Introduction to daily activities of clinical pharmacist.
Drug therapy monitoring,
Medication chart review
Clinical Progress
Pharmacist intervention
Detection and management of ADRs
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INTRODUCTION TO
DAILY ACTIVITIES OF
CLINICAL PHARMACIST
Dr. Ramesh Bhandari
Asst. Professor
Dept. of Pharmacy Practice
KLE College of Pharmacy, Belagavi
Drug Therapy Monitoring
Itinvolvesthereviewofapatient’smedication
regimentoensurethattherapyisappropriate,
safe,efficaciousandcosteffective.
Alsoknownasdrugtherapyreviewor
medicationreview.
Goals of Drug Therapy Monitoring
Identifyingandsolvingdrugrelated
problemsinordertooptimizethedrug
therapyandpatienthealthoutcome.
Toensurealltherapeuticsobjectives
arebeingachieved.
Significance of Drug Therapy Monitoring
Assesswhetherdesiredtherapeutic
outcomesarebeingachieved.
Monitorfordrugrelatedproblems
Ensurerationalandqualityuseofmedicine
Assesspatientcompliance
Assessthecompletenessofmedication
charts
Components of Drug Therapy Monitoring
A.Medicationchartreview(MCR)or
Medicationorderreview(MOR)or
Treatmentcharreview(TCR)
B.Clinicalreview/dailyprogressreview
C.Detectionandmanagementofadverse
drugreactions
1. Collection and interpretation of patient specific
information, including medication history interview
Firststepinsettingthetherapeuticgoal
Needtocollectinformationthatwillassistthemtodetermine
theappropriatenessofdrugtherapy.
Includespatient’sdemographicdetailssuchasage,sexand
bodyweight,socialhistory,presentingcomplaints,past
medicalhistory,allergyandsensitivitystatus,current
medicationsandresultsofrelevantlaboratorytestsandother
investigations.
Enablesthepharmacisttounderstandthepatientdisease
condition,indicationofdrugsanddailyclinicalprogress.
1. Collection and interpretation of patient specific
information, including medication history interview
Sources:Patient,casenotes,medicationchart,
observationalcharts,laboratoryresultsandthrough
discussionswithmedicalandnursingstaff.
Furtherpharmacistcanobtainmoreinformationwhichisof
importancetotheongoingmedicalmanagementofthe
patient.(MedicationHistoryInterview).
Patient’smedicationhistoryshouldbeobtainedatthe
beginningofthehospitaladmissioninordertoprovidethe
additionalusefulinformationtotheprescriber.
1. Collection and interpretation of patient specific
information, including medication history interview
Aspectsofmedicationusewhichmaybeobtainedfrom
Medicationhistoryinterview:
Historyofpreviousallergies/ADRs
Indicationofeachmedications
Dosingregimenincludingdose,route,frequencyand
durationoftherapy
Perceivedsideeffects
Adherencetomedicationregimen
Useofmedicationaids
Treatmentwithothersystemofmedicine(Ayurveda,
siddha,unani)
UseofOTCdrugs
Socialdruguse(tobacco,alcohol,panmasalaetc)
1. Collection and interpretation of patient specific
information, including medication history interview
Followinginterview,datacollectedshouldbecomparedwith
themedicationchartsforanydiscrepancies(medication
reconciliation)inordertoidentifydrug-relatedproblems.
Ifanyproblemexistsconcernedphysicianshouldbe
contactedtoovercomethosedrugrelatedproblemsortodo
anychangesinthemedicationchart.
3. Identification of drug related problems
Reviewingdrugtherapyshouldbeaimedatidentifyingand
resolvinganydrugrelatedproblems.
Adrugrelatedproblemisanyeventorcircumstance
involvingdrugtreatmentthatinterferesorpotentially
interfereswiththepatientachievinganoptimumoutcomeof
medicalcare.
CharlesheplersandLindastrandcategorizedrugrelated
problemsinto8categories.
3. Identification of drug related problems
i.Untreatedindication
ii.Improperdrugselection
iii.Sub-therapeuticdose
iv.Overdosage
v.Adversedrugreactions
vi.Failuretoreceivedrugs
vii.Druginteractions
viii.Drugusewithoutindication
3. Identification of drug related problems
i.UntreatedIndications:
Examples:
RApatientsusingNSAIDsforsymptomsreliefandmaypresent
symptomsofGastritis,thissituationrequiresanadditionaldrug
suchasH2blockersranitidineORPPIOmeprazole,Pantoprazoleto
controlgastritissymptoms.
InTBpatientsINHtherapyadvisedpyridoxinetoprevent
peripheralneuropathycausedbyINH.
3. Identification of drug related problems
ii.Improperdrugselection:
EG:anygivendrugregimenbeconsideredaswrongforaspecific
patientatgiventimeifthedosageformisinappropriate(eg:a55
yearoldpatientwithmildanginareceivingnitoglycerinpatchesto
beappliedondailybasis.
Contraindicationsarepresent(eg:apregnantwomenreceiving
Isotretinoin20mgBDfor2weeksforacnevulgaris.
3. Identification of drug related problems
iii.Subtherapeuticdose:
Anydruggiveninlowerdosethantherecommended.
Eg.,Atwoyearoldchildreceivingamoxicillin40mg
PO(40mg/5ml)forherfirstepisodeofotitismedia.
3. Identification of drug related problems
iv.Overdosage:
Eg.,Anydruggivenmoredosethanrecommendedfor
individualpatient.
