gms | German Medical Science

130. Kongress der Deutschen Gesellschaft für Chirurgie

Deutsche Gesellschaft für Chirurgie

30.04. - 03.05.2013, München

The use of ICG fluorescence microscopy in neurosurgical revision surgery – a pilot study

Meeting Abstract

  • Dirk Lindner - Klinik und Poliklinik für Neurochirurgie, Universitätsmedizin Leipzig, Leipzig
  • Jürgen Meixensberger - Klinik und Poliklinik für Neurochirurgie, Universitätsmedizin Leipzig, Leipzig
  • Alexander Hemprich - Klink für Mund-, Kiefer- und Plastische Gesichtschirurgie, Universitätsmedizin Leipzig, Leipzig
  • Dirk Halama - Klink für Mund-, Kiefer- und Plastische Gesichtschirurgie, Universitätsmedizin Leipzig, Leipzig

Deutsche Gesellschaft für Chirurgie. 130. Kongress der Deutschen Gesellschaft für Chirurgie. München, 30.04.-03.05.2013. Düsseldorf: German Medical Science GMS Publishing House; 2013. Doc13dgch283

doi: 10.3205/13dgch283, urn:nbn:de:0183-13dgch2836

Veröffentlicht: 26. April 2013

© 2013 Lindner et al.
Dieser Artikel ist ein Open Access-Artikel und steht unter den Creative Commons Lizenzbedingungen (http://creativecommons.org/licenses/by-nc-nd/3.0/deed.de). Er darf vervielfältigt, verbreitet und öffentlich zugänglich gemacht werden, vorausgesetzt dass Autor und Quelle genannt werden.


Gliederung

Text

Introduction: Fluorescence microscopy is an innovative tool for the intraoperative evaluation of perfusion in soft tissue structures and chronic inflammatory processes in bone structures. In secondary neurosurgical interventions wound closure is highly endangered by the disturbance of tissue perfusion in scar tissue. If bone sequestration occurs, this method can be supplemented by additional fluorescence microscopy within the range of 400nm.

Material and methods: ICG fluorescence microscopy was applied to three patients (0,3 mg /kg) in the range of 800nm and 400nm (OPMI Pentero, Zeiss). For the infrared video angiography ICG was administered intravenously and the following dynamic tissue perfusion was investigated during the arterial, capillary and venous phase.

Patient 1: explantation of the bone flap due to osteonecrosis and implantation of an individual plastic. Explantation with wound dehiscence, decrease of tissue perfusion in wound margin, implantation of an expander, incision planning with ICG and new skull plastic

Patient 2, craniocervical stabilisation (CerviFix), chronic inflammation process and progressive dehiscence of occiput with exposed osteosynthesis material

Patient 3: titanium implant temporo-occipital, progressive inflammation process of skin and bone in spite of antibiotic treatment

Results: In the first two cases the perfusion of the galea was evaluated and a sufficient wound closure was achieved. Patient 1 intraoperatively showed decreased tissue perfusion under the application of ICG which was macroscopicly inconspicuous (Figure 1 [Fig. 1]). After removal sufficient wound closure was achieved. The combined application of fluorescence in the range of 800nm and 400nm in the third case allowed a reliable distinction between vital and necrotic bone.

Conclusion: Fluorescence microscopy enables the intraoperative diagnosis of tissue perfusion as well as the distinction between vital and necrotic bone structures. Thus it’s essential for the planning, for intraoperative decision making and for the control of results in all interventions with critical tissue perfusion.