Cochrane · systematic review · CD009567

Interventions for treating acute high altitude illness

Simancas‐Racines, D, Arevalo‐Rodriguez, I, Osorio, D, et al. · Cochrane Database of Systematic Reviews · 2018 · Cochrane Library

Emergency and Critical CareAMSTAR 2: not assessed
SoF tableOnly the outcomes this review put in its Summary of Findings table are listed (the Cochrane Handbook caps them at about seven per comparison). Its other analyses are not shown here.
Questions
9
current version
GRADE rated
5
No studies
4
Included studies
NR
No studies 4 · 44.4%Ungraded 0 · 0%Very low 0 · 0%Low 5 · 55.6%Moderate 0 · 0%High 0 · 0%

Ungraded means an effect was reported without a GRADE rating; it is not a gap. No studies means the review found nothing to answer the question. The six categories are a display order, not a score.

Questions and results

Non‐pharmacological interventions for treating acute high altitude illness

Population: people suffering from high altitude illness
5 questions
OutcomeEffectEvidenceStatus / GRADE
Outcomes and intervention
no estimate extractedNRNo studies
All‐cause mortality
no estimate extractedNRNo studies
Complete relief of AMS symptoms
no estimate extractedNRNo studies
Reduction in symptom score severity at 12 hours (Clinical score: ranged from 0 to 11 (worse)) Intervention: Simulated descent of 193 millibars versus 20 millibars
no estimate extracted1 study · 64 participantsLow
Downgraded: risk of bias, imprecision
Adverse effects during treatment Intervention: Hyperbaric chamber/ 160 millibars versus supplementary oxygen
no estimate extracted1 study · 29 participantsLow
Downgraded: risk of bias, imprecision

Pharmacological interventions for treating acute high altitude illness

Population: people suffering from high altitude illness
4 questions
OutcomeEffectEvidenceStatus / GRADE
All‐cause mortality
no estimate extractedNRNo studies
Complete relief of AMS symptoms (12 to 16 hours after treatment) Scale used: Acute Mountain Sickness score (ranged from 0 to 9 (worse))
no estimate extracted1 study · 35 participantsLow
Downgraded: risk of bias
Reduction in symptom score severity Time of measurement: 1 to 48 hours after treatment, end of treatment Scale of measurement: Self‐administered AMS questionnaires (ranged from 0 to 90 (worse)), AMS Symptom Questionnaire (ranged from 0 to 22 (wors...
Mean Difference 1.152 studies · 25 participantsLow
Downgraded: risk of bias, imprecision, inconsistency
Adverse effects Time of measurement: 1 to 48 hours after treatment, end of treatment Scale of measurement:not stated
no estimate extracted1 study · 25 participantsLow
Downgraded: risk of bias, imprecision, inconsistency