Re-Admission/HospitalizationForm (ADM)
|
|
- Helena Carmella Goodwin
- 5 years ago
- Views:
Transcription
1 BloodandMarrow TransplantClinical TrialsNetwork Segment(PROTSEG): DateofAdmission(ADMITDT): Re-Admission/HospitalizationForm (ADM) WebVersion:1.0;4.02; Dateofdischarge:(DISCHDT) (mm/dd/yyyy) 2.Patientdischargestatus:(DISCPTST) 1-Alive 2-Dead IfDead,aDeathForm mustbesubmited. 3.RecordPRIMARYdischargediagnosis:(PHSPREAS) *Specifyorgan:(ADM4SPEC) **Specifyother:(ADM1SPEC) GVHD Relapse/Progression GraftFailure Infection FungalInfection? 4.Recordsecondarydischargediagnoses: a.gvhd:(reasgvhd) b.relapse/progression:(reasrlps) 1-Contributory ncontributory? 1-Contributory ncontributory c.graftfailure:(reasgf) 1-Contributory ncontributory d.infection:(reasinf) 1-Contributory ncontributory e.fever:(reasfvr) 1-Contributory ncontributory f.seizure:(reasszr) 1-Contributory ncontributory g.bleeding/hemorhage:(reasgibl) 1-Contributory ncontributory h.diarhea:(reasdrh) 1-Contributory ncontributory i.nausea/vomiting:(reasnv) 1-Contributory ncontributory j.organfailure:(reasorgf) 1-Contributory ncontributory Specifyorgan:(ADM3SPEC) k.trauma:(reastram) 1-Contributory ncontributory l.psychiatric:(reaspsyc) 1-Contributory ncontributory m.secondarymalignancy:(reasmalg) 1-Contributory ncontributory n.scheduledprocedure/treatment:(reasproc) 1-Contributory ncontributory o.thrombosis/thrombus/embolism:(reastrmb) 1-Contributory ncontributory p.other:(reasothr) Specifyother:(ADM2SPEC) 1-Contributory ncontributory 5.Recordre-admissioninstitution:(ADMCENTR) 1-1-OriginalTransplantCenter 2-2-OtherTransplantCenter 3-3-OtherHospital Comments:(ADMCOMM1)
2 AdditionalSelectionOptionsforADM RecordPRIMARYdischargediagnosis: Non-FungalInfection Fever Seizure Bleeding/Hemorhage Diarhea Nausea/Vomiting OrganFailure(specifyorgan)* Trauma Psychiatric SecondaryMalignancy Transplant ScheduledProcedure/Treatment Thrombosis/Thrombus/Embolism Other(specify)**
3 BloodandMarrow TransplantClinical TrialsNetwork Segment(PROTSEG): DateofOnset(ADVDATE): Eventdescription(ADVENT): Unexpected,Grade3-5AdverseEventForm (AE1) WebVersion:1.0;3.06; Reportactivationstatus:(AVSTATUS) IfOther,specifyreasonfordeactivation:(AESPEC1) 1-1-Keepreportactive 2-2-Deactivate-Reportfiledineror 3-3-Deactivate-Keyfielderor 9-9-Deactivate-Otherreason? 2.Recorddatetransplantcenterbecameawareoftheevent:(AVAWARDT) (mm/dd/yyyy) 3.Indicateweightattimeoftheevent:(AVWGHTKG) (xxx.x) kg 4.Wasthiseventexpectedoranticipated?(AVEXPECT) 5.Recordtheseverityofevent:(AVEVENT) 6.Whatistherelationshiptostudytherapy/intervention:(AVRELAT) 7.Isthereanalternativeetiology:(AVETIOL) 8.Whatistheefectonstudytherapy/interventionschedule:(AVEFFECT)? 1-1-Mild 2-2-Moderate 3-3-Severe 4-4-LifeThreatening 5-5-Fatal 1-1-Unrelated 2-2-Unlikely 3-3-Possible 4-4-Probable 5-5-Definite? 0-0-NoneApparent 1-1-StudyDisease 2-2-OtherPre-ExistingDiseaseorCondition 3-3-Accident,Trauma,orExternalFactors 4-4-ConcurentIlness/Condition(NotPre-Existing) 1-1-NoChange-Completed 2-Change-Ongoing 3-3-DoseModified 4-4-TemporarilyStopped 5-5-PermanentlyStopped 9.Recordthemostsevereoutcomeoftheevent:(AVOUTCOM) 1-1-Resolved,NoResidualEfects 2-2-ResolvedwithSequelae 3-3-PersistentCondition 4-4-ResolvedbyDeath 10.Recordthedateofresolution:(AVRESDT) (mm/dd/yyyy)? 11.Wasthiseventassociatedwith:(AVASSOCI) 0-0-NoneoftheFolowing 1-1-Death 2-2-Life-ThreateningEvent 3-3-Disability 4-4-CongenitalAnomaly??
4 Comments:(AE1COMM)
5 AdditionalSelectionOptionsforAE1 Wasthiseventassociatedwith: 5-5-RequiredInterventiontoPreventPermanentImpairmentorDamage 6-6-Hospitalization(InitialorProlonged) 9-9-OtherSAE
6 BloodandMarrow TransplantClinical TrialsNetwork Segment(PROTSEG): DateofOnset(ADVDATE): Eventdescription(ADVENT): SummaryForm -Unexpected,Grade3-5AdverseEvent(AE2) WebVersion:1.0;3.06; Reportactivationstatus:(AVSTAT_A) 1-1-Keepreportactive 2-2-Deactivate-Reportfiledineror 3-3-Deactivate-Keyfielderor 9-9-Deactivate-Otherreason RelevantPastMedicalHistory 2.Doesthepatienthaveanyrelevanthistory,includingpre-existingmedical conditions?(semedhxs) IfYes,includeanyrelevanthistory,includingpreexistingmedicalconditionsbelow. (SEMEDHX) 3.EventSummary Includeclinicalhistoryofevent,associatedsignsandsymptoms,alternativeetiologiesbeingconsideredandmedicalmanagementbelow. (SESUMM) 4.Initialsubmiter:(SEISUBBY) Name: Date:(SEISUBDT) (mm/dd /yyyy) 5.Authorizedsubmiter:(SEASUBBY) Name: Date:(SEASUBDT) (mm/dd /yyyy)?
7 BloodandMarrow TransplantClinical TrialsNetwork Segment(PROTSEG): DateofOnset(ADVDATE): Eventdescription(ADVENT): TherapyForm -Unexpected,Grade3-5AdverseEvent(AE3) WebVersion:1.0;3.06; Reportactivationstatus:(AVSTAT_B) 1-1-Keepreportactive 2-2-Deactivate-Reportfiledineror 3-3-Deactivate-Keyfielderor 9-9-Deactivate-Otherreason StudyProduct/SuspectMedicationData 2.Wasthepatientreceivinganystudyproducts/suspectmedications?(RCVSP) IfYes,listthestudyproduct/suspectmedicationsthesubjectwastakinginthegridbelow. StudyProductName (Note:Ifblinded,indicate assuch) Doseof StudyProduct(s) atsaeonset Routeof StudyProduct(s) atsae Onset Scheduleof StudyProduct(s) atsaeonset DateStudy Product FirstStarted (mm/dd/yyyy) DateStudy Product LastTaken (mm/dd/yyyy) ReasonforUse (SPNAME1) (SP1DOSE) (SP1ROUTE) (SP1SCHED) (SP1STDT) (SP1SPDT) (SP1REASO) (SPNAME2) (SP2DOSE) (SP2ROUTE) (SP2SCHED) (SP2STDT) (SP2SPDT) (SP2REASO) (SPNAME3) (SP3DOSE) (SP3ROUTE) (SP3SCHED) (SP3STDT) (SP3SPDT) (SP3REASO) (SPNAME4) (SP4DOSE) (SP4ROUTE) (SP4SCHED) (SP4STDT) (SP4SPDT) (SP4REASO) (SPNAME5) (SP5DOSE) (SP5ROUTE) (SP5SCHED) (SP5STDT) (SP5SPDT) (SP5REASO) ConcomitantMedications 3.Wasthepatienttakinganyconcomitantmedications?(RCVCONMD) IfYes,listtheconcomitantmedicationsthepatientwastakingupto1monthpriortoSAEonsetinthegridbelow. Medication StartDate (mm/dd/yyyy) StopDate (mm/dd/yyyy) Dose,Route,Schedule Indication (CONMED1) (CM1STDT) (CM1SPDT) (CM1DOSE) (CM1INDIC) 1-1-Treatmentofadverseevent 9-9-Other (CONMED2) (CM2STDT) (CM2SPDT) (CM2DOSE) (CM2INDIC) 1-1-Treatmentofadverseevent 9-9-Other (CONMED3) (CM3STDT) (CM3SPDT) (CM3DOSE) (CM3INDIC) 1-1-Treatmentofadverseevent 9-9-Other (CONMED4) (CM4STDT) (CM4SPDT) (CM4DOSE) (CM4INDIC) 1-1-Treatmentofadverseevent 9-9-Other (CONMED5) (CM5STDT) (CM5SPDT) (CM5DOSE) (CM5INDIC)
8 1-1-Treatmentofadverseevent 9-9-Other (CONMED6) (CM6STDT) (CM6SPDT) (CM6DOSE) (CM6INDIC) 1-1-Treatmentofadverseevent 9-9-Other (CONMED7) (CM7STDT) (CM7SPDT) (CM7DOSE) (CM7INDIC) 1-1-Treatmentofadverseevent 9-9-Other (CONMED8) (CM8STDT) (CM8SPDT) (CM8DOSE) (CM8INDIC) 1-1-Treatmentofadverseevent 9-9-Other (CONMED9) (CM9STDT) (CM9SPDT) (CM9DOSE) (CM9INDIC) 1-1-Treatmentofadverseevent 9-9-Other (CONMED10) (CM10STDT) (CM10SPDT) (CM10DOSE) (CM10INDI) 1-1-Treatmentofadverseevent 9-9-Other (CONMED11) (CM11STDT) (CM11SPDT) (CM11DOSE) (CM11INDI) 1-1-Treatmentofadverseevent 9-9-Other (CONMED12) (CM12STDT) (CM12SPDT) (CM12DOSE) (CM12INDI) 1-1-Treatmentofadverseevent 9-9-Other (CONMED13) (CM13STDT) (CM13SPDT) (CM13DOSE) (CM13INDI) 1-1-Treatmentofadverseevent 9-9-Other (CONMED14) (CM14STDT) (CM14SPDT) (CM14DOSE) (CM14INDI) 1-1-Treatmentofadverseevent 9-9-Other (CONMED15) (CM15STDT) (CM15SPDT) (CM15DOSE) (CM15INDI) 1-1-Treatmentofadverseevent 9-9-Other (CONMED16) (CM16STDT) (CM16SPDT) (CM16DOSE) (CM16INDI) 1-1-Treatmentofadverseevent 9-9-Other (CONMED17) (CM17STDT) (CM17SPDT) (CM17DOSE) (CM17INDI) 1-1-Treatmentofadverseevent 9-9-Other (CONMED18) (CM18STDT) (CM18SPDT) (CM18DOSE) (CM18INDI) 1-1-Treatmentofadverseevent 9-9-Other (CONMED19) (CM19STDT) (CM19SPDT) (CM19DOSE) (CM19INDI) 1-1-Treatmentofadverseevent 9-9-Other (CONMED20) (CM20STDT) (CM20SPDT) (CM20DOSE) (CM20INDI) 1-1-Treatmentofadverseevent 9-9-Other
9 (CONMED21) (CM21STDT) (CM21SPDT) (CM21DOSE) (CM21INDI) 1-1-Treatmentofadverseevent 9-9-Other (CONMED22) (CM22STDT) (CM22SPDT) (CM22DOSE) (CM22INDI) 1-1-Treatmentofadverseevent 9-9-Other (CONMED23) (CM23STDT) (CM23SPDT) (CM23DOSE) (CM23INDI) 1-1-Treatmentofadverseevent 9-9-Other (CONMED24) (CM24STDT) (CM24SPDT) (CM24DOSE) (CM24INDI) 1-1-Treatmentofadverseevent 9-9-Other (CONMED25) (CM25STDT) (CM25SPDT) (CM25DOSE) (CM25INDI) 1-1-Treatmentofadverseevent 9-9-Other Comments:(AE3COMM)
10 BloodandMarrow TransplantClinical TrialsNetwork Segment(PROTSEG): DateofOnset(ADVDATE): Eventdescription(ADVENT): Laboratory/DiagnosticsForm -Unexpected,Grade3-5AdverseEvent(AE4) WebVersion:1.0;3.05; Reportactivationstatus:(AVSTAT_C) 1-1-Keepreportactive 2-2-Deactivate-Reportfiledineror 3-3-Deactivate-Keyfielderor 9-9-Deactivate-Otherreason LaboratoryTestResults 2.Wererelevantlaboratorytestsperformed?(LABTSTPF) IfYes,recordtherelevantlaboratorytestresultsinthegirdbelow. Test ColectionDate (mm/dd/yyyy) Result (Includeunits) SiteNormal Range (Includeunits) LabValuePrevious tothissae (Includeunits) ColectionDate forpreviouslab (mm/dd/yyyy) (ADLTST1) (ADL1CD) (ADL1RES) (ADL1NORG) (ADL1PRVL) (ADL1PCD) (ADLTST2) (ADL2CD) (ADL2RES) (ADL2NORG) (ADL2PRVL) (ADL2PCD) (ADLTST3) (ADL3CD) (ADL3RES) (ADL3NORG) (ADL3PRVL) (ADL3PCD) (ADLTST4) (ADL4CD) (ADL4RES) (ADL4NORG) (ADL4PRVL) (ADL4PCD) (ADLTST5) (ADL5CD) (ADL5RES) (ADL5NORG) (ADL5PRVL) (ADL5PCD) (ADLTST6) (ADL6CD) (ADL6RES) (ADL6NORG) (ADL6PRVL) (ADL6PCD) (ADLTST7) (ADL7CD) (ADL7RES) (ADL7NORG) (ADL7PRVL) (ADL7PCD) (ADLTST8) (ADL8CD) (ADL8RES) (ADL8NORG) (ADL8PRVL) (ADL8PCD) (ADLTST9) (ADL9CD) (ADL9RES) (ADL9NORG) (ADL9PRVL) (ADL9PCD) (ADLTST10) (ADL10CD) (ADL10RES) (ADL10NRG) (ADL10PVL) (ADL10PCD) DiagnosticTests(EX:MR,CTScan,Ultrasound) 3.Wererelevantdiagnostictestsperformed?(DXSTPF) IfYes,recordtherelevantdiagnostictestresultsinthegridbelow.Submitcopiesofthediagnostictestifavailable. Test DatePerformed (mm/dd/yyyy) Results/Comments
