Background: There are several studies indicating a correlation between trea
tment with hydroxyethyl starch (HES) and pruritus. In order to see whether
there is a possible dose-response relationship between HES and pruritus, we
retrospectively studied 50 patients who had received HES in varying doses
(cumulative dose 500-19500 ml) as hemodilution therapy after subarachnoid h
emorrhage.
Methods: Of 50 consecutive patients, 6 were excluded due to severe neurolog
ical sequelae. A questionnaire was sent to the remaining 44 patients at 6 m
onths (5-12 months) median (range) after the end of HES treatment.
Results: We received answers from 37 patients, of whom 54% reported pruritu
s. On average pruritus lasted for 15 weeks. There was significantly more pr
uritus in patients who received more than 5000 ml of HES versus those who r
eceived less than 5000 ml (1)= 0.023). Pruritus had a delayed onset and app
eared as pruritic crises lasting for 2-30 min. It had a patchy distribution
in most patients and no predilected locations. In 4 patients (20%) the pru
ritus lasted longer than 21 weeks.
Conclusion: Our study indicates that there is a dose-dependency for the inc
idence of HES-induced pruritus, and that in some cases the pruritus may he
severe and long-lasting.