Reevaluating the Role of Corticosteroids in Septic Shock: An Updated Meta-Analysis of Randomized Controlled Trials

What Is Known and Objective. To reevaluate the benefits and risks of corticosteroid treatment in adult patients with septic shock. Methods. This study was performed based on PRISMA guidelines. Randomized controlled trials (RCTs) of corticosteroids versus placebo were retrieved from PubMed, MEDLINE,...

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Veröffentlicht in:BioMed research international 2019-01, Vol.2019 (2019), p.1-14
Hauptverfasser: Wang, S.-H., Liu, Yuanhui, Qin, T.-H., Lian, Z.-Z., Wei, Y.-X., Cao, Y.-S., Huang, D.-Z., Lian, X.-J., He, Pengcheng
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container_end_page 14
container_issue 2019
container_start_page 1
container_title BioMed research international
container_volume 2019
creator Wang, S.-H.
Liu, Yuanhui
Qin, T.-H.
Lian, Z.-Z.
Wei, Y.-X.
Cao, Y.-S.
Huang, D.-Z.
Lian, X.-J.
He, Pengcheng
description What Is Known and Objective. To reevaluate the benefits and risks of corticosteroid treatment in adult patients with septic shock. Methods. This study was performed based on PRISMA guidelines. Randomized controlled trials (RCTs) of corticosteroids versus placebo were retrieved from PubMed, MEDLINE, EMBASE, Web of Science, the Cochrane Central RCTs, and ClinicalTrials.gov from January 1980 to April 2018. We also conducted a trial sequential analysis to indicate the possibility of type I or II errors and calculate the information size. Grading of Recommendations, Assessment, Development and Evaluation approach (GRADE) was applying to assess the certainty of evidence at the primary outcome level. Results. Twenty-one RCTs were identified and analyzed. Patients treated with corticosteroid had a 7% reduction in relative risk in 28-day all-cause mortality compared to controls (RR 0.93, 95% CI 0.88 to 0.99). However, there were no significant differences for the intensive care unit (ICU) mortality (RR 0.97, 95% CI 0.86 to 1.09) or in-hospital mortality (RR 1.01, 95% CI 0.92 to 1.11). Corticosteroids shortened the length of ICU stay by 1.04 days (RR -1.04, 95% CI -1.72 to -0.36) and the length of hospital stay by 2.49 days (RR -2.49, 95% CI -4.96 to -0.02). Corticosteroids increased the risk of hyperglycemia (RR 1.11, 95% CI 1.06 to 1.16) but not gastroduodenal bleeding (RR 1.06, 95% CI 0.82 to 1.37) or superinfection (RR 1.04, 95% CI 0.94 to 1.15). However, some date on secondary outcomes were unavailable because they were not measured or not reported in the included studies which may cause a lack of power or selective outcome reporting. The information size was calculated at 10044 patients. Trial sequential analysis showed that the meta-analysis was conclusive and the risk of type 2 error was minimal. What Is New and Conclusion. Corticosteroids are likely to be effective in reducing 28-day mortality and attenuating septic shock without increasing the rate of life-threatening complications. TSA showed that the risk of type II error in this meta-analysis was minimal and the result was conclusive.