11 (ADDTS1) (AD1DTDAT) (AD1DTRES) (ADDTS2) (AD2DTDAT) (AD2DTRES) (ADDTS3) (AD3DTDAT) (AD3DTRES) (ADDTS4) (AD4DTDAT) (AD4DTRES) (ADDTS5) (AD5DTDAT) (AD5DTRES)
12 (ADDTS6) (AD6DTDAT) (AD6DTRES) (ADDTS7) (AD7DTDAT) (AD7DTRES) (ADDTS8) (AD8DTDAT) (AD8DTRES) (ADDTS9) (AD9DTDAT) (AD9DTRES) (ADDTS10) (AD10DTDT) (AD10DTRS)
13 Comments:(AE4COMM)
14 BloodandMarrow TransplantClinical TrialsNetwork Segment(PROTSEG): DateofOnset(ADVDATE): Eventdescription(ADVENT): Review Form -Unexpected,Grade3-5AdverseEvent(AE5) WebVersion:1.0;3.06; Reportactivationstatus:(AVSTAT_D) 1-1-Keepreportactive 2-2-Deactivate-Reportfiledineror 3-3-Deactivate-Keyfielderor 9-9-Deactivate-Otherreason 2.Reviewed:(AEREVIEW) 3.Reviewedby:(ARFREVBY) 4.Review date:(arfrevdt) (mm/dd/yyyy) 5.Comment1-ForDistribution:(ARCM1DIS) 6.Comment2-AlOtherReviewers/DataCoordinatingCenter(ARCM2ALL)
15 BloodandMarrow TransplantClinical TrialsNetwork Segment(PROTSEG): DateofOnset(ADVDATE): Eventdescription(ADVENT): MedicalMonitorReviewerForm -Unexpected,Grade3-5AdverseEvent(AE6) WebVersion:1.0;5.00; Adverseeventstatus:(AVSTAT_E) 1-1-Keepreportactive 2-2-Deactivate-Reportfiledineror 3-3-Deactivate-Keyfielderor 9-9-Deactivate-Otherreason 2.Hasthiseventbeendeterminedtobeanunexpected,grade3-5adverse event?(amdeter) 3.DoesthisrequireexpeditedreportingtotheDSMB?(AMEXPDSM) 4.Doyourecommendthepatientbewithdrawnfrom furtherprotocol therapy?(amwithdr) 5.Isthereviewcomplete?(AMREVDNE) 6.IfNo,whatadditionalinformationisrequired:(AMREVINF) 7.MedicalMonitoreventdescription:(AMMMEVDS) Comments:(AE6COMM)
16 BloodandMarrow TransplantClinical TrialsNetwork Segment(PROTSEG): VisitNumber(VISNO): Folow UpGVHD Form (CGV) WebVersion:1.0;7.03; Startofassessmentperiod:(DTPRVAST) (mm/dd/yyyy) 2.Endofassessmentperiod:(DTASSESS) (mm/dd/yyyy) Answerquestions3-9relatingtoacuteGVHD. 3.Maximum overalgradeofacutegvhd duringthis assessmentperiod:(grdagvhd) 0-0-NoSymptomsofAcuteGVHD 1-1-I 2-2-I 3-3-I 4-4-IV 4.Didclinicalsignsand/orsymptomsofacuteGVHDdevelop duringthisassessmentperiod?(agvdvlp) 5.Recordmethodusedtodiagnoseacute GVHD:(DGNSAGVH)? 1-1-HistologicEvidence 2-2-ClinicalEvidence 3-3-Both 6.DateofdiagnosisofacuteGVHD:(DTDGNAGV) (mm/dd/yyyy)? 7.WasprophylaxisforGVHD givenduringthisassessment period?(prophimm) DiscontinuedDuringThisAssessmentPeriod 8.Ifyes,specifyalimmunosuppressantsusedforGVHD prophylaxis: a.cyclosporine:(prophcy) b.tacrolimus:(prophtac) c.sirolimus:(prophsir) d.mmf:(prophmmf) e.prednisone:(prophprd) f.other:(prophoth) Specifyotheragentused:(PRPHOTSP) 9.IfGVHD prophylaxiswasdiscontinuedduringthis assessment,recordthedate:(prphdisc) (mm/dd/yyyy) Answerquestions10-20relatingtochronicGVHD. 10.Maximum overalseverityofchronicgvhd duringthis assessmentperiod:(sevcgvhd) 0-0-NoSymptomsofChronicGVHD 1-1-Mild 2-2-Moderate 3-3-Severe 11.Maximum overalgradeofchronicgvhd duringthis assessmentperiod:(grdcgvhd) 12.Didclinicalsignsand/orsymptomsofchronicGVHD develop duringthisassessmentperiod?(cgvdvlp) 13.Recordmethodusedtodiagnosechronic GVHD:(DGNSCGVH) 1-Limited 2-Extensive?? 1-1-HistologicEvidence 2-2-ClinicalEvidence 3-3-Both 14.DateofdiagnosisofchronicGVHD:(DTDGNCGV) (mm/dd/yyyy)?
17 15.Minimum Karnofsky/LanskyScoreattimeof diagnosis:(cgvkrnln) (Normal;NoComplaints/FulyActive) (NormalActivity/MinorRestrictioninStrenuousPlay) (NormalActivitywithEfort/RestrictedinStrenuousPlay) (UnabletoCaryOnNormalActivity/LessTimeSpentinPlay) (RequiresOccasionalAssistance/MinimalActivePlay) 16.Minimum plateletcountattimeofdiagnosis:(pltltcnt) (xxx.x) x10 9 /L 17.Alkalinephosphataseattimeofdiagnosis:(ALKPHOSP) (xxxx) U/L 18.Weightattimeofdiagnosis:(CGVWEIGH) (xxx.x) kg 19.Totalbilirubinattimeofdiagnosis:(BILIRUBN) (xx.x) mg/dl 20.Bodysurfaceareainvolvedwithrashattimeof diagnosis:(bsa) (xxx) %? Indicatethemaximum severityofinvolvementforthefolowingorgansystemsduringthisassessment period. Skin/Hair 21.Extentofskininvolvement:(CGVRASH) 0-0-NoRash 1-1-<25% ofbsainvolvement % ofbsainvolvement 3-3->50% ofbsainvolvement 4-4-GeneralizedInvolvement Ifthereisskininvolvement,indicatethetypeofrash: a.lichenoid:(rashlich)? b.maculopapular:(rashmacu) c.sclerodermatous:(rashsclr) Ocular 22.Xerophthalmia:(DRYEYES) 0-0-NoSymptoms 1-1-DryEyesbutNotRequiringTherapy 2-2-DrynessofEyesorInflammationRequiringTherapy Oral 23.Mucositis/ulcers(functional):(MUCOFXN) 0-0-NoSymptoms 1-1-MinimalSymptoms,NormalDiet 2-2-SymptomaticbutCanEatandSwalowModifiedDiet 3-3-SymptomaticandUnabletoAdequatelyAlimentorHydrateOraly Pulmonary 24.Dyspnea:(CGVDYSPN) 0-0-Asymptomatic 1-1-DyspneawithExertion 2-2-DyspneawithNormalActivities 3-3-DyspneaatRest 25.Pulmonaryfibrosis:(PULMFIBR) 0-0-None 1-1-MinimalRadiographicFindings 2-2-PatchyorBi-basilarRadiographicFindings 3-3-ExtensiveRadiographicFindings 9-9-NotDone 26.Bronchiolitisobliterans:(BRNCOBLT) 1-,Histologicdiagnosis 2-2-Yes,Clinicaldiagnosis 3-3-No 4-4-Unknown 27.FEV1:(CGVFEV1) % 1-1-<90-75% 2-2-<75-50% 3-3-<50-25% 4-4-<25%
18 28.Oxygensaturation:(O2SAT) 0-0-NoSymptoms 1-1-DesaturationwithExercise 2-2-RequiresSupplementalOxygen Gastrointestinal 29.Esophagus:(ESOPHAGS) 0-0-NoChanges 1-1-SymptomaticbutCanEatRegularDiet 2-2-DysphagiaorOdynophagiaRequiringDietaryChanges 3-3-NeedforParenteralNutrition 30.Nauseaandvomiting:(NAUSVOMT) 0-0-NoProtractedNauseaandVomiting 1-1-PersistentNausea,VomitingorAnorexia 31.Diarhea:(CGVDIARH) 0-0-None 1-1-PersistingLessThan2Weeks 2-2-PersistingMoreThan2Weeks 32.Wasdiarheameasuredasnumberofstoolsorvolumeof stools?(diarhmsr) 1-1-NumberofStools 2-2-VolumeofStools 3-3-BothNumberandVolume 33.Diarhea(numberofstools):(DIARHEA1) 1-1-Increaseof<4Stools/dayOverBaseline;MildIncreaseinOstomyOutputComparedtoBaseline 2-2-Increaseof4-6stools/day;IVFluidsIndicated<24Hrs;ModerateIncreaseinOstomyOutput 3-3-Increaseof7orMoreStools/day,IVFluidsfor24orMoreHrs;Hospitalization 4-4-Life-threateningConsequences(e.g.HemodynamicColapse) 5-5-Death UsemL/dayforadultrecipientsandmL/m 2 forpediatricrecipients. 34.Diarhea(volumeofstools):(DIARHEA2) 1-1-DiarheaLessThanorEqualto500mL/dayor<280mL/m^2 2-2-Diarhea>500butLessThanorEqualto1000mL/dayor mL/m^2 3-3-Diarhea>1000butLessThanorEqualto1500mL/dayor mL/m^2 4-4-Diarhea>1500mL/dayor>833mL/m^2 5-5-SevereAbdominalPainwithorwithoutIleus,orStoolwithFrankBloodorMelena 35.Malabsorption:(MALABSRP) 0-0-NoSymptoms 2-2-AlteredDiet;OralTherapiesIndicated(e.g.Enzymes,Medications,DietarySupplements) 3-3-InabilitytoAlimentAdequatelyviaGITract(e.g.TPN Indicated) 4-4-Life-threateningConsequences 5-5-Death Hepatic 36.Bilirubinlevel:(LIVERBIL) 0-0-Bilirubin<2.0mg/dL 1-1-Bilirubin mg/dL 2-2-Bilirubin mg/dL 3-3-Bilirubin mg/dL 4-4-Bilirubin>15.0mg/dL Genitourinary 37.Vaginitis:(VAGNITIS) 0-0-NoSymptomsorNotApplicable 1-1-Mild,InterventionNotIndicated 2-2-Moderate,InterventionIndicated 3-3-Severe,NotRelievedwithTreatment;Ulceration Musculoskeletal 38.Contractures:(CONTRCTR) 0-0-NoSymptoms 2-2-MildJointContractures(DoesnotAfectADL) 3-3-SevereJointContractures(InterfereswithADL) 39.Myositis:(MYOSITIS) Hematologic 40.Eosinophilia:(EOSINPHL)
19 Other 41.Serositis:(SEROSITS) 42.Fascitis:(FASCITIS) 43.Wasthereotherorganinvolvement?(ORGNOTHR) Specifyotherorgan:(ORGSPEC) Answerquestions44-50relatingtobiopsiesperformedduringthisassessmentperiod. 44.Wereanybiopsiesperformedduringthisassessmentperiod forsuspectedgvhd?(biopsy) Ifyes,recordthetype,date,andresultofanybiopsiesperformedforsuspectedGVHDbelow. TypeofBiopsy: IfOther,Specify: DateofBiopsy: ResultofBiopsy: 45.(BIOTYP1) 1-1-SkinBiopsy 2-2-OralBiopsy 3-3-UpperGIBiopsy 4-4-LowerGIBiopsy 5-5-LiverBiopsy (TYP1OSPE) (BIODT1) (mm/dd /yyyy) (BIORSLT1) 1-1-Positive 2-2-Negative 3-3-Equivocal 46.(BIOTYP2) 1-1-SkinBiopsy 2-2-OralBiopsy 3-3-UpperGIBiopsy 4-4-LowerGIBiopsy 5-5-LiverBiopsy (TYP2OSPE) (BIODT2) (mm/dd /yyyy) (BIORSLT2) 1-1-Positive 2-2-Negative 3-3-Equivocal 47.(BIOTYP3) 1-1-SkinBiopsy 2-2-OralBiopsy 3-3-UpperGIBiopsy 4-4-LowerGIBiopsy 5-5-LiverBiopsy (TYP3OSPE) (BIODT3) (mm/dd /yyyy) (BIORSLT3) 1-1-Positive 2-2-Negative 3-3-Equivocal 48.(BIOTYP4) 1-1-SkinBiopsy 2-2-OralBiopsy 3-3-UpperGIBiopsy 4-4-LowerGIBiopsy 5-5-LiverBiopsy (TYP4OSPE) (BIODT4) (mm/dd /yyyy) (BIORSLT4) 1-1-Positive 2-2-Negative 3-3-Equivocal 49.(BIOTYP5) 1-1-SkinBiopsy 2-2-OralBiopsy 3-3-UpperGIBiopsy 4-4-LowerGIBiopsy 5-5-LiverBiopsy (TYP5OSPE) (BIODT5) (mm/dd /yyyy) (BIORSLT5) 1-1-Positive 2-2-Negative 3-3-Equivocal 50.(BIOTYP6) 1-1-SkinBiopsy 2-2-OralBiopsy 3-3-UpperGIBiopsy 4-4-LowerGIBiopsy 5-5-LiverBiopsy (TYP6OSPE) (BIODT6) (mm/dd /yyyy) (BIORSLT6) 1-1-Positive 2-2-Negative 3-3-Equivocal Answerquestions51-54relatingtoGVHD therapy.
