Myasthenia Gravis in Acute Care

Referral Criteria

Urgent

  • Contact on-call neurology registrar at Queen Elizabeth University Hospital (QEUH) via switchboard as soon as possible (including out of hours) for patients with a history of Myasthenia Gravis (MG) who are experiencing MG related issues.

Routine

  • Contact on-call neurology registrar via QEUH switchboard after admission for patients with a history of MG but are not experiencing active MG symptoms.
  • Before / on discharge please consider informing the MG specialist nurse (0141 232 4022) in case there has been a change in medications or patient warrants an earlier review at the MG clinic.

Symptoms of MG 

These include:

  • Difficulty swallowing, speaking or chewing
  • Double vision and ptosis
  • Neck and limb weakness
  • Type 2 respiratory failure.

Important points

  • It is crucial not to withhold MG medicines for any significant length of time, i.e. >2 hours, or to miss any doses of pyridostigmine or steroids as there is a risk of myasthenic crisis.
  • Before prescribing any new medicine, check if the medicine may affect patients with MG by referring to the NHSGGC guideline Myasthenia Gravis or Lambert-Eaton Myasthenia Syndrome, medicines that may affect patients.
  • High risk situations include: nil by mouth status, infection and surgical procedures.

Pyridostigmine

  • It is important for pyridostigmine to be administered at exact times. Ensure no missed doses. For further guidance see NHSGGC's guideline Pyridostigmine for Myasthenia Gravis Q&A.
  • Use free-format prescribing function on HEPMA if pre-fixed times are not suitable.
  • Where a patient does not have an individual supply of pyridostigmine, this must be obtained urgently via pharmacy during working hours or via the local emergency cupboard, hospital co-ordinator or the on-call pharmacist via switchboard if out of hours.
  • Overdose of pyridostigmine can lead to cholinergic crisis. For further guidance, refer to NHSGGC's guideline Pyridostigmine for Myasthenia Gravis Q&A.

Nil by mouth

  • Administration of medication via nasogastric (NG) feeding tube is the preferred option in patients who are unable to swallow. Pyridostigmine and prednisolone (not enteric coated, E/C) tablets can be crushed and mixed with water. See NHSGGC's guideline Pyridostigmine for Myasthenia Gravis Q&A.
  • Any delays in passing NG tube, or if NG insertion is not possible, seek senior medical and neurology advice as soon as possible.
  • If a chest X-ray is required to confirm NG position prior to use (i.e. no aspirate), then this will be reported out-of-hours when time critical medicines (i.e. pyridostigmine) are required.

Infection

Minor infection

  1. Continue regular immunosuppressant drugs.
  2. Stable MG patients may not require any change in steroid dose.

Severe infection or sepsis

  1. Withhold regular immunosuppressant drugs (and discuss with MG team).
  2. Consider increasing steroid dose after consulting with MG/neurology team.

Patients with stable MG can usually revert to baseline steroid dose once infection is treated (provided <3 weeks on higher dose). Patients with active MG may require slower reduction in steroid dose (consult MG team).

Patients undergoing surgical procedures

  • Patients should continue with regular medication for MG pre- and post-operatively.
  • Discuss on a case by case basis with an anaesthetist and MG team.

Note: If unable to access the guidelines linked above, then see alternative ways to access below:

  • Myasthenia Gravis or Lambert-Eaton Myasthenia Syndrome, medicines that may affect patients guideline - NHSGGC's Clinical Guidelines Platform on Right Decisions Service / Central Nervous System / Myasthenia or using the search function.
  •  Pyridostigmine for Myasthenia Gravis Q&A - NHSGGC's Clinical Guidelines Platform on Right Decisions Service / Central Nervous System / Myasthenia or using the search function.

 

Guideline reviewed May 2026
Page updated July 2026



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