doi_str_mv 10.1155/2019/3175047
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To reevaluate the benefits and risks of corticosteroid treatment in adult patients with septic shock. Methods. This study was performed based on PRISMA guidelines. Randomized controlled trials (RCTs) of corticosteroids versus placebo were retrieved from PubMed, MEDLINE, EMBASE, Web of Science, the Cochrane Central RCTs, and ClinicalTrials.gov from January 1980 to April 2018. We also conducted a trial sequential analysis to indicate the possibility of type I or II errors and calculate the information size. Grading of Recommendations, Assessment, Development and Evaluation approach (GRADE) was applying to assess the certainty of evidence at the primary outcome level. Results. Twenty-one RCTs were identified and analyzed. Patients treated with corticosteroid had a 7% reduction in relative risk in 28-day all-cause mortality compared to controls (RR 0.93, 95% CI 0.88 to 0.99). However, there were no significant differences for the intensive care unit (ICU) mortality (RR 0.97, 95% CI 0.86 to 1.09) or in-hospital mortality (RR 1.01, 95% CI 0.92 to 1.11). Corticosteroids shortened the length of ICU stay by 1.04 days (RR -1.04, 95% CI -1.72 to -0.36) and the length of hospital stay by 2.49 days (RR -2.49, 95% CI -4.96 to -0.02). Corticosteroids increased the risk of hyperglycemia (RR 1.11, 95% CI 1.06 to 1.16) but not gastroduodenal bleeding (RR 1.06, 95% CI 0.82 to 1.37) or superinfection (RR 1.04, 95% CI 0.94 to 1.15). However, some date on secondary outcomes were unavailable because they were not measured or not reported in the included studies which may cause a lack of power or selective outcome reporting. The information size was calculated at 10044 patients. Trial sequential analysis showed that the meta-analysis was conclusive and the risk of type 2 error was minimal. What Is New and Conclusion. Corticosteroids are likely to be effective in reducing 28-day mortality and attenuating septic shock without increasing the rate of life-threatening complications. TSA showed that the risk of type II error in this meta-analysis was minimal and the result was conclusive.</description><identifier>ISSN: 2314-6133</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2019/3175047</identifier><identifier>PMID: 31281831</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Adrenal Cortex Hormones - adverse effects ; Adrenal Cortex Hormones - therapeutic use ; Adrenal glands ; Analysis ; Bleeding ; Care and treatment ; Clinical trials ; Complications ; Corticoids ; Corticosteroids ; Error analysis ; Evaluation ; Female ; Fludrocortisone ; Health aspects ; Humans ; Hyperglycemia ; Intensive Care Units ; Length of Stay ; Male ; Mathematical analysis ; Meta-analysis ; Middle Aged ; Mortality ; Patients ; Publication Bias ; Quality ; Randomization ; Randomized Controlled Trials as Topic ; Respiration, Artificial ; Review ; Risk ; Risk Factors ; Sepsis ; Septic shock ; Sequential analysis ; Shock, Septic - drug therapy ; Shock, Septic - mortality ; Superinfection ; Systematic review</subject><ispartof>BioMed research international, 2019-01, Vol.2019 (2019), p.1-14</ispartof><rights>Copyright © 2019 X.-J. Lian et al.</rights><rights>COPYRIGHT 2019 John Wiley &amp; Sons, Inc.</rights><rights>Copyright © 2019 X.-J. Lian et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2019 X.-J. Lian et al. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-d7d88d57ba983237ec86762b419a4c22cf27099437b20f2b66980c897447e83</citedby><cites>FETCH-LOGICAL-c499t-d7d88d57ba983237ec86762b419a4c22cf27099437b20f2b66980c897447e83</cites><orcidid>0000-0003-0317-1203 ; 0000-0001-6103-2493</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6590573/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6590573/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31281831$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Inaba, Hideo</contributor><contributor>Hideo Inaba</contributor><creatorcontrib>Wang, S.-H.</creatorcontrib><creatorcontrib>Liu, Yuanhui</creatorcontrib><creatorcontrib>Qin, T.