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7/23/2018 1 Drug Adjustments in Older Adults Marilyn N. Bulloch PharmD, BCPS, FCCM Associate Clinical Professor Harrison School of Pharmacy Auburn University Disclosures Alabama Medicaid Drug Utilization Board Pharmacy Times Contributor Objectives Discuss age-related physiologic changes and their subsequent impact on medication use in older adults Describe methods for determining need for dose- adjustments based on physiologic changes in older patients Recognize dosage forms that cannot be altered and identify potential alternative drug delivery methods Explain scales and formulas that have been developed to guide medication dose-adjustments

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Page 1: Bulloch Drug Adjustments in Older Adults - ALMDA · 2018-07-24 · 7/23/2018 1 Drug Adjustments in Older Adults Marilyn N. Bulloch PharmD, BCPS, FCCM Associate Clinical Professor

7/23/2018

1

Drug Adjustments in Older Adults

Marilyn N. Bulloch PharmD, BCPS, FCCMAssociate Clinical Professor

Harrison School of Pharmacy

Auburn University

Disclosures

• Alabama Medicaid Drug Utilization Board

• Pharmacy Times Contributor

Objectives

• Discuss age-related physiologic changes and their subsequent impact on medication use in older adults

• Describe methods for determining need for dose-adjustments based on physiologic changes in older patients

• Recognize dosage forms that cannot be altered and identify potential alternative drug delivery methods

• Explain scales and formulas that have been developed to guide medication dose-adjustments

Page 2: Bulloch Drug Adjustments in Older Adults - ALMDA · 2018-07-24 · 7/23/2018 1 Drug Adjustments in Older Adults Marilyn N. Bulloch PharmD, BCPS, FCCM Associate Clinical Professor

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Drug Related Complications

Medication Issue

Polypharmacy

Socioeconomic

Physiologic changesComorbidities

Cognition

Suboptimal Prescribing

Overuse Underuse

Inappropriate use Suboptimal use

Suboptimal Prescribing

Lack of Data In Older Adults

• Few medications have specific dose recommendations for geriatrics

• Only 32% of phase II and III study patients are > 65 years old– Up to 35% published studies specifically excluded geriatrics

• Reasons for exclusions– Comorbidities, ageism, economics, communication barriers

• FDA guidance document recommends, but does not require inclusion of geriatrics

Shenoy et al. Perspect Clin Res.2015;6:184-9Watts G. BMJ 2012;344:e3445Herrera et al. Am J Pub Health. 2010;100:s105-112

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Industry Guidance on Organ Impairment Studies

http://www.appliedclinicaltrialsonline.com/early-phase-clinical-trials-patients-hepatic-or-renal-impairment

Age-Related Physiologic Changes

Turnheim. Drugs and Aging.1998;13:357-79Image credit: https://nursekey.com/8-safe-medication-use/

Receptor down regulationChanges in receptor sensitivity

Altered homeostasis mechanisms

“Synergistic” drug-body effects

Roberts et al. Clin Ger Med.1988;4:127-145

Age-Related Physiologic Changes

Turnheim. Drugs and Aging.1998;13:357-79Image credit: https://nursekey.com/8-safe-medication-use/

Receptor down regulationChanges in receptor sensitivity

Altered homeostasis mechanisms

“Synergistic” drug-body effects

Roberts et al. Clin Ger Med.1988;4:127-145

Page 4: Bulloch Drug Adjustments in Older Adults - ALMDA · 2018-07-24 · 7/23/2018 1 Drug Adjustments in Older Adults Marilyn N. Bulloch PharmD, BCPS, FCCM Associate Clinical Professor

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Drugs Affected By Absorption Changes

Thomas et al. Drugs & Aging.1998;13:199-209Myers et al. Clin Pharmacokin.1989;17:385-95

Others• Pravastatin – H+-coupled monocarboxylic acid-specific transporter• Folate – pH dependent carrier-mediated transporter• Penicillin - ↑ bioavailability due to higher pH; ↓ absorption of IM agent

