Home            Past Issues            About IP            About IAP           Author Information            Subscription            Advertisement              Search  

   
research paper

Indian Pediatr 2019;56: 917-922

Electrocardiographic Parameters in Indian Newborns


SK Md Habibulla1, Arijit Bhowmik2, Jayanta Saha3, Avijit Hazra4, Sanjay K Halder3 and Rakesh Mondal5

From Departments of 1Pediatrics, 2Neonatology, 3Cardiology, and 4Pediatric Medicine, Medical College Kolkata, and 5Department of Pharmacology, IPGMER and SSKM Hospital; Kolkata, West Bengal, India.

Correspondence to: Dr Rakesh Mondal, Premises no 50, Shibrampur Bye Lane, Sarsuna, Kolkata 700061,
West Bengal, India.
Email: [email protected]

Received: August 22, 2018;
Initial review: December 27, 2018;
Accepted: September 03, 2019.

Objective: To generate data of electrocardiogram (ECG) parameters according to gestational age in Indian newborns. Methods: An observational study was carried out over 7 months in neonatology unit of a tertiary care teaching hospital. Following auscultation, ECG parameters were recorded simultaneously in 12 leads, on third day of life, in hemodynamically stable neonates. Data from 364 babies were analyzed, keeping at least 30 records for each gestational age between 30 to 42 weeks. Results: There was no difference in mean heart rate recorded through auscultation and ECG traces. The mean (SD) values recorded were: P wave duration 0.04 (0.01) s, P wave amplitude 1.3 (0.4) mm, T wave duration 0.07 (0.02) s, T wave amplitude 1.1 (0.6) mm, PR interval 0.09 (0.02) s, QRS duration 0.04 (0.01) s, QT interval 0.26 (0.02) s, QTc 0.4 (0.03) s and QRS axis 127 (22) degree. Gestation age-wise percentile charts of different ECG parameters were generated. Conclusion: These gestational age-wise percentile charts of different ECG parameters for Indian newborns can be used as reference for neonatal ECG.

Keywords: Characteristics, Charts, Gestational age, Percentiles.


P
rominent anatomical and physiological changes occur in the cardiovascular system from birth to adolescence [1]. Both term and preterm infants experience cardiorespiratory changes at birth, that coincide with termination of the placental circulation and improved lung compliance. The changes taking place in fetal cardiac physiology during the last part of gestation and perinatal transition are reflected in the evolution of electrocardiographic (ECG) parameters during the neonatal period [1]. In the newborn, ECG recording is necessary for diagnosis of different cardiac ailments, hemodynamic monitoring during intensive care stay and during resuscitation. Survival of even preterm babies has improved because of increasing availability of specialized neonatal care with SpO2 monitors, cardiac monitors etc. The different ECG parameters reflecting cardiac electrophysiological changes need to be compared with gestational age appropriate data for interpretation. Unfortunately, there is a paucity of data on ECG measurements in term and preterm neonates and such data is nonexistent for Indian babies. We therefore conducted a descriptive observational study to generate gestational age wise data of ECG parameters of the newborn from the Indian perspective.

Methods

The study was conducted between March and September 2017 in the neonatology unit of a tertiary-care teaching hospital in Kolkata, India. The research protocol was approved by the institutional ethics committee and written informed consent was obtained.

Healthy term or preterm newborns, admitted for establishment of feeding or observation for neonatal jaundice, or babies kept in the maternity ward with mothers requiring postpartum hospital stay were enrolled. Babies with critical illness, birth asphyxia, major congenital anomaly including cardiac abnormality or with maternal antenatal history of serious illness or maternal medication use, were excluded. Gestational age was estimated from the date of last menstrual period, from antenatal ultrasound or new Ballard score [2] as appropriate. If any discrepancy occurred, the gestational age estimated through new Ballard score was accepted.

ECG was recorded on the third day after birth. A twelve lead simultaneous acquisition ECG machine (ClarityMed ECG 100C; CMRR > 90 dB, dynamic range ± 4.25 mV, frequency response 0.05-150Hz (-3dB), time constant 3.2 sec, input impedance >10 MW on each electrode) was used to record ECG. The American Heart Association (AHA) recommendations for pediatric ECG of 150 Hz as minimum bandwidth cut off and 500 Hz as minimum sampling rate were followed [3]. Disposable electrodes were used. Electrode placement and removal were done cautiously in order to avoid injury to the delicate skin, especially in preterm babies. If needed, the electrodes were trimmed to make them smaller in size without damaging the metal panel. Standard electrode sites were carefully identified and placement done according to AHA recommendations [4]. The recording team comprised one ECG technician who operated the ECG machine using a standardized protocol, one junior resident (pediatric postgraduate student) who placed the electrode following guidelines and maintaining asepsis protocol, and one supervising pediatrician. The team was trained beforehand by a pediatric cardiologist and a neonatologist. The same machine and the same team recorded all the ECGs.

