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Randomized trial to assess the potential role of ascorbic acid and statin for post-contrast acute kidney injury prevention
Purpose To evaluate the effect of using statins and ascorbic acid for the prevention of post-contrast acute kidney injury (PC-AKI) in patients undergoing urologic diagnostic elective contrast-enhanced computed tomography (CECT). Methods This registered trial (NCT03391830) was for statin naïve patien...
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Published in: | International urology and nephrology 2024-02, Vol.56 (2), p.399-405 |
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creator | Hashem, Abdelwahab Laymon, Mahmoud Elgamal, Mostafa Hegazy, Mohammed Elmeniar, A. M. Refaie, Huda Osman, Yasser |
description | Purpose
To evaluate the effect of using statins and ascorbic acid for the prevention of post-contrast acute kidney injury (PC-AKI) in patients undergoing urologic diagnostic elective contrast-enhanced computed tomography (CECT).
Methods
This registered trial (NCT03391830) was for statin naïve patients underwent elective CECT. Patients were randomized allocated to two groups: the first group received atorvastatin 80-mg the day before the study and atorvastatin 40-mg two hours before the CECT and for continue on atorvastatin 40-mg two days after CECT; plus ascorbic acid 500 mg with atorvastatin. The other group received two tablets of placebo once/daily before the procedure and for another 3 days. The primary outcome was to assess the incidence PC-AKI.
Results
The baseline parameters were comparable between both groups. The final median (interquartile range “IQR”) serum creatinine were 0.80 (0.60, 1.00) and 0.80 (0.60, 1.00), respectively, with insignificant
p
-value (
p
= 0.8). The median (IQR) final estimated GFR were 95.2 (72.8, 108.1) and 88.6 (71.9, 111.0) mL/min in placebo and statin plus ascorbic acid groups, respectively (
p
= 0.48). The eGFR difference median (IQR) were − 6.46 (− 11.72, − 4.18) and − 6.57 (− 13.38, − 3.82) ml/min in placebo and statin plus ascorbic acid groups, respectively (
p
= 0.58). PC-AKI occurred in 11 patients (9.8%) in placebo group and in 3 patients (3%) in statin plus ascorbic acid group (
p
= 0.04).
Conclusions
Statin and ascorbic acid did not statistically improve neither serum creatinine nor eGFR values in patient underwent CECT. However, it can decrease the incidence of the clinically insignificant PC-AKI. |
doi_str_mv | 10.1007/s11255-023-03806-8 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10808395</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2918141377</sourcerecordid><originalsourceid>FETCH-LOGICAL-c475t-da2548a33fe6f3d9899fea8c69d23e5b220f0a0639324a4d90e854ac50fdb8613</originalsourceid><addsrcrecordid>eNp9kU9vFSEUxSfGxv7RL-DCkLhxM_YCwwysjGlqa9LExOia8OBOy3MePIFp8vrpZfpqrS5cQTi_e-69nKZ5TeE9BRhOM6VMiBYYb4FL6Fv5rDmiYuAtE7J7_uR-2BznvAYAJQFeNId8GDrGmTxq7r6a4OLG36EjJXkzkRKJyRlzJuUGyTYWDGV5T3FCEscq2phW3hJjvSO1muRiig9kjKniubQ2hpJMLpWYC5If3gXcER_Wc9qRbcLbxTGGl83BaKaMrx7Ok-b7p_NvZ5ft1ZeLz2cfr1rbDaK0zjDRScP5iP3InZJKjWik7ZVjHMWKMRjBQM8VZ53pnAKUojNWwOhWsqf8pPmw993Oqw06i8t0k94mvzFpp6Px-m8l-Bt9HW81BQmSK1Ed3j04pPhzxlz0xmeL02QCxjlrJnvZD5TJBX37D7qOcwp1P80UlbSj9e8rxfaUTTHnhOPjNBT0kq3eZ6trtvo-Wy1r0ZunezyW_A6zAnwP5CqFa0x_ev_H9heAvbIX</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2918141377</pqid></control><display><type>article</type><title>Randomized trial to assess the potential role of ascorbic acid and statin for post-contrast acute kidney injury prevention</title><source>Springer Nature</source><creator>Hashem, Abdelwahab ; Laymon, Mahmoud ; Elgamal, Mostafa ; Hegazy, Mohammed ; Elmeniar, A. M. ; Refaie, Huda ; Osman, Yasser</creator><creatorcontrib>Hashem, Abdelwahab ; Laymon, Mahmoud ; Elgamal, Mostafa ; Hegazy, Mohammed ; Elmeniar, A. M. ; Refaie, Huda ; Osman, Yasser</creatorcontrib><description>Purpose
To evaluate the effect of using statins and ascorbic acid for the prevention of post-contrast acute kidney injury (PC-AKI) in patients undergoing urologic diagnostic elective contrast-enhanced computed tomography (CECT).