Obesity

Barras et al. Australian Prescriber.2017:40:189-193

Obesity

Others• Erythromycin – IBW

• Rifampin – IBW

• Theophylline – IBW

• Carvedilol – max 100 mg dose in ≥ 100 kg

Barras et al. Australian Prescriber.2017:40:189-193

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Protein Binding

Shargel L, Yu AC. Applied Biopharmaceutics & Pharmacokinetics, 7e; 2016 Available at: https://accesspharmacy.mhmedical.com/content.aspx?sectionid=100671709&bookid=1592&Resultclick=2 Accessed: April 02, 2018

Highly Protein Bound Medications

• Indomethacin

• Sulindac

• Ibuprofen

• Naproxen

• Piroxicam

• Phenytoin

• Valproic acid

• Glipizide

• Glyburide

• Digoxin

• Diphenhydramine

• Doxycycline

• Clindamycin

• Dicloxacillin

• Cisplatin

• Vincristine

• Acetazolamide

• Furosemide

• Bumetanide

• Chlorthalidone

• Metolozone

Creatinine Clearance

Image credit: https://www.hepatitisc.uw.edu/go/special-populations-situations/treament-renal-impairment/core-concept/allImage credit: http://www.patientcareonline.com/depression/early-renal-disease

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Adjusting Dose: Decreased Kidney Function

• 2nd generation antihistamines

• H1RAs

• Amantadine

• Gout medications

• Gabapentin

• Pregabalin

• Most antimicrobials

• Fesoterodine

• Hydrophillic beta-blockers- atenolol, bisoprolol, nadolol

• Opioids: morphine, codeine

• ACE-inhibitors

• Statins – rosuvastatin, simvastatin, lovastatin

American Geriatrics Society 2015 Beers Criteria Update Expert Panel. J Am Geriatr Soc. 2015;63:2227-47

Hepatic

• 20% of all medications in patients with chronic hepatic dysfunction are dosed incorrectly.– 30% experience ADRs → 80% ADRs are preventable

• Liver Flashback– Enzymes that metabolize drugs located in most body

tissue BUT are in highest levels and most diverse in liver

Weersink. BMJ Open. 2016;6:e012991

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Liver and Drug Metabolism

Trevor AJ, Katzung BG, Kruidering-Hall M. Katzung & Trevor's Pharmacology: Examination & Board Review, 11e; 2015 Available at: https://accesspharmacy.mhmedical.com/ViewLarge.aspx?figid=95701060 Accessed: April 11, 2018

Brunton LL, Hilal-Dandan R, Knollmann BC. Goodman & Gilman's: The Pharmacological Basis of Therapeutics, 13e; 2017 Available at: https://accesspharmacy.mhmedical.com/ViewLarge.aspx?figid=172473542 Accessed: April 11, 2018

Hepatic

• Liver – primary organ for drug metabolism occurring in hepatocytes– Phase I – oxidation, reduction, hdyrolosis

– Phase II – glucuronidation, sulfation, acetylation, methylation

• First Pass Metabolism – pre-systemic metabolism after oral intake but before entry into systemic circulation. – May be impacted by ↓ intrinsic clearance → increase in absolute oral

bioavailability• Increased blood concentrations – morphine, meperidine, verapamil, metoprolol,

labetalol, carvedilol, midazolam

• Prodrugs – may see decreased conversion to active form– E.g. clopidogrel, enalapril

Weersink. BMJ Open. 2016;6:e012991Pena et al. Exp Rev Clin Pharmacol.2016;9:441-458

Child-Pugh Classification

Pena et al. Exp Rev Clin Pharmacol.2016;9:441-458

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Hepatic Adjustments: EBM Recommendations

• Unsafe in all hepatic dysfunction – avoid– NSAIDs

– Nebivolol

– Isradipine

– Oral Nicardipine

– Triamterene

– Cimetidine

– Lansoprazole

– Pantoprazole

– Budesonide

– Atorvastatin

– DuloxetineWeersink et al. Drug Saf.2018:httos://doi.org/10.1007/s40264-0635-xPena et al. Exp Rev Clin Pharmacol.2016;9:441-458

Hepatic Adjustments: EBM Recommendations

Unsafe

Child-Pugh C Only• ACE inhibitors

• Domperidone

• Clopidogrel

• Rabeprazole

• Omeprazole

• Verapamil

• Felodipine

• Metoprolol

• Carvedilol

• Diazepam (oral)

