diagnosing & treating chronic msk pain in working-aged adults

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1 agnosing & Treating Musculoskeleta Pain In Working-Aged Adults The Importance of Identifying The Central Pain Phenotype 2/5/17 Presented By: Paul C. Coelho, MD

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Page 1: Diagnosing & Treating Chronic MSK Pain in Working-Aged Adults

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Diagnosing & Treating Musculoskeletal Pain In Working-Aged Adults

The Importance of Identifying The Central Pain Phenotype

2/5/17

Presented By:Paul C. Coelho, MD

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Disclosures:Dr. Coelho has no disclosures. He will not be discussing any off-label uses of medications or devices.

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Table of Contents

Early Pain Models

Modern Pain Models

FMS, HA, and LBP

The Central Pain Phenotype

Evidence-Based Treatments

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1980 Model of MSK PainNociceptive Neuropathic

Primarily due to inflammation or tissue damage in the periphery

Damage or entrapment of peripheral nerves.

NSAID/Opioid Responsive Responds to both peripheral and central pharmacotherapy.

Responds to procedures. Does not respond to procedures.

Behavioral factors minor. Behavioral factors minor.Examples: Osteoarthritis, Rheumatoid arthritis, cancer pain.

Examples: Diabetic peripheral neuropathy, post-herpetic neuralgia.

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1829161/

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1990 FMS

https://www.rheumatology.org/Portals/0/Files/1990_Criteria_for_Classification_Fibro.pdf

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US Overdose Deaths1980-2014

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1829161/

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2014

012500250003750050000

Wolfe ACR FMS1990

FDA Approves OxyContin1995

APS Pain as a 5th Vital Sign1996

Wolfe Recants FMS2008

IOM 100M In Pain2011

Peak Incidence of Prescription OD 45-54

Portenoy Portenoy/Foley1986

Portenoy Recants2012

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Variation in Opioid Rx’ing forFMS 2007-2009

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4346177/

Peak Incidence of Prescription OD 45-54

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35% of FMS Pt’s Receive SSDI

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4151179/

Disabled Medicare Beneficiaries Rx’d Opioids

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FMS Patients Report High PainLevels In Spite of High Dosages

https://www.ncbi.nlm.nih.gov/pubmed/24310048

N = 582

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Opioids In FMS: Once StartedSeldom Stopped

https://www.ncbi.nlm.nih.gov/pubmed/26443495

N = 100K, 60% Received Opioids.

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Opioids In FMS: Once StartedSeldom Stopped

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117947/

N = 64K, 44% Received Opioids.

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FMS Is Not Opioid Responsive

https://www.ncbi.nlm.nih.gov/pubmed/26975749

OrganizationAmerican Pain SocietyAmerican Academy of Pain MedicineAmerican Academy of NeurologyEuropean League Against RheumatismCanadian Pain SocietyCanadian Rheumatology AssociationBritish Pain Society

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2017 Model of MSK PainNociceptive Neuropathic Central

Primarily due to inflammation or tissue damage in the periphery

Damage or entrapment of peripheral nerves.

Primarily due to a central disturbance in pain processing.

NSAID/Opioid Responsive

Responds to both peripheral and central pharmacotherapy.

Tricyclic neuro-active compounds. Opioid unresponsive.

Responds to procedures.

Does not respond to procedures.

Does not respond to procedures.

Behavioral factors minor.

Behavioral factors minor.

Behavioral Factors Prominent.

Examples: Osteoarthritis, Rheumatoid arthritis, cancer pain.

Examples: Diabetic peripheral neuropathy, post-herpetic neuralgia.

Examples: FMS, cLBP, cHA, IBS.

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1829161/

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Prevalence of LBP & HA in FMS

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1829161/

2007 Internet Survey of 2596 FMS Pts

Ave Age = 47If due to chance aloneLBP .3 x .05 =1.5% HA: .2 x .05 =1%

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Prevalence of FMS in cLBP 42%

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1829161/

Chance Alone: .3 x .05 = 1.5%

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Prevalence of FMS in Migraineurs 56%

Chance Alone:.2 x .05 += 1%

https://www.ncbi.nlm.nih.gov/pubmed/25994041

N = 1,730

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Comorbid Pain in FMS is the Norm

https://www.ncbi.nlm.nih.gov/pubmed/22364327

Fibromyalgia

Head AcheLow Back Pain

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Comorbid Pain in FMS is the Norm

https://www.ncbi.nlm.nih.gov/pubmed/22364327

Low Back Pain

“Overwhelming evidence reveals that what isoften labeled as a single chronic regional painsyndrome is, upon closer evaluation, a chronicillness beginning much earlier in life, where thepain merely occurs at different points of the bodyat different points in time and is given different labels by subspecialists focusing on “their region” of the body.”

