Tuberculosis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Pulmonary tuberculosis patients undergoing routine tracheoscopy; Gender is not limited; 18 years old <= age <=65 years old; BMI 18.5~23.9 kg/m2; ASA I~? grade; Informed consent, voluntary participation in the experiment, and the informed consent signed by the patient, approved by the hospital ethics committee.
Exclusion criteria
Exclusion criteria: If the examination time is expected to exceed 15min, if the operation is complicated or the tracheoscopy diagnosis and treatment technology is required, the laser or electrotome is required, or the blood loss is expected to be large; After full communication with the tuberculosis doctor, it is considered that the patient (intraoperative treatment may be added, etc.) is not suitable for this clinical study; Complicated with intracranial nervous system disease, intracranial hypertension, complicated with neuromuscular disease, etc.; Patients with severe communication disorders caused by severe hearing degradation; Acute or severe respiratory disease, cardiovascular disease, including but not limited to recent upper respiratory tract infection, severe or extremely severe chronic obstructive ventilation dysfunction, asthma (airway hyperresponsiveness), refractory hypoxemia, intolerance of hypercarbon dioxide, heart failure, hypertrophic cardiomyopathy, dilated cardiomyopathy, etc.; Patients with a full stomach, or with severe gastroesophageal reflux and other diseases with a high risk of aspiration; Difficult airway; Allergy to narcotic drugs; The patient refused.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of hypoxemia;Arterial blood gas tests; | — |
Secondary
| Measure | Time frame |
|---|---|
| Success rate of anesthesia;Induction time of anesthesia;Occupy operating room time;Anesthesia recovery time;Incidence of pharyngialgia; | — |
Countries
China
Contacts
The Second Hospital of Nanjing