TY - JOUR
T1 - Acupoint Transcutaneous Electrical Nerve Stimulation in Hospitalized COPD Patients with Severe Dyspnoea
T2 - A Randomized Controlled Trial
AU - Fernández-Jané, Carles
AU - Vilaró, Jordi
AU - Costa-Tutusaus, Lluís
N1 - Publisher Copyright:
© The Author(s) 2023.
PY - 2023/1/1
Y1 - 2023/1/1
N2 - OBJECTIVE: To evaluate the effect of acupuncture transcutaneous electrical nerve stimulation (acuTENS) on the reduction of dyspnoea during acute exacerbation of chronic obstructive pulmonary disease (AECOPD). METHODS: A multicentric randomized control trial with masked patients and evaluators was carried out. During hospitalization, AECOPD patients received 45 min of acuTENS (experimental group) or sham acuTENS (controls) daily on 5 consecutive days. The trial was conducted at the Hospital del Mar, Barcelona, and Hospital Sant Joan de Déu, Manresa (both in Spain). Dyspnoea and peak expiratory flow were measured daily from the first to fifth days. Length of stay, readmissions at 3 months and adverse events were also analysed. RESULTS: Finally, 19 patients with moderately to severely exacerbated COPD were included. Although some tendencies in dyspnoea during day 1 and length of hospital stay were found favouring acupuncture, no significant differences were shown between groups. CONCLUSIONS: The acuTENS intervention was feasible#well tolerated in AECOPD patients and no important side effects were reported.
AB - OBJECTIVE: To evaluate the effect of acupuncture transcutaneous electrical nerve stimulation (acuTENS) on the reduction of dyspnoea during acute exacerbation of chronic obstructive pulmonary disease (AECOPD). METHODS: A multicentric randomized control trial with masked patients and evaluators was carried out. During hospitalization, AECOPD patients received 45 min of acuTENS (experimental group) or sham acuTENS (controls) daily on 5 consecutive days. The trial was conducted at the Hospital del Mar, Barcelona, and Hospital Sant Joan de Déu, Manresa (both in Spain). Dyspnoea and peak expiratory flow were measured daily from the first to fifth days. Length of stay, readmissions at 3 months and adverse events were also analysed. RESULTS: Finally, 19 patients with moderately to severely exacerbated COPD were included. Although some tendencies in dyspnoea during day 1 and length of hospital stay were found favouring acupuncture, no significant differences were shown between groups. CONCLUSIONS: The acuTENS intervention was feasible#well tolerated in AECOPD patients and no important side effects were reported.
KW - Acupuncture therapy
KW - Aecopd
KW - Dyspnoea
KW - acuTENS
UR - http://www.scopus.com/inward/record.url?scp=85169766188&partnerID=8YFLogxK
U2 - 10.1177/2515690X231198308
DO - 10.1177/2515690X231198308
M3 - Article
C2 - 37671480
AN - SCOPUS:85169766188
SN - 2515-690X
VL - 28
SP - 2515690X231198308
JO - Journal of evidence-based integrative medicine
JF - Journal of evidence-based integrative medicine
M1 - 2515690X231198308
ER -