Exam 2: the old farts Flashcards
what are 4 components that make up frailty?
-chronic malnutrition
-sarcopenia
-decreased metabolic rate and activity
-decreased appetite
frailty + stressor event = _____ & ______
falls and delirium
what are 5 phenotypes model indicators of frailty?
1- weight loss
2-self-reported exhaustion
3- low energy expenditure
4- slow gait speed
5- weak grip strength
Dementia onset, duration, cause and course
-slow and gradual, with an uncertain begining point
-usually permanent
-usually cause by a chronic brain disorder (alzheimers, lewy body dementia, vascular dementia)
-slowly progressing
Dementia effect at night, attention, level of consciousness, & orientation to time and place
-often worse at night
-A & LOC: unimpaired until dementia has become severe
-impaired
dementia use of language, memory & need for medical attention
-sometimes difficulty finding the right word
-lost memory, especially for recent events
-required medical attention but less urgent
Delirium use of language, memory & need for medical attention
-slow, often incoherent + inappropriate
-varies memory loss
-IMMEDIATE medical attention
Delirium effect at night, attention, level of consciousness, & orientation to time and place
-almost always worse at night
-attention is greatly impaired
-LOC & time and place: varies
Delirium onset, duration, cause and course
-sudden, with a definite beginning point
-days to weeks, although it may be longer
-almost alway due to another condition (infection –> UTI, dehydration, use or withdrawal of certain drugs)
-usually reversible
what drugs are not metabolized as well due to dec in hydroxylation?
-alprazolam
-midazolam
-quinidine
-propranolol
-triazolam
-r-warfarin
what drugs are not metabolized as well due to decrease in demethylation?
-imipramine
-sertraline
-verapamil
-therophylline
active metabolites with detrimental effects in excretion:
-norpropoxyphene
-hydroxyaminodapsone
-normeperidine
gastrointestinal absorption changes in the elderly
-unchanged passive diffusion and no change in bioavailability for most drugs
-dec active transport and dec F for some drugs
-dec first pass metabolism, inc F for some drugs and dec F for some prodrugs
distribution changes in the elderly
-dec volume of distribution and inc plasma concentration of water-soluble drugs
-inc volume of distribution and inc terminal disposition t 1/2 life for soluble drugs
hepatic metabolism changes in the elderly
-dec clearance and inc t 1/2 life for some drugs with poor hepatic excretion (capacity-limited metabolism). Phar 1 metabolism may be affected more than phase II
-dec clearance and inc T 1/2 life for drugs with high hepatic extraction ratios (flow-limited metabolism)
renal excretion changes in the elderly
-dec clearance and inc T 1/2 life for renally eliminated drugs and active metabolites
anticholinergic side effects: vision, oral cavity & GI
V: impaired ALD, falls and accidents
OC: decline in nutritional status, increased risk of infection, worsened communication
GI: decline in nutritional status, worsening of disease (constipation), anxiety and pain
anticholinergic side effects: Cardio, urinary tract & CNS
C: worsening of disease, anxiety
UT: incontinence, infection, loss of independence
CNS: cognitive dysfunction, impaired ADL
Anticholinergic: muscle relaxants
-cyclobenzaprine
-methocarbamol
-carisoprodol
-oxybutynin
anticholinergic TCAs
amitriptyline
anticholinergic antispasmodics
-dicyclomine, hyoscyamine, propantheline
anticholinergic antihistamines
-diphenhydramine
-chlorpheniramine
-cyproheptadine
-hydroxyzine
-promethazine
benzodiazepine use in the elderly leads to an increased risk of:
-cognitive impairment, delirium, falls/fractures & motor vehicle crashes
–> MAY be appropriate for seizure disorders, rapid eye movement sleep behavior disorder, benzo withdrawal;, ethanol withdrawal, severe generalized anxiety disorder and periprocedural anesthesia
NSAID: GI toxicity in elders
-ulcer risk 4-5x nonusers
-~4 fold increase mortality related to PUD
-highest risk early
