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Implantatspezifische Zugänge: Activ-L

Keel-Implants: Activ-L

Zusammenfassung

Das Activ-L-Implantat (B. Braun/Aesculap, Tuttlingen, Deutschland) ermöglicht einen minimalinvasiven endoprothetischen Bandscheibenersatz der Lendenwirbelsäule (LWS). Verankerung mittels Spikes, Keel oder einer Kombination aufgrund seines modularen Designs möglich. Translation in begrenztem Ausmaß durch ein UHMWPEInlay möglich. Frühe klinische Ergebnisse sind mit bereits etablierten Implantatkonzepten vergleichbar.

Operationsziel

Restauration der Funktion des lumbalen Bewegungssegments mit anhaltender Schmerzreduktion und normaler Belastbarkeit. Rasche klinische Reintegration des Patienten in Berufs- und Privatleben.

Indikationen

Gescheiterte konservative Behandlung bei nachgewiesener Bandscheibendegeneration eines oder mehrerer Bewegungssegmente und Ausschluss einer nicht diskogenen Schmerzursache.

Kontraindikationen

Spondylitiden und Diszitiden des Segmentes, Frakturen, Wirbelkörpermetastasen, Z. n. Fusionsoperationen, Osteoporose, metabolische Knochenerkrankungen, schwere Allgemeinerkrankungen, allgemeine Kontraindikationen, die gegen einen abdominellen Eingriff sprechen, unklare lumbale Schmerzzustände.

Operationstechnik

Minimalinvasiver ventraler Zugang zur Lendenwirbelsäule, Darstellen der ventralen Zirkumferenz des Segmentes, Ausräumen des Zwischenwirbelraumes, Höhenbestimmung mit dem Probeimplantat, Festlegung, ob Keel- oder Spike-Verankerung individuell für jede Endplatte, Implantation der Prothese in der Mittellinie, Röntgenkontrollen, Wundverschluss.

Weiterbehandlung

Mobilisation 6 Stunden postoperativ, stabilisierende Physiotherapie ab der 3. Woche postoperativ.

Ergebnisse

Veröffentlichte klinische und radiologische Ergebnisse decken sich mit den bereits publizierten Ergebnissen der Literatur für andere Prothesentypen. Publizierte Ergebnisse von In-vitro-Untersuchungen des Polyethylenabriebs zeigen einen signifikant niedrigeren Abrieb als bei vergleichbaren Implantattypen, was unter Umständen am Testverfahren liegen kann.

Abstract

Due to its modular design, the Activ-L total disc replacement (B. Braun/Aesculap, Tuttlingen, Germany) allows for a flexible anchoring concept either with spikes or one or two keels. It has a semiconstraint design which allows for some movement of a UHMWPE inlay. The minimal invasive surgical technique is highly standardized. Early clinical results are comparable to established disc-replacement devices.

Objective

Aim of the surgery is lasting pain relief and complete restauration of segmental mobility without affection of adjacent motion segments.

Indications

Mono- or multisegmental lumbar disc degeneration leading to low-back pain, refractory to conservative treatment.

Contraindications

Infections of vertebra or disc-space, fractures, prior fusion surgery of the affected motion segments, malignancy, osteoporosis, metabolic bone disease, severe conditions affecting general health, conditions prohibitive for anterior abdominal surgery, unclear or non-discogenic low-backpain.

Surgical Technique

Minimal-invasive anterior approach to the lumbar spine, removal of nucleus and cartilagenous endplates, sizing with trial implant, decision about spike or keel anchoring concept, implantation of prosthesis, xray-control, wound closure.

Postoperative Management

Bed-rest for 6 hours, stabilizing physiotherapy 3 weeks postoperative.

Results

Level-3 evidence shows early clinical results comparable with published data from previous implants, particle wear of inlay is significantly lower, possibly due to different testing protocols.

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Literatur

  1. Blumenthal S, McAffee P, Guyer R et al. A prospective, randomized, multicenter Food and Drug Administration Investigational device exemptions study of lumbar total disc replacement with the CHARITÉ™ artificial disc versus lumbar fusion. Part I: evaluation of clinical outcomes. Spine 2005;30:1565–1575.

    PubMed  Article  Google Scholar 

  2. Brücher D, Müller C, Garcia R et al. Initial clinical results of the activ® L lumbar total disc replacement (TDR) prosthesis: A prospective study with 1 year follow-up. Abstract/Poster Spine Arthroplasty Society, 2007.

  3. Carragee EJ, Don AS, Hurwitz EL et al. 2009 ISSLS Prize Winner: Does discography cause accelerated progression of degeneration changes in the lumbar disc: a ten-year matched cohort study. Spine 2009;34:2338–2345.

