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Acute high-altitude illness.


Mr X--a fit and healthy 30-year-old man--joins a group climbing Mount Kilimanjaro, hoping to reach Uhuru Peak (5 895 m above mean sea level). His 6-day, 5-night expedition is following the Rongai route, approaching from the northern side of Kilimanjaro. After flying in from his home at sea level in South Africa (SA), they begin their trek near the Kenyan border at 1 900 m. Despite no previous experience at altitude, he shows no signs of struggling with the ascent, and easily copes during the deliberately slow hikes of the first 3 days to reach Kikelewa Caves (3 675 m). However, on arrival at Mawenzi Tarn camp (4 300 m) at the end of the hot 4th day, Mr X complains of a headache, dizziness and nausea.

The local lead guide offers Mr X 800 mg oral ibuprofen to ease the headache and encourages him to rest. Having no appetite, Mr X skips dinner that night, but does take care to remain well hydrated. In the morning his headache has resolved, but he complains of having had fitful sleep. Routine screening by the guides shows elevated resting breathing and heart rates (respiratory rate 28/min.; heart rate 120/ min.). A portable fingertip pulse oximeter shows that his peripheral arterial oxygen saturation (Sp[O.sub.2]) has dropped to 64%. The guides are nevertheless anxious to push on, and Mr X continues with the group to Kibo Huts (4 714 m).

During the day, his headache returns, and he feels lethargic and breathless. Nonetheless, with his bucket-list goal in sight, he participates in the final summit preparations. The group leaves camp for the summit at midnight. During the relentless climb to the crater rim (5 680 m), Mr X feels increasingly cold, and develops ataxia and tunnel vision. Amid the tired party in the predawn light, his deterioration remains unnoticed. At Gilman's Point on the summit ridge, the group stops for a brief rest. Mr X is disorientated, has lost fine motor control, and speaks incoherently before he collapses.

By this point, the guides have discovered that you are a doctor, and turn to you for help. What is your assessment and action plan? Thinking back, if you were the expedition's doctor, would you have intervened earlier?


Although SA is not traditionally associated with high-altitude climbing, the country is blessed with many beautiful mountain ranges. An increasingly substantial proportion of the population takes part in recreational climbing and mountaineering, both locally and abroad. Many also travel to high-altitude regions worldwide for simple tourism, business or religious pilgrimages. [1] Globally, it has been estimated that >35 million people travel to altitudes of greater than 3 000 m per annum. [2] In southern Africa, several large metropolitan areas are above 1 500 m, and peaks of up to 3 482 m are regularly ascended. Despite this, there is generally a poor level of recognition of the implications and risks of high altitude for healthy travel and recreation among SA doctors. [3]

High altitude is defined as greater than 1 500 m above sea level. At this level, the physiological implications of decreasing ambient pressure (hypobaria) and corresponding decrease in the partial pressure of oxygen (hypoxia) are regularly apparent, although they do not have pathological consequences in healthy individuals. Altitude between 1 500 m and 3 500 m is referred to by some authors as intermediate, and it is within this range that altitude-related illnesses begin to manifest. Very high altitude is defined as being above 3 500 m, where simple physiological compensation is no longer sufficient to maintain oxygenation, and gradual acclimatisation is required. Exposure to extreme altitudes (above 5 500 m) without acclimatisation is highly likely to cause severe illness. The summit of Kilimanjaro (5 895 m) has an ambient pressure of approximately 47 kPa (less than half of sea-level pressure), resulting in arterial oxygen tension (Pa[O.sub.2]) of only 6 kPa, even with ideal acclimatisation (Fig. 1). Blood gases drawn near the summit of Mount Everest have demonstrated the lowest recorded oxygen partial pressures in healthy subjects, with a Pa[O.sub.2] range of 2.55-3.93 kPa. [4]

Acute high-altitude illnesses

Physiology of altitude, acclimatisation and aetiology of high-altitude illnesses

The complex physiological response to altitude is not yet fully understood and beyond the scope of this article. While the concentration (proportion) of oxygen in the atmosphere remains remarkably consistent at 20.9%, the drop in ambient pressure with increasing altitude results in a directly corresponding decline in the partial pressure (P[O.sub.2]). The reduction in inspired P[O.sub.2] is compounded by the unaltered saturated vapour pressure of water in the alveoli, and the unaltered (or increased) metabolic production of carbon dioxide. Although rapid and profound compensation through increased minute ventilation is possible, the inevitable physiological consequence of ascent to high altitude is hypobaric hypoxia. [5] Over time, the combination of hypoxia and hyperventilation-induced respiratory alkalosis triggers a cascade of physiological effects, leading to acclimatisation. These include increased renal excretion of bicarbonate, a 2-3-DPG-mediated shift in the oxygen-haemoglobin dissociation curve, erythropoiesis, and angioneogenesis at the capillary level.

