new and appropriate goals for parkinson disease physical therapy
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8/17/2019 New and Appropriate Goals for Parkinson Disease Physical Therapy.
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Copyright 2016 American Medical Association. All ri ghts reserved.
New and AppropriateGoals for Parkinson Disease
Physical TherapyJ. Eric Ahlskog, PhD, MD
Physical and occupational therapy have long been compo-
nents of Parkinson disease (PD) treatment. Prior to the ad-
vent of levodopa, this was a primary therapeutic modality.What is the current role for physical therapyin PD?Should ev-
eryone with PD be referred? Is it cost-effective? What should
be the therapeutic goals and program content?
In the United Kingdom, cost-effectiveness is an especially
relevantconsiderationin the contextof itssingle-payerNational
Health Service. The cost-effectivenessof routinereferral of pa-
tientswith earlier-stagePD forphysiotherapyand occupational
therapy was addressed in an
article in this edition of JAMA
Neurology. Half of more than
patients with PD from
across the United Kingdomwere randomized to standard prac-ticephysiotherapyand occupationaltherapy (median,; hour-
long therapy sessions). Compared with the control group, this
therapyintervention failed to meaningfully influencethe activi-
tiesof daily living or quality-of-life measures, withfollow-up at
andup to months. Theinvestigators concluded that, “This
evidencedoes notsupport theuse oflow-dose,patient-centered,
goal-directedphysiotherapyandoccupationaltherapyin patients
in the early stages of PD.” The authors cited prior studies that
tended to support this conclusion.
These results should be interpreted with attention to the
study details. Patients in this investigation had mild to mod-
erate PD and the enrollment criteria excluded patients whose
clinicians believed needed physical/occupational therapy.
Thus, one may conclude from this investigation that blanket
referralsof allpatients with earlier-stage PD forroutine physi-
cal or occupation therapy appears to be cost-ineffective.
Intuitively, certainPD-related symptoms shouldbenefitfrom
routinephysical therapystrategies,including problems such as
gaitfreezing,imbalance/fallrisk, or immobilizedlimbs. Patients
withPDwithshortenedstrideorreducedarmswingbenefitfrom
strategiesforconsciouslyincreasingattenuatedmovements.Such
circumscribed problemswere notthe focus of thisinvestigation.
The therapy schemes performed in this investigation are
also notable: “Physiotherapy and [occupationaltherapy] were
delivered…by qualified therapists working within the Na-tional Health Service (NHS) per local practice.” Such routine
physicaltherapy practices areuniversally establishedand have
been used for decadesin treating PD.Per convention,these pri-
marily focus on stretching, balance, posture, gait, and strate-
gies forfacilitatingactivities of daily living. More recently, pro-
tocols forenhancing movement amplitudes have beenadded
(eg, consciously focusing on increasing stride length and arm
movements). However, these conventional physical therapy
practices take no advantageof what has nowbecome increas-
ingly apparent: ongoing aerobic exercise may slow the pro-
gression of PD. Todate,it has not beenpartof physical thera-
pists’ job description to facilitate ongoing aerobic exercise.
The progression of PD extends far beyond dopaminergic
substrates and includes potential for levodopa-refractory de-
mentia, dysautonomia, and medication-unresponsive motorsymptoms. No medications are proven to slow such PD pro-
gression. However, there is substantial, albeit indirect, evi-
dence for regular vigorous exercise and aerobic fitness possi-
bly providing a neurop rotective effect. This comes from a
variety of investigations, which may be summarized as
follows.Animalstudies havedocumented exercise-related in-
creases of brain neurotrophic factors, synapticproteins,neu-
roplasticity factors, hippocampal neurogenesis, hippocam-
pal long-term potentiation, recovery from neurotoxins, and
enhanced memory. Habitually exercising humans have evi-
dence of significantlylargerbrain cognitive regions,bettercor-
tical connectivity (functional magnetic resonance imaging), better cognitive scores, and reduced later frequencies of PD,
dementia, and mild cognitive impairment.
This exerciseliterature posesthe question ofwhether na-
tionalhealth careadministrationsshould endorseand financially
underwrite aerobicexercise programsfor allwithPD.Thiswould
entail far more than single therapy sessions.Our culture tends
to reinforcea sedentarylifestyle,and newexercise habits would
need to be periodically monitored and reinforced. Such a PD
exercise program would necessarily begin with optimized
carbidopa/levodopa treatment, which is often necessary to
allow exercise. The envisioned therapy program would begin
with individualized selection of aerobic exercise routines that
wouldbe toleratedandmaintainedbyeach personwithPD.There
is no one-size-fits-allprogram forexercise and all aerobic exer-
cise options should beon thetable.Such a programwould nec-
essarily start modestly for some but with therapist-guided ad-
vances and, sometimes, with tough love.
A challenge forthoseendorsingsucha structured aerobicex-
ercise protocol is proof of benefit. A randomized clinical trial
among patients withPD is going to be highly susceptibleto con-
founding factors. Manyin our culture aredisinclinedto exercise
even in the absence of neurologic disease; maintaining persis-
tentadequatelevelsofaerobicexercisewillbeachallengeinsuch
people. Such a program wouldrequirepeople toalso exerciseon
their own, wherebadexercise habits canflourish.On theotherhand, motivated patients with PD randomized to the control
group mayrecognizepotential exercisebenefits andengage on
their own. Moreover, sucha controlledstudy of PD progression
would necessarilyrequire prolongedfollow-up (eg,a fewyears),
andtheexpected dropoutratewouldcompromiseinterpretation.