• COX2 inhibitors

• Tapentadol

• Morphine

• Hydromorphone

• Tramadol

• Fentanyl

Child-Pugh B and C

• Codeine

• Ezetimibe

• Lomitapide

• Oxycodone

Weersink et al. Drug Saf.2018:httos://doi.org/10.1007/s40264-0635-xPena et al. Exp Rev Clin Pharmacol.2016;9:441-458Image: https://edrugsearch.com/worst-medications-for-liver/

Hepatic Adjustments: EBM Recommendations

Reduce Dose • Simvastatin

• Rosuvastatin

• Pravastatin

• Fluvastatin

• Omeprazole (CP A/B)

• Rabeprazole(CP A/B)

• Verapamil (CP A/B)

• Felodipine (CP A/B)

• Metoprolol (CP A/B)

• Repaglinide

• Most opioids (CP A/B)

• Most antiarrhythmics

• Escitalopram

• Venalfaxine

• Bupropion

• Fluoxetine

• Lamotrigine

Varies by severity– avoid if possible or reduce dose• Prasugrel

• Ticagrelor

• Dipyridamole

• Gemfibrozil

• Sitagliptin

• Canagliflozin

• Alogliptin

• Fentanyl

• Tigecycline

• Qunidine

• Mexiletine

• LithiumWeersink et al. Drug Saf.2018:httos://doi.org/10.1007/s40264-0635-xPena et al. Exp Rev Clin Pharmacol.2016;9:441-458

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Hepatic Adjustments: EBM Recommendations

SAFE!!

• Acetaminophen

• Ciprofloxacin

• Norfloxacin

• Ofloxacin

• Moxifloxacin

• Amoxicillin

• Amoxicillin/clav• Piperacillin/tazobactam

• SMX/TMP

• Azithromycin

• Erythromycin

• Fosfomycin

• Rifaximin

• Acarbose

• Insulin

• Metformin

• Atenolol

• Labetalol (IV)

• Sotalol

• HCTZ

• Amiloride

• Furosemide

• Bumetanide

• Spironolactone

• Eplerenone

• Prednisolone

• Prednisone

• Lactulose

• Cholestyramine

• Colesevalam

• Bisacodyl

• Ranitidine

• Famotidine

• Empagliflozin

• Saxagliptin

• Acebutolol

Weersink et al. Drug Saf.2018:httos://doi.org/10.1007/s40264-0635-xPena et al. Exp Rev Clin Pharmacol.2016;9:441-458

Hepatic Adjustments: EBM Recommendations

SAFE with Dose Adjustment

• Tolbutamide

• Propranolol

• Carvedilol

• Labetalol (oral)

• Amlodipine

• Nifedipine

• Nimodipine

• Metoclopramide

• Aspirin

• Esomeprazole

Weersink et al. Drug Saf.2018:httos://doi.org/10.1007/s40264-0635-xPena et al. Exp Rev Clin Pharmacol.2016;9:441-458

Dose Adjustments

Pena et al. Exp Rev Clin Pharmacol.2016;9:441-458

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Hepatic Adjustments: When EBM Does Not Exist

Verbeeck. Eur J Clin Pharmacol.2008;64:1147-1161

Characteristic Rationale Dose Adjustment

High EH Oral BA significantly ↑Plasma Cl may be ↓

↓ dose

Low EH and > 90% protein binding

Intrinsic clearance ↓↓ protein binding

Adjust even if dose within normal blood concentrations

Low EH and < 90% protein binding

Intrinsic clearance ↓↓ protein binding

Maintain normal total blood concentrations

Partly excreted unchanged in kidneys

Elimination ↓ ↓ dose

Hydrophilic Vd increased with edema,ascites

↑ loading doses

Narrow Therapeutic Index Avoid as much as possible

EH - hepatic extraction ratio

Special PK Considerations

• HCTZ– ↑ plasma concentrations (related to ↑ half-life and ↓CL)

– More electrolyte issues, but less response with doses > 50 mg

• Triamterene– ↑ Cmax (related to ↓CL)

• Diltiazem– ↓ absorption rate (unknown impact on bioavailability)

