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1.
Clin Orthop Relat Res ; 469(1): 209-17, 2011 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-20625950

RESUMEN

BACKGROUND: Total hip arthroplasty (THA) has been associated with high survival rates, but debate remains concerning the best fixation mode of THA. QUESTIONS/PURPOSES: We conducted a randomized controlled trial (RCT) with 250 patients with a mean age of 64 years between October 1987 and January 1992 to compare the results of cementless and cemented fixation. PATIENTS AND METHODS: Patients were evaluated for revision of either of the components. One hundred twenty-seven patients had died (51%) and 12 (4.8%) were lost to followup. The minimum 17-year followup data (mean, 20 years; range, 17-21 years) for 52 patients of the cementless group and 41 patients of the cemented group were available for evaluation. RESULTS: Kaplan-Meier survivorship analysis at 20 years revealed lower survival rates of cemented compared with cementless THA. The cementless tapered stem was associated with a survivorship of 99%. Age younger than 65 years and male gender were predictors of revision surgery. CONCLUSIONS: The efficacy of future RCTs can be enhanced by randomizing patients in specific patient cohorts stratified to age and gender in multicenter RCTs. Including only younger patients might improve the efficacy of a future RCT with smaller sample sizes being required. A minimum 10-year followup should be anticipated, but this can be expected to be longer if the difference in level of quality between the compared implants is smaller. LEVEL OF EVIDENCE: Level I, therapeutic study. See Guidelines for Authors for a complete description of levels of evidence.


Asunto(s)
Artroplastia de Reemplazo de Cadera/instrumentación , Artroplastia de Reemplazo de Cadera/métodos , Cementos para Huesos/uso terapéutico , Articulación de la Cadera/cirugía , Prótesis de Cadera , Osteoartritis de la Cadera/cirugía , Adulto , Factores de Edad , Anciano , Artroplastia de Reemplazo de Cadera/efectos adversos , Femenino , Estudios de Seguimiento , Articulación de la Cadera/diagnóstico por imagen , Articulación de la Cadera/fisiopatología , Humanos , Estimación de Kaplan-Meier , Masculino , Persona de Mediana Edad , Ontario , Osteoartritis de la Cadera/diagnóstico por imagen , Osteoartritis de la Cadera/fisiopatología , Modelos de Riesgos Proporcionales , Diseño de Prótesis , Falla de Prótesis , Radiografía , Reoperación , Medición de Riesgo , Factores de Riesgo , Factores Sexuales , Factores de Tiempo , Resultado del Tratamiento
2.
Clin Orthop Relat Res ; 468(2): 424-32, 2010 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-19777316

RESUMEN

UNLABELLED: There are two broad-based categories of cementless femoral component designs: proximally porous-coated and fully porous-coated. While both have been widely used, there remains debate regarding differences in clinical outcome scores, relative incidence of thigh pain, and development of stress shielding. We investigated these variables in a multicenter prospective randomized blinded clinical trial of 388 patients from three centers: 198 patients had a proximally porous-coated tapered cementless femoral component and 190 patients had a fully porous-coated cementless femoral component. A minimum followup of 2 years (mean, 6.7 years; range, 2.0-8.65 years) was available in 367 of the 388 patients (95%). We observed no differences in age at surgery, body mass index, or preoperative clinical outcome scores (WOMAC, SF-12, Harris hip score, UCLA activity, thigh pain) with the two groups. We determined serial bone density changes in a subcohort of 72 patients from two of the three centers. The postoperative clinical outcome scores were similar at all followup intervals, and we observed no differences in the incidence of thigh pain at any time. Bone density reduction in Gruen Zone 7 was greater with the fully coated stem than the proximally coated stem (24% versus 15% reduction, respectively). Both fully and proximally coated stems performed well, with no clinical differences at 2 years' followup, except in bone mineral density evaluations. LEVEL OF EVIDENCE: Level I, therapeutic study. See Guidelines for Authors for a complete description of levels of evidence.


