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收稿:2020-05-08,
纸质出版:2020-10-15
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曾媛, 孙建海. 度洛西汀和帕罗西汀联合羟考酮缓释片治疗晚期癌痛伴抑郁的疗效比较[J]. 第三军医大学学报, 2020,42(19):1890-1897.
Yuan ZENG, Jianhai SUN. Curative effect of oxycodone sustained-release tablets combined with duloxetine versus paroxetine in treatment of depression and pain from advanced cancer[J]. Journal of Third Military Medical University, 2020, 42(19): 1890-1897.
曾媛, 孙建海. 度洛西汀和帕罗西汀联合羟考酮缓释片治疗晚期癌痛伴抑郁的疗效比较[J]. 第三军医大学学报, 2020,42(19):1890-1897. DOI: 10.16016/j.1000-5404.202005052.
Yuan ZENG, Jianhai SUN. Curative effect of oxycodone sustained-release tablets combined with duloxetine versus paroxetine in treatment of depression and pain from advanced cancer[J]. Journal of Third Military Medical University, 2020, 42(19): 1890-1897. DOI: 10.16016/j.1000-5404.202005052.
Objective
2
To investigate the efficacy and safety of oxycodone sustained-release tablets combined with different types of antidepressants (duloxetine and paroxetine) in the patients suffering from depression and pain due to advanced cancer.
Methods
2
A total of 108 depressive patients with advanced cancer pain in admitted in Hubei Third People's Hospital from July 2018 to September 2019 were recruited in this study. They were divided into 3 groups single-blindly and randomly
with 36 subjects in each group. The patients from Group A were given oxycodone sustained-release tablets only
those out of Group B the tablets+paroxetine
and those of Group C the tablets+duloxetine. Pain relief
depression
anxiety
dose of oxycodone
sleep quality
quality of life and adverse reactions were compared among the 3 groups after treatment.
Results
2
After treatment of 1 week
the numeric rating scale (NRS) score of Group C was significantly lower than those of Group B and A (
P
<
0.05). The NRS score and self-rating anxiety scale (SAS) score at 2 weeks after treatment
and the self-rating depression scale (SDS) score at 1 week after treatment were significantly decreased in a trend from Group A to Group B to Group C (all
P
<
0.05). But the
re were no obvious differences in the NRS
SAS and SDS scores at 1 and 2 months after treatment
and the SDS score at 2 weeks after treatment between Group C and B (
P
>
0. 05)
and all of these scores were notably lower than those of Group A (
P
<
0. 05). After treatment of 2 months
the average daily oral dose of oxycodone per capita in Group A and B were significantly higher than that before treatment (
P
<
0.05)
but no such difference was seen in Group C (
P
>
0.05). The score of Pittsburgh sleep quality index (PSQI) were remarkably decreased in the 3 groups after treatment (
P
<
0.05). But no significant differences were seen in the average daily oral dose of oxycodone per capita and the PSQI score between Group B and C
but the dose and score were both significantly lower than those of Group A (
P
<
0.05). In 2 months after treatment
the scores of different items of quality of life score were significantly increased in the 3 groups (
P
<
0.05)
but except for the role function score
there were no differences in other scores between Group C and B (
P
>
0.05)
and the scores were significantly higher than those of Group A (
P
<
0.05). After treatment of 2 months
the adverse reactions had no significant differences among the 3 groups (
P
>
0.05)
and were gradually reduced or disappeared after symptomatic treatment or dose adjustment.
Conclusion
2
In the treatment of depressive patients with pain from advanced cancer
oxycodone sustained-release tablets combined with duloxetine is superior to paroxetine in quick onset
effective improvement of pain
depression
anxiety and quality of sleep and life
and reduced dose of oxycodone
and does not increase adverse reactions.
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