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1.
J Paediatr Child Health ; 53(10): 976-980, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28600851

ABSTRACT

AIM: Neonatal surgery in low-income and middle-income countries has a poorer outcome when compared with high-income countries. This study evaluated the management challenges and outcomes of neonatal surgery before and after the introduction of focused interdisciplinary team management in 2013. METHODS: We retrospectively analysed neonatal surgery undertaken at two referral hospitals in Enugu, south-eastern Nigeria from January 2011 to November 2015. Cases managed prior to July 2013 (group A) were compared with those managed from July 2013 (group B). RESULTS: There were 91 cases (group A, 47; group B, 44). The common neonatal conditions were oesophageal atresia (21), anorectal malformation (18) and intestinal atresia (18). The surgical conditions, birthweight, age at presentation and associated anomalies did not differ in the two groups. The treatment was also similar except in oesophageal atresia, where cardiac banding was added to the temporary gastrostomy in late presenting cases with undernutrition in group B. Postoperative complications occurred in 43 (47.3%) cases (group A, 55.3%; group B, 38.6%; P > 0.05), and the overall mortality was 33 (35.3%: group A, 48.9%; group B, 22.7%: P < 0.05). Causes of mortality were unremitting sepsis (group A, 11; group B, 5), anaesthesia complications (group A, 5; group B, 0) and respiratory complication (group A, 7; group B, 5). Delayed presentation, inadequate facilities and defective health insurance scheme were challenges in the two groups. CONCLUSION: Despite the persisting challenges, co-ordinated team management may result in the modest improvement of outcomes of neonatal surgery in our setting. Addressing these challenges may further improve outcomes.


Subject(s)
Interdisciplinary Communication , Patient Care Team , Surgical Procedures, Operative , Delayed Diagnosis , Female , Humans , Infant, Newborn , Male , Nigeria , Postoperative Complications/classification , Retrospective Studies
2.
J Trop Pediatr ; 61(4): 304-9, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26130620

ABSTRACT

Schistosomiasis is an important communicable disease in the developing world. However, testicular schistosomiasis is an extremely rare condition. We report a case of testicular schistosomiasis mimicking testicular tumour in a 13 year old who presented with huge unilateral testicular mass. The dilemma encountered in the diagnosis and treatment of this child is presented to highlight the need for high index of suspicion of this pathology in children with testicular mass presenting from schistosomiasis-endemic areas.


Subject(s)
Schistosomiasis haematobia/diagnosis , Schistosomiasis/diagnosis , Testicular Diseases/diagnosis , Adolescent , Anthelmintics/therapeutic use , Diagnosis, Differential , Humans , Male , Neoplasms, Germ Cell and Embryonal , Praziquantel/therapeutic use , Rare Diseases , Schistosomiasis/drug therapy , Schistosomiasis haematobia/therapy , Testicular Diseases/therapy , Testicular Neoplasms , Treatment Outcome
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