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Weighing The Risks and
Benefits of Treatment in
Older Adults
Do our scales need recalibration?
Debra L. Bynum, MD
Division of Geriatric Medicine
University of North Carolina
??????
What do you think of when
you think of “Geriatrics”……
Quips…
 Benjamen Franklin:

“All would live long, but none would be
old”
 Abraham Lincoln:

“And in the end, its not the years in your
life that count. It’s the life in your years.”
Geriatric “Domains”
 Palliative Care
 Dementia
 Incontinence
 Falls
 Delirium
 Frailty
 Constipation
Geriatric “Catch Phrases”
 Start low and go slow…
 The Dying Patient…. “?Moriatrics…”
 Life expectancy…
 Quality of Life….
 Falls Risk….
 Polypharmacy
Geriatric “Realities”
 “Graying” of America…
 Increasing population of oldest of the old
(number of people over age 80 will increase
form 6.9 million in 1990 to 25 million by year
2050)
Geriatric “Realities”
 With an increase in older adults comes an
increase in chronic diseases
 Many older adults are not “dying” but are
living healthy, active lives with several chronic
diseases…
New Geriatric Domains
 Myocardial Infarction
 Congestive Heart Failure
 Atrial Fibrillation
 Stroke
 Hypertension
 Hyperlipidemia
 Osteoporosis
 Aortic Stenosis
Do we “undertreat” older adults with
chronic conditions?
 Probably Yes….
Outline
 Why we might undertreat older patients
 Problems with clinical trials
 New perspectives on life expectency
 Examples
 Importance of Absolute Risk reduction
and determination of baseline risk
Objectives
 Appreciate the need to individualize care
of older patients with complex medical
problems
 Understand the importance of Baseline
Risk in determining the overall impact, or
absolute risk reduction, that any certain
therapy may have– patients at highest risk
for a bad outcome stand to gain the most
from a treatment that has even modest
benefit!
Why would we undertreat?
 Ageism
 Exclusion of older adults from clinical trials
 Assumption that the older adult may not want




“aggressive” treatment
Ideas based upon Life Expectancy
Concern for Polypharmacy
Concern that relative efficacies may be less for
certain treatments in older subgroups
Overestimation of Risks of Treatment and
underestimation of Benefits of Treatment
Ageism
 Coined 1969 by Dr. Robert Butler (first director of
the National Institute on Aging)
 “Systematic stereotying of and discrimination
against people because they are old”
 Fostered in clinical training
 Students and Residents see older adults from
nursing homes and in the hospital
 The Aging Game…
 The “Unwritten Curriculum”
 Age is NOT EQUAL to Frailty
Exclusion of Older Adults from
Clinical Trials
 1/3 of all major, original research papers in 1997
and 15% in 2004 excluded older people without
justification
 Potential concerns:
 More comorbid illnesses, more difficulty to follow,
higher drop out
 Increased risks with treatment
 Polypharmacy
 Protocol restrictions on comorbidities
 Older population as “vulnerable” study group
 Barriers with transportation and mobility
Assumption that Older Adult may not
want “aggressive” therapy
 Literature suggests that we tend to
underestimate “Quality of Life” equivalents for
others
 Data that physicians tend to assume that
older adults do not want certain treatments,
including ICU care, even though older
patients, when asked, actually do want such
care
Ideas Based upon Life Expectency
 Average Life Expectancy” can be misleading

Overall average 77 years in 2002

But, a 70 year old woman on average can
expect to live another 18 years!

10% of 90 year olds will live to 100
Polypharmacy
 Legitimate concern
 Medications seem to exponentially increase with
each additional Diagnosis!
 Balance standard of care
 Risk for Adverse Drug Event directly related to
number of medications
 Need to actively discontinue any unnecessary
medications
Some Examples
 Acute Coronary Syndrome
 Atrial Fibrillation and anticoagulation
 Lipid lowering therapy in older adults
Common Theme
 Increasing age associated with increased bad
outcome (stroke with afib, death/recurrent MI
with acute coronary syndrome,
cardiovascular event with hyperlipidemia)
 With increase in age, there is a decrease in
the number of eligible patients who receive
the standard of care treatment
Acute Coronary Syndrome
% Eligible AMI patients given ASA in ED
(Annals Em Med 2005)
100
90
80
70
60
50
40
30
20
10
0
<50
(n=169)
50-59
60-69
70-79
80-89
(n=461)
>90
Treatment with Aspirin
 Aspirin:
 Same relative benefit in older patients