Asunto(s)
Artroplastia de Reemplazo de Cadera/instrumentación , Materiales Biocompatibles Revestidos , Fémur/cirugía , Articulación de la Cadera/cirugía , Prótesis de Cadera , Absorciometría de Fotón , Artroplastia de Reemplazo de Cadera/efectos adversos , Densidad Ósea , Canadá , Método Doble Ciego , Femenino , Fémur/diagnóstico por imagen , Articulación de la Cadera/diagnóstico por imagen , Articulación de la Cadera/fisiopatología , Humanos , Louisiana , Masculino , Persona de Mediana Edad , Dolor/etiología , Dolor/prevención & control , Dimensión del Dolor , Porosidad , Estudios Prospectivos , Diseño de Prótesis , Falla de Prótesis , Recuperación de la Función , Estrés Mecánico , Propiedades de Superficie , Factores de Tiempo , Resultado del Tratamiento
3.
Clin Orthop Relat Res ; 467(11): 2895-900, 2009 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-19412648

RESUMEN

UNLABELLED: Restoration of femoral offset and acetabular inclination may have an effect on polyethylene (PE) wear in THA. We therefore assessed the effect of femoral offset and acetabular inclination (angle) on acetabular conventional (not highly cross-linked) PE wear in uncemented THA. We prospectively followed 43 uncemented THAs for a minimum of 49 months (mean, 64 months; range, 49-88 months). Radiographs were assessed for femoral offset, acetabular inclination, and conventional PE wear. The mean (+/- standard deviation) linear wear rate in all THAs was 0.14 mm/year (+/- 0.01 mm/year) and the mean volumetric wear rate was 53.1 mm(3)/year (+/- 5.5 mm(3)/year). In THAs with an acetabular angle less than 45 degrees , the mean wear was 0.12 mm/year (+/- 0.01 mm/year) compared with 0.18 mm/year (+/- 0.02 mm/year) in those with a reconstructed acetabular angle greater than 45 degrees . Reproduction of a reconstructed femoral offset to within 5 mm of the native femoral offset was associated with a reduction in conventional PE wear (0.12 mm/year versus 0.16 mm/year). Careful placement of the acetabular component to ensure an acetabular angle less than 45 degrees in the reconstructed hip allows for reduced conventional PE wear. LEVEL OF EVIDENCE: Level II, prospective study. See Guidelines for Authors for a complete description of levels of evidence.


Asunto(s)
Artroplastia de Reemplazo de Cadera/métodos , Prótesis de Cadera , Inestabilidad de la Articulación/prevención & control , Polietileno/farmacología , Falla de Prótesis , Estrés Mecánico , Acetábulo/diagnóstico por imagen , Acetábulo/cirugía , Anciano , Artroplastia de Reemplazo de Cadera/efectos adversos , Análisis de Falla de Equipo , Femenino , Cabeza Femoral/diagnóstico por imagen , Estudios de Seguimiento , Humanos , Inestabilidad de la Articulación/etiología , Masculino , Persona de Mediana Edad , Osteoartritis de la Cadera/diagnóstico por imagen , Osteoartritis de la Cadera/cirugía , Probabilidad , Estudios Prospectivos , Diseño de Prótesis , Radiografía , Medición de Riesgo , Factores de Tiempo , Resultado del Tratamiento , Soporte de Peso
4.
Can J Surg ; 52(4): 295-301, 2009 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-19680514

RESUMEN

BACKGROUND: In recent years, the use of low molecular weight heparins such as dalteparin has become attractive because of their ease of administration and superiority in preventing venous thromboembolism (VTE) compared with traditional agents. The primary purpose of our study was to evaluate the impact of dalteparin use on blood loss and transfusion rates in patients undergoing primary total joint arthroplasty. We also evaluated the effect of patient sex, releasing the tourniquet in knee arthroplasty and the turnover of house staff. METHODS: Using our hospital transfusion database, we prospectively studied the mean reduction in hemoglobin and transfusion rates of 1642 consecutive patients who underwent primary total hip arthroplasty (THA) or total knee arthroplasty (TKA) between January 2004 and December 2005. In 2004, warfarin was used exclusively for VTE prevention; however, in 2005, following the release of the 2004 American College of Chest Physicians' guidelines, our centre began using dalteparin for VTE prophylaxis. We analyzed the impact of dalteparin use and the effect of patient sex, tourniquet release in TKA and house staff turnover months on blood loss and transfusion rates. RESULTS: The use of dalteparin for postoperative VTE prevention in patients undergoing THA and TKA in 2005 was associated with a significantly greater mean reduction in hemoglobin compared with warfarin use in 2004 (p = 0.014 for patients undergoing THA, p < 0.001 for patients undergoing TKA). The use of dalteparin in 2005 was not associated with a significant increase in allogeneic blood transfusions compared with the use of warfarin in 2004, except in women (p < 0.001). Although we observed no significant differences in mean reduction in hemoglobin between men and women undergoing THA, women undergoing THA had significantly higher transfusion rates regardless of the method of VTE prophylaxis (p = 0.037 for warfarin, p < 0.001 for dalteparin). Intraoperative tourniquet release in patients undergoing TKA was associated with a significantly lower mean reduction in hemoglobin than release after wound closure (p = 0.005). Although house staff turnover months were associated with a significantly greater mean reduction in hemoglobin levels than non-turnover months (p = 0.039), these months were not associated with a significant increase in allogeneic blood transfusions (p = 0.59). CONCLUSION: Low molecular weight heparins such as dalteparin are the most common form of VTE prophylaxis in Canada. Our results suggest that dalteparin use, timing of tourniquet release and house staff turnover can all influence transfusion rates and/or blood loss in patients undergoing primary total joint arthroplasty. This study also emphasizes that women undergoing THA are at particularly high risk for blood transfusion.

