<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-13T01:14:03Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:11351/11373" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:11351/11373</identifier><datestamp>2025-10-24T10:34:00Z</datestamp><setSpec>com_2072_378070</setSpec><setSpec>com_2072_378040</setSpec><setSpec>col_2072_378092</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Invasive Treatment Strategy in Adults With Frailty and Non–ST-Segment Elevation Myocardial Infarction: A Secondary Analysis of a Randomized Clinical Trial</dc:title>
   <dc:creator>Sanchis, Juan</dc:creator>
   <dc:creator>BUENO, HECTOR</dc:creator>
   <dc:creator>García-Blas, Sergio</dc:creator>
   <dc:creator>Alegre, Oriol</dc:creator>
   <dc:creator>Martí, David</dc:creator>
   <dc:creator>Martinez-Selles, Manuel</dc:creator>
   <dc:creator>García del Blanco, Bruno</dc:creator>
   <dc:subject>Angiografia</dc:subject>
   <dc:subject>Infart de miocardi - Tractament</dc:subject>
   <dc:subject>ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Therapeutics::Conservative Treatment</dc:subject>
   <dc:subject>ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Diagnosis::Diagnostic Techniques and Procedures::Diagnostic Imaging::Cardiac Imaging Techniques::Coronary Angiography</dc:subject>
   <dc:subject>DISEASES::Pathological Conditions, Signs and Symptoms::Pathologic Processes::Frailty</dc:subject>
   <dc:subject>DISEASES::Cardiovascular Diseases::Heart Diseases::Myocardial Ischemia::Myocardial Infarction::Non-ST Elevated Myocardial Infarction</dc:subject>
   <dc:subject>TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::terapéutica::tratamiento conservador</dc:subject>
   <dc:subject>TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::diagnóstico::técnicas y procedimientos diagnósticos::diagnóstico por imagen::técnicas de imagen cardíaca::angiografía coronaria</dc:subject>
   <dc:subject>ENFERMEDADES::afecciones patológicas, signos y síntomas::procesos patológicos::fragilidad</dc:subject>
   <dc:subject>ENFERMEDADES::enfermedades cardiovasculares::enfermedades cardíacas::isquemia miocárdica::infarto de miocardio::infarto de miocardio sin elevación del ST</dc:subject>
   <dcterms:abstract>Invasive treatment; Myocardial infarction; ST-segment</dcterms:abstract>
   <dcterms:abstract>Tractament invasiu; Infart de miocardi; Segment ST</dcterms:abstract>
   <dcterms:abstract>Tratamiento invasivo; Infarto de miocardio; Segmento ST</dcterms:abstract>
   <dcterms:abstract>Importance  The MOSCA-FRAIL randomized clinical trial compared invasive and conservative treatment strategies in patients with frailty with non–ST-segment elevation myocardial infarction (NSTEMI). It showed no differences in the number of days alive and out of the hospital at 1 year.&#xd;
Objective  To assess the outcomes of the MOSCA-FRAIL trial during extended follow-up.&#xd;
Design, Setting, and Participants  The MOSCA-FRAIL randomized clinical trial was conducted at 13 hospitals in Spain between July 7, 2017, and January 9, 2021, and included 167 adults (aged ≥70 years) with frailty (Clinical Frailty Scale score ≥4) and NSTEMI. In this preplanned secondary analysis, follow-up was extended to January 31, 2023. Data analysis was performed from April 5 to 29, 2023, using the intention-to-treat principle.&#xd;
Interventions  Patients were randomized to a routine invasive (coronary angiography and revascularization if feasible [n = 84]) or a conservative (medical treatment with coronary angiography only if recurrent ischemia [n = 83]) strategy.&#xd;
Main outcomes and measures  The primary end point was the difference in restricted mean survival time (RMST). Secondary end points included readmissions for any cause, considering recurrent readmissions.&#xd;
Results  Among the 167 patients included in the analysis, the mean (SD) age was 86 (5) years; 79 (47.3%) were men and 88 (52.7%) were women. A total of 93 deaths and 367 readmissions accrued. The RMST for all-cause death over the entire follow-up was 3.13 (95% CI, 2.72-3.60) years in the invasive and 3.06 (95% CI, 2.84-3.32) years in the conservative treatment groups. The RMST analysis showed inconclusive differences in survival time (invasive minus conservative difference, 28 [95% CI, −188 to 230] days). Patients under invasive treatment tended to have shorter survival in the first year (−28 [95% CI, −63 to 7] days), which improved after the first year (192 [95% CI, 90-230] days). Kaplan-Meier mortality curves intersected, displaying higher mortality to 1 year in the invasive group that shifted to a late benefit (landmark analysis hazard ratio, 0.58 [95% CI, 0.33-0.99]; P = .045). Early harm was more evident in the subgroup with a Clinical Frailty Scale score greater than 4. No differences were found for the secondary end points.&#xd;
Conclusions and Relevance  In this extended follow-up of a randomized clinical trial of patients with frailty and NSTEMI, an invasive treatment strategy did not improve outcomes at a median follow-up of 1113 (IQR, 443-1441) days. However, a differential distribution of deaths was observed, with early harm followed by later benefit. The phenomenon of depletion of susceptible patients may be responsible for this behavior.&#xd;
Trial registration  ClinicalTrials.gov Identifier: NCT03208153</dcterms:abstract>
   <dcterms:abstract>This study was supported by grants FIS 17/01736 and FIS 17/00899 from Spain’s Ministry of Science and Innovation through the Carlos III Health Institute: Fondo Europeo de Desarrollo Regional and by grant 16/11/00420 from Centro de Investigación Biomédica en Red Enfermedades Cardiovaculares.</dcterms:abstract>
   <dcterms:dateAccepted>2025-10-24T10:34:00Z</dcterms:dateAccepted>
   <dcterms:available>2025-10-24T10:34:00Z</dcterms:available>
   <dcterms:created>2025-10-24T10:34:00Z</dcterms:created>
   <dcterms:issued>2024-04-25T10:05:40Z</dcterms:issued>
   <dcterms:issued>2024-04-25T10:05:40Z</dcterms:issued>
   <dcterms:issued>2024-03-04</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>http://hdl.handle.net/11351/11373</dc:identifier>
   <dc:relation>JAMA Network Open;7(3)</dc:relation>
   <dc:relation>https://doi.org/10.1001/jamanetworkopen.2024.0809</dc:relation>
   <dc:rights>Attribution 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>American Medical Association</dc:publisher>
   <dc:source>Scientia</dc:source>
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