Performance of pulse oximetry screening for detection of congenital heart diseases in neonates at two  health facilities in Yaounde, Cameroon

Authors

  • Tony Nengom J Mother and Child Center of Chantal
  • Epée Ngoué J Faculty of Medicine and Biomedical Sciences
  • Nguefack F Yaounde Gyneco-Obstetric and Pediatric Hospital
  • Tchouasseu Mbiake C University of the Mountains
  • Kago D Yaounde Gyneco-Obstetric and Pediatric Hospital
  • Chelo D Mother and Child Center of Chantal

Keywords:

Pulse oximetry, congenital heart disease, neonatal screening, Cameroon

Abstract

Background: Early detection of congenital heart diseases (CHD) remains challenging in resource-limited settings. This study aimed to determine the diagnostic performance of pulse oximetry screening in detecting congenital heart diseases in neonates.
Methods: This was a test validity study conducted over 8 months at two referral hospitals in Yaoundé. Newborns with gestational age >35 weeks underwent pulse oximetry screening after 24 hours of life. Oxygen saturation (SpO₂) was measured at four limbs to determine whether there is a difference in saturation between the upper and lower limbs. The test was considered positive if SpO₂ <95% or if the difference between preductal (right hand) and post-ductal (lower limb) measurements >3%. All newborns subsequently underwent echocardiography.
Results: Fifty newborns were included in the study. The prevalence of CHD  as 22% (11/50). Among newborns with SpO₂ <95%, 6 out of 7 had CHD  confirmed by echocardiography. The identified cardiac malformations included atrial septal defects (n=2), ventricular septal defect (n=1),  atrioventricular canal defect (n=1), bicuspid aortic valve (n=3), pulmonary valve stenosis (n=3), and combined pulmonary valve stenosis with bicuspid aortic valve (n=1). Pulse oximetry demonstrated a sensitivity of 54.54%,  specificity of 97.43%, positive predictive value of 85.71%, and negative predictive value of 83.37%. There was a statistically significant relationship between oxygen saturation <95% and the presence of CHD (OR 20.5, 95%  CI: 5.30-79.21; p<0.001). 
Conclusion: Pulse oximetry is a valuable, non-invasive screening tool for detecting CHD in neonates. Its high specificity and positive predictive value support its systematic implementation in resource- limited settings to improve early diagnosis and management of CHD.  

Author Biographies

  • Tony Nengom J, Mother and Child Center of Chantal

    Mother and Child Center of Chantal
    Biya’s Foundation

  • Epée Ngoué J, Faculty of Medicine and Biomedical Sciences


    Faculty of Medicine and Biomedical
    Sciences of Yaounde I University

  • Nguefack F, Yaounde Gyneco-Obstetric and Pediatric Hospital

    Yaounde Gyneco-Obstetric and
    Pediatric Hospital

  • Tchouasseu Mbiake C, University of the Mountains

    University of the Mountains,
    Cameroon

  • Kago D, Yaounde Gyneco-Obstetric and Pediatric Hospital

    Yaounde Gyneco-Obstetric and
    Pediatric Hospital

  • Chelo D, Mother and Child Center of Chantal

    Mother and Child Center of Chantal
    Biya’s Foundation

References

1. Van der Linde D, Konings EE, Slager MA, Witsenburg M, Helbing WA, Takkenberg JJ, et al. Birth prevalence of congenital heart disease worldwide: a systematic review and meta-analysis. J Am Coll Cardiol. 2011;58(21):2241-7.

2. Hoffman JI, Kaplan S. The incidence of congenital heart disease. J Am Coll Cardiol. 2002;39(12):1890-900.

3. Gilboa SM, Salemi JL, Nembhard WN, Fixler DE, Correa A. Mortality resulting from congenital heart disease among children and adults in the United States, 1999 to 2017. Circulation. 2020;142 (11):1034-49.

4. Tennant PW, Pearce MS, Bythell M, Rankin J. 20-year survival of children born with congenital anomalies: a population- based study. Lancet. 2010;375(9715):649-56.

