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dc.contributor.authorHalvorsen, Lene Vernås
dc.contributor.authorSøraas, Camilla Lund
dc.contributor.authorLarstorp, Anne Cecilie Kjeldsen
dc.contributor.authorHjørnholm, Ulla
dc.contributor.authorKjær, Vibeke Norheim
dc.contributor.authorLiestøl, Knut
dc.contributor.authorAune, Arleen
dc.contributor.authorOlsen, Erik
dc.contributor.authorBrobak, Karl Marius
dc.contributor.authorBergland, Ola Undrum
dc.contributor.authorRognstad, Stine
dc.contributor.authorAarskog, Nikolai Ravn
dc.contributor.authorHeimark, Sondre
dc.contributor.authorFadl Elmula, Fadl Elmula M.
dc.contributor.authorGerdts, Eva
dc.contributor.authorMo, Rune
dc.contributor.authorSolbu, Marit Dahl
dc.contributor.authorOpdal, Mimi Stokke
dc.contributor.authorKjeldsen, Sverre
dc.contributor.authorRostrup, Morten
dc.contributor.authorHøieggen, Aud
dc.date.accessioned2024-10-01T12:31:42Z
dc.date.available2024-10-01T12:31:42Z
dc.date.issued2024-01-07
dc.description.abstractBACKGROUND - Drug concentration in blood or urine is an acknowledged method to detect nonadherence. Observational studies suggest that informing patients about low or absent serum drug levels improves blood pressure (BP). We performed a multicenter randomized clinical trial to test the hypothesis that therapeutic drug monitoring (TDM) could improve drug adherence and BP in patients with uncontrolled hypertension (HT).<p> <p>METHODS - Patients were ≥18 years on stable treatment with at least 2 antihypertensive agents. We planned to randomize 80 nonadherent patients with a systolic daytime ambulatory BP ≥135 mm Hg to TDM intervention or not. The control group and the study personnel who measured BP remained uninformed about serum drug measurements throughout. All patients and physicians were blinded for BPs. Lifestyle advice and detailed information on the disease process and the importance of BP treatment were given to both groups.<p> <p>RESULTS - From 2017 to 2022, we randomized 46 diagnosed nonadherent from a total of 606 patients with uncontrolled HT. The TDM group had a 6.7 (±14.5) mm Hg reduction from 147.9 (±10.3) to 141.1 (±14.1) mm Hg, and the control group experienced a 7.3 (±13.2) mm Hg reduction from 147.1 (±9.2) to 139.1 (±17.4) mm Hg, P = 0.9 between groups. Adherence improved in both groups, 73% in the TDM group and 59% in the control group became adherent at 3 months, P = 0.51.<p> <p>CONCLUSIONS - In our prospective multicenter clinical trial of uncontrolled and nonadherent hypertensive patients, we found no additional effect of TDM on BP and drug adherence compared with standard care.en_US
dc.identifier.citationHalvorsen, Søraas, Larstorp, Hjørnholm, Kjær, Liestøl, Aune, Olsen, Brobak, Bergland, Rognstad, Aarskog, Heimark, Fadl Elmula, Gerdts, Mo, Solbu, Opdal, Kjeldsen, Rostrup, Høieggen. Effect of Therapeutic Drug Monitoring on Adherence and Blood Pressure: A Multicenter Randomized Clinical Trial. American Journal of Hypertension. 2024;37(10):826-836en_US
dc.identifier.cristinIDFRIDAID 2305000
dc.identifier.doi10.1093/ajh/hpae059
dc.identifier.issn0895-7061
dc.identifier.issn1941-7225
dc.identifier.urihttps://hdl.handle.net/10037/34958
dc.language.isoengen_US
dc.publisherOxford University Pressen_US
dc.relation.journalAmerican Journal of Hypertension
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2024 The Author(s)en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.rightsAttribution 4.0 International (CC BY 4.0)en_US
dc.titleEffect of Therapeutic Drug Monitoring on Adherence and Blood Pressure: A Multicenter Randomized Clinical Trialen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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Attribution 4.0 International (CC BY 4.0)
Med mindre det står noe annet, er denne innførselens lisens beskrevet som Attribution 4.0 International (CC BY 4.0)