TY - JOUR A1 - Streit, Sven A1 - Verschoor, Marjolein A1 - Rodond, Nicolas A1 - Bonfim, Daiana A1 - Burman, Robert Anders A1 - Collins, Claire A1 - Gerasimovska Kitanovska, Biljana A1 - Gintere, Sandra A1 - Gómez Bravo, Raquel A1 - Hoffmann, Kathryn A1 - Iftode, Claudia A1 - Johansen, Kasper A1 - Kerse, Ngaire A1 - Koskela, Tuomas H. A1 - Kreitmayer Peštić, Sanda A1 - Kurpas, Donata A1 - Mallen, Christian David A1 - Maisoneuve, Hubert A1 - Merlo, Christoph A1 - Müller, Yolanda A1 - Muth, Christiane A1 - Šter, Marija Petek A1 - Petrazzuoli, Ferdinando A1 - Rosemann, Thomas A1 - Sattler, Martin A1 - Švadlenková, Zuzana A1 - Tatsioni, Athina A1 - Thulesius, Hans A1 - Tkachenko, Victoria A1 - Torzsa, Peter A1 - Tsopra, Rosy A1 - Canan, Tuz A1 - Viegas, Rita P. A. A1 - Vinker, Shlomo A1 - Margot W. M. de, Waal A1 - Zeller, Andreas A1 - Gussekloo, Jacobijn A1 - Poortvliet, Rosalinde K. E. T1 - Variation in GP decisions on antihypertensive treatment in oldest-old and frail individuals across 29 countries T2 - BMC geriatrics N2 - Background: In oldest-old patients (>80), few trials showed efficacy of treating hypertension and they included mostly the healthiest elderly. The resulting lack of knowledge has led to inconsistent guidelines, mainly based on systolic blood pressure (SBP), cardiovascular disease (CVD) but not on frailty despite the high prevalence in oldest-old. This may lead to variation how General Practitioners (GPs) treat hypertension. Our aim was to investigate treatment variation of GPs in oldest-olds across countries and to identify the role of frailty in that decision. Methods: Using a survey, we compared treatment decisions in cases of oldest-old varying in SBP, CVD, and frailty. GPs were asked if they would start antihypertensive treatment in each case. In 2016, we invited GPs in Europe, Brazil, Israel, and New Zealand. We compared the percentage of cases that would be treated per countries. A logistic mixed-effects model was used to derive odds ratio (OR) for frailty with 95% confidence intervals (CI), adjusted for SBP, CVD, and GP characteristics (sex, location and prevalence of oldest-old per GP office, and years of experience). The mixed-effects model was used to account for the multiple assessments per GP. Results: The 29 countries yielded 2543 participating GPs: 52% were female, 51% located in a city, 71% reported a high prevalence of oldest-old in their offices, 38% and had >20 years of experience. Across countries, considerable variation was found in the decision to start antihypertensive treatment in the oldest-old ranging from 34 to 88%. In 24/29 (83%) countries, frailty was associated with GPs’ decision not to start treatment even after adjustment for SBP, CVD, and GP characteristics (OR 0.53, 95%CI 0.48–0.59; ORs per country 0.11–1.78). Conclusions: Across countries, we found considerable variation in starting antihypertensive medication in oldest-old. The frail oldest-old had an odds ratio of 0.53 of receiving antihypertensive treatment. Future hypertension trials should also include frail patients to acquire evidence on the efficacy of antihypertensive treatment in oldest-old patients with frailty, with the aim to get evidence-based data for clinical decision-making. KW - Hypertension KW - Oldest-old KW - Clinical variation KW - General practitioners KW - Frailty KW - Elderly Y1 - 2017 UR - http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/44118 UR - https://nbn-resolving.org/urn:nbn:de:hebis:30:3-441182 SN - 1471-2318 N1 - © The Author(s). 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated VL - 17 IS - 1, Art. 93 SP - 1 EP - 7 PB - BioMed Central CY - London ER -