モリモト サトシ
Morimoto Satoshi
森本 聡 所属 医学部 医学科(東京女子医科大学病院) 職種 准教授 |
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論文種別 | 原著 |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | Risk factors of normal ankle-brachial index and low toe-brachial index in hemodialysis patients. |
掲載誌名 | 正式名:Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy 略 称:Ther Apher Dial ISSNコード:17449987/17449979 |
掲載区分 | 国外 |
巻・号・頁 | 13(2),pp.103-7 |
著者・共著者 | Morimoto Satoshi†*, Nakajima Fumitaka, Yurugi Takatomi, Morita Tatsuyori, Jo Fusakazu, Nishikawa Mitsushige, Iwasaka Toshiji, Maki Kei |
担当区分 | 筆頭著者,責任著者 |
発行年月 | 2009/04 |
概要 | The prevalence of peripheral arterial occlusive disease is high in patients with terminal renal failure, and it is a major problem in those on dialysis. A low ankle-brachial index (ABI) suggests the presence of arterial stenotic lesions between the aorta and the ankle joint, while a low toe-brachial index (TBI) suggests stenotic lesions between the aorta and the toes. Therefore, a normal ABI (> or =0.9) and a low TBI (<0.6) may indicate the presence of stenotic lesions located only on the peripheral side of the ankle joint. In the present study, risk factors of normal ABI/low TBI were investigated. In 115 patients on maintenance dialysis, the ABI and TBI were simultaneously measured, and the background factors and laboratory data of patients with normal ABI/low TBI (L group) and those with normal ABI/normal TBI (> or =0.6) (N group) were compared. Low ankle-brachial and toe-brachial indices were detected in 13% and 22% of the patients, respectively. Comparison of the background factors and laboratory data between the N and L groups showed that the ratio of diabetes mellitus, interdialytic body weight gain, and Hb(A1c) values were significantly higher in the L group than in the N group. It was clarified that diabetes and excess body weight gain are involved as risk factors in dialysis patients with normal ABI/low TBI. |
DOI | 10.1111/j.1744-9987.2009.00663.x |
PMID | 19379148 |