Pediatric Resident in her 2nd year at Maimonides Medical Center
Abstracts:
1) RACIAL DISPARITIES IN ACQUISITION OF LIVER TRANSPLANT IN PATIENTS OF SHORT BOWEL SYNDROME AND OTHER CAUSES OF INTESTINAL FAILURE THROUGH DESCRIPTIVE ANALYSIS OF NATIONAL INPATIENT SAMPLE 2021.
Objectives:
1) to identify, quantify, and understand the racial and socioeconomic disparities in the outcomes of pediatric liver transplantation and intestinal failure management,
2)To inform policy changes and develop targeted interventions aimed at reducing these disparities, ensuring equitable access to transplantation, and improving healthcare delivery and outcomes for all children, regardless of their racial, ethnic, or socioeconomic background.
Methods:
We conducted a descriptive analysis using the National Inpatient Sample (NIS) 2021 to examine the demographic distribution of pediatric patients undergoing liver transplants and those diagnosed with short bowel syndrome and other forms of intestinal malabsorption. The analysis utilized ICD-10 codes for liver transplants, short bowel syndrome, Whipple's disease, intestinal failure, and other causes of intestinal malabsorption.
Results:
Our analysis of the National Inpatient Sample (NIS) 2021 identified 2105 pediatric patients with liver transplants and 6275 patients with short bowel syndrome. Pediatric patients who needed liver transplant due to short bowel syndrome were 130 in number. The demographic breakdown for race/Ethnicity was: 15% White, 35% Black, 35% Hispanic, 15% Other
he demographic breakdown for race/Ethnicity for liver transplant alone was: 40% White, 17% Black, 30% Hispanic, 13% Other
he demographic breakdown for race/Ethnicity was: 40% White, 26% Black, 24% Hispanic, 10% Other
On subgroup analysis for median household income, there was no racial disparity based on household income status, p value 0.33
Conclusion:
The data highlight significant racial disparities in pediatric patients undergoing liver transplants due to short bowel syndrome, with Black and Hispanic patients being overrepresented in this group. However, advancements in IRPs and innovative treatments have improved survival rates and reduced the need for transplants. The analysis found no significant racial disparity based on median household income status (p value 0.33), suggesting that the observed disparities may not be solely due to economic factors but could be influenced by other systemic or healthcare access issues.
2) EARLY DIAGNOSIS OF CHOLEDOCHAL CYST DUE TO BETA THALASSEMIA MINOR, A RARE PRESENTATION.
Objective
To present an unusual case of CC in a 3-year-old girl with beta thalassemia minor, highlighting the atypical presentation of CC and the potential interplay between these conditions.
Design/Method
This is a case report. The information on the patient's clinical presentation does not contain any identifying information. A literature review was conducted using PubMed, focusing on studies published within the last decade.
Result
Our patient had intrahepatic and extrahepatic cystic dilatation measuring 2cm, which if had been un-influenced by other factors would have likely remained asymptomatic till adulthood. Most childhood presentations of cysts are due to large size of cyst compared to patient's body habitus which causes abdominal pain and swelling. However, our patient had beta thalassemia minor which contributed to the biliary stasis already caused by the CC which caused the choledocholithiasis. Of note, patient had a brief episode of sickness consistent with a viral upper respiratory tract infection 1 week prior to presentation that could have lead to mild hemolysis and subsequent hyperbilirubinemia due to underlying thalassemia. Removal of CC before 18 years of age, has an almost negligent risk of development into cholangiocarcinoma later in life. After 18 years of age, even complete cyst resection has a small risk of development of cholangiocarcinoma. Thus patient's beta thalassemia turned out to be a serendipitious.
Conclusion
This case report highlights an unusual presentation of choledochal cyst in a young patient with beta thalassemia minor. The interplay between these conditions led to early detection and treatment, potentially reducing the long-term risk of cholangiocarcinoma. This case underscores the importance of considering underlying hematological disorders in pediatric patients presenting with biliary symptoms.
3) Work In Progress: Prevalence Of GDM In Mothers of Children Diagnosed With MASLD, A Case Control Study, currently pending IRB approval.
-Currently a second year pediatric resident at Maimonides Medical Center
-I was interested in Pediatric GI after a rotation during intern year, I realized I enjoy helping children improve their bowel health and manage constipation effectively, nutrition and optimizing it for different health states, especially the effect nutrition has on liver, in the manner of MASLD. Very interested in hepatology in general.
- I also enjoy General Pediatrics, talking to families and watching children grow and reach their full potential.
4001, New Utrecht Avenue, 11219, Brooklyn