Over a period of days to weeks, the body gradually adjusts to optimise oxygen delivery to the tissues, maintaining the oxygen cascade from atmosphere to mitochondrion. Indeed, given sufficient time to acclimatise, the human organism is remarkably capable of function despite low Pa[O.sub.2], as is eloquently demonstrated by a visit to any paediatric cardiology ward, where children with cyanotic congenital heart disease play alongside their well-oxygenated counterparts. However, a sudden decrease in Pa[O.sub.2] without adequate time for acclimatisation is highly likely to manifest as acute illness. In the context of ascent to altitude, simple respiratory compensation is no longer sufficient from ~3 500 m. This explains the sudden increase in high-altitude illnesses (HAIs) and particularly acute mountain sickness (AMS) seen above this point (Table 1). The exact aetiology of AMS, widely considered a precursor to more severe altitude illnesses, is also poorly understood. [6-9]

Acute mountain sickness, high-altitude cerebral oedema and high-altitude pulmonary oedema

Altitude illness is characterised by tissue hypoxia and oedema, particularly in the brain and lungs. This is the result of a complex interplay of hydrostatic pressure differences due to hypoxic vasomotor changes, and increased capillary permeability through release of agents such as vascular endothelial growth factor and hypoxia-inducible factor 1-alpha (HIF-1-[alpha]). The predominant symptom complex includes headaches, nausea and loss of appetite, dizziness or lightheadedness, fatigue or weakness, and sleep disturbance. It is diagnosed clinically, because of the typical lack of advanced investigations in the context of high-altitude expeditions and the multifactorial nature of the disease (see 'Clinical diagnosis' below). Similarly, high-altitude pulmonary oedema (HAPE) and high-altitude cerebral oedema (HACE) are commonly considered advanced forms of AMS and diagnosed on clinical signs, but can and do occur independently.

Onset of altitude-related illness is indiscriminate, and can occur at relatively low altitudes (instances of AMS have been reported at as low as 2 000-2 500 m), but is most common after rapid ascent to above 3 500 m. Prior safe ascent to altitude is no guarantee of avoiding AMS on subsequent exposure. [8] Physical fitness, gender and youth are not reliably predictive, although there is a protective association with increased age. A genetic predisposition is being researched. [10-12]

Typical altitudes for onset of development of HAPE and HACE are 3 000 m and 4 500 m, respectively. While AMS is usually diagnosed within a day of reaching a new elevation, HAPE and HACE (considered to be advanced manifestations or complications of AMS) commonly present after more than 24 hours at altitude. [6,13,14]

Prevention of high-altitude illness

AMS, HACE and HAPE are the most commonly encountered altitude-induced illnesses during ascent above 2 500 m, but are also nearly entirely preventable. [6,7] Up to altitudes of 6 000 m, the occurrence of HAI is the direct result of inadequate acclimatisation. Depending on individual physiology and ascent profile, up to 70% of mountaineers develop symptoms of AMS. [14] The foremost approach to AMS, HAPE and HACE is prevention through education, supporting conservative ascent profiles to allow sufficient acclimatisation, and promoting adequate hydration, caloric intake and exposure protection. [3,14] Within the African context, AMS is very prevalent on Kilimanjaro owing to the lack of a sufficiently long approach trek and rapid ascent profiles followed by local tour operators. [15] Kilimanjaro climbs of <7 days' duration are therefore considered 'high risk' profiles (Table 2), which contribute to the 3-8 reported but avoidable deaths out of about 30 000 trekkers on the mountain each year. [3,13,15-19]

The single most effective method of prevention is gradual acclimatisation, paired with adequate hydration and caloric intake. After reaching an elevation of 2 500-3 000 m, sleeping altitudes should not increase by more than 300-500 m each day, with a rest day at the same altitude for each 1 000 m ascent. [3,13,14] Sleeping elevation contributes more significantly to adequate acclimatisation than physical exercise and altitude gain during the day. [13] Where terrain necessitates occasional elevation gains in excess of suggested safe ascent profiles, additional rest days must be incorporated into the itinerary to keep the average rate of ascent within safe parameters. [13] Adequate hydration (estimated in the field by maintaining frequent micturition and keeping urine colourless) is imperative to allow the elimination of bicarbonate necessary for physiological acclimatisation. Although loss of appetite is a common feature, care should be taken to consume sufficient carbohydrate-rich meals to compensate for increased metabolic loads and improve the respiratory exchange ratio. [5] Minimising loss of body fat has the benefit of helping cope with low temperatures at high altitude; a more significant risk of poor nutrition is subsequent loss of muscle mass.