-risks increase ~4% per year of age > 65
NSAID induced injury prevention: Misoprostil
-800 mcg/day needed
-lower doses do have less diarrhea but less effective
NSAID induced injury prevention: H2- RA
-use double doses to be effective
NSAID induced injury prevention: PPI
-standard dose effective
NSAID induced injury prevention: HIGH risk GI pts
-COX2 alone or NSAID + PPI: offer similar but potentially insufficient protection
-COX-2 + PPI: can be considered
NSAIDs and cardiovascular risk
-all NSAIDs increase the risk of acute mirtrocardial infarction
FDA warning: NSAIDS can cause heart attacks or strokes
NSAID renal effects in elders
-reductions in renal blood flow
-sodium and water retention
-concern for combinations with ACEI or diuretics commonly used in elders (can cause a decrease in renal blood flow and acute renal injury)
–> 2 fold increase in hospitalizations for CHF in pts on NSAIDs and diuretics
Beers list: common anticholinergic drugs to avoid (1st gen antihistamines)
-diphenhydramine
-doxylamine
-hydroxyzine
-promethazine
-pyrilamine
-tiprolidine
Beers list: antiparkinsonian agents to avoid
-benztropine
-trihexyphenidyl
Beers list: antispasmodics to avoid
-atropine (excludes ophthalmic)
-belladonna alkaloids
-clidnium-chlordiazepoxide
-dicyclomine homatropoine (not ophthalmic)
-hyoscyamine
-methoscopolamine
-propantheline
-scopolamine
Beers list: antithrombotics to avoid
-dipyridamole- oral short acting –> does not apply to the extended release combo with aspirin
Beers list: anti infective to avoid
nitrofurantoin
Beers list: cardiovascular drugs to avoid
–> peripheral alpha-1 blockers for tx of hypertension
-doxazosin
-prazosin
-terazosin
-clonidine
Beers list: cardiovascular drugs to avoid - other CNS alpha agonists
-guanabenz
-guanfacine
-methyldopa
-reserpine
-disopyramide
-dronedarone
-digoxin
-nefedipine
-amiodarone
Beers list: CNS antidepressants to avoid
-amitrptyline
-amoxapine
-clomipramine
-desipramine
-doxepin > 6 mg/day
-imipramine
-nortriptyline
-paroxetine
-protriptyline
-tripipramine
Beers list: barbiturates to avoid
-amobarbital
-butaburbital
-butalbital
-mephorbarbital
-secobarbital
Beers list: short and intermediate benzos to avoid
-alprazolam
-estazolam
-lorazepam
-oxazepam
-temazopam
-trazolam
Beers list: long acting benzos to avoid
-chlordiazepoxide
-clonazepate
-diazepam
-flurazepam
-quazepam
-random: meprobamate
Beers list: z-drugs to avoid
-eszocipiclone
-zalepion
-zolpidem
Beers list: endocrine related drugs to avoid
-methyltestosterone, testosterone
-desiccated thyroid
-estrogens w or w/o progestins
-growth hormone
-insulin (sliding scale- hypoglycemia)
-megestrol
Beers list: sulfonylureas to avoid
-chlorprapamide
-glimepiride
-glyburide
Beers list: GI meds to avoid
-metaclopramide
-mineral oil (given oral)
-PPIs
Beers list: main meds to avoid (non selective NSAIDs)
-mependine
-aspirin > 325 mg/day
-diclofenac
-diflurisal
-etodlac
-fenoprofen
-ibuprofen
-ketoprofen
-meclofenamate
-mefeamic acid
-meloxicam
-nabumentone
-naproxen
-oxaprozin
-piroxicam
-sulindac
-tolmetin
-indomethacin
-ketorolac
Beers list: muscle relaxants to avoid
-carisopeodol
-chlorzoxazone
-cyclobenzaprine
-metaxalone
-metocarbamol
-orphenadrine
Beers list: genitourinary drug to avoid
desmopressin
Deprescribing
-the systematic process of identifying and discontinuing drugs in instances in which existing potential harms outweigh existing or potential benefits within the context of an individual patients care goals, current level of functioning, life expectancy, values and preferences
Goal: to reduce medication burden and harm while maintaining or improving QOL
Process of deprescribing ( 5 steps)
1) ascertain all drugs the patient is currently taking and the reasons for each one
2) consider overall risk of drug-induced harm in individual pts to determine the required intensity of deprescribing intervention
3) assess each drug for its eligibility to be discontinued
4) prioritize drugs for discontinuation
5) implement and monitor drug discontinuation regimen
what is ascertain?
