AI-model voorspelt overlijden en complicaties na hartingreep
Voor de zorgverleners en patiënten Historisch gezien hebben zowel patiënten als clinici de voordelen van procedures zoals coronaire angiografie en PCI overschat en de risico's onderschat. Dit heeft geleid tot beperkingen in de adoptie van strategieën om bloedingen en contrast-geassocieerde acute kidney injury (acute nierbeschadiging; AKI) te vermijden bij patiënten met het hoogste risico. Het […]

Aanbevolen

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Nieuwe techniek ter behandeling van urinewegstenen
Patiënten met urinewegstenen komen vaak op de spoedeisende hulp. Indien mogelijk wordt meestal als eerste gekozen voor observatie met een poging tot ...
Non-Hodgkin lymfoom (NHL) na niertransplantatie
Non-Hodgkin lymfoom Non-Hodgkin lymfoom (NHL) dat zich ontwikkelt na niertransplantatie behoort tot de post-transplantatie lymfoproliferatieve aandoen...

Nefrologie nieuws

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Pushing kidney-stone fragments reduces stones' recurrence
sciencedaily.com
Researchers found that patients who underwent the stone-moving ultrasound procedure had a 70% lower risk of such a recurrence.
Higher thiazide doses shown to reduce kidney stone events
sciencedaily.com
Higher thiazide doses are associated with greater reductions in urine calcium, which in turn correlate with fewer symptomatic kidney stone events, according to a new study.
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Oncologie

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Water/elektrolytstoornissen

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Homozygosity for a Rare FASTKD2 Variant Resulting in an Adult Onset Autosomal Recessive Mitochondrial Podocytopathy
ajkd.org
Mitochondrial cytopathies can have kidney involvement in up to half of cases. Their diagnosis is challenging due to phenotypic variability, lack of noninvasive tests to assess mitochondrial dysfunction and genetic heterogeneity. We report on a young adult male with hypertrophic cardiomyopathy (HCM) and chronic kidney disease (CKD) with sub-nephrotic proteinuria, who presented to the emergency department with kidney failure and hypervolemia requiring dialysis. A kidney biopsy showed focal segmental and global glomerulosclerosis, extensive foot process effacement, and abnormal mitochondria in podocytes and tubular epithelial cells; the genetic workup identified a rare FASTKD2 exon 2 variant, c.29G>C p.(Ser10Thr), in homozygosity; and functional mitochondrial assays in cultured skin fibroblasts showed reduction in FASTKD2 protein expression and moderate combined impairment in mitochondrial respiratory chain (MRC) assembly and function.
Homozygosity for a Rare FASTKD2 Variant Resulting in an Adult Onset Autosomal Recessive Mitochondrial Podocytopathy
ajkd.org
Mitochondrial cytopathies can have kidney involvement in up to half of cases. Their diagnosis is challenging due to phenotypic variability, lack of noninvasive tests to assess mitochondrial dysfunction and genetic heterogeneity. We report on a young adult male with hypertrophic cardiomyopathy (HCM) and chronic kidney disease (CKD) with sub-nephrotic proteinuria, who presented to the emergency department with kidney failure and hypervolemia requiring dialysis. A kidney biopsy showed focal segmental and global glomerulosclerosis, extensive foot process effacement, and abnormal mitochondria in podocytes and tubular epithelial cells; the genetic workup identified a rare FASTKD2 exon 2 variant, c.29G>C p.(Ser10Thr), in homozygosity; and functional mitochondrial assays in cultured skin fibroblasts showed reduction in FASTKD2 protein expression and moderate combined impairment in mitochondrial respiratory chain (MRC) assembly and function.
Clesrovimab Protects Against RSV-Associated Disease in Infants, Study Shows
empr.com
Topline results were announced from a phase 2b/3 study investigating clesrovimab as a preventive therapy for respiratory syncytial virus (RSV)-associa...