Clinical diagnosis: Symptoms and the Lake Louise symptom score

Secondary only to proper acclimatisation, early recognition of AMS is key to allowing individuals to take simple corrective measures before the risks of complications increase.

AMS is defined by the presence of a high-altitude headache (onset of headache within 24 hours of ascent to above 2 500 m) and at least one other symptom of sleep disorder, gastrointestinal upset (nausea, vomiting or loss of appetite), dizziness or lightheadedness, and lethargy, fatigue or weakness. Frequently, this is accompanied by peripheral oedema, shortness of breath and tachycardia, which often worsen at night. [8-14-0] Being nonspecific, these symptoms are often mistaken for non-consequential ailments such as flu, a cold or dehydration--all common travel complaints. [6] However, AMS should always be assumed until proven otherwise. [3] Although the diagnosis of AMS is symptomatic and clinical, determining its severity is largely subjective. As participants focus on expedition goals, symptoms are often under-reported, which leads to an underestimation of severity. This can result in a lack of appropriate medical intervention, such as the climber being advised to discontinue an ascent. Furthermore, under-reporting of AMS symptoms such as severe headaches and drowsiness may lead to the early warning signs of HACE being missed.

To objectively standardise diagnosis and quantify the severity of AMS, the Lake Louise Symptom Questionnaire and Clinical Scores were established (LLSQ and LLS-C, respectively). This allows for both monitoring of symptoms by lay mountaineers, and field research of AMS by expedition doctors (Fig. 2). [13,20,21] Each of the five symptoms and three clinical signs are assigned a severity-related score from 0 (absent) to 3 (severe or incapacitating). Inability to stand for an ataxia test carries a score of 4. AMS is considered present with a score of [greater than or equal to] 3 for the LLSQ, and >5 for the LLS-C. It is advisable that the LLSQ is performed twice daily by team members (in the mornings after waking, and in the evenings once settled into camp), and the LLS-C independently by the team physician.

For HAPE, AMS symptoms are typically aggravated by dyspnoea at rest or with light workloads, impaired exercise performance, coughing, tachycardia, subjective chest tightness, ronchi/rales, cyanosis, mild fever and (in extreme cases) foamy bloodstained sputum. [7,14,22] Importantly, HAPE may occur without the precedence of AMS symptoms. [23]

HACE commonly presents with severe headaches that remain unresponsive to analgesics, ataxia, altered level of consciousness and loss of insight. A simple field test for ataxia is to observe an individual walking heel-to-toe on a straight line drawn on the ground. [14-24]

Complications of AMS in the form of HAPE or HACE may be lethal, and early clinical recognition is vital in austere environments to allow suitable and effective treatment. Research into the use of point-of-care ultrasound scans of the lung and optic nerve sheath diameter is a promising new modality for screening, prediction and early diagnosis of HAPE and HACE respectively, but is still at the experimental stage. [25,26]


Although widely advised, the prophylactic intake of the carbonic anhydrase inhibitor acetazolamide (Diamox 125-250 mg twice daily) is debated in the literature. [2,13,27] By increasing renal bicarbonate excretion, it can improve the rate of acclimatisation, but has limited or no effect if the ascent profile is too rapid. [7,14,19,28] Acetazolamide can result in side-effects that mimic AMS (nausea, vomiting, anorexia and dizziness) and blurred vision, severe paraesthesia and odd tastes in the mouth. Individuals wishing to take acetazolamide for high-risk ascent profiles should ideally take several test doses at home before the ascent. It is contraindicated for use in diabetes and sulphonamide allergy. [13,14]

Use of dexamethasone as prophylaxis (2 mg 6-hourly or 4 mg 12-hourly) is similarly debated, mainly because of concerns regarding masking symptoms of AMS, and its side-effect profile. [13,28] However, it is used selectively in groups making very short rapid high-altitude ascents, such as rescue teams.