    PubMed  Article  Google Scholar 

  4. Derby R, Kim BJ, Lee SH et al. Comparison of discographic findings in asymptomatic subject discs and the negative discs of chronic LBP patients: can discography distinguish asymptomatic discs among morphologically abnormal discs? Spine J 2005;5:389–394.

    PubMed  Article  Google Scholar 

  5. Galbusera F, Bellini C, Zweig T et al. Design concepts in lumbar total disc arthroplasty. Eur Spine J 2008;17:1635–1650.

    PubMed  Article  Google Scholar 

  6. Garcia R, Yue J: Early Clinical and Radiographic Outcome with the activ® L Total Disc Replacement: Data from Two Centers in the US IDE Trial. Abstract/Poster on Spine Arthroplasty Society, 2008.

  7. Garcia R, Yue J. Prospective randomized US trial comparing an unconstrained, semi-constrained, and constrained TDR in the treatment of single level discogenic pain: radiograhic results from 2 centers in an FDA IDE Study. Abstract/Oral Presentation, Spine Arthroplasty Society, 2009.

  8. Grupp T, Yue J, Garcia R et al. Biotribological evaluation of artificial disc arthroplasty devices: Influence of loading and kinematic patterns during in vitro wear simulation; Eur Spine J 2009;18:98–108.

    PubMed  Article  Google Scholar 

  9. Leary S, Regan J, Lanman T et al. Revision and explantation strategies involving the CHARITÉ lumbar artificial disc replacement. Spine 2007;32:1001–1011.

    PubMed  Article  Google Scholar 

  10. McAfee P, Cunningham B, Holsapple G et al. A prospective, randomized, multicenter Food and Drug Administration investigational device exemption study of lumbar total disc replacement with the CHARITÉ™ artificial disc versus lumbar fusion. Part II: Evaluation of radiographic outcomes and correlation of surgical technique accuracy with clinical outcomes. Spine 2005;30:1576–1583.

    PubMed  Article  Google Scholar 

  11. McAfee P, Geisler F, Saidey S et al. Revisability of the CHARITÉ artificial disc replacement. Analysis of 688 patients enrolled in the U.S. IDE study of the CHARITÉ artificial disc. Spine 2006;31:1217–1226.

    PubMed  Article  Google Scholar 

  12. Moumene M, Geisler FH. Comparison of biomechanical function at ideal and varied surgical placement for two lumbar artificial disc implant designs: mobile-core versus fixed-core. Spine 2007;32:1840–1851.

    PubMed  Article  Google Scholar 

  13. Nabhan A, Al-Yhary A, Ishak B, et al. Analysis of spinal kinematics following implantation of lumbar spine disc prostheses versus fusion: radiological study. J Long Term Eff Med Implants. 2007;17:207–216.

    CAS  PubMed  Google Scholar 

  14. Nechtow W, Hintner M, Bushelow M, et al. Inter-vertebral disc replacement mechanical performance depends strongly on input parameters. Abstract. 52nd Orthopaedic Research Society Chicago, 2006.

  15. Rousseau MA, Bradford DS, Bertagnoli R, et al. Disc arthroplasty design influences intervertebral kinematics and facet forces. Spine J 2006;6:258–266.

    PubMed  Article  Google Scholar 

  16. Sola S, Hebecker R, Mann S, et al. Clinical evaluation of a new lumbar artificial disc (activ L). Abstract/Poster, Spine Arthroplasty Society, 2008.

  17. Yue J, Garcia R, Morreale J. Volumetric analysis of foraminal parameters following lumbar total disc replacement: A radiographic and clinical comparison of 3 biomechanical types of lumbar disc replacements: A semi-constrained device, a controlled translation device (CTD) and an unconstrained device; Abstract/Oral Presentation, Spine Arthroplasty Society, 2009.

  18. Zigler J, Delamarter R, Spivak J, et al. Results of the prospective, randomized, multicenter Food and Drug Administration investigational device exemption study of the ProDisc-L total disc replacement versus circumferential fusion for the treatment of 1-level degenerative disc disease. Spine 2007;32:1155–1162.

    PubMed  Article  Google Scholar 

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Correspondence to Karsten Wiechert.

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Zeichner: Rüdiger Himmelhan, Heidelberg

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Wiechert, K. Implantatspezifische Zugänge: Activ-L. Orthop Traumatol 22, 608–619 (2010). https://doi.org/10.1007/s00064-010-1005-3

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  • DOI: https://doi.org/10.1007/s00064-010-1005-3

Schlüsselwörter

  • Lendenwirbelsäule
  • Bandscheibenersatz
  • Activ-L
  • Operationstechnik

Key Words

  • Lumbar spine
  • Total disc replacement
  • Activ-L disc
  • Surgery