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Cardiovascular autonomic regulation in preterm infants: the effect of atropine
Peter Andriessen1, Ben J A Janssen, Ralph C M Berendsen
1Máxima Medical Center, Neonatal Intensive Care Unit, Veldhoven, P.O. Box 7777, 5500 MB, The Netherlands. P.Andriessen@mmc.nl
Insights
Atropine significantly alters heart rate (HR) and blood pressure (BP) variability in preterm infants. This suggests parasympathetic control is crucial for cardiovascular regulation in neonates, even during respiratory distress.
Area of Science:
- Neonatal physiology
- Autonomic nervous system function
- Cardiovascular research
Background:
- Cardiovascular autonomic control is critical in preterm infants.
- Understanding autonomic regulation aids in managing cardiorespiratory instability.
- Preterm infants often experience respiratory insufficiency, impacting autonomic function.
Purpose of the Study:
- To investigate the effects of atropine on heart rate (HR) and blood pressure (BP) variability in preterm infants.
- To assess baroreceptor reflex (BR) functioning before and after atropine administration.
- To determine the role of parasympathetic control in cardiovascular regulation in this population.
Main Methods:
- Assessed 12 preterm infants (26-32 wk gestation) before intubation.
- Administered atropine sulfate (0.01 mg/kg).
- Utilized spectral power analysis of R-R interval and systolic BP (SBP) series (LF and HF bands) and transfer function analysis for BR assessment.
Main Results:
- Atropine increased steady-state HR by 12% (p < 0.01) but did not change SBP.
- Total spectral power of R-R interval decreased 6-fold, primarily in the LF band (16-fold reduction).
- Total spectral power of SBP series increased by 25% (p < 0.05), with increased HF power. Baroreceptor reflex sensitivity (LF transfer gain) significantly decreased post-atropine.
Conclusions:
- Atropine modulates HR and BP variability in preterm infants, even those in respiratory distress.
- Parasympathetic control, mediated by the baroreceptor reflex, plays a significant role in cardiovascular regulation in preterm neonates.
- Findings highlight the importance of autonomic nervous system assessment in neonatal care.
Abstract:
To study cardiovascular autonomic control, we assessed the effect of atropine on heart rate (HR) and blood pressure (BP) variability in 12 preterm infants (range 26-32 wk) before intubation for respiratory insufficiency. Spectral power analysis of R-R interval and systolic BP (SBP) series were estimated in a low-frequency (LF; 0.04-0.15 Hz) and high-frequency (HF; 0.4-1.5 Hz) band and evaluated for a 10-min period before and a 10-min period after atropine sulfate (0.01 mg/kg). Baroreceptor reflex (BR) functioning was estimated using transfer function analysis at LF (coherence, gain, and phase). Atropine resulted in a significant 12% increase in steady-state HR (p < 0.01) and unchanged SBP. For R-R interval series, the total spectral power decreased 6-fold (p < 0.01), which was predominantly due to a reduction in the LF band (16-fold; p < 0.01). In contrast, we observed a significant increase (25%; p < 0.05) in total spectral power of SBP series partly as a result of an increase in HF power. The LF power of SBP series was not altered. The median LF transfer gain (BR sensitivity) between SBP and R-R interval decreased from 4.2 to 1.4 ms/mm Hg (p < 0.01) after atropine. The LF phase relationship (BP leads R-R interval fluctuations by approximately 4 s) was not changed after atropine. In conclusion, even in preterm infants in distress, atropine modulates HR and BP variability, suggesting that BR-mediated parasympathetic control of heart rate is of significance for cardiovascular control at that age.
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