Studies have shown that intravenous infusion and nebulized dexmedetomidine can improve lung function in mechanically ventilated patients, including those with preoperative COPD, exerting lung protection. However, these studies are based on mechanical ventilation patients under general anesthesia, and more intuitive research is needed on whether dexmedetomidine can also exercise pulmonary precaution in awake patients. Pulmonary function monitoring is the most direct way to evaluate changes in lung function in awake patients. Portable pulmonary function machines can assess lung function in a variety of settings. In addition, compared with intravenous administration, nebulized inhalation administration directly acts on the mucosa of the respiratory tract, does not involve invasive operations, and has higher safety and comfort. Therefore, this study intends to use portable pulmonary function instruments and non-invasive ambulatory respiratory monitors to evaluate the effect of nebulized dexmedetomidine on lung function in COPD patients to guide the perioperative management of COPD patients.
Chronic obstructive pulmonary disease (COPD) is a common respiratory disease that seriously endangers the physical and mental health of patients. Surgical patients with COPD will increase the risk of postoperative pulmonary complications and the risk of complications of extrapulmonary organs such as heart and kidney, and lead to prolonged hospital stay, increased medical costs, and increased perioperative mortality. Therefore, it is necessary to explore drugs with lung protection effects to improve the perioperative safety of COPD patients. Dexmedetomidine (Dex) is a new type of highly selective α2-adrenergic receptor agonist, which has the effects of sedative-hypnotic, anti-inflammatory, stress reduction, hemodynamic stabilization, analgesia, and organ protection, and has little inhibitory effect on respiratory function. In recent years, studies have found that dexmedetomidine may have the effect of improving lung function. In addition, human studies have found that intravenous infusion of dexmedetomidine (loading dose 0.5 to 1 μg/kg or 0.5 to 0.7 μg/kg/hour) can reduce inflammation levels, improve oxidative stress, reduce plateau pressure, peak airway pressure, airway resistance, and improve lung compliance, thereby improving oxygenation and postoperative pulmonary complications, and promoting patient recovery. In obese patients undergoing laparoscopic gastric reduction, intraoperative intravenous dexmedetomidine infusion (loading dose of 1 μg/kg, followed by 1 μg/kg/hour) improves lung compliance and oxygenation. One study found that intraoperative intravenous infusion of dexmedetomidine (loading dose of 1 μg/kg, followed by 0.5 μg/kg/hour) increased forced expiratory volume in one second and improved postoperative oxygenation on days 1 and 2 after one-lung ventilation. Another study found that nebulized inhalation of 0.5 μg/kg, 1 μg/kg, and 2 μg/kg dexmedetomidine in one-lung ventilation for thoracic surgery improved lung compliance and oxygenation. These studies have shown that intravenous infusion and nebulized dexmedetomidine can improve lung function in mechanically ventilated patients, including those with preoperative COPD, exerting lung protection. However, these studies are based on mechanical ventilation patients under general anesthesia, and more intuitive research is needed on whether dexmedetomidine can also exercise pulmonary precaution in awake patients. Pulmonary function monitoring is the most direct way to evaluate changes in lung function in awake patients. Portable pulmonary function machines can assess lung function in a variety of settings. In addition, compared with intravenous administration, nebulized inhalation administration directly acts on the mucosa of the respiratory tract, does not involve invasive operations, has limited effect, high safety, fewer side effects, and higher comfort. Therefore, this study intends to use portable pulmonary function instruments and non-invasive ambulatory respiratory monitors to evaluate the effect of nebulized dexmedetomidine on lung function in COPD patients to guide the perioperative management of COPD patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
6
Participants inhale the atomized 0.5 μg/kg dexmedetomidine in 2 ml of 0.9% saline.
Participants inhale the atomized 1 μg/kg dexmedetomidine in 2 ml of 0.9% saline.
Participants inhale atomized 2 ml 0.9% saline.
The Second Affiliated Hospital of Chongqing Medical University
Chongqing, Chongqing Municipality, China
FVC
Forced vital capacity
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
FEV1
Forced expiratory volume in one second
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
FEV1/FVC%
Forced expiratory volume in one second/Forced vital capacity
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
MMEF
maximal mid-expiratory flow curve
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
PEF
Peak expiratory flow
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
BEV
Back-extrapolation volume
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
FET
Forced expiratory time
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
VC
Vital capacity
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
FEV1/VC
Forced expiratory volume in one second/vital capacity
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
FEF25%,FEF50%,FEF75%,
forced expiratory flow at 25%, 50%, and 75% of FVC exhaled
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
PIF
peak inspiratory flow
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
FIVC
forced inspiratory vital capacity
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
FIF25, FIF50, FIF75
forced inspiratory flow at 25%, 50%, and 75% of FIVC
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
FIV1
forced inspiratory volume in 1 second
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
MVV
maximal ventilatory volume
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
Richmond Agitation-Sedation Scale (RASS)
RASS is a 10-point scale, with four levels of anxiety or agitation (+1 to +4 \[combative\]), one level to denote a calm and alert state (0), and 5 levels of sedation (-1 to -5) culminating in unarousable (-5).
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
heart rate
heart rate (beat per min)
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
Systolic and diastolic blood pressures
Systolic and diastolic blood pressures (mmHg)
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
SPO2
Pulse oximetry (SpO2)
Time frame: 10 minutes and 30 minutes after administration of nebulized drugs
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