-H.</creatorcontrib><creatorcontrib>Lian, Z.-Z.</creatorcontrib><creatorcontrib>Wei, Y.-X.</creatorcontrib><creatorcontrib>Cao, Y.-S.</creatorcontrib><creatorcontrib>Huang, D.-Z.</creatorcontrib><creatorcontrib>Lian, X.-J.</creatorcontrib><creatorcontrib>He, Pengcheng</creatorcontrib><title>Reevaluating the Role of Corticosteroids in Septic Shock: An Updated Meta-Analysis of Randomized Controlled Trials</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><description>What Is Known and Objective. To reevaluate the benefits and risks of corticosteroid treatment in adult patients with septic shock. Methods. This study was performed based on PRISMA guidelines. Randomized controlled trials (RCTs) of corticosteroids versus placebo were retrieved from PubMed, MEDLINE, EMBASE, Web of Science, the Cochrane Central RCTs, and ClinicalTrials.gov from January 1980 to April 2018. We also conducted a trial sequential analysis to indicate the possibility of type I or II errors and calculate the information size. Grading of Recommendations, Assessment, Development and Evaluation approach (GRADE) was applying to assess the certainty of evidence at the primary outcome level. Results. Twenty-one RCTs were identified and analyzed. Patients treated with corticosteroid had a 7% reduction in relative risk in 28-day all-cause mortality compared to controls (RR 0.93, 95% CI 0.88 to 0.99). However, there were no significant differences for the intensive care unit (ICU) mortality (RR 0.97, 95% CI 0.86 to 1.09) or in-hospital mortality (RR 1.01, 95% CI 0.92 to 1.11). Corticosteroids shortened the length of ICU stay by 1.04 days (RR -1.04, 95% CI -1.72 to -0.36) and the length of hospital stay by 2.49 days (RR -2.49, 95% CI -4.96 to -0.02). Corticosteroids increased the risk of hyperglycemia (RR 1.11, 95% CI 1.06 to 1.16) but not gastroduodenal bleeding (RR 1.06, 95% CI 0.82 to 1.37) or superinfection (RR 1.04, 95% CI 0.94 to 1.15). However, some date on secondary outcomes were unavailable because they were not measured or not reported in the included studies which may cause a lack of power or selective outcome reporting. The information size was calculated at 10044 patients. Trial sequential analysis showed that the meta-analysis was conclusive and the risk of type 2 error was minimal. What Is New and Conclusion. Corticosteroids are likely to be effective in reducing 28-day mortality and attenuating septic shock without increasing the rate of life-threatening complications. TSA showed that the risk of type II error in this meta-analysis was minimal and the result was conclusive.</description><subject>Adrenal Cortex Hormones - adverse effects</subject><subject>Adrenal Cortex Hormones - therapeutic use</subject><subject>Adrenal glands</subject><subject>Analysis</subject><subject>Bleeding</subject><subject>Care and treatment</subject><subject>Clinical trials</subject><subject>Complications</subject><subject>Corticoids</subject><subject>Corticosteroids</subject><subject>Error analysis</subject><subject>Evaluation</subject><subject>Female</subject><subject>Fludrocortisone</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Hyperglycemia</subject><subject>Intensive Care Units</subject><subject>Length of Stay</subject><subject>Male</subject><subject>Mathematical analysis</subject><subject>Meta-analysis</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Patients</subject><subject>Publication Bias</subject><subject>Quality</subject><subject>Randomization</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Respiration, Artificial</subject><subject>Review</subject><subject>Risk</subject><subject>Risk Factors</subject><subject>Sepsis</subject><subject>Septic shock</subject><subject>Sequential analysis</subject><subject>Shock, Septic - drug therapy</subject><subject>Shock, Septic - mortality</subject><subject>Superinfection</subject><subject>Systematic review</subject><issn>2314-6133</issn><issn>2314-6141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkctvEzEQxlcIRKvQG2dkiQsSLPX7wQEpinhJRUhJOVterzdxcexgb4rKX49XCSlwwpcZeX7-PDNf0zxF8DVCjF1iiNQlQYJBKh4055gg2nJE0cNTTshZc1HKDaxHIg4Vf9ycEYQlkgSdN3np3K0JezP6uAbjxoFlCg6kASxSHr1NZXQ5-b4AH8HK7eoVWG2S_fYGzCP4uuvN6Hrw2Y2mnUcT7oov0-OliX3a-p-1tkhxzCmEml5nb0J50jwaanAXxzhrVu_fXS8-tldfPnxazK9aS5Ua2170UvZMdEZJgolwVnLBcUeRMtRibAcsoFKUiA7DAXecKwmtVIJS4SSZNW8Pqrt9t3W9dbULE_Qu-63JdzoZr_-uRL_R63SrOVOQCVIFXhwFcvq-d2XUW1-sC8FEl_ZFY8yIxEyqCX3-D3qT9rmuY6Ioo7y6xO-ptQlO-zik-q-dRPWcIwwJZFVy1rw6UDanUrIbTi0jqCfP9eS5Pnpe8Wd_jnmCfztcgZcHYONjb374_5RzlXGDuacRphQL8gu9DbvS</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Wang, S.