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Altitude Medicine updates and controversies

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Title: Altitude Medicine updates and controversies


1
Altitude Medicine updates and controversies
  • Corinne Michèle Hohl R3
  • Royal College Emergency
  • Medicine Training Program

2
  • Millions of visitors per year to high altitude
  • destinations world wide, increasing trends
  • gt20000 British trekkers to Nepal annually
  • 90000 nights spent in huts gt 2500m in
    Switzerland/yr
  • Ski industry.
  • Aviation industry.
  • Pathophysiologic modelling of hypoxic processes
    in health indivisuals.
  • Military operations.

Thorung La Pass, 5467m
3
  • Physics

Himalayan Peaks over Kathmandu, Nepal
4
Physics
  • Hypobaric hypoxia
  • Alveolar gas equation
  • PAO2 (PB-PH2O) FiO2 - PaCO2 /R
    (0.003PaO2)
  • PAO2 varies proportionally to PB, as it declines
    PaO2declines.

Himalayan Peaks over Kathmandu, Nepal
5
Physics
  • Further from the earths surface gravitational
    pull diminishes affecting gas density, pressure
    and volume.
  • Hypobaria PB PiO2 O2 sat
  • Sealevel 760mmHg 160mmHg 100
  • 1829m 608mmHg (80) 128mmHg 94
  • 5486m 380mmHg (50) 80mmHg 78
  • 8848m 240mmHg (31) 43mmHg 56
  • .

Himalayan Peaks over Kathmandu, Nepal
6
Adaptive mechanisms
  • As PaO2 declines to 60mmHg chemosensors in the
    carotid body trigger an increase in minute
    ventilation
  • Hypoxic Ventilatory vesponse (HVR)
  • PCO2 drops --gt resp alkalosis --gt limits HVR.
  • Low HVR at SL predicts increased susceptibility.
  • (Krieger Holz, 1999, Fagan Weil, 2001)

Himalayan Peaks over Kathmandu, Nepal
7
Adaptive mechanisms
  • 24-48h bicarbonate diuresis --gt compensatory
    metabolic acidosis --gt minute ventilation
    increases.
  • Catecholmine release --gt increase in HR and PAP.
    Acclimatization correlates with return of resting
    HR to baseline except at extreme altitude.
  • Increase in cerebral blood flow offset by the
    vaso-constrictive effect of hypocapnea.
  • 4-5days hematopeisis after 4-5 days. (Lundby et
    al. 2001)

Himalayan Peaks over Kathmandu, Nepal
8
AMSAcuteMountainSickness
Trekkers on the Annapurna Circuit
9
AMSEpidemiology
  • Maggiorini et al. 1990 visitors to Swiss
    mountain huts 34
  • 2850-3050m 9-13
  • 3650m 34
  • 4559m 52 (11 with HAPE or HACE)
  • Houston. 1985 and Hackett et al. 2001 Colorado
    skiers
  • 1850-2800m 12 - 22
  • Montgomery et al. 1989 Rocky Mountains
  • 2000m 25
  • Hackett et al. 1976 Trekkers in Nepal
  • 4200m 43-52 AMS

Trekkers on the Annapurna Circuit
10
AMS - Pathophysiology
11
AMS Pathophysiologycerebral autoregulation
12
AMS Pathophysiology cerebral autoregulation
Jansen et al. Cerebral Autoregulation in Subjects
Adapted and Not Adapted to High Altitude. Stroke
2000. Methods 10 subjects at SL 9 sherpas 10
newcomers at 4243m w/o AMS. Phenylephrine
infusion to increase MABP (20-30mmHg) and
challenge CA. Measured Vmca (MCA blood flow) by
transcranial doppler as a measure of
CA. Results SL No change in Vmca after
phenylephrine in any group --gt intact CA. 4243m
In both sherpas and newcomers increase in MABP
triggered an increase in Vmca at altitude (124
in sherpas vs. 111 in newcomers -
NS). Conclusion Both sherpas and newcomers w/o
AMS have impaired CA at altitude. Is AMS a
reflection of an individuals adaptability to
impaired CA?
13
AMS - Signs Symptoms
  • Lake Louise Consensus 1993
  • Headache in an unacclimatized individual who
    recently arrived at gt 2500m plus one or more
  • n/v, anorexia, insomnia, dizziness or fatigue.
  • 1-10h after ascent, remits in 4-8days.
  • No diagnostic physical findings except low O2sat.
  • (Hackett Roach, 2001, Forwand et al. 1968)