20 51.WasaspecifictherapyusedtotreatGVHD duringthis assessmentperiod?(thrpyusd) 1-,InitiatedthisAssessmentPeriod 2-2-Yes,Continuingfrom PreviousAssessmentPeriod 3-3-No? Ifyes,indicatewhetherornottheagentslistedbelowwereusedtotreatGVHD duringthisassessmentperiod: a.als,alg,ats,atg:(thrpyatg) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven b.azathioprine:(thrpyaza) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven c.cyclosporine:(thrpycyc) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven d.systemiccorticosteroids:(thrpysco) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven e.topicalcorticosteroids:(thrpytco) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven f.thalidomide:(thrpytha) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven g.tacrolimus(fk 506,Prograf):(THRPYTAC) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven h.mycophenolatemofetil(mmf,celcept):(thrpymmf) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven i.puva(psoralenanduva):(thrpypuv) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven j.ecp(extra-corporealphotopheresis):(thrpyecp) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven k.sirolimus(rapamycin):(thrpysir) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven l.etretinate:(thrpyetr) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven m.lamprene:(thrpylam) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven n.etanercept:(thrpyeta) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven o.zenapax(daclizumab):(thrpyzen) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven p.chloroquinephosphate:(thrpycph) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven
21 q.invivoantit-lymphocytemonoclonal Antibody:(THRPYMAB) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven SpecifyinvivoantiT-lymphocytemonoclonalantibody used:(mabagnt) r.invivoimmunotoxin:(thrpyimm) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven Specifyinvivoimmunotoxinused:(IMMAGNT) s.other:(thrpyoth) 1-,StilTakingDrug 2-2-Yes,NoLongerTakingDrug 3-3-No,DrugNotGiven Specifyotheragentused:(OTHAGNT) 52.Hastreatmentbeendiscontinued?(ONGTRT) 53.Ifyes,enterdateofdiscontinuation:(TRTSTOP) (mm/dd/yyyy) 54.IndicatethebestresponsetoGVHD therapyduringthis assessmentperiod:(thrpyrsp) 1-1-CompleteResolutionofSymptoms 2-2-PartialResolutionofSymptoms 3-3-StableSymptoms 4-4-ProgressionofSymptoms? Answerquestions55-58relatingtocurrentpatientstatus. 55.AresymptomsofGVHD stilpresent?(gvhdsymp) 56.CurentKarnofsky/LanskyScore:(CURKRNLN) (Normal;NoComplaints/FulyActive) (NormalActivity/MinorRestrictioninStrenuousPlay) (NormalActivitywithEfort/RestrictedinStrenuousPlay) (UnabletoCaryOnNormalActivity/LessTimeSpentinPlay) (RequiresOccasionalAssistance/MinimalActivePlay) 57.Curentplateletcount:(CURPLTCT) (xxx.x) x10 9 /L 58.Curentweight:(CURWGHT) (xxx.x) kg Comments:(CGVCOMM)
22 AdditionalSelectionOptionsforCGV Minimum Karnofsky/LanskyScoreattimeofdiagnosis: (RequiresConsiderableAssistance/NoActivePlay) (Disabled/AbletoInitiateQuietActivities) (SeverelyDisabled/NeedsAssistanceforQuietPlay) (VerySick/LimitedtoVeryPassiveActivity) (Moribund;CompletelyDisabled) BiopsyType1 6-6-LungBiopsy 7-7-Other,Specify CurentKarnofsky/LanskyScore: (RequiresConsiderableAssistance/NoActivePlay) (Disabled/AbletoInitiateQuietActivities) (SeverlyDisabled/NeedsAssistanceforQuietPlay) (VerySick/LimitedtoVeryPassiveActivity) (Moribund;CompletelyDisabled) (Dead)
23 BloodandMarrow TransplantClinical TrialsNetwork Demographics(DEM) WebVersion:1.0;6.00; NameCode:(NAMECODE) 2.IUBMID #(ifavailable):(iubmid) 3.CRID #(CIBMTRRecipientID):(CRIDNUM) (xxxxxxxxxx) 4.Gender:(GENDER) DoNOTuseIUBMID/UPN numbersinthecridfield. 1-Male 2-Female 5.DateofBirth:(DOB) (mm/dd/yyyy) 6.Ethnicity:(ETHNIC) 1-1-HispanicorLatino 2-tHispanicorLatino 8-8-Unknown 9-9-NotAnswered 7.Race:(RACE) -White White(NotOtherwiseSpecified) European(NotOtherwiseSpecified) Mediteranean WhiteNorthAmerican Specifyrace:(RACESP) 8.SecondaryRace:(RACE2) -White White(NotOtherwiseSpecified) European(NotOtherwiseSpecified) Mediteranean WhiteNorthAmerican Specifysecondaryrace:(RACE2SP) Comments:(DEMCOMM1)
24 AdditionalSelectionOptionsforDEM Race: SouthorCentralAmerican EasternEuropean NorthernEuropean WesternEuropean WhiteCaribbean 82-8rthCoastofAfrica MiddleEastern -Black Black(NotOtherwiseSpecified) AfricanAmerican AfricanBlack(BothParentsBorninAfrica) CaribbeanBlack SouthorCentralAmericanBlack Black,OtherSpecify -Asian Asian(NotOtherwiseSpecified) Indian/SouthAsian Filipino(Pilipino) Japanese Korean Chinese OtherSoutheastAsian Vietnamese -AmericanIndianorAlaskaNative NativeAmerican(NotOtherwiseSpecified) NativeAlaskan/Eskimo/Aleut AmericanIndian(NotOtherwiseSpecified) NorthAmericanIndian SouthorCentralAmericanIndian CaribbeanIndian -NativeHawaianorOtherPacificIslander NativePacificIslander(NotOtherwiseSpecified) Guamanian Hawaian Samoan -Other Unknown Other,Specify NotAnswered
25 BloodandMarrow TransplantClinical TrialsNetwork DeathForm (DTH) WebVersion:1.0;4.06; Recorddateofdeath:(DTHDT) (mm/dd/yyyy) 2.Wasanautopsyperformed?(AUTPERF) Ifyes,submitautopsyreporttoDCC Enterappropriatecauseofdeathcodebelow.Listinorderofdecreasingseverity. 3.Primarycauseofdeath:(CZDTHPRM) GraftRejectionorFailure -Infection(OtherthanInterstitialPneumonia) AutologousRecovery Rejection Bacterial? Specifyother:(DTHSPEC1) 4.Secondarycauseofdeath:(SCNDCZ1) GraftRejectionorFailure -Infection(OtherthanInterstitialPneumonia) AutologousRecovery Rejection Bacterial Specifyother:(DTHSPEC2) 5.Secondarycauseofdeath:(SCNDCZ2) GraftRejectionorFailure -Infection(OtherthanInterstitialPneumonia) AutologousRecovery Rejection Bacterial Specifyother:(DTHSPEC3) 6.Secondarycauseofdeath:(SCNDCZ3) GraftRejectionorFailure -Infection(OtherthanInterstitialPneumonia) AutologousRecovery Rejection Bacterial Specifyother:(DTHSPEC4) 7.Secondarycauseofdeath:(SCNDCZ4) GraftRejectionorFailure -Infection(OtherthanInterstitialPneumonia) AutologousRecovery Rejection Bacterial Specifyother:(DTHSPEC5) Comments:(DTCMMNTS)
26 AdditionalSelectionOptionsforDTH Primarycauseofdeath: Fungal Viral Protozoal Other,SpecifyBelow Organism NotIdentified -InterstitialPneumonia Viral,CMV Viral,Other Pneumocystis Other,SpecifyBelow Idiopathic AdultRespiratoryDistressSyndrome AcuteGVHD ChronicGVHD RecurenceorPersistenceofLeukemia/Malignancy/MDS PersistentDisease -OrganFailure(NotDuetoGVHDorInfection) Liver Cardiac(Cardiomyopathy) Pulmonary CNS Renal Other,SpecifyBelow MultipleOrganFailure,SpecifyBelow SecondaryGraftFailure SecondaryMalignancy EBV Other,SpecifyBelow -Hemorhage Pulmonary Intracranial Gastrointestinal HemorhageNotSpecified Other,SpecifyBelow -Vascular Thromboembolic DisseminatedIntravascularCoagulation(DIC) Gastrointestinal ThromboticThrombocytopenicPurpura VascularNotSpecified Other,SpecifyBelow AccidentalDeath Other,SpecifyBelow
27 BloodandMarrow TransplantClinical TrialsNetwork 0402A(ENR) WebVersion:1.0;6.02; GVHD Prophylaxis-SegmentA 1.Recordthedatepatient'sinformedconsentform was signed:(cn0402dt) (mm/dd/yyyy) 2.Patient'sbirthdate:(PTDBTDT) (mm/dd/yyyy) 3.Recordtheproposedstartdateofconditioning:(CONDDT) (mm/dd/yyyy) 4.Conditioningregimen:(CONDREG) 1-1-CyclophosphamideandTotalBodyIradiation(CY-TBI) 2-2-EtoposideandTotalBodyIradiation(VP16-TBI) InclusionCriteria 5.Recordtheparticipant'sprimarydiagnosis:(PRIMDX) 6.IfAML,recordthediseasestage:(AML402SG) 7.IfALL,recordthediseasestage:(ALL402SG) 8.IfCML,recordthediseasestage:(CML402SG) 9.IfMDS,recordthediseasestage:(MDS402SG) 10.IfAcuteBiphenotypicLeukemia,recordthedisease stage:(abl402sg) 11.IfAcuteBiphenoytpicLeukemia,perwhichhistologywasthe patientbeingtreated?(abl402ht) 1-1-AcuteMyelogenousLeukemia(AML) 2-2-AcuteLymphoblasticLeukemia(ALL) 3-3-ChronicMyelogenousLeukemia(CML) 4-4-MyelodysplasticSyndrome(MDS) 5-5-AcuteBiphenotypicLeukemia 1-1-FirstRemission 2-2-SecondRemission 3-3-SubsequentRemission 1-1-FirstRemission 2-2-SecondRemission 3-3-SubsequentRemission 1-1-ChronicPhase 2-2-AcceleratedPhase 1-1-RefractoryAnemia 2-2-RefractoryAnemiawithRingedSideroblasts 3-3-RefractoryCytopeniawithMultilineageDysplasia 4-4-RefractoryCytopeniawithMultilineageDysplasiaandRingedSideroblasts 5-5-RefractoryAnemiawithExcessBlasts1(5-10% blasts) 1-1-FirstRemission 2-2-SecondRemission 3-3-SubsequentRemission 1-1-AcuteMyelogenousLeukemia(AML) 2-2-AcuteLymphoblasticLeukemia(ALL) 12.Performancestatusscaleusedtoevaluatepatient(Lanskyfor patients<16yearsold;karnofskyforpatients>16years old):(ptkarlan) 13.Recordthepatient'sperformancestatus:(PTKLSCR) 14.Ifthepatientis<18yearsold,indicateifhe/sheiswilingandableto takeoralmedications:(oralmed) 1-Karnofsky 2-Lansky (Normal;NoComplaints/FulyActive) (NormalActivity/MinorRestrictioninStrenuousPlay) (NormalActivitywithEfort/RestrictedinStrenuousPlay) (UnabletoCaryOnNormalActivity/LessTimeSpentinPlay) (RequiresOccasionalAssistance/MinimalActivePlay) 3-NotApplicable MostRecentValue LLNforyourInstitution ULN foryourinstitution DateSampleObtained
