesis

Objetivo El genu valgo artrósico severo (> 20°) puede presentar distintos grados de insuficiencia del ligamento colateral medial e inestabilidad articular. El objetivo de este trabajo retrospectivo evalúa nuestra experiencia en el tratamiento del genu valgo severo con prótesis de estabilidad aumentada y propone un método para la evaluación y clasificación del genu valgo artrósico. Material y métodos A 27 pacientes (28 rodillas) con genu valgo artrósico severo se les realizó una artroplastia total de rodilla primaria con un implante de estabilidad aumentada, y un seguimiento promedio de 6.2 años. Se confeccionó una nueva clasificación del genu valgo artrósico que contempla la suficiencia ligamentaria y por lo tanto relaciona el tipo de rodilla con el tipo de implante necesario. Resultados Se utilizó una prótesis constreñida en 17 pacientes con un eje promedio de 22,7° y el ligamento colateral medial atenuado. En 11 casos con un eje promedio de 28,1°, LCM incompetente y/o recurvatum, se optó por bisagras rotatorias. Se confeccionó una nueva clasificación del genu valgo artrósico que considera el desgaste y estabilidad articular, el grado de deformidad de la rodilla y la suficiencia ligamentaria. Discusión Las prótesis constreñidas deben utilizarse en pacientes que presenten inestabilidad exclusivamente en el plano coronal, aún en genu valgo severo, con LCM atenuado. Debe reservarse el uso de bisagras rotatorias a aquellos pacientes que presentan incompetencia ligamentaria, inestabilidad combinada (recurvatum) y/o déficit neuro-muscular severo.

Purpose This retrospective level 2 analysis evaluates the prosthesis type selected in our department for the treatment of the severe valgus knee and proposes a new classification for the valgus knee osteoarthritis. Material and methods A total knee arthroplasty with a constrained or hinged knee prosthesis was performed in 28 valgus knees. The average follow-up was 6.2 years. A new classification that considerates the ligament sufficiency status was developed in order to relate the different knee types with the different type of eventually needed implants. Results Constrained prosthesis was used in 17 patients with an attenuated medial collateral ligament, and a rotating hinge in 11 patients with incompetent medial collateral ligament and/or recurvatum. The postoperatory Knee Society Score was of 85 points. The valgus knee was classified in 5 types considering the knee valgus deformity, the ligament sufficiency and joint stability and wear. Discussion The classification proposed clearly defines the ligament status and valgus knee types, and it seems to be a comprehensive tool to select the appropriate prosthesis. Constrained prosthesis must be used on patients who present coronal instability with attenuated medial collateral ligament. Rotating hinges must be reserved for those patients who have medial collateral ligament incompetence, recurvatum, combined instability and/or severe muscular deficiency.

Cerclaje con alambre en fracturas subtrocantéricas de cadera. Análisis de beneficios y complicaciones / Cerclage wiring in subtrochanteric hip fractures. Analysis of benefits and complications

Introducción: El objetivo de este estudio retrospectivo fue evaluar si la reducción abierta con cerclaje de alambre afectó la consolidación, la tasa de complicaciones y de reoperaciones en pacientes con fracturas subtrocantéricas de cadera, tratadas con clavos cefalomedulares. materiales y métodos:Se evaluó a todos los pacientes operados consecutivamente entre enero de 2010 y diciembre de 2017. Se comparó a los tratados con cerclaje (Grupo A) o sin cerclaje (Grupo B) de alambre en términos de tipo de fractura, estancia hospitalaria, tiempo quirúrgico, necesidad de transfusiones, calidad de la reducción, consolidación y complicaciones (infección, seudoartrosis, reoperaciones). Resultados:Se incluyó a 58 pacientes. El grupo A estaba conformado por 20 pacientes y el grupo B, por 38. El tipo de fractura más frecuente fue 3A (p = 0,0004). La estancia hospitalaria fue similar (9.0 vs. 10.6 días; p = 0,81), el tiempo quirúrgico y la necesidad de transfusiones fue mayor en el grupo A (p<0,0001 y p = 0,58, respectivamente). La tasa de consolidación fue similar en ambos grupos (90 vs. 92,1%, respectivamente; p = 0,09). Los desejes se observaron solo en el grupo tratado sin lazadas (5-13,5%; p = 0,01). Las tasas de complicaciones (15 vs. 18,4%) y de reopera-ciones (15 vs. 15,8%) fueron similares (p = 0,99). Conclusiones: El uso de lazadas de alambre en fracturas subtrocantéricas de cadera tratadas con clavos cefalomedulares generó un aumento significativo del tiempo quirúrgico, y disminuyó significativamente la incidencia de desejes. La incidencia de reoperaciones fue menor, aunque no significativamente. Nivel de Evidencia: III

Background: The aim of this retrospective study was to assess whether open reduction with cerclage wire affected the union and/or complication rate in subtrochanteric hip fractures treated with cephalomedullary nails. materials and methods: We analyzed all patients who had undergone surgery in our center between January 2010 and December 2017. We comparatively analyzed those treated with (Group A) and without (Group B) cerclage wire in terms of fracture type, hospital stay, surgical time, blood transfusions, malalignment, union, and complications (infection rates, non-union, and reoperations). Results: Fifty-eight patients were included. Group A consisted of 20 patients and Group B of 38. The most frequent type of fracture was 3A (p 0.0004). The mean hospital stay was similar (9 vs 10.6 days p 0.81), the surgical time and transfusions were higher in group A (p<0.0001 and p 0.58 respectively). The union rate was similar (90 vs 92.1%; p 0.09, respectively). Malalignment was only observed in group B (5 - 13.5%; p 0.01). The complication (15 vs 18.4%) and reoperation (15 vs 15.8%) rates were similar (p 0.99). Conclusions: The use of cerclage wire in subtrochanteric hip fractures treated with cephalomedullary nails generated a significant increase in surgical time and a lower rate of malalignment. It allowed a lower rate of re-operation, although it was not significant. Level of Evidence: III