Ibuprofen has been shown in randomised controlled trials to be more effective than placebo in decreasing the incidence of AMS, but this has been contested in light of the fact that it reduces headache, which is essential for the clinical diagnosis. [29,30] Alternative prophylactic substances such as ginkgo biloba and coca-derived products have shown contradictory results. [13,29,31]

Individuals at elevated risk or with previous episodes of HAPE can be treated with nifedipine (20 mg slow-release preparation 8-hourly) or sildenafil (20-50 mg 8-hourly) prophylactically. As both drugs can cause postural hypotension, a trial at home before departure is recommended.

Field management

For mild to moderate symptoms of AMS (LLSQ 3-5 or LLS-C >5), primary treatment takes the form of rest days without any physical exertion at the current altitude, until all symptoms resolve [13] (Fig. 3). Additional supportive treatment with oral anti-emetics, simple analgesia, adequate hydration and sleeping with a slightly elevated upper body are effective. If symptoms do not improve within 24 hours, the patient should descend to an altitude where the symptoms are not present. Acetazolamide (250 mg orally twice daily) may be administered (particularly if symptoms worsen and descent is delayed). [13] Should the presenting altitude be situated in a 'terrain trap'--a location which demands some ascent before descent can be commenced --then early descent before exacerbation of symptoms must be considered. 0nce symptoms have progressed further, a terrain trap may preclude descent, leading to a serious or fatal outcome. Other scenarios that may hamper immediate descent worsening weather, other injuries or difficult terrain--deserve the same considerations.

In the presence of severe symptoms (LLSQ score >5), HACE should be suspected and integrated into the treatment plan. [3] Immediate action takes the form of refraining from any further ascent, administration of oxygen if available, enforced rest and protection against cold. Descent by any safe means should be initiated. Supporting treatment as described may be provided. Dexamethasone should be considered in severe AMS and used in all cases of HACE (8 mg orally every 6 hours, or 4 mg intramuscularly/intravenously every 4 hours). [13,14] As soon as the patient's condition allows (able to safely navigate the terrain), descent must be started, going down to the altitude at which the patient was last completely well, or if that altitude is unknown, at least 500-1 000 m. ["8321 Descent should avoid terrain traps and the patient should not carry any loads. If descent is delayed because of environmental conditions, a portable hyperbaric chamber (PHC) is strongly advised. [314] A PHC is an inflatable, lightweight, airtight capsule into which a patient is placed while the capsule is inflated by a foot pump to increase the internal pressure, simulating descent (Fig. 4). Pumping must be continuous to maintain air flow, making the use of a PHC extremely strenuous at high altitude. PHC treatment is to be continued for 2-4 hours to stabilise severely ill patients before descending. [24,33] PHCs are rare in the African context, but are carried by some high-altitude expeditions.

For HAPE patients, immediate rest (with the upper body elevated), protection against cold, supplementary [O.sub.2], acetazolamide and dexamethasone followed by slow-release nifedipine (20 mg orally) are recommended. This can be supplemented with sildenafil (50 mg orally) and inhaled salbutamol or salmeterol, which improves pulmonary interstitial oedema by stimulating the sodium/potassium pump. Antidiuretics should be avoided, and use of a PHC should be considered, if available.

All patients with severe AMS, HAPE or HACE should be evacuated to lower altitudes, preferably by passive evacuation using a stretcher, beast of burden or helicopter. Adequate treatment equipment must accompany the patient during descent. The patient must be continuously monitored for deterioration, and must be safely managed and assisted in navigating the terrain once ambulant. This task should be performed by adequately trained and equipped medical personnel, rather than being deferred to guides or porters.

Re-ascent should not be considered until patients are completely asymptomatic after cessation of treatment. [13] Should it be difficult to differentiate between AMS, HAPE and HACE, treat for all three conditions. However, care must be taken in HACE to not inadvertently lower mean arterial pressure by using nifedipine, which could worsen cerebral oxygenation by lowering cerebral perfusion pressure. [8,33,34]

Scenario resolution

Faced with Mr X's collapse on the summit ridge, you regret not speaking up at Mawenzi Tarn, 1 500 m below, although the differential diagnosis for his symptoms at that stage was broad, including simple dehydration or heat stroke. You recognise that the combination of headache, loss of appetite and poor sleep already constituted a clinical diagnosis of mild AMS. At Kibo, his breathlessness and lethargy should have alerted the expedition leadership that he should descend, or at least commence treatment for AMS. In the setting of his acute collapse, you recognise that the differential includes exhaustion, hypothermia, hypoglycaemia, dehydration and various other medical conditions, but a presumptive diagnosis of severe AMS and high-altitude cerebral oedema must be made. Knowing that only the most rudimentary field rescue facilities and no helicopter are available, which will undoubtedly delay definitive medical care, you urgently administer doses of oral acetazolamide and intravenous dexamethasone as well as supplemental oxygen from the guide's cylinder, and initiate a rapid descent. Foregoing the summit, you monitor his condition on an ongoing basis. By the time Mr X reaches Kibo he is able to walk unaided, and you push on down to Horombo Huts (3 700 m). Other than tiredness and a slight cough, Mr X is feeling well. He thanks you for sacrificing your summit bid to assist him and affirms his intention to return to the mountain again with a more prudent acclimatisation profile.