-ask patient (and caregiver) about all prescribed, OTC, complementary and alt meds, and supps they currently take
–> assess adherence to current regimen with special attention paid to drugs not being taken and the reasons why
Potential drug induced harm: drug factors
-number of medication prescribed
-use of potentially inappropriate or “high risk” meds
-past or current toxicity
-NNT/NNH
Potential drug induced harm: patient factors
-age > 80y/o
-cognitive impairment
-multiple comorbidities
-substance abuse
-multiple prescribers
medications that would be good candidates for discontinuation include:
-no valid indication
-part of a prescribing cascade
-harm clearly outweights potential benefit
-time to benefit/time to harm
-drugs imposing unacceptable treatment burden
–> important to ask pts about treatment emergent side effects
–> consider patient preference
prioritizing when it comes to deprescribing
-decision on what to recommend stopping first should be based on integration of the criteria:
1) those with the likelihood of greatest harm and least benefit
2) those easiest to d/c (lowest likelihood of withdrawal reactions or disease rebound)
3) those that the patient is most willing to d/c first (to gain buy-in to deprescribing other drugs)
–> suggested approach is to rank drugs from high harm/low benefit t low harm/high benefit anf d/c in sequntial order
Implement and monitor deprescribing
-gain pt buy in before attempting d/c
-d/c one agent at a time
-taper meds more likely to cause withdrawal symptoms
-communicate plan for deprescribing to all care givers and healthcare professionals involved in pts care
-clearly document rationale and outcomes of deprescribing
Physiologic changes with aging that can lead to increased fall risk
-dec lean body mass
-dec myocardial sensitivity to B-adrenergic stimulation
-dec baroreceptor activity
-dec cardiac output
-alterations in several aspects of cognition
-pulmonary issues
-dec accommodation of the lens of the eye = causing farsightedness
-dec conduction velocity
-loss of skeletal bone mass (osteopenia)
intrinsic (non modifiable) risk factors for falls
-muscle weakness
-impaired balance, mobility and activities of daily living
-arthritis, stroke, diabetes, HTN, heart disease and dementia
Extrinsic (modifiable) risk factors for falls
-medication use
-poor foot care
-impaired vision
-unsafe footwear
-hearing problems
-an unsafe environment
drug burden index and falls
-DBI is a method for measuring an individual’s total exposure to anticholinergic and sedative drugs
fall risk increasing drugs
-any psychotropic drug
-antidepressants
-benzos
-antipsychotics
-sedative hypnotics
-tranquilizers
Common causes of Incontinence
-urethral obstruction: BPH/strictures/stenosis
-impair bladder contraction: DM/MS/Spinal injuries/detrusor hyperactivity
-incompetent sphincter: stress incontinence/cystocele
-bladder inflammation: UTI/interstitial cystitis
-bladder stones: obstruction/metabolic disease/UTI
-malgnancy: bladder CA, carcinoma in situ, invasive CA
meds that affect continence
-alpha agonists/antagonists
-alcohol
-anticholinergics
-cholinesterase inhibitors
-CCBs
-diuretics
-narcotics
-antidepressants
-antipsychotics
-sedative/hypnotic
Desmopressin nasal spray in nocturnal polyuria dosing
indication: nocturnal polyuria in adults, awaken > 2 x/night to void
age 50-65: 1 spray (1.66) either nostril ~ 30 mins before bed
age >/ 65: 1 spray (0.83) either nostril ~30 mins before bed (inc to 1.66 after 1 week if Na stays wnl)
Desmopressan nasal spray warnings & CI
warning: fluid retention, hyponatremia, nasal conditions (beers list “avoid”)
CI: hyponatremia, polydipsia, primary nocturnal enuresis, concomitant use w/ loop diuretics or systemic glucocorticoids. eGFR < 50