Abstract
Background: In adults, heart rate variability triangular index (HRVi) is a highly reproducible measure of heart rate variability (HRV), which makes it more suitable for use in longitudinal studies. Although normative data have been published for newborns, studies in infants with pathological conditions are lacking.
Methods: From 1997 to 2000, within the first 4 days of life, we prospectively evaluated HRVi in cocaine‐exposed asymptomatic newborns (N = 97) by Holter monitoring. Their data were compared with infants from two control groups (one with no in utero drug exposure, N = 102; the other with exposure to alcohol, nicotine, or marijuana but no cocaine, N = 111).
Results: In assessing concordance between and within operators for HRVi, the intraclass correlations were 0.983 (95% Cl: 0.958, 0.994) and 0.997 (95% Cl: 0.984, 0.999), respectively. Infants with in utero cocaine exposure had significantly (P < 0.0001) lower HRVi than those exposed to other drugs and to no drugs in utero. If abnormal HRVi is defined as < fifth percentile for the no drug exposed group (HRVi < 8), 10% of the cocaine‐exposed newborns, in contrast to 2% in each of the control groups (P = 0.003) had abnormal values.
Conclusion: HRVi is a reliable measure to study heart rate variability in newborns. Asymptomatic infants with in utero cocaine exposure have lower HRVi. Our study supports the clinical use of an abnormal HRVi as a value < 8 for newborn infants. A.N.E. 2002;7(4):374–378
Keywords: autonomic nervous system, vagal tone, Holter monitoring
REFERENCES
- 1. Rosen H, Craelius W, Curcie D, et al. Spectral analysis of heart rate variability in the newborn infant. Biol Neonate 2000;77:224–229. [DOI] [PubMed] [Google Scholar]
- 2. Veerappan S, Rosen H, Craelius W, et al. Spectral analysis of heart rate variability in premature infants with feeding bradycardia. Pediatr Res 2000;47: 659–662. [DOI] [PubMed] [Google Scholar]
- 3. Massin M, von Bernuth G. Normal ranges of heart rate variability during infancy and childhood. Pediatr Cardiol 1997;18:297–302. [DOI] [PubMed] [Google Scholar]
- 4. Lotze U, Kober A, Kaepplinger S, et al. Cardiac sympathetic activity as measured by myocardial 123‐I‐metaiodobenzyl‐guanidine uptake and heart rate variability in idiopathic dilated cardiomyopathy. Am J Cardiol 1999;831548–1551. [DOI] [PubMed]
- 5. Deligiannis A, Kouidi E, Tourkantonis A. Effects of physical training on heart rate variability in patients on hemodialy‐sis. Am J Cardiol 1999;84197–202. [DOI] [PubMed]
- 6. Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology. Heart rate variability. Circulation 1996;93: 1043–1065. [PubMed] [Google Scholar]
- 7. Yi G, Gallagher MM, Yap YG, et al. Consistency of multi‐center measurements of heart rate variability in survivors of acute myocardial infarction. Pacing Clin Electrophysiol 2000;23:157–164. [DOI] [PubMed] [Google Scholar]
- 8. Ziegler D, Piolot R, Strassburger K, et al. Normal ranges and reproducibility of statistical, geometric, frequency domain, and nonlinear measures of 24‐hour heart rate variability. Horm Metab Res 1999;31: 672–679. [DOI] [PubMed] [Google Scholar]
- 9. Mehta SK, Super DM, Connuck D, et al. Heart rate variability in healthy newborn infants. Am J Cardiol 2002;89: 50–53. [DOI] [PubMed] [Google Scholar]
- 10. Akinci A, Celiker A, Baykal E et al. Heart rate variability in diabetic children: Sensitivity of the time and frequency domain methods. Pediatr Cardiol 1993;14:140–146. [DOI] [PubMed] [Google Scholar]
- 11. Heragu NP, Scott WA. Heart rate variability in healthy children and in those with congenital heart disease both before and after operation. Am J Cardiol 1999;83:1654–1657. [DOI] [PubMed] [Google Scholar]
- 12. Massin M, von Bermuth G. Clinical and hemodynamic correlates of heart rate variability in children with congenital heart disease. Eur J Pediatr 1998;157:967–971. [DOI] [PubMed] [Google Scholar]
- 13. Hseu SS, Yien Hw, Du F, et al. Heart rate variability in neonatal rats after perinatal cocaine exposure. Neurotoxicol Teratol 1998;20:601–605. [DOI] [PubMed] [Google Scholar]
- 14. Mehta SK, Super DM, Salvator A, et al. Heart rate variability in cocaine‐exposed newborn infants. Am Heart J 2001;142:828–832. [DOI] [PubMed] [Google Scholar]
- 15. Singer L, Arendt R, Farkas K. et al. Relationship of prenatal cocaine exposure and maternal postpartum psychological distress to child developmental outcome. Dev Psychopath 1997;9:473–489. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16. Streissguth AP, Barr H, Martin D. Alcohol exposure in utero and neonatal habituation assessed with the Brazelton Scale. Child Dev 1983;54:1109–111S. [PubMed] [Google Scholar]
- 17. Streissguth AP. The behavior teratology of alcohol: Performance, behavioral, and intellectual deficits in prenatally exposed children In West J.R. (Ed.), Alcohol and Brain Development. New York : Oxford Univ. Press; 1986, pp. 3–44. [Google Scholar]
- 18. Singer LT, Arendt RA, Fagan JF, et al. Neonatal visual information processing in cocaine‐exposed and nonexposed infants. Inf Beh Dev 1999;11:1–15. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19. SAS version 8.1. Cary , NC : SAS Institute Inc., 1999. [Google Scholar]
- 20. Haycock GB, Schwartz GJ, Wisotsky DH. Geometric method for measuring body surface area: A height‐weight formula validated in infants, children, and adults. J Pediatr 1978;93:62–66. [DOI] [PubMed] [Google Scholar]
- 21. Malik M, Xia R, Odemuyiwa O, et al. Influence of the recognition artifact in automatic analysis of long‐term electrocardiograms on time‐domain measurement of heart rate variability. Med Biol Eng Comput 1993;31:639–644. [DOI] [PubMed] [Google Scholar]
- 22. Leshner Al. Molecular mechanisms of cocaine addiction N Engl J Med 1996;335: 128–129. [DOI] [PubMed] [Google Scholar]
- 23. Hoffman RS, Thompson T, Henry GC, et al. Variation in human plasma cholinesterase activity during low‐dose cocaine administration. J Toxicol Clin Toxicol 1998;36:3–9. [DOI] [PubMed] [Google Scholar]
- 24. Sternfeld M, Rachmilewitz J. Loewenstein‐Lichtenstein Y, et al. Normal and atypical butyrylcholinesterases in placen‐tal development, function, and malfunction. Cell Mol Neu robiol 1997;17:315–332. [DOI] [PMC free article] [PubMed] [Google Scholar]
