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Sertraline plus deanxit to treat patients with depression and anxiety in chronic somatic diseases: a randomized controlled trial
BACKGROUND: Patients in chronic somatic diseases are often accompanied with depression and anxiety, remission of which may be observed in the third or fourth week after applying common antidepressant medications. We investigate the efficacy and safety of sertraline plus deanxit on patients with depr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4403889/ https://www.ncbi.nlm.nih.gov/pubmed/25879863 http://dx.doi.org/10.1186/s12888-015-0449-2 |
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author | Wang, Limin Zhong, Zhuoyuan Hu, Jingyang Rong, Xiaoming Liu, Jun Xiao, Songhua Liu, Zhonglin |
author_facet | Wang, Limin Zhong, Zhuoyuan Hu, Jingyang Rong, Xiaoming Liu, Jun Xiao, Songhua Liu, Zhonglin |
author_sort | Wang, Limin |
collection | PubMed |
description | BACKGROUND: Patients in chronic somatic diseases are often accompanied with depression and anxiety, remission of which may be observed in the third or fourth week after applying common antidepressant medications. We investigate the efficacy and safety of sertraline plus deanxit on patients with depression and anxiety in chronic somatic diseases. METHODS: 75 Patients who met the criteria were randomly assigned to deanxit group or placebo group: sertraline (75 mg/day) plus deanxit (one piece/day) (N = 38), or sertraline (75 mg/day) plus placebo (one piece/day) (N = 37) for 2 weeks, both groups received sertraline (75 mg/day) in the following 2 weeks. Changes from baseline to day 4, day 8, day 15, and day 29 in Hamilton Rating Scale for Depression (HAM-D) and Hamilton Rating Scale for Anxiety (HAM-A) total scores were the efficacy measures. Adverse events were monitored and registered systematically during the trial. RESULTS: Response rates for HAM-D scores in deanxit group and placebo group were significantly different on day 8(55.26% ± 2.56% VS 24.32% ± 2.19%, p = 0.006) and day 15(78.95% ± 3.89% VS 40.54% ± 4.18%, p = 0.001), while no statistical differences were observed on day 4 and day 29. Respectively, response rates for HAM-A scores on day 4 (34.21% ± 2.21% VS 8.11% ± 1.37%, p = 0.006), day 8 (57.89% ± 3.56% VS 18.92% ± 2.68%, p = 0.001) and day 15 (78.95% ± 4.37% VS 43.24% ± 4.68%, p = 0.002), favoring the deanxit group. However, HAM-A scores were not remarkably different at the end point. The overall safety profile of both groups was favorable with no distinct differences. CONCLUSIONS: The efficacy was exhibited in the deanxit group, with evidence for similar safety. The rapid onset of sertraline plus short-term deanxit indicated that it might be an inspiring strategy to manage depression and anxiety within the first two weeks in chronic somatic diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12888-015-0449-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4403889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44038892015-04-21 Sertraline plus deanxit to treat patients with depression and anxiety in chronic somatic diseases: a randomized controlled trial Wang, Limin Zhong, Zhuoyuan Hu, Jingyang Rong, Xiaoming Liu, Jun Xiao, Songhua Liu, Zhonglin BMC Psychiatry Research Article BACKGROUND: Patients in chronic somatic diseases are often accompanied with depression and anxiety, remission of which may be observed in the third or fourth week after applying common antidepressant medications. We investigate the efficacy and safety of sertraline plus deanxit on patients with depression and anxiety in chronic somatic diseases. METHODS: 75 Patients who met the criteria were randomly assigned to deanxit group or placebo group: sertraline (75 mg/day) plus deanxit (one piece/day) (N = 38), or sertraline (75 mg/day) plus placebo (one piece/day) (N = 37) for 2 weeks, both groups received sertraline (75 mg/day) in the following 2 weeks. Changes from baseline to day 4, day 8, day 15, and day 29 in Hamilton Rating Scale for Depression (HAM-D) and Hamilton Rating Scale for Anxiety (HAM-A) total scores were the efficacy measures. Adverse events were monitored and registered systematically during the trial. RESULTS: Response rates for HAM-D scores in deanxit group and placebo group were significantly different on day 8(55.26% ± 2.56% VS 24.32% ± 2.19%, p = 0.006) and day 15(78.95% ± 3.89% VS 40.54% ± 4.18%, p = 0.001), while no statistical differences were observed on day 4 and day 29. Respectively, response rates for HAM-A scores on day 4 (34.21% ± 2.21% VS 8.11% ± 1.37%, p = 0.006), day 8 (57.89% ± 3.56% VS 18.92% ± 2.68%, p = 0.001) and day 15 (78.95% ± 4.37% VS 43.24% ± 4.68%, p = 0.002), favoring the deanxit group. However, HAM-A scores were not remarkably different at the end point. The overall safety profile of both groups was favorable with no distinct differences. CONCLUSIONS: The efficacy was exhibited in the deanxit group, with evidence for similar safety. The rapid onset of sertraline plus short-term deanxit indicated that it might be an inspiring strategy to manage depression and anxiety within the first two weeks in chronic somatic diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12888-015-0449-2) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-14 /pmc/articles/PMC4403889/ /pubmed/25879863 http://dx.doi.org/10.1186/s12888-015-0449-2 Text en © Wang et al.; licensee BioMed Central. 2015 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Wang, Limin Zhong, Zhuoyuan Hu, Jingyang Rong, Xiaoming Liu, Jun Xiao, Songhua Liu, Zhonglin Sertraline plus deanxit to treat patients with depression and anxiety in chronic somatic diseases: a randomized controlled trial |
title | Sertraline plus deanxit to treat patients with depression and anxiety in chronic somatic diseases: a randomized controlled trial |
title_full | Sertraline plus deanxit to treat patients with depression and anxiety in chronic somatic diseases: a randomized controlled trial |
title_fullStr | Sertraline plus deanxit to treat patients with depression and anxiety in chronic somatic diseases: a randomized controlled trial |
title_full_unstemmed | Sertraline plus deanxit to treat patients with depression and anxiety in chronic somatic diseases: a randomized controlled trial |
title_short | Sertraline plus deanxit to treat patients with depression and anxiety in chronic somatic diseases: a randomized controlled trial |
title_sort | sertraline plus deanxit to treat patients with depression and anxiety in chronic somatic diseases: a randomized controlled trial |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4403889/ https://www.ncbi.nlm.nih.gov/pubmed/25879863 http://dx.doi.org/10.1186/s12888-015-0449-2 |
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