Estudio retrospectivo comparativo entre aspirina y dabigatrán en la incidencia de efectos tromboembólicos en pacientes con artroplastia de cadera y rodilla / Comparative retrospective study between aspirin and dabigatran in the incidence of thromboembolic events in hip and knee arthroplasty

Objetivo: Analizar la incidencia de eventos tromboembólicos extrahospitalarios luego de un reemplazo total de rodilla o cadera primario en los primeros 90 días posoperatorios, utilizando como tromboprofilaxis ácido acetilsalicílico o dabigatrán. El objetivo secundario fue evaluar el costo de la terapia antiagregante y de la anticoagulante. Materiales y Métodos: Se realizó un estudio observacional retrospectivo en el posoperatorio de reemplazos totales de cadera y rodilla primarios sobre la incidencia de eventos tromboembólicos extrahospitalarios, durante los primeros 90 días posteriores a la cirugía, en dos grupos. Se administró ácido acetilsalicílico (325 mg/día) o dabigatrán (150-220 mg/día) por 35 días. Resultados: La serie incluyó a 224 pacientes (media de la edad 68.5 años), el 44,2% eran hombres. El 51,3% era un reemplazo total de cadera. El 64,3% continuó la tromboprofilaxis con dabigatrán y el 35,7%, con aspirina. La incidencia total de eventos tromboembólicos fue del 1,3%; 1,4% con dabigatrán y 1,3% con aspirina (p = 0,9). El costo de la tromboprofilaxis fue de USD 3,6 con aspirina 325 mg y USD 130 o 175 con dabigatrán, según la presentación de 75 y 110 mg. Conclusiones:La aspirina como tromboprofilaxis tras un reemplazo total de cadera o rodilla en pacientes con bajo riesgo de sufrir eventos tromboembólicos ha logrado resultados clínicos similares a los del dabigatrán. Se puede recomendar un protocolo multimodal basado en el uso de aspirina. Este mejora el cumplimiento de la terapia antitrombótica por parte de los pacientes, debido al bajo costo de la profilaxis con aspirina. Nivel de Evidencia: III

Objective: To analyze the incidence of out-of-hospital thromboembolic events after a primary total knee or hip replacement in the first 90 postoperative days, using acetylsalicylic acid or dabigatran as thromboprophylaxis. As a secondary objective, to evaluate the cost of antiplatelet therapy compared to anticoagulants. Materials and Methods: A retrospective observational study was carried out in the postoperative period of primary total hip and knee replacement on the incidence of out-of-hospital thromboembolic events during the first 90 postoperative days in two groups of patients. Acetylsalicylic acid (325 mg per day) or dabigatran (150 to 220 mg per day) were used as thromboprophylaxis for 35 days. Results: The series consisted of 224 patients aged 68.5 years (38-95 years), 44.2% male. 51.3% corresponded to total hip replacement. 64.3% continued thromboprophylaxis with dabigatran and 35.7% with aspirin. The total incidence of thromboembolic events was 1.3%. In the patients who received dabigatran it was 1.4% and in those who received aspirin, 1.3% (p = 0.9). The cost of thromboprophylaxis with aspirin 325 mg was US $ 3.6 while with dabigatran it was US $ 130 or $ 175, according to its presentation, 75 and 110 mg. Conclusion: Aspirin as thromboprophylaxis after total hip or knee replacement in individuals at low risk of thromboembolic events has shown similar clinical outcomes as dabigatran, and a multimodal protocol based on the use of aspirin can be recommended. This improves patient adherence to antithrombotic therapy, due to the low cost of aspirin prophylaxis. Level of Evidence: III

Comportamiento de los tallos no cementados recubiertos con hidroxiapatita colocados con alineación coronal inadecuada en la artroplastia primaria de cadera. Resultados del seguimiento a largo plazo / Behavior of hydroxyapatite-coated cementless stems placed with coronal malalignment in primary hip arthroplasty. Long-term follow-up results

Introducción: La mala alineación de los tallos femorales no cementados sigue siendo un tema controvertido. Algunos autores han comunicado una inadecuada osteointegración y hundimiento en los tallos en varo y otros no encontraron dichos efectos adversos, pese a la incorrecta alineación. Los objetivos de este estudio fueron determinar la prevalencia de tallos no cementados con cobertura total de hidroxiapatita en deseje coronal y mostrar los resultados clínico-radiográficos a largo plazo. materiales y métodos: Estudio retrospectivo entre 2006 y 2009. Se analizaron 220 reemplazos totales de cadera primarios con tallos no cementados con cobertura completa de hidroxiapatita. La alineación coronal fue analizada con radiografías anteroposteriores de ambas caderas en 10° de rotación interna. Se registraron datos, como osteointegración, hundimiento, osteólisis femoral proximal e hipertrofia cortical. Para el análisis clínico se utilizó el Harris Hip Score. El análisis de supervivencia contempló la necesidad de revisión por cualquier causa. Resultados: La prevalencia de tallos en deseje fue del 32,3%, con mayoría de implantes en varo (73,3%). El Harris Hip Score tuvo un incremento estadísticamente significativo (41,05 ± 6,5 vs. 90,05 ± 2,5; p <0,01). El 73,1% de los tallos desarrollaron una fijación ósea estable. Se observó osteólisis femoral proximal en el 3% de los casos. Hubo un 3% de fracturas periprotésicas femorales. La supervivencia de la prótesis fue del 100% a los 10.9 años. Conclusión: Los tallos no cementados con cobertura total de hidroxiapatita toleran adecuadamente la alineación coronal en varo/valgo a largo plazo. Nivel de Evidencia: IV

