Effects of Safflower Yellow on the Treatment of Severe Sepsis and Septic Shock: A Randomized Controlled Clinical Trial
Objective. To evaluate the clinical effect of safflower yellow on the treatment of severe sepsis and septic shock. Methods. 85 patients with severe sepsis and septic shock were randomly selected to receive either therapy according to the international guidelines for management of severe sepsis and s...
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Series: | Evidence-Based Complementary and Alternative Medicine |
Online Access: | http://dx.doi.org/10.1155/2016/3948795 |
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doaj-f179bc8c5d714fdd98d6b748d6f8dd2d2020-11-24T21:47:08ZengHindawi LimitedEvidence-Based Complementary and Alternative Medicine1741-427X1741-42882016-01-01201610.1155/2016/39487953948795Effects of Safflower Yellow on the Treatment of Severe Sepsis and Septic Shock: A Randomized Controlled Clinical TrialXiao-jin Li0Ru-rong Wang1Yan Kang2Jin Liu3Yun-xia Zuo4Xue-feng Zeng5Gong Cheng6Department of Anesthesiology, West China Hospital of Sichuan University, Chengdu 610041, ChinaDepartment of Anesthesiology, West China Hospital of Sichuan University, Chengdu 610041, ChinaDepartment of Intensive Care Unit, West China Hospital of Sichuan University, Chengdu 610041, ChinaDepartment of Anesthesiology, West China Hospital of Sichuan University, Chengdu 610041, ChinaDepartment of Anesthesiology, West China Hospital of Sichuan University, Chengdu 610041, ChinaDepartment of Respiratory Medicine, The People’s Hospital of Pujiang County, Sichuan 611630, ChinaDepartment of Nephrology, The People’s Hospital of Pujiang County, Sichuan 611630, ChinaObjective. To evaluate the clinical effect of safflower yellow on the treatment of severe sepsis and septic shock. Methods. 85 patients with severe sepsis and septic shock were randomly selected to receive either therapy according to the international guidelines for management of severe sepsis and septic shock (Surviving Sepsis Campaign 2012) (control group, n = 45) or conventional therapy plus safflower yellow (study group, n = 40). The 28-day mortality and 28-day Kaplan-Meier survival curves were compared as primary outcomes. Results. The 28-day mortality from all causes and in-hospital mortality were significantly lower in the study group (50%, 17.5%) as compared to the control group (78.58%, 54.76%) (P = 0.007, all causes, P < 0.001, in-hospital), and the 28-day Kaplan-Meier survival curve was higher in the study group than in the control group (P = 0.008, all causes, P < 0.001, in-hospital, Log Rank). 72 hours after treatment, secondary outcomes including heart rate, leukocyte counts, lactate levels, and platelet counts of patients in the study group were ameliorated significantly as compared with the control group. Conclusion. This study offers a potential new strategy employing safflower yellow to more effectively treat patients with severe sepsis and septic shock. This trial is registered with identifier ChiCTR-TRC-14005196.http://dx.doi.org/10.1155/2016/3948795 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xiao-jin Li Ru-rong Wang Yan Kang Jin Liu Yun-xia Zuo Xue-feng Zeng Gong Cheng |
spellingShingle |
Xiao-jin Li Ru-rong Wang Yan Kang Jin Liu Yun-xia Zuo Xue-feng Zeng Gong Cheng Effects of Safflower Yellow on the Treatment of Severe Sepsis and Septic Shock: A Randomized Controlled Clinical Trial Evidence-Based Complementary and Alternative Medicine |
author_facet |
Xiao-jin Li Ru-rong Wang Yan Kang Jin Liu Yun-xia Zuo Xue-feng Zeng Gong Cheng |
author_sort |
Xiao-jin Li |
title |
Effects of Safflower Yellow on the Treatment of Severe Sepsis and Septic Shock: A Randomized Controlled Clinical Trial |
title_short |
Effects of Safflower Yellow on the Treatment of Severe Sepsis and Septic Shock: A Randomized Controlled Clinical Trial |
title_full |
Effects of Safflower Yellow on the Treatment of Severe Sepsis and Septic Shock: A Randomized Controlled Clinical Trial |
title_fullStr |
Effects of Safflower Yellow on the Treatment of Severe Sepsis and Septic Shock: A Randomized Controlled Clinical Trial |
title_full_unstemmed |
Effects of Safflower Yellow on the Treatment of Severe Sepsis and Septic Shock: A Randomized Controlled Clinical Trial |
title_sort |
effects of safflower yellow on the treatment of severe sepsis and septic shock: a randomized controlled clinical trial |
publisher |
Hindawi Limited |
series |
Evidence-Based Complementary and Alternative Medicine |
issn |
1741-427X 1741-4288 |
publishDate |
2016-01-01 |
description |
Objective. To evaluate the clinical effect of safflower yellow on the treatment of severe sepsis and septic shock. Methods. 85 patients with severe sepsis and septic shock were randomly selected to receive either therapy according to the international guidelines for management of severe sepsis and septic shock (Surviving Sepsis Campaign 2012) (control group, n = 45) or conventional therapy plus safflower yellow (study group, n = 40). The 28-day mortality and 28-day Kaplan-Meier survival curves were compared as primary outcomes. Results. The 28-day mortality from all causes and in-hospital mortality were significantly lower in the study group (50%, 17.5%) as compared to the control group (78.58%, 54.76%) (P = 0.007, all causes, P < 0.001, in-hospital), and the 28-day Kaplan-Meier survival curve was higher in the study group than in the control group (P = 0.008, all causes, P < 0.001, in-hospital, Log Rank). 72 hours after treatment, secondary outcomes including heart rate, leukocyte counts, lactate levels, and platelet counts of patients in the study group were ameliorated significantly as compared with the control group. Conclusion. This study offers a potential new strategy employing safflower yellow to more effectively treat patients with severe sepsis and septic shock. This trial is registered with identifier ChiCTR-TRC-14005196. |
url |
http://dx.doi.org/10.1155/2016/3948795 |
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