5.
Lancet ; 370(9597): 1508-19, 2007 Oct 27.
Artículo en Inglés | MEDLINE | ID: mdl-17964352

RESUMEN

In the 1960s, total hip replacement revolutionised management of elderly patients crippled with arthritis, with very good long-term results. Today, young patients present for hip-replacement surgery hoping to restore their quality of life, which typically includes physically demanding activities. Advances in bioengineering technology have driven development of hip prostheses. Both cemented and uncemented hips can provide durable fixation. Better materials and design have allowed use of large-bore bearings, which provide an increased range of motion with enhanced stability and very low wear. Minimally invasive surgery limits soft-tissue damage and facilitates accelerated discharge and rehabilitation. Short-term objectives must not compromise long-term performance. Computer-assisted surgery will contribute to reproducible and accurate placement of implants. Universal economic constraints in healthcare services dictate that further developments in total hip replacement will be governed by their cost-effectiveness.


Asunto(s)
Artroplastia de Reemplazo de Cadera , Cementos para Huesos , Prótesis de Cadera/tendencias , Procedimientos Quirúrgicos Mínimamente Invasivos , Anciano , Artroplastia de Reemplazo de Cadera/historia , Artroplastia de Reemplazo de Cadera/métodos , Artroplastia de Reemplazo de Cadera/tendencias , Historia del Siglo XIX , Historia del Siglo XX , Humanos , Persona de Mediana Edad , Procedimientos Quirúrgicos Mínimamente Invasivos/métodos , Procedimientos Quirúrgicos Mínimamente Invasivos/tendencias , Osteoartritis de la Cadera/cirugía
6.
J Biomech ; 41(4): 907-11, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18096170

RESUMEN

In this study, a new radiostereometric analysis (RSA) calibration cage was developed with the aim of improving the accuracy and precision of RSA. This development consisted of three steps: a numerical simulation technique was first used to design the new cage; a synthetic imaging method was then implemented to predict the performance of the designed cage before it was actually fabricated; and an experimental phantom test was finally conducted to verify the actual performance of the new cage and compare with two currently widely used cages. Accuracy was calculated as the 95% prediction intervals from regression analyses between the measured and actual displacements, and precision was defined as the standard deviation of repeated measurements. The final experimental phantom tests showed that the accuracy and precision of the new calibration cage were improved by about 40% over an existing biplanar cage and by about 70% compared to a uniplanar cage design. This new cage can be used with any skeletal joints, in either static or kinematic examination, which is helpful for the standardization of the RSA application.


Asunto(s)
Radiografía/normas , Calibración/normas , Simulación por Computador , Fémur/diagnóstico por imagen , Humanos , Modelos Biológicos , Fantasmas de Imagen , Radiografía/métodos , Tibia/diagnóstico por imagen
7.
Clin Orthop Relat Res ; 466(11): 2612-6, 2008 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-18800216

RESUMEN

UNLABELLED: Gender-specific total knee replacement design is a recent and debated topic. We determined the survivorship and clinical outcomes of a large primary total knee arthroplasty cohort, specifically assessing any differences between gender groups. A consecutive cohort of 3817 patients with 5279 primary total knee replacements (3100 female, 2179 male) with a minimum of 2 years followup were evaluated. Preoperative, latest, and change in clinical outcome scores (WOMAC, SF-12, KSCRS) were compared. While men had higher raw scores preoperatively, women had greater improvement in all WOMAC domains including pain (29.87 versus 27.3), joint stiffness (26.78 versus 24.26), function (27.21 versus 23.09), and total scores (28.35 versus 25.09). There were no gender differences in improvements of the SF-12 physical scores. Men had greater improvement in Knee Society function (22.1 versus 18.63) and total scores (70.01 versus 65.42), but not the Knee Society knee score (47.83 versus 46.64). Revision rates were 10.2% for men and 8% for women. Women demonstrated greater implant survivorship, greater improvement in WOMAC scores, equal improvements in SF-12 scores, and less improvement in only the Knee Society function and total scores. The data refute the hypothesis of inferior clinical outcome for women following total knee arthroplasty when using standard components. LEVEL OF EVIDENCE: Level II, prognostic study. See the Guidelines for Authors for a complete description of levels of evidence.


