1
artÃculo
Publicado 2017
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We present the first case of application of therapeutic hypothermia in a newborn with a diagnosis of moderate ischemic hypoxic encephalopathy with the inclusion criterias. Risk factors, diagnostic criteria, evolution and monitoring during hypothermia and the followed-up post-discharge, are reported in our institution.
2
artÃculo
Publicado 2017
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We present the first case of application of therapeutic hypothermia in a newborn with a diagnosis of moderate ischemic hypoxic encephalopathy with the inclusion criterias. Risk factors, diagnostic criteria, evolution and monitoring during hypothermia and the followed-up post-discharge, are reported in our institution.
3
artÃculo
Publicado 2024
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ABSTRACTMaple syrup urine disease is a congenital metabolic disorder, commonly presenting as acute neonatal encephalopathy.Case 1. A 7-day-old neonate exhibited somnolence and refusal to breastfeed, later developing respiratory failure, neurological impairment, metabolic acidosis, and death. Elevated levels of branched-chain amino acids and a confirmatorygenetic test established the diagnosis. Case 2. A 10-day-old neonate was admitted with breastfeeding refusal, hypoglycemia, and seizures. Elevated branched-chain amino acids confirmed the diagnosis genetically. The patient receivedparenteral nutrition and a special formula, leading to progressive neurological improvement. Currently, at 2 years and 7months, the patient remains under multidisciplinary follow-up. Conclusion. Early detection of maple syrup urine diseasethrough neonatal screening significantly improves neurological outcomes.Â...
4
artÃculo
Publicado 2024
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ABSTRACTMaple syrup urine disease is a congenital metabolic disorder, commonly presenting as acute neonatal encephalopathy.Case 1. A 7-day-old neonate exhibited somnolence and refusal to breastfeed, later developing respiratory failure, neurological impairment, metabolic acidosis, and death. Elevated levels of branched-chain amino acids and a confirmatorygenetic test established the diagnosis. Case 2. A 10-day-old neonate was admitted with breastfeeding refusal, hypoglycemia, and seizures. Elevated branched-chain amino acids confirmed the diagnosis genetically. The patient receivedparenteral nutrition and a special formula, leading to progressive neurological improvement. Currently, at 2 years and 7months, the patient remains under multidisciplinary follow-up. Conclusion. Early detection of maple syrup urine diseasethrough neonatal screening significantly improves neurological outcomes.Â...
5
artÃculo
Publicado 2016
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El objetivo del estudio fue analizar el uso de la punción lumbar (PL) en las sospechas de sepsis neonatal tardÃa. Se utilizó una cohorte de 414 neonatos con peso al nacer <2000 g en tres hospitales de Lima. Se realizó la PL en 45/214 (21,0%) sospechas de sepsis y en 13/48 (27,1%) sepsis confirmadas por hemocultivo. Se diagnosticó meningitis en 8/214 (3,7%) sospechas y en 8/45 (17,5%) episodios en los que se realizó la PL. El tiempo de tratamiento de los episodios sin PL fue similar a los episodios de sepsis con meningitis descartada y menor a los episodios de meningitis. El uso de la PL es bajo, lo que puede resultar en meningitis no diagnosticadas y tratadas inadecuadamente.
6
artÃculo
Publicado 2018
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We report the first successful case of fetal surgery for spina bifida repair in Peru. A pregnant woman was referred to our center at 23 weeks’ gestation because of prenatal diagnosis of spina bifida. We formed a multidisciplinary international team with the goal of performing the first open intrauterine surgery in Peru. We performed a successful intrauterine surgery at 25 weeks of gestation and a healthy infant was born by cesarean section at 37 weeks of gestation. We demonstrated the feasibility of this complex intrauterine surgery in our local setting.