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Effect of Azilsartan on clinical blood pressure reduction compared to other angiotensin receptor blockers: a systematic review and meta-analysis
Hypertension has significantly contributed to morbidity and mortality, necessitating effective management. Angiotensin receptor blockers (ARBs) have emerged as a cornerstone in hypertension treatment. Azilsartan, a relatively recent addition to the ARB family, offers unique characteristics, includin...
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Published in: | Annals of medicine and surgery 2024-02, Vol.86 (2), p.958-967 |
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container_title | Annals of medicine and surgery |
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creator | Khan, Qaisar Ali Sharma, Shalini Mulk, Ittehad Ul Li, David Belay, Naod F Afzal, Muhammad Farrukh, Ameer Mustafa Asad, Muhammad Baqi, Abdul Semakieh, Bader |
description | Hypertension has significantly contributed to morbidity and mortality, necessitating effective management. Angiotensin receptor blockers (ARBs) have emerged as a cornerstone in hypertension treatment. Azilsartan, a relatively recent addition to the ARB family, offers unique characteristics, including prodrug activation. This systematic review and meta-analysis aimed to evaluate Azilsartan's role in reducing clinical blood pressure compared to other ARBs and determine the most effective dosage.
Following PRISMA guidelines, a comprehensive literature search was conducted in Medline, Web of Science, Cochrane Library, and clinicaltrials.gov. Eligible studies included adult hypertensive patients receiving Azilsartan compared to other ARBs, with clinical systolic blood pressure (SBP) and diastolic blood pressure (DBP) outcomes. Data extraction and quality assessment were performed, and statistical analysis employed comprehensive meta-analysis (CMA) software.
Eleven randomized controlled trials encompassing 18 studies involving 6024 patients were included. Azilsartan demonstrated significant reductions in clinical SBP (mean difference=-2.85 mmHg) and DBP (mean difference=-2.095 mmHg) compared to other ARBs. Higher doses of Azilsartan showed greater efficacy, with 80 mg exhibiting the most substantial reduction in SBP. The analysis emphasized the need for more studies investigating lower Azilsartan doses (10 and 20 mg).
This systematic review and meta-analysis underscore Azilsartan's effectiveness in reducing SBP and DBP. Dose-dependent effects emphasize the importance of optimal dosing when prescribing Azilsartan. These findings provide valuable insights for clinicians in managing hypertension effectively and call for further research, primarily focusing on lower Azilsartan doses and a more diverse patient population. |
doi_str_mv | 10.1097/MS9.0000000000001547 |
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Following PRISMA guidelines, a comprehensive literature search was conducted in Medline, Web of Science, Cochrane Library, and clinicaltrials.gov. Eligible studies included adult hypertensive patients receiving Azilsartan compared to other ARBs, with clinical systolic blood pressure (SBP) and diastolic blood pressure (DBP) outcomes. Data extraction and quality assessment were performed, and statistical analysis employed comprehensive meta-analysis (CMA) software.
Eleven randomized controlled trials encompassing 18 studies involving 6024 patients were included. Azilsartan demonstrated significant reductions in clinical SBP (mean difference=-2.85 mmHg) and DBP (mean difference=-2.095 mmHg) compared to other ARBs. Higher doses of Azilsartan showed greater efficacy, with 80 mg exhibiting the most substantial reduction in SBP. The analysis emphasized the need for more studies investigating lower Azilsartan doses (10 and 20 mg).