3. Identification of drug related problems
v.Adversedrugreactions:
a)Eg:Ofloxacininducedthrombocytopenicpurpura
b)Insulininducedhypoglycemia
c)Penicillininducedhypersensitivity
3. Identification of drug related problems
vi.Failuretoreceivedrugs:
a)Eg.,Despitetheprescriberorder,dutynursemayfailto
administerthedrugs.
b)Duetohighcostofthedrugpatientmaynotpurchasethe
medication.
c)Duetoforgetfulnesssometimepatientmayforgettotakethe
drugs.
3. Identification of drug related problems
vii.Druginteractions:
a)Eg,Ciprofloxacinandantacidsconcomitantusecancausefailure
ofciprofloxacintherapy.
b)Mostofthedrugswithgrapesjuicecancausetoxicityofthe
drugs.
3. Identification of drug related problems
viii.Drugusewithoutindication:
EG:Nebulizationsalbutamol200mcgTID+Budesonide100mcg
BID,thenpatientalsoRxwithTabpantoprazole40mgODfor10
days,patienthasnotcomplainedanysymptomsofgastritisorPUD
B. CLINICAL/DAILY PROGRESS REVIEW
Integral componentof medication review
It is the review of the patient’s progressfor
the purpose of assessing therapeutic outcome.
Performed on daily basis
Goals of Clinical/Daily Progress Review
Assess the responseto drug treatment
Evaluate the safetyof the treatment
Assess the progress of the disease and the need for
any change in therapy
Assess the need for monitoring (if any)
Assess the convenienceof therapy (to improve
compliance)
Procedure for Clinical/Daily Progress Review
Ideally, clinical review should be done routinelyfor
all patients.
Usually carried out by attending doctorswhile
evaluating their patients to monitor the patient
outcome to drug therapy.
While evaluating, the pharmacist may need to review
biochemical, haematological, microbiological and
other investigationsas appropriate.
Procedure for Clinical/Daily Progress Review
Information obtained must be interpretedand
evaluated with reference to
Clinical featuresof the existing disease
Need for a laboratory investigation
Aspects related to the drug effects
Past Medication history of the patient
Desired therapeutic outcome(s)
Procedure for Clinical/Daily Progress Review
If therapeutic objectives are not being achieved, the
clinical pharmacist should re-evaluatethe
appropriateness of the treatment and discussany
relevant issues with the clinicians.
C. Detection and management of Adverse Drug
Reaction
One of the most important causes of morbidity and
mortality.
Hence, it is essential that clinical pharmacist should
have knowledge of ADRs including their predictability,
preventability, frequency, severity, predisposing
factors and recognition their causality assessment,
management and prevention.
Definition of ADR
Anyresponsetoadrugwhichisnoxiousand
unintended,andwhichoccursatdosesnormallyused
inmanforprophylaxis,diagnosisortherapyof
disease,orforthemodificationofphysiological
function.(WHO)
Goal of ADR Management
1)Identification and monitoring of patients susceptible
to ADRs
2)Detection and assessment of ADRs
3)Assisting in the management of ADRs
4)Documentation and prevention of ADRs
1) Identification and monitoring of Patient susceptible to
ADRs
Patients who are most susceptible to develop an ADR
should be identified and monitored on daily basis.
These can be identified during MCR, clinical review or
at the time of medication history interview.
1) Identification and monitoring of Patient susceptible to
ADRs
Patients who are at high risk of developing an ADR;
Those with Polypharmacy
with multiple disease process
Geriatric and paediatric patients
Those with intercurrentdiseases (renal/hepatic diseases)
Those treated with highly toxic drugs
Those who are treated with narrow therapeutic index drugs
Those who are treated with drugs that have potential to interacts with
other drugs.
2) Detection and assessment of ADRs
ADRsmaybeidentifiedduringwardroundswiththemedicalteamand
reviewofpatient’schart.
Itshouldconsideredaspartofthebroaderdiagnosishence,the
differentialdiagnosisshouldincludethepossibilityofanADR.
Causalityrelationshipbetweenasuspecteddrugandareaction,a
temporalorpossibleassociationissufficientforareporttobemade.
TheassessmentofacausalityrelationshipbetweenadrugandanADR
isoftenhighlysubjective,basedontheclinician’sjudgmentand
experience.
2) Detection and assessment of ADRs
IfanADRissuspected,theassessmentofADRstartswiththe
collectionofallrelevantdatapertainingto:
Patientdemographics
Medicationsincludingnon-prescriptiondrugs(OTC)
ComprehensiveADRdetails(descriptionofthereaction,timeof
onset,anddurationofthereaction,complication,treatmentofthe
reactionandoutcomeofthetreatment)
Relevantinvestigationreports
Byusingoneormoreavailablecausalityassessmentscales,
correlationofsuspecteddrugwithanADRcanbeestablished.
3) Assisting in the management of ADRs
BasedontheseverityofanADR,rapidtreatmentisnecessary.ForEg:,
anaphylacticshock.
Iftheculpritdrugisobvious,risk-benefitdecisionneedstobetaken
abouttheneedforthedrug.
Ifseveralmedicinesmaybeduetothenon-essentialmedicinesshould
bewithdrawn.
Ifthereactionislikelytobedoserelated,dosereductionshouldbe
done.
Ifthedrugisnecessarythensymptomaticreliefmaybegivenwhile
continuingtheessentialtreatment.
4) Documentation and Prevention of ADRs
Necessarytopreventre-exposurefromthesamedrug/class
Attendingpharmacistshouldcompleteappropriatedocumentationinthe
patientmedicalrecordincludingalertcardsorplacingsheetinthefront
ofthepatientcasenotes.
Essentialthatmedicalstaff,includingtheoriginalprescriberarenotified
ofsuspectedADRs