Machhapuchhre, 6993m
14
AMS - Signs Symptoms
  • Risk factors
  • Prior history
  • Residence below 900m
  • Exertion
  • Preexisting cardiopulmonary disorders
  • Younger individuals (lt50)
  • Men more susceptible to HAPE but not AMS
  • Dehydration
  • (Hackett Roach, 2001, Basnyat, 1999)

Machhapuchhre, 6993m
15
AMS - Signs Symptoms
  • Fitness is NOT protective
  • Roach et al. 2000
  • Cross-over design, n7, exposed to simulated
    alt.(4800m) x10h.
  • Symptom scores of AMS 4.4 ( 1.0) with exercise
    (50 max workload) vs. 1.3 ( 0.4) when
    sedentary.
  • Normoxic controls who exercised had no symptoms
    of AMS.
  • Sa O2 during exercise 76 vs 81.
  • C Does exercise-induced exaggeration of
    hypoxemia worsen AMS?
  • (Roach et al, 2000 Hackett Roach, 2001)

Machhapuchhre, 6993m
16
AMS - Signs Symptoms
  • Is there a way to predict individual
    susceptibility?
  • Prior history of AMS/HAPE is most reliable.
  • Low HVR too much overlap with the range of
    normal.
  • High PAP with exposure to hypoxia or exercise
    poor sensitivity and specificity.
  • Avoid by prevention and ascent rates to lt
    300m/day above 2000m in first exposure to
    altitude or susceptible individuals.
  • (Bärtsch P et al. 2001)

Machhapuchhre, 6993m
17
AMS - DDx
  • acute psychosis hangover seizures
  • AV malformation hypoglycemia stroke
  • brain tumor hyponatremia TIA
  • CO poisoning hypothermia viral infection
  • CNS infection drugs bact. infection
  • Dehydration EtOH exhaustion
  • DKA migraine
  • (Hackett Roach, 2001)

Machhapuchhre, 6993m
18
AMS Prevention
  • Graded Ascent
  • Prior hypoxic exposure
  • Oxygen
  • Acetazolamide
  • Dexamethasone
  • Nifedipine
  • Antioxidants

Bhulebhule, 840m
19
AMS - Prevention normobaric hypoxia
  • Burse et al. Acute Mountain Sickness at 4500m Is
    Not Altered by Repeated Eight-Hour Exposures to
    3200-3550m Normobaric Hypoxic Equivalent. Aviat
    Space Environ Med 1988.
  • Methods
  • Single-blinded design. Exposed 10 soldiers to
    normobaric hypoxia (FiO2 12, 3960m equivalent)
    and 10 soldiers to SL conditions (FiO2 21)
    with a portable altitude simulator for 8h/day for
    10 d prior simulated ascent.
  • Results
  • Trend towards higher PetO2 and lower PCO2 in
    experimental group (NS).
  • Trend towards lower symptom scores in exp grp
    (1.0 0.4 vs 1.6 0.4).
  • Conclusion
  • No ventilatory advantage.
  • There may be a marginal benefit of
    acclimatization with respect toAMS scores.
  • A benefit of longer or more intense program
    cannot be ruled out.

Bhulebhule, 840m
20
AMS - Prevention Acetazolamide
  • Forwand et al. Effect of Acetazolamide on Acute
    Mountain Sickness. NEJM 1968.
  • Hypothesis
  • Studies in the 30s showed improvement of AMS
    symptoms and respiratory alkalosis with CO2
    inhalation.
  • Acetazolamide inhibits renal carbonic anhydrase
    and increases bicarbonate excretion resulting in
    metabolic acidosis.
  • Methods
  • RCT, n 43 male soldiers.
  • Acetazolamide 250mg q8h vs. placebo 32h prior
    ascent to 12800 ft, continued for 40h.
  • Results
  • Tx group lower serum HCO3-, lower blood pCO2,
    higher minute ventilation, and no significant
    change in blood pH from SL.
  • HCO3- in tx and placebo group approximated on
    days 4 and 5.

