Validation of a New Scoring Method to Assess the Efficacy of Rapid Initiation and Titration of Combination Pharmacotherapy for Patients Hospitalized with Acute Decompensated Heart Failure with Reduced and Mildly Reduced Ejection Fraction
: Despite the encouragement of early initiation and titration of guideline-directed medical therapy (GDMT) for the treatment of heart failure (HF), most patients do not receive an adequate type and dose of pharmacotherapy in the real world. : This study aimed to determine the efficacy of titrating c...
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creator | Asano, Takaaki Maeno, Yoshio Nakano, Masataka Taguri, Masataka Miyasaka, Masaki Nakai, Daisuke Miyazaki, Itaru Nasu, Takahito Tanimoto, Shuzou Masuda, Naoki Morino, Yoshihiro Isshiki, Takaaki Ogata, Nobuhiko |
description | : Despite the encouragement of early initiation and titration of guideline-directed medical therapy (GDMT) for the treatment of heart failure (HF), most patients do not receive an adequate type and dose of pharmacotherapy in the real world.
: This study aimed to determine the efficacy of titrating composite GDMT in patients with HF with reduced and mildly reduced ejection fraction and to identify patient conditions that may benefit from titration of GDMT.
: This was a two-center, retrospective study of consecutive patients hospitalized with acute decompensated heart failure (ADHF). Patients were classified into two groups according to a scoring scale determined by combination and doses of four types of HF agents (ACEis/ARBs/ARNis, BBs, MRAs, and SGLT2is) at discharge. A score of 5 or greater was defined as titrated GDMT, and a score of 4 or less was regarded as sub-optimal medical therapy (MT).
: A total of 979 ADHF patients were screened. After 553 patients were excluded based on exclusion criteria, 426 patients (90 patients in the titrated GDMT group and 336 patients in the sub-optimal MT group) were enrolled for the analysis. The median follow-up period was 612 (453-798) days. Following statistical adjustment using the propensity score weighting method, the 2-year composite endpoint (composite of cardiac death and HF rehospitalization) rate was significantly lower in the titrated GDMT group, at 19%, compared with the sub-optimal MT group: 31% (score 3-4 points) and 43% (score 0-2 points). Subgroup analysis indicated a marked benefit of titrated GDMT in particular patient subgroups: age < 80 years, BMI 19.0-24.9, eGFR > 20 mL/min/1.73 m
, and serum potassium level ≤ 5.5 mmol/L.
: Prompt initiation and dose adjustment of multiple HF medications, with careful monitoring of the patient's physiologic and laboratory values, is a prerequisite for improving the prognosis of patients with heart failure. |
doi_str_mv | 10.3390/jcm13102775 |
format | Article |
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: This study aimed to determine the efficacy of titrating composite GDMT in patients with HF with reduced and mildly reduced ejection fraction and to identify patient conditions that may benefit from titration of GDMT.
: This was a two-center, retrospective study of consecutive patients hospitalized with acute decompensated heart failure (ADHF). Patients were classified into two groups according to a scoring scale determined by combination and doses of four types of HF agents (ACEis/ARBs/ARNis, BBs, MRAs, and SGLT2is) at discharge. A score of 5 or greater was defined as titrated GDMT, and a score of 4 or less was regarded as sub-optimal medical therapy (MT).
: A total of 979 ADHF patients were screened. After 553 patients were excluded based on exclusion criteria, 426 patients (90 patients in the titrated GDMT group and 336 patients in the sub-optimal MT group) were enrolled for the analysis. The median follow-up period was 612 (453-798) days. Following statistical adjustment using the propensity score weighting method, the 2-year composite endpoint (composite of cardiac death and HF rehospitalization) rate was significantly lower in the titrated GDMT group, at 19%, compared with the sub-optimal MT group: 31% (score 3-4 points) and 43% (score 0-2 points). Subgroup analysis indicated a marked benefit of titrated GDMT in particular patient subgroups: age < 80 years, BMI 19.0-24.9, eGFR > 20 mL/min/1.73 m
, and serum potassium level ≤ 5.5 mmol/L.
