| Literature DB >> 35634054 |
Yunjiao Sheng1, Yang Li2, Ting Feng3.
Abstract
Objective: The main objective is to investigate the effect of Yifei-Huoxue decoction combined with tiotropium on the inflammatory cytokine levels, pulmonary function, and quality of life in patients with chronic obstructive pulmonary disease (COPD).Entities:
Mesh:
Substances:
Year: 2022 PMID: 35634054 PMCID: PMC9135534 DOI: 10.1155/2022/5740181
Source DB: PubMed Journal: Comput Intell Neurosci
Comparison of the general data (n = 49).
| Observed indexes | Reference group | Study group | X2/ |
|
|---|---|---|---|---|
| Age (years old) | 64.72 ± 6.08 | 65.13 ± 6.15 | 0.332 | 0.741 |
| BMI (kg/m2) | 23.12 ± 3.01 | 23.24 ± 2.85 | 0.203 | 0.840 |
| Course of disease (years) | 9.05 ± 3.26 | 9.17 ± 3.15 | 0.185 | 0.853 |
| Sex | ||||
| Male | 29 (59.18) | 31 (63.27) | 0.172 | 0.678 |
| Female | 20 (40.82) | 18 (36.73) | ||
| Smoker | 23 (46.94) | 22 (44.90) | 0.041 | 0.839 |
| Drinker | 25 (51.02) | 24 (48.98) | 0.041 | 0.840 |
| Education level | ||||
| Under junior high school | 21 (42.86) | 19 (38.78) | 0.169 | 0.681 |
| Junior high school | 16 (32.65) | 17 (34.69) | 0.046 | 0.831 |
| Above junior high school | 12 (24.49) | 13 (26.53) | 0.054 | 0.817 |
| Place of residence | ||||
| Urban areas | 31 (63.27) | 33 (67.35) | 0.180 | 0.671 |
| Rural areas | 18 (36.73) | 16 (32.65) | ||
Patients' inflammatory cytokine levels.
| Observed indexes | Reference group ( | Study group ( |
|
| |
|---|---|---|---|---|---|
| TNF- | Before treatment | 34.22 ± 3.17 | 34.56 ± 3.20 | 0.528 | 0.599 |
| After treatment | 29.45 ± 2.17 | 25.94 ± 2.15 | 8.043 | <0.001 | |
|
| |||||
| CRP (mg/L) | Before treatment | 7.12 ± 0.85 | 7.10 ± 0.84 | 0.117 | 0.907 |
| After treatment | 4.88 ± 0.52 | 3.46 ± 0.51 | 13.647 | <0.001 | |
|
| |||||
| IL-6 (ng/L) | Before treatment | 70.85 ± 4.73 | 70.52 ± 4.52 | 0.353 | 0.725 |
| After treatment | 51.06 ± 3.34 | 26.75 ± 3.29 | 36.291 | <0.001 | |
Patients' pulmonary function indexes.
| Observed indexes | Reference group ( | Study group ( |
|
| |
|---|---|---|---|---|---|
| FVC (L) | Before treatment | 2.16 ± 0.22 | 2.14 ± 0.20 | 0.471 | 0.639 |
| After treatment | 2.50 ± 0.21 | 2.75 ± 0.24 | 5.488 | <0.001 | |
|
| |||||
| FEV1 (L) | Before treatment | 1.26 ± 0.29 | 1.25 ± 0.31 | 0.165 | 0.869 |
| After treatment | 1.55 ± 0.34 | 1.86 ± 0.32 | 4.678 | <0.001 | |
|
| |||||
| FEV1/FVC (%) | Before treatment | 55.33 ± 4.62 | 55.51 ± 4.58 | 0.194 | 0.847 |
| After treatment | 60.82 ± 5.11 | 74.10 ± 5.20 | 12.751 | <0.001 | |
Patients' ESR levels (mm/h).
| Group |
| Before treatment | After treatment |
|---|---|---|---|
| Reference group | 49 | 78.83 ± 7.25 | 60.17 ± 6.79 |
| Study group | 49 | 78.49 ± 7.17 | 37.65 ± 6.92 |
|
| 0.233 | 16.267 | |
|
| 0.816 | <0.001 |
Figure 1Patients' SF-36 scores.