Bhulebhule, 840m
21
AMS - Prevention Acetazolamide
Acetazolamide
HCO3
Blood pCO2
Acetazolamide
pH
Acetazolamide
Bhulebhule, 840m
22
AMS - Prevention Acetazolamide
  • Forwand et al. 1968.
  • Headache, gastrointestinal symptoms and insomnia
    significantly reduced in Acetazolamide group.
  • Correlation of AMS symptoms with pCO2 levels
  • high pCO2 levels correlated with greater AMS
    symptoms.
  • Remission of AMS in both treatment and control
    levels correlated with decrease in serum pCO2.
  • Conclusions
  • Acetazolamide 250mg q8h reduces symptoms of AMS,
    and reduces metabolic derangements at altitude.
  • No side effects reported.

Bhulebhule, 840m
23
AMS - Prevention Dexamethasone
  • Johnson et al. Prevention of Acute Mountain
    Sickness by Dexamethasone. NEJM 1984.
  • Hypothesis
  • If AMS is caused by vasogenic cerebral edema
    dexamethasone should be effective.
  • Methods
  • RTC, double-blind, cross-over.
  • n12 4 did not complete crossover.
  • Simulated altitude (4570m) for 42h in
    decompression chamber.
  • Dexamethasone 4mg q6h vs placebo starting day
    prior to decompression until recompression.
  • Symptom evaluation 5 times during decompression.

Tal, 1680m
24
AMS - Prevention Dexamethasone
  • Johnson et al. 1984.
  • Results Placebo Dexanethasone
  • AMS - C 1.09 0.18 0.26 0.08 plt 0.05
  • AMS -R 0.64 0.09 0.31 0.06 plt 0.05
  • Clinical 1.1 0.11 0.28 0.07 p0.01
  • Conclusions
  • Dexamethasone reduced AMS symptom scores during
    decompression.
  • Dexamethasone associated with decreased retinal
    artery width.
  • No side effects noted.
  • What about real altitude? Rebound effects? Longer
    exposures?
  • What about those individuals who did not complete
    crossover?

Tal, 1680m
25
AMS - Prevention acetazolamide vs. dexamethasone
  • Reid et al. Acetazolamide or dexamethasone for
    prevention of acute mountain sickness a
    meta-analysis. J Wild Med, 1994.
  • Methods
  • Computerized lit search, 23 databases and
    contacted authors. N 20.
  • Placebo controlled trials acetazolamide or
    dexamethasone for AMS prophylaxis.
  • Studies evaluated by 2 reviewers, quality
    assessed by Chalmers criteria and weighted
    accordingly.
  • Outcomes incidence of AMS, AMS score by ESQ and
    GHAQ, and symptoms of AMS.
  • Acetazolamide dose ranges 500-750mg qd, one
    study used 1000mg.
  • Dexamethasone dose ranges 0.25mg q12 - 4mg
    q6-8h.

Tal, 1680m
26
AMS - Prevention acetazolamide vs. dexamethasone
  • Reid et al. 1994.
  • Results
  • ES acetazolamide vs. placebo (n680) -0.61
    (-0.29 to -0.93)
  • ES dexamethasone vs. placebo (n237) -0.32
    (0.38 to -1.02)
  • ES for chamber studies much greater than field
    studies (-2.4 vs -0.5) however higher doses,
    greater ascent rates. Dexamethasone seemed more
    effective than acetazolamide in chamber studies
    only.
  • Conclusions
  • AMS prophylaxis with acetazolaminde or
    dexamethasone effective.
  • ES greater for acetazolamide however,
    comparisons were not under same experimental
    conditions from study to study and dosages
    varied.
  • Field studies favored acetazolamide, chamber
    studies dexamethasone.
  • Given efficacy of acetazolamide and benign side
    effect profile compared to dexamethasone,
    acetazolamide should probably be the agent of
    choice for chemoprophylaxis dexamethasone for
    very rapid ascent rates (i.e. rescue or military
    operations).

