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1.
Clin Orthop Relat Res ; 469(1): 138-45, 2011 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-20848243

RESUMEN

BACKGROUND: A dramatic increase in the demand for TKA is expected. The current burden of revision TKA is well known but the incidence and etiology of nonrevision reoperations after primary TKA is not. QUESTIONS/PURPOSES: We determined the rate, reason, timing, and predictors of nonrevision reoperation after TKA. METHODS: Using our institutional joint arthroplasty database, we identified 10,188 TKA performed on 7,613 patients between April 2000 and March 2008. A nonrevision reoperation was defined as any procedure requiring anesthetic in which components with bony interfaces were not removed or exchanged. Procedures after revision TKA were excluded. Potential risk factors investigated included age, gender, laterality, and simultaneous bilateral versus staged bilateral versus unilateral TKA. The minimum followup was 1 year (median, 4.1 years; range, 1.1 to 9.1 years). RESULTS: Three hundred fifty-three patients of 7,613 (4.6%) underwent 434 nonrevision reoperations on 384 of 10,188 (3.8%) knees. The most common indication for nonrevision reoperation was stiffness (58%; 252 of 434), followed by patellar clunk (12%; 53), infection (12%; 52), wound revision (6%; 26), hematoma (4.4%; 19), among others. The median time to reoperation was 74.5 days (range, 1-3058 days) but varied widely. Younger patients and those with unilateral TKA were more likely to have a nonrevision reoperation. CONCLUSIONS: The majority of nonrevision reoperations are performed for stiffness. Patellar clunk and infection also result in a large number of nonrevision reoperations. In weighing the future economic and workforce burden of TKA, nonrevision reoperations need to be acknowledged, and preventive measures need to be implemented. LEVEL OF EVIDENCE: Level II, prognostic study. See the Guidelines for Authors for a complete description of levels of evidence.


Asunto(s)
Artroplastia de Reemplazo de Rodilla , Complicaciones Posoperatorias/cirugía , Anciano , Artroplastia de Reemplazo de Rodilla/efectos adversos , Artroplastia de Reemplazo de Rodilla/instrumentación , Distribución de Chi-Cuadrado , Femenino , Hematoma/etiología , Hematoma/cirugía , Humanos , Prótesis de la Rodilla , Masculino , Philadelphia , Complicaciones Posoperatorias/etiología , Infecciones Relacionadas con Prótesis/etiología , Infecciones Relacionadas con Prótesis/cirugía , Sistema de Registros , Reoperación , Estudios Retrospectivos , Medición de Riesgo , Factores de Riesgo , Factores de Tiempo , Resultado del Tratamiento
2.
J Arthroplasty ; 25(3): 410-5, 2010 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-20149582

RESUMEN

Pain management after total hip arthroplasty has improved dramatically in the past decade. However, most protocols use opioid medications for pain control. In the current study, 100 patients were prospectively selected to receive a traditional narcotic-based patient-controlled analgesia protocol or a nonnarcotic oral protocol for pain management after primary total hip arthroplasty. Therapy programs were similar for both groups. Postoperatively, patients were followed daily for opioid use, medication adverse effects, pain control, and overall satisfaction. The nonnarcotic oral group showed lower mean pain scores during the first 24 hours after surgery. The satisfaction rate was high in both groups. Both protocols provided adequate pain control after total hip arthroplasty; the nonnarcotic pain management protocol resulted in significantly decreased opioid consumption and fewer adverse effects.


Asunto(s)
Analgésicos no Narcóticos/uso terapéutico , Artroplastia de Reemplazo de Cadera/efectos adversos , Prótesis de Cadera , Narcóticos/uso terapéutico , Dolor Postoperatorio/tratamiento farmacológico , Acetaminofén/efectos adversos , Acetaminofén/uso terapéutico , Adulto , Anciano , Anciano de 80 o más Años , Analgésicos no Narcóticos/efectos adversos , Celecoxib , Dextropropoxifeno/efectos adversos , Dextropropoxifeno/uso terapéutico , Femenino , Fentanilo/efectos adversos , Fentanilo/uso terapéutico , Humanos , Masculino , Persona de Mediana Edad , Narcóticos/efectos adversos , Oxicodona/efectos adversos , Oxicodona/uso terapéutico , Dolor Postoperatorio/etiología , Satisfacción del Paciente , Pregabalina , Estudios Prospectivos , Pirazoles/efectos adversos , Pirazoles/uso terapéutico , Sulfonamidas/efectos adversos , Sulfonamidas/uso terapéutico , Encuestas y Cuestionarios , Resultado del Tratamiento , Ácido gamma-Aminobutírico/efectos adversos , Ácido gamma-Aminobutírico/análogos & derivados , Ácido gamma-Aminobutírico/uso terapéutico
3.
J Long Term Eff Med Implants ; 17(4): 359-65, 2007.
Artículo en Inglés | MEDLINE | ID: mdl-19267690

RESUMEN

Thromboembolic disease is common after orthopaedic surgery. In an effort to minimize the risk of pulmonary embolism and deep vein thrombosis (DVT), anticoagulation administration has become a common practice. Both the American College of Chest Physicians (ACCP) and the American Association of Orthopaedic Surgeons (AAOS) have published guidelines recommending antithrombotic protocols. The ACCP guidelines are excessive and do not adequately evaluate the complications resulting from aggressive anticoagulation. These complications include, but are not limited to, major and minor bleeding events, thrombocytopenia, subsequent periprosthetic infection, and complications with spinal or epidural anesthesia. The AAOS guidelines generated by a group of orthopedic surgeons evaluate the efficacy of various agents in preventing pulmonary embolus and not distal DVT. They differ from the AACP guidelines in some aspects. The AAOS guidelines accept the use of aspirin combined with mechanical compression devices, and low-dose warfarin therapy. We believe that the AAOS guidelines for thromboprophylaxis take into account all risks associated with anticoagulation therapy and may prove to be a safer option for our patients.


Asunto(s)
Anticoagulantes/uso terapéutico , Artroplastia de Reemplazo/efectos adversos , Guías de Práctica Clínica como Asunto/normas , Tromboembolia/prevención & control , Humanos , Tromboembolia/etiología , Resultado del Tratamiento , Estados Unidos
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