Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2004 Apr 2;4(1):6.
doi: 10.1186/1471-2393-4-6.

Dependency of magnetocardiographically determined fetal cardiac time intervals on gestational age, gender and postnatal biometrics in healthy pregnancies

Affiliations

Dependency of magnetocardiographically determined fetal cardiac time intervals on gestational age, gender and postnatal biometrics in healthy pregnancies

Peter Van Leeuwen et al. BMC Pregnancy Childbirth. .

Abstract

BACKGROUND: Magnetocardiography enables the precise determination of fetal cardiac time intervals (CTI) as early as the second trimester of pregnancy. It has been shown that fetal CTI change in course of gestation. The aim of this work was to investigate the dependency of fetal CTI on gestational age, gender and postnatal biometric data in a substantial sample of subjects during normal pregnancy. METHODS: A total of 230 fetal magnetocardiograms were obtained in 47 healthy fetuses between the 15th and 42nd week of gestation. In each recording, after subtraction of the maternal cardiac artifact and the identification of fetal beats, fetal PQRST courses were signal averaged. On the basis of therein detected wave onsets and ends, the following CTI were determined: P wave, PR interval, PQ interval, QRS complex, ST segment, T wave, QT and QTc interval. Using regression analysis, the dependency of the CTI were examined with respect to gestational age, gender and postnatal biometric data. RESULTS: Atrioventricular conduction and ventricular depolarization times could be determined dependably whereas the T wave was often difficult to detect. Linear and nonlinear regression analysis established strong dependency on age for the P wave and QRS complex (r2 = 0.67, p < 0.001 and r2 = 0.66, p < 0.001) as well as an identifiable trend for the PR and PQ intervals (r2 = 0.21, p < 0.001 and r2 = 0.13, p < 0.001). Gender differences were found only for the QRS complex from the 31st week onward (p < 0.05). The influence on the P wave or QRS complex of biometric data, collected in a subgroup in whom recordings were available within 1 week of birth, did not display statistical significance. CONCLUSION: We conclude that 1) from approximately the 18th week to term, fetal CTI which quantify depolarization times can be reliably determined using magnetocardiography, 2) the P wave and QRS complex duration show a high dependency on age which to a large part reflects fetal growth and 3) fetal gender plays a role in QRS complex duration in the third trimester. Fetal development is thus in part reflected in the CTI and may be useful in the identification of intrauterine growth retardation.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Number of recordings Number of FMCG recordings obtained between the 12th and 42nd week of gestation. Viable recordings were available as early as the 15th week and, from the 20th week on, all recordings could be evaluated (no signal = signal-to-noise ratio too low for the identification of fetal QRS complexes; signal = sufficient signal quality for evaluation).
Figure 2
Figure 2
Averaged FMCG signal FMCG signal traces from 4 selected channels of the averaged data of a recording performed in the 39th week of gestation. The vertical lines show how the signal onsets and ends were set and used to determine the cardiac time intervals. (B = magnetic field strength)
Figure 3
Figure 3
Scatter plots of fetal CTI vs. gestational age Duration of CTI with respect to gestational age: disjunct intervals (P wave, PQ interval, QRS complex, ST segment, T wave) in the top two rows, composite intervals (PR, QT and QTc interval) in the bottom row (males ◊, females +).

References

    1. Quinn A, Weir A, Shahani U, Bain R, Maas P, Donaldson G. Antenatal fetal magnetocardiography: a new method for fetal surveillance? Br J Obstet Gynaecol. 1994;101:866–870. - PubMed
    1. Van Leeuwen P, Schüβler M, Bettermann H, Lange S, Hatzmann W. Magnetocardiography for assessment of fetal heart actions. Geburtshilfe Frauenheilkd. 1995;55:642–646. - PubMed
    1. Menendez T, Achenbach S, Moshage W, Flüg M, Beinder E, Kollert A, Bittel A, Bachmann K. Prenatal recording of fetal heart action with magnetocardiography. Z Kardiol. 1998;87:111–118. doi: 10.1007/s003920050162. - DOI - PubMed
    1. Leuthold A, Wakai RT, Martin CB. Noninvasive in utero assessment of PR and QRS intervals from the fetal magnetocardiogram. Early Hum Dev. 1999;54:235–243. doi: 10.1016/S0378-3782(98)00100-5. - DOI - PubMed
    1. Horigome H, Takahashi MI, Asaka M, Shigemitsu S, Kandori A, Tsukada K. Magnetocardiographic determination of the developmental changes in PQ, QRS and QT intervals in the foetus. Acta Paediatr. 2000;89:64–67. doi: 10.1080/080352500750029086. - DOI - PubMed

LinkOut - more resources