Chronic obstructive pulmonary emphysema
Conditions
Interventions
Experimental group and control group:NO
Sponsors
Fuling Central Hospital of Chongqing
Eligibility
Sex/Gender
All
Age
40 Years to 70 Years
Inclusion criteria
Inclusion criteria: 1. The patients volunteered to participate in the study and signed the informed consent; 2. The diagnosis of COPD in the observation group was clear, but not in the control group; 3. Those aged 40-70 years, with cardiac function grades I-II and ASA II-III, without long-term smoking history or quitting smoking for more than 5 years; (4) The operation time was less than 4 hours and the bleeding was less than 100 ml.
Exclusion criteria
Exclusion criteria: 1. Sinusitis, allergic diseases, sleep apnea syndrome; 2. Stroke history, psychosis, epilepsy, Parkinson's disease history, MMSE 11.1 mmol/L); (2) Patients with acute myocardial infarction within 1 month; (3) According to the New York Heart Association (NYHA) classification, cardiac function (> III); 5. unable to communicate accurately with words.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Exhaled nitric oxide; | — |
Secondary
| Measure | Time frame |
|---|---|
| pulmonary function;Serum inflammatory blood markers; | — |
Countries
China
Contacts
Public ContactKeyu He
Fuling Central Hospital of Chongqing
Outcome results
None listed