Referral

ME/Chronic Fatigue Service - Plymouth

Scope

NICE GUIDELINES:

The NICE guidelines for ME/CFS recommend referral to specialist ME/CFS when patients are experiencing all 4 key ME/CFS symptoms, for a minimum of 3 months. The appropriate investigations must show that these symptoms cannot be explained by another condition, excessive working hours or ongoing exertion.

  • This guidance covers the referral criteria (please see below) to the Plymouth Chronic Fatigue Service. Referrals submitted without this information may be returned.
  • This service covers West Devon including; Plymouth, Ivybridge, Kingsbridge
  • Specialist ME/CFS services are designed to provide an individualised, person-centred programme that aims to offer guidance on fatigue management strategies that support patient goals, depending on the patient’s preferences and priorities. Our service is commissioned to provide the treatment strategies outlined in the NICE guideline for this condition.

The treatment pathway is delivered as follows:

    • A holistic assessment will be carried out following referral from a GP to ascertain the suitability of the service.
    • Following assessment, patients can engage in a set number of telephone consultation sessions, providing self-management strategies on an individual basis.
    • Due to limited resources, we are unable to offer long-term contact with patients, or to conduct home assessments. If patients have severe ME/CFS and are bedbound or housebound, it is appropriate for their GP to refer them to Adult Social Care/Intermediate Care Teams, with their agreement, as a care package and equipment may be required. We would then liaise with these services to offer a combined treatment approach.

Out of scope

  • Patients under 18 years of age
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Signs and Symptoms

Following the release of the updated NICE guidelines NG206, the criteria for diagnosis and considering a referral to a specialist ME/CFS service is now more stringent. Patients should only be referred if they are experiencing all 4 symptoms outlined below, for 3 months or more.
The symptoms are as follows:

  1. Debilitating fatigue that is worsened by activity, is not caused by excessive cognitive, physical, emotional or social exertion, and is not significantly relieved by rest.
  2. Post-exertional malaise after activity in which the worsening of symptoms:
    • Is often delayed in onset by hours or days
    • Is disproportionate to the activity
    • Has a prolonged recovery time that may last hours, days, weeks or longer.
  3. Unrefreshing sleep or sleep disturbance (or both), which may include:
    • Feeling exhausted
    • Feeling flu-like and stiff on waking
    • Broken or shallow sleep
    • Altered sleep pattern or hypersomnia.
  4. Cognitive difficulties (sometimes described as ‘brain fog’), which may include:
    • Problems finding words or numbers
    • Difficulty in speaking
    • Slowed responsiveness
    • Short-term memory problems, and difficulty concentrating or multitasking.

ME/CFS should be suspected, if a patient has had all of the 4 key symptoms persisting for a minimum of 6 weeks (4 weeks in children). However, a diagnosis of ME/CFS can only be made when a patient has had all 4 key symptoms, persisting for a minimum of 3 months or more, and the symptoms should be:

  • Of definite onset (i.e. not lifelong) but chronic.
  • Not the result of ongoing exertion (or over-activity)
  • Not the result of excessive working hours
  • Not substantially relieved by rest
  • Causing a substantial reduction in effectiveness of occupational, educational, social or personal activities.
  • Not explained by another condition

Diagnosis

In many cases, a diagnosis of ME/CFS can be made confidently in primary care. However, it is important to know that there is currently no diagnostic test for ME/CFS and it is recognised on clinical grounds alone, when all other causes for the debilitating fatigue and other symptoms have been excluded. In order to do this it is recommended that people undergo thorough medical assessment by their GP first, including blood tests, prior to being assessed for ME/CFS. Please see the updated NICE guidelines (NG206) for a full list of suggested tests to be carried out, prior to referral.

Be aware that the following symptoms may also be associated with, but are not exclusive to, ME/CFS:

  • Orthostatic intolerance and autonomic dysfunction, including dizziness, palpitations, fainting, nausea on standing or sitting upright from a reclining position
  • Temperature hypersensitivity resulting in profuse sweating, chills, hot flushes, or feeling very cold
  • Neuromuscular symptoms, including twitching and myoclonic jerks
  • Flu-like symptoms, including sore throat, tender glands, nausea, chills or muscle aches
  • Intolerance to alcohol, or to certain foods and chemicals
  • Heightened sensory sensitivities, including to light, sound, touch, taste and smell
  • Pain, including pain on touch, myalgia, headaches, eye pain, abdominal pain or joint pain without acute redness, swelling or effusion.