Tal, 1680m
27
AMS - Prevention nifedipine
  • Hohenhaus E et al. Nifedipine Does Not Prevent
    Acute
  • Mountain Sickness. Am J Resp Crit Care Med 1994.
  • Hypothesis
  • Because AMS and HAPE share common
    pathophysiologic mechanisms nifedipine may be
    beneficial in the prevention of AMS as it is
    effective in the prophylaxis and treatment of
    HAPE.
  • Methods
  • RCT, n 27 HAPE-R mountaineers, rapid ascent to
    4559m.
  • Nifedipine SR 20mg tid vs placebo.
  • Results
  • Subjects with AMS had significantly lower O2 sat
    (75.9 1.5 vs. 82 1.4), higher A-a gradients
    than asymptomatic subjects. PAP and PCO2 did not
    differ significantly between subjects with AMS
    and without.

Bagarchhap, 2080m
28
AMS - Prevention nifedipine
  • Hohenhaus E et al. 1994.
  • AMS scores were almost identical btw nifedipine
    and control subjects.
  • Nifedipine was associated with significantly
    lower PAP pressures. No hypotension occurred.
  • Nifedipine had no effect on O2 sat.
  • Conclusions
  • Nifedipine is ineffective for AMS prevention, or
    has a marginal benefit not detected with this
    study.
  • The exaggerated hypoxemia seen with AMS in
    contrast to subjects who are well at altitude
    cannot be explained by changes in PAP, as no
    significant different in PAP was noted btw AMS
    and well subjects. This could be explained by V/Q
    mismatch, interstitial edema or lower hypoxic
    ventilatory drive (trend towards higher PCO2.)

Bagarchhap, 2080m
29
AMS - Prevention Antioxidants
  • Bailey et al. Acute Mountain Sickness
    Prophylactic
  • Benefit of Antioxidant Vitamin Supplementation at
    High
  • Altitude. High Alt Med Biol, 2001.
  • Hypothesis Free-radical mediated damage to BBB
    may be implicated in pathophysiology of AMS.
    Benefit of dexamethasone may be related to
    antioxidant properties which helps maintain BBB
    vascular integrity.
  • Methods
  • RCT, double-blinded, placebo controlled, n18.
  • AO (ascorbic acid, dl-? tocopherol, ? -lipoic
    acid) qid vs placebo starting 3 wks prior ascent,
    continued until 10d at altitude (5180m)
  • Results
  • Trend towards decreased incidence of AMS in AO
    (5/9) vs. 9/9 in the placebo group (NS).
  • AMS scores 2.3 0.9 in AO vs. 3.5 0.4 in
    placebo grp (p0.03).

Bagarchhap, 2080m
30
AMS - Prevention Antioxidants
  • Bailey et al. 2001.
  • Higher O2sat in the AO group (89 5 vs. 85
    5, p0.04)
  • Lower satiety scores and higher caloric intake in
    the AO group-however, did not measure baseline
    satiety or caloric intake at sealevel.
  • Conclusions
  • This study indicates that AO may be effective in
    preventing AMS as well as reducing symptom scores
    ? via AO mediated improvement in BBB integrity?
  • Possible hyperphagic effect?
  • No side effects reported.
  • Larger studies warranted.

Bagarchhap, 2080m
31
AMS - Prevention
  • Dumont et al. Efficacy and harm of
    pharmacological prevention of acute mountain
    sickness quantitative systematic review. BMJ
    2000.
  • Methods
  • Systematic Search for all RTCs on efficacy and
    harm of pharmacological prevention of AMS.
  • 33 trials, n 523 pharmacologic intervention, n
    519 placebo
  • Endpoints prevention of AMS prevention of AMS
    sxs.
  • Results
  • Final altiudes 4050 - 5885m. Mean AMS
  • event rate 67.
  • Incidence correlated with rate of ascent,
  • not final altitude
  • NNTs high with low ascent rates
  • decreased with increasing altitudes.

Ascent rate (m/h)
AMS incidence in control groups
Manang, 3440m
32
AMS - Prevention
  • Dumont et al. BMJ 2000
  • Meta-anlysis - dexamethasone
  • 8 trials, mean altitude 4000m.
  • 0.5-2mg qd had no effect on AMS.
  • 8-16mg qd was effective in preventing AMS.
  • RR 2.5 (CI 1.7-3.6) NNT 2.8 (2.0-4.6).
  • Trend towards decreasing headache and nausea, not
    statistically significant. Significant decrease
    in dizziness RR 2.14 (1.01-4.5).
  • Adverse reactions when weaned RR 4.45 (1.9-9.3),
  • NNT 3.7.
  • Adverse reactions depression.