Daniel Clauw, MD

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Central Sensitivity Spectrum Disorders

https://www.ncbi.nlm.nih.gov/pubmed/17350675

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Overlapping Chronic Pain Conditions

https://www.ncbi.nlm.nih.gov/pubmed/27586833

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Prescribers are Poor at DiagnosingCentral Pain Syndromes

https://www.ncbi.nlm.nih.gov/pubmed/23071343

23% Sensitivity

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Prescribers are Poor at DiagnosingCentral Pain Syndromes

https://www.ncbi.nlm.nih.gov/pubmed/23071343

27% Specificity

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Prescribers are Poor at DiagnosingCentral Pain Syndromes

https://www.ncbi.nlm.nih.gov/pubmed/20461781

“You cannot guess at the extent of fatigue, unrefreshed sleep, cognitive problems, multiplicity of symptoms, and extent of pain without a detailed interview. The new criteria obligate you to pay careful attention to the patient if you want to diagnose fibromyalgia.”

Fredrick Wolfe

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Diagnosing Central Sensitivity Spectrum Disorders

https://www.ncbi.nlm.nih.gov/pubmed/26266995

1. Pain in many body regions. 2. Higher current and lifetime history of chronic pain in several body regions.3. Multiple somatic symptoms (e.g., fatigue, memory difficulties, sleep problems, mood disturbance)4. More sensitive to other sensory stimuli (e.g., bright light, loud noises, odors, other sensations in internal organs)5. 1.5 to 2x more common in women.6. Strong family history of chronic pain.7. High self-reported pain & distress (VAS/NPS/PSD/PCS)8. Pain triggered or exacerbated by stressors.9. Peak prevalence of FMS age 50-59 (working-age).*10. Essentially normal physical examination +/- diffuse tenderness.

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2016 Fibromyalgia Screening Questionnaire (FSQ)

https://www.ncbi.nlm.nih.gov/pubmed/26266995

96% Sensitivity, 92% Specificity

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Why Is Dx’ing FMS/CSS Important?

https://www.ncbi.nlm.nih.gov/pubmed/26266995

1. It is opioid unresponsive.2. Prognosis: It does not improve with time.3. When present, it is the primary source of morbidityIn chronic non-cancer pain.

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FMS Is Opioid Unresponsive

https://www.ncbi.nlm.nih.gov/pubmed/26975749

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Natural Hx of FMS

https://www.ncbi.nlm.nih.gov/pubmed/21765102

N = 1,555 11yr f/u

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Natural Hx of FMS

https://www.ncbi.nlm.nih.gov/pubmed/28077978

N = 762yr f/u

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FMS is the Primary Source of Morbidity in CNP

https://www.ncbi.nlm.nih.gov/pubmed/27049402

N = 383, 76 FMS+

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Evidence-Based Treatments of FMS

https://www.ncbi.nlm.nih.gov/pubmed/28077978

Treatment Evidence Level

Patient Education 1AGraded Exercise 1ACBT 1ATricyclics 1ASNRI’s 1AGabapentenoids 1ANSAIDS 5DOpioids 5D

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Evidence-Based Treatments for FMS

https://www.youtube.com/watch?v=pgCfkA9RLrM

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Evidence-Based Treatments for FMS

https://fibroguide.med.umich.edu/

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Centralized Pain Pt Handout

https://www.painscience.com/articles/central-sensitization.php

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ResourcesFibromyalgia Screening Questionnairehttp://www.slideshare.net/101N/pcp-pain-screening-tool

Evidence-Based Treatments for FMS, Dr. Clauw JAMAhttp://www.slideshare.net/101N/fibromyalgia-clinical-review

Daniel Clauw, MD Youtube Video for patientshttps://www.youtube.com/watch?v=pgCfkA9RLrM&t=6s

Salmple Centralized Pain Patient Handouthttp://www.slideshare.net/101N/central-sensitization-70569194