5. Tantchou Tchoumi JC, Ambassa JC, Giamberti A, Butera G. Occurrence, aetiology and challenges in the management of congenital heart disease in a developing country: a prospective study. Cardiovasc Diagn- Ther. 2013;3(4):236-43.

6. Narvey M, Wong KK, Fournier A. La saturométrie pour mieux dépister la cardiopathie congénitale grave chez les nouveaunés. Paediatr Child Health. 2017;22(8):499-503.

7. Jullien S. Newborn pulse oximetry screening for critical congenital heart defects. BMC Paediatr. 2021;21(1):305.

8. Wong K, Fournier A, Fruitman DS, Graves L, Human DG, Narvey M. Canadian Cardiovascular Society/Canadian Paediatric Cardiology Association Position Statement on Pulse Oximetry Screening in Newborns to Enhance Detection of Critical Congenital Heart Disease. Can J Cardiol. 2017;33 (2):199-208.92

9. Chelo D, Nguefack F, Menanga AP, Ngo Um S, Gody JC, Tatah SA, et al. Spectrum of heart diseases in children: an echocardiographic study of 1,666 subjects in a paediatric hospital, Yaounde, Cameroon. Cardiovasc Diagn Ther. 2016;6(1):10-9.

10. Ndongo-Amougou S, Jingi AM, Otseng Abe A, Owona A, Hamadou B, Chelo D, et al. Aspects Épidémiologiques, Cliniques et Thérapeutiques des Cardiopathies Congénitales dans Deux Hôpitaux de Yaoundé. Health Sci Dis. 2022;23(1):32-51.

11. Iselin M. Cardiopathies congénitales. In: Le Manuel Du Résidanat Pédiatrie. Paris: Elsevier Masson SAS; 2017. p. 300.

12. Dhem A. Développement du coeur. In: Embryologie humaine de Larsen. 3e édition. De Boeck Supérieur; 2023. p. 159 -95.

13. Thangaratinam S, Brown K, Zamora J, Khan KS, Ewer AK. Pulse oximetry screening for critical congenital heart defects in asymptomatic newborn babies: a systematic review and meta- analysis. Lancet. 2012;379(9835):2459-64.

14. Ewer AK, Middleton LJ, Furmston AT, Bhoyar A, Daniels JP, Thangaratinam S, et al. Pulse oximetry screening for congenital heart defects in newborn infants (PulseOx): a test accuracy study. Lancet. 2011;378(9793):785-94.

15. de-Wahl Granelli A, Wennergren M, Sandberg K, Mellander M, Bejlum C, Inganäs L, et al. Impact of pulse oximetry screening on the detection of duct-dependent congenital heart disease: a Swedish prospective screening study in 39,821 newborns. BMJ. 2009;338:a3037.

16. Riede FT, Wörner C, Dähnert I, Möckel A, Kostelka M, Schneider P. Effectiveness of neonatal pulse oximetry screening for detection of critical congenital heart disease in daily clinical routine-- results from a prospective multicentre study. Eur J Pediatr. 2010;169(8):975-81.

17. Liu Y, Chen S, Zühlke L, Black GC, Choy MK, Li N, et al. Global birth revalence of congenital heart defects 1970- 2017: updated systematic review and meta-analysis of 260 studies. Int J Epidemiol. 2019;48(2):455-63.

18. Narayen IC, Blom NA, Bourgonje MS, Haak MC, Smit M, Posthumus F, et al. Pulse oximetry screening for critical congenital heart disease after home birth and early discharge. J Paediatr. 2016;170:188-92.

19. Klausner R. Evaluation of pulse oximetry as a screen for critical congenital heart disease in newborns [dissertation]. New Haven: Yale University; 2018.

20. Arvind B, Saxena A, Ramakrishnan S. Utility of pulse oximetry screening in newborns with nonductus dependent cyanotic congenital heart defects: a reason to alarm? Ann Pediatr Cardiol. 2022;15(1):41-3.

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Published

2026-05-07

How to Cite

Performance of pulse oximetry screening for detection of congenital heart diseases in neonates at two  health facilities in Yaounde, Cameroon. (2026). JOURNAL OF AFRICAN NEONATOLOGY, 4(2), 88-92. https://janeonatology.org/index.php/jan/article/view/319

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