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2.
Saudi J Kidney Dis Transpl ; 26(3): 549-55, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26022026

RESUMEN

Acute kidney injury (AKI) is a complex disorder with clinical manifestations ranging from mild dysfunction to complete kidney failure. The published literature on the incidence and outcome of AKI in the critically ill neonatal population is scarce. The aim of this study was to evaluate the types, the associated risk factors and short-term outcome of AKI in the critically ill neonates. A cohort study was conducted including 100 critically ill neonates successively admitted to the Neonatal Intensive Care Unit. The inclusion criteria were a gestational age ≥28 weeks and body weight ≥1 kg. Exclusion criteria included those with multiple congenital anomalies or on drugs altering glomerular filtration rate or AKI developing postoperatively. Neonates were evaluated for the development of AKI [creatinine >1.5 mg/dL and/or blood urea nitrogen (BUN) >20 mg/dL] and were assigned as group A (who developed AKI) and group B (who did not develop AKI). Forty-one patients developed AKI (group A) among whom nine (22%) showed oliguric AKI. The most common risk factors among group A patients were sepsis (75.6%) and nephrotoxic drug administration (75.6%), followed by shock (39%). There were no statistically significant differences between both groups except for male sex predominance and necrotizing enterocolitis (NEC), which were significantly higher among group A (P <0.05). Use of continuous positive airway pressure (CPAP) ventilation was significantly higher in neonates without AKI (13.6% vs 0.0%, P = 0.02). The mortality rate among group A reached 51.2%. Various risk factors including gender, gestational age, birth weight, shock, NEC, sepsis, nephrotoxic drugs, oliguria and mechanical ventilation were studied as regards outcome of group A, and all factors except gender and oliguria proved to be significantly higher in deceased neonates. Male sex and NEC were important risk factors for developing AKI that was predominantly non-oliguric. CPAP ventilation may have a protective effect against AKI. The mortality rate was more than three times higher in the AKI group.

3.
J Egypt Public Health Assoc ; 88(3): 148-52, 2013 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-24374948

RESUMEN

BACKGROUND: Thyroid dysfunction is a known complication of transfusion-dependent ß-thalassemia. However, information on its frequency and risk factors among Egyptian Children is still unclear. OBJECTIVE: We aimed to determine the frequency of functional thyroid abnormalities among young patients with ß-thalassemia and compare the thyroid function status among patients with ß-thalassemia major (TM) and ß-thalassemia intermedia (TI). MATERIALS AND METHODS: This was a cross-sectional study that included 52 ß-thalassemia children [27 boys and 25 girls; 34 (65.4%) with TM and 18 (34.6%) with TI]. Their mean age was 16.0±1.91 (range: 12-18) years. Thyroid function and iron load status were assessed by measurement of free tetraiodothyronine, free triiodothyronine, thyroid stimulating hormone (TSH), and serum ferritin concentrations. RESULTS: Serum TSH of the studied cases ranged from 0.28 to 25 µIU/ml with a mean of 4.5±4.8 µIU/ml. None of the studied cases had overt primary hypothyroidism and the frequency of subclinical hypothyroidism was 19.2%. No risk factors for thyroid dysfunction could be identified among our cases. The thyroid profile was comparable in TM and TI patients (P>0.05) and the frequency of subclinical hypothyroidism among TM cases was 20.6% and it was comparable to the 16.7% found among TI patients (P>0.05). No correlations were found between TSH, serum ferritin, chelation therapy, and frequency of blood transfusion. CONCLUSION AND RECOMMENDATIONS: Both TM and TI patients are at risk for subclinical thyroid failure regardless of their iron overload status. Early evaluation of thyroid function in ß-thalassemia children and thyroid replacement therapy for subclinical hypothyroidism should be introduced in the treatment protocols.


Asunto(s)
Sobrecarga de Hierro , Talasemia beta , Niño , Estudios Transversales , Humanos , Hipotiroidismo/sangre , Talasemia beta/sangre
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