Journal of Traditional Chinese Medicine ›› 2026, Vol. 46 ›› Issue (1): 195-204.DOI: 10.19852/j.cnki.jtcm.2026.01.018
• Original Articles • Previous Articles Next Articles
XU Huanfang1, LI Jiashan1, YANG Li1, WU Wenzhong2, YANG Jun3, ZHANG Wei4, LI Hui5, QU Nini, WANG Rui7, WANG Landi8, YANG Hongzhi9, ZHANG Lihua10, HE Yong11, XIONG Guanyu12, LIU Baoyan13(
), FANG Yigong1(
)
Received:2024-11-27
Accepted:2025-06-09
Online:2026-02-15
Published:2026-01-28
Contact:
Prof. FANG Yigong, Acupuncture and Moxibustion Hospital, Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing 100700, China. About author:Supported by:XU Huanfang, LI Jiashan, YANG Li, WU Wenzhong, YANG Jun, ZHANG Wei, LI Hui, QU Nini, WANG Rui, WANG Landi, YANG Hongzhi, ZHANG Lihua, HE Yong, XIONG Guanyu, LIU Baoyan, FANG Yigong. Effect of point application therapy for bronchial asthma: a multicenter randomized controlled trial[J]. Journal of Traditional Chinese Medicine, 2026, 46(1): 195-204.
| Characteristic | PAT (n = 418) | Placebo PAT (n = 417) |
|---|---|---|
| Female Sex [n (%)] | 257 (61.48) | 253 (64.99) |
| Age ($\bar{x} \pm s$, years) | 52.5±12.5 | 52.7±12.6 |
| Smoker [n (%)] | 63 (15.07) | 77 (18.47) |
| Duration of disease ($\bar{x} \pm s$, years) | 10.4±6.1 | 10.1±6.0 |
| Patients with comorbidities [n (%)] | 46 (11.08) | 45 (10.87) |
| Number of asthma exacerbation [median (Q1, Q3)] | 4.00 (2.00, 7.00) | 4.00 (2.00, 8.00) |
| Severity of asthma exacerbation [n (%)]a | ||
| Mild | 1718 (77.04) | 1654 (75.42) |
| Moderate | 436 (19.55) | 451 (20.57) |
| Severe | 76 (3.41) | 88 (4.01) |
| Lung function | ||
| FEV1%pred ($\bar{x} \pm s$, %) | 74.4±23.4 | 73.1±23.4 |
| FEV1/FVC ($\bar{x} \pm s$) | 70.4±15.5 | 68.3±15.4 |
| PEF ($\bar{x} \pm s$, L/s) | 4.1±2.8 | 3.8±2.5 |
| ACT score ($\bar{x} \pm s$) | 20.5±3.0 | 20.6±2.9 |
| Patients using reliever medications [n (%)] | 355 (84.93) | 334 (80.10) |
| Use of reliever [n (%)] | ||
| Corticosteroids | 235 (56.22) | 242 (58.03) |
| β2 receptor agonist | 224 (53.59) | 228 (54.68) |
| Others | 69 (16.51) | 75 (17.99) |
| AEs [n (%)] | 20 (4.78) | 20 (4.80) |
Table 1 Baseline characteristics of the participants
| Characteristic | PAT (n = 418) | Placebo PAT (n = 417) |
|---|---|---|
| Female Sex [n (%)] | 257 (61.48) | 253 (64.99) |
| Age ($\bar{x} \pm s$, years) | 52.5±12.5 | 52.7±12.6 |
| Smoker [n (%)] | 63 (15.07) | 77 (18.47) |
| Duration of disease ($\bar{x} \pm s$, years) | 10.4±6.1 | 10.1±6.0 |
| Patients with comorbidities [n (%)] | 46 (11.08) | 45 (10.87) |
