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| Name | Class |
|---|---|
| Fu Jen Catholic University | OTHER |
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The purpose of this study is to assess the efficacy of Heated Humidified High-Flow Nasal Cannula compared with noninvasive positive-pressure ventilation in the prevention of extubation failure in patients with prolonged mechanical ventilation.
There have been many clinical trials comparing the role of Heated Humidified High-Flow Nasal Cannula or Noninvasive positive pressure ventilation in the prevention of extubation failure.
These review all have similar results summarized here:
Compared with Noninvasive positive pressure ventilation, Heated Humidified High-Flow Nasal Cannula provides better patient comfort, fewer oxygen desaturation episodes, lower likelihood of interface displacement, and, lower reintubation rate than Noninvasive positive pressure ventilation.
However, most of these clinical trials focused on participants experiencing acute respiratory failure.
Investigators of this study want to find something difference between oh these two groups.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Noninvasive Ventilation group | Experimental | Noninvasive Ventilation group initial setting: Insp. Pressure:12 ~ 16 centimeter of water Exp. Pressure : 4 ~ 6 centimeter of water FiO2:Keep oxygen saturation measured by pulse oximeter:> 92% By condition, gradually tap 2~3 centimeter of water inspiratory positive airway pressure Keep Tidal volume:6~10 ml/kg |
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| Heated Humidified High-Flow Nasal Cannula group | Active Comparator | Heated Humidified High-Flow Nasal Cannula group initial setting: Flow setting: 50 L/m FiO2:Keep oxygen saturation measured by pulse oximeter > 92% temperature:37 ℃ By condition, gradually tap Flow 5 L/m |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Heated Humidified High-Flow Nasal Cannula | Device | Participants using of invasive ventilator more than 14 days, maybe considered transferred to the Respiratory Care Center(RCC), participants enrolled to this study and also written informed consent from participants or their family; After extubation, the difficult weaning patients were allocated to two treatment groups, and randomly assigned to Heated Humidified High-Flow Nasal Cannula or Noninvasive Ventilation devices. |
| Measure | Description | Time Frame |
|---|---|---|
| Re-intubation rate | Any placement of an endotracheal tube for any indication within 72 hours of extubation, censored at the first of hospital discharge or 72 hours after extubation. | within 72 hours of extubation |
| Measure | Description | Time Frame |
|---|---|---|
| Mortality rate | Mortality rate, or death rate is a measure of the number of deaths | up to 3 months |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Chen-Chun Lin, MD | Shin Kong Wu Ho-Su Memorial Hospital | Study Chair |
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| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 36949116 | Derived | Tseng CW, Chao KY, Wu HL, Lin CC, Hsu HS. Effectiveness of high-flow nasal cannulae compared with noninvasive positive-pressure ventilation in preventing reintubation in patients receiving prolonged mechanical ventilation. Sci Rep. 2023 Mar 22;13(1):4689. doi: 10.1038/s41598-023-31444-8. |
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| ID | Term |
|---|---|
| D063087 | Noninvasive Ventilation |
| ID | Term |
|---|---|
| D012121 | Respiration, Artificial |
| D058109 | Airway Management |
| D013812 | Therapeutics |
| D012138 | Respiratory Therapy |
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