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1.
Clin Transplant ; 38(3): e15272, 2024 03.
Article in English | MEDLINE | ID: mdl-38445550

ABSTRACT

COVID-19 is a heterogenous infection-asymptomatic to fatal. While the course of pediatric COVID-19 infections is usually mild or even asymptomatic, individuals after adult heart transplantation are at high risk of a severe infection. We conducted a retrospective, multicenter survey of 16 pediatric heart transplant centers in Germany, Austria and Switzerland to evaluate the risk of a severe COVID-19 infection after pediatric heart transplantation between 02/2020 and 06/2021. Twenty-six subjects (11 male) with a median age of 9.77 years at time of transplantation and a median of 4.65 years after transplantation suffered from COVID-19 infection. The median age at time of COVID-10 infection was 17.20 years. Fourteen subjects had an asymptomatic COVID-19 infection. The most frequent symptoms were myalgia/fatigue (n = 6), cough (n = 5), rhinitis (n = 5), and loss of taste (n = 5). Only one subject showed dyspnea. Eleven individuals needed therapy in an outpatient setting, four subjects were hospitalized. One person needed oxygen supply, none of the subjects needed non-invasive or invasive mechanical ventilation. No specific signs for graft dysfunction were found by non-invasive testing. In pediatric heart transplant subjects, COVID-19 infection was mostly asymptomatic or mild. There were no SARS-CoV-2 associated myocardial dysfunction in heart transplant individuals.


Subject(s)
COVID-19 , Heart Transplantation , Adult , Humans , Male , Child , Adolescent , COVID-19/epidemiology , Austria/epidemiology , Switzerland/epidemiology , Retrospective Studies , Heart Transplantation/adverse effects , Germany/epidemiology
2.
JPEN J Parenter Enteral Nutr ; 42(8): 1288-1294, 2018 Nov.
Article in English | MEDLINE | ID: mdl-29603266

ABSTRACT

BACKGROUND: Preterm infants are at risk of oxidative stress from neonatal intensive care interventions. 8-Oxo-2'-deoxyguanosine (8-oxodG), generated by oxygen radical attack on DNA, is a potential marker of oxidative stress. The aim of the present study was to investigate the impact of quality and source of enteral nutrition (EN) on renal excretion of 8-oxodG in preterm infants. METHODS: Spontaneous urine samples were collected on postnatal days 26-31 in 33 preterm infants. Infants were fed either breast milk (BM), formula (FM), or BM/FM mixtures. Daily iron (Fe) supplementation was started day 28 ± 1 postnatally. 8-oxodG was determined by highperformance liquid chromatography-electrochemical detection (HPLC-EC). RESULTS: The 8-oxodG/creatinine ratio was significantly higher in infants fed FM vs FM/BM (38.7 ± 28.7 vs 16.7 ± 12.2 nmol 8-oxodG/mmol creatinine, P < 0.0001) or BM (11.6 ± 10.4 nmol 8-oxodG/mmol creatinine, P < 0.0001). There was no significant effect of Fe supplementation (P = 0.547). 8-OxodG excretion showed significant interindividual variation but was similar within pairs of twins. CONCLUSION: Quality and source of EN seem to influence oxidative stress in preterm infants. The underlying pathophysiological mechanism is unclear and needs further investigation. It may be speculated that other mechanisms than Fe supplementation contribute to oxidative stress, such as cow's milk protein-mediated up-regulation of the intestinal inflammatory cascade.


Subject(s)
Deoxyguanosine/analogs & derivatives , Enteral Nutrition/adverse effects , Infant Formula , Infant, Premature , Iron, Dietary , Milk , Oxidative Stress , 8-Hydroxy-2'-Deoxyguanosine , Animals , Biomarkers/urine , Cattle , Creatinine/urine , Deoxyguanosine/urine , Dietary Supplements/adverse effects , Enteral Nutrition/methods , Female , Humans , Infant Nutritional Physiological Phenomena , Infant, Newborn , Intensive Care, Neonatal , Iron, Dietary/adverse effects , Male , Milk/adverse effects , Milk, Human , Prospective Studies , Twins
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