Statistical analysis plan for the Standard versus Accelerated Initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) trial
Background: The Standard versus Accelerated Initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) trial is a multinational randomised controlled trial that will enrol a minimum of 2866 patients comparing two strategies for initiating renal replacement therapy in critically ill...
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Veröffentlicht in: | Critical care and resuscitation 2019-09, Vol.21 (3), p.162-170 |
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description | Background: The Standard versus Accelerated Initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) trial is a multinational randomised controlled trial that will enrol a minimum of 2866 patients comparing two strategies for initiating renal replacement therapy in critically ill patients with acute kidney injury.
Objective: To describe a pre-specified statistical analysis plan (SAP) for the STARRT-AKI trial before completion of patient recruitment and data collection.
Methods: The SAP was designed by the principal investigators and statisticians and approved by the international STARRT-AKI Steering Committee. The primary and secondary outcomes are defined, the approach to safety monitoring and data collection are summarised, and a detailed description of the planned statistical analyses, including pre-specified subgroup and secondary analyses, is described.
Results: We have developed the SAP for the STARRT-AKI trial, including a mock CONSORT diagram, figures and tables. The primary outcome is 90-day all-cause mortality. The primary analysis will be reported as a relative risk (95% CI), absolute risk difference (95% CI), and tested with the 'X'2 test. Secondary analyses of the primary outcome will include adjustment for baseline covariates and site, and evaluation for heterogeneity in treatment effect. Pre-specified subgroups will include patient sex, baseline kidney function, illness acuity, surgical status, presence of sepsis, and geographic location.
Conclusion: To align with best practice standards for rigour, internal validity and transparency, we have developed a SAP for the STARRT-AKI trial before trial completion. The analysis will adhere to the SAP to avoid bias arising from knowledge of trial results. |
doi_str_mv | 10.1016/S1441-2772(23)00524-0 |
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Objective: To describe a pre-specified statistical analysis plan (SAP) for the STARRT-AKI trial before completion of patient recruitment and data collection.
Methods: The SAP was designed by the principal investigators and statisticians and approved by the international STARRT-AKI Steering Committee. The primary and secondary outcomes are defined, the approach to safety monitoring and data collection are summarised, and a detailed description of the planned statistical analyses, including pre-specified subgroup and secondary analyses, is described.
Results: We have developed the SAP for the STARRT-AKI trial, including a mock CONSORT diagram, figures and tables. The primary outcome is 90-day all-cause mortality. The primary analysis will be reported as a relative risk (95% CI), absolute risk difference (95% CI), and tested with the 'X'2 test. Secondary analyses of the primary outcome will include adjustment for baseline covariates and site, and evaluation for heterogeneity in treatment effect. Pre-specified subgroups will include patient sex, baseline kidney function, illness acuity, surgical status, presence of sepsis, and geographic location.
Conclusion: To align with best practice standards for rigour, internal validity and transparency, we have developed a SAP for the STARRT-AKI trial before trial completion. The analysis will adhere to the SAP to avoid bias arising from knowledge of trial results.</description><identifier>ISSN: 1441-2772</identifier><identifier>DOI: 10.1016/S1441-2772(23)00524-0</identifier><identifier>PMID: 31462203</identifier><language>eng</language><publisher>Australia</publisher><subject>Acute Kidney Injury - therapy ; Acute renal failure ; Clinical trials ; Critical Illness ; Critically ill ; Data Collection ; Hospital utilization ; Humans ; Kidneys ; Length of stay ; Medical care ; Patient Selection ; Practice Guidelines as Topic - standards ; Renal Replacement Therapy ; Sepsis ; Statistics ; Statistics as Topic ; Transplantation</subject><ispartof>Critical care and resuscitation, 2019-09, Vol.21 (3), p.162-170</ispartof><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c437t-a6835a73062d3fc099436fbe2d24812888a5daf0aff9598504f34f801b949dbf3</citedby><cites>FETCH-LOGICAL-c437t-a6835a73062d3fc099436fbe2d24812888a5daf0aff9598504f34f801b949dbf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31462203$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bagshaw, Sean</creatorcontrib><creatorcontrib>Wald, Ron</creatorcontrib><creatorcontrib>STARRT-AKI Investigators</creatorcontrib><title>Statistical analysis plan for the Standard versus Accelerated Initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) trial</title><title>Critical care and resuscitation</title><addtitle>Crit Care Resusc</addtitle><description>Background: The Standard versus Accelerated Initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) trial is a multinational randomised controlled trial that will enrol a minimum of 2866 patients comparing two strategies for initiating renal replacement therapy in critically ill patients with acute kidney injury.
Objective: To describe a pre-specified statistical analysis plan (SAP) for the STARRT-AKI trial before completion of patient recruitment and data collection.
Methods: The SAP was designed by the principal investigators and statisticians and approved by the international STARRT-AKI Steering Committee. The primary and secondary outcomes are defined, the approach to safety monitoring and data collection are summarised, and a detailed description of the planned statistical analyses, including pre-specified subgroup and secondary analyses, is described.
Results: We have developed the SAP for the STARRT-AKI trial, including a mock CONSORT diagram, figures and tables. The primary outcome is 90-day all-cause mortality. The primary analysis will be reported as a relative risk (95% CI), absolute risk difference (95% CI), and tested with the 'X'2 test. Secondary analyses of the primary outcome will include adjustment for baseline covariates and site, and evaluation for heterogeneity in treatment effect. Pre-specified subgroups will include patient sex, baseline kidney function, illness acuity, surgical status, presence of sepsis, and geographic location.
