Post-infection syndrome Flashcards

1
Q

Post-infection syndrome also known as chronic fatigue syndrome/ myalgic encephalomyelitis

What is definition?

A

It is a complex, chronic medical condition affecting multiple body systems.

Pathophysiology is unclear

Extreme fatigue that is worsened by physical or mental exertion. Also included myalgia, impaired memory, insomnia, impaired concentration

Experienced in aftermath of infection

can have significant impact on quality of life

symptoms can fluctuate

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2
Q

How do CFS/ME NICE 2020 guidelines relate to post-viral fatigue in COVID19?

A

Guidelines drafted in 2020 based on evidence reviewed before COVID19. So recommendations do not apply to those who have fatigue due to COVID19

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3
Q

What is general approach to delivering care when speaking to patient with CFS?

A

ackowledge their symptoms

take time to build a supportive, trusting, empathetic relationship

person-centred approach

involve family members/ carers

early diagnose can help patients get appropriate help for their symptoms

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4
Q

When to suspect CFS/ME?

How long should patient have had symptoms before diagnosis can be made?

A

Must have had symptoms for 3 months to diagnose.
If had symptoms for 6 weeks, we can suspect it.

debilitating fatigability that is not caused by excessive cognitive, physical, emotional or social exertion, and is not relieved by rest

post-exertional symptom exacerbation after activity, that is disproportionate to the activity, and has prolonged recovery time

unrefreshed sleep

constant flu-like symptoms

cognitive difficulties

as soon as provisional diagnosis is made, do not delay. Refer patient for symptom management

Need 3x clinic appointments before can confirm diagnosis

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5
Q

What are other rarer symptoms of CFS/ME?

A

severe constant pain

GI upset - nausea, constipation, bloating

double vision/ dizziness

postural orthostatic tachycardia syndrome POTS

sensitive to stimulus - light/ noise

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6
Q

What is involved in initial CFS/ ME assessment?

A

comprehensive clinical history

physical examination

psychological wellbeing - impact on daily life

investigations to exclude other diagnoses

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7
Q

You diagnose patient with CFS/ME.

They ask what the condition is, and how it may change over time.

How do you explain this?

A

Fluctuating medical condition which affects everyone differently

symptoms can change, and severity can change over days or weeks

often involves remission/ relapse

small proportion never fully recover

can have triggers e.g physical injury, stress

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8
Q

CFS/ME treatment is about supporting the patient.

How can this be achieved?

A

Reduce stress/ stimuli - e.g light/ noise/ pain

refer to social care

mobility aids

home adaptations

work adjustments under Equality Act 2010 - offer to liaise with employer

energy management - flexible tailored approach to activities - could include physiotherapy. Graduated exercise therapy is not a treatment

symptom management - e.g analgesia for headaches/ neuropathic pain

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9
Q

CFS/ME patients with severely reduced mobility are at risk of certain diseases. What are examples?

A

DVT

pressure ulcer

contractures

cardiovascular disease

osteoporosis

vitamin deficiencies - no evidence to support routine vitamin supplementation as does not help with symptoms

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10
Q

CBT is not a treatment for CFS/ME, but can help with symptoms.

How do you explain what CBT is to patient?

A

involves collaborating with a therapist, to understand the main difficulties a person faces

exploring their personal meaning of symptoms and illness, and how this might relate to how the manage their symptoms

developing a self management plan

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11
Q

What is a CFS/MS flare?

A

Sustained exacerbation of symptoms to a greater level than person’s normal symptoms

patient should reduce their activity levels, and identify possible triggers e.g acute illness

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12
Q

What is a CFS/MS relapse?

A

Sustained period of exacerbation, lasting longer than a flare.

patient should reduce their activity levels, and identify possible triggers e.g acute illness

re-assess patient holistically, and agree plan of management

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13
Q

What is difference between mild/ moderate/ severe CFS/ ME?

A

Mild - mobile, can perform light activities, usually still in work/ school. But limited in activity

Moderate - reduced mobility, restricted in all activities of daily living. Usually stopped school/ work. Need rest periods.

Severe - severely affected ADLs, need wheelchair, spend most time in bed, sensitive to light/ noise

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