Asunto(s)
Artralgia/fisiopatología , Osteoartritis de la Rodilla/cirugía , Dolor Postoperatorio/fisiopatología , Distribución por Edad , Anciano , Artralgia/epidemiología , Distinciones y Premios , Índice de Masa Corporal , Femenino , Estudios de Seguimiento , Humanos , Incidencia , Masculino , Ontario/epidemiología , Ortopedia , Osteoartritis de la Rodilla/fisiopatología , Dimensión del Dolor , Dolor Postoperatorio/epidemiología , Periodo Posoperatorio , Estudios Prospectivos , Rango del Movimiento Articular/fisiología , Índice de Severidad de la Enfermedad , Factores Sexuales , Sociedades Médicas , Factores de Tiempo , Resultado del Tratamiento
8.
J Arthroplasty ; 23(6): 795-800, 2008 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-18534516

RESUMEN

Five hundred fifty patients who underwent primary total knee arthroplasty between 1987 and 2004 with a primary diagnosis of osteoarthritis and 1-year outcome data (Western Ontario and McMaster Osteoarthritis Index [WOMAC]) were evaluated. Patients were stratified into body mass index categories based on the World Health Organization classification of obesity. Patients were dichotomized into a class III morbidly obese group and a non-morbidly obese group. Independent t test and multivariable linear regression were used to determine if a difference existed in the 1-year WOMAC outcome between morbidly obese patients and all other patients. Although 1-year outcomes were worse for morbidly obese patients (P < .05), they showed greater improvement in function compared with non-morbidly obese patients. Morbid obesity does not affect 1-year outcomes in patients who have had a total knee arthroplasty.


Asunto(s)
Artroplastia de Reemplazo de Rodilla , Obesidad Mórbida/fisiopatología , Obesidad Mórbida/psicología , Osteoartritis de la Rodilla/cirugía , Evaluación de Resultado en la Atención de Salud , Anciano , Femenino , Humanos , Modelos Lineales , Masculino , Persona de Mediana Edad , Osteoartritis de la Rodilla/fisiopatología , Osteoartritis de la Rodilla/psicología , Estudios Prospectivos , Estudios Retrospectivos , Resultado del Tratamiento
9.
J Bone Joint Surg Am ; 89(4): 814-8, 2007 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-17403805

RESUMEN

UNLABELLED: We previously reported the ten to fifteen-year results for 195 matte-finished Harris Design-2 total hip replacements that had been inserted with cement by two surgeons in 166 patients with osteoarthritis. The purpose of the present report is to update that study and report the twenty to twenty-five-year outcomes. The patients were followed prospectively on the basis of clinical assessment with use of the Harris hip score and radiographic analysis. One hundred and forty-nine patients (90%) had a functioning implant at the time of death or, if living, at twenty to twenty-five years of follow-up. A total of ten patients (ten hips; 5%) underwent a revision because of aseptic loosening of the acetabular component (two hips; 1%), the femoral component (four hips; 2%), or both components (four hips; 2%). At twenty-five years, Kaplan-Meier analysis revealed a survival rate of 83% +/- 6% with revision for any reason as the end point. The survival rate was 86% +/- 6% for the femoral component and 93% +/- 3% for the acetabular component with aseptic loosening as the end point. LEVEL OF EVIDENCE: Therapeutic Level IV. See Instructions to Authors for a complete description of levels of evidence.


Asunto(s)
Artroplastia de Reemplazo de Cadera/métodos , Prótesis de Cadera , Adulto , Anciano , Anciano de 80 o más Años , Cementos para Huesos , Femenino , Estudios de Seguimiento , Articulación de la Cadera/diagnóstico por imagen , Articulación de la Cadera/cirugía , Humanos , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Diseño de Prótesis , Radiografía , Factores de Tiempo
10.
J Am Acad Orthop Surg ; 15(1): 53-64, 2007 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-17213382

RESUMEN

Osteolysis induced by wear debris of ultra-high-molecular-weight polyethylene has emerged as a significant problem after total knee arthroplasty. The generation of polyethylene wear and the development of osteolysis around total knee arthroplasty are caused by a combination of patient, implant, and surgical factors. Activity level over time may be the most important patient factor affecting the loads placed on a total knee replacement, but it is the most difficult to manage. Multiple factors related to the manufacturing of the polyethylene implant influence the extent of wear, and surgeons should be cautious in considering enhanced polyethylenes pending results of further investigations. The optimal design of the articular bearing surface remains controversial but needs to be considered with respect to the stresses imparted on component-bone and modular tibial backside interfaces. Surgical factors, including restoration of alignment and ligament balance, are important for long-term durability of the implant. Methods of measuring the wear of total knee implants are still evolving. Thus, when confronted with a worn total knee implant and developing osteolysis, the surgeon should consider each of these factors in selecting the best management option to eliminate the source of debris and minimize the potential for wear and osteolysis following revision.


