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Title: | Profile of Infective Endocarditis in Nigerian Children |
Authors: | Ige, O. O. Yilgwan, C. S. Diala, U. Akhiwu, H. O. Baba, F. Bok, M. Bode-Thomas, F. |
Keywords: | congenital heart disease infective endocarditis rheumatic heart disease |
Issue Date: | 2017 |
Publisher: | Journal of Advances in Medicine and Medical Research |
Series/Report no.: | Vol.22;Iss.8: Pp 1-9 |
Abstract: | Background: Infective endocarditis (IE) was initially thought to be uncommon in children but is on
the increase due to improved cardiac services in the developing world.
Aims: Aims of this study is to describe the profile of IE in children in Jos, Nigeria and identify the
peculiarities of the disease in the locality.
Methods: Case records of children diagnosed with IE based on the modified Duke’s criteria over a
seven year period were retrospectively reviewed in a tertiary hospital. Their clinical manifestations,
blood culture isolates, presence or absence of vegetations and clinical outcomes were
documented and analyzed using Epi Info 7.
Results: Case records of thirty children were reviewed. The number of children managed
increased yearly with 10 (33.3%) of them seen in the last year of the study. The clinical features
were mainly non-specific - fever (70.0%), congestive cardiac failure (63.3%) and anorexia (63.3%)
being the major findings. Staphylococcus aureus was the commonest isolate, present in 5 (45.5%)
of the 11 blood culture-positive cases. Other organisms isolated were Klebsiella species in 3 (27.3%), Pseudomonas aeruginosa in 2 (18.2%) and Acinetobacter baumami in 1 (9.1%) child.
Vegetations were detected in 12 (40.0%) children, most of them located on the mitral valve.
Mortality occurred in 8 (26.7%) children and was significantly higher in males – P = 0.02.
Conclusion: There is a marked increase in the number of children admitted and managed for IE in
the last year of the study possibly due to an increased index of clinical suspicion of IE. A high index
of suspicion is required for diagnosis because many children presented with nonspecific clinical
features. |
URI: | http://hdl.handle.net/123456789/2225 |
ISSN: | 2231-0614 |
Appears in Collections: | Paediatrics
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