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<channel><title><![CDATA[EMERGENCY MEDICINE GUIDEWIRE - Pediatric EM Shownotes]]></title><link><![CDATA[https://www.emguidewire.com/pediatric-em-shownotes]]></link><description><![CDATA[Pediatric EM Shownotes]]></description><pubDate>Mon, 16 Feb 2026 20:32:02 -0800</pubDate><generator>Weebly</generator><item><title><![CDATA[Pediatric UTI]]></title><link><![CDATA[https://www.emguidewire.com/pediatric-em-shownotes/pediatric-uti]]></link><comments><![CDATA[https://www.emguidewire.com/pediatric-em-shownotes/pediatric-uti#comments]]></comments><pubDate>Fri, 15 Feb 2019 16:50:30 GMT</pubDate><category><![CDATA[Uncategorized]]></category><guid isPermaLink="false">https://www.emguidewire.com/pediatric-em-shownotes/pediatric-uti</guid><description><![CDATA[Why is this important:&nbsp;UTI is the most frequent bacterial infection in children &lt; 2 yearsClinical presentation is non-specific and urine sample cannot be obtained without invasive measures so dx is often delayed&nbsp;Who created these guidelines:&nbsp;revision of practice parameters published in 1999committee included gen peds, epidemiology/informatics, peds ID, radiology, peds urology.&nbsp;Guidelines were further reviewed by multiple subgroups within AAP and 5 external organizations in [...] ]]></description><content:encoded><![CDATA[<div><div id="200766646487573751" align="left" style="width: 100%; overflow-y: hidden;" class="wcustomhtml"><iframe style="border: none" src="//html5-player.libsyn.com/embed/episode/id/8662046/height/90/theme/custom/thumbnail/yes/direction/backward/render-playlist/no/custom-color/68a0e1/" height="90" width="100%" scrolling="no" allowfullscreen="" webkitallowfullscreen="" mozallowfullscreen="" oallowfullscreen="" msallowfullscreen=""></iframe></div></div><div><div style="height: 20px; overflow: hidden; width: 100%;"></div><hr class="styled-hr" style="width:100%;"><div style="height: 20px; overflow: hidden; width: 100%;"></div></div><div class="paragraph"><strong>Why is this important:&nbsp;</strong><br><ul><li>UTI is the most frequent bacterial infection in children &lt; 2 years</li><li>Clinical presentation is non-specific and urine sample cannot be obtained without invasive measures so dx is often delayed&nbsp;</li></ul><br><strong>Who created these guidelines:&nbsp;</strong><br><ul><li>revision of practice parameters published in 1999</li><li>committee included gen peds, epidemiology/informatics, peds ID, radiology, peds urology.&nbsp;</li><li>Guidelines were further reviewed by multiple subgroups within AAP and 5 external organizations in the US and Canada.&nbsp;</li></ul><br><strong>Guideline objectives:&nbsp;</strong><br><ul><li>Focuses on the dx/management of initial UTI in febrile children &lt; 2 years&nbsp;</li><li>studies suggest that incidence of UTI can be as high as 5% in &lt; 2 yr with unexplained fever</li><li>Neonates &lt; 2 months were excluded&nbsp;</li><li>Children w/ obvious neuro or anatomic abnormality leading to recurrent UTI were excluded</li></ul><br><strong>Diagnosis:&nbsp;</strong><br><ul><li>Febrile infant w/ no other source of infection requiring abx 2/2 to toxic nature<ul><li>obtain UA/Culture before abx</li></ul></li><li>Febrile infant w/ no other source of infection who are non-toxic:&nbsp;<ul><li>MD should assess likelihood of UTI<ul><li>Low: clinical follow up without testing&nbsp;</li><li>High (&gt;2%): 2 options&nbsp;:<ul><li>1. Obtain UA/culture via cath or SPA&nbsp;</li><li>2. Obtain urine via bag, complete UA and if UA is suggestive of UTI obtain 2ndsample via cath or SPA. If negative, monitor clinically w/o abx</li></ul></li></ul></li></ul></li><li>To establish dx of UTI, MD should require both UA suggestive of infection (pyuria and bacteriuria) and 50K CFU of uropathogen cultured from non-bagged sample</li></ul><br><strong>What is a (+) UA</strong><br><ul><li>UA: nitrates not good for children, LE has high SN, WBC threshold should be 5WBC/HPF</li><li>Bacteriuria: the presence of bacteria correlates with 10^5 CFU on cx</li></ul><br><strong>Who should be tested</strong> (&nbsp;Low risk vs. not):<br><ul><li>Females: <strong>age &lt; 12 months;&nbsp;white race;&nbsp;fever &gt; 39;&nbsp;duration &gt; 2 days;&nbsp;no other ssx of infection</strong><ul><li>&le; 1% chance of UTI &le;1 risk factor&nbsp;&nbsp;</li><li>&le;2% chance &le; 2 risk factors&nbsp;</li></ul></li><li>Males: <strong>nonblack race; fever &gt; 39;&nbsp;duration &gt; 24 hours;&nbsp;no other ssx of infection</strong><ul><li>Uncircumcised: &le;2% chance only if they have no risk factors&nbsp;</li><li>Circumcised:<ul><li>&le;1% chance: &le; 2 risk factors</li><li>&le;2% chance: &le; 3 risk factors&nbsp;</li></ul></li></ul></li></ul><br><strong>How should we test them?