28 15. Serum Creatinine: (SCRESCR) (x.x) mg/dl (SCRELLN) (x.x) mg/dl (SCREULN) mg/dl (x.x) (SCREDT) (mm/dd/yyyy) 16. CalculatedCreatinine Clearance: (CRECLSCR) (xxx) ml/min N/A N/A (CRECLDT) (mm/dd/yyyy) 17. DirectBilirubin: (BILISCR) (x.x) mg/dl 18. ALT: (ALTSCR) (xxx) Units/L N/A (BI402ULN) (x.x) mg/dl N/A (AL402ULN) (xx) Units/L (BILIDT) (mm/dd/yyyy) (ALTDAT) (mm/dd/yyyy) 19. AST: (ASTSCR) (xxx) Units/L N/A (AS402ULN) (xxx) Units/L (ASTDAT) (mm/dd/yyyy) 20. Cholesterol: (CHOLSCR) (xxx) mg/dl 21. Triglycerides: (TRIGSCR) (xxx) mg/dl N/A N/A (CHOLDT) (mm/dd/yyyy) N/A N/A (TRIGDT) (mm/dd/yyyy) 22.Werepulmonaryfunctiontestsperformed?(PULFTST) IfPFT'swerenotperformed,thenanO 2saturationmustbeobtained. MostRecentValueCorectedforHemoglobin DateSampleObtained 23. FVC: (FVCSCR) (xxx) % ofpredictedvalue (FVCDAT) (mm/dd/yyyy) 24. FEV1: (FEV1SCR) (xxx) % ofpredictedvalue (FEV1DAT) (mm/dd/yyyy) 25.O2saturationonroom air:(o2sattst) (xxx) % DateO 2saturationwasobtained:(O2SATDT) (mm/dd/yyyy) 26.Recordthetypeoffractiontestperformed:(FR0402TY) 1-1-LeftVentricularEjectionFraction(LVEF) 2-2-ShorteningFraction 27.Recordtheleftventricularejectionfraction:(EJTFRSCR) (xxx) % Dateejectionfractionperformed:(EJTFRDT) (mm/dd/yyyy) 28.Recordtheshorteningfractionatrest:(SHTFRSCR) (xxx) % Dateshorteningfractionperformed:(SHTFRDT) (mm/dd/yyyy) ExclusionCriteria 29.Hastheparticipanthadaprioralogeneicorautologous transplant?(priortxp) 30.IsthepatientHIVseropositive?(HIVSCR) 31.Isthepatientdiagnosedwithanuncontroledviral,bacterial,orfungal infection?(vibafuif) 32.Isthepatientpregnant(positiveserum orurineβ-hcg)orbreast feeding?(pregscr) 33.Doesthepatienthaveadocumentedalergyto Sirolimus?(SIROALG) 34.IsthepatientcurentlyreceivingVoriconazole?(VORIRX) 35.Isthepatientreceivinganinvestigationaldrug?(INVSDG) 3-NotApplicable Yes,ApprovedbyStudyChair/MM 3-3-No 36.Dateapprovedbystudychair/medicalmonitor:(DGAPPDT) (mm/dd/yyyy) 37.Doesthepatienthaveahistoryofpriormalignanciesotherthan resectedbasalcelcarcinoma,treatedcarcinomainsituorcancer treatedwithcurativeintent>5yearspreviously?(maligscr) 38.Doesthepatienthaveacancertreatedwithcurativeintent<5years previously?(malig5yr) Yes,ApprovedbyStudyChair/MM 3-3-No 39.Dateapprovedbystudychair/medicalmonitor:(MAAPPDT) (mm/dd/yyyy) HLATyping TypeofHLAMatchrequiredbythisprotocol:(HLAMATCH) DNA_HIGH-HighLevelDNA DNA_LOW-Low LevelDNA SEROLOGY-Serologic AB_SEROLOGY_DRB1_DNA_LOW-LociA,B:Serologic,LocusDRB1:LowLevelDNA AB_DNA_LOW_DRB1_DNA_HIGH-LociA,B:LowLevelDNA,LocusDRB1:HighLevelDNA
29 40. RecipientHLATyping HLA-A Typingmethod:(RHLAAMET) Antigens/alelesprovided:(RHLAANUM) 1-1-DNATechnology 2-2-Serology 1-1-One 2-2-Two 1st: (RHLAA11X) (RHLAA12X) / (RHLAA13X) / (RHLAA14X) / (RHLAA15X) (RHLAA16X) / (RHLAA17X) / (RHLAA18X) / 2nd: (RHLAA21X) (RHLAA22X) / (RHLAA23X) / (RHLAA24X) / (RHLAA25X) (RHLAA26X) / (RHLAA27X) / (RHLAA28X) / HLA-B Typingmethod:(RHLABMET) Antigens/alelesprovided:(RHLABNUM) 1-1-DNATechnology 2-2-Serology 1-1-One 2-2-Two 1st: (RHLAB11X) (RHLAB12X) / (RHLAB13X) / (RHLAB14X) / (RHLAB15X) (RHLAB16X) / (RHLAB17X) / (RHLAB18X) / 2nd: (RHLAB21X) (RHLAB22X) / (RHLAB23X) / (RHLAB24X) / (RHLAB25X) (RHLAB26X) / (RHLAB27X) / (RHLAB28X) / HLA-DRB1 Typingmethod:(RHLADMET) Antigens/alelesprovided:(RHLADNUM) 1-1-DNATechnology 2-2-Serology 1-1-One 2-2-Two 1st: (RHLAD11X) (RHLAD12X) / (RHLAD13X) / (RHLAD14X) / (RHLAD15X) (RHLAD16X) / (RHLAD17X) / (RHLAD18X) / 2nd: (RHLAD21X) (RHLAD22X) / (RHLAD23X) / (RHLAD24X) / (RHLAD25X) (RHLAD26X) / (RHLAD27X) / (RHLAD28X) / 41. DonorHLATyping HLA-A Typingmethod:(DHLAAMET) Antigens/alelesprovided:(DHLAANUM) 1-1-DNATechnology 2-2-Serology 1-1-One 2-2-Two 1st: (DHLAA11X) (DHLAA12X) / (DHLAA13X) / (DHLAA14X) / (DHLAA15X) (DHLAA16X) / (DHLAA17X) / (DHLAA18X) / 2nd: (DHLAA21X) (DHLAA22X) / (DHLAA23X) / (DHLAA24X) / (DHLAA25X) (DHLAA26X) / (DHLAA27X) / (DHLAA28X) / HLA-B Typingmethod:(DHLABMET) Antigens/alelesprovided:(DHLABNUM) 1-1-DNATechnology 2-2-Serology 1-1-One 2-2-Two 1st: (DHLAB11X) (DHLAB12X) / (DHLAB13X) / (DHLAB14X) / (DHLAB15X) (DHLAB16X) / (DHLAB17X) / (DHLAB18X) /
30 2nd: (DHLAB21X) (DHLAB22X) / (DHLAB23X) / (DHLAB24X) / (DHLAB25X) (DHLAB26X) / (DHLAB27X) / (DHLAB28X) / HLA-DRB1 Typingmethod:(DHLADMET) 1-1-DNATechnology 2-2-Serology Antigens/alelesprovided:(DHLADNUM) 1-1-One 2-2-Two 1st: (DHLAD11X) (DHLAD12X) / (DHLAD13X) / (DHLAD14X) / (DHLAD15X) (DHLAD16X) / (DHLAD17X) / (DHLAD18X) / 2nd: (DHLAD21X) (DHLAD22X) / (DHLAD23X) / (DHLAD24X) / (DHLAD25X) (DHLAD26X) / (DHLAD27X) / (DHLAD28X) / Locus-AcalculatedHLAMatchScore(SCORE_A) Locus-BcalculatedHLAMatchScore(SCORE_B) Locus-DRB1calculatedHLAMatchScore(SCORE_D) TotalcalculatedHLAMatchScore(HLASCORE) DoyouagreewiththecalculatedHLAMatchScore?(HLAAGREE) Indicateyourinstitution'sHLAMatchScoreforthis participant:(sitescr) 0/6-0/6 1/6-1/6 2/6-2/6 3/6-3/6 4/6-4/6 Comments(COMMENTS)
31 AdditionalSelectionOptionsforENR IfMDS,recordthediseasestage: 6-6-RefractoryAnemiawithExcessBlasts-2(10-20% blasts) 7-7-MyelodysplasticSyndrome,Unclassified 8-8-MDSAssociatedwithIsolatedDel(5q) 9-9-ChronicMyelomonocyticLeukemia Recordthepatient'sperformancestatus: (RequiresConsiderableAssistance/NoActivePlay) (Disabled/AbletoInitiateQuietActivities) (SeverelyDisabled/NeedsAssistanceforQuietPlay) (VerySick/LimitedtoVeryPassiveActivity) (Moribund;CompletelyDisabled) TypeofHLAMatchrequiredbythisprotocol: AB_SEROLOGY_DRB1_DNA_HIGH-LociA,B:Serologic,LocusDRB1:HighLevelDNA ABC_DNA_LOW_DRB1_DNA_HIGH-LociA,B,C:LowLevelDNA,LocusDRB1:HighLevelDNA ABCDQ_DNA_LOW_DRB1_DNA_HIGH-LociA,B,C,DQ:Low LevelDNA,LocusDRB1:HighLevelDNA Indicateyourinstitution'sHLA MatchScoreforthisparticipant: 5/6-5/6 6/6-6/6 0/8-0/8 1/8-1/8 2/8-2/8 3/8-3/8 4/8-4/8 5/8-5/8 6/8-6/8 7/8-7/8 8/8-8/8
32 BloodandMarrow TransplantClinical TrialsNetwork Segment(PROTSEG): VisitNumber(VISNO): Folow UpStatusForm (FUS) WebVersion:1.0;12.01; Dateoflastcontact:(LASTCTDT) (mm/dd/yyyy) Sincethedateofthelastvisitindicateifanyofthefolowinghaveoccurred: 2.Hasthepatientdied?(DIED) IfYes,aDeathForm mustbesubmited. 3.Dateofpatientdeath:(DEATHDT) (mm/dd/yyyy) 4.Hasthepatientrelapsedorexperienceddiseaseprogression?(RELAPSE) IfYes,aRelapseForm mustbesubmited. 5.Dateofrelapseorprogression:(RELAPSDT) (mm/dd/yyyy) 6.Hasthepatientexperiencedsecondarygraftfailure?(SECGRFAL) 7.Hasthepatientexperiencedsecondarygraftfailure?(SECGRFAL) IfYes,aSecondaryGraftFailureForm mustbesubmited. 8.Dateofsecondarygraftfailure:(SCGRFLDT) (mm/dd/yyyy) 9.Dateofsecondarygraftfailure:(SCGRFLDT) (mm/dd/yyyy) Hasthepatientexperiencedanynew clinicalysignificantinfections?(newinfx) IfYes,anInfectionForm mustbesubmited. 12.Dateofinfection:(INFDT) (mm/dd/yyyy) 13.Hasthepatientbeenhospitalized?(HOSPITAL) 14.Dateofhospitalization:(HOSPTLDT) IfYes,aRe-AdmissionForm mustbesubmited. (mm/dd/yyyy) 15.Hasthepatientreceivedanon-protocolspecifiedtransplant?(TRANSTWO) 16.Dateofnon-protocolspecifiedtransplant:(DATRANSP) (mm/dd/yyyy) Comments:(FUS1COMM)
33 BloodandMarrow TransplantClinical TrialsNetwork Segment(PROTSEG): VisitNumber(VISNO): AcuteGVHDForm (GVH) WebVersion:1.0;10.04; Dateofstaging:(STAGEDT) (mm/dd/yyyy) StartofGVHD AssessmentPeriod:(GVASSTDT) (mm/dd/yyyy) EndofGVHD AssessmentPeriod:(GVASENDT) (mm/dd/yyyy) 2.Recordthestudydrugassignment:(GVHTRAS) 1-Sirolimus/Tacrolimus 2-Tacrolimus/Methotrexate Theassessmentforwhichyouareenteringdatamusthavetakenplacewithintheabovedates.Ifthepatientwasnotseenduringtheassessmentperiodspecifiedabove, pleaseexittheform andrequestanexceptionforthisform. 3.Immunosuppressant(prophylaxis)received:(IMMUNORC) 0-0-Prednisone 1-1-Cyclosporine 2-2-Tacrolimus 3-3-Nottakenduringassessment 4.Recordmostrecentbloodlevelofimmunosuppressant (prophylaxis):(troughlv) (xxxx.x) ng/ml 5.Recorddatebloodsampleobtained:(TROUGHDT) (mm/dd/yyyy)? 6.Recordmostrecentbloodlevelofsirolimus:(GVHSIRLV) (xxxx.x) ng/ml 7.Recorddatebloodsampleobtained:(GVHSIRDT) (mm/dd/yyyy) Recordthehighestleveloforganabnormalities,theetiologiescontributingtotheabnormalitiesandanybiopsyresultsduringtheassessmentperiod. 8.Skinabnormalities:(GVHSKINA) 9.Skinetiologies: 0-0-NoRash 1-1-MaculopapularRash,<25% ofbodysurface 2-2-MaculopapularRash,25-50% ofbodysurface 3-3-GeneralizedErythroderma 4-4-GeneralizedErythrodermawithBulusFormationandDesquamation? GVHD DrugReaction ConditioningRegimenToxicity (SETGVHD)? (SETDRGRX) (SETCRTOX) Infection Other (SETINFCT) (SETOTHER) Specifyotherskinetiologies:(GVHSKNSP) 10.SkinbiopsyforGVHD:(GVHSKINB) 1-1-Positive 2-2-Negative 3-3-Equivocal 4-4-NotDone 11.UpperGIabnormalities:(GVHUPGIA) 0-0-NoProtractedNauseaandVomiting 1-1-PersistentNausea,VomitingorAnorexia 12.Upperintestinaltractetiologies: GVHD DrugReaction ConditioningRegimenToxicity (UGIETGVH) (UGIETDRG) (UGIETCON) TPN Infection Other (UGIETTPN) (UGIETINF) (UGIETOTH)
