{"id":4040,"date":"2025-03-31T18:11:56","date_gmt":"2025-03-31T18:11:56","guid":{"rendered":"https:\/\/kidneydiseaseclinic.net\/kdc\/gentamicin-txt\/"},"modified":"2025-03-31T18:11:56","modified_gmt":"2025-03-31T18:11:56","slug":"gentamicin-txt","status":"publish","type":"post","link":"https:\/\/kidneydiseaseclinic.net\/kdc\/gentamicin-txt\/","title":{"rendered":"Gentamicin.txt"},"content":{"rendered":"<h1>  Gentamicin   <\/h1>\n<p><H3>  CLINICAL USE <\/H3><br \/>\nAntibacterial agent<H3> DOSE IN NORMAL RENAL FUNCTION  <\/H3>Once daily dose: 5\u20137 mg\/kg, dose is then  adjusted according to levelsEndocarditis: 1 mg\/kg every 8 hours Intrathecal: 1\u20135 mg daily PD peritonitis: see local policy <H3>  PHARMACOKINETICS    <\/H3><LI> Molecular weight &amp;nbsp  &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp  &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp :477.6<\/li>\n<li>  %Protein binding  &amp;nbsp &amp;nbsp &amp;nbsp  &amp;nbsp  &amp;nbsp  &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp :0\u201330<\/li>\n<li>  %Excreted unchanged in urine &amp;nbsp &amp;nbsp : 90<\/li>\n<p><LI> Volume of distribution (L\/kg) &amp;nbsp &amp;nbsp &amp;nbsp :0.3<\/li>\n<p><LI>half-life \u2013 normal\/ESRD (hrs)&amp;nbsp &amp;nbsp &amp;nbsp :2\u20133\/20<H3>  DOSE IN RENAL IMPAIRMENT <\/H3> <H4>GFR (mL\/MIN)<\/H4>30\u201370 3\u20135 mg\/kg daily and monitor levels10\u201330 2\u20133 mg\/kg daily and monitor levels5\u201310 2 mg\/kg every 48\u201372 hours according to levels<H3> DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES  <\/H3><LI> CAPD  &amp;nbsp &amp;nbsp &amp;nbsp  &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp:Dialysed. <LI> CAPD  &amp;nbsp &amp;nbsp &amp;nbsp  &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp: clearance is about 3 mL\/min. Dose as in GFR=5\u201310 mL\/min. Monitor levels<\/p>\n<li> HD &amp;nbsp  &amp;nbsp &amp;nbsp  &amp;nbsp &amp;nbsp  &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp :Dialysed. Dose as in GFR=5\u201310 mL\/min. Give after dialysis<LI>HDF\/high flux  &amp;nbsp :Dialysed. Dose as in GFR=5\u201310 mL\/min. Give after dialysis<LI>CAV\/VVHD  &amp;nbsp &amp;nbsp &amp;nbsp:Dialysed. Dose in GFR= 30\u201370 mL\/min according to severity of infection, and measure levels<H3> IMPORTANT DRUG INTERACTIONS  <\/H3>Potentially hazardous interactions with other drugsBotulinum toxin: neuromuscular block  enhanced \u2013 risk of toxicity\n<li>Ciclosporin: increased risk of  nephrotoxicityCytotoxics: increased risk of  nephrotoxicity and possibly of ototoxicity with platinum compounds\n<li>    Diuretics: increased risk of ototoxicity  with loop diureticsMuscle relaxants: effects of non- depolarising muscle relaxants and suxamethonium enhancedParasympathomimetics: antagonism of  effect of neostigmine and pyridostigmine\n<li>  Tacrolimus: increased risk of  nephrotoxicity<H3> ADMINISTRATION  <\/H3><H4> Reconstition<\/H4>\u2013<H4>  Route  <\/H4>IV, IM, IP, intrathecal <H4>  Rate of Administration  <\/H4>Bolus IV: over not less than 3 minutes Short infusion: 20\u201330 minutes Once daily large infusions over 30\u2013 60 minutes<H4>Comments<\/H4>Can be added to sodium chloride or  glucose 5%<H4>  OTHER INFORMATION  <\/H4>Concurrent penicillins may result in sub- therapeutic blood levelsMonitor blood levels. 1 hour post-dose  peak levels must not exceed 10 mg\/L. Pre-dose trough levels should be less than 2 mg\/LIP therapy commonly used for PD  peritonitis. Dose varies according to local protocol and whether <LI> CAPD  &amp;nbsp &amp;nbsp &amp;nbsp  &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp: or APD dialysis. Monitoring of blood levels is advisable, as absorption is increased by inflamed peritoneumPotential nephrotoxicity of the drug may  worsen residual renal functionLong-term concurrent use of gentamicin  with teicoplanin causes additive ototoxicity.<br \/>\n","protected":false},"excerpt":{"rendered":"<p>Gentamicin CLINICAL USE Antibacterial agent DOSE IN NORMAL RENAL FUNCTION<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[7],"class_list":["post-4040","post","type-post","status-publish","format-standard","hentry","category-blog","tag-post-by-auto-php"],"_links":{"self":[{"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/posts\/4040","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/comments?post=4040"}],"version-history":[{"count":0,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/posts\/4040\/revisions"}],"wp:attachment":[{"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/media?parent=4040"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/categories?post=4040"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/tags?post=4040"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}