mms survey & consensus criteria results
TRANSCRIPT
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Sumit Parikh Md
The North American Mitochondrial Disease Survey (2012) and Consensus Project (2013)Practice Patterns and Challenges
Mitochondrion 2013Genetics in Medicine 2015
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How is mitochondrial medicine practiced in North America?
Is there consensus?
Is there a need for consensus criteria?
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Invitations sent to CNS, SIMD, MMS, metab-l and Child Neurology
list-serv members
37 initial volunteers
5 stopped participating
32 completed all surveys
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Practice LocationsLittle Rock, ArkansasSan Diego, CaliforniaStanford, CaliforniaVancouver, BC, CanadaHamilton, Ontario, CanadaAurora, ColoradoWashington, DCAtlanta, GeorgiaIndianapolis, IndianaNew Orleans, LouisianaBaltimore, MarylandBethesda, MarylandBoston, MassachusettsDetroit, MichiganRochester, MinnesotaAkron, OhioCleveland, OhioColumbus, OhioNashville, TennesseeHouston, TexasPhiladelphia, PennsylvaniaPittsburgh, PennsylvaniaSeattle, WashingtonMilwaukee, Wisconsin
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6%
9%
9%
16% 28%
31%
Biochemical genetics Neurometabolism/NeurogeneticsChild Neurology Clinical GeneticsNeuromuscular Other
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of physicians surveyed, while pediatric trained, see both adults and pediatric patients
81%
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90-120 minutes25%
60-90 minutes50%
< 60 minutes25%
50 minutes
Average time of a follow-up
visit
New Patient Consult Visit Time
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30-60 minutes38%
Variable16%
90-120 minutes13%
60-90 minutes19%
< 30 minutes16%
New Patient Preparation Time
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Mitochondrial clinics require
Prescreening of patients Advance review of records
Multiple specialty appointmentsAdditional preparation time > 30 minutes
Physician ExtendersCase Review with colleagues
66%94%69%69%90%88%
50% cancel visit if no records received
Time !!!
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LactateOrganic Acids, urine
CMPAmino Acids, plasma
AcylcarnitinesCBC
UrinalysisPyruvate
Amino Acids, urineCK
MMACarnitine, urine
Physicians surveyed
0 8 16 24 32 38%
38%
100%100%
47%38%
6%
94%
28%
54%
3%
31%
91%84%
Biochemical studies obtained
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38%
38%
84%100%
mtDNA point mutation first
mtDNA genome first
Nuclear Gene Panel, Selective
Nuclear Gene Panel, 100 genes
Nuclear Gene Panel, > 100 genes
Exome, if needed
Physicians surveyed
0 8 16 24 32
28%Perceived pressure to
perform mtDNA sequencing
59%
38%
15%
63%
34%
50%
Genetic studies obtained
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38%
38%
Perception of various laboratories that perform mitochondrial testing
bit.ly/mms paper supplement
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53%obtain a muscle
biopsy when faced with normal
biochemical screening
46%wait until a child is at least a year old prior to obtaining a muscle biopsy (if not longer)
97%prefer the quadricep
muscle
84%obtain at least ETC
enzymology, histology and electron
microscopy
Only 31%establish whether an ETC abnormality is
significant via diagnostic criteria
Only 43%measure muscle
Coenzyme Q10 levels
Only 48%obtain mtDNA
sequencing, deletion and duplication
analysis
78%feel mitochondrial testing in skin is of
limited value
81%obtain liver biopsy if
there is hepatic disease
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of physicians surveyed use diagnostic criteria
63%
60% 20% 20% NijmegenModified Bernier NAMDC
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of physicians surveyed require a genetic diagnosis
37%
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believe in secondary mitochondrial dysfunction
100%
need to treat secondary dysfunction
34%
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unsure if Autism related mitochondrial dysfunction is a primary or secondary phenomenon
88%
unsure what symptoms represents mitochondrial autism
78%
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% o
f phy
sici
ans s
urve
yed
0
14
28
< 5% 5-10% 10-20% >20% Unable to assess
19%16%16%
28%
19%
Perceived Muscle Biopsy False-Positive Rate
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% o
f phy
sici
ans s
urve
yed
0
15
30
< 5% 5-20% 20-30% 30-50% >50% Unable to assess
22%19%
6%
28%
22%
3%
Perceived Muscle Biopsy False-Negative Rate
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% o
f phy
sici
ans s
urve
yed
0
25
50
< 5% 5-10% 10-20% 20-40% >40% Unable to assess
16%
50%
28%
3%3%0%
Perceived Skin Biopsy False-Negative Rate
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38%
38%
Part 2Treatment and Preventative Care
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100%
84%
Creatine