Introduction: Coronal malalignment of non-cemented stems remains controversial. It's been reported that femoral stems implanted with varus or valgus developed subsidence and lack of integration with femoral bone. The purpose of this study was to calculate prevalence of coronal malalignment in cementless, fully coated with hydroxialapatyte (HA) femoral stems focusing in their long-term clinical and radiographic outcomes. Materials and methods: A retrospective study was performed, assessing 220 primaries total hip replacements with non-cemented, fully coated with HA, femoral stems between 2006 and 2009. Coronal alignment was assessed with hips antero-posterior views with 10º of internal rotation of lower limbs. We registered data about subsidence, proximal femoral osteolysis and cortical hipertrophy. Functional outcomes were assessed with Harris Hip Score (HHS). Free revision rate implant survival was calculated. Results: Prevalence of femoral stems with malalignment was 32.3%. HHS showed an statistically significant increase after surgery (41.05 ± 6.5 versus 90.05 ± 2.5; p <0.01). There were 73.1% of femoral stems that achieved a bone stable fixation. We observed proximal femoral osteolysis in 3.0% of the patients and there were 3% of periprosthetic fractures. Free-revision survival rate was 100% at 10.9 years of follow-up. Conclusion: Cementless, fully coated with HA femoral stems with varus/valgus malalignment achieves good long-term clinical and radiographic outcomes. Level of Evidence: IV

Colgajo neurocutáneo safeno y recambio de espaciador de cemento en el manejo de una artroplastia de rodilla infectada con defecto de cobertura cutánea. Reporte de un caso / Saphenous neurocutaneous flap and cement spacer replacement in the management of arthroplasty of an infected knee with a soft tissue coverage defect. Case report

Los defectos de cobertura asociados a una infección de la prótesis son un desafío al cual nos enfrentamos los cirujanos ortopédicos en el posoperatorio de un reemplazo articular. El objetivo de este artículo es comunicar un caso de defecto de cobertura tratado con un colgajo neurocutáneo safeno por una artroplastia de rodilla infectada. Se recambió el espaciador y se cubrió el defecto tegumentario con colgajo neurocutáneo safeno en un mismo tiempo. Conclusiones:El colgajo neurocutáneo safeno proporciona una adecuada cobertura en la cara anterior de la rodilla y permite tratar defectos tegumentarios asociados a una infección de la prótesis. Nivel de Evidencia: IV

Soft tissue defects in the setting of periprosthetic joint infection represent serious problems for orthopaedic surgeons following total joint replacement. This report aims is to show our experience using the proximal-based saphenous neurocutaneous flap for the reconstruction of a wound defect in the treatment of a periprosthetic knee infection. A new cement spacer was placed and a neurocutaneous saphenous flap was performed in the same stage. Conclusions: Soft tissue defects around the knee can be effectively solved with the neurocutaneous saphenous flap, which provides an adequate coverage to this joint within the context of infected arthroplasty. Level of Evidence: IV

Vástagos estriados cónicos modulares en revisión de artroplastia total de cadera. Estudio multicéntrico. Resultados y complicaciones a mediano plazo / Modular fluted tapered stems in revision total hip arthroplasty. Multicenter study. Medium-term results and complication rate

Introducción: Debido al crecimiento exponencial del número de artroplastias de cadera, se espera una mayor cantidad de re-visiones en las próximas décadas. Los vástagos cónicos estriados modulares se han vuelto populares en la última década por sus resultados favorables. El objetivo de este estudio es evaluar los resultados, las complicaciones y la tasa de supervivencia de estos vástagos en las revisiones de cadera, con un seguimiento a mediano plazo. materiales y métodos: Estudio multicéntrico, retrospectivo. Se incluyeron 182 pacientes a quienes se les realizó una cirugía de revisión de cadera entre 2007 y 2017. Se colo-caron 185 vástagos cónicos estriados de fijación distal. El déficit de stock óseo femoral se clasificó según Paprosky y Burnett; y las facturas periprotésicas, según la clasificación de Vancouver. Se evaluó a los pacientes clínicamente con el Harris Hip Score (HHS) y con radiografías a los 3 meses y anualmente para evaluar la estabilidad del vástago, la subsidencia y el aflojamiento, así como la consolidación de la osteotomía. Resultados: Seguimiento medio 55.18 meses. El HHS posoperatorio tuvo una media de 80,28 (DE = 12,8, IC95% 78,5-82,97). No hubo complicaciones posoperatorias en el 75,4% de los pacientes. Las complicaciones más frecuentes fueron inestabilidad (7,6%) y subsidencia del implante (11,5%). Al final del seguimiento, el 95,05% de los pacientes tenía un implante estable. Conclusiones: Los vástagos cónicos estriados modulares de fijación distal proporcionan una solución confiable, reproducible y duradera para el manejo de revisiones de componentes femorales a medio plazo. Nivel de Evidencia: IV

