Optimizing Cirrhosis Emergency Care

A
Archita Desai, MD

Primary Investigator

Enrolling By Invitation
18 years - 100 years
All
Phase N/A
1 participants needed
6 Locations

Brief description of study

What is the purpose of this study?

Within our IU health system, utilizing retrospective data we developed a clinical decision instrument based on ED visits, named it as Cirrhosis Risk Instrument for Stratifying Post Emergency Department mortality (CRISPE) tool. This tool was designed to identify predictors of 14-day and 30-day mortality in individuals with cirrhosis. However, given the retrospective nature of our study, certain limitations exist, particularly regarding data collection, as it relies on chart reviews. To enhance the reliability of this tool, we aim to validate it prospectively in individuals with cirrhosis who present to the ED. Secondarily, we aim to collect patient-reported outcomes (PROs) and test the utility of these in predicting healthcare utilization (HCU) after an ED visit.

THIS STUDY IS ENROLLING BY INVITATION ONLY -   Participants will be recruited from among patients being seen at an IU Emergency Department and will be contacted in one of two ways: by telephone or in person at an IU Health clinic visit.

Detailed description of study

What will happen during the study?

  • Our study is a prospective study including patient population with cirrhosis who experienced an ED visits.
  • After informed consent, patient-reported outcomes (surveys attached) will be collected within one week of ED discharge or post-ED hospitalization discharge.
  • Each survey tool will be accessible electronically or via paper for completion and all assessments are expected to take no more than 60–90 minutes.
  • For participants who complete the study in person, a member of the study team will conduct a subject interview including several measures to assess each subject’s demographics and quality of life as well as frailty and strength testing via a grip strength test, a sit to stand test and a balance test.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Cirrhosis
  • Age: 18 years - 100 years
  • Gender: All

INCLUSION CRITERIA:
1.Age > 18 years 
2. Individuals who had cirrhosis identified by:
a.  ICD 10 codes 
b. liver biopsy
c. nodular liver on imaging with ascites OR varices/collaterals OR hepatocellular carcinoma OR  splenomegaly AND thrombocytopenia
3. ED visit at an IU Health facility


EXCLUSION CRITERIA:
•    Incarcerated
•    Post-liver transplant at time of ED visit
•    Under hospice care or discharge to hospice
•    Pregnant
•    Unable to provide consent

Updated on 07 May 2025. Study ID: GI-IIR-ED, 26810
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