Differential Diagnoses

The following conditions would EXCLUDE a diagnosis of ME/CFS and should be screened prior to referral:

  • Established medical disorders known to cause chronic fatigue. This is especially important in the elderly in whom cardiac, respiratory and neurological causes of fatigue can be frequently missed
  • Psychosis e.g. schizophrenia, bipolar disorder
  • Alcohol or substance abuse
  • Eating disorders, anorexia, bulimia or severe obesity with a BMI greater than 40 or less than 18
  • Adults with behaviour or conditions which prevent engagement with the service
  • Exclude FIBROMYALGIA where Fibromyalgia is the primary diagnosis, or where pain dominates fatigue.
  • Severe depressive illness with psychotic or melancholic features (but not anxiety states or mild to moderate depression)
  • Somatisation disorder
  • Possible dementia

  • a medical assessment (including symptoms and history, comorbidities, overall physical and mental health)
  • a physical examination
  • an assessment of the impact of symptoms on psychological and social wellbeing
  • investigations to exclude other diagnoses, for example (but not limited to):
    • urinalysis for protein, blood and glucose
    • full blood count
    • urea and electrolytes
    • liver function
    • thyroid function
    • erythrocyte sedimentation rate or plasma viscosity
    • C-reactive protein
    • calcium and phosphate
    • HbA1c
    • serum ferritin
    • coeliac screening
    • creatine kinase.
  • Use clinical judgement to decide on additional investigations to exclude other diagnoses (for example, vitamin D, vitamin B12 and folate levels; serological tests if there is a history of infection; and 9am cortisol for adrenal insufficiency).

“In many cases, a diagnosis of ME/CFS can be made confidently in primary care.” I think we need to add some management advice.

Advice for people with suspected ME/CFS

When ME/CFS is suspected, give people personalised advice about managing their symptoms. Also advise them:

  • not to use more energy than they perceive they have − they should manage their daily activity and not 'push through' their symptoms
  • to rest and convalesce as needed (this might mean making changes to their daily routine, including work, school and other activities)
  • to maintain a healthy balanced diet, with adequate fluid intake.

Explain to people with suspected ME/CFS that their diagnosis can only be confirmed after 3 months of persistent symptoms. Reassure them that they can return for a review before that if they develop new or worsened symptoms and ensure that they know who to contact for advice.

Referral Criteria

Referrals may be returned to the referrer if not on the correct Referral form

Referrals are accepted from GP's or Consultants only, following investigations outlined in the NICE guidelines.

It is essential that referrals include information on the duration of fatigue, any precipitating factors and impact on functional ability. It is not possible to triage referrals effectively when this information is not provided. Therefore, it will be requested prior to accepting the referral.

  • Symptoms have persisted for:
    • At least 3 months but not lifelong
    • Patients should be 18 or over to access the service
    • Debilitating, persistent or relapsing fatigue for at least 3 months but not lifelong, that is new or of definite onset. It is not the result of ongoing exertion and is not substantially alleviated by rest. Severe enough to cause a substantial reduction of previous levels of social, occupational, educational or personal activities.

The NICE guidelines state that it is essential that the 4 key symptoms are all present as stated in the Assessment section above.

Referrals submitted without this information may be returned.

Service Outline
  • To provide a specialist service for patients with Myalgic Encephalomyelitis (ME) / Chronic Fatigue Syndrome (CFS) who are 18 and over, based on the NICE guidelines 2021
  • To Support local clinicians in the continued management of the condition, where this proves appropriate.
  • This service is based at Plymouth Science Park, Unit 1 delivering assessment. This is followed by a set number of hourly telephone consultations, providing energy management advice, with the provision of written resources for future guidance following discharge. These sessions are designed to provide an individualised, person-centred programme that aims to support personal goals based on the patient’s preferences and priorities.
  • Due to limited resources we are unable to offer long-term contact with patients, or to conduct home assessments or visits. The team consists of 6 hours of medical input and 2 part-time therapists, covering West Devon.
  • Primary care, social care/ employment/ housing or benefits services should continue to be involved whilst the patient is seen within the specialist service to ensure continuity of care and a seamless service upon discharge
  • If patients have severe ME/CFS and are bedbound or housebound, it is appropriate for their GP to refer them to Adult Social Care/Intermediate Care Teams with their agreement, as a care package and equipment may be required. We would then liaise with these services to offer a combined treatment approach.

Contact Details for the service

  • Telephone Number: 01752 435205
  • Email: SHS.SentinelCFS@nhs.net
  • ME/CFS service, Sentinel Healthcare Southwest CIC, Plymouth Science Park, Derriford, Plymouth PL6 8BU
  • This is a part-time service operating from: 09:00 am - 4:30 pm on Monday, Tuesday and Wednesday
  • This service is commissioned by the Healthcare Commissioning organisations covering Plymouth and provided by Sentinel.


Referral Instructions

  • Refer using the e-Referral Service
    • Specialty: General Medicine
    • Clinic Type: General Medicine
    • Service: D DRSS-Western-General Med-Devon ICB-15N

Referral Form

ME/Chronic Fatigue referral form - No merge fields

ME/Chronic Fatigue referral form - EMIS WEB

ME/Chronic Fatigue referral form – SystmOne

Patient Information

Action for ME

ME Association

Improving Lives Plymouth - Long Term Conditions Self-Management Programme

  • for patient support with any long-term physical or low level mental health condition.

GP Information

NICE guideline (NG206)

Evidence

Myalgic encephalomyelitis (or encephalopathy)/chronic fatigue syndrome: diagnosis and management. NICE clinical guidelines (NG206). October 2021.

Pathway Group

This guideline has been signed off on behalf of NHS Devon

Publication date: January 2018
Updated: August 2023