Overall 20+ % lower death rate in patients
who receive ASA after MI

GREATER absolute benefit in older patients
because of higher ABSOLUTE risk of bad
outcomes

ARR of death 4.5 % in > 65 vs 3.3 % in those
younger than 65
% given Beta Blockers in ED
(Ann Em Med 2005)
80
70
60
50
40
30
20
10
0
<50
50-59
60-69
70-79
80-89
>90
% Eligible AMI patients given
reperfusion (Ann Em Med 2005)
90
80
70
60
50
40
30
20
10
0
<50
(n=62)
50-59
(n=96)
60-69
(n=107)
70-79
(n=117)
80-89
(n=69)
>90
(n=9)
Who has an Acute MI? Numbers from
the ED…
 8%
 15%
 20%
 30%
 22%
5%
younger than 50
50-59
60-69
70-79
80-89
>90
Ischemic Heart Disease in the Elderly
 Leading cause of death
 35% of all deaths in people over age 65
 Among people who die of IHD, 83% are over
age 65
 CV mortality and morbidity rates increase
exponentially after age 75


6% US population over age 75
60% MI related deaths in people over age 75
Pitfalls… Trial Patients are Different
 Skewed Numbers in trials:
 Patients over 85 = 2% of trial patients with ACS but
for 11% of ACS events in community registries
 Older patients in trials are different than
community elders who have Acute Coronary
Events

Older trial patients have lower traditional CV risk
factors, less comorbidity, better hemodynamics,
and better renal function than community elders
with ACS AND than younger trial patients!
Pitfalls… Delay in Diagnosis
 Increased prevalence of Atypical symptoms


Dyspnea, syncope, n/v
Increased prevalence of acute heart failure
 Increased prevalence of nondiagnostic EKG

34 % people over age 85 have baseline LBBB
Risk Stratification
 Age is huge risk factor for bad outcomes (even
when controlled for)
 ACC/AHA guidelines: patients over age 75 are at
high risk for death/recurrent MI
 Patients < 65 with NSTE ACS have 1% hospital
mortality
 Patients > 85 have 10% hospital mortality with
NSTE ACS
 Complications of recurrent MI, CHF, bleeding
increase with age
Atrial Fibrillation and Anticoagulation
 Prevalence: 5% of people over age 65
 10% of people over age 80
 50% of all patients with afib are over age 80
 Dreaded outcome: Stroke
 Strokes with afib have higher mortality/disability
Age and Stroke Risk
 Incidence of Stroke with afib increases with
age:

1.3 %/year in patients 50-59
2.2 %/year in 60-69
4.2 %/year in 70-79
5.1 %/year in 80-89

But it is much more complicated…



Predicting Risk of Stroke
 CHADS2
 CHF: 1 point
 HTN: 1 point
 Age over 75: 1 point
 DM: 1 point
 Prior Stroke/TIA: 2 point