Background: The number of arthroplasties performed every year is increasing; therefore, a greater number of revisions is expected in the coming decades. Modular fluted tapered stems have become the gold standard for their results in different series of patients. The objective of this article is to evaluate the results, complications and the survival rate of these stems in hip revisions with a medium-term follow-up. Materials and Methods: Retrospective, multicenter analysis. One hundred eighty-two patients who had undergone hip revision surgery between 2007 and 2017 were included. One hundred eighty-five modular fluted tapered stems were placed. Femoral bone stock defects were classified according to Paprosky and Burnett; and periprosthetic femur fractures according to Vancouver classification. Patients were evaluated clinically with Harris Hip Score (HHS) and radiographically 3 months after surgery and every year to assess stem stability, subsidence and loosening, as well as osteotomy healing. Results: Average follow-up was 55.18 months. Postoperative HHS had an average of 80.28 (SD = 12.8, 95% CI = [78.5, 82.97]). There were no postoperative complications in 75.4% of the patients. The most frequent complications were instability in 7.6% and implant subsidence in 11.5%. At the end of the follow-up, 95.05% of the patients had a stable implant. Conclusion: Modular fluted tapered stems provide a reliable, reproducible solution for the management of femoral component revisions at medium-term. Level of Evidence: IV

Paciente con síndrome de Klippel-Trenaunay. Reporte de un caso de reemplazo articular de cadera suspendido durante la cirugía / Patient with Klippel-Trenaunay syndrome. Case report of an intraoperatively aborted hip joint replacement

El síndrome de Klippel-Trenaunay es un trastorno congénito infrecuente. Por lo general, afecta uno de los miembros inferiores. Los hallazgos típicos son angiomas, malformaciones venosas, várices hipertróficas con comunicaciones arteriovenosas e hipertrofia del miembro afectado que, en algunos casos, altera la estructura ósea. El objetivo de esta presentación es describir el caso de un paciente de 54 años en el que se programó un reemplazo articular de la cadera izquierda durante un año y la cirugía debió suspenderse por el riesgo de exanguinación, y analizar la bibliografía al respecto. Nivel de Evidencia: IV

Klippel-Trenaunay Syndrome is a rare congenital disorder. It usually affects one of the lower limbs. It is characterized by the presence of angiomas, venous malformations, hypertrophic varices with arteriovenous communications and hypertrophy of the affected limb, altering in some cases the bone structure. The aim of this presentation is to describe the case of a 54-year-old patient for whom a joint replacement of the left hip had been scheduled for one year and the surgery had to be aborted due to the risk of exsanguination of the patient, and to analyze the literature in this regard. Level of Evidence: IV

Estudio prospectivo comparativo del manejo de la analgesia preventiva en pacientes sometidos a artroplastia total de rodilla primaria / Comparative prospective study of the management of preventive analgesia in patients undergoing primary total knee arthroplasty

Introducción: La analgesia preventiva es aquella que se administra horas o días antes de una artroplastia total de rodilla con el fin de reducir el dolor posoperatorio. El objetivo de este estudio fue comparar y analizar la eficacia clínica de la analgesia preventiva en los pacientes sometidos a un reemplazo total de rodilla. materiales y métodos: Noventa y seis pacientes, divididos en dos grupos de 48 pacientes, fueron evaluados prospectivamente y comparados entre noviembre de 2018 y marzo de 2019. El grupo A recibió analgesia preoperatoria con una combinación de etoricoxib, tramadol y paracetamol, por vía oral, 2 horas antes de la cirugía. El grupo B de control no recibió analgesia. El dolor posoperatorio de los pacientes se evaluó de acuerdo con sus propios registros en una escala analógica visual a las 12, 24, 48, 72 h y una semana después de la cirugía. Resultados: Se observó una diferencia significativa a las 24 h entre ambos grupos, el dolor fue significativamente menor en el grupo A (p = 0,001), a las 48 h la diferencia fue estadísticamente menor que a las 24 h (p = 0,016). También se observó que el grupo de control requirió más cantidad de rescates, aunque la diferencia solo fue significativa a las 24 h (p = 0,047). Conclusión: La combinación de etoricoxib, tramadol y paracetamol es eficaz, segura, económica y fácil de administrar, y la tasa de efectos adversos de la analgesia es baja; por lo tanto, representa un esquema adecuado para el manejo de la analgesia preventiva. Nivel de Evidencia: IIb

Background and Objective: Preventive analgesia is one that is administered hours or days before a total knee arthroplasty in or-der to reduce postoperative pain. The objective of this study was to compare and analyze the clinical efficacy of the use of preven-tive analgesia in patients undergoing total knee replacement. materials and methods: Ninety-six patients, divided into two groups of 48 patients, were evaluated prospectively and comparatively between November 2018 and March 2019. Group A received preoperative analgesia with a combination of etoricoxib, tramadol, and paracetamol, orally, 2 hours before surgery. Control group B, did not receive anything. The postoperative pain of the patients was evaluated according to their own records on a visual analog scale at 12, 24, 48, 72 hours and one week after surgery. Results: A significant difference was observed at 24 hours between both groups, pain was significantly less for group A (p = 0.001), at 48 hours the difference was statistically lower than at 24 hours (p = 0.016). It was also observed that the control group required a greater number of rescues, although the difference was only significant at 24 hours (p = 0.047). Conclusion: The combination of etoricoxib, tramadol and paracetamol represents an effective, safe, economical, easy to administer form with a low rate of analgesia adverse effects; which represents an adequate scheme for the management of preventive analgesia.Key words: Knee arthrosplasty; pain; preemptive analgesia. Level of evidence: IIb