Methods
This registered trial (NCT03391830) was for statin naïve patients underwent elective CECT. Patients were randomized allocated to two groups: the first group received atorvastatin 80-mg the day before the study and atorvastatin 40-mg two hours before the CECT and for continue on atorvastatin 40-mg two days after CECT; plus ascorbic acid 500 mg with atorvastatin. The other group received two tablets of placebo once/daily before the procedure and for another 3 days. The primary outcome was to assess the incidence PC-AKI.
Results
The baseline parameters were comparable between both groups. The final median (interquartile range “IQR”) serum creatinine were 0.80 (0.60, 1.00) and 0.80 (0.60, 1.00), respectively, with insignificant
p
-value (
p
= 0.8). The median (IQR) final estimated GFR were 95.2 (72.8, 108.1) and 88.6 (71.9, 111.0) mL/min in placebo and statin plus ascorbic acid groups, respectively (
p
= 0.48). The eGFR difference median (IQR) were − 6.46 (− 11.72, − 4.18) and − 6.57 (− 13.38, − 3.82) ml/min in placebo and statin plus ascorbic acid groups, respectively (
p
= 0.58). PC-AKI occurred in 11 patients (9.8%) in placebo group and in 3 patients (3%) in statin plus ascorbic acid group (
p
= 0.04).
Conclusions
Statin and ascorbic acid did not statistically improve neither serum creatinine nor eGFR values in patient underwent CECT. However, it can decrease the incidence of the clinically insignificant PC-AKI.</description><identifier>ISSN: 1573-2584</identifier><identifier>ISSN: 0301-1623</identifier><identifier>EISSN: 1573-2584</identifier><identifier>DOI: 10.1007/s11255-023-03806-8</identifier><identifier>PMID: 37742328</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Acids ; Acute Kidney Injury - chemically induced ; Acute Kidney Injury - epidemiology ; Acute Kidney Injury - prevention & control ; Ascorbic acid ; Ascorbic Acid - therapeutic use ; Atorvastatin ; Atorvastatin - adverse effects ; Computed tomography ; Contrast Media - adverse effects ; Creatinine ; Epidermal growth factor receptors ; Humans ; Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects ; Kidneys ; Medicine ; Medicine & Public Health ; Nephrology ; Placebos ; Statins ; Urology ; Urology - Original Paper</subject><ispartof>International urology and nephrology, 2024-02, Vol.56 (2), p.399-405</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-da2548a33fe6f3d9899fea8c69d23e5b220f0a0639324a4d90e854ac50fdb8613</citedby><cites>FETCH-LOGICAL-c475t-da2548a33fe6f3d9899fea8c69d23e5b220f0a0639324a4d90e854ac50fdb8613</cites><orcidid>0000-0002-0664-3504</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37742328$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hashem, Abdelwahab</creatorcontrib><creatorcontrib>Laymon, Mahmoud</creatorcontrib><creatorcontrib>Elgamal, Mostafa</creatorcontrib><creatorcontrib>Hegazy, Mohammed</creatorcontrib><creatorcontrib>Elmeniar, A. M.</creatorcontrib><creatorcontrib>Refaie, Huda</creatorcontrib><creatorcontrib>Osman, Yasser</creatorcontrib><title>Randomized trial to assess the potential role of ascorbic acid and statin for post-contrast acute kidney injury prevention</title><title>International urology and nephrology</title><addtitle>Int Urol Nephrol</addtitle><addtitle>Int Urol Nephrol</addtitle><description>Purpose
To evaluate the effect of using statins and ascorbic acid for the prevention of post-contrast acute kidney injury (PC-AKI) in patients undergoing urologic diagnostic elective contrast-enhanced computed tomography (CECT).