– ↓ CL and ↑ half-life

– Start with lower doses

• Verapamil– ↓ CL and ↑ half-life

– Start with lower doses

Facts and ComparisonsPiepho et al. Drugs & Aging.1991;1:194-211

Special PK Considerations

• Nifedipine– ↓ absorption rate but ↑ bioavailability

– ↓ Cmax and ↑AUC

– ↑ half-life ↓ CL

• Amlodipine– ↓ CL : start with lower doses

Facts and ComparisonsPiepho et al. Drugs & Aging.1991;1:194-211

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Pharmacogenomics

• Identification of phenotypes for certain genes

• Data required in labeling by FDA

• May help guide need to: Adjust dose, use with caution, or use an alternative agent

• Some identify patients at risk for hypersensitivity reaction

• Phenotypes– Poor Metabolizers

– Intermediate Metabolizers

– Extensive Metabolizers

– Ultra-Rapid Metabolizers

https://www.cms.gov/medicare-coverage-database/details/lcd-details.aspx?LCDId=35332&ver=11&CntrctrSelected=228*2&Cntrctr=228&s=22&DocType=All&LCntrctr=140*2&bc=AggAAAIBAAAA&Finkelstein et al. Pharmacogenomics and Personalized Medicine.2016;9:31-45Image: Mayo Clinic

Pharmacogenomics Testing Availability

• Allopurinol

• Aspirin

• TCAs

• Antipsychotics

• Carisoprodol

• Carbamazepine

• Oxcarbazepine

• Clopidogrel

• Donepezil

• Opioids

• SSRIs

• SNRIs

• Ivacaftor

• PPIs

• NSAIDs

• Brivaracetam

• Glimepiride

• Glipizide

• Fluoroquinolones

• Nitrofurantoin

• Bactrim

• Aminoglycosides

• Ondansetron

• Phenytoin

• Tacrolimus

• Tamoxifen

• Tramadol

• Voriconazole

• Valproic acid

• Warfarin

• Carvedilol

• Clozapine

• Diazepam

• Dolasetron

• Flecanide

• Haloperidol

• Metoprolol

• Propafenone

• Propranolol

• Tamsulosin

• Tiotropium

• Tolterodine

• Digoxin

• Salmeterol

• ACE-Is

• Statins

• Bisphosphonates

• Budesonide

• Furosemidde

• Galantamine

• HCTZ

• Lamotrigine

• Latanoprost

• Metformin

• Metoclopramide

• Spironolactone

• Hydralazine

• Isosorbide dinitrate

https://cpicpgx.org/genes-drugs/

Pharmacogenomics Medicare Coverage

• CYP2C19 – metabolizes 15% of medications

• Covered– Clopidogrel – for patients with ACS undergoing PCI

• Not covered– PPIs

– SSRIs

– Amitriptyline

– Warfarin

– Clopidogrel for other indications (including ACS without PCI)

https://www.cms.gov/medicare-coverage-database/details/lcd-details.aspx?LCDId=35332&ver=11&CntrctrSelected=228*2&Cntrctr=228&s=22&DocType=All&LCntrctr=140*2&bc=AggAAAIBAAAA&

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Pharmacogenomics Medicare Coverage

• CYP2D6 – metabolizes 20-25% of all drugs

• Covered– Amitriptyline and nortriptyline for depression

– Tetrabenazine doses > 50 mg/day

• Not covered– Tamoxifen

– Antidepressants (except above)

– Codeine

– Antipsychotics

– Donepezil

– Galantamine

https://www.cms.gov/medicare-coverage-database/details/lcd-details.aspx?LCDId=35332&ver=11&CntrctrSelected=228*2&Cntrctr=228&s=22&DocType=All&LCntrctr=140*2&bc=AggAAAIBAAAA&

Pharmacogenomics Medicare Coverage

• CYP2C9 – metabolized 10% of medications

• Covered– Warfarin (with strict restrictions)

• Not covered– NSAIDs

– Flovoxamine

https://www.cms.gov/medicare-coverage-database/details/lcd-details.aspx?LCDId=35332&ver=11&CntrctrSelected=228*2&Cntrctr=228&s=22&DocType=All&LCntrctr=140*2&bc=AggAAAIBAAAA&

