Evaluation of pulse oximetry screening in Middle Tennessee: cases for consideration before universal screening
1Division of Neonatology, Monroe Carell Jr Children's Hospital at Vanderbilt, Nashville, TN 37232-9550, USA. bill.walsh@vanderbilt.edu
Insights
Pulse oximetry screening for critical congenital heart disease (CHD) in newborns showed a low positive predictive value. The study highlights issues with false positives and the need for improved care systems before universal implementation.
Area of Science:
- Neonatal Medicine
- Public Health Screening
- Cardiology
Background:
- Pulse oximetry screening is proposed for detecting critical congenital heart disease (CHD) in asymptomatic newborns.
- This study evaluates the effectiveness and challenges of this screening in a real-world, non-research setting.
Purpose of the Study:
- To assess the performance of pulse oximetry screening for critical CHD in a public health program.
- To identify practical issues and limitations encountered during screening implementation.
Main Methods:
- Evaluation of an elective, state-directed pulse oximetry screening program for 14,564 infants in Middle Tennessee.
- Screening conducted by nurses in local hospitals after 24 hours of age and before discharge.
- Analysis of screening results, including positive predictive value and false positive rates.
Main Results:
- The positive predictive value for critical CHD was less than 1% (1 true positive, 112 false positives).
- The single true positive case was not referred for evaluation.
- Antenatal diagnosis combined with physical examination identified 43 of 44 critical CHD cases.
Conclusions:
- Current pulse oximetry screening protocols in this setting yielded a high rate of false positives.
- Significant challenges exist regarding educational and referral systems for screening.
- A defined system of care is necessary before considering universal implementation of newborn screening for critical CHD.
Objective:
Pulse oximetry screening of asymptomatic newborns is suggested as a life-saving procedure for the timely detection of critical congenital heart disease (CHD) in asymptomatic newborns. We evaluated this screening and report cases that demonstrate problems with screening in a non-research setting.
Study Design:
An elective state-directed public health screening program was evaluated in Middle Tennessee; 14 564 infants were screened after 24 h of age and before discharge. The screening was performed in a non-research setting by nurses at the local hospitals. A parallel investigation of the methods and timing of diagnosis in Middle Tennessee revealed a surprisingly high incidence of antenatal diagnosis (66%).
Result:
Using a saturation value of 94% as the defined normal, the positive predictive value was less than 1%, with 112 infants having a false positive case and 1 having a true positive case identified (incidence 1/34 775). The one true positive case was not referred for evaluation. One false-positive case resulted in a costly referral and hospitalization. Antenatal diagnosis when combined with physical examination detected 43 of 44 infants with critical CHD during the year-long evaluation.
Conclusion:
Before universal screening can be implemented, a system of care must be defined to address the educational and referral issues raised by this report.
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