Schroeder JB, Marian T, Muhle P, Claus I, Thomas C, Ruck T, Wiendl H, Warnecke T, Suntrup-Krueger S, Meuth S, Dziewas R
Forschungsartikel (Zeitschrift) | Peer reviewedIntroduction: Although patients with Guillain–Barré syndrome frequently require orotracheal intubation and tracheostomy, the incidence and relevance of neurogenic dysphagia prior to intubation and risk factors for prolonged requirement for a tracheal cannula have not yet been identified. Methods: Retrospective analysis of the medical records of 88 patients was performed. Clinical characteristics were compared between intubated and nonintubated patients and between immediately decannulated and not immediately decannulated patients. Results: Thirty-five (39.7%) patients required tracheostomy. Neuromuscular weakness and related respiratory insufficiency were the main reasons for intubation. In the subgroup of tracheotomized patients, immediate decannulation after completed respiratory weaning was possible in 14 (40%) patients. The severity of dysphagia, in particular pharyngolaryngeal hypesthesia, was related to the length of cannulation. Discussion: Respiratory muscle weakness is the main reason for intubation, whereas neurogenic dysphagia is the main risk factor for persisting cannulation. Dysphagia after weaning is most frequently characterized by severe laryngeal sensory deficit.
| Claus, Inga | Klinik für Neurologie |
| Dziewas, Rainer | Klinik für Neurologie |
| Marian, Thomas | Klinik für Neurologie |
| Meuth, Sven | Klinik für Neurologie |
| Muhle, Paul | Klinik für Neurologie |
| Ruck, Tobias | Klinik für Neurologie |
| Schröder, Jens Burchard | Klinik für Neurologie |
| Suntrup-Krüger, Sonja | Klinik für Neurologie |
| Thomas, Christian | Institut für Neuropathologie |
| Warnecke, Tobias | Klinik für Neurologie |
| Wiendl, Heinz Siegfried | Klinik für Neurologie |