<?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>2026-08-29T14:25:13Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/17628" metadataPrefix="mets">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/17628</identifier><datestamp>2024-02-08T14:41:49Z</datestamp><setSpec>com_20.500.12105_15322</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_16927</setSpec></header><metadata><mets xmlns="http://www.loc.gov/METS/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" ID="&#xa;&#x9;&#x9;&#x9;&#x9;DSpace_ITEM_20.500.12105-17628" TYPE="DSpace ITEM" PROFILE="DSpace METS SIP Profile 1.0" xsi:schemaLocation="http://www.loc.gov/METS/ http://www.loc.gov/standards/mets/mets.xsd" OBJID="&#xa;&#x9;&#x9;&#x9;&#x9;hdl:20.500.12105/17628">
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                  <mods:namePart>Pérez-Belmonte, Luis M</mods:namePart>
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                  <mods:namePart>Gómez-Doblas, Juan J</mods:namePart>
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                  <mods:namePart>Millán-Gómez, Mercedes</mods:namePart>
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                  <mods:namePart>López-Carmona, María D</mods:namePart>
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                  <mods:namePart>Guijarro-Merino, Ricardo</mods:namePart>
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                  <mods:namePart>Carrasco-Chinchilla, Fernando</mods:namePart>
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                  <mods:namePart>de Teresa-Galván, Eduardo</mods:namePart>
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                  <mods:namePart>Jiménez-Navarro, Manuel</mods:namePart>
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                  <mods:namePart>Bernal-López, M Rosa</mods:namePart>
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                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Gómez-Huelgas, Ricardo</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-02-08T14:41:49Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2018-09-11</mods:dateIssued>
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               <mods:identifier type="doi">10.3390/jcm7090271</mods:identifier>
               <mods:identifier type="issn">2077-0383</mods:identifier>
               <mods:identifier type="journal">Journal of clinical medicine</mods:identifier>
               <mods:identifier type="other">http://hdl.handle.net/10668/12937</mods:identifier>
               <mods:identifier type="pubmedID">30208631</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/17628</mods:identifier>
               <mods:abstract>The use of noninsulin antihyperglycaemic drugs in the hospital setting has not yet been fully described. This observational study compared the efficacy and safety of the standard basal-bolus insulin regimen versus a dipeptidyl peptidase-4 inhibitor (linagliptin) plus basal insulin in medicine department inpatients in real-world clinical practice. We retrospectively enrolled non-critically ill patients with type 2 diabetes with mild to moderate hyperglycaemia and no injectable treatments at home who were treated with a hospital antihyperglycaemic regimen (basal-bolus insulin, or linagliptin-basal insulin) between January 2016 and December 2017. Propensity score was used to match patients in both treatment groups and a comparative analysis was conducted to test the significance of differences between groups. After matched-pair analysis, 227 patients were included per group. No differences were shown between basal-bolus versus linagliptin-basal regimens for the mean daily blood glucose concentration after admission (standardized difference = 0.011), number of blood glucose readings between 100⁻140 mg/dL (standardized difference = 0.017) and >200 mg/dL (standardized difference = 0.021), or treatment failures (standardized difference = 0.011). Patients on basal-bolus insulin received higher total insulin doses and a higher daily number of injections (standardized differences = 0.298 and 0.301, respectively). Basal and supplemental rapid-acting insulin doses were similar (standardized differences = 0.003 and 0.012, respectively). There were no differences in hospital stay length (standardized difference = 0.003), hypoglycaemic events (standardized difference = 0.018), or hospital complications (standardized difference = 0.010) between groups. This study shows that in real-world clinical practice, the linagliptin-basal insulin regimen was as effective and safe as the standard basal-bolus regimen in non-critical patients with type 2 diabetes with mild to moderate hyperglycaemia treated at home without injectable therapies.</mods:abstract>
               <mods:language>
                  <mods:languageTerm authority="rfc3066">eng</mods:languageTerm>
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               <mods:subject>
                  <mods:topic>diabetes mellitus</mods:topic>
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               <mods:subject>
                  <mods:topic>hospital care</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>inpatient hyperglycaemia</mods:topic>
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               <mods:subject>
                  <mods:topic>linagliptin</mods:topic>
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                  <mods:title>Use of Linagliptin for the Management of Medicine Department Inpatients with Type 2 Diabetes in Real-World Clinical Practice (Lina-Real-World Study).</mods:title>
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               <mods:genre>research article</mods:genre>
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