Literature DB >> 32552526

Association between hospital admissions and healthcare provider communication for individuals with sickle cell disease.

Robert M Cronin1,2,3, Manshu Yang4,5, Jane S Hankins6, Jeannie Byrd7, Brandi M Pernell7,8, Adetola Kassim9, Patricia Adams-Graves10, Alexis A Thompson11, Karen Kalinyak12, Michael DeBaun7, Marsha Treadwell13.   

Abstract

Objective: To test the hypothesis that caregivers' or adult participants' low ratings of provider communication are associated with more hospital admissions among adults and children with sickle cell disease (SCD), respectively. Secondarily, we determined whether there was an association between the caregivers' or participants' health literacy and rating of providers' communication.
Methods: Primary data were collected from participants through surveys between 2014 and 2016, across six sickle cell centers throughout the U.S. In this cross-sectional cohort study, 211 adults with SCD and 331 caregivers of children with SCD completed surveys evaluating provider communication using the Consumer Assessment of Healthcare Providers and Systems (CAHPS), healthcare utilization, health literacy, and other sociodemographic and behavioral variables. Analyses included descriptive statistics, bivariate analyses, and logistic regression.
Results: Participants with better ratings of provider communication were less likely to be hospitalized (odds ratio (OR) = 0.54, 95% confidence interval (CI) = [0.35, 0.83]). Positive ratings of provider communication were associated with fewer readmissions for children (OR = 0.23, 95% CI = [0.09, 0.57]). Participants with better ratings of provider communication were less likely to rate their health literacy as lower (regression coefficient (B) = -0.28, 95% CI = [-0.46, -0.10]). Conclusions: Low ratings of provider communication were associated with more hospitalizations and readmissions in SCD, suggesting the need for interventions targeted at improving patient-provider communication which could decrease hospitalizations for this population.

Entities:  

Keywords:  Provider communication; consumer assessment of healthcare providers and systems; health care surveys; shared decision-making; sickle cell anemia; vulnerable populations

Year:  2020        PMID: 32552526      PMCID: PMC7440685          DOI: 10.1080/16078454.2020.1780737

Source DB:  PubMed          Journal:  Hematology        ISSN: 1024-5332            Impact factor:   2.269


  47 in total

Review 1.  Evolution of sickle cell disease from a life-threatening disease of children to a chronic disease of adults: The last 40 years.

Authors:  Shruti Chaturvedi; Michael R DeBaun
Journal:  Am J Hematol       Date:  2016-01       Impact factor: 10.047

2.  Emergency department visits made by patients with sickle cell disease: a descriptive study, 1999-2007.

Authors:  Hussain R Yusuf; Hani K Atrash; Scott D Grosse; Christopher S Parker; Althea M Grant
Journal:  Am J Prev Med       Date:  2010-04       Impact factor: 5.043

3.  Barriers and facilitators to research participation among adults, and parents of children with sickle cell disease: A trans-regional survey.

Authors:  Robert M Cronin; Jane S Hankins; Patricia Adams-Graves; Alexis A Thompson; Karen Kalinyak; Jeannie Byrd; Brandi McClain; Adetola Kassim; Michael DeBaun; Marsha Treadwell
Journal:  Am J Hematol       Date:  2016-08-04       Impact factor: 10.047

Review 4.  Minireview: Clinical severity in sickle cell disease: the challenges of definition and prognostication.

Authors:  Charles T Quinn
Journal:  Exp Biol Med (Maywood)       Date:  2016-03-23

5.  Hydroxyurea adherence and associated outcomes among Medicaid enrollees with sickle cell disease.

Authors:  Sean D Candrilli; Sarah H O'Brien; Russell E Ware; Milap C Nahata; Eric E Seiber; Rajesh Balkrishnan
Journal:  Am J Hematol       Date:  2011-02-15       Impact factor: 10.047

Review 6.  Advances in the use of hydroxyurea.

Authors:  Russell E Ware; Banu Aygun
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2009

7.  The cost of health care for children and adults with sickle cell disease.

Authors:  Teresa L Kauf; Thomas D Coates; Liu Huazhi; Nikita Mody-Patel; Abraham G Hartzema
Journal:  Am J Hematol       Date:  2009-06       Impact factor: 10.047

8.  Validation of screening questions for limited health literacy in a large VA outpatient population.

Authors:  Lisa D Chew; Joan M Griffin; Melissa R Partin; Siamak Noorbaloochi; Joseph P Grill; Annamay Snyder; Katharine A Bradley; Sean M Nugent; Alisha D Baines; Michelle Vanryn
Journal:  J Gen Intern Med       Date:  2008-03-12       Impact factor: 5.128

9.  Quality of care in sickle cell disease: Cross-sectional study and development of a measure for adults reporting on ambulatory and emergency department care.

Authors:  Christian T Evensen; Marsha J Treadwell; San Keller; Roger Levine; Kathryn L Hassell; Ellen M Werner; Wally R Smith
Journal:  Medicine (Baltimore)       Date:  2016-08       Impact factor: 1.889

10.  The Mid-South clinical Data Research Network.

Authors:  S Trent Rosenbloom; Paul Harris; Jill Pulley; Melissa Basford; Jason Grant; Allison DuBuisson; Russell L Rothman
Journal:  J Am Med Inform Assoc       Date:  2014-05-12       Impact factor: 4.497

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