&nbsp;</strong><br><ul><li>Catheterization or suprapubic aspiration (SPA)&nbsp;</li></ul><ul><li>Dx of UTI cannot be made through urine cx collected in bag; these have an unacceptably high false positive rate and are valid only when negative. SP is only 63%</li></ul><br><strong>Treatment:</strong><br><ul><li>Base choice of route of abx practically&nbsp;&#61664;if toxic appearing or not tolerating PO, then tx parentally, otherwise PO&nbsp;</li><li>Base choice of agent on <strong>local biograms</strong></li><li>Adjust abx as needed based on culture SN results&nbsp;</li><li>Tx for 7-14 days (no difference found between 7,10, or 14 days but 1-3 days was inferior)</li></ul><br><strong>Follow up studies:</strong><br><ul><li>Febrile infants with UTI should undergo RUS; if toxic recommended within first 2 days of dx, if well defer to later date.&nbsp;</li><li>Nuclear scans not recommended&nbsp;</li><li>VCUG are not recommended after first UTI unless RUS is abnormal&nbsp;</li></ul>&nbsp;<br></div>]]></content:encoded></item><item><title><![CDATA[Hyperemesis gravidarum]]></title><link><![CDATA[https://www.emguidewire.com/pediatric-em-shownotes/hyperemesis-gravidarum]]></link><comments><![CDATA[https://www.emguidewire.com/pediatric-em-shownotes/hyperemesis-gravidarum#comments]]></comments><pubDate>Fri, 27 Jul 2018 16:45:26 GMT</pubDate><category><![CDATA[Uncategorized]]></category><guid isPermaLink="false">https://www.emguidewire.com/pediatric-em-shownotes/hyperemesis-gravidarum</guid><description><![CDATA[ [...] ]]></description><content:encoded><![CDATA[<div><div id="153523154974415248" align="left" style="width: 100%; overflow-y: hidden;" class="wcustomhtml"><iframe style="border: none" src="//html5-player.libsyn.com/embed/episode/id/6857719/height/90/theme/custom/autoplay/no/autonext/no/thumbnail/yes/preload/no/no_addthis/no/direction/backward/render-playlist/no/custom-color/68a0e1/" height="90" width="100%" scrolling="no" allowfullscreen="" webkitallowfullscreen="" mozallowfullscreen="" oallowfullscreen="" msallowfullscreen=""></iframe></div></div><div><div style="height: 20px; overflow: hidden; width: 100%;"></div><hr class="styled-hr" style="width:100%;"><div style="height: 20px; overflow: hidden; width: 100%;"></div></div>]]></content:encoded></item><item><title><![CDATA[Pediatric DKA and Fluid Management]]></title><link><![CDATA[https://www.emguidewire.com/pediatric-em-shownotes/pediatric-dka-and-fluid-management]]></link><comments><![CDATA[https://www.emguidewire.com/pediatric-em-shownotes/pediatric-dka-and-fluid-management#comments]]></comments><pubDate>Tue, 17 Jul 2018 21:48:51 GMT</pubDate><category><![CDATA[Uncategorized]]></category><guid isPermaLink="false">https://www.emguidewire.com/pediatric-em-shownotes/pediatric-dka-and-fluid-management</guid><description><![CDATA[Kuppermann&nbsp;N&nbsp;et al.&nbsp;Clinical Trial of Fluid Infusion Rates for Pediatric Diabetic Ketoacidosis.&nbsp;www.nejm.org/doi/full/10.1056/NEJMoa1716816N Engl J Med.&nbsp;2018 Jun 14;378(24):2275-228Cerebral edema is an uncommon complication in DKA in pediatrics.This study did not find any significant difference in adverse neurological outcomes when comparing slightly slower vs slightly faster infusion rates.The infusion rates they studied were at the upper and lower boundaries of current [...] ]]></description><content:encoded><![CDATA[<div><div id="441889409972396335" align="left" style="width: 100%; overflow-y: hidden;" class="wcustomhtml"><iframe style="border: none" src="//html5-player.libsyn.com/embed/episode/id/6822602/height/90/theme/custom/autoplay/no/autonext/no/thumbnail/yes/preload/no/no_addthis/no/direction/backward/render-playlist/no/custom-color/68a0e1/" height="90" width="100%" scrolling="no" allowfullscreen="" webkitallowfullscreen="" mozallowfullscreen="" oallowfullscreen="" msallowfullscreen=""></iframe></div></div><div><div style="height: 20px; overflow: hidden; width: 100%;"></div><hr class="styled-hr" style="width:100%;"><div style="height: 20px; overflow: hidden; width: 100%;"></div></div><div class="paragraph"><font color="#2A2A2A" size="2">Kuppermann&nbsp;N<span style="font-weight:400">&nbsp;et al.&nbsp;Clinical Trial of Fluid Infusion Rates for Pediatric Diabetic Ketoacidosis.&nbsp;<a href="https://www.nejm.org/doi/full/10.1056/NEJMoa1716816" target="_blank">www.nejm.org/doi/full/10.1056/NEJMoa1716816</a></span><a href="https://www.ncbi.nlm.nih.gov/pubmed/29897851#">N Engl J Med.</a>&nbsp;2018 Jun 14;378(24):2275-228<br></font></div><div class="paragraph"><ul><li><font size="3"><strong><a href="http://pedemmorsels.com/cerebral-edema-diabetic-ketoacidosis/" target="_blank">Cerebral edema</a></strong> is an uncommon complication in DKA in pediatrics.</font></li><li><font size="3">This study <strong>did not find any significant difference</strong> in adverse neurological outcomes when comparing slightly slower vs slightly faster infusion rates.</font></li><li><font size="3">The infusion rates they studied were at the upper and lower boundaries of currently adopted protocols.&nbsp; We do not know what the results who have been if they had compared even faster infusion rates to the current protocols.</font></li><li><font size="3"><strong>Resuscitation of the DKA patient should be based on the clinical presentation</strong> of the patient along with currently accepted protocols.</font></li></ul></div>]]></content:encoded></item></channel></rss>