Asunto(s)
Artroplastia de Reemplazo de Rodilla , Prótesis de la Rodilla , Osteólisis/etiología , Osteólisis/cirugía , Falla de Prótesis , Remoción de Dispositivos , Humanos , Prótesis de la Rodilla/efectos adversos , Polietilenos/efectos adversos , Diseño de Prótesis , Reoperación , Factores de Riesgo , Propiedades de Superficie
11.
J Bone Joint Surg Am ; 88(5): 959-63, 2006 May.
Artículo en Inglés | MEDLINE | ID: mdl-16651569

RESUMEN

BACKGROUND: Postoperative analgesia with the use of parenteral opioids or epidural analgesia can be associated with troublesome side effects. Good perioperative analgesia facilitates rehabilitation, improves patient satisfaction, and may reduce the hospital stay. We investigated the analgesic effect of locally injected drugs around a total knee prosthesis. METHODS: Sixty-four patients undergoing total knee arthroplasty were randomized either to receive a periarticular intraoperative injection containing ropivacaine, ketorolac, epimorphine, and epinephrine or to receive no injection. The perioperative analgesic regimen was standardized. All patients in both groups received patient-controlled analgesia for twenty-four hours after the surgery, and this was followed by standard analgesia. Visual analog scores for pain, during activity and at rest, and for patient satisfaction were recorded preoperatively and postoperatively and at the six-week follow-up examination. The consumption of patient-controlled analgesia at specific postoperative time-points and the overall analgesic requirement were measured. RESULTS: The patients who had received the injection used significantly less patient-controlled analgesia at six hours, at twelve hours, and over the first twenty-four hours after the surgery. In addition, they had higher visual analog scores for patient satisfaction and lower visual analog scores for pain during activity in the post-anesthetic-care unit and four hours after the operation. No cardiac or central nervous system toxicity was observed. CONCLUSIONS: Intraoperative periarticular injection with multimodal drugs can significantly reduce the requirements for patient-controlled analgesia and improve patient satisfaction, with no apparent risks, following total knee arthroplasty.


Asunto(s)
Amidas/administración & dosificación , Analgesia , Analgésicos/administración & dosificación , Artroplastia de Reemplazo de Rodilla , Epinefrina/administración & dosificación , Ketorolaco/administración & dosificación , Morfina/administración & dosificación , Anciano , Anciano de 80 o más Años , Quimioterapia Combinada , Femenino , Humanos , Inyecciones Intraarticulares , Masculino , Persona de Mediana Edad , Dimensión del Dolor , Estudios Prospectivos , Ropivacaína , Método Simple Ciego
12.
Instr Course Lect ; 55: 263-77, 2006.
Artículo en Inglés | MEDLINE | ID: mdl-16958462

RESUMEN

Osteolysis is the greatest threat to the viability of modern acetabular implants. The etiology and natural history of osteolysis remain unknown. Patients with cementless implants who have osteolysis are challenging to treat. There are no standards for follow-up methods or frequency, and there is little evidence to support timing of the decision to begin treatment in these patients. The natural history of proposed treatment options is also unknown. Reconstruction of the acetabulum in the presence of bone loss is difficult. Classifications have been developed to guide management. Multiple options exist for revision acetabular surgery, and it is important to understand the rationale and data in support of these options. A review of the literature was undertaken and algorithms were developed to help address acetabular bone loss in patients undergoing revision surgery.


Asunto(s)
Acetábulo , Artroplastia de Reemplazo de Cadera/efectos adversos , Conservadores de la Densidad Ósea/uso terapéutico , Difosfonatos/uso terapéutico , Osteólisis/tratamiento farmacológico , Osteólisis/cirugía , Humanos , Osteólisis/etiología , Reoperación/métodos , Resultado del Tratamiento
13.
Instr Course Lect ; 54: 131-41, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-15948440

RESUMEN

Inadequate soft-tissue balancing is a major yet often underemphasized cause of failure for primary and revision total hip arthroplasty. Accordingly, contemporary cemented and cementless hip prostheses have been designed with consideration of this issue, and this has substantially increased the long-term survival of total hip replacements. Therefore, it is important for orthopaedic surgeons to be familiar with the rationale, biomechanical principles, and clinical implications associated with soft-tissue balancing of the hip as well as strategies to avoid inadequate soft-tissue balancing and systematic techniques to restore adequate soft-tissue tensioning during total hip arthroplasty.


