{"id":3809,"date":"2025-03-31T18:11:50","date_gmt":"2025-03-31T18:11:50","guid":{"rendered":"https:\/\/kidneydiseaseclinic.net\/kdc\/carboplatin-txt\/"},"modified":"2025-03-31T18:11:50","modified_gmt":"2025-03-31T18:11:50","slug":"carboplatin-txt","status":"publish","type":"post","link":"https:\/\/kidneydiseaseclinic.net\/kdc\/carboplatin-txt\/","title":{"rendered":"Carboplatin.txt"},"content":{"rendered":"<h1>Carboplatin<\/h1>\n<p><H3>  CLINICAL USE <\/H3><br \/>\nAntineoplastic agent:<\/p>\n<li>Ovarian carcinoma of epithelial origin\n<li>Small cell carcinoma of the lung <H3> DOSE IN NORMAL RENAL FUNCTION  <\/H3>Dose = Target AUC \u00d7 [GFR (mL\/min) + 25]where AUC is commonly 5 or 6 depending on protocol used (Calvert equation)<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 :371.2<\/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 :29\u201389<\/li>\n<li>  %Excreted unchanged in urine &amp;nbsp &amp;nbsp : 32\u201370<\/li>\n<p><LI> Volume of distribution (L\/kg) &amp;nbsp &amp;nbsp &amp;nbsp :0.23\u20130.28<\/li>\n<p><LI>half-life \u2013 normal\/ESRD (hrs)&amp;nbsp &amp;nbsp &amp;nbsp :1.5\u20136\/ Increased<H3>  DOSE IN RENAL IMPAIRMENT <\/H3> <H4>GFR (mL\/MIN)<\/H4><LI> 20 to 50  &amp;nbsp &amp;nbsp : Dose as in normal renal function. See \u2018Other Information\u2019<LI> 10 to 20  &amp;nbsp &amp;nbsp : Dose as in normal renal function. See \u2018Other Information\u2019<LI> &lt;10 &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp : Dose as in normal renal function. See \u2018Other Information\u2019<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:Unknown dialysability. Dose as in GFR &lt;10 mL\/min<\/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<LI> &lt;10 &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp : mL\/min<LI>HDF\/high flux  &amp;nbsp :Dialysed. Dose as in GFR<LI> &lt;10 &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp &amp;nbsp : mL\/min<LI>CAV\/VVHD  &amp;nbsp &amp;nbsp &amp;nbsp:Unknown dialysability. Dose as in GFR 10 to 20   mL\/min <H3> IMPORTANT DRUG INTERACTIONS  <\/H3>Potentially hazardous interactions with other drugs\n<li>Aminoglycosides: increased risk of  nephrotoxicity and possibly ototoxicity with aminoglycosides, capreomycin, polymyxins or vancomycin\n<li>Antipsychotics: avoid concomitant  use with clozapine, increased risk of agranulocytosis<H3> ADMINISTRATION  <\/H3><H4> Reconstition<\/H4>\u2013<H4>  Route  <\/H4>IV <H4>  Rate of Administration  <\/H4><H4> IV infusion  <\/H4> over 15\u201360 minutes <H4>Comments<\/H4>\n<li>Therapy should not be repeated until  4 weeks after the previous carboplatin course\n<li>May be diluted with glucose 5%, or sodium  chloride 0.9% to concentrations as low as 0.5 mg\/mL<H4>  OTHER INFORMATION  <\/H4>\n<li>Patients with abnormal kidney function  or receiving concomitant therapy with nephrotoxic drugs are likely to experience more severe and prolonged myelotoxicity\n<li>Blood counts and renal function should be  monitored closely\n<li>Some units still use a dose in normal renal  function of 400 mg\/m2. In this instance, the dose should be reduced to 50% of normal for a GFR of 10 to 20  mL\/min, and to 25% of normal for a GFR &lt;10 mL\/min\n<li>There is little, if any, true metabolism of  carboplatin. Excretion is primarily by glomerular filtration in the urine, with most of the drug excreted in the first 6 hours. Approximately 32% of the dose is excreted unchanged.\n<li>Platinum from carboplatin slowly becomes  protein bound, and is subsequently excreted with a terminal half-life of 5 days or more.<br \/>\n","protected":false},"excerpt":{"rendered":"<p>Carboplatin CLINICAL USE Antineoplastic agent: Ovarian carcinoma of epithelial origin<\/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-3809","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\/3809","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=3809"}],"version-history":[{"count":0,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/posts\/3809\/revisions"}],"wp:attachment":[{"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/media?parent=3809"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/categories?post=3809"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/kidneydiseaseclinic.net\/kdc\/wp-json\/wp\/v2\/tags?post=3809"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}