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A study on respiratory management in acute postoperative period by nasal high flow for patients undergoing surgery under general anesthesia

In head and neck surgery where the oropharyngeal area is the operative field, postoperative respiratory depression and upper airway obstruction are common. Therefore, supplemental oxygen is administered to prevent severe postoperative early hypoxemia. However, a high concentration of oxygen increase...

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Detalles Bibliográficos
Autores principales: Kurata, Shinji, Mishima, Gaku, Sekino, Motohiro, Sato, Shuntaro, Pinkham, Maximilian, Tatkov, Stanislav, Ayuse, Takao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7402890/
https://www.ncbi.nlm.nih.gov/pubmed/32756204
http://dx.doi.org/10.1097/MD.0000000000021537
Descripción
Sumario:In head and neck surgery where the oropharyngeal area is the operative field, postoperative respiratory depression and upper airway obstruction are common. Therefore, supplemental oxygen is administered to prevent severe postoperative early hypoxemia. However, a high concentration of oxygen increases the likelihood of secondary complications, such as carbon dioxide (CO(2)) narcosis. Nasal high-flow (NHF) therapy generates high flows (≤60 L/min) of heated and humidified gas delivered via nasal cannula and provides respiratory support by generating positive airway pressure, clearance of dead space and reduction of work of breathing. This study aims to determine whether the postoperative hypoxemia and hypercapnia can be prevented by NHF without the requirement of supplemental oxygen. The study will recruit adult patients undergoing planned oral surgery under general anesthesia at Nagasaki University Hospital. It is a randomized parallel group comparative study with 3 groups: NHF with room air only and no supplemental oxygen, no respiratory support, and face mask oxygen administration. The study protocol will begin at the time that the patient is returned to the general ward and will finish 3 hours later. The primary endpoint is the time-weighted average of transcutaneous O(2) over the 180 minutes and secondary endpoints are the time-weighted average of transcutaneous CO(2) (tcpCO(2)), SpO(2), and respiratory rate, incidence rate of marked hypercapnia (tcpCO(2) ≥60 mm Hg for 5 minutes or longer), incidence rate of moderate hypercapnia (tcpCO(2) ≥50 mm Hg for 5 minutes or longer) and the percentage of time that SpO(2) is <90%. Included also is a group in which the postoperative management is performed only by spontaneous breathing without performing respiratory support such as oxygen administration, to investigate the efficacy and necessity of conventional oxygen administration. This exploratory study will investigate the use of NHF without supplemental oxygen as an effective respiratory support during the acute postoperative period. TRIAL REGISTRATION: The study was registered the jRCTs072200018. URL https://jrct.niph.go.jp/latest-detail/jRCTs072200018