Levo-Carnitine
CoQ10
L-Arginine for strokes
Physicians surveyed
0 8 16 24 32
75%
94%
100%
100%
Supplement used most commonly
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50% 50%
Start cocktailStart individual supplement
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42%
10%
48%
UbiqunolUbiquinoneDoes not matter
Ubiquinol vs Ubiquinone
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47%53%
Follow levelsDo not follow levels
Following CoQ10 levels
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12%
41%
47%
Leukocyte levelsSerum levelsNo preference
Following CoQ10 levels
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22%
78%
Recommend exerciseNo recommendation
Use of exercise as a treatment
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12%
48%
40%
Land, water and resistanceLand and resistancePer therapist
Type of exercise recommended
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38%
38%
Lab work checked preventatively
Electrolytes
Transaminases
HgbA1C
Thyroid function
Amino acids, urine
CoQ10
Lipids
Adrenal function
Physicians surveyed
0 6.25 12.5 18.75 25
80%obtain screening every 1-2 years
100%
100%
84%
72%
68%
56%
52%
28%
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EKGEcho
OphthalmologyCardiology Consultaton
AudiogramsSleep studies, if fatigue
Immnologic testsRepeat MRIRepeat CSF
Stress testResting metabolic rate
Physicians surveyed
0 8 16 24 32
81%81%81%
69%63%
47%38%
22%13%
6%6%
Preventative Testing obtained routinely
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38%
38%
Educational talks to families
Advisory Board
Educational talks to physicians
Fundraising
Political Advocacy
Walkathon participation
Physicians surveyed
0 8 16 24 32
60%
69%
50%
28%
34%
47%
Clinician Participation Levels
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Similarities in practice but a general lack of consensus
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Agreement in care
Clinic structures and organization
Physician perceptions of various diagnostic laboratories
Care requires significantly more time
Shortage of adult trained experts
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Variability in care
Diagnostic approaches used
Extent of testing sent
Interpretation of test results How a diagnosis of mitochondrial disease is arrived upon
Treatment variability
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Officers of the MMS, 2012-2014
Sumit Parikh
Mary Kay Koenig
Greg Enns
Fernando Scaglia
Amy Goldstein
Russ Saneto
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Methods to develop consensus
✤ Evidence-based
✤ Eminence based (grey heads in the room)
✤ Committee based (may the strongest personality win)
✤ NIH style consensus (non-experts decide)
✤ Individual (I’ll decide)
borrowed from Georgianne Arnold
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Oxford Levels of Evidence
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Delphi Method
“Pooled intelligence enhances individual judgement and captures the collective opinion of a
group of experts”
Developing consensus in the absence of sufficient evidence utilizing a committee
of 15-25 content experts
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Delphi Method “Pooled intelligence enhances individual judgement and captures the collective
opinion of a group of experts”
Consensus?SurveyCommittee
forms subgroups
Literature review and
data summary
Items without
consensus
Survey with group’s
responses revealed
Consensus?Face-to-face discussion
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Delphi Method
✤ Quantifiable consensus
✤ Less personality based; results driven to the group mean
✤ Leaves room for dissent
✤ Panel size allows for functional and geographic diversity
borrowed from Georgianne ArnoldThe Good
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Delphi Method
✤ The “Mean” is not Scientific Truth
✤ Panel selection is a source of bias (having people who all agree)
✤ Consensus not always reached
✤ Managing groups of physicians is like “herding a group of cats”
borrowed from Georgianne ArnoldThe Bad
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Consensus Criteria Working Group
Kathie Simms
Andrea Gropman
Bruce Cohen
Mark Tarnopolsky
Irina Anselm Marni FalkSalvatore DiMauro
Michio HiranoRichard HaasCarol Greene
Johan Van HovePhil Morgan Lynne Wolfe
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5%5%
11%
16%32%
32%
Neurometabolism/Neurogenetics NeurologyBiochemical genetics Clinical GeneticsAnesthesia Nurse Practioner
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Consensus Criteria
✤ Biochemical Testing in Blood, Urine and Spinal fluid
✤ Genetic Testing
✤ Pathology and Biochemical Testing of Tissue
✤ Neuroimaging
✤ Treatment of Acute Stroke
✤ Exercise
✤ Anesthesia
✤ Treatment During Illness
✤ Treatment with vitamins and xenobiotics
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Next?
✤Preventative Care Guidelines?