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Convened under the auspicious of esteemed endorsers - ISTA

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polymerization, <strong>the</strong> outer mold is pealed from around <strong>the</strong> cemented stem; D. combinedfemoral stem with its cement mantle that match <strong>the</strong> femoral canal diameter.The final construct is cemented in place with antibiotic-impregnated polymethylmethacrylateand inserted during <strong>the</strong> late stages <strong>of</strong> polymerization to minimize osseous interdigitation t<strong>of</strong>acilitate later removal in <strong>the</strong> second stage. As regards <strong>the</strong> femoral component, cementation islimited to <strong>the</strong> proximal 3cm <strong>of</strong> <strong>the</strong> femoral canal. Modular head that achieves stability is <strong>the</strong>napplied. Extramedullary rod formed <strong>of</strong> K-wire with antibiotic-impregnatedpolymethylmethacrylate cured around is inserted sub-muscular to provide elution <strong>of</strong> antibioticextramedullary, followed by closure in layers (Fig 5)Fig 5 A. acetabular component after cementation; B. Femoral component insertion withcementation limited to <strong>the</strong> proximal 3 cm <strong>of</strong> <strong>the</strong> femoral canal; C. extramedullary K-wirewith antibiotic-impregnated polymethylmethacrylate investing itIn septic hip arthritis <strong>the</strong> same technique is used after osteotomy <strong>of</strong> <strong>the</strong> neck and debridement <strong>of</strong><strong>the</strong> infected and devitalized tissues.In <strong>the</strong> first stage, all necrotic and devitalised tissues are removed, and <strong>the</strong> functional temporarypros<strong>the</strong>sis is inserted using <strong>the</strong> technique described. Tissue biopsy (5-6 specimens fromacetabulum and femur) are collected and sent for culture. Extended cultures for 2 weeks is ourprotocol to approve <strong>the</strong> results <strong>of</strong> culture with infection best predicted when three or more <strong>of</strong> <strong>the</strong>intraoperative cultures show growth <strong>of</strong> a consistent microorganism [3]. Even if we thought that<strong>the</strong> positive growth on culture was a contaminant, as is <strong>the</strong> case when only one <strong>of</strong> five culturespecimens is positive, we counted <strong>the</strong> case as a confirmed infection. This approach was taken toensure <strong>the</strong> safety <strong>of</strong> <strong>the</strong> procedure.During <strong>the</strong> interval period between <strong>the</strong> two stages: patient is allowed to mobilize and ambulatepartial weight-bearing with frame <strong>the</strong> day after surgery, intravenous antibiotics are administeredfor a minimum <strong>of</strong> 6 weeks, combined with oral rifampicin. The patient is followed clinicallyand radiologically; provided wound healing and inflammatory mediators (ESR and C-RP)levels are satisfactory, antibiotics discontinued and second stage performed. Numerousintraoperative samples are obtained for microbiological analysis during <strong>the</strong> second stage. Afile:///E|/<strong>ISTA</strong>2010-Abstracts.htm[12/7/2011 3:15:47 PM]

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