ALTERED CARDIOVASCULAR AUTONOMIC REGULATION AFTER 2-WEEK INHALED SALBUTAMOL TREATMENT IN ASTHMATIC-CHILDREN

Citation
Tt. Jartti et al., ALTERED CARDIOVASCULAR AUTONOMIC REGULATION AFTER 2-WEEK INHALED SALBUTAMOL TREATMENT IN ASTHMATIC-CHILDREN, European journal of pediatrics, 156(11), 1997, pp. 883-888
Citations number
32
Categorie Soggetti
Pediatrics
ISSN journal
03406199
Volume
156
Issue
11
Year of publication
1997
Pages
883 - 888
Database
ISI
SICI code
0340-6199(1997)156:11<883:ACARA2>2.0.ZU;2-F
Abstract
We studied the effects of therapeutic 2-week inhaled salbutamol treatm ent on the cardiovascular and respiratory autonomic nervous regulation in eight children with asthma. In this randomized: double-blind, plac ebo-controlled crossover study our test subjects inhaled 200 mu g salb utamol or placebo thrice daily for 14 days. After the 14-day treatment we continuously measured electrocardiogram, finger systolic arterial pressure (SAP) and flow-volume spirometry at baseline and the response to a single 600 mu g salbutamol inhalation. The periodic variability components of R-R intervals (the time between successive heart beats) and SAP in relation to respiration were assessed using spectral analys is. Two-week salbutamol treatment increased baseline low frequency (LF ) variability (P < 0.05) and low frequency/high frequency (LF/HF) vari ability ratio of R-R intervals (P < 0.05) when compared to the placebo treatment. As a response to the single salbutamol inhalation the incr ease in LF/HF ratio of R-R intervals was smaller after the 2-week salb utamol treatment (P < 0.01). No significant differences were found in the bronchodilatory response after the treatment period. Conclusion Tw o-week salbutamol treatment shifts the cardiovascular autonomic regula tion to a new level characterized by greater sympathetic responsivenes s and slight beta(2)-receptor tolerance. Because these effects were ev ident 18 h after cessation of the therapy they are likely to reflect t he adaptation of organ responses to regular therapy or altered central autonomic regulation rather than direct drug effect. A slight toleran ce developed in the sympathovagal cardiac response but not in the bron chodilatory response.