Fractura del poste tibial en la artroplastia total de rodilla estabilizada a posterior. Presentación de dos casos / Fracture of a polyethylene tibial post in posterior stabilized total knee replacement. Two case reports

La fractura del poste tibial luego de un reemplazo total de rodilla es una complicación poco frecuente e incapacitante. Presentamos a dos pacientes con fractura del poste tibial no traumática, que acudieron con dolor más inestabilidad en recurvatum, de forma repentina, después de reemplazos articulares con buen funcionamiento previo. El primer paciente se presentó a los 12 años del reemplazo total de rodilla primario y el segundo, a los 14 meses. Ambos tenían el mismo modelo de prótesis estabilizada a pos-terior. Los dos pacientes fueron sometidos a una revisión con prótesis abisagrada rotatoria (Endo-Model NR®, Waldemar Link, EEUU), sin recidiva de la deformidad. Nivel de Evidencia: IV

Tibial post fracture after posterior stabilized total knee replacement (TKR) is a uncommon and disabling complication. We report two cases of non-traumatic tibial post fracture, which presented with sudden pain and recurvatum instability in joint replacements with good previous function. For the first case, the presentation time was 12 years from the primary TKR, and for the second it was 14 months. Both presented the same model of a posterior stabilized prosthesis. In both cases, a revision TKR was performed witha rotating hinge prosthesis (Endo-Model NR®, Waldemar Link), without recurrence of the deformity. Level of Evidence: IV

Artroplastia total de rodilla posterior a osteotomía tibial alta. Estudio retrospectivo comparativo entre osteotomías sustractivas y aditivas / Total knee replacement after high tibial osteotomy. Retrospective comparative study between subtractive and additive osteotomies

Introducción: El reemplazo total de rodilla luego de una osteotomía tibial alta plantea dificultades técnicas adicionales. El objetivo de este estudio fue analizar los resultados clínicos y radiográficos de la conversión a reemplazo total de rodilla luego de una osteotomía tibial alta y comparar la evolución de los pacientes con una osteotomía de cierre (sustractiva) o de apertura (aditiva) previa. Materiales y Métodos: Se analizó retrospectivamente una serie de 46 artroplastias de rodilla realizadas entre 1997 y 2019, en 39 pacientes con antecedente de osteotomía tibial alta. Se evaluaron los parámetros clínicos y radiográficos antes de la artroplastia y después, determinando el eje femorotibial, la caída tibial posterior, el valor de Insall-Salvati y el Knee Society Score. También se compararon los resultados en pacientes con antecedente de osteotomía tibial sustractiva vs. aditiva. Resultados:El seguimiento promedio fue de 5.72 años (mín. 1, máx. 19). El Knee Society Score de la serie tuvo una mejoría promedio de 42,3 a 79,8. La caída tibial posterior y el índice de Insall-Salvati no sufrieron grandes modificaciones luego de la cirugía. La supervivencia promedio de la osteotomía aditiva hasta la conversión a reemplazo total de rodilla fue de 5.5 años, mientras que la de la sustractiva, de 13.5 años.Conclusiones:Pese a la dificultad técnica que puede plantear, el reemplazo total de rodilla luego de una osteotomía tibial alta valguizante tuvo una buena evolución clínico-radiográfica a corto y mediano plazo, y el tipo de osteotomía no repercutió en los resultados luego de la artroplastia. Nivel de Evidencia: IV

Introduction: Total knee replacement after a high tibial osteotomy presents additional technical difficulties. The objective of this study was to analyze the clinical and radiological outcomes of conversion to total knee replacement after a high tibial osteotomy and to compare the evolution of patients with a history of a closing (subtractive) versus opening (additive) osteotomy. Materials and Methods: A series of 46 knee arthroplasties performed between 1997 and 2019 in 39 patients with a history of a high tibial osteotomy was retrospectively analyzed. The clinical and radiographic parameters were evaluated before and after the arthroplasty by measuring the femorotibial axis, the posterior tibial slope, the Insall Salvati value, and the Knee Society Score. At the same time, the results were compared in patients with a history of subtractive versus additive tibial osteotomy. Results:In the series of 46 patients, an average follow-up of 5.72 years was achieved (minimum 1, maximum 19). The Knee Society Score for the entire series had an average improvement from 42.3 to 79.8 points. The posterior tibial slope and the IS value did not show great modifications after surgery. In this series, the average survival of additive osteotomy until conversion to total knee replacement was 5.5 years, while for the subtractive one it was 13.5 years. Conclusions:Despite the technical difficulty that it may present, total knee replacement after a valgus high tibial osteotomy presented a good clinical-radiological evolution in the short and medium term and the type of osteotomy did not affect the results obtained after arthroplasty. Level of Evidence: IV

Prótesis bipolares en pacientes añosos con fractura lateral inestable de cadera. Resultados funcionales y tasa de reoperación luego de los primeros 100 casos / Bipolar prosthesis in elderly patients with unstable intertrochanteric hip fractures. Functional outcomes and reoperation rate after the first 100 cases