Score 0 = annual stroke risk <1% (ASA alone)
2 or more: annual stroke risk over 4%: warfarin
Score 1= individualized treatment decision
Score 5 = over 10%/year stroke rate
Score 6 = over 15%/year stroke rate
Benefit of Warfarin
 Overall decreases risk of stroke by 60-70%,
ARR of 2.7-3 %/year
 Beneficial in all age groups, even those over
age 75
 ?Quality of life of preventing a stroke
Risks of Warfarin
 Risk of warfarin associated bleeding
increases with age
 Risk ICH: .34 %/year in age less than 60,
.76% /year in those over 80
 Absolute risk of major bleeding = 2.2% /year
(increases to near 3% in those on warfarin
plus asa)
Warfarin use…
 Older patients less likely to receive
anticoagulation
 Older patients more likely to be
“underanticoagulated” -- even though data is
clear that there is no significant stroke
protection at an INR of less than 2
 Overestimation of “Falls Risk”
Warfarin in older patients: Bigger
Bang for the Buck…
 Patients under age 65 with afib and risk factors
for stroke: warfarin decreases risk of stroke from
4.9 %/year to 1.7 %/year
 In patients over 75 with risk factors (highest risk
group), warfarin reduces risk of stroke from 12
%/year to 2-4 % /year
 Those at highest risk for stroke (older, prior
stroke, chf, dm, htn) are less likely to be given
warfarin because of concerns for their
“comorbidities”
Lipid lowering therapy in older
adults…
Lipid lowering therapy in High Risk
Elderly Patients (JAMA 2004)
 Retrospective cohort study
 Databases of over 1 million elderly in
Ontario, study looked at nearly 400,000
over age 66 with history of CV disease or
DM (SECONDARY PREVENTION)
 Outcome: likelihood of statin use for each
CV risk group
Results
 Only 19% prescribed statins
 Likelihood of statin prescription was 6.4%
lower for each year of increased age AND
each 1% increase in predicted 3 year
mortality risk
Likelihood of statin prescription: Ages 6674
Low CV risk
(7.8% 3 year
mortality)
37.7%
Intermediate
Baseline Risk
High Baseline
Risk
(12.8% 3 year
mortality)
(34.4 % 3 year
mortality)
26.7%
23.4%
Likelihood of statin Rx: ages 75-80
Low CV risk
(13.7% 3 year
mortality)
29%
Intermediate
risk
(21% 3 year
mortality)
19%
High risk
(43% 3 year
mortality)
15%
Likelihood of statin Rx: age > 80
Low risk
Intermediate
risk
High risk
(25% 3 year
mortality)
( 40% mortality)
(60 % 3 year
mortality)
13%
6%
4%
Treatment-Risk Paradox
 Those at the highest risk of certain outcome
(CV mortality) are often those NOT treated
because of fear of risk of treatment
 Highest risk population may see the greatest
ABSOLUTE benefit in reduction of events
given the high baseline risk
Importance of Absolute Risk Reduction
and Number Needed to Treat (NNT)

NNT to prevent one patient from having event

Clinically more meaningful than relative risk

1/ absolute risk reduction (example: 10 % ARR =
1/.10 = NNT of 10)

RRR of 50 % may be good or not so good,
depending on the number at risk
 Decrease events from 2% to 1% (ARR of 1%)

Decrease from 30 % to 15 % (ARR of 15%)
Risk Reduction
 In high risk populations, the BASELINE RISK
has MORE impact than relative efficacy of a
treatment on determining the absolute risk
reduction and NNT
Relation between baseline risk and NNT by various
relative efficacies of treatment (Alter, Am J Med 2004)
Age
Group
NNT with
relative
efficacy
of 25%
175
NNT with
relative
efficacy
of 50%
<50
1 year
NNT with
mortality relative
efficacy
%
of 10%
2.3
437
50-64
4.8
209
84
42
65-74
11.1
90
36
18
>74
27
37
15
7
87
What does this all mean?
Take Home Points
 Age is only one factor; frailty and age are not
the same
 There need to be increased numbers of older
adults included in trials, and these patients
should be of similar to older community
patients and younger trial patients
Take Home Points…
 Care of complicated older patients with
multiple chronic comorbidities must be
individualized and cannot be totally driven by
standard guidelines
 But guidelines and standards of care should
not be ignored in patients just because they
are older
Take Home Points…
 Weighing Risks and Benefits in treatment of an
individual older patient requires:




Knowing risks and benefits of a therapy (not
overestimating risk or underestimating benefit)
Looking at the ARR and NNT
Understanding the impact that Baseline Risk
has upon absolute risk reduction
Those at highest risk stand to gain the most –
and risk of treatment may be completely
outweighed by this potential gain
P.S.
 Case Study: Just to complicate matters






85 healthy man with distant history of TURP and HTN
was admitted 2 weeks prior with a NSTEMI that was
uncomplicated; he had early catheterization and a stent
to his RCA, was placed on aspirin, clopidogrel
He returned a few days later with a nosocomial
pneumonia and atrial fibrillation, was started on
warfarin. In the CCU, he had a foley catheter placed.
He again returned a few days later with E coli UTI and
sepsis syndrome
He again returned a few days later with gross hematuria
He stayed in the hospital for over a month with bleeding,
urologic procedures
?Did he need the cath or intervention? The
anticoagulation?