: Prompt initiation and dose adjustment of multiple HF medications, with careful monitoring of the patient's physiologic and laboratory values, is a prerequisite for improving the prognosis of patients with heart failure.</description><identifier>ISSN: 2077-0383</identifier><identifier>EISSN: 2077-0383</identifier><identifier>DOI: 10.3390/jcm13102775</identifier><identifier>PMID: 38792317</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Blood pressure ; Cardiac output ; Care and treatment ; Demographics ; Diagnosis ; Drug dosages ; Drug therapy ; Ejection fraction ; Evaluation ; Heart failure ; Heart rate ; Hospitalization ; Medical records ; Mortality ; Observational studies ; Patients ; Physiology ; Potassium ; Software</subject><ispartof>Journal of clinical medicine, 2024-05, Vol.13 (10), p.2775</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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><cites>FETCH-LOGICAL-c309t-b7abaaa55a69f57b9366309240fb0786733627dab4d3b27e106913e5d768bd803</cites><orcidid>0000-0001-9922-1548</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38792317$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Asano, Takaaki</creatorcontrib><creatorcontrib>Maeno, Yoshio</creatorcontrib><creatorcontrib>Nakano, Masataka</creatorcontrib><creatorcontrib>Taguri, Masataka</creatorcontrib><creatorcontrib>Miyasaka, Masaki</creatorcontrib><creatorcontrib>Nakai, Daisuke</creatorcontrib><creatorcontrib>Miyazaki, Itaru</creatorcontrib><creatorcontrib>Nasu, Takahito</creatorcontrib><creatorcontrib>Tanimoto, Shuzou</creatorcontrib><creatorcontrib>Masuda, Naoki</creatorcontrib><creatorcontrib>Morino, Yoshihiro</creatorcontrib><creatorcontrib>Isshiki, Takaaki</creatorcontrib><creatorcontrib>Ogata, Nobuhiko</creatorcontrib><title>Validation of a New Scoring Method to Assess the Efficacy of Rapid Initiation and Titration of Combination Pharmacotherapy for Patients Hospitalized with Acute Decompensated Heart Failure with Reduced and Mildly Reduced Ejection Fraction</title><title>Journal of clinical medicine</title><addtitle>J Clin Med</addtitle><description>: Despite the encouragement of early initiation and titration of guideline-directed medical therapy (GDMT) for the treatment of heart failure (HF), most patients do not receive an adequate type and dose of pharmacotherapy in the real world.
: This study aimed to determine the efficacy of titrating composite GDMT in patients with HF with reduced and mildly reduced ejection fraction and to identify patient conditions that may benefit from titration of GDMT.
: This was a two-center, retrospective study of consecutive patients hospitalized with acute decompensated heart failure (ADHF). Patients were classified into two groups according to a scoring scale determined by combination and doses of four types of HF agents (ACEis/ARBs/ARNis, BBs, MRAs, and SGLT2is) at discharge. A score of 5 or greater was defined as titrated GDMT, and a score of 4 or less was regarded as sub-optimal medical therapy (MT).
: A total of 979 ADHF patients were screened. After 553 patients were excluded based on exclusion criteria, 426 patients (90 patients in the titrated GDMT group and 336 patients in the sub-optimal MT group) were enrolled for the analysis. The median follow-up period was 612 (453-798) days. Following statistical adjustment using the propensity score weighting method, the 2-year composite endpoint (composite of cardiac death and HF rehospitalization) rate was significantly lower in the titrated GDMT group, at 19%, compared with the sub-optimal MT group: 31% (score 3-4 points) and 43% (score 0-2 points). Subgroup analysis indicated a marked benefit of titrated GDMT in particular patient subgroups: age < 80 years, BMI 19.0-24.9, eGFR > 20 mL/min/1.73 m
, and serum potassium level ≤ 5.5 mmol/L.
