Effect of Ceftriaxone Dosage and Albumin–Bilirubin Score on the Risk of Ceftriaxone-Induced Liver Injury

The albumin–bilirubin (ALBI) score is an index of hepatic functional reserve and is calculated from serum albumin and total bilirubin levels. However, the relationship between ceftriaxone (CTRX)-induced liver injury and ALBI score remains unknown. Therefore, we aimed to elucidate the risk of CTRX-in...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biological & pharmaceutical bulletin 2023/12/01, Vol.46(12), pp.1731-1736
Hauptverfasser: Ooi, Hayahide, Asai, Yuki, Koriyama, Yoshiki, Takahashi, Masaaki
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1736
container_issue 12
container_start_page 1731
container_title Biological & pharmaceutical bulletin
container_volume 46
creator Ooi, Hayahide
Asai, Yuki
Koriyama, Yoshiki
Takahashi, Masaaki
description The albumin–bilirubin (ALBI) score is an index of hepatic functional reserve and is calculated from serum albumin and total bilirubin levels. However, the relationship between ceftriaxone (CTRX)-induced liver injury and ALBI score remains unknown. Therefore, we aimed to elucidate the risk of CTRX-induced liver injury based on the ALBI scores and CTRX dosage. This was a single-center, retrospective, case-control study of 490 patients and the primary outcome was CTRX-induced liver injury. We performed a COX regression analysis using age ≥75 years, male sex, alanine aminotransferase levels, ALBI score, and CTRX dosage regimen (4 ≥2 or 1 g/d) as explanatory factors. We also performed 1 : 1 propensity score matching between non-liver injury and liver injury groups. The incidence of liver injury was 10.0% (49/490). In COX regression analysis, CTRX 4 g/d was an independent risk factor for liver injury (95% coefficient interval: 1.05–6.96, p = 0.04). Meanwhile, ALBI score ≥−1.61 was an independent factor for liver injury (95% coefficient interval: 1.03–3.22, p = 0.04) with the explanatory factor of ≥2 and 1 g/d. The Kaplan–Meier curve indicated that the cumulative risk for CTRX-induced liver injury was significantly higher in the ALBI score ≥−1.61 group than in the ALBI score
doi_str_mv 10.1248/bpb.b23-00469
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2897489230</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2914393018</sourcerecordid><originalsourceid>FETCH-LOGICAL-c521t-fadfa301da8f77d4ff422aa914ae05811b8bf2f523dcbd08cf06260dd25969283</originalsourceid><addsrcrecordid>eNpdkLlOAzEURS0EEmEp6S3R0Ax4mcVTQggQKRISS215vBAPEzvYMwg6_oE_5EtwCEqR5rl45z5fHQBOMDrHJGcXzbI5bwjNEMrLegeMMM2rrCC42AUjVGOWlbhg--AgxhYhVCFCR6CdGKNlD72BY236YMWHdxpe-yheNBROwcuuGRbW_Xx9X9nOhqGxDj5KHzT0DvZzDR9sfN3KZ1OnBqkVnNl3HeDUtUP4PAJ7RnRRH_-_h-D5ZvI0vstm97fT8eUsk6lrnxmhjKAIK8FMVancmJwQIWqcC40KhnHDGkNMQaiSjUJMGlSSEilFirqsCaOH4Gx9dxn826Bjzxc2St11wmk_RE5YXeWsJhQl9HQLbf0QXGrHSfqQ1qnH6mC2pmTwMQZt-DLYhQifHCO-Ms-TeZ7M8z_zib9e823sk8UNLUJvZaf_6LxMydXcxDZrOReBa0d_AV2IkAI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2914393018</pqid></control><display><type>article</type><title>Effect of Ceftriaxone Dosage and Albumin–Bilirubin Score on the Risk of Ceftriaxone-Induced Liver Injury</title><source>J-STAGE Free</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Free Full-Text Journals in Chemistry</source><creator>Ooi, Hayahide ; Asai, Yuki ; Koriyama, Yoshiki ; Takahashi, Masaaki</creator><creatorcontrib>Ooi, Hayahide ; Asai, Yuki ; Koriyama, Yoshiki ; Takahashi, Masaaki</creatorcontrib><description>The albumin–bilirubin (ALBI) score is an index of hepatic functional reserve and is calculated from serum albumin and total bilirubin levels. However, the relationship between ceftriaxone (CTRX)-induced liver injury and ALBI score remains unknown. Therefore, we aimed to elucidate the risk of CTRX-induced liver injury based on the ALBI scores and CTRX dosage. This was a single-center, retrospective, case-control study of 490 patients and the primary outcome was CTRX-induced liver injury. We performed a COX regression analysis using age ≥75 years, male sex, alanine aminotransferase levels, ALBI score, and CTRX dosage regimen (4 ≥2 or 1 g/d) as explanatory factors. We also performed 1 : 1 propensity score matching between non-liver injury and liver injury groups. The incidence of liver injury was 10.0% (49/490). In COX regression analysis, CTRX 4 g/d was an independent risk factor for liver injury (95% coefficient interval: 1.05–6.96, p = 0.04). Meanwhile, ALBI score ≥−1.61 was an independent factor for liver injury (95% coefficient interval: 1.03–3.22, p = 0.04) with the explanatory factor of ≥2 and 1 g/d. The Kaplan–Meier curve indicated that the cumulative risk for CTRX-induced liver injury was significantly higher in the ALBI score ≥−1.61 group than in the ALBI score &lt;−1.61 group before propensity score matching (p = 0.032); however, no significant differences were observed after propensity score matching (p = 0.791). These findings suggest that in patients treated with CTRX with ALBI score ≥−1.61, frequent liver function monitoring should be considered.</description><identifier>ISSN: 0918-6158</identifier><identifier>EISSN: 1347-5215</identifier><identifier>DOI: 10.1248/bpb.b23-00469</identifier><language>eng</language><publisher>Tokyo: The Pharmaceutical Society of Japan</publisher><subject>Alanine transaminase ; Albumin ; albumin–bilirubin score ; Antibiotics ; Bilirubin ; Ceftriaxone ; Dosage ; drug-induced liver injury ; Liver ; Regression analysis ; Risk factors</subject><ispartof>Biological and Pharmaceutical Bulletin, 2023/12/01, Vol.46(12), pp.1731-1736</ispartof><rights>2023 The Pharmaceutical Society of Japan</rights><rights>Copyright Japan Science and Technology Agency 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c521t-fadfa301da8f77d4ff422aa914ae05811b8bf2f523dcbd08cf06260dd25969283</citedby><cites>FETCH-LOGICAL-c521t-fadfa301da8f77d4ff422aa914ae05811b8bf2f523dcbd08cf06260dd25969283</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1876,27903,27904</link.rule.ids></links><search><creatorcontrib>Ooi, Hayahide</creatorcontrib><creatorcontrib>Asai, Yuki</creatorcontrib><creatorcontrib>Koriyama, Yoshiki</creatorcontrib><creatorcontrib>Takahashi, Masaaki</creatorcontrib><title>Effect of Ceftriaxone Dosage and Albumin–Bilirubin Score on the Risk of Ceftriaxone-Induced Liver Injury</title><title>Biological &amp; pharmaceutical bulletin</title><description>The albumin–bilirubin (ALBI) score is an index of hepatic functional reserve and is calculated from serum albumin and total bilirubin levels. However, the relationship between ceftriaxone (CTRX)-induced liver injury and ALBI score remains unknown. Therefore, we aimed to elucidate the risk of CTRX-induced liver injury based on the ALBI scores and CTRX dosage. This was a single-center, retrospective, case-control study of 490 patients and the primary outcome was CTRX-induced liver