Manang, 3440m
33
AMS - Prevention
  • Dumont et al. BMJ 2000
  • Meta-anlysis - acetazolamide
  • 9 trials, mean altitude 4478m.
  • 500mg trend towards less AMS RR 1.2 (0.93-1.59)
    NNT 7(3.3-54).
  • 750mg decreased AMS RR 2.18 (1.5-3.1) NNT 2.9
    (2.0-5.2).
  • Bias lower ascent rates used for 500mg, making
    500mg less likely to work.
  • Significant less insomnia, headache and nausea
    than placebo.
  • Significantly more adverse drug effects
    polyuria, paresthesias and taste disturbance than
    placebo groups.
  • Conclusion
  • Dexamethasone 8-16mg qd and acetazolamide 750mg
    qd equally effective in preventing AMS above
    4000m with ascent rates gt500m/day (NNTs lt 3).
  • Prophylaxis is worth while when ascent rates are
    high.

Manang, 3440m
34
AMS - Prevention
Dexamethasone
  • Dumont et al. BMJ 2000

Incidence of AMS in placebo groups
other drugs
Acetazolamide
Incidence of AMS in intervention group
Manang, 3440m
35
AMSTreatment
  • Oxygen, carbon dioxide enriched air
  • Descent
  • Dexamethasone
  • Acetazolamide
  • Symptomatic treatment

Gangapurna, 7454m
36
AMS - treatment Gamow Bag
  • Early uncontrolled studies in Himalayan trekkers
    indicated short and long term benefit of portable
    hyperbaric chambers in the treatment of AMS.
  • Pollard. Treatment of acute mountain sickness.
    BMJ 1995.
  • Lay press anecdotal reports of symptomatic
    relief has led to widespread use of portable
    hypobaric chambers by trekking/expedition
    companies.
  • Unfortunately, there is confusion among the
    public about the therapeutic role of these
    portable hypobaric chambers. At least one
    potentially avoidable death has occurred. In 1991
    a European trekker died at 5100, in Nepal after
    three days of intermittent treatment in a
    portable hyperbaric chamber without an attempt at
    descent. Descent might have been life saving.

Gangapurna, 7454m
37
AMS - treatment Gamow Bag
  • Bärtsch et al. Treatment of acute mountain
    sickness by simulated descent a randomised
    controlled trial. BMJ 1993.
  • Hypothesis
  • Hyperbaric tx reduces the symptoms of AMS - for
    how long? rebound?
  • Methods
  • Single-blinded RTC.
  • n 64 mountaineers exposed to 4559m (430 mm Hg)
    with AMS.
  • One hour of treatment in a portable hyperbaric
    chamber at 193mbar (simulated descent of 2250m)
    vs. treatment in a portable hyperbaric chamber at
    20mbar (300m, control) vs. bed rest.
  • Outcomes AMS symptoms before, immediately after
    and 12h post tx.
  • Intake of analgesics and antiemetics.

Gangapurna, 7454m
38
AMS - treatment Gamow Bag
  • Bärtsch et al. 1993
  • Results
  • Increase in O2 sat in tx group and short-term
    improvement in AMS score
  • 193mbar 20mbar rest
  • O2 sat during 90(88-91) 70(67-75) 68
    (61-75 ) (plt0.001)
  • O2 sat 12h post 72(68-76) 74 (70-77)
    74(70-79)
  • AMS prior tx 4.1(3.7-4.5) 4.3 (3.7-4.8) 4.5
    (4.0-5.0)
  • AMS after tx 1.4 (1.1-1.6) 2.7 (2.1-3.4)
    2.7 (2.1-3.3) (plt0.001)
  • AMS 12h post 2.5 (1.8-3.2) 3.1 (2.4-3.9)
    2.3 (2.1-3.3)
  • Conclusion
  • Portable hyperbaric chambers can alleviate AMS
    symptoms and hypoxia rapidly but have no
    prolonged effect.on AMS or oxygenation.
  • Chambers should be used only to FACILITATE but
    NOT delay descent.
  • Prolonged tx? Repeated tx? Rebound?