34 Specifyotherupperintestinaltractetiologies:(UGIETSPC) 13.UpperintestinaltractbiopsyforGVHD:(UGIBIORS) 1-1-Positive 2-2-Negative 3-3-Equivocal 4-4-NotDone 14.LowerGIabnormalities:(GVHINTA) 0-0-NoDiarhea 1-1-DiarheaLessThanorEqualto500mL/dayor<280mL/m^2 2-2-Diarhea>500butLessThanorEqualto1000mL/dayor mL/m^2 3-3-Diarhea>1000butLessThanorEqualto1500mL/dayor mL/m^2 4-4-Diarhea>1500mL/dayor>833mL/m^2? 15.Lowerintestinaltractetiologies: UsemL/dayforadultpatientsandmL/m 2 forpediatricpatients GVHD DrugReaction ConditioningRegimenToxicity (LGIETGVH) (LGIETDRG) (LGIETCON) TPN Infection Other (LGIETTPN) (LGIETINF) (LGIETOTH) Specifyotherlowerintestinaltractetiologies:(LGIETSPC) 16.LowerintestinaltractbiopsyforGVHD:(LGIBIORS) 1-1-Positive 2-2-Negative 3-3-Equivocal 4-4-NotDone 17.Liverabnormalities:(GVHLIVRA) 0-0-Bilirubin<2.0mg/dL 1-1-Bilirubin mg/dL 2-2-Bilirubin mg/dL 3-3-Bilirubin mg/dL 4-4-Bilirubin>15.0mg/dL 18.Liveretiologies: GVHD DrugReaction ConditioningRegimenToxicity TPN (LIVETGVH) (LIVETDRG) (LIVETCND) (LIVETTPN) Infection VOD Other (LIVETINF) (LIVETVOD) (LIVETOTH) Specifyotherliveretiologies:(GVHLIVRS) 19.LiverbiopsyforGVHD:(GVHLIVRB) 1-1-Positive 2-2-Negative 3-3-Equivocal 4-4-NotDone ')} ThisonlyappliestoTREATMENTforGVHD.IfGVHD prophylaxiswastheonlymodificationduringthisassessmentperiod,thisquestionshouldbeanswered"". 20.Ifyes,specifyagentname:(GVHAGENT) 1-1-CSA 2-2-FK TopicalSteroids 4-4-Prednisone 5-5-ATG Specifyotheragent:(GVHAGNSP)
35 21.Indicatetreatmentmodification:(GVHTRMOD) 1-1-Started 2-2-Stopped 4-4-Tapered 5-5-Increased Comments:(GVHCOMM)
36 AdditionalSelectionOptionsforGVH LowerGIabnormalities: 5-5-SevereAbdominalPainwithorwithoutIleus,orStoolwithFrankBloodorMelena Ifyes,specifyagentname: 6-6-MMF 7-7-Daclizumab 8-8-Methylprednisolone 9-9-Other
37 BloodandMarrow TransplantClinical TrialsNetwork Segment(PROTSEG): VisitNumber(VISNO): MyeloablativeHematopoiesisForm (HEM) WebVersion:1.0;7.01; DidthepatientachieveANC recovery>500/mm 3 onthreeconsecutive days?(engrft1) 3-PreviouslyReported 2.Recordneutrophilcountandspecimencolectiondates: Day1: (ANCDAY1) (xxxxx) /mm 3 (ANC1DT) (mm/dd/yyyy) Day2: (ANCDAY2) (xxxxx) /mm 3 (ANC2DT) (mm/dd/yyyy) Day3: (ANCDAY3) (xxxxx) /mm 3 (ANC3DT) (mm/dd/yyyy) RecordChimerism AssayDataforMarrow and/orblood Marow 3.Wasachimerism performedonamarowsample?(mrwdone) 4.Datespecimencolected:(MRWDT2) (mm/dd/yyyy) 5.Methodofevaluation:(MTHOD1) 1-1-StandardCytogenetics 2-2-FluorescentInSituHybridization(FISH) 3-3-RestrictionFragment-LengthPolymorphisms(RFLP) 4-4-PolymeraseChainReaction(PCR) 5-5-HLASerotyping Specifyother:(MRWSPEC) 6.Celtype:(MRWCLTYP) 7.Marowassayresults:(MRWASSAY) 1-Unmanipulated 1-1-AlHostCels 2-2-AlDonorCels 3-3-HostandDonor 2-Granulocytes 8.% Donor:(PCNTDNR1) (xx) % Blood 9.Wasachimerism performedonabloodsample?(blddone) 10.Datespecimencolected:(BLDCHMDT) 11.Methodofevaluation:(MTHOD2) (mm/dd/yyyy) 1-1-StandardCytogenetics 2-2-FluorescentInSituHybridization(FISH) 3-3-RestrictionFragment-LengthPolymorphisms(RFLP) 4-4-PolymeraseChainReaction(PCR) 5-5-HLASerotyping Specifyother:(BLDSPEC) 12.Celtype:(BLDCLTYP) 13.Bloodassayresults:(BLDASSAY) 1-Unmanipulated 1-1-AlHostCels 2-2-AlDonorCels 3-3-HostandDonor 2-Granulocytes 14.% Donor:(PCNTDNR2) (xx) % TCelChimerism 15.Wasachimerism performedonatcelsample?(tcldone) 16.Typeofsample:(TCLSMPL) 1-Blood 2-Marow 17.Datespecimencolected:(TCLDATE) (mm/dd/yyyy)
38 18.Methodofevaluation:(MTHOD3) 1-1-StandardCytogenetics 2-2-FluorescentInSituHybridization(FISH) 3-3-RestrictionFragment-LengthPolymorphisms(RFLP) 4-4-PolymeraseChainReaction(PCR) 5-5-HLASerotyping Specifyother:(TCLSPEC) 19.Tcelassayresults:(TCLASSAY) 1-1-AlHostCels 2-2-AlDonorCels 3-3-HostandDonor 20.% Donor:(PCNTDNR3) (xx) % 21.Didthepatientreceiveastem celre-infusionduetoinadequatehematopoietic function?(reinfuse) 22.Recorddateofinfusion:(INFUSEDT) (mm/dd/yyyy) Comments:(HEMCOMM1)
39 AdditionalSelectionOptionsforHEM Methodofevaluation: 9-9-Other,specify
40 BloodandMarrow TransplantClinical TrialsNetwork Segment(PROTSEG): InfectionSite(INFSITE): InfectionStartDate(INFSTDT): InfectionForm (INF) WebVersion:1.0;4.00; INFECTION I 1.Typeofinfection:(INFTYP01) B-B-Bacteria V-V -Viral F-F-Fungal P-P-Protozoal O-O -Other 2.Organism I:(ORGN01) Ifotherspecify:(INFSPEC1) 3.Recordthelevelofcertaintyofthefungalinfectiondiagnosis:(CERTNTY1) 4.Severityofinfection:(SVRTY01) B01-B01-Acinetobacter(baumani,calcoaceticus,lwofi,otherspecies) B02-B02-Agrobacterium radiobacter B03-B03-Alcaligenesxylosoxidans B04-B04-Anaerobicbacteria(NOS,exceptforBacteroides,Clostridium) B05-B05-Bacilus(cereus,otherspecies) 1-1-ProvenFungalInfection 2-2-ProbableFungalInfection 3-3-PossibleFungalInfection 1-1-Moderate 2-2-Severe 3-3-Life-Threatening/Fatal? INFECTION I 5.Typeofinfection:(INFTYP02) B-B-Bacteria V-V -Viral F-F-Fungal P-P-Protozoal O-O -Other 6.Organism I:(ORGN02) Ifotherspecify:(INFSPEC2) 7.Recordthelevelofcertaintyofthefungalinfectiondiagnosis:(CERTNTY2) B01-B01-Acinetobacter(baumani,calcoaceticus,lwofi,otherspecies) B02-B02-Agrobacterium radiobacter B03-B03-Alcaligenesxylosoxidans B04-B04-Anaerobicbacteria(NOS,exceptforBacteroides,Clostridium) B05-B05-Bacilus(cereus,otherspecies) 1-1-ProvenFungalInfection 2-2-ProbableFungalInfection 3-3-PossibleFungalInfection 8.Severityofinfection:(SVRTY02) 1-1-Moderate 2-2-Severe 3-3-Life-Threatening/Fatal INFECTION I 9.Typeofinfection:(INFTYP03) B-B-Bacteria V-V -Viral F-F-Fungal P-P-Protozoal O-O -Other
41 10.Organism I:(ORGN03) B01-B01-Acinetobacter(baumani,calcoaceticus,lwofi,otherspecies) B02-B02-Agrobacterium radiobacter B03-B03-Alcaligenesxylosoxidans B04-B04-Anaerobicbacteria(NOS,exceptforBacteroides,Clostridium) B05-B05-Bacilus(cereus,otherspecies) Ifotherspecify:(INFSPEC3) 11.Recordthelevelofcertaintyofthefungalinfectiondiagnosis:(CERTNTY3) 1-1-ProvenFungalInfection 2-2-ProbableFungalInfection 3-3-PossibleFungalInfection 12.Severityofinfection:(SVRTY03) 1-1-Moderate 2-2-Severe 3-3-Life-Threatening/Fatal 13.Wasanagent(s)administeredtotreattheinfection(s)?(TRTINF) Provideagent(s)administeredforthisinfectiousperiod: st agent:(agent1) abacavir-abacavir(ziagen) acyclovir-acyclovir(zovirax) albendazole-albendazole(albenza) amantadine-amantadine(symmetrel,symadine) amikacin-amikacin(amikin) Ifotherspecify:(AGTSPEC1) nd agent:(agent2) abacavir-abacavir(ziagen) acyclovir-acyclovir(zovirax) albendazole-albendazole(albenza) amantadine-amantadine(symmetrel,symadine) amikacin-amikacin(amikin) Ifotherspecify:(AGTSPEC2) rd agent:(agent3) abacavir-abacavir(ziagen) acyclovir-acyclovir(zovirax) albendazole-albendazole(albenza) amantadine-amantadine(symmetrel,symadine) amikacin-amikacin(amikin) Ifotherspecify:(AGTSPEC3) 17.Wereadditionalagentsadministeredforthisinfectiousperiod?(ADDAGENT) Ifyes,specifyadditionalagentsadministered:(INFSPEC4) Comments:(INFCOM)
42 AdditionalSelectionOptionsforINF InfectionSite(INFSITE)(keyfield): Blood/BufyCoat Disseminated-Generalized,Isolatedat2orMoreDistinctSites Brain SpinalCord MeningesandCSF CentralNervousSystem Unspecified Lips Tongue,OralCavity,andOro-Pharynx Esophagus Stomach GalbladderandBiliaryTree(NotHepatitis),Pancreas SmalIntestine LargeIntestine Feces/Stool Peritoneum Liver GastrointestinalTractUnspecified UpperAirwayandNasopharynx Larynx LowerRespiratoryTract(Lung) PleuralCavity,PleuralFluid Sinuses RespiratoryTractUnspecified Kidneys,RenalPelvis,UretersandBladder Prostate Testes FalopianTubes,Uterus,Cervix Vagina Genito-UrinaryTractUnspecified GenitalArea Rash,Pustules,orAbscessesNotTypicalofAnyoftheAbove SkinUnspecified Woundsite CatheterTip Eyes Ears Joints BoneMarow BoneCortex(Osteomyelitis) Muscle(ExcludingCardiac) Cardiac(Endocardium,Myocardium,Pericardium) LymphNodes Spleen OtherUnspecified Organism I: B06-B06-Bacteroides(gracilis,uniformis,vulgaris,otherspecies) B07-B07-Borrelia(Lymedisease) B08-B08-BranhameliaorMoraxelacatarhalis(otherspecies) B09-B09-Campylobacter(alspecies) B11-B11-Chlamydia B12-B12-Citrobacter(freundi,otherspecies) B13-B13-Clostridium (alspeciesexceptdificile) B14-B14-Clostridium dificile B15-B15-Corynebacterium (alnon-diptheriaspecies) B16-B16-Coxiela B17-B17-Enterobacter B18-B18-Enterococcus(alspecies) B19-B19-Escherichia(alsoE.coli) B20-B20-Flavimonasoryzihabitans B21-B21-Flavobacterium B22-B22-Fusobacterium nucleatum B23-B23-Gram NegativeDiplococci(NOS) B24-B24-Gram NegativeRod(NOS) B25-B25-Gram PositiveCocci(NOS) B26-B26-Gram PositiveRod(NOS) B27-B27-Haemophilus(alspeciesincludinginfluenzae) B28-B28-Helicobacterpylori B29-B29-Klebsiela B30-B30-Lactobacilus(bulgaricus,acidophilus,otherspecies) B31-B31-Legionela B32-B32-Leptospira B33-B33-Leptotrichiabuccalis B34-B34-Leuconostoc(alspecies) B35-B35-Listeria B36-B36-Methylobacterium B37-B37-Micrococcus(NOS) B38-B38-Mycobacteria(avium,bovium,haemophilum,intercelulare) B39-B39-Mycoplasma B40-B40-Neisseria(gonorhoea,meningitidis,otherspecies) B41-B41-Nocardia B42-B42-Pharyngeal/RespiratoryFlora B43-B43-Propionibacterium (acnes,avidum,
