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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004403naa a2200373 4500
001oai:DiVA.org:oru-68592
003SwePub
008180827s2018 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-685922 URI
024a https://doi.org/10.1007/s00198-018-4465-12 DOI
040 a (SwePub)oru
041 a engb eng
042 9 SwePub
072 7a vet2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Axelsson, K. F.u Geriatric Medicine, Sahlgrenska Academy, University of Gothenburg, Mölndal, Sweden4 aut
2451 0a Fracture Risk After Gastric Bypass Surgery :b A Retrospective Cohort Study
264 c 2018-07-27
264 1b Springer London,c 2018
338 a print2 rdacarrier
520 a Objectives: Gastric bypass surgery constitutes the most common and effective bariatric surgery to treat obesity. Gastric bypass leads to bone oss but fracture risk following surgery has been insufficiently studied. Our objective was to investigate if gastric bypass surgery in obese patients, with and without diabetes, was associated with fracture risk, and if the fracture risk was associated with post-surgery weight loss or insufficient calcium and vitamin D supplementation.Methods: Using large databases, 38 971 obese patients undergoing gastric bypass were identified, 7758 with diabetes and 31 213 without. Through multivariable 1:1 propensity score matching, well-balanced controls were identified. The risk of fracture and fall injury was investigated using Cox proportional hazards and flexible parameter models. Fracture risk according to weight loss and degree of calcium and vitamin D supplementation one year post-surgery was investigated.Results: 77 942 patients had a median and total follow-up time of 3.1 (IQR 1.7-4.6) and 251 310 person-years, respectively. Gastric bypass was associated with increased risk of any fracture, in patients with diabetes and without diabetes using a multivariable Cox model (HR 1.26, 95%CI 1.05-1.53 and HR 1.32, 95%CI 1.18-1.47, respectively). The risk of fall injury without fracture was also increased after gastric bypass, both in patients with (HR 1.26 95%CI 1.04-1.52) and without diabetes (HR 1.24 95%CI 1.12-1.38). Weight loss or degree of calcium and vitamin D supplementation after gastric bypass were not associated with fracture risk.Conclusions: Gastric bypass was associated with an increased risk of fracture and fall injury. Weight loss or calcium and vitamin D supplementation following surgery were not associated with fracture risk. These findings indicate that gastric bypass increases fracture risk, which could at least partly be due to increased susceptibility to falls.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Endokrinologi och diabetes0 (SwePub)302052 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Endocrinology and Diabetes0 (SwePub)302052 hsv//eng
700a Werling, M.u Department of Gastrosurgical Research & Education, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden4 aut
700a Eliasson, B.u Department of Molecular a nd Clinical Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, sweden4 aut
700a Szabo, Eva,d 1973-u Örebro universitet,Institutionen för medicinska vetenskaper,Region Örebro län,Department of Surgery4 aut0 (Swepub:oru)eso
700a Näslund, I.u Department of Surgery, Faculty of Medicine and Health, Örebro University, Örebro, Sweden4 aut
700a Wedel, H.u Health Metrics, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden4 aut
700a Lundh, D.u School of Bioscience, University of Skövde, Skövde, Sweden4 aut
700a Lorentzon, M.u Geriatric Medicine, Sahlgrenska Academy, University of Gothenburg, Mölndal, Sweden4 aut
710a Geriatric Medicine, Sahlgrenska Academy, University of Gothenburg, Mölndal, Swedenb Department of Gastrosurgical Research & Education, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden4 org
773t Osteoporosis Internationald : Springer Londong 29:Suppl. 1, s. S491-S491q 29:Suppl. 1<S491-S491x 0937-941Xx 1433-2965
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-68592
8564 8u https://doi.org/10.1007/s00198-018-4465-1

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