Gangapurna, 7454m
39
AMS - treatment simulated descent vs.
dexamethasone
  • Keller et al. Simulated descent v dexamethasone
    in treatment of acute mountain sickenss a
    randomised trial. BMJ 1995.
  • Methods
  • RTC non-blinded.
  • n31 mountaineers with AMS at 4559m.
  • Random assignment to hyperbaric chamber (193mbar,
    2250m descent) for one hour vs. dexamethasone 8mg
    first dose, then 4mg q6h.
  • Outcome AMS symptoms at 1hour and 11h.
  • Results
  • 1h Trend towards greater relief of AMS at one
    hour with hyperbaric tx (- 4.0 1.9 vs. - 2.5
    1.8) as opposed to Dexamethasone.

Letdar, 4230m
40
AMS - treatment simulated descent vs.
dexamethasone
  • Keller et al. 1995.
  • 11h Dexamethasone group suffered significantly
    less AMS than the hyperbaric tx group (-7.0
    3.6 vs. -1.6 3.0)
  • O2 sat Trend towards increasing sat with
    dexamethasone at 11h.
  • Similar intake of analgesics.
  • Conclusion
  • Hyperbaric treatment has a short-term beneficial
    effect on AMS, but no long term effect.
  • Dexamethasone has less short-term but a longer
    term clinical improvement.

Letdar, 4230m
41

AMS - treatment Acetazolamide
  • Grissom et al. Acetazolamide in the Treatment of
    Acute
  • Mountain Sickness Clinical Efficacy and Effect
    on Gas
  • Exchange. Ann Int Med, 1992.
  • Methods
  • RCT, placebo controlled, double-blinded, n12
    with AMS who presented to a medical research
    center at 4200m on Mt McKinley.
  • Acetazolamide 250mg q8h, 2 doses vs. placebo.
  • Results
  • At 24h 1/6 climbers receiving acetazolamide vs.
    6/6 receiving placebo still met criteria for AMS
    (p0.015).
  • PaO2 improved in acetazolamide group and worsened
    in placebo group (2.9 0.8mmHg vs. -1.3
    2.8mmHg, p0.045).
  • Conclusions
  • In AMS acetazolamide relieves symptoms and
    improves oxygenation.

High Camp, 4750m
42
HAPE - Epidemiology
  • Most common fatal manifestation of altitude
    illness.
  • 1-2 of healthy individuals which ascending over
    4000m.
  • 10 of HAPE-R and 60 of HAPE -S individuals who
    ascend to over 4000m in 24h develop HAPE.
  • Risk factors
  • Strenuous exercise - absence of pulmonary artery
  • Cold - pulmonary hypertension
  • Recent URTI - reentry
  • Prior HAPE
  • (Bärtsch et at. 1991)

On the way to Thorung La 5000m
43
HAPE - signs symptoms
  • Symptoms most often superimposed on AMS
  • Cough - Tachypnea - SOBOE, rest
  • Tachycardia - Orthopnea - Fever
  • Cyanosis - Rales - Watery sputum
  • 2-4d after rapid ascent, often during the night.
  • CXR (fluffly patchy perihilar infiltrates,
    sparing of lung bases periphery, usually
    affects the RML first.
  • ECG RBBB, RAD, tall R precordial leads, S
    lateral leads.
  • (Jerome Severinghaus, 1996.)

On the way to Thorung La 5000m
44
HAPE - signs symptoms
  • In those with HAPE severe hypoxemia can lead to
    the rapid progression of AMS to HACE.
  • Mortality
  • 11 with treatment.
  • when descent impossible and no supplemental O2
    available mortality rate 44 - 50.
  • An effective portable medical regimen for the
    treatment of HAPE is desirable for when immediate
    descent it not an option.
  • (Oelz et al, 1989 Bärtsch et al. 1991, Hackett
    Roach, 2001)

On the way to Thorung La 5000m
45
HAPE - prevention
  • Slow ascent (HAPE-S lt300m/day over 2000m)
  • Nifedipine
  • Garlic