Introducción: Se realizó un estudio retrospectivo para evaluar los resultados funcionales, las complicaciones y las reoperaciones del tratamiento con prótesis bipolar en adultos mayores con fracturas intertrocantéricas inestables de cadera. Materiales y Métodos: Se evaluó a pacientes >70 años con fracturas laterales inestables de cadera operados entre 2002 y 2013. Las fracturas se clasificaron según la OTA/AO. Se analizaron los días de internación, el índice de Charlson, el día que comenzaron la marcha, la necesidad de asistencia para deambular, toda complicación relacionada con el procedimiento y la tasa de reoperaciones. Resultados: Se incluyeron 100 pacientes (84 mujeres y 16 hombres) con 101 fracturas. La edad promedio era de 82.4 años (rango 72-102). Cincuenta y nueve fracturas eran del subtipo A2.2 y 42, del A2.3. El índice de Charlson promedio fue de 6,23 (rango 4-9) y el tiempo promedio de internación, de 6.95 días (rango 5-18). El 87% comenzó la marcha al segundo día poscirugía. El HHS promedio fue de 84,7 (rango 69-92) y el seguimiento promedio, de 28.4 meses (rango 12-40). Hubo 7 (6,93%) complicaciones: 2 (1,98%) trombosis venosas profundas, 1 (0,99%) tromboembolismo pulmonar, 3 infecciones (2,97%) y 1 (0,99%) luxación. La tasa de reoperaciones fue del 2,97%. Las complicaciones se relacionaron significativamente con la edad (p = 0,005) y el índice de Charlson (odds ratio 2,8071; IC95% 1,4105-5,58669). Conclusiones: El tratamiento con prótesis bipolar permitió una rápida rehabilitación con puntajes funcionales buenos o excelentes en el 93% de la serie, asociados a una baja tasa de complicaciones y de reoperaciones

Introduction: The purpose of this retrospective study was to evaluate the functional outcomes, complications, and reoperations for the treatment of unstable intertrochanteric hip fractures by bipolar hip arthroplasty in elderly patients. Materials and Methods: We analyzed >70-year-old patients with unstable intertrochanteric hip fractures undergoing surgery between 2002 and 2013. Fractures were classified according to the OTA/AO classification. The analysis included length of hospital stay (LOS), Charlson comorbidity index (CCI), time to weight-bearing, need for weight-bearing assistance, all complications related to the procedure, and the reoperations rate. Results: Study population consisted of 100 patients (84 females, 16 males), with 101 fractures. Average age was 82.4 years (range, 72-102 years). Fractures were categorized as A2.2 in 59 cases and A2.3 in 42 cases. The average CCI was 6.23 (range, 4-9). The average LOS was 6.95 days (range, 5-18). Weight-bearing ambulation started on postoperative day 2 in 87.12% of cases. The average Harris hip score (HHS) was 84.7 (range, 69-92). The average follow-up period was 28.4 months (range, 12-40). There were 7 (6.93%) complications: 2 (1.98%) deep venous thrombosis, 1 (0.99%) pulmonary thromboembolism, 3 (2.97%) periprosthetic infections and 1 (0.99%) dislocation. The reoperation rate was 2.97%. Complications were significantly related to age (P=0.005) and to ICC (odds ratio [OR]: 2.8071; 95% confidence interval [CI]: 1.4105-5.58669). Conclusions: Bipolar prostheses allowed for early rehabilitation with acceptable functional outcomes, associated with a low complication rate (6.93%) and a low reoperation rate (2.97%)

The W.A.I.O.T. Definition of Peri-Prosthetic Joint Infection: A Multi-center, Retrospective Validation Study.

Peri-prosthetic joint infection (PJI) definition plays an important role in diagnostic and therapeutic decisions. However, while several criteria have been proposed by eminent institutions to define a PJI in the last decade, their clinical validation has been rarely performed. Aim of the present multicenter, international, retrospective study was to validate the World Association against Infection in Orthopedics and Trauma (WAIOT) pre/intra-operative PJI definition with post-operative confirmatory tests. A total of 210 patients, undergoing hip (n = 86) or knee (n = 124) revision surgery for any reason in six orthopedic centers in Africa, Asia, Europe and South America, were retrospectively evaluated at a two years minimum follow-up after surgery. All the available pre-, intra- and post-operative findings were collected and analyzed according to the WAIOT criteria, which include a set of tests to confirm (Rule In) or to exclude (Rule Out) a PJI. On average, patients were investigated pre/intra-operatively with 3.1 ± 1.1 rule out and 2.7 ± 0.9 rule in tests; the presence of a fistula or exposed implant was reported in 37 patients (17.6%). According to pre/intraoperative findings, 36.2% of the patients were defined as affected by high-grade PJI (n = 76; average score: 2.3 ± 0.8), 21.9% by low-grade PJI (n = 46; average score: 0.8 ± 0.8), 10.5% by biofilm-related implant malfunction (n = 22; average score: -1.6 ± 0.8), 2.9% as contamination (n = 6; average score: -3.5 ± 1.0), and 28.6% as no infection (n = 60; average score: -3.0 ± 1.4). Pre/intra-operative PJI definitions matched post-operative confirmatory tests, in 97.1% of the patients. This is, to our knowledge, one of the largest study ever conducted to validate a PJI definition The retrospective analysis in different centers was greatly facilitated by the structure of the WAIOT definition, that allows to include different tests on the basis of their sensitivity/specificity, while the comparison between pre/intra-operative and post-operative findings offered the internal validation of the scoring system. Our results authenticate the WAIOT definition as a reliable, simple tool to identify patients affected by PJI prior to joint revision surgery.

