prophylactic (preventative) measures against development of mountain sickness

Last edited 04/2022 and last reviewed 07/2022

It is advised that climbers should acclimatise if climbing to high altitude.

  • if above 3000m (10,000 feet), no more than 300m (1000 feet) should be climbed per 24 hour period (1)
    • if a climber develops symptoms of mild altitude sickness then he/she should rest for 24 hours at that altitude
    • if a climber has more severe symptoms then he/she must descend to the last altitude at which they felt well. This should occur whether or not they use drugs
    • if rapid ascent is unavoidable then acetozolamide is beneficial
    • a rest day every 3 days or 1000 m

Prevention of acute mountain sickness (AMS) (2)

  • acetazolamide can be used for preventing AMS according to the National Travel and Health Network Centre and Fit For Travel recommendations (not licensed for this this indication)
  • acetazolamide prevents AMS by mimicking the body naturally adjusting to a change in environment
  • a Cochrane review demonstrated acetazolamide reduced the risk of AMS vs placebo by a factor of 0.47 (n=2,301, 16 studies). Acetazolamide was administered one to five days prior to ascent with doses of up to 500mg/day to adults at risk of AMS

    • prescribing and dosing
      • use acetazolamide 125mg twice daily (off-label).
      • smaller doses of acetazolamide can be given by halving 250mg tablets which are scored.
      • prescribe acetazolamide one to two days before gradual ascent to high altitude and continue acetazolamide for at least two days after reaching the highest point.
      • advise people to take the second dose of acetazolamide at dinnertime rather than at bedtime as it is a diuretic.
      • trial acetazolamide for two days before ascent to high altitude because side effects can resemble the symptoms of AMS
      • check local guidelines for processes on prescribing acetazolamide for travel
    • cautions
      • take into account the contraindications and cautions of acetazolamide and check if it is appropriate for the person
      • avoid acetazolamide in people with a history of anaphylaxis or severe allergy to suphonamide as it is a sulphonamide derivative

  • the NHS review did not recommend any other medications for use in AMS prophylaxis
    • overall, evidence for the use of the medicines listed below to prevent AMS is inconclusive and for some, side effects are a concern:
      • aspirin
      • dexamethasone
        • Using dexamethasone has been suggested by some organisations to help prevent AMS. However, the Cochrane review (n=176) assessing four parallel studies comparing dexamethasone with placebo found dexamethasone does not prevent AMS at any dose and does not aid acclimatisation.
      • ibuprofen
      • iron supplements
      • magnesium citrate
      • spironolactone
      • sumatriptan

Notes:

  • if acetazolamide is used, treatment should be started at least one day before ascent and continued until adequate acclimatisation is judged to have occurred
    • side effects, which include paraesthesia and mild diuresis, are common but usually well tolerated
    • acetazolamide is a sulphonamide, and allergic reactions can occur
    • acetazolamide is not a substitute for acclimatisation

  • phosphodiesterase Inhibitors as prophylaxis for altitude sicknes: tadalafil and sildenafil (3)
    • because of its pulmonary vasodilatory effects, the phosphodiesterase inhibitor tadalafil can be used for prevention of high altitude pulmonary edema (HAPE)
      • it has been demonstrated that tadalafil prevents the disease in known HAPE-susceptible individuals. No studies have examined whether the drug can also be used to treat HAPE
      • although no systematic studies have examined whether sildenafil is effective in the prevention and treatment of HAPE, it is worth considering this medication as well because it has a similar mechanism of action and should exert a similar benefit as tadalafil and because there are reports of its use in clinical practice as treatment for HAPE or prevention in children with underlying cardiopulmonary disease and HAPE

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