OTHER DRUG DELIVERY CONSIDERATIONS

When Patients Cannot Swallow Pills

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Dysphagia in LTC

• > 60% of all active pharmaceutical ingredients are developed and intended for oral administration– Rationale: ease of administration, increased product

stability, cheaper to manufacturer

• 40-80% of patients in nursing homes may have difficulty swallowing

• 33-60% non-dysphagic ambulatory patients have some difficulty swallowing oral dosage forms

Logrippo et al. Clin Int Age.2017;12:241-51Schiele et al. Dysphagia.2015;30”571-82Carvajal et al. Farm Hosp.2016;40:514-28Manrique et al J Pharm Pharm Sci 2014;17:207-19

Pill Manipulation

• Tablet crushing or capsule opening

• Dispersion/dissolution of material in water, beverages, gels, or food– May allow better deglutition

– Administered orally or via PEG tube

• Any manipulation of approved product is considered an “off-label use” unless outlined in labeling– Technically – prescribers, nurses, and pharmacists can be legally

liable for ADRs resulting from medication administration and use

• Frequent occurrence in LTC

• Up to 42% of medications crushed in LTC should not be

Logrippo et al. Clin Int Age.2017;12:241-51Carvajal et al. Farm Hosp.2016;40:514-28Manrique et al. J Pharm Pharm Sci.2014;17:207-19

Pill Manipulation: Stroke Study

• German study of stroke patients in acute care ward or rehab

• 42.3% of solid oral dosage forms (154/364) prescribed for 25 patients were crushed

• 1/5 inadequately crushed– 47% could have been put into suspension

– 53% had pharmaceutical equivalents or therapeutically equivalent dosage forms suitable for crushing or suspending

• 1/3 required crushing just before administration due to stability concerns

• 38 drugs with unjustified crushing: Pantoprazole, metoprolol SR, probiotics, others

Schiele et al. Dysphagia.2015;30”571-82

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Avoid Crushing: Narrow Therapeutic Window Drugs

Problems

• Imprecise dose

• ↓stability in solution

• Impacted stability when mixed with food, drinks, or vicious gels

Examples

• Warfarin

• Carbamazepine

• Digoxin

• Lithium

• Theophylline

• Phenytoin

Logrippo et al. Clin Int Age.2017;12:241-51

Avoid Crushing: Modified –Release Dosage Forms

Problems

• Altered amount of API released over time– Dose dumping

• Altered API release site –impact absorption

Examples

• Pantoprazole

• Rabeprazole

• Quetiapine

• Tamsulosin

• Levodopa/carbidopa

• Pentoxifylline

Logrippo et al. Clin Int Age.2017;12:241-51

Avoid Crushing: Prolonged/Slow Release

• Nifedipine

• Aggrenox

• Allegra-D

• Lovastatin

• Lubiprostone

• Dutasteride

• Brivaracetam

• Duloxetine

• Divalproex

• Topiramate

• Rivaroxaban

• Isosorbide

• Guanfacine

• Paliperidone

• Hyoscyamine

• Guaifenesin

• Mirabegron

• Felodipine

• Ranolazine

• Benzonate

• Extended release

ISMP: Oral Dosage Forms That Should Not be Crushed 2016

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Avoid Crushing: Enteric Coated Formulations

Problems

• APIs are often acid-labile – designed to be absorbed in intestines

• Drug inactivated by gastric acid

Examples

• Prolonged-release drugs

• Brivaracetam

• Diltiazem

• Pancrelipase

• Bisacodyl

• Erythromycin

• Tamsulosin

• Exceptions– Microencapsulated

oxycodone

Logrippo et al. Clin Int Age.2017;12:241-51

Avoid Crushing: Enteric Coated GI Irritants

Problems

• Safety– Diarrhea

– Mucosal damage

– Perforation

– Hemorrhage

• Efficacy– Delayed absorption/onset

– Inactivated

Examples

• Ferrous sulfate

• Bisphosphonates

• KCL

• NSAIDs

• Tetracyclines

• Clindamycin

• Valganciclovir

Logrippo et al. Clin Int Age.2017;12:241-51

Alternatives in Dysphagia

• Orally disintegrating tablets

• Transdermal patches

• Pulmonary delivery– Under development – levodopa

• Intranasal– Under development - donepezil

• Compounds

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DRUG INTERACTIONS

American Geriatrics Society 2015 Beers Criteria Update Expert Panel. J Am Geriatr Soc. 2015;63:2227-47