| Number of asthma exacerbation [median (Q1, Q3)] | 4.00 (2.00, 7.00) | 4.00 (2.00, 8.00) |
| Severity of asthma exacerbation [n (%)]a | ||
| Mild | 1718 (77.04) | 1654 (75.42) |
| Moderate | 436 (19.55) | 451 (20.57) |
| Severe | 76 (3.41) | 88 (4.01) |
| Lung function | ||
| FEV1%pred ($\bar{x} \pm s$, %) | 74.4±23.4 | 73.1±23.4 |
| FEV1/FVC ($\bar{x} \pm s$) | 70.4±15.5 | 68.3±15.4 |
| PEF ($\bar{x} \pm s$, L/s) | 4.1±2.8 | 3.8±2.5 |
| ACT score ($\bar{x} \pm s$) | 20.5±3.0 | 20.6±2.9 |
| Patients using reliever medications [n (%)] | 355 (84.93) | 334 (80.10) |
| Use of reliever [n (%)] | ||
| Corticosteroids | 235 (56.22) | 242 (58.03) |
| β2 receptor agonist | 224 (53.59) | 228 (54.68) |
| Others | 69 (16.51) | 75 (17.99) |
| AEs [n (%)] | 20 (4.78) | 20 (4.80) |
| Variable | PAT | Placebo PAT | P value |
|---|---|---|---|
| 12 months | 0.062 | ||
| Mild | 630 (79.85) | (75.51) | |
| Moderate | 148 (18.76) | 217 (22.14) | |
| Severe | 11 (1.39) | 23 (2.35) | |
| 24 months | < 0.001 | ||
| Mild | 473 (85.53) | (74.56) | |
| Moderate | 68 (12.30) | 171 (23.01) | |
| Severe | 12 (2.17) | 18 (2.42) |
Table 2 Severity of asthma exacerbations [n (%)]
| Variable | PAT | Placebo PAT | P value |
|---|---|---|---|
| 12 months | 0.062 | ||
| Mild | 630 (79.85) | (75.51) | |
| Moderate | 148 (18.76) | 217 (22.14) | |
| Severe | 11 (1.39) | 23 (2.35) | |
| 24 months | < 0.001 | ||
| Mild | 473 (85.53) | (74.56) | |
| Moderate | 68 (12.30) | 171 (23.01) | |
| Severe | 12 (2.17) | 18 (2.42) |
| Variable | PAT (n = 418) | Placebo PAT (n = 417) | Difference (95% CI) | P value |
|---|---|---|---|---|
| FEV1%pred ($\bar{x} \pm s$, %) | ||||
| 12 months | 76.5±20.4 | 73.3±23.9 | 2.92 (-0.79, 6.23) | 0.120 |
| 24 months | 76.4±18.7 | 73.4±23.0 | 3.05 (-0.35, 6.45) | 0.039 |
| FEV1/FVC ($\bar{x} \pm s$, %) | ||||
| 12 months | 71.6±15.8 | 67.8±15.6 | 4.11 (1.76, 6.47) | 0.001 |
| 24 months | 77.2±16.7 | 72.2±18.1 | 4.61 (1.72, 7.51) | 0.001 |
| PEF ($\bar{x} \pm s$, L/s) | ||||
| 12 months | 4.2±2.8 | 4.2±2.7 | -0.03 (-0.37, 0.30) | 0.755 |
| 24 months | 4.2±2.7 | 4.07±2.6 | 0.25 (-0.09, 0.58) | 0.645 |
| ACT score ($\bar{x} \pm s$) | ||||
| 12 months | 21.7±2.4 | 21.5±2.3 | 0.26 (-0.05, 0.58) | 0.269 |
| 24 months | 22.1±2.2 | 21.5±2.5 | 0.60 (0.33, 0.87) | 0.005 |
| Patients using reliever medications [n (%)] | ||||
| 12 months | 186 (44.50) | 218 (52.28) | 0.024 | |
| 24 months | 159 (38.04) | 175 (41.97) | 0.037 | |
| Use of relievera [n (%)] | ||||
| 12 months | ||||
| Corticosteroid | 109 (26.08) | 129 (30.94) | 0.050 | |