Data were captured on a structured case report form. Weight, gender and heart rate determined by auscultation, were recorded. Data extracted from the ECG traces were heart rate (bpm), P wave duration (s), P wave amplitude (mm), R wave amplitude in lead V1 (mm), S wave in V1 (mm), R wave in V6 (mm), S wave in V6 (mm), T wave duration (s), T wave amplitude (mm), PR segment interval (s), QRS complex duration (s), QT segment interval (s), QTc (s), and QRS complex axis (degree)

No formal sample size calculation was done beforehand but the target was to recruit at least 30 babies born in each gestational week between weeks 28 to 42. Sampling was purposive and consecutive babies were recruited as far as possible, provided informed consent was available.

Statistical analysis: Descriptive statistics, namely mean, standard deviation (SD), 95% confidence interval (CI), and 10th, 25th, 50th, 75th and 90th percentile values were calculated for the whole cohort and gestational age based weekly subcohorts. Numerical variables were compared between male and female subgroups by Mann-Whitney U test with two-sided P<0.05 as the cut-off for statistical significance. Significance of change across gestational age was assessed by Kruskal-Wallis analysis of variance (ANOVA). Correlation between variables was quantified by calculating Spearman’s rank correlation coefficient rho, after verifying from scatter plots that an approximately linear relationship exists. Statistica version 6 (Tulsa, Oklahoma: StatSoft Inc., 2001) and MedCalc version 11.6 (Mariakreke, Belgium: MedCalc Software, 2011) software were used for statistical analyses.

Results

Although 511 babies were screened, 364 ECG traces could be analyzed. The exclusions occurred stepwise – 27 babies were excluded at screening (19 failed exclusion criteria; 8 refused consent), 26 were excluded due to difficulties in lead placement, 39 excluded due to poor ECG recording and finally, 55 traces were discarded because the preset criterion of at least 30 records for each gestational week were not met. The babies included were healthy and those born preterm were all ensured to be hemodynamically stable. There were 212 babies (58.2%) in the analyzed cohort who were born before 37 completed weeks. Male babies numbered 191 (52.5%). The mean (SD) birth weight of the whole cohort was 2.11 (0.73 kg) (95% CI 2.03-2.18 kg) and for preterm cohort (n=212) was 1.60 (0.13) kg (95% CI 1.55-1.66 kg).

The mean (SD) values were: P duration, 0.04 (0.01) s; P amplitude, 1.3 (0.4) mm; T duration 0.07 (0.02) s; T amplitude, 1.1 (0.6) mm; PR interval, 0.09 (0.02) s, QRS duration, 0.04 (0.01) s; QT interval, 0.26 (0.02) s, QTc interval, 0.4 (0.03) s; and QRS axis, 127 (22) degree. There were no statistically significant gender differences in birthweight, heart rate and ECG parameters.

The gestation age-wise (30 weeks to 41 weeks) summary of the ECG measurements (mean with SD), has been presented in Table I. Detailed percentile values as per gestation are available in Web Table I. Among the ECG parameters, heart rate, R and S wave amplitudes and QT interval and QTc showed significant variation with gestational age (P<0.001), but the overall range was narrow, as can be seen from the 10th and 90th percentile values, other than for heart rate.

