However, it is difficult to compare these data, as the study methods differ and no other studies used clients of a travel clinic as a research population. We found a significantly higher risk for women, which confirms the results of Dallimore, Gaillard, and Murdoch, although several other studies found both sexes to be equally affected or even that women
were less affected.4,15–17 Like many previous studies we found that a high maximum overnight altitude and a prior history of AMS are important risk factors, while the risk decreases with age and days of acclimatization at a moderate altitude.4,18–21 Hackett and others found that the rate of altitude increase is an important factor.18,22 Although we also found a significant association between the average increase in altitude and AMS incidence in a univariate analysis, multivariate analysis showed that it was not an independent risk factor. The risk increase related to a higher CAL-101 nmr average climbing rate was in fact due to the higher maximum altitude that was associated with it. Our results confirm those of Wagner, as he too found that the rate of ascent
was not significant.19 Similarly, Davies in his observational study on the Kilimanjaro showed that an extra resting day at 3,700 m (which reduced the average ascent rate) did this website not decrease the risk of AMS.23 We found no higher risk for cardiopulmonary conditions, which confirms Hackett’s results that hypertension and mild chronic obstructive pulmonary disease do not appear to affect the susceptibility Tideglusib to AMS.11 Although most of our travelers reported to have read and understood the information, many did not follow the advice we stressed the most: do not climb further while having AMS symptoms. This might be due, at least partially, to a relatively fixed itinerary, especially in organized groups, as Murdoch argues.12 The fact that the mean climbing rate was higher than advised may be because of a shortage of suitable sleeping places, especially at very high altitude (>3,500 m). Compared with the Paz study, more of our travelers brought acetazolamide along, but fewer actually took
it when AMS developed.5 Clinical trials proved the preventive effect of acetazolamide. However, Hacket found that acetazolamide 250 mg bid taken at 3,440 m for 4 days reduced AMS incidence in those who climbed 2,800 m, but not in those who hiked up there from Katmandu.18 Davies found that acetazolamide prevention in doses ranging from 250 to 750 mg/d reduced the incidence of AMS in trekkers on the Kilimanjaro who took the 5-day ascent, but not in trekkers who took the 4-day ascent.23 Regarding the low dose, Basnyat and colleagues demonstrated a preventive effect of 125 mg acetazolamide bid, started at 3,440 and 4,243 m, respectively, in trekkers who were already several days at high altitude and who did not have any symptoms of AMS until then.
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