Asunto(s)
Artroplastia de Reemplazo de Cadera/métodos , Fenómenos Biomecánicos , Articulación de la Cadera/fisiología , Prótesis de Cadera , Humanos , Diferencia de Longitud de las Piernas/prevención & control , Diseño de Prótesis
14.
J Clin Epidemiol ; 56(11): 1046-54, 2003 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-14614995

RESUMEN

OBJECTIVE: The purpose is to examine the responsiveness of the Health Utilities Index Mark 2 (HUI2), Mark 3 (HUI3), and other generic and disease-specific measures in osteoarthritis patients undergoing total hip arthroplasty (THA). METHODS: Ninety patients (mean age=68.13; SD=8.15) on a waiting list for THA completed measures that included the standard gamble, HUI2, HUI3, SF-36, Harris Hip Scale, WOMAC, and MACTAR. before and after THA. Responsiveness statistics (effect size, standardized response mean, Guyatt's responsiveness statistic, paired-sample t-tests, and relative efficiency statistic) were calculated. RESULTS: The disease-specific measures were more responsive than the generic measures. Rankings of the degree of responsiveness varied depending on the responsiveness statistic used. CONCLUSIONS: Disease-specific measures are the most responsive in THA patients. However, the SF-36, HUI2, and HUI3 had summary scores and domain/attributes scores that were also responsive and provided additional information. Among the generic measures, HUI3 was the most responsive.


Asunto(s)
Artroplastia de Reemplazo de Cadera , Indicadores de Salud , Osteoartritis de la Cadera/cirugía , Animales , Femenino , Estudios de Seguimiento , Humanos , Masculino , Osteoartritis de la Cadera/rehabilitación , Sensibilidad y Especificidad
15.
J Bone Joint Surg Am ; 84(10): 1823-8, 2002 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-12377914

RESUMEN

BACKGROUND: This study was designed to compare the fixation of a Mallory-Head total hip prosthesis with and without cement. METHODS: Two hundred and fifty patients with osteoarthritis of the hip were randomized to receive a Mallory-Head total hip prosthesis designed for insertion with cement or the same prosthesis designed for insertion without cement. Neither the patient nor the outcomes assessor was aware of the type of prosthesis. Outcomes were assessed with respect to mortality, revision arthroplasty, health-related quality of life (evaluated with the Harris hip score, Merle d'Aubign and Postel hip score, McMaster-Toronto Arthritis Patient Preference Disability Questionnaire (MACTAR), Western Ontario and McMaster University Osteoarthritis Index (WOMAC), and the time trade-off technique), and the six-minute-walk test. Patients were seen at three, six, and twelve months and yearly thereafter. RESULTS: The prosthesis was inserted with cement in 124 patients and without cement in 126 patients. The mean age of the patients was sixty-four years, 48% were female, and the mean duration of follow-up was 6.3 years. There were thirteen revisions in the group that had fixation with cement and six in the group that had fixation without cement (p = 0.11), and more femoral components were revised in the group that had fixation with cement (twelve versus one; p = 0.002). All health-related quality-of-life measures improved postoperatively in both groups. CONCLUSIONS: In this randomized trial, the group that had the cemented Mallory-Head hip prostheses required more revisions of the femoral component than did the group with the cementless Mallory-Head prostheses, which was perhaps related to the titanium-alloy femoral stem. Our findings are specific to the implants evaluated in this study.


Asunto(s)
Artroplastia de Reemplazo de Cadera/métodos , Osteoartritis de la Cadera/cirugía , Calidad de Vida , Anciano , Artroplastia de Reemplazo de Cadera/efectos adversos , Cementos para Huesos , Femenino , Estudios de Seguimiento , Humanos , Masculino , Persona de Mediana Edad , Dimensión del Dolor , Probabilidad , Diseño de Prótesis , Ajuste de Prótesis , Rango del Movimiento Articular/fisiología , Recuperación de la Función , Reoperación/estadística & datos numéricos , Muestreo , Resultado del Tratamiento
16.
J Bone Joint Surg Am ; 86(9): 1931-5, 2004 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-15342755