Methods
This registered trial (NCT03391830) was for statin naïve patients underwent elective CECT. Patients were randomized allocated to two groups: the first group received atorvastatin 80-mg the day before the study and atorvastatin 40-mg two hours before the CECT and for continue on atorvastatin 40-mg two days after CECT; plus ascorbic acid 500 mg with atorvastatin. The other group received two tablets of placebo once/daily before the procedure and for another 3 days. The primary outcome was to assess the incidence PC-AKI.
Results
The baseline parameters were comparable between both groups. The final median (interquartile range “IQR”) serum creatinine were 0.80 (0.60, 1.00) and 0.80 (0.60, 1.00), respectively, with insignificant
p
-value (
p
= 0.8). The median (IQR) final estimated GFR were 95.2 (72.8, 108.1) and 88.6 (71.9, 111.0) mL/min in placebo and statin plus ascorbic acid groups, respectively (
p
= 0.48). The eGFR difference median (IQR) were − 6.46 (− 11.72, − 4.18) and − 6.57 (− 13.38, − 3.82) ml/min in placebo and statin plus ascorbic acid groups, respectively (
p
= 0.58). PC-AKI occurred in 11 patients (9.8%) in placebo group and in 3 patients (3%) in statin plus ascorbic acid group (
p
= 0.04).
Conclusions
Statin and ascorbic acid did not statistically improve neither serum creatinine nor eGFR values in patient underwent CECT. However, it can decrease the incidence of the clinically insignificant PC-AKI.</description><subject>Acids</subject><subject>Acute Kidney Injury - chemically induced</subject><subject>Acute Kidney Injury - epidemiology</subject><subject>Acute Kidney Injury - prevention & control</subject><subject>Ascorbic acid</subject><subject>Ascorbic Acid - therapeutic use</subject><subject>Atorvastatin</subject><subject>Atorvastatin - adverse effects</subject><subject>Computed tomography</subject><subject>Contrast Media - adverse effects</subject><subject>Creatinine</subject><subject>Epidermal growth factor receptors</subject><subject>Humans</subject><subject>Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects</subject><subject>Kidneys</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Nephrology</subject><subject>Placebos</subject><subject>Statins</subject><subject>Urology</subject><subject>Urology - Original Paper</subject><issn>1573-2584</issn><issn>0301-1623</issn><issn>1573-2584</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kU9vFSEUxSfGxv7RL-DCkLhxM_YCwwysjGlqa9LExOia8OBOy3MePIFp8vrpZfpqrS5cQTi_e-69nKZ5TeE9BRhOM6VMiBYYb4FL6Fv5rDmiYuAtE7J7_uR-2BznvAYAJQFeNId8GDrGmTxq7r6a4OLG36EjJXkzkRKJyRlzJuUGyTYWDGV5T3FCEscq2phW3hJjvSO1muRiig9kjKniubQ2hpJMLpWYC5If3gXcER_Wc9qRbcLbxTGGl83BaKaMrx7Ok-b7p_NvZ5ft1ZeLz2cfr1rbDaK0zjDRScP5iP3InZJKjWik7ZVjHMWKMRjBQM8VZ53pnAKUojNWwOhWsqf8pPmw993Oqw06i8t0k94mvzFpp6Px-m8l-Bt9HW81BQmSK1Ed3j04pPhzxlz0xmeL02QCxjlrJnvZD5TJBX37D7qOcwp1P80UlbSj9e8rxfaUTTHnhOPjNBT0kq3eZ6trtvo-Wy1r0ZunezyW_A6zAnwP5CqFa0x_ev_H9heAvbIX</recordid><startdate>20240201</startdate><enddate>20240201</enddate><creator>Hashem, Abdelwahab</creator><creator>Laymon, Mahmoud</creator><creator>Elgamal, Mostafa</creator><creator>Hegazy, Mohammed</creator><creator>Elmeniar, A. M.</creator><creator>Refaie, Huda</creator><creator>Osman, Yasser</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>C6C</scope><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>7QP</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0664-3504</orcidid></search><sort><creationdate>20240201</creationdate><title>Randomized trial to assess the potential role of ascorbic acid and statin for post-contrast acute kidney injury prevention</title><author>Hashem, Abdelwahab ; Laymon, Mahmoud ; Elgamal, Mostafa ; Hegazy, Mohammed ; Elmeniar, A. M. ; Refaie, Huda ; Osman, Yasser</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-da2548a33fe6f3d9899fea8c69d23e5b220f0a0639324a4d90e854ac50fdb8613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Acids</topic><topic>Acute Kidney Injury - chemically induced</topic><topic>Acute Kidney Injury - epidemiology</topic><topic>Acute Kidney Injury - prevention & control</topic><topic>Ascorbic acid</topic><topic>Ascorbic Acid - therapeutic use</topic><topic>Atorvastatin</topic><topic>Atorvastatin - adverse effects</topic><topic>Computed