Trusted Resources: Evidence & Education
Scientific literature and patient education texts
Health care utilization, patient trust, and satisfaction with care in adults with sickle cell disease
source: American Society of Pediatric Hematology/Oncology
year: 2017
authors: Jacquelyn Baskin, Anne Nord, Dawn Canada, Kelly LC. Russell, Payal Shah, Thomas D. Coates, Arch G. Mainous III
summary/abstract:Background:
Transition from pediatric to adult centered care for emerging adults with sickle cell disease (SCD) has previously been unsuccessful due to lack of connection to adult providers with experience with SCD, physician mistrust, poor patient preparation, and difficulty navigating the adult health care system. The resulting gaps in medical care lead to decreased out-patient visits and increased Emergency Department (ED) visits and hospitalizations, contributing to fragmented care and poor outcomes.
Objectives:
To assess barriers that adults with SCD face when accessing adult care, satisfaction and trust with medical providers, and health care utilization.
Results:
Only 62% of the 34 survey participants, ages 22-39 years, identified having an adult PCP and/or hematologist. Patients’ general satisfaction with care increased as their trust increased in both their adult hematologist (p=0.001) and PCP (p<0.001). Patients had greater trust in their hematologist (mean score 79.4 vs 65.1, p = 0.0376) and trended towards improved general satisfaction with care (mean score 3.8 vs 3.2, p=0.128) when compared to their PCP. For complications related to SCD, 62% of all participants had been to the ED and 50% had been hospitalized in the previous 6 months. Of those utilizing the ED, 60% had negative comments regarding their care, including delays and sub-optimal dosing in pain management and lack of provider experience with SCD. Regarding their transition experience, 50% were dissatisfied and more than 50% reported they were not prepared for adult care.
Conclusion:
Almost 40% of patients are not receiving regular medical care for their SCD with a significant portion relying on emergency departments, which can lead to fragmented medical care. There was a higher level of trust and general satisfaction with adult hematologists, which may reflect patients’ confidence in their specialists’ ability to manage their disease. Based on participant feedback, medical care improved when their adult provider was involved in their hospital care, indicating the importance of the connection with an adult provider familiar with their disease, which can lead to improved long-term outcomes.
Related Content
-
Hydroxyurea to Lower Transcranial Doppler Velocities and Prevent Primary Stroke: The Uganda NOHARM Sickle Cell Anemi...In sub-Saharan Africa, sickle cell anemi...
-
RARE Patient Advocacy SummitEach year, Global Genes convenes one of ...
-
Results of a Multicenter Pilot Investigation of Bone Marrow Transplantation in Adults with Sickle Cell Disease (STRI...Background: Hematopoietic cell transplan...
-
PSA Safe Grocery Shopping & Take-Out Food in COVID-19 Pandemichttps://www.youtube.com/watch?v=sjDuwc9K...
-
2018 World Sickle Cell Day “In Good Spirits & Good Health” EventTuesday June 19th is World Sickle Cell D...
-
Children’s Healthcare of Atlanta Sickle Cell Disease ProgramChildren's Healthcare of Atlanta's Sickl...
-
Guy’s and St Thomas’ NHS Foundation TrustOur haemoglobinopathies service sees chi...
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.