Alvin Jay Freeman

Dr. Alvin Jay Freeman

orcid

Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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29 October 2022 in Journal of Cystic Fibrosis
Verified
Journal Article
Closed access
BMBaha Moshiree
Baha Moshiree
AFAlvin Jay Freeman
Alvin Jay Freeman
PVPhuong T. Vu
Phuong T. Vu
UKUmer Khan
Umer Khan
CUCarmen Ufret-Vincenty
Carmen Ufret-Vincenty
MSMeghana Nitin Sathe
Meghana Nitin Sathe

2 February 2021 in Journal of Pediatric Gastroenterology and Nutrition
Verified
Journal Article
Closed access
AFAlvin Jay Freeman
Alvin Jay Freeman
AMAsim Maqbool
Asim Maqbool
MBMelena D. Bellin
Melena D. Bellin
KGKenneth R. Goldschneider
Kenneth R. Goldschneider
AGAmit S. Grover
Amit S. Grover
MAMaisam Abu‐El‐Haija
Maisam Abu‐El‐Haija

1 November 2017 in Journal of Cystic Fibrosis
Verified
Journal Article
Closed access
AFAlvin Jay Freeman
Alvin Jay Freeman
KOKeith Ooi
Keith Ooi

1 August 2016 in Pediatric Clinics of North America
Verified
Journal Article
Closed access
MSMeghana Nitin Sathe
Meghana Nitin Sathe
AFAlvin Jay Freeman
Alvin Jay Freeman

13 January 2021 in Journal of Cystic Fibrosis
Verified
Journal Article
Closed access
AFAlvin Jay Freeman
Alvin Jay Freeman
MSMeghana Sathe
Meghana Sathe
EAEnid Aliaj
Enid Aliaj
DBDrucy Borowitz
Drucy Borowitz
BFBarbra Fogarty
Barbra Fogarty
BMBaha Moshiree
Baha Moshiree

22 March 2024 in American Journal of Gastroenterology
Verified
Journal Article
Closed access
AFAlvin Jay Freeman
Alvin Jay Freeman
KNKenneth Ng
Kenneth Ng
FWFuchenchu Wang
Fuchenchu Wang
MAMaisam A. Abu-El-Haija
Maisam A. Abu-El-Haija
ACAnkur Chugh
Ankur Chugh
AUAliye Uc
Aliye Uc
INTRODUCTION: Among children who suffer from acute recurrent pancreatitis (ARP) or chronic pancreatitis (CP), acute pancreatitis (AP) episodes are painful, often require hospitalization, and contribute to disease complications and progression. Despite this recognition, there are currently no interventions to prevent AP episodes. In this retrospective cohort study, we assessed the impact of pancreatic enzyme therapy (PERT) use on clinical outcomes among children with pancreatic-sufficient ARP or CP. METHODS: Children with pancreatic-sufficient ARP or CP in the INSPPIRE-2 cohort were included. Clinical outcomes were compared for those receiving vs not receiving PERT, as well as frequency of AP before and after PERT. Logistic regression was used to study the association between development of AP episodes after starting PERT and response predictors. RESULTS: Among 356 pancreatic-sufficient participants, 270 (76%) had ARP, and 60 (17%) received PERT. Among those on PERT, 42% did not have a subsequent AP episode, during a mean 2.1 years of follow-up. Children with a SPINK1 mutation (P = 0.005) and those with ARP (compared with CP, P = 0.008) were less likely to have an AP episode after starting PERT. After initiation of PERT, the mean AP annual incidence rate decreased from 3.14 down to 0.71 (P < 0.001). DISCUSSION: In a retrospective analysis, use of PERT was associated with a reduction in the incidence rate of AP among children with pancreatic-sufficient ARP or CP. These results support the need for a clinical trial to evaluate the efficacy of PERT to improve clinical outcomes among children with ARP or CP.