Artroplastia total de rodilla en pacientes con secuela de fracturas articulares: Resultados del seguimiento a mediano plazo / Total knee arthroplasty in patients with joint fracture sequela: Mid-term follow-up outcomes

Introducción: Las fracturas articulares de rodilla son frecuentes y pueden evolucionar a gonartrosis postraumática. El tratamiento en su estadio final es el reemplazo total de rodilla (RTR). Cuando se indica, el especialista se enfrenta a situaciones que predisponen a resultados menos satisfactorios. El objetivo de este estudio fue evaluar los resultados del RTR en pacientes con secuela de fracturas articulares de rodilla, con un seguimiento mínimo de 4 años. Materiales y Métodos: Estudio retrospectivo observacional, entre mayo de 1999 y enero de 2013. Se evaluaron 25 RTR en 24 pacientes (edad promedio 67.1 años) con secuela de fractura articular de rodilla y un seguimiento promedio de 6.1 años. Tres (12%) tenían cirugías anteriores al RTR. Ocho se resolvieron en dos tiempos. Se empleó un implante constreñido en 4 pacientes (16%). Se determinaron el KSS, el KSSf y el rango de movilidad preoperatorios y del último control. Se documentó la supervivencia del implante. Resultados: El KSS se incrementó de 38,5 en el preoperatorio a 82,8 en promedio. El KSSf posoperatorio mejoró de 48 a 85. El rango de movilidad aumentó de un promedio de 7,5-76° a 1-102,4° en el posoperatorio. Cuatro casos fueron reoperados. La supervivencia de la prótesis fue del 92% a los 6.1 años. Conclusiones: El RTR es adecuado para la gonartrosis postraumática en su estadio final, con buenos resultados a mediano plazo. Si se logran una adecuada alineación posoperatoria y un correcto posicionamiento de los componentes, los resultados son satisfactorios y se asemejan a los del RTR por gonartrosis idiopática. Nivel de Evidencia: IV

Introduction: Knee joint fractures are common in Orthopedics, and may evolve to post-traumatic Osteoarthritis (PTOA). Total Knee Arthroplasty (TKA) is an effective treatment for the end-stage of this process. When indicated, orthopedic surgeons face many situations that may cause unsatisfactory results and affect prosthesis survival. The purpose of our study was to evaluate TKA outcomes on Osteoarthritis secondary to distal femoral and proximal tibial joint fractures, in cases with a minimum follow-up period of 4 years. Materials and Methods: We carried out an observational, retrospective study on TKA patients treated between May 1999 and January 2013. We evaluated 25 TKAs, performed on 24 patients, with knee fracture sequela, with an average follow-up of 6.1 years and an average age of 67.1 years. Three cases (12%) had required additional surgeries before TKA. Eight cases (32%) were 2-stage surgeries. Constrained implants were used in four cases (16%). The Knee Society Score (KSS), the Functional KSS (KSSf) and the Range of Motion (ROM) were evaluated preoperatively and at the last follow-up. Prosthesis survival evaluation was documented. Results: KSS increased from a preoperative average of 38.5 to a postoperative average of 82.8. Postoperative KSSf increased on average from 48 to 85. ROM increased on average from 7.5°-76° to 1°-102.4°. Four patients required a second surgical procedure. Prosthesis survival was 92% at a 6.1-year average follow-up. Conclusion: TKA is an appropriate treatment for advanced PTOA, with good mid-term outcomes. If adequate postoperative alignment and correct component positioning is achieved, expected outcomes are satisfactory and similar to those with TKA in primary osteoarthritis. Level of Evidence: IV

Loud and silent epidemics in the third millennium: tuning-up the volume.

The media play a key role in promoting public health and influencing debate regarding health issues; however, some topics seem to generate a stronger response in the public, and this may be related to how the media construct and deliver their messages. Mass media coverage of COVID-19 epidemic has been exceptional with more than 180,000 articles published each day in 70 languages from March 8 to April 8, 2020. One may well wonder if this massive media attention ever happened in the past and if it has been finally proven to be beneficial or even just appropriate. Surgical site and implant-related infections represent a substantial part of health care-associated infections; with an estimated overall incidence of 6% post-surgical infection, approximately 18 million new surgical site infections are expected each year globally, with 5 to 10% mortality rate and an astounding economic and social cost. In the current mediatic era, orthopaedic surgeons need to refocus some of their time and energies from surgery to communication and constructive research. Only raising mediatic awareness on surgical site and implant-related infections may tune up the volume of silent epidemics to a level that can become audible by governing institutions.

Errores de osteosíntesis en fracturas laterales de cadera tratadas con placa/tornillo deslizante / Failed internal fixation of intertrochanteric hip fractures with dynamic hip screws

Introducción: El uso de los sistemas placa/tornillo deslizante para fracturas intertrocantéricas ha demostrado ser un método de fijación eficaz, pero no está exento de fallas. El propósito de este estudio fue evaluar las causas de falla en los pacientes con fracturas laterales de cadera, tratados con placa/tornillo deslizante, puntualizando los defectos técnicos en la colocación. Materiales y Métodos: En nuestro centro, se trató a 177 pacientes por fractura lateral de cadera, a 151 de ellos se les practicó osteosíntesis con placa/tornillo deslizante. Se analizaron la adecuada reducción posoperatoria, la medición de la distancia punta a vértice, la posición del tornillo cefálico en la cabeza femoral y las posibles complicaciones. Resultados: La serie quedó conformada por 143 pacientes. El seguimiento promedio fue de 18 meses (rango 12-48). La tasa de fallas fue del 8,4% (n = 12): 7 (4,8%) por migración cefálica (cut-out) del tornillo proximal, 2 (1,4%) por migración medial (cut-through), 2 (1,4%) presentaron seudoartrosis y un caso (0,70%) de reducción inadecuada en varo. El porcentaje de una segunda operación fue del 7,7% (n = 11). La peor posición fue la superior/posterior con un 100% de migración (n = 4) (p <0,001, diferencia estadísticamente significativa). Conclusión: El posicionamiento superior/posterior del tornillo cefálico podría incrementar la posibilidad de migración y, en consecuencia, la tasa de falla del sistema. Nivel de Evidencia: IV