This systematic review and meta-analysis underscore Azilsartan's effectiveness in reducing SBP and DBP. Dose-dependent effects emphasize the importance of optimal dosing when prescribing Azilsartan. These findings provide valuable insights for clinicians in managing hypertension effectively and call for further research, primarily focusing on lower Azilsartan doses and a more diverse patient population.</description><identifier>ISSN: 2049-0801</identifier><identifier>EISSN: 2049-0801</identifier><identifier>DOI: 10.1097/MS9.0000000000001547</identifier><identifier>PMID: 38333313</identifier><language>eng</language><publisher>England: Lippincott Williams & Wilkins</publisher><subject>Reviews</subject><ispartof>Annals of medicine and surgery, 2024-02, Vol.86 (2), p.958-967</ispartof><rights>Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc.</rights><rights>Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c288t-c80c05fafee07979e2af06f1e463e4b88105e57e47ce5b75a6cc9de5f27469113</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10849446/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10849446/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38333313$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Khan, Qaisar Ali</creatorcontrib><creatorcontrib>Sharma, Shalini</creatorcontrib><creatorcontrib>Mulk, Ittehad Ul</creatorcontrib><creatorcontrib>Li, David</creatorcontrib><creatorcontrib>Belay, Naod F</creatorcontrib><creatorcontrib>Afzal, Muhammad</creatorcontrib><creatorcontrib>Farrukh, Ameer Mustafa</creatorcontrib><creatorcontrib>Asad, Muhammad</creatorcontrib><creatorcontrib>Baqi, Abdul</creatorcontrib><creatorcontrib>Semakieh, Bader</creatorcontrib><title>Effect of Azilsartan on clinical blood pressure reduction compared to other angiotensin receptor blockers: a systematic review and meta-analysis</title><title>Annals of medicine and surgery</title><addtitle>Ann Med Surg (Lond)</addtitle><description>Hypertension has significantly contributed to morbidity and mortality, necessitating effective management. Angiotensin receptor blockers (ARBs) have emerged as a cornerstone in hypertension treatment. Azilsartan, a relatively recent addition to the ARB family, offers unique characteristics, including prodrug activation. This systematic review and meta-analysis aimed to evaluate Azilsartan's role in reducing clinical blood pressure compared to other ARBs and determine the most effective dosage.
Following PRISMA guidelines, a comprehensive literature search was conducted in Medline, Web of Science, Cochrane Library, and clinicaltrials.gov. Eligible studies included adult hypertensive patients receiving Azilsartan compared to other ARBs, with clinical systolic blood pressure (SBP) and diastolic blood pressure (DBP) outcomes. Data extraction and quality assessment were performed, and statistical analysis employed comprehensive meta-analysis (CMA) software.
Eleven randomized controlled trials encompassing 18 studies involving 6024 patients were included. Azilsartan demonstrated significant reductions in clinical SBP (mean difference=-2.85 mmHg) and DBP (mean difference=-2.095 mmHg) compared to other ARBs. Higher doses of Azilsartan showed greater efficacy, with 80 mg exhibiting the most substantial reduction in SBP. The analysis emphasized the need for more studies investigating lower Azilsartan doses (10 and 20 mg).
This systematic review and meta-analysis underscore Azilsartan's effectiveness in reducing SBP and DBP. Dose-dependent effects emphasize the importance of optimal dosing when prescribing Azilsartan. These findings provide valuable insights for clinicians in managing hypertension effectively and call for further research, primarily focusing on lower Azilsartan doses and a more diverse patient population.</description><subject>Reviews</subject><issn>2049-0801</issn><issn>2049-0801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpdUU1v1DAQtRCIVkv_AUI-ckmxEyexuaCqKhSpiANwtmadcWtw7GA7Rcuv4CfXq5ZqYS4zo3lvvh4hLzk75UyNbz59UafswHgvxifkuGVCNUwy_vQgPiInOX_fg1jfDYN8To462VXj3TH5c2EtmkKjpWe_nc-QCgQaAzXeBWfA062PcaJLwpzXhDThtJri9og4L1BTWiKN5QYThXDtYsGQXag4g0uJac83PzDltxRo3uWCMxRnav3W4a9KmeiMBRoI4HfZ5RfkmQWf8eTBb8i39xdfzy-bq88fPp6fXTWmlbI0RjLDegsWkY1qVNiCZYPlKIYOxVbKeiz2I4rRYL8dexiMURP2th3FoDjvNuTdfd9l3c44GQwlgddLcjOknY7g9L-V4G70dbzVnEmhRB2zIa8fOqT4c8Vc9OyyQe8hYFyzblXbs_rm-vUNEfdQk2LOCe3jHM70XlBdBdX_C1pprw53fCT9la-7A6--n-s</recordid><startdate>20240201</startdate><enddate>20240201</enddate><creator>Khan, Qaisar