injury. We performed a COX regression analysis using age ≥75 years, male sex, alanine aminotransferase levels, ALBI score, and CTRX dosage regimen (4 ≥2 or 1 g/d) as explanatory factors. We also performed 1 : 1 propensity score matching between non-liver injury and liver injury groups. The incidence of liver injury was 10.0% (49/490). In COX regression analysis, CTRX 4 g/d was an independent risk factor for liver injury (95% coefficient interval: 1.05–6.96, p = 0.04). Meanwhile, ALBI score ≥−1.61 was an independent factor for liver injury (95% coefficient interval: 1.03–3.22, p = 0.04) with the explanatory factor of ≥2 and 1 g/d. The Kaplan–Meier curve indicated that the cumulative risk for CTRX-induced liver injury was significantly higher in the ALBI score ≥−1.61 group than in the ALBI score &lt;−1.61 group before propensity score matching (p = 0.032); however, no significant differences were observed after propensity score matching (p = 0.791). These findings suggest that in patients treated with CTRX with ALBI score ≥−1.61, frequent liver function monitoring should be considered.</description><subject>Alanine transaminase</subject><subject>Albumin</subject><subject>albumin–bilirubin score</subject><subject>Antibiotics</subject><subject>Bilirubin</subject><subject>Ceftriaxone</subject><subject>Dosage</subject><subject>drug-induced liver injury</subject><subject>Liver</subject><subject>Regression analysis</subject><subject>Risk factors</subject><issn>0918-6158</issn><issn>1347-5215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdkLlOAzEURS0EEmEp6S3R0Ax4mcVTQggQKRISS215vBAPEzvYMwg6_oE_5EtwCEqR5rl45z5fHQBOMDrHJGcXzbI5bwjNEMrLegeMMM2rrCC42AUjVGOWlbhg--AgxhYhVCFCR6CdGKNlD72BY236YMWHdxpe-yheNBROwcuuGRbW_Xx9X9nOhqGxDj5KHzT0DvZzDR9sfN3KZ1OnBqkVnNl3HeDUtUP4PAJ7RnRRH_-_h-D5ZvI0vstm97fT8eUsk6lrnxmhjKAIK8FMVancmJwQIWqcC40KhnHDGkNMQaiSjUJMGlSSEilFirqsCaOH4Gx9dxn826Bjzxc2St11wmk_RE5YXeWsJhQl9HQLbf0QXGrHSfqQ1qnH6mC2pmTwMQZt-DLYhQifHCO-Ms-TeZ7M8z_zib9e823sk8UNLUJvZaf_6LxMydXcxDZrOReBa0d_AV2IkAI</recordid><startdate>20231201</startdate><enddate>20231201</enddate><creator>Ooi, Hayahide</creator><creator>Asai, Yuki</creator><creator>Koriyama, Yoshiki</creator><creator>Takahashi, Masaaki</creator><general>The Pharmaceutical Society of Japan</general><general>Japan Science and Technology Agency</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20231201</creationdate><title>Effect of Ceftriaxone Dosage and Albumin–Bilirubin Score on the Risk of Ceftriaxone-Induced Liver Injury</title><author>Ooi, Hayahide ; Asai, Yuki ; Koriyama, Yoshiki ; Takahashi, Masaaki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c521t-fadfa301da8f77d4ff422aa914ae05811b8bf2f523dcbd08cf06260dd25969283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Alanine transaminase</topic><topic>Albumin</topic><topic>albumin–bilirubin score</topic><topic>Antibiotics</topic><topic>Bilirubin</topic><topic>Ceftriaxone</topic><topic>Dosage</topic><topic>drug-induced liver injury</topic><topic>Liver</topic><topic>Regression analysis</topic><topic>Risk factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ooi, Hayahide</creatorcontrib><creatorcontrib>Asai, Yuki</creatorcontrib><creatorcontrib>Koriyama, Yoshiki</creatorcontrib><creatorcontrib>Takahashi, Masaaki</creatorcontrib><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biological &amp; pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ooi, Hayahide</au><au>Asai, Yuki</au><au>Koriyama, Yoshiki</au><au>Takahashi, Masaaki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Ceftriaxone Dosage and Albumin–Bilirubin Score on the Risk of Ceftriaxone-Induced Liver Injury</atitle><jtitle>Biological &amp; pharmaceutical bulletin</jtitle><date>2023-12-01</date><risdate>2023</risdate><volume>46</volume><issue>12</issue><spage>1731</spage><epage>1736</epage><pages>1731-1736</pages><artnum>b23-00469</artnum><issn>0918-6158</issn><eissn>1347-5215</eissn><abstract>The albumin–bilirubin (ALBI) score is an index of hepatic functional reserve and is calculated from serum albumin and total bilirubin levels. However, the relationship between ceftriaxone (CTRX)-induced liver injury and ALBI score remains unknown. Therefore, we aimed to elucidate the risk of CTRX-induced liver injury based on the ALBI scores and CTRX dosage. This was a single-center, retrospective, case-control study of 490 patients and the primary outcome was CTRX-induced liver injury. We performed a COX regression analysis using age ≥75 years, male sex, alanine aminotransferase levels, ALBI score, and CTRX dosage regimen (4 ≥2 or 1 g/d) as explanatory factors. We also performed 1 : 1 propensity score matching between non-liver injury and liver injury groups. The incidence of liver injury was 10.0% (49/490). In COX regression analysis, CTRX 4 g/d was an independent risk factor for liver injury (95% coefficient interval: 1.05–6.96, p = 0.04). Meanwhile, ALBI score ≥−1.61 was an independent factor for liver injury (95% coefficient interval: 1.03–3.22, p = 0.04) with the explanatory factor of ≥2 and 1 g/d. The Kaplan–Meier curve indicated that the cumulative risk for CTRX-induced liver injury was significantly higher in the ALBI score ≥−1.61 group than in the ALBI score &lt;−1.61 group before propensity score matching (p = 0.032); however, no significant differences were observed after propensity score matching (p = 0.791). These findings suggest that in patients treated with CTRX with ALBI score ≥−1.61, frequent liver function monitoring should be considered.</abstract><cop>Tokyo</cop><pub>The Pharmaceutical Society of Japan</pub><doi>10.1248/bpb.b23-00469</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0918-6158
ispartof Biological and Pharmaceutical Bulletin, 2023/12/01, Vol.46(12), pp.1731-1736
issn 0918-6158
1347-5215
language eng
recordid cdi_proquest_miscellaneous_2897489230
source J-STAGE Free; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Free Full-Text Journals in Chemistry
subjects Alanine transaminase
Albumin
albumin–bilirubin score
Antibiotics
Bilirubin
Ceftriaxone
Dosage
drug-induced liver injury
Liver
Regression analysis
Risk factors
title Effect of Ceftriaxone Dosage and Albumin–Bilirubin Score on the Risk of Ceftriaxone-Induced Liver Injury
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T04%3A09%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effect%20of%20Ceftriaxone%20Dosage%20and%20Albumin%E2%80%93Bilirubin%20Score%20on%20the%20Risk%20of%20Ceftriaxone-Induced%20Liver%20Injury&rft.jtitle=Biological%20&%20pharmaceutical%20bulletin&rft.au=Ooi,%20Hayahide&rft.date=2023-12-01&rft.volume=46&rft.issue=12&rft.spage=1731&rft.epage=1736&rft.pages=1731-1736&rft.artnum=b23-00469&rft.issn=0918-6158&rft.eissn=1347-5215&rft_id=info:doi/10.1248/bpb.b23-00469&rft_dat=%3Cproquest_cross%3E2914393018%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2914393018&rft_id=info:pmid/&rfr_iscdi=true