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Predicting the Occurrence of Hypotension in Stable Patients With Nonvariceal Upper Gastrointestinal Bleeding: Point-of-Care Lactate Testing

Authors
Ko, Byuk SungKim, Won YoungRyoo, Seung MokAhn, ShinSohn, Chang HwanSeo, Dong WooLee, Yoon-SeonLim, Kyoung SooJung, Hwoon-Yong
Issue Date
Nov-2015
Publisher
Wolters Kluwer Health
Keywords
hypotension; nonvariceal upper gastrointestinal bleeding; point-of-care testing of lactate
Citation
Critical Care Medicine, v.43, no.11, pp.2409 - 2415
Indexed
SCIE
SCOPUS
Journal Title
Critical Care Medicine
Volume
43
Number
11
Start Page
2409
End Page
2415
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/155875
DOI
10.1097/CCM.0000000000001275
ISSN
0090-3493
Abstract
Objectives: It is difficult to assess risk in normotensive patients with upper gastrointestinal bleeding. The aim of this study was to evaluate whether the initial lactate value can predict the inhospital occurrence of hypotension in stable patients with acute nonvariceal upper gastrointestinal bleeding. Design: Retrospective, observational, single-center study. Setting: Emergency department of a tertiary-care, university-affiliated hospital during a 5-year period. Patients: Medical records of 3,489 patients with acute upper gastrointestinal bleeding who were normotensive at presentation to the emergency department. We analyzed the ability of point-of-care testing of lactate at emergency department admission to predict hypotension development (defined as systolic blood pressure <90 mm Hg) within 24 hours after emergency department admission. Interventions: None. Measurements and Main Results: Of the 1,003 patients with acute nonvariceal upper gastrointestinal bleeding, 157 patients experienced hypotension within 24 hours. Lactate was independently associated with hypotension development (odds ratio, 1.6; 95% CI, 1.4.1.7), and the risk of hypotension significantly increased as the lactate increased from 2.5.4.9 mmol/L (odds ratio, 2.2) to 5.0.7.4 mmol/L (odds ratio, 4.0) and to greater than or equal to 7.5 mmol/L (odds ratio, 39.2) (p < 0.001). Lactate elevation (. 2.5 mmol/L) was associated with 90% specificity and an 84% negative predictive value for hypotension development. When the lactate levels were greater than 5.0 mmol/L, the specificity and negative predictive value increased to 98% and 87%, respectively. Conclusions: Point-of-care testing of lactate can predict in-hospital occurrence of hypotension in stable patients with acute nonvariceal upper gastrointestinal bleeding. However, subsequently, prospective validate research will be required to clarify this.
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