Objectives: The use of dynamic hip screws (DHS) for intertrochanteric fractures has proven to be an effective, but infalible, fixation method. The purpose of this study was to evaluate the reason behind fixation failure in patients with this type of hip fracture treated with a DHS. Materials and Methods: 177 patients were treated in our center for intertrochanteric hip fractures. A DHS was placed in 151 of them. Our analysis included quality of reduction after surgery, tip-apex distance, femoral head lag screw position, and possible complications. Results: The series included 143 patients. The average follow-up was 18 months (range 12-48). The failure rate was 8.4% (n = 12): 7 (4.8%) cases were due to intrapelvic migration of the lag screw ("cut-out") and 2 (1.4%) were due to medial perforation ("cut-through"), while 2 (1.4%) cases presented with pseudarthrosis and 1 (0.70%) with varus deformity after reduction. The revision rate was 7.7% (n = 11). Lag screws placed in a superior/posterior position had the highest failure rate (100% migration rate) (n = 4) (p <0.001, statistically significant difference). Conclusions: Superior/posterior positioning of the lag screw may increase the possibility of migration and, consequently, the failure rate of the DHS system. Level of Evidence: IV

Indicación y resultados de la prótesis con estabilidad aumentada en la artroplastia primaria de rodilla / Constrained prosthesis in primary total knee arthroplasty

Introducción: El objetivo de este estudio retrospectivo fue mostrar los criterios de indicación para implantes con una estabilidad superior a la estabilización posterior en la artroplastia total de rodilla primaria, puntualizando su estabilidad y resultados funcionales. Materiales y Métodos: Se analizaron 43 artroplastias totales de rodilla en 40 pacientes, con seguimiento promedio de 6.2 años; 38 casos con deseje valgo y 5 en varo. La suficiencia de los ligamentos colaterales se definió como suficiente, atenuada o incompetente, mediante maniobras y radiografías con estrés varo-valgo. Los resultados funcionales se evaluaron mediante el KSS. Resultados: Se utilizaron 28 prótesis con estabilización posterior plus en pacientes con deseje coronal promedio de 15,9° (21 presentaron ligamentos suficientes y 5 atenuados). Prótesis constreñidas en 7 pacientes con deseje valgo promedio de 21,6° (2 con ligamentos suficientes y 5 atenuados). Se utilizaron 8 prótesis abisagradas rotatorias, 5 en pacientes con genu valgo promedio de 24,6° (3 asociados a recurvatum), 4 con ligamentos incompetentes y 1 con ligamentos atenuados, y 3 genu varo de 16° promedio. El KSS promedio posoperatorio fue de 84 (rango 73-94). No se detectaron inestabilidades. La supervivencia protésica fue del 100% al final del seguimiento. Conclusiones: Se recomienda utilizar las prótesis estabilizadas plus en desejes < 20°, con ligamentos colaterales suficientes en ausencia de defectos óseos y las prótesis constreñidas en pacientes con grandes desejes con ligamentos colaterales y algún grado de suficiencia (a lo sumo atenuados). Las prótesis abisagradas rotatorias se reservan para rodillas con incompetencia ligamentaria colateral o multidireccional, grandes defectos óseos o deformidades severas en artritis reumatoide o de origen neuropático. Nivel de Evidencia: IV

Introduction: The objective of this retrospective study was to show the functional results and indication criteria for prostheses for primary TKA with more constraint than posterior stabilization. Methods: Forty-three TKA were analyzed in 40 patients, with an average follow-up of 6.2 years. Preoperative diagnoses were valgus osteoarthritis (38 cases) and varus osteoarthritis (5 cases). Sufficiency of the collateral ligaments was classified as sufficient, attenuated or incompetent, through physical examination and X-rays with varus-valgus stress. Functional results were evaluated using the KSS. Results: Posterior-stabilized plus implants were used in 28 cases, with an average alignment of 15.9°: 26 were valgus knees, 21 of which presented sufficient and 5 attenuated ligaments. Constrained prostheses were used in 7 patients with an average valgus alignment of 21.6° (2 with sufficient and 5 with attenuated ligaments). Rotating-hinge prostheses were used in 8 patients, 5 with an average valgus alignment of 24.6° (3 of them associated with recurvatum), 4 with incompetent ligaments and one with attenuated ligaments. The average post-operative KSS was 84 (range 73-94) points. No instabilities were detected and prosthetic survival was 100% at the end of the follow-up. Conclusions: We recommend using posterior-stabilized plus implants in deformities <20°, with sufficient collateral ligaments and no bone defects; constrained prosthesis in patients with greater deformity (>20°) and collateral ligaments with some degree of sufficiency (attenuated at the most); and rotating-hinge implants in knees with collateral or multidirectional ligament insufficiency, associated with recurvatum, significant bone defects or severe deformities in rheumatoid arthritis or with neuropathic origin. Level of Evidence: IV