Z Gastroenterol 2011; 49(12): 1529-1534
DOI: 10.1055/s-0031-1282025
Originalarbeit
© Georg Thieme Verlag KG Stuttgart · New York

Probe-based Confocal Laser Endomicroscopy in Double Balloon Enteroscopy

Sondenbasierte Endomikroskopie während der Doppelballonenteroskopie
S. Miehlke
1   Center for Digestive Diseases, Cooperation of Internal Medicine, Hamburg, Germany
,
A. Morgner
2   Strategic Management, University Hospital, Dresden, Germany
,
D. Aust
3   Institute for Pathology, University Hospital, Dresden, Germany
,
G. Baretton
3   Institute for Pathology, University Hospital, Dresden, Germany
,
A. Madisch
4   Department of Internal Medicine, Siloah Hospital, Hannover, Germany
› Author Affiliations
Further Information

Publication History

14 June 2011

09 October 2011

Publication Date:
02 December 2011 (online)

Zusammenfassung

Hintergrund: Die sondenbasierte konfokale Endomikroskopie (pCLE) erlaubt die Darstellung der gastrointestinalen Mukosaarchitektur während der Endoskopie. Wir untersuchten die Machbarkeit und Sicherheit der pCLE während der Doppelballonenteoskopie (DBE).
Methoden: Während der DBE (Fujinon EN-450P5) wurde die pCLE (Cellvizio-GI®, Mauna Kea Technologies) nach intravenöser Injektion von 5–10 ml Fluorescein 1 % mit einer 1,8 mm dünnen Sonde (GastroFlex/ColoFlex Z-probe) am tiefsten Punkt der DBE-Insertion und im Fall einer pathologischen Läsion durchgeführt. Der primäre Endpunkt war technischer Erfolg der pCLE, definiert als (i) erfolgreicher Vorschub der Sonde am tiefsten Punkt der DBE-Insertion und (ii) erfolgreiche endomikroskopische Darstellung der intestinalen Mukosa. Sekundärer Endpunkt war die Sicherheit der pCLE.
Ergebnisse: Bei 16 Patienten wurden 27 DBE-Prozeduren (14 antegrad) durchgeführt. Die mittleren Insertionstiefen betrugen 255 cm für die antegrade und 130 cm für die retrograde DBE. Der technische Erfolg der pCLE betrug 96,3 % (antegrad 92,8 %, retrograd 100 %). Es traten keine pCLE-bedingten Nebenwirkungen auf. Die endomikroskopische Darstellung der Dünndarmmukosa gelang in allen Fällen. Pathologische Befunde wie Zottenatrophie, Kryptenhyperplasie, fortgeschrittene Neoplasie oder entzündliche Läsionen konnten erfolgreich dargestellt werden.
Schlussfolgerung: Die Studie demonstriert erstmals die Machbarkeit und Sicherheit der pCLE im Rahmen der Doppelballon-Enteroskopie. Weitere Studien sind wünschenswert, um den klinische Nutzen der pCLE in der Diagnostik von Dünndarmerkrankungen zu evaluieren.

Abstract

Background: Probe-based confocal laser endomicroscopy (pCLE) allows in-vivo assessment of the gastrointestinal mucosal architecture during ongoing endoscopy. We investigated the feasibility and safety of pCLE during double balloon enteroscopy (DBE).
Methods: DBE was performed using the Fujinon EN-450P5. pCLE (Cellvizio-GI®, Mauna Kea Technologies) was performed after intravenous injection of 5–10 mL fluorescein 1 % using a 1.8-mm probe (GastroFlex/ColoFlex Z-probe) at the deepest point of DBE insertion and in case of any pathological lesion. Primary outcome measure was technical success, defined as (i) successful advancement of the probe at the deepest DBE insertion and (ii) successful pCLE imaging of the intestinal mucosa. Secondary outcome was safety of the pCLE procedure.
Results: 27 DBE procedures (14 antegrade) were performed in 16 patients. The mean depth of small bowel insertion was 255 cm for antegrade and 130 cm for retrograde DBE. Technical success of pCLE was achieved in 96.3 % (antegrade 92.8 %, retrograde 100 %). One technical failure occurred (incomplete probe advancement). There were no adverse events related to the pCLE procedure. pCLE imaging of the small bowel mucosal architecture was possible in all cases. Pathological conditions within the small bowel such as loss of villi, crypt hyperplasia, advanced neoplasia, or increased blood flow due to inflammation tissue could be successful visualized.
Conclusion: This study is the first to demonstrate successful and safe application of pCLE in the deep small bowel during double balloon enteroscopy. Further studies are needed to determine the clinical benefit of pCLE in the management of patients with small bowel diseases.

 
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