Thorung La, 5415m
46
HAPE - prevention
  • Bärtsch P et al. Prevention of High Altitude
    Pulmonary Edema by Nifedipine. NEJM 1991.
  • Methods
  • RCT, double blinded, n 21 with prior hx of HAPE
    acscent to 4559m.
  • Nifedipine SR 20mg q8h vs. placebo 3d prior
    ascent to 4th day at altitude.
  • Results
  • 7/11 subjects with placebo vs. 1/10 with
    nifedipine developed HAPE (p0.01).
  • Placebo arm terminated early because too sick, 2
    of developed HACE.
  • Significantly lower PAPs (41 8 vs. 53
    16mmHg), A-a gradients (6.6 3.8 vs. 11.8 4.4)
    and lower symptom scores with nifedipine. Trend
    towards higher O2sat with nifedipine.
  • Conclusions
  • Nifedipine prophylaxis lowers PAP and HAPE
    incidence when taken prophylactically in HAPE S
    individuals. No side effects reported.

Thorung La, 5415m
47
HAPE - prevention
  • Fallon et al. Garlic prevents hypoxic pulmonary
    hypertension in rats. Am. J. Physiol. 1998.
  • Hypothesis Hypoxic pulmonary vasoconstriction
    underlies the development of HAPE. Anecdotal
    evidence suggest a benefit of garlic in
    preventing altitude induced symptoms.
  • Methods Gave rats garlic gavage (100mg/kg body
    weight!) for 5 days, then subjected them to
    normobaric hypoxia.
  • Results Complete inhibition of acute hypoxic
    pulmonary vasoconstriction in garlic gavage group
    compared with controls. Nitric oxide synthase
    inhibitor inhibited the vasodilatory effects of
    garlic.
  • Conclusion Garlic may prevent hypoxic pulmonary
    vasoconstriction by upregulating NO synthesis.
    Garlic may be beneficial in HAPE.

Thorung La, 5415m
48
HAPE - treatment
  • Descent
  • Postural Maneuver
  • Oxgen
  • NO
  • Nifedipine
  • EPAP

Heading towards Muktinath, 5000m
49
HAPE - postural drainage?
  • Bock et al. Emergency Maneuver in High-Altitude
  • Pulmonary Edema. JAMA 1986.
  • 33yr old mountaineer with prior hx of HAPE
    trekking at 5100m.
  • SOB, cough,watery sputum, felt as if he were
    drowning and that death was imminent
  • Evacuation route involved crossing over a 5800m
    pass.
  • Relieved when kneeling with head on the ground
    and his buttocks in the air, his trunk upside
    down.
  • He got his companion to straddle him, applying
    pressure on abdomen which with a deep breath
    triggered paroxysm of cough and increase sputum
    volume. After 20-30minutes of coughing, felt less
    SOB.

Heading towards Muktinath, 5000m
50
HAPE - treatment O2 vs. NO
  • Anand et al. Effects of Inhaled Nitric Oxide and
    Oxygen
  • in High-Altitude Pulmonary Edema. Circulation
    1998.
  • Methods
  • RTC - NO vs. oxygen vs. NO oxygen.
  • N 14 soldiers with HAPE transported to a high
    altitude research center and hospital at 3600m in
    t Western Himalayas.
  • Each patient was exposed to the 3 gas mixtures
    for 30min sequentially with washout periods of
    room air. Measurements were performed in the last
    10min of each gas inhalation. After the protocol
    was over all patients were treated with oxygen
    and descent.
  • Results
  • NO inhalation reduced PAP by 11mmHg 1.5, and
    pulmonary vascular resistance by 36. O2sat
    increased from 67 3.5 to 72 3.6.
  • FiO2 50 caused a greater rise in O2sat than NO,
    but a similar drop in PAP.

Heading towards Muktinath, 5000m
51
HAPE - treatment O2 vs. NO
  • Anand et al. 1998.
  • NO with FiO2 of 50 caused the largest decrease
    in PAP (36 2.4 vs. 16 1.7mmHg) and greatest
    rise in O2sat (68 3.6 vs. 96 1.3) - although
    this treatment was 3h into the treatment
    protocol.
  • Conclusions
  • NO and oxygen may have additive effects in the
    treatment of HAPE.