: Prompt initiation and dose adjustment of multiple HF medications, with careful monitoring of the patient's physiologic and laboratory values, is a prerequisite for improving the prognosis of patients with heart failure.</description><subject>Blood pressure</subject><subject>Cardiac output</subject><subject>Care and treatment</subject><subject>Demographics</subject><subject>Diagnosis</subject><subject>Drug dosages</subject><subject>Drug therapy</subject><subject>Ejection fraction</subject><subject>Evaluation</subject><subject>Heart failure</subject><subject>Heart rate</subject><subject>Hospitalization</subject><subject>Medical records</subject><subject>Mortality</subject><subject>Observational studies</subject><subject>Patients</subject><subject>Physiology</subject><subject>Potassium</subject><subject>Software</subject><issn>2077-0383</issn><issn>2077-0383</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNptklFv0zAQxyMEYtPYE-_IEi9IqMOOGzt5rEpLJ20wjcFrdLEvq6vEzmxHU_nOfAfcdZSBsB989v93_ztZl2WvGT3jvKIfNqpnnNFcyuJZdpxTKSeUl_z5k_goOw1hQ9Mqy2nO5MvsiJeyyjmTx9nP79AZDdE4S1xLgHzGe_JVOW_sLbnEuHaaREdmIWAIJK6RLNrWKFDbHX4Ng9Hk3Jpo9hZgNbkx0R8M565vjN1fr9bge1AuuXgYtqR1nlwlCW0MZOXCYGJq5gdqcm_imszUGJF8ROX6AW2AmIQVgo9kCaYbPe6xa9SjStKu9KXpdLc9PC02qB4qLz08BK-yFy10AU8fz5Ps23JxM19NLr58Op_PLiaK0ypOGgkNABQFiKotZFNxIZKQT2nbUFkKybnIpYZmqnmTS2RUVIxjoaUoG11SfpK92_sO3t2NGGLdm6Cw68CiG0PNqaBc0lLKhL79B9240dvUXaKKaipYntM_1C10WBvbuvTHamdaz2RV8IoJUSTq7D9U2hp7o5zF1qT3vxLe7xOUdyF4bOvBmx78tma03s1X_WS-Ev3msdWx6VEf2N_TxH8BL83Muw</recordid><startdate>20240508</startdate><enddate>20240508</enddate><creator>Asano, Takaaki</creator><creator>Maeno, Yoshio</creator><creator>Nakano, Masataka</creator><creator>Taguri, Masataka</creator><creator>Miyasaka, Masaki</creator><creator>Nakai, Daisuke</creator><creator>Miyazaki, Itaru</creator><creator>Nasu, Takahito</creator><creator>Tanimoto, Shuzou</creator><creator>Masuda, Naoki</creator><creator>Morino, Yoshihiro</creator><creator>Isshiki, Takaaki</creator><creator>Ogata, Nobuhiko</creator><general>MDPI AG</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9922-1548</orcidid></search><sort><creationdate>20240508</creationdate><title>Validation of a New Scoring Method to Assess the Efficacy of Rapid Initiation and Titration of Combination Pharmacotherapy for Patients Hospitalized with Acute Decompensated Heart Failure with Reduced and Mildly Reduced Ejection Fraction</title><author>Asano, Takaaki ; Maeno, Yoshio ; Nakano, Masataka ; Taguri, Masataka ; Miyasaka, Masaki ; Nakai, Daisuke ; Miyazaki, Itaru ; Nasu, Takahito ; Tanimoto, Shuzou ; Masuda, Naoki ; Morino, Yoshihiro ; Isshiki, Takaaki ; Ogata, Nobuhiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c309t-b7abaaa55a69f57b9366309240fb0786733627dab4d3b27e106913e5d768bd803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Blood pressure</topic><topic>Cardiac output</topic><topic>Care and treatment</topic><topic>Demographics</topic><topic>Diagnosis</topic><topic>Drug dosages</topic><topic>Drug therapy</topic><topic>Ejection fraction</topic><topic>Evaluation</topic><topic>Heart failure</topic><topic>Heart rate</topic><topic>Hospitalization</topic><topic>Medical records</topic><topic>Mortality</topic><topic>Observational