Ali</creator><creator>Sharma, Shalini</creator><creator>Mulk, Ittehad Ul</creator><creator>Li, David</creator><creator>Belay, Naod F</creator><creator>Afzal, Muhammad</creator><creator>Farrukh, Ameer Mustafa</creator><creator>Asad, Muhammad</creator><creator>Baqi, Abdul</creator><creator>Semakieh, Bader</creator><general>Lippincott Williams & Wilkins</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20240201</creationdate><title>Effect of Azilsartan on clinical blood pressure reduction compared to other angiotensin receptor blockers: a systematic review and meta-analysis</title><author>Khan, Qaisar Ali ; Sharma, Shalini ; Mulk, Ittehad Ul ; Li, David ; Belay, Naod F ; Afzal, Muhammad ; Farrukh, Ameer Mustafa ; Asad, Muhammad ; Baqi, Abdul ; Semakieh, Bader</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c288t-c80c05fafee07979e2af06f1e463e4b88105e57e47ce5b75a6cc9de5f27469113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Reviews</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Khan, Qaisar Ali</creatorcontrib><creatorcontrib>Sharma, Shalini</creatorcontrib><creatorcontrib>Mulk, Ittehad Ul</creatorcontrib><creatorcontrib>Li, David</creatorcontrib><creatorcontrib>Belay, Naod F</creatorcontrib><creatorcontrib>Afzal, Muhammad</creatorcontrib><creatorcontrib>Farrukh, Ameer Mustafa</creatorcontrib><creatorcontrib>Asad, Muhammad</creatorcontrib><creatorcontrib>Baqi, Abdul</creatorcontrib><creatorcontrib>Semakieh, Bader</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Annals of medicine and surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Khan, Qaisar Ali</au><au>Sharma, Shalini</au><au>Mulk, Ittehad Ul</au><au>Li, David</au><au>Belay, Naod F</au><au>Afzal, Muhammad</au><au>Farrukh, Ameer Mustafa</au><au>Asad, Muhammad</au><au>Baqi, Abdul</au><au>Semakieh, Bader</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Azilsartan on clinical blood pressure reduction compared to other angiotensin receptor blockers: a systematic review and meta-analysis</atitle><jtitle>Annals of medicine and surgery</jtitle><addtitle>Ann Med Surg (Lond)</addtitle><date>2024-02-01</date><risdate>2024</risdate><volume>86</volume><issue>2</issue><spage>958</spage><epage>967</epage><pages>958-967</pages><issn>2049-0801</issn><eissn>2049-0801</eissn><abstract>Hypertension has significantly contributed to morbidity and mortality, necessitating effective management. Angiotensin receptor blockers (ARBs) have emerged as a cornerstone in hypertension treatment. Azilsartan, a relatively recent addition to the ARB family, offers unique characteristics, including prodrug activation. This systematic review and meta-analysis aimed to evaluate Azilsartan's role in reducing clinical blood pressure compared to other ARBs and determine the most effective dosage.
Following PRISMA guidelines, a comprehensive literature search was conducted in Medline, Web of Science, Cochrane Library, and clinicaltrials.gov. Eligible studies included adult hypertensive patients receiving Azilsartan compared to other ARBs, with clinical systolic blood pressure (SBP) and diastolic blood pressure (DBP) outcomes. Data extraction and quality assessment were performed, and statistical analysis employed comprehensive meta-analysis (CMA) software.
Eleven randomized controlled trials encompassing 18 studies involving 6024 patients were included. Azilsartan demonstrated significant reductions in clinical SBP (mean difference=-2.85 mmHg) and DBP (mean difference=-2.095 mmHg) compared to other ARBs. Higher doses of Azilsartan showed greater efficacy, with 80 mg exhibiting the most substantial reduction in SBP. The analysis emphasized the need for more studies investigating lower Azilsartan doses (10 and 20 mg).
This systematic review and meta-analysis underscore Azilsartan's effectiveness in reducing SBP and DBP. Dose-dependent effects emphasize the importance of optimal dosing when prescribing Azilsartan. These findings provide valuable insights for clinicians in managing hypertension effectively and call for further research, primarily focusing on lower Azilsartan doses and a more diverse patient population.</abstract><cop>England</cop><pub>Lippincott Williams & Wilkins</pub><pmid>38333313</pmid><doi>10.1097/MS9.0000000000001547</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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title | Effect of Azilsartan on clinical blood pressure reduction compared to other angiotensin receptor blockers: a systematic review and meta-analysis |
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