P622 Stress echocardiography for liver transplant evaluation

2003 ◽  
Vol 24 (5) ◽  
pp. 108
Author(s):  
A VIEIRA
2001 ◽  
Vol 71 (6) ◽  
pp. 818 ◽  
Author(s):  
Jeffrey S. Plotkin ◽  
Lynt B. Johnson ◽  
Vinod K. Rustgi ◽  
Paul C. Kuo ◽  
Amy D. Liu

2018 ◽  
Vol 28 (4) ◽  
pp. 361-367
Author(s):  
David Snipelisky ◽  
Justin Shipman ◽  
Nicole Olson ◽  
Patricia Pellikka ◽  
Bashar Aqel ◽  
...  

Introduction: Dobutamine stress echocardiography (DSE) is frequently used to screen for obstructive coronary artery disease in the pre-liver transplant evaluation. Although atropine is a commonly used adjunctive medication, no study has evaluated its side effect profile in patients with end-stage liver disease (ESLD). Research Question: What is the safety of atropine in candidates undergoing pre-liver transplant evaluation when atropine is used in stress testing? Design: This multicenter, prospective study enrolled patients over a 6-month period undergoing pre-liver transplant evaluation. Each patient completed a questionnaire assessing anticholinergic-related symptoms within 24 hours of testing and 48 hours following. Comparisons were made among patients receiving any atropine dose versus those who did not and among patients receiving at least 1 mg atropine and those receiving less/none. Results: Forty patients were evaluated, and 32 (80%) had adjunctive atropine administered. No differences in clinical characteristics were noted. In comparisons among patients receiving any dose of atropine with those who did not, questionnaire results indicated a higher rate of nausea prior to testing and higher overall symptom severity following testing in patients not receiving atropine. In comparisons among patients receiving less than 1 mg atropine with those receiving at least 1 mg atropine, no difference in pre- or posttesting questionnaire responses was present. No patient in the study required reversal agents or hospitalization within 7 days of testing. Conclusions: Atropine, a hepatically metabolized medication, did not predispose patients with ESLD to an increased symptom burden, and clinical outcomes related to DSE were unaffected.


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