Hines et al. Am J Geriatr Pharmacother. 2011;9:364-377

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Hines et al. Am J Geriatr Pharmacother. 2011;9:364-377

Hines et al. Am J Geriatr Pharmacother. 2011;9:364-377

Hines et al. Am J Geriatr Pharmacother. 2011;9:364-377

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MATH AND SCALES

Anticholinergic Burden Calculator

http://www.anticholinergicscales.es/calculate

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Scales• Anticholinergic Risk Scale (ARS)

– Rudolph JL, Salow MJ, Angelini MC, McGlinchey RE. The anticholinergic risk scale and anticholinergic adverse effects in older persons. Arch Intern Med. 2008; 168(5):508-13.

• Chew’s scale (Chew)

– Chew ML, Mulsant BH, Pollock BG, Lehman ME, Greenspan A, Mahmoud RA, et al. Anticholinergic activity of 107 medications commonly used by older adults. J Am Geriatr Soc. 2008; 56(7):1333-41.

• Anticholinergic Drug Scale (ADS)

– Carnahan RM, Lund BC, Perry PJ, Pollock BG, Culp KR. The Anticholinergic Drug Scale as a measure of drug-related anticholinergic burden: associations with serum anticholinergic activity. J Clin Pharmacol. 2006; 46:1481-6.- Update ADS score 2013

• Anticholinergic Activity Scale (AAS)

– Ehrt U, Broich K, Larsen JP, Ballard C, Aarsland D. Use of drugs with anticholinergic effect and impact on cognition in Parkinson's disease: a cohort study. J Neurol Neurosurg Psychiatry. 2010; 81(2):160-5.

• Anticholinergic Load Scale (ALS)

– Sittironnarit G, Ames D, Bush A, Faux N, Flicker L, Foster J, et al. Effects of anticholinergic drugs on cognitive function in older Australians: results from the AIBL study. Dement Geriatr CognDisord. 2011; 31(3):173-8.

http://www.anticholinergicscales.es/calculate

Scales

• Clinician-Rated Anticholinergic Scale (CrAS) – Han L, Agostini JV, Allore HG, Abrahamowicz M, Primeau F, Élie M. Cumulative anticholinergic exposure is associated with

poor memory and executive function in older men. J Am Geriatr Soc. 2008; 56:2203-10.

• Duran’s scale (Duran) – Durán CE, Azermai M, Vander Stichele RH. Systematic review of anticholinergic risk scales in older adults. Eur J Clin

Pharmacol. 2013; 69(7):1485-96.

• Anticholinergic Burden Classification (ABC) – Ancelin ML, Artero S, Portet F, Dupuy AM, Touchon J, Ritchie K. Non-degenerative mild cognitive impairment in elderly

people and use of anticholinergic drugs: longitudinal cohort study. BMJ. 2006; 332:455-9.

• Drug Burden Index (DBI) – Hilmer SN, Mager DE, Simonsick EM, Cao Y, Ling SM, Windham BG, et al. A drug burden index to define the functional

burden of medications in older people. Arch Intern Med. 2007; 167 (8): 781-7.- Dispennette R, Elliott D, Nguyen L, Richmond R. Drug Burden Index score and anticholinergic risk scale as predictors of readmission to the hospital. Consult Pharm. 2014; 29(3):158-68.- Spanish Agency of Medicines and Medical Devices – AEMPS

– A.M. Villalba-Moreno, et al., Systematic review on the use of anticholinergic scales in poly pathological patients, Arch. Gerontol. Geriatr. (2015), http://dx.doi.org/10.1016/j.archger.2015.10.002d

http://www.anticholinergicscales.es/calculate

Ultimate Rules for Drug Dosing

• Start Low and Go Slow

• Trust Nothing

• Look up everything!

• Look up everything often.

• Treat each new symptom as an ADR until proven otherwise.

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QUESTIONS?