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[11.] MacInnis MJ, Rupert JL. 'Ome on the range: Altitude adaptation, positive selection, and Himalayan genomics. High Alt Med Biol 2011;12(2):133-139.

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[17.] Jackson SJ, Varley J, Sellers C, et al. Incidence and predictors of acute mountain sickness among trekkers on Mount Kilimanjaro. High Alt Med Biol 2010;11(3):217-222.

[18.] Davies AJ, Kalson NS, Stokes S, et al. Determinants of summiting success and acute mountain sickness on Mt Kilimanjaro (5 895 m). Wilderness Environ Med 2009;20(4):311-317. http://dx.doi. org/10.1580/1080-6032-020.004.0311

[19.] Nicol LG, Evans HE. Walk high, sleep low: An observational cohort study of altitude symptoms and physiological profiles over a 6 day ascent of Mount Kilimanjaro. Wilderness Environ Med 2014;25(3):354.

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R Hofmeyr, (1,2) MB ChB, DipPEC, DA, MMed (Anaes), FCA, FAWM; G Tolken, (2,3) MA, STB; R De Decker, (4) MSc, MB ChB, DCH (UK), FCPaeds (SA), Cert Med Genetics (Paeds)

(1) Department of Anaesthesia and Perioperative Medicine, Faculty of Health Sciences, University of Cape Town, South Africa

(2) WildMedix, Cape Town, South Africa

(3) Mountain Rescue, Hottentots-Holland Section--Mountain Club of South Africa, Cape Town, South Africa

(4) Department of Paediatrics and Child Health, University of Cape Town and Red Cross War Memorial Children's Hospital, Cape Town, South Africa

Corresponding author: R Hofmeyr (

Caption: Fig. 1. Altitudes of well-known peaks and African locations, with the approximate alveolar partial pressure of oxygen and minimum duration of safe acclimatisation (SAMJ, [3] with permission).

Caption: Fig. 3. Flow diagram for the management of acute high-altitude illness (adapted from Davis et al. [35]). (AMS = acute mountain sickness; LOC = level of consciousness; DMZ = dexamethasone (first dose intravenously then intramuscularly); ACT. = oral acetazolamide; nifedipine = sustained-release; HAPE = high-altitude pulmonary oedema; HACE = high-altitude cerebral oedema; LLS = Lake Louise Score.)

Caption: Fig. 4. The authors training expedition doctors and mountain guides discussing the use of a portable hyperbaric chamber at 4 800 m on Kilimanjaro (photo: Dr Chanel Rossouw, with permission).
Table 1. Consequences of acute exposure to high altitude

High altitude           Very high altitude      Extreme altitude
(1 500 - 3 500 m)       (3 500 - 5 500 m)       (5 500 - 8 850 m)

HAI occurs with         Most common             Abrupt ascent always
rapid ascent above      range for HAI           causes severe HAI
2 500 m                 (AMS, HAPE, HACE)

[down arrow] Exercise   Requires                Progressive
performance             acclimatisation for     physiological
[up arrow]              physical effort to      deterioration
Ventilation             be tolerated            outstrips

Minor decrease in       Sp[O.sub.2]: 75 - 85%   Sp[O.sub.2]: 55 - 75%
SpO, (usually                                   Severe hypocarbia
[greater than or
equal to] 90%)

Pa[O.sub.2]:            Pa[O.sub.2]:            Pa[O.sub.2]:
7 - 10 kPa              5 - 8 kPa               3.5 - 5 kPa

Severe hypoxia          Extreme hypoxia may     Always requires
unlikely in the         occur during sleep,     acclimatisation to
absence of underlying   exercise or illness     avoid illness
illness or HAPE

HAI = high-altitude illness; AMS = acute mountain sickness;
HAPE = high-altitude pulmonary oedema; HACE = high-altitude
cerebral oedema.

