Interactive Transcript
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So our last section that we're gonna cover in our head
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to toe or north, north to south imaging
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of newborns in the NICU is genital urinary imaging.
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And a lot of this we're gonna be focused on the kidneys.
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So let's talk about congenital hydronephrosis
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or neonatal hydronephrosis.
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So in this part of this review,
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we're gonna talk about why this is important.
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We're gonna talk about the consensus nomenclature.
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Currently we're gonna know when
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to call a kidney normal in the setting
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of congenital hydronephrosis,
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and then we'll learn how to appropriately grade, um,
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urinary tract dilatation postnatally.
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So, uh, prenatal urinary tract dilatation is a big deal
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because it's pretty common, uh, finding
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that is found on prenatal imaging in up
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to 2% of all pregnancies.
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So this leads to a lot of imaging costs, not
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to mention parental anxiety, um, of a mom who has a baby
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who might have a congenital anomaly of the kidney
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and urinary tract.
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These are expensive because of prenatal
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and postnatal imaging, not to mention patients who have
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to go on to voiding, cysto urethrogram, uh,
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or contrast enhance voiding cystogram plus slash minus
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antibiotic therapy.
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So the goal of imaging the kidneys in patients
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with suspected congenital, um, hydronephrosis is
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to identify complications
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or anomalies rather prior to complications such
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as urinary tract infection or stone formation.
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The good news is most cases
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of in utero congenital hydronephrosis resolve spontaneously.
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And so we'll get a follow-up postnatal renal ultrasound
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and the hydronephrosis will spontaneously resolve.
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So a group of multidisciplinary urologic imagers urologists,
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um, fetal imagers came together
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to create some consensus guidelines for how to appropriately
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classify and care for infants
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with congenital hydro necrosis.
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Um, so there are both antenatal presentation
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and postnatal presentations of urinary tract dilatation, um,
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where we will appropriately classify patients into low risk
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versus high risk.
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And the higher the number, the greater the likelihood
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that there will be an abnormality
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that will require surgical intervention.
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Um, so management is based on the severity.
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So ANTENATALLY is the UTDA system where one is low risk
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and two slash three is moderate to intermediate
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or moderate to high risk.
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Rather, these patients will get two ultrasounds postnatally,
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one after 40 hours of life to one month of life,
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and then a second, six months later
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if there's bilateral hydronephrosis follow up is based on
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the more severe side.
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Importantly, the recommendations are to do ultrasound
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after 48 hours of life,
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to not underestimate the degree of dilation.
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Infants have physiologic
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Oliguria, um, prior to 48 hours of life.
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So we wanna wait to make sure
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that we're not underestimating the severity
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of hydro necrosis.
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Um, I also wanna say that in patients who have, uh,
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severe antenatal abnormalities, seen sonographic, um,
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you don't wait four, eight hours to image those patients.
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Those patients go straight to, uh,
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renal ultrasound immediately following birth.
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And then you don't wanna wait too long
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before you image patients postnatally
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because if there's a severe abnormality,
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you wanna diagnose it sooner rather than later.
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In this consensus guidelines, the recommendation is to image
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and prone 'cause you want the degree of hydronephrosis to be
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as severe as possible.
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So in infants, typically the renal pelvis is located as sort
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of oriented more anterior to posterior.
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And in the prone position,
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a collecting system will open up a little bit
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and look more severe in prone compared to supine.
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So you wanna grade the hydronephrosis, uh, when it's
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as severe as possible,
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which is in the prone position typically.