-H.</creator><creator>Liu, Yuanhui</creator><creator>Qin, T.-H.</creator><creator>Lian, Z.-Z.</creator><creator>Wei, Y.-X.</creator><creator>Cao, Y.-S.</creator><creator>Huang, D.-Z.</creator><creator>Lian, X.-J.</creator><creator>He, Pengcheng</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</general><general>John Wiley &amp; 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To reevaluate the benefits and risks of corticosteroid treatment in adult patients with septic shock. Methods. This study was performed based on PRISMA guidelines. Randomized controlled trials (RCTs) of corticosteroids versus placebo were retrieved from PubMed, MEDLINE, EMBASE, Web of Science, the Cochrane Central RCTs, and ClinicalTrials.gov from January 1980 to April 2018. We also conducted a trial sequential analysis to indicate the possibility of type I or II errors and calculate the information size. Grading of Recommendations, Assessment, Development and Evaluation approach (GRADE) was applying to assess the certainty of evidence at the primary outcome level. Results. Twenty-one RCTs were identified and analyzed. Patients treated with corticosteroid had a 7% reduction in relative risk in 28-day all-cause mortality compared to controls (RR 0.93, 95% CI 0.88 to 0.99). However, there were no significant differences for the intensive care unit (ICU) mortality (RR 0.97, 95% CI 0.86 to 1.09) or in-hospital mortality (RR 1.01, 95% CI 0.92 to 1.11). Corticosteroids shortened the length of ICU stay by 1.04 days (RR -1.04, 95% CI -1.72 to -0.36) and the length of hospital stay by 2.49 days (RR -2.49, 95% CI -4.96 to -0.02). Corticosteroids increased the risk of hyperglycemia (RR 1.11, 95% CI 1.06 to 1.16) but not gastroduodenal bleeding (RR 1.06, 95% CI 0.82 to 1.37) or superinfection (RR 1.04, 95% CI 0.94 to 1.15). However, some date on secondary outcomes were unavailable because they were not measured or not reported in the included studies which may cause a lack of power or selective outcome reporting. The information size was calculated at 10044 patients. Trial sequential analysis showed that the meta-analysis was conclusive and the risk of type 2 error was minimal. What Is New and Conclusion. Corticosteroids are likely to be effective in reducing 28-day mortality and attenuating septic shock without increasing the rate of life-threatening complications. TSA showed that the risk of type II error in this meta-analysis was minimal and the result was conclusive.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>31281831</pmid><doi>10.1155/2019/3175047</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-0317-1203</orcidid><orcidid>https://orcid.org/0000-0001-6103-2493</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adrenal Cortex Hormones - adverse effects
Adrenal Cortex Hormones - therapeutic use
Adrenal glands
Analysis
Bleeding
Care and treatment
Clinical trials
Complications
Corticoids
Corticosteroids
Error analysis
Evaluation
Female
Fludrocortisone
Health aspects
Humans
Hyperglycemia
Intensive Care Units
Length of Stay
Male
Mathematical analysis
Meta-analysis
Middle Aged
Mortality
Patients
Publication Bias
Quality
Randomization
Randomized Controlled Trials as Topic
Respiration, Artificial
Review
Risk
Risk Factors
Sepsis
Septic shock
Sequential analysis
Shock, Septic - drug therapy
Shock, Septic - mortality
Superinfection
Systematic review
title Reevaluating the Role of Corticosteroids in Septic Shock: An Updated Meta-Analysis of Randomized Controlled Trials
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