43 granulosum,otherspecies) B44-B44-Pseudomonas(alspeciesexcept cepaciaandmaltophilia) B45-B45-PseudomonasorBurkholderiacepacia B46-B46-PseudomonasorStenotrophomonasorXanthomonasmaltophilia B47-B47-Rhodococcus B48-B48-Ricketsia B49-B49-Salmonela(alspecies) B50-B50-Serratiamarcescens B51-B51-Shigela B52-B52-Staphylococcus(coag-) B53-B53-Staphylococcus(coag+) B54-B54-Staphylococcus(NOS) B55-B55-Stomatococcusmucilaginosis B56-B56-Streptococcus(alspeciesexceptEnterococcus) B57-B57-Treponema(syphilis) B58-B58-Tuberculosis(NOS,AFB,acidfastbacilus,Kochbacilus) B59-B59-TypicalTuberculosis(TB,Tuberculosis) B60-B60-Vibrio(alspecies) B99-B99-OtherBacteria V01-V01-HerpesSimplex(HSV1,HSV2) V02-V02-HerpesZoster(Chickenpox,Varicela) V03-V03-Cytomegalovirus(CMV) V04-V04-Adenovirus V05-V05-Enterovirus(Coxsackie,Echo,Polio) V06-V06-HepatitisA(HAV) V07-V07-HepatitisB(HBV,Australianantigen) V08-V08-HepatitisC (includesnon-aandnon-b,hcv) V09-V09-HIV-1,HITLV-I V10-V10-Influenza(Flu) V11-V11-Measles(Rubeola) V12-V12-Mumps V13-V13-Papovavirus V14-V14-RespiratorySyncytialvirus(RSV) V15-V15-Rubela(GermanMeasles) V16-V16-Parainfluenza V17-V17-HHV-6(HumanHerpesVirus) V18-V18-Epstein-BarVirus(EBV) V19-V19-Polyomavirus V20-V20-Rotavirus V21-V21-Rhinovirus(CommonCold) V22-V22-OtherViral P01-P1-Pneumoncystis(PCP) P02-P2-Toxoplasma P03-P3-Giardia P04-P4-Cryptosporidium P05-P5-Amebiasis P06-P6-Echinocoocalcyst P07-P7-Trichomonas(eithervaginalorgingivitis) P08-P8-OtherProtozoal(Parasite) O01-O1-Mycobacterium Tuberculosis O02-O2-OtherMycobacterium O03-O3-Mycoplasma O04-O4-OtherOrganism F01-F01-CandidaAlbicans F02-F02-CandidaKrusei F03-F03-CandidaParasilosis F04-F04-CandidaTropicalis F05-F05-TorulopsisGalbrata(asubspeciesofCandida) F06-F06-Candida(NOS) F07-F07-AsperguilusFlavus F08-F08-AsperguilusFumigatus F09-F09-AsperguilusNiger F10-F10-Asperguilus(NOS) F11-F11-CryptococcusSpecies F12-F12-Fusarium Species F13-F13-Mucormycosis(Zygomycetes,Rhizopus) F14-F14-Yeast(NOS) F15-F15-OtherFungus 1 st agent: amoxicilin/clavulanate-amoxicilin/clavulanate(augmentin) amphotericinb-amphotericinb(abelcet,amphotec,fungizone) ampicilin-ampicilin(omnipen,polycilin) ampicilin/sulbactam-ampicilin/sulbactam (Unasyn) amprenavir-amprenavir(agenerase) atovaquone-atovaquone(meprone) azithromycin-azithromycin(zithromax,z-pack) cefaclor-cefaclor(ceclor) cefadroxil-cefadroxil(duricef,ultracef) cefazolin-cefazolin(ancef,kefzol) cefdinir-cefdinir(omnicef) cefepime-cefepime(maxipime) cefixime-cefixime(suprax) cefoperazone-cefoperazone(cefobid) cefotaxime-cefotaxime(claforan) cefotetan-cefotetan(cefotan)
44 cefoxitin-cefoxitin(mefoxin) cefpodoxime-cefpodoxime(vantin) cefprozil-cefprozil(cefzil) ceftazidime-ceftazidime(fortaz,tazicef) ceftriaxone-ceftriaxone(rocephin) cefuroxime-cefuroxime(ceftin,kefurox,zinacef) cephalexin-cephalexin(keflet,keflex,keftab) chloramphenicol-chloramphenicol(chloromycetin) cidofovir-cidofovir(vistide) ciprofloxacin-ciprofloxacin(cipro) clarithromycin-clarithromycin(biaxin) clindamycin-clindamycin(cleocin) clotrimazole-clotrimazole(mycelex,lotrimin) clotrimoxazole/betamethasone-clotrimoxazole/betamethasone(lotrisone) co-trimoxazole-co-trimoxazole(bactrim,septra,sulfamethoprim) dapsone-dapsone(dds) dicloxacilin-dicloxacilin(dycil,dynapen,pathocil) didanosine-didanosine(videx,ddi) doxycycline-doxycycline(vibramycin) efavirenz-efavirenz(sustiva) erythromycin-erythromycin(ery-tab,ilosone,pediamycin) erythromycin/sulfisoxazole-erythromycinethyl/sulfisoxazole(pediazole) erythromycintopical-erythromycintopical(akne-mycin,eryderm) ethambutol-ethambutol(myambutol) famciclovir-famciclovir(famvir) fluconazole-fluconazole(diflucan) flucytosine-flucytosine(ancobon) foscarnet-foscarnet(foscavir) ganciclovir-ganciclovir(cytovene) gatifloxacin-gatifloxacin(tequin) gentamicin-gentamicin(garamycin,gentacidin) grepafloxacin-grepafloxacin(raxar) hepatitisavaccine-hepatitisavaccine(havrix,vaqta) hepatitisbvaccine-hepatitisbvaccine(recombivaxhb,engerix-b) hepatitiscvaccine-hepatitiscvaccine imipenem /cilastatin-imipenem /cilastatin(primaxin) imiquimod-imiquimod(aldara) indinavir-indinavir(crixivan) interferonalfacon-1-interferonalfacon-1(infergen) interferonbeta-1a-interferonbeta-1a(avonex) interferonbeta-1b-interferonbeta-1b(betaseron) isoniazid-isoniazid(inh,lanizid,nydrazid) itraconazole-itraconazole(sporonox) ivermectin-ivermectin(stromectol) kanamycin-kanamycin(kantrex) ketoconazole-ketoconazole(nizoral) lamivudine-lamivudine(epivir,3tc) levofloxacin-levofloxacin(levaquin) linezolid-linezolid(zyvox) lopinavir/ritonavir-lopinavir/ritonavir(kaletra) mefloquine-mefloquine(larium) meropenem-meropenem (Merem I.V.) metronidazole-metronidazole(flagyl,protostat) minocycline-minocycline(arestin) moxifloxacinhydrochloride-moxifloxacinhydrochloride(avelox) mupirocin-mupirocin(bactroban) nafcilin-nafcilin(nalpen,unipen) nelfinavir-nelfinavir(viracept) neomycin-neomycin(mycifradin,myciguent) neomycin/polymxin/hydrocortisone-neomycin/polymxin/hydrocortisone(cortisporin) nevirapine-nevirapine(viramune) nitrofurantoin-nitrofurantoin(macrobid) nystatin-nystatin(mycostatin) oseltamivir-oseltamivir(tamiflu) oxacilin-oxacilin(bactocil) palivizumab-palivizumab(synagis) peniciling-peniciling(bicilin) penicilinvk-penicilinvk(v-cilink,veetids) pentamidine-pentamidine(pentam 300) piperacilin-piperacilin(pipracil) piperacilin/tazobactam-piperacilin/tazobactam (Zosyn) podofilox-podofilox(condylox) polymyxin-polymyxin(ak-sporeh.c.,cortisporinophthalmicsuspension) ppd-ppd skintest(mantouxtest,tinetest) pyrazinamide-pyrazinamide(rifater) pyrimethamine-pyrimethamine(daraprim) quinidinegluconate-quinidinegluconate(duraquin,cardioqiuin) quinupristin/dalfopristin-quinupristin/dalfopristin(synercid) respiratorysyncytialimmuneglobulin-respiratorysyncytialimmuneglobulin(respigam) ribavirin-ribavirin(virazole) rifampin-rifampin(rifadin,rimactane) rifampin/isoniazid-rifampin/isoniazid(rifamate,rimactane/inh) rifampin/isoniazid/pyrazinamide-rifampin/isoniazid/pyrazinamide(rifater) rimantadine-rimantadine(flumadine) ritonavir-ritonavir(norvir) saquinavirmesylate-saquinavirmesylate(fortovase,invirase) stavudine-stavudine(d4t,zerit)
Re-Admission/HospitalizationForm (ADM)
BloodandMarrow TransplantClinical TrialsNetwork Segment(PROTSEG): DateofAdmission(ADMITDT): Re-Admission/HospitalizationForm (ADM) WebVersion:1.0;4.02;06-09-11 1.Dateofdischarge:(DISCHDT) (mm/dd/yyyy)
More informationChapter 46. Learning Objectives (cont d)
Chapter 46 Antimicrobial Agents Learning Objectives Explain the major action and effects of drugs used to treat infectious diseases Identify criteria used to select an effective antimicrobial agent Identify
More informationAMR Industry Alliance Antibiotic Discharge Targets
AMR Industry Alliance Antibiotic Discharge Targets List of Predicted No-Effect Concentrations (PNECs) The members of the AMR Industry Alliance have developed a unified approach to establishing discharge
More informationFreedom of Information Act 2000 Request Reference FoI/16/226 Companies Supplying Antibiotics
Freedom of Information Act 2000 Request Reference FoI/16/226 Companies Supplying Antibiotics Request details Under the Freedom of Information Act 2000 please could you provide me with the following: 1.
More information21 st Expert Committee on Selection and Use of Essential Medicines Peer Review Report Antibiotics Review
(1) Have all important studies/evidence of which you are aware been included in the application? Yes No Please provide brief comments on any relevant studies that have not been included: (2) For each of
More informationHelp with moving disc diffusion methods from BSAC to EUCAST. Media BSAC EUCAST
Help with moving disc diffusion methods from BSAC to EUCAST This document sets out the main differences between the BSAC and EUCAST disc diffusion methods with specific emphasis on preparation prior to
More informationChildrens Hospital Antibiogram for 2012 (Based on data from 2011)
Childrens Hospital Antibiogram for 2012 (Based on data from 2011) Prepared by: Department of Clinical Microbiology, Health Sciences Centre For further information contact: Andrew Walkty, MD, FRCPC Medical
More informationPerichondritis: Source: UpToDate Ciprofloxacin 10 mg/kg/dose PO (max 500 mg/dose) BID Inpatient: Ceftazidime 50 mg/kg/dose q8 hours IV
Empiric Antibiotics for Pediatric Infections Seen in ED NOTE: Choice of empiric antibiotic therapy must take into account local pathogen frequency and resistance patterns, individual patient characteristics,
More information2015 Antibiotic Susceptibility Report
Citrobacter freundii Enterobacter aerogenes Enterobacter cloacae Escherichia coli Haemophilus influenzenza Klebsiella oxytoca Klebsiella pneumoniae Proteus mirabilis Pseudomonas aeruginosa Serratia marcescens
More information2016 Antibiotic Susceptibility Report
Fairview Northland Medical Center and Elk River, Milaca, Princeton and Zimmerman Clinics 2016 Antibiotic Susceptibility Report GRAM-NEGATIVE ORGANISMS 2016 Gram-Negative Non-Urine The number of isolates
More information- the details, where possible, of the antibiotic products these companies supply or have supplied.
Under the Freedom of Information Act 2000 please could you provide me with a list of all companies currently supplying antibiotics - or that have supplied antibiotics in the last three years - to Royal
More information* gender factor (male=1, female=0.85)
Usual Doses of Antimicrobials Typically Not Requiring Renal Adjustment Azithromycin 250 500 mg Q24 *Amphotericin B 1 3-5 mg/kg Q24 Clindamycin 600 900 mg Q8 Liposomal (Ambisome ) Doxycycline 100 mg Q12
More informationTable 1. Commonly encountered or important organisms and their usual antimicrobial susceptibilities.
Table 1. Commonly encountered or important organisms and their usual antimicrobial susceptibilities. Gram-positive cocci: Staphylococcus aureus: *Resistance to penicillin is almost universal. Resistance
More informationI am writing in response to your request for information made under the Freedom of Information Act 2000 in relation to Antibiotics.