RESUMEN

BACKGROUND: Unicompartmental knee arthroplasty has become a popular treatment alternative for osteoarthritis that is confined to the medial part of the knee. Excellent intermediate-term results recently have been reported in association with the Miller-Galante unicompartmental implant. The purpose of the present study was to report on our longer-term experience with the Miller-Galante medial unicompartmental knee implant. METHODS: We evaluated the results of 113 medial unicompartmental knee arthroplasties that had been performed with use of the Miller-Galante implant in eighty-four patients between 1989 and 2000. The mean age of the patients at the time of surgery was sixty-eight years. Forty-five patients were men, and thirty-nine were women. Thirteen patients (sixteen knees) died at a mean of seven years after the index arthroplasty. No patient was lost to follow-up. The remaining seventy-one patients (ninety-seven knees) were followed for a mean of ten years and were evaluated with use of the Knee Society clinical and radiographic rating system. RESULTS: Eleven knees were revised at a mean of four years after the index procedure. The mean Knee Society knee and function scores for the sixty-one patients (eighty-six knees) who were living and who had not had a revision improved from 48 and 53 points preoperatively to 93 and 80 points at the time of the most recent evaluation. The five and ten-year rates of survival were 94% and 90%, respectively, with revision to tricompartmental knee arthroplasty as the end point and 93% and 86%, respectively, with revision or radiographic loosening as the end point. CONCLUSIONS: The Miller-Galante medial unicompartmental knee arthroplasty provided excellent pain relief and restoration of function in carefully selected patients and demonstrated durable implant survival at ten years.


Asunto(s)
Artroplastia de Reemplazo de Rodilla/métodos , Prótesis de la Rodilla , Adulto , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Masculino , Persona de Mediana Edad , Diseño de Prótesis , Factores de Tiempo
17.
J Bone Joint Surg Am ; 86(6): 1179-85, 2004 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-15173290

RESUMEN

BACKGROUND: Revision of the femoral component of a total hip replacement with use of cement has been associated with early mechanical failure due to aseptic loosening. The purpose of the present study was to determine the long-term survival after revision of the femoral component with cement and to identify factors that were predictive of failure. METHODS: The results of 129 revision total hip arthroplasties that had been performed with use of a cemented femoral stem were reviewed to determine component survival. Ninety-seven hips that had been followed for a minimum of five years were included in survival analysis and tests of significance. Harris hip scores were used to quantify clinical outcomes. Clinical and surgical factors were analyzed to determine whether they were predictive of failure. RESULTS: The mean Harris hip score improved from 52 points preoperatively to 71 points at the time of the most recent follow-up (p < 0.001). The ten-year survival rate was 91% with rerevision of the femoral component because of aseptic loosening as the end point and 71% with mechanical failure as the end point. Patients who were more than sixty years old had greater long-term component survival and less pain than younger patients did (p < 0.05). A good-quality postoperative cement mantle was associated with better long-term radiographic signs of fixation (p < 0.001). Poor femoral bone quality was associated with an increased rate of rerevision for aseptic loosening (p = 0.021). CONCLUSIONS: Revision with use of a cemented femoral component remains an option for selected patients, with an acceptable ten-year survival rate and fair radiographic evidence of fixation. Our patients had acceptable clinical outcomes at ten years, and few had notable pain. The best results may be achieved in older patients (those who are sixty years old or more) with adequate bone stock who are managed with modern cementing techniques.


Asunto(s)
Artroplastia de Reemplazo de Cadera , Cementos para Huesos , Anciano , Cementación/métodos , Femenino , Estudios de Seguimiento , Articulación de la Cadera/diagnóstico por imagen , Humanos , Complicaciones Intraoperatorias/epidemiología , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Diseño de Prótesis , Falla de Prótesis , Radiografía , Reoperación , Estudios Retrospectivos , Factores de Tiempo
18.
J Bone Joint Surg Am ; 85(3): 505-11, 2003 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-12637439

