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Patency of paediatric endotracheal tubes for airway instrumentation.
Elfgen, J; Buehler, P K; Thomas, J; Kemper, M; Imach, S; Weiss, M.
Afiliação
  • Elfgen J; Department of Anaesthesia, University Children's Hospital, Zurich, Switzerland.
  • Buehler PK; Department of Anaesthesia, University Children's Hospital, Zurich, Switzerland.
  • Thomas J; Department of Anaesthesia, University Children's Hospital, Zurich, Switzerland.
  • Kemper M; Department of Anaesthesia, University Children's Hospital, Zurich, Switzerland.
  • Imach S; Department of Anaesthesia, University Children's Hospital, Zurich, Switzerland.
  • Weiss M; Department of Anaesthesia, University Children's Hospital, Zurich, Switzerland.
Acta Anaesthesiol Scand ; 61(1): 46-52, 2017 Jan.
Article em En | MEDLINE | ID: mdl-27868188
BACKGROUND: Airway exchange catheters (AEC) and fiberoptic bronchoscopes (FOB) for tracheal intubation are selected so that there is only a minimal gap between their outer and inner diameter of endotracheal tube (ETT) to minimize the risk of impingement during airway instrumentation. This study aimed to test the ease of passage of FOBs and AECs through paediatric ETT of different sizes and from different manufacturers when using current recommendations for dimensional equipment compatibility taken from text books and manufacturers information. METHODS: Twelve different brands of cuffed and uncuffed ETT sized ID 2.5 to 5.0 mm were evaluated in an in vitro set-up. Ease of device passage as well as the locations of an impaired passage within the ETT were assessed. Redundant samples were used for same sized ETT and all measurements were triple-checked in randomized order. RESULTS: In total, 51 paired samples of uncuffed as well as cuffed paediatric ETT were tested. There were substantial differences in the ease of ETT passage concordantly for FOBs and AECs among different manufacturers, but also among the product lines from the same manufacturer for a given ID size. Restriction to passage most frequently was found near the endotracheal tube tip or as a gradually increasing resistance along the ETT shaft. CONCLUSIONS: Current recommendations for dimensional equipment compatibility AECs and FOBs with ETTs do not appear to be completely accurate for all ETT brands available. We recommend that specific equipment combinations always must be tested carefully together before attempting to use them in a patient.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Intubação Intratraqueal Tipo de estudo: Clinical_trials Limite: Child / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Intubação Intratraqueal Tipo de estudo: Clinical_trials Limite: Child / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article