Ref: FOI/CAD/ID 3459 27 June 2017 Please reply to: FOI Administrator Trust Management Maidstone Hospital Hermitage Lane Maidstone Kent ME16 9QQ Email: mtw-tr.foiadmin@nhs.net Freedom of Information Act
More informationEAGAR Importance Rating and Summary of Antibiotic Uses in Humans in Australia
EAGAR Importance Rating and Summary of Antibiotic Uses in Humans in Australia Background The Expert Advisory Group on Antimicrobial Resistance of the NH&MRC provides advice to Australian governments and
More informationCompliance of manufacturers of AST materials and devices with EUCAST guidelines
Compliance of manufacturers of AST materials and devices with EUCAST guidelines Data are based on questionnaires to manufacturers of materials and devices for antimicrobial susceptibility testing. The
More informationEUCAST recommended strains for internal quality control
EUCAST recommended strains for internal quality control Escherichia coli Pseudomonas aeruginosa Staphylococcus aureus Enterococcus faecalis Streptococcus pneumoniae Haemophilus influenzae ATCC 59 ATCC
More informationMercy Medical Center Des Moines, Iowa Department of Pathology. Microbiology Department Antibiotic Susceptibility January December 2016
Mercy Medical Center Des Moines, Iowa Department of Pathology Microbiology Department Antibiotic Susceptibility January December 2016 These statistics are intended solely as a GUIDE to choosing appropriate
More informationa. 379 laboratories provided quantitative results, e.g (DD method) to 35.4% (MIC method) of all participants; see Table 2.
AND QUANTITATIVE PRECISION (SAMPLE UR-01, 2017) Background and Plan of Analysis Sample UR-01 (2017) was sent to API participants as a simulated urine culture for recognition of a significant pathogen colony
More information2018 OPTIONS FOR INDIVIDUAL MEASURES: REGISTRY ONLY. MEASURE TYPE: Process
Quality ID #116 (NQF 0058): Avoidance of Antibiotic Treatment in Adults With Acute Bronchitis National Quality Strategy Domain: Efficiency and Cost Reduction 2018 OPTIONS FOR INDIVIDUAL MEASURES: REGISTRY
More informationRoutine internal quality control as recommended by EUCAST Version 3.1, valid from
Routine internal quality control as recommended by EUCAST Version.1, valid from 01-01-01 Escherichia coli Pseudomonas aeruginosa Staphylococcus aureus Enterococcus faecalis Streptococcus pneumoniae Haemophilus
More informationAdvanced Practice Education Associates. Antibiotics
Advanced Practice Education Associates Antibiotics Overview Difference between Gram Positive(+), Gram Negative(-) organisms Beta lactam ring, allergies Antimicrobial Spectra of Antibiotic Classes 78 Copyright
More informationRational management of community acquired infections
Rational management of community acquired infections Dr Tanu Singhal MD, MSc Consultant Pediatrics and Infectious Disease Kokilaben Dhirubhai Ambani Hospital, Mumbai Why is rational management needed?
More informationANTIMICROBIALS 1. Gentamicin 2. Intermediate spectrum (2nd generation) cephalosporins include all of the following except 3.
ANTIMICROBIALS 1. Gentamicin a. Can be mixed in the same administration set as penicillin b. Most streptococci are sensitive to gentamicin c. If organisms are resistant to gentamicin they will also be
More information1. The preferred treatment option for an initial UTI episode in a 22-year-old female patient
1 Chapter 79, Self-Assessment Questions 1. The preferred treatment option for an initial UTI episode in a 22-year-old female patient with normal renal function is: A. Trimethoprim-sulfamethoxazole B. Cefuroxime
More informationAntimicrobial Stewardship 101
Antimicrobial Stewardship 101 Betty P. Lee, Pharm.D. Pediatric Infectious Disease/Antimicrobial Stewardship Pharmacist Lucile Packard Children s Hospital Stanford Disclosure I have no actual or potential
More informationJanuary 2014 Vol. 34 No. 1
January 2014 Vol. 34 No. 1. and Minimum Inhibitory Concentration (MIC) Interpretive Standards for Testing Conditions Medium: diffusion: Mueller-Hinton agar (MHA) Broth dilution: cation-adjusted Mueller-Hinton
More informationCompliance of manufacturers of AST materials and devices with EUCAST guidelines
Compliance of manufacturers of AST materials and devices with EUCAST guidelines Data are based on questionnaires to manufacturers of materials and devices for antimicrobial susceptibility testing. The
More informationJanuary 2014 Vol. 34 No. 1
January 2014 Vol. 34 No. 1. and Minimal Inhibitory Concentration (MIC) Interpretive Standards for Testing Conditions Medium: diffusion: Mueller-Hinton agar (MHA) roth dilution: cation-adjusted Mueller-Hinton
More informationAntibiotics 1. Lecture 8
Antibiotics 1 Lecture 8 Overview of antibiotics What am I treating? Viral, bacterial, fungal, mycobacterial, etc. Who am I treating? Host factors: age, genetic factors, co-morbidities (renal and liver
More informationMeasure #20 (NQF 0270): Perioperative Care: Timing of Prophylactic Parenteral Antibiotic Ordering Physician
Measure #20 (NQF 0270): Perioperative Care: Timing of Prophylactic Parenteral Antibiotic Ordering Physician 2014 PQRS OPTIONS FOR INDIVIDUAL MEASURES: CLAIMS, REGISTRY DESCRIPTION: Percentage of surgical
More informationReport on the Point Prevalence Survey of Antimicrobial Prescribing in Secondary Care in Wales November/December 2009
Report on the Point Prevalence Survey of Antimicrobial Prescribing in Secondary Care in Wales November/December 2009 Authors: Maggie Heginbothom Robin Howe Version: 1 Antimicrobial PPS - Wales Date: 26/04/2010
More informationNational Clinical Guideline Centre Pneumonia Diagnosis and management of community- and hospital-acquired pneumonia in adults
National Clinical Guideline Centre Antibiotic classifications Pneumonia Diagnosis and management of community- and hospital-acquired pneumonia in adults Clinical guideline 191 Appendix N 3 December 2014
More information56 Clinical and Laboratory Standards Institute. All rights reserved.
Table 2C 56 Clinical and Laboratory Standards Institute. All rights reserved. Table 2C. Zone Diameter and Minimal Inhibitory Concentration Breakpoints for Testing Conditions Medium: Inoculum: diffusion:
More informationINFECTIOUS DISEASES DIAGNOSTIC LABORATORY NEWSLETTER
INFECTIOUS DISEASES DIAGNOSTIC LABORATORY NEWSLETTER University of Minnesota Health University of Minnesota Medical Center University of Minnesota Masonic Children s Hospital May 2017 Printed herein are
More informationGuidelines for Antimicrobial treatment for treatment of confirmed infections adults
Guidelines for Antimicrobial treatment for treatment of confirmed infections adults This guideline gives recommendations for treatment of confirmed infections in adults for children please see the Paediatric
More informationINFECTIONS IN CHILDREN-ANTIMICROBIAL MANAGEMENT
INFECTIONS IN CHILDREN-ANTIMICROBIAL MANAGEMENT Name & Title Of Authors: Dr M Milupi, Consultant Microbiologist Dr N Rao,Consultant Paediatrician Dr V Desai Consultant Paediatrician Date Revised: DEC 2015
More informationAntimicrobial susceptibility
Antimicrobial susceptibility PATTERNS Microbiology Department Canterbury ealth Laboratories and Clinical Pharmacology Department Canterbury District ealth Board March 2011 Contents Preface... Page 1 ANTIMICROBIAL
More informationTB Grand Rounds. MDR-TB: Management of Adverse Drug Reactions. Reynard J. McDonald, M.D. September 18, Patient History
TB Grand Rounds MDR-TB: Management of Adverse Drug Reactions Reynard J. McDonald, M.D. September 18, 2007 Patient History This 30 y/o H/M was born in Ecuador and immigrated to the US in 2001 On 11-22-05
More informationUpdated recommended treatment regimens for gonococcal infections and associated conditions United States, April 2007
Updated recommended treatment regimens for gonococcal infections and associated conditions United States, April 2007 1 Ongoing data from CDC 's Gonococcal Isolate Surveillance Project (GISP), including
More informationAntimicrobial Susceptibility Patterns
Antimicrobial Susceptibility Patterns KNH SURGERY Department Masika M.M. Department of Medical Microbiology, UoN Medicines & Therapeutics Committee, KNH Outline Methodology Overall KNH data Surgery department
More informationApproach to pediatric Antibiotics
Approach to pediatric Antibiotics Gassem Gohal FAAP FRCPC Assistant professor of Pediatrics objectives To be familiar with common pediatric antibiotics o Classification o Action o Adverse effect To discus
More informationSuggestions for appropriate agents to include in routine antimicrobial susceptibility testing
Suggestions for appropriate agents to include in routine antimicrobial susceptibility testing These suggestions are intended to indicate minimum sets of agents to test routinely in a diagnostic laboratory
More informationAppendix Table 1. Dosage form codes for oral and injected drugs. Appendix Table 3. Number of beneficiaries meeting each inclusion criterion.
Appendix Olesen SW, Barnett ML, MacFadden DR, et al. Trends in outpatient antibiotic prescribing practice among US older adults, 2011-2015: an observational study. Appendix Table 1. Dosage form codes for
More informationAntibiotic Abyss. Discussion Points. MRSA Treatment Guidelines
Antibiotic Abyss Fredrick M. Abrahamian, D.O., FACEP, FIDSA Professor of Medicine UCLA School of Medicine Director of Education Department of Emergency Medicine Olive View-UCLA Medical Center Sylmar, California
More informationجداول میکروارگانیسم های بیماریزای اولویت دار و آنتی بیوتیک های تعیین شده برای آزمایش تعیین حساسیت ضد میکروبی در برنامه مهار مقاومت میکروبی
جداول میکروارگانیسم های بیماریزای اولویت دار و آنتی بیوتیک های تعیین شده برای آزمایش تعیین حساسیت ضد میکروبی در برنامه مهار مقاومت میکروبی ویرایش دوم بر اساس ed., 2017 CLSI M100 27 th تابستان ۶۹۳۱ تهیه
More informationEuropean Committee on Antimicrobial Susceptibility Testing
European Committee on Antimicrobial Susceptibility Testing Routine and extended internal quality control as recommended by EUCAST Version 5.0, valid from 015-01-09 This document should be cited as "The
More informationEuropean Committee on Antimicrobial Susceptibility Testing
European Committee on Antimicrobial Susceptibility Testing Routine and extended internal quality control for MIC determination and disk diffusion as recommended by EUCAST Version 8.0, valid from 018-01-01
More informationChapter 14. Antimicrobial Agents. Mosby items and derived items 2008, 2002 by Mosby, Inc., an affiliate of Elsevier Inc.
Chapter 14 Antimicrobial Agents Principles of Antimicrobial Therapy Identification of the pathogen Gram stain Acid-fast stain Enzyme-linked immunosorbent assay (ELISA) Principles of Antimicrobial Therapy
More informationPinni Meedha Mojutho Ammanu Dengina Koduku Part 1 Kama Kathalu
Search for: Search Search Does levaquin cover anaerobes Pinni Meedha Mojutho Ammanu Dengina Koduku Part 1 Kama Kathalu Levofloxacin, sold under the trade names Levaquin among others, is an antibiotic.
More informationAntimicrobial Susceptibility Testing: Advanced Course
Antimicrobial Susceptibility Testing: Advanced Course Cascade Reporting Cascade Reporting I. Selecting Antimicrobial Agents for Testing and Reporting Selection of the most appropriate antimicrobials to
More informationEinheit für pädiatrische Infektiologie Antibiotics - what, why, when and how?
Einheit für pädiatrische Infektiologie Antibiotics - what, why, when and how? Andrea Duppenthaler andrea.duppenthaler@insel.ch Limping patient local pain swelling tenderness warmth fever acute Osteomyelitis
More informationWhat s new in EUCAST methods?
What s new in EUCAST methods? Derek Brown EUCAST Scientific Secretary Interactive question 1 MIC determination MH-F broth for broth microdilution testing of fastidious microorganisms Gradient MIC tests
More informationSMART WORKFLOW SOLUTIONS Introducing DxM MicroScan WalkAway System* ...
SMART WORKFLOW SOLUTIONS Introducing DxM MicroScan WalkAway System* The next-generation MicroScan WalkAway System combines proven technology and reliability with enhanced ease-of-use features to streamline
More informationCONTAGIOUS COMMENTS Department of Epidemiology
VOLUME XXIX NUMBER 3 November 2014 CONTAGIOUS COMMENTS Department of Epidemiology Bugs and Drugs Elaine Dowell SM MLS (ASCP), Marti Roe SM MLS (ASCP), Sarah Parker MD, Jason Child PharmD, and Samuel R.
More informationINFECTIONS IN CHILDREN-ANTIMICROBIAL MANAGEMENT
INFECTIONS IN CHILDREN-ANTIMICROBIAL MANAGEMENT Name & Title Of Authors: Dr M Milupi, Consultant Microbiologist Dr N Rao,Consultant Paediatrician Dr V Desai Consultant Paediatrician Date Revised: APRIL
More informationAberdeen Hospital. Antibiotic Susceptibility Patterns For Commonly Isolated Organisms For 2015
Aberdeen Hospital Antibiotic Susceptibility Patterns For Commonly Isolated s For 2015 Services Laboratory Microbiology Department Aberdeen Hospital Nova Scotia Health Authority 835 East River Road New
More informationIntrinsic, implied and default resistance
Appendix A Intrinsic, implied and default resistance Magiorakos et al. [1] and CLSI [2] are our primary sources of information on intrinsic resistance. Sanford et al. [3] and Gilbert et al. [4] have been
More informationnumber Done by Corrected by Doctor
number 28 Done by Dina Yaseen Corrected by حسام أبو عوض Doctor مالك الزحلف Cephalosporins -Cephalosporins are β-lactam antibiotics isolated from a strain of Streptomyces. -They are bactericidal and work
More informationAntimicrobial Update. Alison MacDonald Area Antimicrobial Pharmacist NHS Highland April 2018
Antimicrobial Update Alison MacDonald Area Antimicrobial Pharmacist NHS Highland alisonc.macdonald@nhs.net April 2018 Starter Questions Setting the scene... What if antibiotics were no longer effective?
