ME/CFS Flashcards

1
Q

what is myalgic encephalomyelitis/chronic fatigue syndrome?

A

dysregulation of CNS, immune system, cellular energy metabolism, ion transport, CV abnormalities
hypometabolic state - measured with seahorse technology

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

presentation of ME/CFS needed for Dx

A

impairment of daily function
post exertion malaise
unrefreshing sleep

plus one of:
cognitive impairment
orthostatic intolerance

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Canadian consensus criteria for ME/CFS

A
pathological fatigue
post exertion malaise 
unrefreshing sleep 
chronic pain 
neurocognitive symptom 
autonomic symptom (difficulty standing) 
endocrine symtoms (temp control)
immune symptoms (flu, sensitivity)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

how to measure post-exertional malaise

A

unable to perform as well on dy 2 of a 2-day maximal cardiopulmonary test protocol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

goals of treatment for ME/CFS

A

increase QoL
treat orthostatic intolerance
add salt
help sleep

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

major differences between CFS and fibromyalgia

A

ME/CFS is more severe
people with FM benefit from moderate activity, in CFS it is not
FM is chronic widespread pain and fatigue

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

difference bw CFS and depression

A

immune, autonomic and endocrine symptoms are not seen in depression

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what is polymyalgia rheumatica?

A

inflammatory disease
proximal muscle pain and stiffness with rest
flu-like symptoms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

PE findings of polymyalgia rheumatica?

A

no loss of muscle bulk
unable to raise arms, standing up from seated/bed position
reduced shoulder ROM

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

lab findings of polymyalgia rheumatica?

A

elevated ESR (inflammation)
normal muscle enzymes
normal EMG

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

management of PE?

A

prednisone maintenance dose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

presentation of giant cell arteritis

A

fatigue, scalp tenderness, jaw claudication, fever

new onset severe headache

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

PE findings of giant cell arteritis

A

temporal artery is tender tot ouch or has decreased pulsation
occipital artery may be tender

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

lab findings of giant cell arteritis

A

ESR elevated
temporal artery biopsy is abnormal (skip lesions, mononuclear cells and granulomatous inflammation)
US: halo sign

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Tx for giant cell arteritis

A

prednisone
DMARDs
biologics

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

golfer’s elbow is pain over

A

medial epicondyle

wrist flexors

17
Q

tennis elbow is pain over

A

lateral epicondyle

18
Q

what is fibromyalgia

A

widespread pain on both sides of the body
pain in 11/18 tender points on digital palpation
not a muscle, immunologic, psychological or arthritic disease

19
Q

epi of fibromyalgia

A

F > M

40-50yr

20
Q

Tx for fibromyalgia

A

no specific drug therapy
medication for sleep can be beneficial
exercise could help symptoms

21
Q

fibromyalgia is a:

a. Muscle disease
b. Form of arthritis
c. Psychiatric disorder
d. Chronic pain disorder

A

Chronic pain disorder

22
Q

Fibromyalgia is caused by

a. A virus
b. Trauma or injury
c. Stress
d. Severe illness
e. None of the above

A

none of the above

23
Q

Fibromyalgia symptoms respond to:

a. Anti-inflammatory medications
b. Narcotic medications
c. Inactivity
d. None of the above

A

None of the above

24
Q

what is Marfan syndrome?

A

genetic disorder of connective tissue

single gene mutation (AD) of fibrillin gene

25
Q

pathophysiology of Marfan syndrome

A

abnormal TGF-beta signalling
breakdown of connective tissue
breakdown of vasculature

26
Q

clinical manifestation of Marfan syndrome

A
Arachnodactyly 
Steinberg/Thumb sign 
Walker-Murdoch sign 
Foot deformities 
Scoliosis 
Pectus carinatum/excavatum 
(Protruding/in-pouching of chest wall) 
High palate inside mouth 
Ectopia lentis (pathognomonic for this disease)
27
Q

investigations for Marfan syndrome

A

CBC, cre, lytes, LFT, autoimmune disease
annual optho exam
annual echo

28
Q

Tx for Marfan syndrome

A

low impact exercise
BP control
ortho surgery

29
Q

what is achondroplasia?

A

single gene mutation (AD)
physeal dysplasia (abnormal growth)
increased mortality

30
Q

clinical manifestations of achondroplasia

A
macrocephaly 
midface hypoplasia 
otitis media
short limbs 
flexion contractures 
lumbar lordosis, scoliosis 
spinal stenosis 
high BMI
31
Q

Tx for achondroplasia

A

no good drug therapies
research for inhibition of FGFR3
vosoritide (cartilage natriuretic peptide)
surgical: limb lengthening, spinal surgery

32
Q

what is Ehlers-Danlos syndrome?

A

structural abnormalities of skin, ligaments, blood vessels

presentation of hypermobility, dislocations, stretchy skin, bruising, mitral value prolapse