TABLE I  Descriptive Statistics of ECG Parameters in the Newborn Stratified by Gestational Age in Weeks
Gestation Heart P dura- P ampli- R ampli- S  ampli- R ampli- S ampli- T dura- T ampli- PR inter- QRS dura- QT inter- QTc QRS axis
Rate tion tude tude in tude in tude in tude in tion   tude val tion (sec) val (sec) (degree)
(bpm) (sec) (mm)  V1 (mm)  V1 (mm)  V6 (mm) V6 (mm) (sec) (mm) (sec)
30 weeks
Mean 159 0.04 1.2 7.1 5.1 8.3 9.8 0.05 1.1 0.09 0.04 0.25 0.41 129
(SD) (17) (0.01) (0.3) (2.8) (2.3) (2.7) (3.8) (0.01) (0.2) (0.01) (0.01) (0.02) (0.03) (26)
Median 159 0.04 1.0 6.8 4.8 7.8 9.0 0.04 1.0 0.08 0.04 0.25 0.40 130
31 weeks
Mean 144 0.04 1.2 7.5 5.3 7.5 8.9 0.06 1.2 0.09 0.04 0.26 0.4 127
(SD) (17) (0.01) (0.3) (3.0) (2.6) (3.1) (3.2) (0.02) (0.2) (0.01) (0.01) (0.02) (0.03) (24)
Median 147 0.04 1.0 7.0 5.0 7.0 8.8 0.06 1.0 0.08 0.04 0.26 0.40 127
32 weeks
Mean 137 0.04 1.2 7.6 5.1 7.5 7.8 0.06 1.1 0.09 0.04 0.26 0.4 125
(SD) (16) (0.01) (0.3) (3.3) (2.8) (2.9) (3.1) (0.02) (0.2) (0.02) (0.01) (0.02) (0.04) (23)
Median 139 0.04 1.0 7.5 4.5 7.0 8.3 0.06 1.0 0.08 0.04 0.26 0.39 125
33 weeks
Mean 148 0.04 1.3 7.5 5.9 7.9 9.4 0.06 1.0 0.09 0.04 0.25 0.38 119
(SD) (20) (0.01) (0.4) (3.3) (2.5) (2.5) (3.5) (0.01) (0.2) (0.01) (0.01) (0.02) (0.03) (23)
Median 145 0.04 1.0 6.8 5.5 7.0 8.0 0.06 1.0 0.08 0.04 0.24 0.39 120
34 weeks
Mean 144 0.05 1.3 7.3 5.3 7.6 8.9 0.06 1.1 0.09 0.04 0.26 0.4 123
(SD) (15) (0.01) (0.4) (3.1) (1.7) (2.4) (3.4) (0.01) (0.3) (0.01) (0.01) (0.02) (0.02) (23)
Median 143 0.04 1.0 6.5 5.3 7.0 8.3 0.06 1.0 0.08 0.04 0.26 0.40 125
35 weeks
Mean 139 0.04 1.4 8.3 5.9 5.5 5.9 0.07 1.2 0.09 0.04 0.27 0.41 125
(SD) (15) (0.01) (0.4) (3.5) (1.9) (1.7) (2.0) (0.01) (0.3) (0.01) (0.01) (0.02) (0.03) (23)
Median 136 0.04 1.5 7.8 6.0 5.5 5.5 0.07 1.0 0.08 0.04 0.27 0.41 125
36 weeks
Mean 138 0.04 1.23 10.1 7.2 4.4 2.9 0.07 1.2 0.09 0.04 0.26 0.39 127
(SD) (15) (0.01) (0.3) (3.9) (2.7) (1.4) (1.2) (0.01) (0.2) (0.01) (0.01) (0.02) (0.03) (19)
Median 137 0.04 1.0 9.3 6.5 4.0 3.0 0.06 1.0 0.08 0.04 0.26 0.39 125
37 weeks
Mean 135 0.05 1.3 11.5 7.8 4.9 3.3 0.07 1.1 0.09 0.04 0.27 0.41 128
(SD) (14) (0.01) (0.4) (3.7) (2.6) (1.6) (1.3) (0.01) (0.3) (0.01) (0.01) (0.02) (0.03) (19)
Median 136 0.04 1.0 11.3 8.0 5.0 3.0 0.06 1.0 0.08 0.04 0.28 0.40 130
38 weeks
Mean 132 0.04 1.3 12.2 7.8 4.5 3.1 0.07 1.1 0.09 0.04 0.27 0.4 131
(SD) (16) (0.01) (0.4) (4.8) (2.6) (1.5) (1.3) (0.01) (0.3) (0.02) (0.01) (0.02) (0.03) (19)
Median 133 0.04 1.0 12.0 8.3 4.5 3.0 0.08 1.0 0.08 0.04 0.28 0.40 130
39 weeks
Mean 134 0.05 1.4 12.1 8.4 4.6 3.3 0.08 1.1 0.1 0.04 0.27 0.39 130
(SD) (18) (0.01) (0.4) (4.8) (2.4) (1.8) (1.5) (0.02) (0.3) (0.02) (0.01) (0.02) (0.03) (23)
Median 133 0.04 1.5 11.8 8.5 4.8 3.5 0.08 1.0 0.10 0.04 0.27 0.39 130
40 weeks
Mean 122 0.04 1.2 12 8.5 4.5 3.4 0.07 1.1 0.09 0.04 0.28 0.4 131
(SD) (15) (0.01) (0.5) (5.1) (2.6) (1.9) (1.3) (0.01) (0.2) (0.01) (0.01) (0.02) (0.02) (23)
Median 123 0.04 1.0 12.3 8.3 4.3 3.5 0.07 1.0 0.08 0.04 0.28 0.40 130
41 weeks
Mean 131 0.05 1.2 12.3 8.8 4.9 3.3 0.07 1.1 0.09 0.04 0.27 0.4 130
(SD) (14) (0.01) (0.4) (4.5) (2.4) (1.8) (1.4) (0.01) (0.2) (0.02) (0.01) (0.02) (0.03) (20)
Median 134 0.04 1.0 12.0 9.0 5.0 3.3 0.06 1.0 0.08 0.04 0.26 0.40 130
(Note: n = 32 for gestational age of 40 weeks, 31 for weeks 32 and 33 and 30 for all other weeks)

Gestational age showed moderate inverse correlation with heart rate (–0.40) and strong inverse correlation with S wave amplitude in Lead V6 (–0.71). The QT interval showed good inverse correlation with heart rate (–0.55). Birth weight also showed good inverse correlation with S wave amplitude in V6 (–0.68). Correlation was near perfect (0.99) between auscultated heart rate and that derived from ECG.

Discussion

The gestation age-wise (30 to 41 weeks) summary of the ECG measurements, including percentile values were generated. Heart rate, R and S wave amplitudes and QT interval and QTc showed significant variation with gestational age (P<0.001).

This study has limitations, including the relatively small sample size and lack of prospective follow-up of ECG and clinical data. Our analysis does not include ECG data of babies below 30 weeks and over 41 weeks as we did not get sufficient numbers. Logistic limitations prevented us from generating gestation-wise ECG data from babies in the community rather than in hospital. Difficulties were encountered in adhering to chest lead placement following AHA guidelines in babies with small chests and a sizeable number of ECG records had to be discarded owing to lead loosening artefacts caused by movement in the babies.

Most studies on neonatal ECGs done in the 1970s [5,6] do not provide gestation-wise data. Gestational age-specific ECG data is lacking in literature, including from India. Until recently, the most comprehensive study of ECG variability in children was that of Davignon, et al. [5] based on measurements made from 2141 White children in Quebec, Canada. Normal limits were presented for few parameters and there were no gestational age-wise stratification attempted. For available parameters, percentile values of ECG parameters in our study are quite comparable to that study [5]. This applies to heart rate, mean QRS axis, QRS duration, R and V amplitude in leads V1 and V6. However, our result differ, to some extent, with respect to P wave duration, QRS duration and QRS axis from figures reported in the study by Rijnbeek, et al. [7], where the study population comprised children aged 11 days to 16 years.

The most recent guidelines for interpretation of normal ECG in newborns have been provided by the Task Force for Interpretation of the Neonatal Electro-cardiogram of the European Society of Cardiology in 2002 [8]. However, these do not provide gestational age-wise stratification of data. Except the mean P amplitude value, S in V1, R in V6, S in V6, other ECG parameters in our study are comparable with these guidelines. It suggests that Western data may not be appropriate to interpret ECG in Indian babies. Heart rate assessment at birth by ECG may be reasonable according to the 2015 guidelines on neonatal resuscitation from American Heart Association (AHA) [9] and European Resuscitation Council (ERC) [10] since clinical and pulse oximetry assessment are sometimes found to be both inaccurate and unreliable [11-14] in the newborn. Therefore availability of data on heart rate by ECG, stratified by gestational age, will be useful in following the resuscitation protocol. The influence of gender on some electrocardiographic variables has been noted in some reports [15,16], unlike the results of our study.

Notwithstanding the above limitations, in conclusion, we have provided normative data of ECG parameters according to gestational age in Indian scenario. This data need to be validated at other centers and in the community. These values, validated through additional studies, can serve as reference for interpretation of neonatal ECG, both in term and preterm babies.

Contributors: MHSk: primary investigator, data collection, manuscript drafting and review; AB: data collection, patient management, literature search; JS: study design, patient management, data interpretation; AH: literature search, statistical analysis, manuscript review; SKH: technical inputs in data Collection, data interpretation; RM: study conception and design, literature search, manuscript review and corresponding author. MHS,RM: shall act as guarantor of the study.

Funding: None; Competing Interest: None stated.

 

What This Study Adds?

Gestational age-wise percentile charts of different electrocardiographic parameters have been derived for Indian newborn babies.

 

References

1. Allen HD, Gutgesell HP, Clark EB, Driscoll DJ, editors. Moss and Adams’ heart disease in infants, children, and adolescents including the fetus and young adult. 6th ed. Vol 1 and 2. Philadelphia: Lippincott Williams and Wilkins; 2001.

2. Donovan EF, Tyson JE, Ehrenkranz RA, Verter J, Wright LL, Korones SB, et al. Inaccuracy of Ballard scores before 28 weeks’ gestation. Network J Pediatr. 1999;135: 147-52.

3. Bailey JJ, Berson AS, Garson A Jr, Horan LG, Macfarlane PW, Mortara DW, et al. Recommendations for Standardization and Specifications in Automated Electrocardiography: Bandwidth and Digital Signal Processing. A report for Health Professionals by an Ad Hoc Writing Group of the Committee on Electrocardiography and Cardiac Electrophysiology of the Council on Clinical Cardiology, American Heart Association. Circulation. 1990;81:730-9.

4. Kligfield P, Gettes LS, Bailey JJ, Childers R, Deal BJ, Hancock EW, et al. for American Heart Association Electrocardiography and Arrhythmias Committee, Council on Clinical Cardiology; American College of Cardiology Foundation; Heart Rhythm Society. Recommendations for the Standardization and Interpretation of the Electro-cardiogram: Part I: the Electrocardiogram and its Technology: A Scientific Statement from the American Heart Association Electrocardiography and Arrhythmias Committee, Council on Clinical Cardiology; the American College of Cardiology Foundation; and the Heart Rhythm Society Endorsed by the International Society for Computerized Electrocardiology. J Am Coll Cardiol. 2007;49:1109-27.

5. Davignon A, Rautaharju P, Boiselle E, Soumis F, Megelas M, Choquette A. Normal ECG standards for infants and children. Pediatr Cardiol. 1979;1:123-31.

6. Haistraiter AR, Abella JB. The electrocardiogram in the newborn period. J Pediatrics. 1971;78:146-56.

7. Rijnbeek PR, Witsenburg M, Schrama E, Hess J, Kors JA. New normal limits for the paediatric electrocardiogram. Eur Heart J. 2001;22:702-11.

8. Schwartz PJ, Garson A Jr, Paul T, Stramba-Badiale M, Vetter VL, Wren C. Guidelines for the Interpretation of the Neonatal Electrocardiogram. A Task Force of the European Society of Cardiology Report. Eur Heart J. 2002;17: 1329-44.

9. Wyckoff MH, Aziz K, Escobedo MB, Kapadia VS, Kattwinkel J, Perlman JM, et al. Neonatal Resuscitation: 2015 American Heart Association Guidelines Update for Cardiopulmonary Resuscitation and Emergency Cardio-vascular Care. Circulation 2015;132:S543-60.

10. Wyllie J, Bruinenberg J, Roehr CC, Rüdiger M, Trevisanuto D, Urlesberger B. European Resuscitation Council Guidelines for Resuscitation 2015. Resuscitation 2015;95:249-63.

11. Dawson JA, Saraswat A, Simionato L, Thio M, Kamlin CO, Owen LS, et al. Comparison of heart rate and oxygen saturation measurements from Masimo and Nellcor pulse oximeters in newly born term infants. Acta Paediatr. 2013;102:955-60.

12. Kamlin CO, Dawson JA, O’Donnell CP, Morley CJ, Donath SM, Sekhon J, et al. Accuracy of pulse oximetry measurement of heart rate of newborn infants in the delivery room. J Pediatr. 2008;152:756-60.

13. Kamlin CO, O’Donnell CP, Everest NJ, Davis PG, Morley CJ. Accuracy of clinical assessment of infant heart rate in the delivery room. Resuscitation. 2006;71:319-21.

14. Mizumoto H, Tomotaki S, Shibata H, Ueda K, Akashi R, Uchio H, et al. Electrocardiogram shows reliable heart rates much earlier than pulse oximetry during neonatal resuscitation. Pediatr Int. 2012;54:205-7.

15. Dickinson DF. The normal ECG in childhood and adolescence. Heart. 2005;91:1626-30.

16. Macfarlane PW, McLaughlin SC, Devine B, Yang TF. Effects of age, sex and race on ECG interval measurements. J Electrocardiol. 1994;27:14-9.

 

Copyright © 1999-2019 Indian Pediatrics