| β2 receptor agonist | 109 (26.08) | 137 (32.85) | ||
| Others | 56 (13.40) | 75 (17.99) | ||
| 24 months | ||||
| Corticosteroid | 91 (21.78) | 105 (25.18) | 0.039 | |
| β2 receptor agonist | 91 (21.78) | 109 (26.14) | ||
| Others | 38 (9.10) | 41 (9.83) | ||
| Blindness assessmentb [n (%)] | ||||
| Yes | 28 (75.67) | 25 (67.56) | 0.688 | |
| No | 3 (8.11) | 5 (13.51) | ||
| Unknown | 6 (16.22) | 7 (18.92) | ||
Table 3 Other secondary outcomes
| Variable | PAT (n = 418) | Placebo PAT (n = 417) | Difference (95% CI) | P value |
|---|---|---|---|---|
| FEV1%pred ($\bar{x} \pm s$, %) | ||||
| 12 months | 76.5±20.4 | 73.3±23.9 | 2.92 (-0.79, 6.23) | 0.120 |
| 24 months | 76.4±18.7 | 73.4±23.0 | 3.05 (-0.35, 6.45) | 0.039 |
| FEV1/FVC ($\bar{x} \pm s$, %) | ||||
| 12 months | 71.6±15.8 | 67.8±15.6 | 4.11 (1.76, 6.47) | 0.001 |
| 24 months | 77.2±16.7 | 72.2±18.1 | 4.61 (1.72, 7.51) | 0.001 |
| PEF ($\bar{x} \pm s$, L/s) | ||||
| 12 months | 4.2±2.8 | 4.2±2.7 | -0.03 (-0.37, 0.30) | 0.755 |
| 24 months | 4.2±2.7 | 4.07±2.6 | 0.25 (-0.09, 0.58) | 0.645 |
| ACT score ($\bar{x} \pm s$) | ||||
| 12 months | 21.7±2.4 | 21.5±2.3 | 0.26 (-0.05, 0.58) | 0.269 |
| 24 months | 22.1±2.2 | 21.5±2.5 | 0.60 (0.33, 0.87) | 0.005 |
| Patients using reliever medications [n (%)] | ||||
| 12 months | 186 (44.50) | 218 (52.28) | 0.024 | |
| 24 months | 159 (38.04) | 175 (41.97) | 0.037 | |
| Use of relievera [n (%)] | ||||
| 12 months | ||||
| Corticosteroid | 109 (26.08) | 129 (30.94) | 0.050 | |
| β2 receptor agonist | 109 (26.08) | 137 (32.85) | ||
| Others | 56 (13.40) | 75 (17.99) | ||
| 24 months | ||||
| Corticosteroid | 91 (21.78) | 105 (25.18) | 0.039 | |
| β2 receptor agonist | 91 (21.78) | 109 (26.14) | ||
| Others | 38 (9.10) | 41 (9.83) | ||
| Blindness assessmentb [n (%)] | ||||
| Yes | 28 (75.67) | 25 (67.56) | 0.688 | |
| No | 3 (8.11) | 5 (13.51) | ||
| Unknown | 6 (16.22) | 7 (18.92) | ||
| AEsa | PAT (n = 418) | Placebo PAT (n = 417) |
|---|---|---|
| Totalb | 81 (19.4) | 21 (5) |
| SAEs | 0 | 0 |
| Blister | 3 (0.7) | 4 (1.0) |
| Asthma aggravation | 3 (0.7) | 1 (0.2) |
| Cough | 1 (0.2) | 2 (0.5) |
| Skin allergyb | 74 (17.7) | 14 (3.4) |
Table 4 Treatment-related AEs [n (%)]
| AEsa | PAT (n = 418) | Placebo PAT (n = 417) |
|---|---|---|
| Totalb | 81 (19.4) | 21 (5) |
| SAEs | 0 | 0 |
| Blister | 3 (0.7) | 4 (1.0) |
| Asthma aggravation | 3 (0.7) | 1 (0.2) |
| Cough | 1 (0.2) | 2 (0.5) |
| Skin allergyb | 74 (17.7) | 14 (3.4) |
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