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1.
J Bone Jt Infect ; 3(4): 203-206, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-30416944

RESUMEN

According to the relevant literature, prosthetic joint infections caused by Listeria monocytogenes require two stage revision surgery or prosthesis removal for a successful outcome. We present the case of a patient who suffered such an infection after Total Knee Replacement surgery and was successfully treated with antibiotics, joint lavage, debridement and retention of the prosthesis.

2.
J Arthroplasty ; 29(2): 416-21, 2014 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-23871706

RESUMEN

Peri-prosthetic pseudotumor formation can be a severe complication following Metal-on-Metal hip resurfacing arthroplasty (MoMHRA), with limited data on the optimal management of this complication. The aims of this study were (1) to evaluate the prevalence and severity of pseudotumors in a consecutive cohort of 248 MoMHRA (214 patients, mean follow-up 4.6 years, range: 1 - 8.2), and (2) to present a clinical guideline for their treatment based on severity grading with Metal Artefact Reduction Sequence Magnetic Resonance Imaging, metal ion levels and symptoms. Pseudotumor prevalence was 36.3%: 61 mild, 25 moderate and four were graded severe. Five revisions followed, all in symptomatic patients with elevated metal ion levels. Pseudotumor severity grading allowed us to be conservative with revision surgery for mild and moderate MoM disease.


Asunto(s)
Artroplastia de Reemplazo de Cadera/efectos adversos , Granuloma de Células Plasmáticas/sangre , Granuloma de Células Plasmáticas/cirugía , Adulto , Anciano , Artroplastia de Reemplazo de Cadera/instrumentación , Materiales Biocompatibles , Cromo/sangre , Cobalto/sangre , Femenino , Granuloma de Células Plasmáticas/diagnóstico , Granuloma de Células Plasmáticas/etiología , Humanos , Iones/sangre , Imagen por Resonancia Magnética , Masculino , Metales , Persona de Mediana Edad , Diseño de Prótesis , Reoperación
3.
J Arthroplasty ; 28(2): 375.e13-5, 2013 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-22810005

RESUMEN

Fungal prosthetic joint infections are rare and difficult to treat. There is an ongoing discussion about the type and duration of antifungal treatment and the necessity of prosthesis removal. We report the first European case of an infected total knee arthroplasty with Coccidioides immitis. Treatment consisted of lifelong treatment with oral fluconazole at a dose of 400 mg/d, without total knee arthroplasty removal. After 6 months, the initial complaints of pain and swelling were completely resolved. This case report clearly states that a travel history and culturing for fungi are helpful in patients with persisting complaints after joint arthroplasty.


Asunto(s)
Antifúngicos/administración & dosificación , Artroplastia de Reemplazo de Rodilla/efectos adversos , Coccidioides , Coccidioidomicosis/tratamiento farmacológico , Fluconazol/administración & dosificación , Infecciones Relacionadas con Prótesis/tratamiento farmacológico , Anciano , Esquema de Medicación , Femenino , Humanos , Prótesis de la Rodilla/efectos adversos , Prótesis de la Rodilla/microbiología , Infecciones Relacionadas con Prótesis/microbiología , Viaje
4.
Hip Int ; 23(3): 243-9, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23233174

RESUMEN

We intensified our screening protocol for the presence of pseudotumours in a consecutive series of patients with a hip resurfacing arthroplasty (HRA), to establish whether we should be alert to the presence of 'silent' pseudotumours. Patients categorised with high risk (11 hips) and low risk (10 hips) for pseudotumour development and a control group (23 hips) were screened with metal artefact reduction sequence (MARS) magnetic resonance imaging (MRI). The Anderson classification to grade any metal-on-metal (MoM) disease present on MARS-MRI images was used. In 15 out of 44 MRI scans pseudotumours were observed (34.1%), of which six were graded with mild (13.6%), eight with moderate (18.2%) and one with severe MoM disease (2.3%). Twelve pseudotumours were present in asymptomatic patients (27.3%). Metal ion levels were normal in 80% of the MARS-MRI screened patients. As a consequence of our intensified screening protocol, one patient was revised for pseudotumour formation and another patient was scheduled for revision. Silent pseudotumours were observed in all three groups. Before our intensified screening protocol was initiated, no pseudotumours were encountered in our cohort of 289 HRAs. We concluded that clinical outcomes and plain radiographs for screening MoM patients underestimates the presence of pseudotumours in MoM patients. The true clinical relevance of these pseudotumours is still unclear.


Asunto(s)
Artroplastia de Reemplazo de Cadera/efectos adversos , Granuloma de Células Plasmáticas/epidemiología , Prótesis de Cadera/efectos adversos , Imagen por Resonancia Magnética/métodos , Adulto , Anciano , Progresión de la Enfermedad , Femenino , Estudios de Seguimiento , Granuloma de Células Plasmáticas/diagnóstico , Granuloma de Células Plasmáticas/etiología , Humanos , Incidencia , Masculino , Persona de Mediana Edad , Países Bajos/epidemiología , Pronóstico , Diseño de Prótesis , Reoperación , Estudios Retrospectivos
5.
BMC Musculoskelet Disord ; 13: 247, 2012 Dec 13.
Artículo en Inglés | MEDLINE | ID: mdl-23234268

RESUMEN

BACKGROUND: The purpose of our study was to prospectively report the clinical results of 280 consecutive hips (240 patients) who received a ReCap Hip Resurfacing System implant (Biomet Inc., Warsaw, USA) in a single district general hospital. Literature reports a large variation in clinical results between different resurfacing designs and published results using this particular design are scarce. METHODS: Mean follow up was 3.3 years (1.0 to 6.3) and four patients were lost to follow-up. All patients were diagnosed with end-stage hip osteoarthritis, their mean age was 54 years and 76.4% of all patients were male. RESULTS: There were 16 revisions and four patients reported a Harris Hip Score <70 points at their latest follow up. There were no pending revisions. Kaplan-Meier implant survival probability, with revision for any reason as endpoint, was 93.5% at six years follow-up (95%-CI: 88.8-95.3). There were no revisions for Adverse Reactions to Metal Debris (ARMD) and no indications of ARMD in symptomatic non-revised patients, although diagnostics were limited to ultrasound scans. CONCLUSIONS: This independent series confirms that hip resurfacing is a demanding procedure, and that implant survival of the ReCap hip resurfacing system is on a critical level in our series. In non-revised patients, reported outcomes are generally excellent. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT00603395.


Asunto(s)
Artroplastia de Reemplazo de Cadera/instrumentación , Artroplastia de Reemplazo de Cadera/métodos , Hospitales de Distrito/tendencias , Hospitales Generales/tendencias , Osteoartritis de la Cadera/diagnóstico por imagen , Osteoartritis de la Cadera/cirugía , Adulto , Anciano , Femenino , Estudios de Seguimiento , Humanos , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Radiografía , Resultado del Tratamiento
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