studies</topic><topic>Patients</topic><topic>Physiology</topic><topic>Potassium</topic><topic>Software</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Asano, Takaaki</creatorcontrib><creatorcontrib>Maeno, Yoshio</creatorcontrib><creatorcontrib>Nakano, Masataka</creatorcontrib><creatorcontrib>Taguri, Masataka</creatorcontrib><creatorcontrib>Miyasaka, Masaki</creatorcontrib><creatorcontrib>Nakai, Daisuke</creatorcontrib><creatorcontrib>Miyazaki, Itaru</creatorcontrib><creatorcontrib>Nasu, Takahito</creatorcontrib><creatorcontrib>Tanimoto, Shuzou</creatorcontrib><creatorcontrib>Masuda, Naoki</creatorcontrib><creatorcontrib>Morino, Yoshihiro</creatorcontrib><creatorcontrib>Isshiki, Takaaki</creatorcontrib><creatorcontrib>Ogata, Nobuhiko</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Asano, Takaaki</au><au>Maeno, Yoshio</au><au>Nakano, Masataka</au><au>Taguri, Masataka</au><au>Miyasaka, Masaki</au><au>Nakai, Daisuke</au><au>Miyazaki, Itaru</au><au>Nasu, Takahito</au><au>Tanimoto, Shuzou</au><au>Masuda, Naoki</au><au>Morino, Yoshihiro</au><au>Isshiki, Takaaki</au><au>Ogata, Nobuhiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Validation of a New Scoring Method to Assess the Efficacy of Rapid Initiation and Titration of Combination Pharmacotherapy for Patients Hospitalized with Acute Decompensated Heart Failure with Reduced and Mildly Reduced Ejection Fraction</atitle><jtitle>Journal of clinical medicine</jtitle><addtitle>J Clin Med</addtitle><date>2024-05-08</date><risdate>2024</risdate><volume>13</volume><issue>10</issue><spage>2775</spage><pages>2775-</pages><issn>2077-0383</issn><eissn>2077-0383</eissn><abstract>: Despite the encouragement of early initiation and titration of guideline-directed medical therapy (GDMT) for the treatment of heart failure (HF), most patients do not receive an adequate type and dose of pharmacotherapy in the real world.
: This study aimed to determine the efficacy of titrating composite GDMT in patients with HF with reduced and mildly reduced ejection fraction and to identify patient conditions that may benefit from titration of GDMT.
: This was a two-center, retrospective study of consecutive patients hospitalized with acute decompensated heart failure (ADHF). Patients were classified into two groups according to a scoring scale determined by combination and doses of four types of HF agents (ACEis/ARBs/ARNis, BBs, MRAs, and SGLT2is) at discharge. A score of 5 or greater was defined as titrated GDMT, and a score of 4 or less was regarded as sub-optimal medical therapy (MT).
: A total of 979 ADHF patients were screened. After 553 patients were excluded based on exclusion criteria, 426 patients (90 patients in the titrated GDMT group and 336 patients in the sub-optimal MT group) were enrolled for the analysis. The median follow-up period was 612 (453-798) days. Following statistical adjustment using the propensity score weighting method, the 2-year composite endpoint (composite of cardiac death and HF rehospitalization) rate was significantly lower in the titrated GDMT group, at 19%, compared with the sub-optimal MT group: 31% (score 3-4 points) and 43% (score 0-2 points). Subgroup analysis indicated a marked benefit of titrated GDMT in particular patient subgroups: age < 80 years, BMI 19.0-24.9, eGFR > 20 mL/min/1.73 m
, and serum potassium level ≤ 5.5 mmol/L.
: Prompt initiation and dose adjustment of multiple HF medications, with careful monitoring of the patient's physiologic and laboratory values, is a prerequisite for improving the prognosis of patients with heart failure.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>38792317</pmid><doi>10.3390/jcm13102775</doi><orcidid>https://orcid.org/0000-0001-9922-1548</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Blood pressure Cardiac output Care and treatment Demographics Diagnosis Drug dosages Drug therapy Ejection fraction Evaluation Heart failure Heart rate Hospitalization Medical records Mortality Observational studies Patients Physiology Potassium Software |
title | Validation of a New Scoring Method to Assess the Efficacy of Rapid Initiation and Titration of Combination Pharmacotherapy for Patients Hospitalized with Acute Decompensated Heart Failure with Reduced and Mildly Reduced Ejection Fraction |
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