PMID- 28488370 OWN - NLM STAT- MEDLINE DCOM- 20171204 LR - 20181202 IS - 1365-2036 (Electronic) IS - 0269-2813 (Linking) VI - 46 IP - 2 DP - 2017 Jul TI - Patients with cirrhosis who have coronary artery disease treated with cardiac stents have high rates of gastrointestinal bleeding, but no increased mortality. PG - 183-192 LID - 10.1111/apt.14121 [doi] AB - BACKGROUND: Patients with coronary artery disease (CAD) treated with stents require dual antiplatelet therapy (DAPT). For cirrhotics, who often have varices and coagulopathy, it is not clear if the risk of gastrointestinal bleeding (GIB) should preclude use of DAPT. AIM: To compare GIB and mortality rates in cirrhotics with CAD treated medically or with stents. METHODS: Using institutional databases, we identified patients with cirrhosis and CAD treated with stents or medical therapy between January 2000-September 2015. Primary outcomes were GIB and mortality. RESULTS: We identified 148 cirrhotics with CAD; 68 received stents (cases), 80 were treated with medical therapy (controls). Cases and controls had similar demographics, comorbidities, MELD scores and clinical presentation; DAPT was used in 98.5% of cases vs 5% of controls. The incidence of GIB was significantly higher in cases than controls (22.1% vs 5% at 1 year, P=.003; 27.9% vs 5% at 2 years, P=.0002), whereas all-cause mortality was similar (20.6% vs 21.3%). No patient required surgery or angiography for GIB, and no known patients died due to GIB. Multivariate analysis revealed use of a proton pump inhibitor (PPI) was highly protective against GIB (OR=0.26, 95%CI=0.08-0.79). CONCLUSIONS: CAD treatment with stents in our cirrhotics was associated with a significantly increased risk of GIB, but no adverse effects on survival. Although it remains unclear whether the cardiovascular benefits of stents outweigh the GIB risk, our findings suggest that DAPT should not be withheld from stented cirrhotics for fear of GIB. Moreover, the use of a PPI should be strongly considered. CI - (c) 2017 John Wiley & Sons Ltd. FAU - Krill, T AU - Krill T AD - Division of Digestive and Liver Disease, VA North Texas Healthcare System, Dallas, TX, USA. AD - Division of Digestive and Liver Diseases, University of Texas Southwestern Medical Center, Dallas, TX, USA. FAU - Brown, G AU - Brown G AD - Division of Digestive and Liver Disease, VA North Texas Healthcare System, Dallas, TX, USA. AD - Division of Digestive and Liver Diseases, University of Texas Southwestern Medical Center, Dallas, TX, USA. FAU - Weideman, R A AU - Weideman RA AD - Department of Pharmacy, VA North Texas Healthcare System, Dallas, TX, USA. FAU - Cipher, D J AU - Cipher DJ AD - College of Nursing and Health Innovation, University of Texas at Arlington, Arlington, TX, USA. FAU - Spechler, S J AU - Spechler SJ AD - Division of Digestive and Liver Disease, VA North Texas Healthcare System, Dallas, TX, USA. AD - Division of Digestive and Liver Diseases, University of Texas Southwestern Medical Center, Dallas, TX, USA. FAU - Brilakis, E AU - Brilakis E AD - Division of Cardiology, VA North Texas Healthcare System, Dallas, TX, USA. AD - Division of Cardiology, University of Texas Southwestern Medical Center, Dallas, TX, USA. FAU - Feagins, L A AU - Feagins LA AUID- ORCID: 0000-0001-7758-3257 AD - Division of Digestive and Liver Disease, VA North Texas Healthcare System, Dallas, TX, USA. AD - Division of Digestive and Liver Diseases, University of Texas Southwestern Medical Center, Dallas, TX, USA. LA - eng PT - Journal Article DEP - 20170509 PL - England TA - Aliment Pharmacol Ther JT - Alimentary pharmacology & therapeutics JID - 8707234 RN - 0 (Platelet Aggregation Inhibitors) RN - 0 (Proton Pump Inhibitors) SB - IM CIN - Aliment Pharmacol Ther. 2017 Sep;46(6):639. PMID: 28805330 CIN - Aliment Pharmacol Ther. 2017 Sep;46(6):638-639. PMID: 28805332 CIN - Aliment Pharmacol Ther. 2017 Oct;46(7):709. PMID: 28880447 CIN - Aliment Pharmacol Ther. 2017 Oct;46(7):710. PMID: 28880452 MH - Aged MH - Case-Control Studies MH - Coronary Artery Disease/*epidemiology/*surgery MH - Drug Therapy, Combination MH - Female MH - Gastrointestinal Hemorrhage/*etiology MH - Humans MH - Liver Cirrhosis/*epidemiology MH - Male MH - Middle Aged MH - Platelet Aggregation Inhibitors/administration & dosage/*adverse effects MH - Proton Pump Inhibitors/therapeutic use MH - Retrospective Studies MH - *Stents OTO - NOTNLM OT - aspirin OT - cirrhosis OT - gastrointestinal haemorrhage OT - thienopyridine EDAT- 2017/05/11 06:00 MHDA- 2017/12/05 06:00 CRDT- 2017/05/11 06:00 PHST- 2017/02/05 00:00 [received] PHST- 2017/02/19 00:00 [revised] PHST- 2017/04/08 00:00 [accepted] PHST- 2017/05/11 06:00 [pubmed] PHST- 2017/12/05 06:00 [medline] PHST- 2017/05/11 06:00 [entrez] AID - 10.1111/apt.14121 [doi] PST - ppublish SO - Aliment Pharmacol Ther. 2017 Jul;46(2):183-192. doi: 10.1111/apt.14121. Epub 2017 May 9.