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Volume 139, Issue 4, Pages 997-1000 (April 2010)


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Endobronchial tumor debulking with a flexible cryoprobe for immediate treatment of malignant stenosis

Christian Schumann, MDaCorresponding Author Informationemail address, Martin Hetzel, MDb, Alexander J. Babiak, MDb, Jürgen Hetzel, MDc, Tobias Merk, MDa, Thomas Wibmer, MDa, Philipp M. Lepper, MDd, Stefan Krüger, MDae

Received 16 March 2009; received in revised form 9 May 2009; accepted 20 June 2009. published online 28 August 2009.

Objective

In addition to use of a laser, argon plasma coagulation, electrocautery, or coring with a rigid bronchoscope, tumor debulking with a flexible cryoprobe is used for therapeutic bronchoscopy with an immediate effect for endobronchial pathologies. We performed this analysis to determine the usefulness, efficacy, and safety of the flexible cryorecanalization in a large population under routine conditions.

Methods

We identified 225 bronchoscopic interventions that were done as cryorecanalization with a flexible cryoprobe. All patients had symptomatic airway stenosis. We determined the endoscopic success rate and safety (bleeding and perforation) of the procedure.

Results

Successful cryorecanalization was achieved in 205 (91.1%) of 225 patients. The flexible cryoprobe was used with all patients, in most patients in combination with flexible bronchoscopy and only in a minority (n = 31, 13.8%) in combination with a rigid bronchoscope. Additional interventional techniques used were endobronchial stents (n = 11, 4.9%) and argon plasma coagulation (n = 37, 16.4%). Mild bleeding (if ice-cold NaCl or epinephrine solution was necessary) occurred in 9 (4.0%) patients, moderate bleeding (if argon plasma coagulation or a bronchus blocker was required) occurred in 18 (8.0%) patients, and severe bleeding (events with hemodynamic instability) never occurred.

Conclusions

Cryorecanalization with the flexible cryoprobe for treatment of symptomatic endobronchial tumor stenosis is a safe technique with a high success rate and immediate treatment effect.

CTSNet classification10, 15

a Center of Internal Medicine, Clinic of Internal Medicine II, University of Ulm, Ulm, Germany

b Clinic of Pneumology and Internal Medicine, Red Cross Hospital, Stuttgart, Germany

c Department of Internal Medicine II, University of Tübingen, Tübingen, Germany

d Department of Pneumology, University Hospital of Bern (Inselspital) and University of Bern, Bern, Switzerland

e Medical Clinic I, University Clinic Aachen, Aachen, Germany

Corresponding Author InformationAddress for reprints: Christian Schumann, MD, University of Ulm, Clinic of Internal Medicine II, Albert-Einstein-Allee 23, 89081 Ulm, Germany.

 Disclosures: M.H., A.J.B., and J.H. report lecture fees from ERBE, the manufacturer of the cryoprobe.

 C.S., M.H., and J.H contributed equally to this article.

PII: S0022-5223(09)00877-0

doi:10.1016/j.jtcvs.2009.06.023


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