More informationAntibiotic. Antibiotic Classes, Spectrum of Activity & Antibiotic Reporting
Antibiotic Antibiotic Classes, Spectrum of Activity & Antibiotic Reporting Any substance of natural, synthetic or semisynthetic origin which at low concentrations kills or inhibits the growth of bacteria
More informationAntibiotic Updates: Part II
Antibiotic Updates: Part II Fredrick M. Abrahamian, DO, FACEP, FIDSA Health Sciences Clinical Professor of Emergency Medicine David Geffen School of Medicine at UCLA Los Angeles, California Financial Disclosures
More informationTreatment of Respiratory Tract Infections Prof. Mohammad Alhumayyd Dr. Aliah Alshanwani
Treatment of Respiratory Tract Infections Prof. Mohammad Alhumayyd Dr. Aliah Alshanwani 30-1-2018 1 Objectives of the lecture At the end of lecture, the students should be able to understand the following:
More informationSimilar to Penicillins: -Chemically. -Mechanism of action. -Toxicity.
Similar to Penicillins: -Chemically. -Mechanism of action. -Toxicity. Cephalosporins are divided into Generations: -First generation have better activity against gram positive organisms. -Later compounds
More informationCONTAGIOUS COMMENTS Department of Epidemiology
VOLUME XXXII NUMBER 6 September 2017 CONTAGIOUS COMMENTS Department of Epidemiology Bugs and Drugs Elaine Dowell SM MLS (ASCP), Stacey Hamilton MT SM (ASCP), Samuel Dominguez MD PhD, Sarah Parker MD, and
More informationPIPERACILLIN- TAZOBACTAM INJECTION - SUPPLY PROBLEMS
PIPERACILLIN- TAZOBACTAM INJECTION - SUPPLY PROBLEMS The current supply of piperacillin- tazobactam should be reserved f Microbiology / Infectious Diseases approval and f neutropenic sepsis, severe sepsis
More informationLiofilchem. ID-AST systems
Liofilchem ID-AST systems Systems for ID and AST directly from clinical specimens page 1 Integral Systems for ID and AST from isolated colonies page 4 Systems for ID from isolated colonies page 6 Systems
More informationValbazen Giardia 12 mg/lb Twice a day for two days. Amoxi-Drops, Biomox, Polymox Bacterial infections 5-10 mg/lb Once to twice a day
Dosages for drugs commonly 0.4536 used in treating cats. kg) Dosages of body weight, are given except per pound as noted. ( WARNING: Not be Albendazole Valbazen Giardia 12 mg/lb Twice a day for two days
More informationMASTDISCS AST. Leading the field with a complete solution for AST and Identification disc testing. Comprehensive range. Premium quality products
IVD solutions through partnership MASTDISCS AST Leading the field with a complete solution for AST and Identification disc testing Comprehensive range Premium quality products Compatible with EUCAST and
More informationAntimicrobial Susceptibility Testing: The Basics
Antimicrobial Susceptibility Testing: The Basics Susan E. Sharp, Ph.D., DABMM, FAAM Director, Airport Way Regional Laboratory Director, Regional Microbiology and Molecular Infectious Diseases Laboratories
More informationMicroScan Microbiology Systems MORE CHOICES MORE ANSWERS. MicroScan GRAM NEGATIVE AND GRAM POSITIVE PANELS
MicroScan Microbiology Systems MORE CHOICES MORE ANSWERS MicroScan GRAM NEGATIVE AND GRAM POSITIVE PANELS LABORATORIES ON THE FRONT LINE From the National Action Plan for Combating Antibiotic Resistant
More informationAntibiotic Usage Guidelines in Hospital
SUPPLEMENT TO JAPI december VOL. 58 51 Antibiotic Usage Guidelines in Hospital Camilla Rodrigues * Use of surveillance data information of Hospital antibiotic policy guidelines from Hinduja Hospital. The
More informationErythromycin Ethylsuccinate 800mg PO QID x7 days Erythromycin Ethylsuccinate 400mg PO QID x14 days
2010 Sexually Transmitted Diseases Treatment Guideline Partial Summary Adapted from CDC, MMWR Dec 17, 2010 Changes in recommendations highlighted in green Arial font http://www.cdc.gov/std/treatment/default.htm
More informationSection 6.2 Antibacterials including Access, Watch and Reserve Lists of antibiotics
Consideration of antibacterial medicines as part of the revisions to 2017 WHO Model List of Essential Medicines for adults (EML) and Model List of Essential Medicines for children (EMLc) Section 6.2 Antibacterials
More informationPrinciples of Antibiotics Use & Spectrum of Some
Principles of Antibiotics Use & Spectrum of Some Rabee Adwan. MD Infectious Diseases Consultant (Pediatric and Adult) Head Of ID Unit and IPAC Committee- AL-Makassed Hospital-AlQuds Head of IPAC Committee
More informationThe β- Lactam Antibiotics. Munir Gharaibeh MD, PhD, MHPE School of Medicine, The University of Jordan November 2018
The β- Lactam Antibiotics Munir Gharaibeh MD, PhD, MHPE School of Medicine, The University of Jordan November 2018 Penicillins. Cephalosporins. Carbapenems. Monobactams. The β- Lactam Antibiotics 2 3 How
More informationANTIBIOTIC SIDE EFFECTS
ANTIBIOTIC THERAPY, PART I1 0025-7125/01 $15.00 +.OO ANTIBIOTIC SIDE EFFECTS Burke A. Cunha, MD Antimicrobial side effects present as adverse drug reactions involving one or more organ systems. Although
More informationPerformance Information. Vet use only
Performance Information Vet use only Performance of plates read manually was measured in three sites. Each centre tested Enterobacteriaceae, streptococci, staphylococci and pseudomonas-like organisms.
More informationVibrio vulnificus. Vibrio vulnificus V. vulnificus. pectinata japonica)
2006 1 Vibrio vulnificus 1 1) 1) 1) 2) 1) 1) 2) 17 5 16 17 11 17 Vibrio vulnificus V. vulnificus 7 9 11 79 2004 11 14 (Atrina pectinata japonica) 3 11 17 16 A B 20 11 17 V. vulnificus 7 9 11 Key words:
More information2018 OPTIONS FOR INDIVIDUAL MEASURES: REGISTRY ONLY. MEASURE TYPE: Process
Quality ID #65 (NQF 0069): Appropriate Treatment for Children with Upper Respiratory Infection (URI) National Quality Strategy Domain: Efficiency and Cost Reduction 2018 OPTIONS FOR INDIVIDUAL MEASURES:
More informationPrinciples of Antimicrobial therapy
Principles of Antimicrobial therapy Laith Mohammed Abbas Al-Huseini M.B.Ch.B., M.Sc, M.Res, Ph.D Department of Pharmacology and Therapeutics Antimicrobial agents are chemical substances that can kill or
More informationCreating a global community for clinical drug repurposing and development. Leonard Sacks Center for drug evaluation and research FDA
Creating a global community for clinical drug repurposing and development Leonard Sacks Center for drug evaluation and research FDA Neglected tropical diseases 1) Repurposing and developing new drugs 2)
More informationAntibiotic Stewardship Program (ASP) CHRISTUS SETX
Antibiotic Stewardship Program (ASP) CHRISTUS SETX Program Goals I. Judicious use of antibiotics Decrease use of broad spectrum antibiotics and deescalate use based on clinical symptoms Therapeutic duplication:
More informationREVOLUTIONARY. MMinimum. BBiofilm EEradication Concentration. inimizing WE HAVE FOUND THE ANSWER.
REVOLUTIONARY. Are recurrent bacterial infections a frustration in your practice? WE HAVE FOUND THE ANSWER. MMinimum inimizing BBiofilm EEradication C oncentration Concentration www.becscreen.com WHY BIOFILM
More informationANTIBIOTICS. Orbit s ANTIBIOTICS. Portfolio
ANTIBIOTICS Orbit s ANTIBIOTICS Portfolio ANTIBIOTICS Antibiotics (from ancient Greek αντιβιοτικά, antibiotiká), also called antibacterials, are a type of antimicrobial drug used in the treatment and prevention
More informationAminoglycosides. Spectrum includes many aerobic Gram-negative and some Gram-positive bacteria.
Aminoglycosides The only bactericidal protein synthesis inhibitors. They bind to the ribosomal 30S subunit. Inhibit initiation of peptide synthesis and cause misreading of the genetic code. Streptomycin
More informationAntimicrobial Stewardship Programs (ASPs) Metrics Examples
Antimicrobial Stewardship Programs (ASPs) Metrics Examples The following table contains examples of metrics used in ASPs. This table is not all-inclusive; additional metrics have been used or proposed.
More informationColor: Black/Tan NO GROWTH ON SOLID MEDIA IN 48 HRS. NO GROWTH ON SOLID MEDIA IN 24 HRS.
11/10/2015 L RD Microbiology results from Antech Diagnostics FINAL RPT 11/12/2015 PRELIM 1 11/11/2015 Ascn: IRBE51114588 Profile: Urine MIC Culture RE: 3099 SOURCE Urine RE: 3196 - (Not Stated) NO GROWTH
More information3 party manufacturing PRODUCT LIST. Category : ANTI BIOTIC
rd 3 party manufacturing PRODUCT LIST Category : ANTI BIOTIC ANTI BIOTIC SR.NO. COMPOSTION DRUG/FOOD DOSAGE PACKING 1 Amikacin Sulphate IP 500mg/2ml DRUG LIQUID INJ. VIAL 2 Amoxicillin 200mg & Clavulanic
More informationEUCAST-and CLSI potency NEO-SENSITABS
EUCASTand CLSI potency NEOSENSITABS Neo Sensitabs Page 1 / 6 Document: 6.2.0 Fastidious organisms EUCAST Interpretation zones and MIC breakpoints according to recommendations by the "Comité de l'antibiogramme
More informationPrinciples of Infectious Disease. Dr. Ezra Levy CSUHS PA Program
Principles of Infectious Disease Dr. Ezra Levy CSUHS PA Program I. Microbiology (1) morphology (e.g., cocci, bacilli) (2) growth characteristics (e.g., aerobic vs anaerobic) (3) other qualities (e.g.,
More informationQuality ID #66: Appropriate Testing for Children with Pharyngitis National Quality Strategy Domain: Efficiency and Cost Reduction
Quality ID #66: Appropriate Testing for Children with Pharyngitis National Quality Strategy Domain: Efficiency and Cost Reduction 2018 OPTIONS FOR INDIVIDUAL MEASURES: REGISTRY ONLY MEASURE TYPE: Process
More informationQUICK REFERENCE. Pseudomonas aeruginosa. (Pseudomonas sp. Xantomonas maltophilia, Acinetobacter sp. & Flavomonas sp.)
Pseudomonas aeruginosa (Pseudomonas sp. Xantomonas maltophilia, Acinetobacter sp. & Flavomonas sp.) Description: Greenish gray colonies with some beta-hemolysis around each colony on blood agar (BAP),
More informationChallenges Emerging resistance Fewer new drugs MRSA and other resistant pathogens are major problems
Micro 301 Antimicrobial Drugs 11/7/12 Significance of antimicrobial drugs Challenges Emerging resistance Fewer new drugs MRSA and other resistant pathogens are major problems Definitions Antibiotic Selective
More informationAntibiogram SAMPLES RECEIVED IN UTI ARE ; URINE OR FOLEY'S TIP Processing of specimen-
Antibiogram SAMPLES RECEIVED IN UTI ARE ; URINE FOLEY'S TIP Processing of specimen- Urine is processed by semiquantitative method of i.e. Calibrated loop method. samples are screened for significant bacteriuria
More informationChapter 51. Clinical Use of Antimicrobial Agents
Chapter 51 Clinical Use of Antimicrobial Agents History of antimicrobial therapy Early 17 th century Cinchona bark was used as an important historical remedy against malaria. 1909 Paul Ehrlich sought a
More informationAntimicrobial Stewardship Program
Antimicrobial Stewardship Program David R. Woodard, MSc, FSHEA, CIC CDC: Antibiotic Resistance Threats in the United States, 2013 http://www.cdc.gov/drugresistance/threat-report-2013/pdf/ CDC Threat Levels
More informationQUALITY HEALTH CARE YOUR PREFERRED PARTNER IN. For better health
YOUR PREFERRED PARTNER IN QUALITY HEALTH CARE For better health Manufacturer of Pharmaceutical Products Eka Pharma 308, Samanvay Zillion, Gotri - Sevasi Road, Opp. Shaishav School, Vadodara-391 101, (Guj.)
More informationAntimicrobial Susceptibility Summary 2011
Antimicrobial Susceptibility Summary 2011 Clinical Microbiology Department of Pathology & Laboratory Medicine 45 Antimicrobial Susceptibility Summary Clinical Microbiology Department of Pathology and Laboratory
More informationAppropriate Management of Common Pediatric Infections. Blaise L. Congeni M.D. Akron Children s Hospital Division of Pediatric Infectious Diseases
Appropriate Management of Common Pediatric Infections Blaise L. Congeni M.D. Akron Children s Hospital Division of Pediatric Infectious Diseases It s all about the microorganism The common pathogens Viruses
More information