The Cirrhosis Outpatient Optimization, Readmission & Safety Study
Status: | Terminated |
---|---|
Conditions: | Gastrointestinal |
Therapuetic Areas: | Gastroenterology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 10/28/2017 |
Start Date: | April 2015 |
End Date: | March 2018 |
COORS: The Cirrhosis Outpatient Optimization, Readmission & Safety Study
A prospective series comparing care incorporating home monitoring and liver care coordination
to conventional care for patients with cirrhosis.
to conventional care for patients with cirrhosis.
Telemonitoring has been suggested to have potential benefits in patients with cirrhosis.
However, to date, no prospective studies exist to support this idea. Hence, the investigators
study would like to explore the use of home telemonitoring devices with vital sign capturing
capabilities in recently-discharged patients with cirrhosis to decrease 30-day readmissions,
mortality and costs.
This is prospective, randomized controlled trial comparing two strategies of post-discharged
care in patients with cirrhosis-related hospitalizations.
First treatment arm will incorporate the Vivify home monitoring device into post hospital
care.Home monitoring kits include a tablet with wireless internet and vital sign monitoring
capabilities (temperature, blood pressure, heart rate, weight and pulse oximetry if needed)
and the device has the ability to trigger an alert to the "liver care coordinator."
Second treatment arm will continue the standard of care therapy that all post- hospitalized
patients receive upon discharge, i.e. return to clinic appointments, education regarding any
signs or worsening symptoms to watch for, as well as contact numbers to connect with their
doctor or nurse.
However, to date, no prospective studies exist to support this idea. Hence, the investigators
study would like to explore the use of home telemonitoring devices with vital sign capturing
capabilities in recently-discharged patients with cirrhosis to decrease 30-day readmissions,
mortality and costs.
This is prospective, randomized controlled trial comparing two strategies of post-discharged
care in patients with cirrhosis-related hospitalizations.
First treatment arm will incorporate the Vivify home monitoring device into post hospital
care.Home monitoring kits include a tablet with wireless internet and vital sign monitoring
capabilities (temperature, blood pressure, heart rate, weight and pulse oximetry if needed)
and the device has the ability to trigger an alert to the "liver care coordinator."
Second treatment arm will continue the standard of care therapy that all post- hospitalized
patients receive upon discharge, i.e. return to clinic appointments, education regarding any
signs or worsening symptoms to watch for, as well as contact numbers to connect with their
doctor or nurse.
Inclusion Criteria:
1. Ascites requiring paracentesis during the hospitalization
2. Hepatic encephalopathy defined as altered mental status that improves after treatment
with lactulose
3. Variceal hemorrhage, defined as clinically significant gastrointestinal bleed
(tachycardia, hypotension, requirement for blood transfusion, or >2g drop in
hemoglobin) and varices seen on endoscopy
4. Spontaneous bacterial peritonitis defined as >250 polymorphonuclear cells per
high-power field and/or monomicrobial culture in the ascetic fluid
5. Renal failure in the presence of ascites, defined as a rise in the serum creatinine by
0.5mg/dl (to >1.5mg/dl), with ascites documented on physical exam or ultrasound, or
admitted on diuretics for the treatment of ascites
6. Hyponatremia, defined by serum sodium <130 on admission labs
7. Hepatocellular carcinoma as seen on arterial phase MRI or liver biopsy, if tumor is
treated and fits within Milan criteria
Exclusion Criteria:
- Admissions for scheduled or elective procedures
- Patients with a comorbid conditions with a life expectancy of less than 12 months or
ones that may confound a patient's clinical course
- Hepatocellular carcinoma
- Hepatorenal syndrome
- Hepatopulmonary syndrome
- Metastatic cancer
- Chronic kidney disease (pre-dialysis, dialysis)
- Congestive heart failure
- Diagnosed dementia
- HIV/AIDS
- Pregnancy or planned pregnancy during the study
- Those managed by palliative care
- Patients with liver transplants prior to or during the index hospitalization
- Patients unable to understand study procedures/instructions/use of the home
monitoring device
- Patients unable to stand for <1 minute
- Patients living in nursing homes or similar institutions
We found this trial at
1
site
Los Angeles, California 90095
Principal Investigator: Daniel Hommes, MD PhD
Phone: 310-825-1793
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