Realistically, perhapsthe bestwe can do is baseour PD exercise
recommendations on the existing published literature.
To summarize, first, current physical/occupation therapy
referralsfor those with PD shouldbe for specificproblemsthat
arelikely to benefit. Second, physical therapypractices should
beginto incorporate facilitationof ongoing aerobic exercise and
fitness.
Relatedarticle page 291
Editorial Opinion
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Copyright 2016 American Medical Association. All ri ghts reserved.
ARTICLE INFORMATION
AuthorAffiliation: Department of Neurology,
MayoClinic, Rochester, Minnesota.
Corresponding Author: J.Eric Ahlskog, PhD, MD,
MayoClinic, Department of Neurology, Gonda8,
Rochester,MN 55905 ([email protected]).
Published Online: January 19,2016.
doi:10.1001/jamaneurol.2015.4449.
Conflict of Interest Disclosures:Nonereported.
REFERENCES
1. ClarkeCE, Patel S,Ives N, et al.Physiotherapy
andoccupationaltherapy vs no therapy in mild to
moderate Parkinsondisease: a randomizedclinical
trial [published online January 19,2016]. JAMA
Neurol . doi:10.1001/jamaneurol.2015.4452.
2. Ahlskog JE.Does vigorous exercisehavea
neuroprotective effect in Parkinsondisease?
Neurology . 2011;77(3):288-294.
3. Ahlskog JE.Cheaper, simpler, andbetter: tipsfor
treating seniors with Parkinsondisease.Mayo Clin
Proc . 2011;86(12):1211-1216.
Implementing Recommendations
for Depression Screeningof Adults
HowCanNeurology Contribute to the Dialogue?Helen S. Mayberg, MD
TheUSPreventiveServicesTaskForce(USPSTF)hasofferedits
updated recommendations for the screening for depression in
adults. Thedocument, publishedthis week in JAMA, updates
a review ofthe evidence as tothe net benefit ofaccurate
diagnosis,effectivetreatment,
and appropriate follow-up af-
ter depression screening for
adults older than years,
including pregnant and postpartum women, complementing
previousrecommendations fordepression screeningin children
and adolescents (http://www.uspreventiveservicetaskforce
.org). There is no question that primary care screeningoffers a
first-line medical opportunity to identify patients with an
undiagnosed major depressive episode. Use of standardized
screening instruments and evidence-based treatments are a
critical first step. Thatsaid, an unsettlingrealityremains:how,
even with improved efficiency of screening and more timely
diagnoses, do we secure the necessaryresourcesto ensure that
depressed patients not only receive treatment and follow-up,
but that the tre atm ent selected is bot h appropri ate and
optimized for the individual. Compounding these challenges,
neurological patients with depression, even when identified,
maybe reticent toacceptpsychiatrictreatment,andlikeinternal
medicine and primary care, the time and resources needed to
address the behavioral “symptoms” are often eclipsed by core
demands of the principal neurological or medical condition.For a patient presenting with major depressive episode, an
antidepressant medication or evidence-based psycho-
therapyis currently recommendedas first-line treatment, with
remissionratesto these options roughly equivalentin allpa-
tients except the mostseverely ill.With thisperceivedequiva-
lency, treatmentselection is oftenbasedon factors such as pa-
tient and health care professional preference, cost and
accessibility, and potential adverse effects. However, the odds
are actually against remission in patients currently treated
using this approach. At best, % of patients achieve remis-
sion with a first treatment, and the “wrong” first choice has
significantindividual andsocietal costs due to continued dis-
tress, risk of suicide, loss of productivity, and wasted re-sources associated with to months of an ineffective treat-
ment. Moreover, among theroughly %to %of depressed
patients who do not remit with their first treatment, many do
not return to explore other options, with potential lethal
consequences.These sameconcernshold fordepression pre-
senting in patients with neurological diseases and othermedi-
cal illnesses where the combined presence of a mood disor-
der has a magnified effect on disability.
Clearly, treatments are highly effective in some individu-
als, but there is no reliable way to match patients to their best
treatment option or to avoid those that are unlikely to be ef-
fective, even in the setting of equal access. Developing reli-
able biomarkers that can stratify individual patients to spe-
cific treatments is essential to achieve the goal of a more
personalized level of care forpatients withdepressionand all
neuropsychiatric disorders.Manymedical specialtiessuch as
those treating heart diseaseand cancer nowroutinely use pa-
tient-level biological measures to subtype and stratify pa-
tients to treatments, andto guide treatmentmodificationswith
disease progression or categories of disease risk, substan-
tially improving patient outcomes.
Toward a “precision medicine” approach for depres-
sion, various strategies have been tested, including clinical,
imaging, genetic, electroencephalographic, and immuno-
logical metrics, but with limited clinical impact thus far.Motivated to translate ongoing advances in functional and
structural neuroimaging methods and mounting evidence
of () distinct patterns of brain dysfunction across clinically
defined depression subgroups, () regional correlates of spe-
cific mood, motor, and cognitive syndrome dimensions, and
() differential change patterns with mechanistically dis-
tinct treatments, investigations of brain-based biomarkers
that predict treatment outcomes to standard first-line treat-
ments have been initiated. Recent studies have identified
some initial promising imaging biomarker candidates that
predict remission and nonresponse to cognitive behavioral
therapy or a standard selective serotonin reuptake inhibitor
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Opinion Editorial
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