Conclusion: To align with best practice standards for rigour, internal validity and transparency, we have developed a SAP for the STARRT-AKI trial before trial completion. The analysis will adhere to the SAP to avoid bias arising from knowledge of trial results.</description><subject>Acute Kidney Injury - therapy</subject><subject>Acute renal failure</subject><subject>Clinical trials</subject><subject>Critical Illness</subject><subject>Critically ill</subject><subject>Data Collection</subject><subject>Hospital utilization</subject><subject>Humans</subject><subject>Kidneys</subject><subject>Length of stay</subject><subject>Medical care</subject><subject>Patient Selection</subject><subject>Practice Guidelines as Topic - standards</subject><subject>Renal Replacement Therapy</subject><subject>Sepsis</subject><subject>Statistics</subject><subject>Statistics as Topic</subject><subject>Transplantation</subject><issn>1441-2772</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kc1u1DAUhbMA0VJ4BJCX00WK_-MsRxXQUSshzQwSO8vxD-NREg-2UylPwSvjdMpsbMn3O-foHlfVJwTvEET8yw5RimrcNHiFyS2EDNMavqmuL89X1fuUjhDilvLmXXVFEOUYQ3Jd_d1llX3KXqseqFH1c_IJnHo1AhciyAcLCjEaFQ14tjFNCay1tr2NKlsDNqPPvhiEEQQHtrYYlLPItR3smMH-UMDTDPxYZFO24NGb0c5Fd5ziDFa7_Xq73dfrx80tyNGr_kP11qk-2Y-v903189vX_f1D_fTj--Z-_VRrSppcKy4IUw2BHBviNGxbSrjrLDaYCoSFEIoZ5aByrmWtYJA6Qp2AqGtpazpHbqrV2fcUw5_JpiwHn8peZXEbpiQxFpi2XDSsoOyM6hhSitbJU_SDirNEUC79y5f-5VK0xES-9C9h0X1-jZi6wZqL6n_5Bfh1BuLgs9Sh761eqkxHlZNMVkV9kH4s_7DMQ_wtTfBSdWkJJqQEX4YcQ0Ea3lDEBWOY_AP6uqKY</recordid><startdate>20190901</startdate><enddate>20190901</enddate><creator>Bagshaw, Sean</creator><creator>Wald, Ron</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20190901</creationdate><title>Statistical analysis plan for the Standard versus Accelerated Initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) trial</title><author>Bagshaw, Sean ; Wald, Ron</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c437t-a6835a73062d3fc099436fbe2d24812888a5daf0aff9598504f34f801b949dbf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acute Kidney Injury - therapy</topic><topic>Acute renal failure</topic><topic>Clinical trials</topic><topic>Critical Illness</topic><topic>Critically ill</topic><topic>Data Collection</topic><topic>Hospital utilization</topic><topic>Humans</topic><topic>Kidneys</topic><topic>Length of stay</topic><topic>Medical care</topic><topic>Patient Selection</topic><topic>Practice Guidelines as Topic - standards</topic><topic>Renal Replacement Therapy</topic><topic>Sepsis</topic><topic>Statistics</topic><topic>Statistics as Topic</topic><topic>Transplantation</topic><toplevel>online_resources</toplevel><creatorcontrib>Bagshaw, Sean</creatorcontrib><creatorcontrib>Wald, Ron</creatorcontrib><creatorcontrib>STARRT-AKI Investigators</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Critical care and resuscitation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bagshaw, Sean</au><au>Wald, Ron</au><aucorp>STARRT-AKI Investigators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Statistical analysis plan for the Standard versus Accelerated Initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) trial</atitle><jtitle>Critical care and resuscitation</jtitle><addtitle>Crit Care Resusc</addtitle><date>2019-09-01</date><risdate>2019</risdate><volume>21</volume><issue>3</issue><spage>162</spage><epage>170</epage><pages>162-170</pages><issn>1441-2772</issn><abstract>Background: The Standard versus Accelerated Initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) trial is a multinational randomised controlled trial that will enrol a minimum of 2866 patients comparing two strategies for initiating renal replacement therapy in critically ill patients with acute kidney injury.
Objective: To describe a pre-specified statistical analysis plan (SAP) for the STARRT-AKI trial before completion of patient recruitment and data collection.
Methods: The SAP was designed by the principal investigators and statisticians and approved by the international STARRT-AKI Steering Committee. The primary and secondary outcomes are defined, the approach to safety monitoring and data collection are summarised, and a detailed description of the planned statistical analyses, including pre-specified subgroup and secondary analyses, is described.
Results: We have developed the SAP for the STARRT-AKI trial, including a mock CONSORT diagram, figures and tables. The primary outcome is 90-day all-cause mortality. The primary analysis will be reported as a relative risk (95% CI), absolute risk difference (95% CI), and tested with the 'X'2 test. Secondary analyses of the primary outcome will include adjustment for baseline covariates and site, and evaluation for heterogeneity in treatment effect. Pre-specified subgroups will include patient sex, baseline kidney function, illness acuity, surgical status, presence of sepsis, and geographic location.
Conclusion: To align with best practice standards for rigour, internal validity and transparency, we have developed a SAP for the STARRT-AKI trial before trial completion. The analysis will adhere to the SAP to avoid bias arising from knowledge of trial results.</abstract><cop>Australia</cop><pmid>31462203</pmid><doi>10.1016/S1441-2772(23)00524-0</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Acute Kidney Injury - therapy Acute renal failure Clinical trials Critical Illness Critically ill Data Collection Hospital utilization Humans Kidneys Length of stay Medical care Patient Selection Practice Guidelines as Topic - standards Renal Replacement Therapy Sepsis Statistics Statistics as Topic Transplantation |
title | Statistical analysis plan for the Standard versus Accelerated Initiation of Renal Replacement Therapy in Acute Kidney Injury (STARRT-AKI) trial |
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