Heading towards Muktinath, 5000m
52
HAPE - treatment NO
  • Oelz et al. Nifedipine for High Altitude
    Pulmonary
  • Edema. Lancet, 1989.
  • Methods
  • n6 subjects with HAPE, 12-36hrs after ascent to
    4559m in 24h.
  • All subjects were treated with Nifedipine 10mg
    S/L and 20mg po q6h. If SBP did not drop by
    10mmHg after the first dose another 10mg S/L was
    administered.
  • Controls with AMS but no HAPE!
  • Results
  • Drop in AMS score from 9.2 ( 1.6) pretx to 5.7
    ( 1.8) at 1h, and 2.5
  • ( 0.8) 14h post tx (plt0.001).
  • O2 sat 65 pretx to 73 1h post tx to 69 14h
    post tx (NS).

above Muktinath, 4800m
53
HAPE - treatment nifedipine
  • Oelz et al. 1989.
  • PAP decreased with nifedipide from 133mmHg pretx
    to 73mmHg 1h post tx, to 58mmHg 14h post tx.
  • (Controls without HAPE had PAPs of 63mmHg.)
  • Radiographic scores decreased from 7.7 to 4.0 14h
    post tx (plt0.05).
  • All subjects with HAPE reported SOB and chest
    pressure prior tx, which was relieved 1h post
    nifedipine.
  • Subjects were able to continue mountain climbing
    activities.
  • Conclusion
  • Nifedipine may be effective.
  • Properly controlled, randomised studies are
    needed.

above Muktinath, 4800m
54
HAPE - treatment CPAP
  • Schoene et al. High Altitude Pulmonary Edema and
    Exercise at 4400m on Mount McKinnley Effect of
    Positive Airway Pressure. Chest, 1985.
  • Methods
  • n4 climbers with HAPE, n12 healthy climbers at
    4400m.
  • All sujects put on EPAP, healthy subjects made to
    exercise, HAPE subjects rested.
  • Mask on with no end expiratory pressure vs. 5 and
    10cm H2O.
  • Results
  • EPAP increased O2 sat in HAPE subjects (54 to
    61, p0.005) as well in healthy subjects (85 to
    88, plt0.01).
  • Conclusions
  • Positive end expiratory pressure may be
    beneficial in HAPE.

above Muktinath, 4800m
55
HACE - epidemiology, pathophysiology
  • Fatal HACE has been reported as low as 2500m.
  • lt1 of mountain climbers.
  • AMS may progress to HACE in 12h.
  • Develops 1-9days after ascent.

56
HACE - signs and symptoms
  • Preexisting AMS or HAPE with severe h/a, n/v
  • Ataxia (cerebellar) - sensitive sign for early
    recognition
  • Altered level of consciousness, global
    encephalopathy.
  • seizures
  • Focal neurological signs, cranial nerve palsies,
    slurred speech
  • Associated with retinal hemorrhages
  • Papilledema, elevated ICP
  • Cuase of death herniation
  • (Hackett Roach, 2001)

Muktinath, 3760m
57
HACE - prevention
  • As for AMS - graded ascent most important

Muktinath, 3760m
58
HACE - treatment
  • Immediate descent
  • Bed rest
  • Hyperbaric Chamber
  • Oxygen
  • Dexamethasone 8mg IV, then 4mg q6h
  • Measures to decrease ICP once in hospital center

Manang valley, 3000m
59
HACE - treatment
  • Dexamethasone 8mg IV, then 4mg q6h
  • Supportive therapy
  • Anecdotal reports only
  • May work by improving capillary membrane
    integrity and causing vasoconstriction.
  • (Levine et al, 1989)

Manang valley, 3000m
60
Thorung La, 5415m
AMS Prevention
Graded Ascent Prior hypoxic exposure Oxygen N
ifedipine Dexamethasone Furosemide,
Spironolactone Antioxidants Narcotics Acetazola
mide ADH
61
Thorung La, 5415m
AMS Treatment

Oxygen CO2 enriched air Descent symptomatic
therapy Dexamethasone nifedipine Acetazolamide
62
Thorung La, 5415m
HAPE Prevention

Slow ascent (HAPE-S lt300m/day over
2000m) Nifedipine Garlic
63
Thorung La, 5415m
HAPE Treatment

Descent EPAP Postural Maneuver Nifedipine Oxgen
NO
64
Thorung La, 5415m
HACE Prevention Treatment

AMS Dexamethasone Supportive therapy
65
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66
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