tomography</topic><topic>Contrast Media - adverse effects</topic><topic>Creatinine</topic><topic>Epidermal growth factor receptors</topic><topic>Humans</topic><topic>Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects</topic><topic>Kidneys</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Nephrology</topic><topic>Placebos</topic><topic>Statins</topic><topic>Urology</topic><topic>Urology - Original Paper</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hashem, Abdelwahab</creatorcontrib><creatorcontrib>Laymon, Mahmoud</creatorcontrib><creatorcontrib>Elgamal, Mostafa</creatorcontrib><creatorcontrib>Hegazy, Mohammed</creatorcontrib><creatorcontrib>Elmeniar, A. M.</creatorcontrib><creatorcontrib>Refaie, Huda</creatorcontrib><creatorcontrib>Osman, Yasser</creatorcontrib><collection>SpringerOpen</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International urology and nephrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hashem, Abdelwahab</au><au>Laymon, Mahmoud</au><au>Elgamal, Mostafa</au><au>Hegazy, Mohammed</au><au>Elmeniar, A. M.</au><au>Refaie, Huda</au><au>Osman, Yasser</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Randomized trial to assess the potential role of ascorbic acid and statin for post-contrast acute kidney injury prevention</atitle><jtitle>International urology and nephrology</jtitle><stitle>Int Urol Nephrol</stitle><addtitle>Int Urol Nephrol</addtitle><date>2024-02-01</date><risdate>2024</risdate><volume>56</volume><issue>2</issue><spage>399</spage><epage>405</epage><pages>399-405</pages><issn>1573-2584</issn><issn>0301-1623</issn><eissn>1573-2584</eissn><abstract>Purpose
To evaluate the effect of using statins and ascorbic acid for the prevention of post-contrast acute kidney injury (PC-AKI) in patients undergoing urologic diagnostic elective contrast-enhanced computed tomography (CECT).
Methods
This registered trial (NCT03391830) was for statin naïve patients underwent elective CECT. Patients were randomized allocated to two groups: the first group received atorvastatin 80-mg the day before the study and atorvastatin 40-mg two hours before the CECT and for continue on atorvastatin 40-mg two days after CECT; plus ascorbic acid 500 mg with atorvastatin. The other group received two tablets of placebo once/daily before the procedure and for another 3 days. The primary outcome was to assess the incidence PC-AKI.
Results
The baseline parameters were comparable between both groups. The final median (interquartile range “IQR”) serum creatinine were 0.80 (0.60, 1.00) and 0.80 (0.60, 1.00), respectively, with insignificant
p
-value (
p
= 0.8). The median (IQR) final estimated GFR were 95.2 (72.8, 108.1) and 88.6 (71.9, 111.0) mL/min in placebo and statin plus ascorbic acid groups, respectively (
p
= 0.48). The eGFR difference median (IQR) were − 6.46 (− 11.72, − 4.18) and − 6.57 (− 13.38, − 3.82) ml/min in placebo and statin plus ascorbic acid groups, respectively (
p
= 0.58). PC-AKI occurred in 11 patients (9.8%) in placebo group and in 3 patients (3%) in statin plus ascorbic acid group (
p
= 0.04).
Conclusions
Statin and ascorbic acid did not statistically improve neither serum creatinine nor eGFR values in patient underwent CECT. However, it can decrease the incidence of the clinically insignificant PC-AKI.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>37742328</pmid><doi>10.1007/s11255-023-03806-8</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-0664-3504</orcidid><oa>free_for_read</oa></addata></record> |
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source | Springer Nature |
subjects | Acids Acute Kidney Injury - chemically induced Acute Kidney Injury - epidemiology Acute Kidney Injury - prevention & control Ascorbic acid Ascorbic Acid - therapeutic use Atorvastatin Atorvastatin - adverse effects Computed tomography Contrast Media - adverse effects Creatinine Epidermal growth factor receptors Humans Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects Kidneys Medicine Medicine & Public Health Nephrology Placebos Statins Urology Urology - Original Paper |
title | Randomized trial to assess the potential role of ascorbic acid and statin for post-contrast acute kidney injury prevention |
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