Table 2. Risk categories for AMS
(Wilderness Medical Society consensus guidelines) [13]

Risk category   Description

Low             Individuals with no prior history of altitude
                illness and ascending to [less than or equal to]
                2 800 m

                Individuals taking >2 days to arrive at 2 500 -
                3 000 m with subsequent increases in sleeping
                elevation <500 m/day and an extra day for
                acclimatisation every 1 000 m

Moderate        Individuals with a prior history of AMS and
                ascending to 2 500 - 2 800 m in 1 day
                No history of AMS and ascending to
                >2 800 m in 1 day
                All individuals ascending >500 m/day
                (increase in sleeping elevation) at altitudes
                >3 000 m but with an extra day for
                acclimatisation every 1 000 m

High            Individuals with a history of AMS and ascending
                to >2 800 m in 1 day
                All individuals with a prior history of HACE
                All individuals ascending to >3 500 m in 1 day
                All individuals ascending >500 m/day
                (increase in sleeping elevation)
                >3 000 m without extra days for acclimatisation
                Very rapid ascents (e.g. <7 day ascents
                of Mount Kilimanjaro)

AMS = acute mountain sickness; HACE = high-altitude cerebral oedema.

Altitudes reter to the altitude at which the person sleeps; ascent
is assumed to start trom elevations < 1 200 m; risk categories
pertain to unacclimatised individuals.

Fig. 2. Diagnostic criteria for acute HAI,
incorporating the Lake Louise Symptom and Clinical Scores.
Graphic representation from WildMedix Mountain Expedition
Medicine course materials, used with permission. (AMS = acute
mountain sickness; HAPE = high-altitude pulmonary oedema;
HACE = high-altitude cerebral oedema; Gr = grade; LOC = level
of consciousness; HR = heart rate; RR = respiratory rate.)


Increase in altitude above 2 500 m in last 4 days
AND headache plus at least one other symptom

           Score                       0                 1

Weakness   Headache                  None               Mild

           tract Fatigue/            None          Poor appetite
           weakness                                or mild nausea

                                     None               Mild

           Dizziness                 None               Mild

Clinical   Sleep                    Normal          Not as good
                                                      as usual

Symptoms alone: [greater than or equal to] 3 = mild AMS
4-5 = moderate AMS [greater than or equal to] 6 = severe AMS

           Mental status            Normal           Lethargy/

           Ataxia (heel-toe)         None            Manoeuvres
                                                     to balance

                               Patient unable to
                               stand for ataxia
                                   test = 4

           Peripheral oedema         None           One location

Symptoms + clincal score: [greater
than or equal to] 5 = AMS


Increase in altitude above 2 500 m in last 4 days
AND headache plus at least one other symptom

           Score                      2                    3

Weakness   Headache                Moderate             Severe/
           Gastrointestinal                         incapacitating

           tract Fatigue/       Nausea and/or           Severe/
           weakness                vomiting         incapacitating

                                   Moderate             Severe/

           Dizziness               Moderate             Severe/

Clinical   Sleep               Woke many times      Unable to sleep

Symptoms alone: [greater than or equal to] 3 = mild AMS
4-5 = moderate AMS [greater than or equal to] 6 = severe AMS

           Mental status        Disorientated/    Difficult to rouse/
                                   confused           unconscious

           Ataxia (heel-toe)    Steps off line        Falls down

           Peripheral oedema   [greater than or
                                 equal to] 2

Symptoms + clincal score: [greater
than or equal to] 5 = AMS

AMS with ataxia OR decreased LOC


Ataxia AND decreased LOC in absence of AMS


Clinical diagnosis ([greater than or equal to] 2 symptoms
AND [greater than or equal to] 2 signs)

Symptoms                                 Signs

Dyspnoea at rest                 Crackles or wheezing
                                  in [greater than or
                                equal to] 1 lung field

Cough                              Central cyanosis

Weakness and/or                       Tachypnoea
[down arrow] exercise

Chest tightness or                    Tachycardia

Gr 1 (mild): only              Gr2 (moderate): ambulant,
symptoms with exertion;         but limited. Rales may
no limitation of function             be present

Gr 3 (serious): symptoms        Gr 4 (severe): comatose
at rest, [+ or -] confused.    or obtunded. Frank oedema
Rales, [up arrow] HR
[up arrow] RR
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Author:Hofmeyr, R.; Tolken, G.; De Decker, R.
Publication:South African Medical Journal
Article Type:Disease/Disorder overview
Date:Jul 1, 2017
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