Evidence map›Paper›PMID 40913723›Full record

ArticleDigestive diseases and sciences2026

Socioeconomic Factors Impact the Perception of Healthcare Experiences in Patients with Cirrhosis.

Nicole Ng, Subhanik Purkayastha, Xiaohan Ying, Arun Jesudian, Russell Rosenblatt

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Article in Digestive diseases and sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Nicole NgDepartment of Internal Medicine, NewYork-Presbyterian Hospital/Weill Cornell, New York, NY, USA.
Subhanik PurkayasthaWeill Cornell Medical College, New York, NY, USA.
Xiaohan YingDepartment of Internal Medicine, NewYork-Presbyterian Hospital/Weill Cornell, New York, NY, USA.
Arun JesudianDivision of Gastroenterology and Hepatology, Weill Cornell Medicine, 1305 York Avenue, 4th Floor, New York, NY, 10021, USA.
Russell RosenblattDivision of Gastroenterology and Hepatology, Weill Cornell Medicine, 1305 York Avenue, 4th Floor, New York, NY, 10021, USA. rur9017@med.cornell.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSuboptimal patient-provider relationship is a significant contributor to healthcare disparities. Minority populations report fewer favorable interactions, which may lead to poorer outcomes and engagement in care. Patients with chronic diseases are especially at risk.

aimsWe aimed to study perceptions of healthcare providers and experience among those with cirrhosis.

methodsThe nationally representative database, All of Us, was queried. The primary outcome was "favorable healthcare experiences," defined as whether providers asked for opinions, demonstrated respect, and were easy to understand. The secondary outcome was "unfavorable healthcare experiences," defined as whether patients felt they were treated with less courtesy, received poorer service, or not listened to. We compared the experience between income levels and other demographic variables. Multivariable logistic regression was adjusted for a priori covariates.

results5753 patients with cirrhosis were included with a mean age of 58. The majority were male (51%), White (52%), and US-born (84%). On multivariable analysis, compared to those earning > $150 k annually, participants with $10-35 k and < $10 k reported significantly lower odds of finding providers easy to understand (OR 0.40 [0.17-0.96] and OR 0.37 [0.15-0.94], respectively) and higher odds of feeling they were treated with less courtesy (OR 3.10 [1.06-9.03] and OR 4.13 [1.30-13.1], respectively). After further controlling for education, participants with an annual income of $10-35 k and < $10 k still reported higher odds of feeling they received poorer service than others (OR 3.87 [1.09-13.71] and OR 5.01 [1.26-19.8], respectively). Compared to men, women felt that they were not listened to (OR 1.90 [1.37-2.63]).

conclusionPatients with cirrhosis from various backgrounds report significantly different experiences with providers. Notably, those with lower income endorsed more unfavorable interactions. We identified areas for interventions to strengthen the patient-provider relationship among patients with chronic liver disease.

Indexed as

Healthcare DisparitiesLiver CirrhosisPhysician-Patient RelationsAdultAgedFemaleHumansMaleMiddle AgedPerceptionSocioeconomic FactorsUnited StatesChronic liver diseasePatientProvider behaviorProvider communicationProvider interactionsProvider relationship

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.