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Effect of Buteyko breathing technique on clinical and functional parameters in adult patients with asthma: a randomized, controlled study.
Vagedes, Katrin; Kuderer, Silja; Ehmann, Rainer; Kohl, Matthias; Wildhaber, Johannes; Jörres, Rudolf A; Vagedes, Jan.
Afiliación
  • Vagedes K; ARCIM Institute (Academic Research in Complementary and Integrative Medicine), Filderstadt, Germany.
  • Kuderer S; ARCIM Institute (Academic Research in Complementary and Integrative Medicine), Filderstadt, Germany.
  • Ehmann R; Asthma Center, Outpatient Pulmonology, Stuttgart, Germany.
  • Kohl M; Institute of Precision Medicine, University Furtwangen, Villingen-Schwenningen, Germany.
  • Wildhaber J; Division of Pediatrics, University and HFR, Fribourg, Switzerland.
  • Jörres RA; Institute and Outpatient Clinic for Occupational, Social and Environmental Medicine, LMU Hospital, LMU Munich, Comprehensive Pneumology Center Munich (CPC-M), Member of the German Center for Lung Research (DZL), Munich, Germany.
  • Vagedes J; ARCIM Institute (Academic Research in Complementary and Integrative Medicine), Filderstadt, Germany. j.vagedes@arcim-institute.de.
Eur J Med Res ; 29(1): 42, 2024 Jan 11.
Article en En | MEDLINE | ID: mdl-38212823
ABSTRACT

BACKGROUND:

The established therapy of asthma might be supported by additional non-pharmaceutical measures, such as the Buteyko breathing technique (BBT); however, the available data are mixed. To clarify the effects of BBT in patients with asthma, we investigated whether it led to clinical improvements with correlation to functional parameters.

METHODS:

Using a randomized, controlled design, we studied two groups (n = 30 each) of patients with asthma under either BBT or usual therapy (UT) w/o BBT over a period of 3 months. The primary outcome comprised the voluntary control pause (CP) after 3 months, secondary outcomes an additional breathhold parameter, forced expiratory volume in 1 s (FEV1), capnovolumetry, exhaled nitric oxide (FeNO), Asthma Control Questionnaire (ACQ) and Nijmegen Questionnaire (NQ), and the use of medication (ß2-agonists; inhaled corticosteroids, ICS).

RESULTS:

CP showed significant time-by-group interaction [F(1,58.09) = 28.70, p < 0.001] as well as main effects for study group [F(1,58.27) = 5.91, p = 0.018] and time [F(1,58.36) = 17.67, p < 0.001]. ACQ and NQ scores were significantly (p < 0.05 each) improved with BBT. This was associated with reductions in the use of ß2-agonists and ICS (p < 0.05 each) by about 20% each. None of these effects occurred in the UT group. While FEV1 and the slopes of the capnovolumetric expiratory phases 2 and 3 did not significantly change, the capnovolumetric threshold volume at tidal breathing increased (p < 0.05) with BBT by about 10 mL or 10%, compared to baseline, suggesting a larger volume of the central airways. No significant changes were seen for FeNO.

CONCLUSIONS:

BBT was clinically effective, as indicated by the fact that the improvement in symptom scores and the small increase in bronchial volume occurred despite the significant reduction of respiratory pharmacotherapy. As the self-controlled Buteyko breathing therapy was well-accepted by the participants, it could be considered as supporting tool in asthma therapy being worth of wider attention in clinical practice. Trial registration Retrospectively registered on 10 March 2017 at ClinicalTrials.gov (NCT03098849).
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Asma Tipo de estudio: Clinical_trials Límite: Adult / Humans Idioma: En Revista: Eur J Med Res Asunto de la revista: MEDICINA Año: 2024 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Asma Tipo de estudio: Clinical_trials Límite: Adult / Humans Idioma: En Revista: Eur J Med Res Asunto de la revista: MEDICINA Año: 2024 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido