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Consequences of electrocardiography screening for prolonged QTc in neonates-A systematic review
Anna Leppänen1, Emmi Helle2, Ilari Kuitunen3
1Kuopio Pediatric Research Unit, University of Eastern Finland, Kuopio, Finland.
Insights
Neonatal electrocardiography (ECG) screening for prolonged corrected QT (QTc) interval shows wide incidence rates. Few infants with prolonged QTc are diagnosed with long QT syndrome (LQTS), indicating a need for further research.
Area of Science:
- Neonatal cardiology
- Clinical electrophysiology
- Genetics
Background:
- Effectiveness of neonatal electrocardiography (ECG) screening for long QT syndrome (LQTS) remains under discussion.
- Current screening practices may lead to varied interpretations and outcomes.
Purpose of the Study:
- To systematically review the consequences of ECG screening for prolonged corrected QT (QTc) interval in neonates.
- To analyze incidence rates, QTc normalization, LQTS diagnoses, and sudden infant death syndrome (SIDS) in screened infants.
Main Methods:
- Systematic literature search of PubMed, Scopus, and Web of Science databases (June 2024).
- Calculation of incidence rates for prolonged QTc (>450 ms) per 1000 neonates.
- Analysis of QTc normalization, LQTS diagnosis, and SIDS outcomes in included studies.
Main Results:
- Incidence of prolonged QTc varied widely based on QTc cutoff values (>450 ms, >460 ms, >470 ms).
- QTc normalization occurred in 57.1%–95.2% of neonates with prolonged QTc.
- Only 0.04% of neonates were diagnosed with LQTS; prolonged QTc was noted in SIDS cases.
Conclusions:
- Neonatal ECG screening for prolonged QTc yields highly variable incidence rates.
- A small fraction of neonates with prolonged QTc are ultimately diagnosed with LQTS.
- Standardized research factors and genetic analysis are crucial to define the utility of neonatal ECG screening for LQTS.
Background:
An ongoing discussion has been the effectiveness of neonatal electrocardiography (ECG) screening for long QT syndrome (LQTS).
Objective:
The aim of this systematic review was to assess the consequences of ECG screening for prolonged corrected QT (QTc) interval in infants younger than 1 month.
Methods:
We searched the PubMed, Scopus, and Web of Science databases in June 2024. The incidence rates of prolonged QTc, defined as >450 ms, were calculated per 1000 neonates. Prolonged QTc cases, including normalization during follow-up, LQTS diagnosis, and sudden infant death syndrome (SIDS), were analyzed.
Results:
Eight studies were included. Five studies using a cutoff QTc >450 ms reported incidences ranging from 5 (95% confidence interval [CI], 5-6) to 79 (CI, 60-102) per 1000 neonates. Six studies with a cutoff of >460 ms reported incidences ranging from 1 (CI, 1-2) to 53 (CI, 50-57). Five studies (cutoff QTc >470 ms) had incidences varying from 1 (CI, 0-1) to 28 (CI, 21-35). In 6 studies, QTc normalization during follow-up occurred in 57.1% to 95.2% of neonates with prolonged QTc. The diagnosis of LQTS was reported in 4 studies, with 21 of 51,817 (0.04%) neonates later diagnosed with LQTS. Two studies reported SIDS outcomes, finding prolonged QTc in 8 of 24 and 3 of 3 SIDS cases.
Conclusion:
The incidence of prolonged QTc varied widely across studies. Only a small proportion of neonates with prolonged QTc were diagnosed with LQTS during follow-up. Further research with standardized study factors and comprehensive genetic analysis is needed to determine the utility of and indications for neonatal ECG screening.
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