Theguidelinescontainedinthisapplicationaredesignedtoprovideextensive,easy-to-readinformationregardingthedialyzabilityofdrugs.Numerousliteraturesourceshavebeenusedinpreparingtheguidelines.Formanydrugs,includingnewly-approvedmedications,investigationalagentsandmedicationsavailableinothercountries,therehavebeennodialysispharmacokineticstudies.Insomecases,theavailabledatamayconflict.Conditionsofdialysisusedinpublishedstudiesmaynotreflectcurrentdialysispracticeandtechnology.Variationsinthedurationofdialysis,bloodanddialysateflowrates,dialysismembranes,andwhetherperitonealdialysisiscontinuousorintermittent,willallaffectdrugremoval.Theseguidelinesdistinguishbetweenconventionalhemodialysisandhighpermeability(high-flux)hemodialysiswheresuchdataareavailable.Noinformationisprovidedondrugdialyzabilitywithcontinuousrenalreplacementtherapy(CRRT)orwithplasmapheresis.Foradditionalinformationonspecificdrugs,thereadershouldconsulttheprimaryliterature.
Usersofthisapplicationarereferredtowww.renalpharmacyconsultants.comforbackgroundandexplanatorymaterialtoassistintheinterpretationofthetabulardata.Thewebsiteprovidesspecificinformationaboutfactorsthatinfluencedrugdialyzabilityandspecialconsiderations,suchasCRRT,plasmapheresisanddrugsofabuse.Usersmustbefamiliarwiththisinformationpriortousingthecontentofthisapplication.Thewebsitealsoincludesatablepresentingsievingcoefficientdatafrominvitroandinvivoevaluations,whichcanbeusedtopredictdosingrequirementsinCRRT,andatableregardingremovalofdrugsofabuse.
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