Heparin Use in Hemodialysis Patients following Gastrointestinal Bleeding

被引:6
|
作者
Shen, Jenny I. [1 ,3 ]
Mitani, Aya A. [2 ]
Winkelmayer, Wolfgang C. [1 ,4 ]
机构
[1] Stanford Univ, Sch Med, Dept Med, Div Nephrol, Palo Alto, CA 94304 USA
[2] Stanford Univ, Sch Med, Dept Med, Div Gen Med Disciplines, Palo Alto, CA 94304 USA
[3] Harbor UCLA Med Ctr, Div Nephrol & Hypertens, Dept Med, Los Angeles Biomed Res Inst, Torrance, CA 90502 USA
[4] Baylor Coll Med, Dept Med, Nephrol Sect, Houston, TX 77030 USA
关键词
Anti-coagulation; Gastrointestinal bleeding; Hemodialysis; Heparin; ATRIAL-FIBRILLATION; SAFETY; ANTICOAGULATION;
D O I
10.1159/000367901
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Heparin is commonly given during hemodialysis (HD). Patients undergoing HD have a high rate of gastrointestinal bleeding (GIB). It is unclear whether or when it is safe to give heparin after acute GIB. We describe the patterns and safety of heparin use with outpatient HD following an acute GIB. Methods: We identified patients aged >= 67 who, from 2004-2008, experienced GIB requiring hospitalization within 2 days of receiving maintenance HD with heparin. We used Cox regression to estimate the risk of recurrent GIB and death associated with receiving heparin the day they resumed outpatient HD post-GIB. Results: Of the 1,342 patients who had GIB, 1,158 (86%) received heparin at a median dose of 4,000 units with their first outpatient HD session after discharge from GIB. On average, their post-GIB doses were slightly lower than their pre-GIB doses (mean change: -214 +/- 3,266 units, p < 0.02). However, only 27% of patients had a decrease in their dose, while 21% had their dose increased. We did not find an increased risk of death or recurrent GIB associated with using heparin post-GIB (HR; 95% confidence interval (CI), for death: 1.01; 0.69-1.48; for recurrent GIB: 0.78; 0.39-1.57). Conclusions: The vast majority of these high-risk patients received heparin on the very first day they resumed outpatient HD post-GIB, and the majority at unchanged doses to those received pre-GIB. Even if the practice was not associated with increased risks of death or re-bleeding, it highlights an area for possible system-based improvement to the care for patients on HD. (C) 2014 S. Karger AG, Basel
引用
收藏
页码:300 / 307
页数:8
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