RESUMEN

BACKGROUND: Three-dimensional radiographic techniques have been developed to estimate in vivo polyethylene wear of total hip replacements. We are not aware of any published study examining the accuracy of these in vivo methods. Our objective was to validate two radiographic techniques by comparing their results with those obtained directly from retrieved specimens. METHODS: A coordinate measuring machine was used to probe the interior bearing surface of seventeen acetabular liners that had been retrieved at revision surgery. Solid models were created to determine volumetric polyethylene loss and linear depth and direction of wear. Two in vivo radiographic techniques (PolyWare and the Martell Hip Analysis Suite) were used to calculate two-dimensional linear, three-dimensional linear, and volumetric wear. The radiographic analysis was done independently, and the results were compared with the known values of polyethylene wear derived with use of the coordinate measuring machine. RESULTS: Correlation coefficients comparing the values for two-dimensional and three-dimensional linear wear and volumetric wear derived with the PolyWare radiographic technique with the values derived with the coordinate measuring machine were r(2) = 0.78, r(2) = 0.75, and r(2) = 0.91, respectively (all p < 0.001), and the correlation coefficients comparing the values derived with the Martell Hip Analysis Suite radiographic technique with those derived with the coordinate measuring machine were r(2) = 0.80, r(2) = 0.84, and r(2) = 0.91, respectively (p < 0.001). The average absolute difference between the radiographic estimates and the results derived with the coordinate measuring machine was approximately 19% (range, 13% to 24%). CONCLUSIONS: There was good agreement between the wear estimates made with both in vivo techniques and the measurements of the retrieved polyethylene liners made with the coordinate measuring machine. Two-dimensional wear analysis (based on anteroposterior radiographs) accounted for most of the polyethylene wear, while one technique of three-dimensional wear analysis (PolyWare) demonstrated some additional wear in the lateral plane.


Asunto(s)
Artroplastia de Reemplazo de Cadera , Prótesis de Cadera , Procesamiento de Imagen Asistido por Computador , Imagenología Tridimensional , Polietileno , Falla de Prótesis , Humanos , Técnicas In Vitro , Radiografía , Jabones
19.
J Am Acad Orthop Surg ; 11(4): 238-47, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-12889862

RESUMEN

Extensor mechanism complications are the most commonly reported reasons for revision surgery after total knee arthroplasty and are a frequent source of postoperative morbidity. Patellofemoral instability is the most commonly reported extensor mechanism complication and has multiple etiologies, including prosthetic malalignment and soft-tissue imbabalce. Patellar fracture or rupture of either the quadriceps or patellar tendon can cause catastrophic disruption of the extensor mechanism. Although some stable fractures can be successfully managed nonsurgically, displaced fractures or tendon rupture often lead to poor results. Other complications include patellar clunk and soft-tissue adhesions, prosthetic wear or loosening, and osteonecrosis. Increased understanding of implant alignment, rotation, and soft-tissue balance, as well as improved design of the trochlear groove of femoral implants and patellar components, has resulted in a decline in extensor mechanism complications. Appropriate prosthetic selection and meticulous surgical technique remain the keys to avoiding unsatisfactory results and revision surgery.


Asunto(s)
Artroplastia de Reemplazo de Rodilla/efectos adversos , Inestabilidad de la Articulación/etiología , Prótesis de la Rodilla , Músculo Esquelético/fisiopatología , Traumatismos de los Tendones/complicaciones , Tendones/fisiopatología , Artroplastia de Reemplazo de Rodilla/métodos , Femenino , Estudios de Seguimiento , Humanos , Inestabilidad de la Articulación/prevención & control , Masculino , Osteoartritis de la Rodilla/diagnóstico , Osteoartritis de la Rodilla/cirugía , Diseño de Prótesis , Falla de Prótesis , Rango del Movimiento Articular , Recuperación de la Función , Reoperación , Medición de Riesgo , Rotura Espontánea
20.
Instr Course Lect ; 53: 207-15, 2004.
Artículo en Inglés | MEDLINE | ID: mdl-15116615

RESUMEN

Instability is a relatively common cause of failure of total knee arthroplasty. In the management of the unstable total knee, the need for constraint must be anticipated. Careful preoperative planning including history and physical examination of the ligamentous support of the knee is mandatory. A thorough study of current and previous radiographs is important to determine wear, component migration, and bone loss. As a general rule, it is recommended that the minimum amount of constraint necessary to achieve stability should be used. Most of the time, stability can be achieved using a posterior-stabilized or a nonlinked implant, such as a varus-valgus constrained or constrained-condylar knee implant. Occasionally, a hinge prosthesis may be indicated, particularly in a patient with an absent and nonreconstructable medial collateral ligament. Increasing constraint is not without its problems, however, as forces across the knee may be transmitted to the stem-bone interface, resulting in radiographic loosening of stemmed components. Fortunately, these observations of radiographic loosening around stems of revision components have not so far correlated with reports of clinical failure.


Asunto(s)
Artroplastia de Reemplazo de Rodilla , Inestabilidad de la Articulación/cirugía , Articulación de la Rodilla , Prótesis de la Rodilla , Complicaciones Posoperatorias/cirugía , Diseño de Equipo , Humanos , Inestabilidad de la Articulación/diagnóstico , Complicaciones Posoperatorias/diagnóstico , Reoperación
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