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...
Gespeichert in:
Veröffentlicht in: | Biological & pharmaceutical bulletin 2023/12/01, Vol.46(12), pp.1731-1736 |
---|---|
Hauptverfasser: | , , , |
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 <−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 & 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 <−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 & 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 & 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 & 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 <−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 |