WHO monographs on selected medicinal plants - travolekar.ru
WHO monographs on selected medicinal plants - travolekar.ru
WHO monographs on selected medicinal plants - travolekar.ru
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Cortex Salicis<br />
Daily c<strong>on</strong>sumpti<strong>on</strong> of the extract with 240.0 mg salicin per day affected<br />
platelet aggregati<strong>on</strong> to a lesser extent than acetylsalicylate (27).<br />
Chr<strong>on</strong>ic lower back pain<br />
Standardized extracts of the bark exhibited analgesic effects similar to<br />
those of higher doses of acetylsalicylic acid. A daily dose of 1572.0 mg of<br />
an extract of the c<strong>ru</strong>de d<strong>ru</strong>g (standardized to 15.2% salicin or 240.0 mg<br />
salicin per day) was superior to placebo in the treatment of pain in patients<br />
with osteoarthritis of the hip and the knee, and in patients with<br />
exacerbati<strong>on</strong>s of chr<strong>on</strong>ic low back pain. In two open studies, unspecified<br />
extracts of the c<strong>ru</strong>de d<strong>ru</strong>g exhibited similar efficacy to the normal treatment<br />
regime of n<strong>on</strong>steroidal antirheumatic d<strong>ru</strong>gs and the efficacy was<br />
similar to that of refecoxib (18).<br />
A randomized placebo-c<strong>on</strong>trolled clinical study evaluated the efficacy<br />
of a willow bark extract in 210 patients with chr<strong>on</strong>ic lower back pain. The<br />
patients were assigned to receive an orally administered willow bark extract<br />
with either 120.0 mg (low dose) or 240.0 mg (high dose) of salicin, or<br />
a placebo, with tramadol as the sole rescue medicati<strong>on</strong>, in the 4-week trial.<br />
The principal outcome measure was the proporti<strong>on</strong> of patients who were<br />
pain-free without tramadol for at least 5 days during the final week of the<br />
study. A total of 191 patients completed the study. The number of painfree<br />
patients in the last week of treatment was 27 (39%) of 65 in the group<br />
receiving high-dose extract, 15 (21%) of 67 in the group receiving lowdose<br />
extract, and 4 (6%) of 59 in the group treated with placebo (p < 0.001).<br />
The resp<strong>on</strong>se in the group treated with the high dose was evident after<br />
<strong>on</strong>ly 1 week of treatment. Significantly more patients in the group receiving<br />
the placebo required tramadol during each week of the study<br />
(p < 0.001). One patient in the treatment group suffered a severe allergic<br />
reacti<strong>on</strong> (14).<br />
An open, n<strong>on</strong>-randomized study (postmarketing surveillance) assessed<br />
the efficacy of an extract of the c<strong>ru</strong>de d<strong>ru</strong>g in three groups of patients aged<br />
18–80 years presenting over an 18-m<strong>on</strong>th period with acute exacerbati<strong>on</strong>s<br />
of low back pain. The first group of 115 patients was prescribed a daily<br />
dose of the extract c<strong>on</strong>taining 120.0 mg of salicin. A sec<strong>on</strong>d group of<br />
112 patients was prescribed the extract equivalent to 240.0 mg salicin per<br />
day. A third “c<strong>on</strong>trol” or “comparator” group of 224 patients received<br />
c<strong>on</strong>venti<strong>on</strong>al therapy. In the patients who had received c<strong>on</strong>venti<strong>on</strong>al therapy,<br />
the exacerbati<strong>on</strong>s had been shorter but the pain was more intense as<br />
judged by Arhus Index and Total Pain Index. After 4 weeks of treatment,<br />
about 40% of patients in the group treated with the extract equivalent to<br />
240 mg salicin per day were free of pain. In the group treated with extract<br />
c<strong>on</strong>taining 120.0 mg of salicin, as a whole, about 19% of patients were<br />
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