Zusammenfassung
Operationsziel
Explantation einer aseptisch gelockerten Endoprothese am oberen Sprunggelenk (OSG), Augmentation der bestehenden knöchernen Defekte und achskorrekte, definitive OSG-Versteifung zur Schmerzlinderung eines periprothetischen Lockerungsprozesses und für eine belastbare untere Extremität.
Indikationen
Symptomatische, aseptische Lockerung einer OSG-Endoprothese mit/ohne signifikante ossäre Defekte des tibialen und/oder talaren Knochenlagers.
Kontraindikationen
Allgemeine chirurgische oder anästhesiologische Kontraindikationen, implantatassoziierte, lokale oder systemische Infektionen, chirurgisch/interventionell nicht beherrschbare Weichteilproblematiken.
Operationstechnik
Explantation der einliegenden Prothesenkomponente über bestehenden Zugang. Sorgfältiges Débridement des Knochenlagers auf tibialer und talarer Seite. Knöcherne Augmentation der Defekte mit autologer/homologer Spongiosa, ggf. Verwendung von strukturellen Allografts. Arthrodese in Doppelplattentechnik.
Nachbehandlung
Postoperativ Anlage eines wattegepolsterten Verbands. Medikamentöse Thromboembolieprophylaxe. Mobilisation ab dem 1. postoperativen Tag mit 15-kg-Teilbelastung in stabiler Orthese oder Unterschenkelgips für 6–8 Wochen. Bei regelrechtem postoperativem Verlauf und gesicherter fortschreitender ossärer Konsolidierung schrittweise Vollbelastung 6–8 Wochen postoperativ nach klinischer und radiologischer Verlaufskontrolle.
Ergebnisse
Revision der OSG-Prothese mit Konversion zur OSG-Arthrodese bei 9 Patienten (6 Männer, 3 Frauen, mittleres Alter 56,4 ± 7,0 Jahre; Spanne 47,8–66,0 Jahre) zwischen Januar 2007 und Dezember 2012. Zwischen ursprünglicher endoprothetischer Versorgung und Revisionseingriff lagen im Mittel 4,5 ± 2,4 Jahre (Spanne 1,2–7,9 Jahre). Postoperativ oberflächliche Wundinfektion bei einem Patienten sowie ein Fall einer verzögerten ossären Konsolidierung der Arthrodese nach 11 Monaten.
Abstract
Objective
To remove loosened prosthesis components, to perform augmentation, to address osseous defects, to perform neutrally aligned ankle arthrodesis, and to achieve postoperative pain relief.
Indications
Symptomatic, aseptic loosening of total ankle replacement (TAR) with/without substantial bone defect of the tibial and/or talar bone stock.
Contraindications
General surgical or anesthesiological risks, periprosthetic infection, local or systemic infection, nonmanageable soft tissue problems.
Surgical technique
Removal of both prosthesis components using the previous incision (mostly using anterior ankle approach). Careful debridement of bone stock at the tibial and talar side. Osseous augmentation of defects using autologous or homologous cancellous bone, if needed, using structural allografts.
Postoperative management
A soft wound dressing is used. Thromboprophylaxis is recommended. Patient mobilization starts on postoperative day 1 with 15 kg partial weight bearing using a stabilizing walking boot or cast for 6–8 weeks. Following clinical and radiographic follow-up at 6 weeks, full weight bearing is initiated gradually after progressive osseous healing has been confirmed.
Results
Between January 2007 and December 2012, ankle arthrodesis was performed in 9 patients with failed TAR (6 men and 3 women, mean age 56.4 ± 7.0 years, range 47.8–66.0 years). The mean time between the initial TAR and revision surgery was 4.5 ± 2.4 years (range 1.2–7.9 years). In one patient irrigation and debridement was performed due to superficial wound infection. Another patient had a delayed osseous healing 11 months after the revision surgery.
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M. D. Wimmer, M. Hettchen, M.M. Plöger, D.C. Wirtz und A. Barg geben an, dass kein Interessenkonflikt besteht. B. Hintermann hat eine Beratertätigkeit bei Firma Integra Life Science.
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T. Mittlmeier, Rostock
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R. Himmelhan, Mannheim
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Wimmer, M.D., Hettchen, M., Ploeger, M.M. et al. Aseptische Lockerung einer OSG‑Endoprothese und Konversion zur OSG‑Arthrodese. Oper Orthop Traumatol 29, 207–219 (2017). https://doi.org/10.1007/s00064-017-0492-x
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DOI: https://doi.org/10.1007/s00064-017-0492-x