Payam Saadai
Overview
Explore the profile of Payam Saadai including associated specialties, affiliations and a list of published articles.
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Articles
52
Citations
233
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0
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Recent Articles
1.
Ramjist J, Dubljevic T, Lapidus-Krol E, Grace R, Heeney M, Oni M, et al.
J Pediatr Surg
. 2025 Feb;
60(4):162229.
PMID: 39999712
Purpose: Hereditary Spherocytosis (HS) is a common genetic hematological disorder causing a life-long hemolytic anemia, with sequela of hemolysis. Children with severe HS commonly undergo partial or total splenectomy (PS,...
2.
Srinivas S, Smith C, Austin K, Avansino J, Badillo A, Calkins C, et al.
J Pediatr Surg
. 2025 Feb;
60(4):162149.
PMID: 39919338
Background: Individually collected social determinants of health (SDOH) have been associated with negative outcomes in children with anorectal malformations (ARMs). Our aim was to assess whether the Child Opportunity Index...
3.
Alexander A, Short S, Austin K, Avansino J, Badillo A, Calkins C, et al.
J Pediatr Surg
. 2024 Dec;
60(3):162078.
PMID: 39657363
Background: Hirschsprung associated enterocolitis (HAEC) is a challenging problem in a subset of children with Hirschsprung disease (HD). In refractory cases, fecal diversion may be required. The aim of this...
4.
Kwon E, Kreiss J, Nicassio L, Austin K, Avansino J, Badillo A, et al.
J Pediatr Surg
. 2024 May;
59(8):1638-1642.
PMID: 38760309
Purpose: Antegrade colonic enemas (ACE) can be an effective management option for defecation disorders and improve quality of life. Best practice regarding channel placement is unclear and variation may exist...
5.
Saenz Z, Austin K, Avansino J, Badillo A, Calkins C, Durham M, et al.
J Pediatr Surg
. 2024 May;
59(8):1652-1656.
PMID: 38735806
Purpose: Congenital anorectal stenosis is managed by dilations or operative repair. Recent studies now propose use of dilations as the primary treatment modality to potentially defer or eliminate the need...
6.
Ullrich S, Austin K, Avansino J, Badillo A, Calkins C, Crady R, et al.
J Pediatr Surg
. 2024 Apr;
59(7):1250-1255.
PMID: 38677965
Background: Hirschsprung Disease (HD) is a rare cause of functional bowel obstruction in children. Patients are typically diagnosed in the neonatal period and undergo pull-through (PT) soon after diagnosis. The...
7.
McNevin K, Nicassio L, Rice-Townsend S, Katz C, Goldin A, Avansino J, et al.
J Pediatr Surg
. 2024 Feb;
59(5):997-1002.
PMID: 38365475
Background: Anorectal malformations (ARM) are rare and heterogenous which creates a challenge in conducting research and offering recommendations for best practice. The Pediatric Colorectal and Pelvic Learning Consortium (PCPLC) was...
8.
Lee S, Du Y, Hassan A, Brown E, Saadai P, Hirose S, et al.
Fetal Diagn Ther
. 2023 Jul;
50(6):491-500.
PMID: 37393899
Spina bifida is the most common congenital anomaly of the central nervous system and the first non-fatal fetal lesions to be addressed by fetal intervention. While research in spina bifida...
9.
Iantorno S, Rollins M, Austin K, Avansino J, Badillo A, Calkins C, et al.
J Pediatr Surg
. 2023 May;
58(8):1588-1593.
PMID: 37173214
Background: The incidence and optimal management of rectal prolapse following repair of an anorectal malformation (ARM) has not been well-defined. Methods: A retrospective cohort study was performed utilizing data from...
10.
Lee S, Jackson J, Hassan A, Kurzrock E, McLennan A, Hirose S, et al.
Fetal Diagn Ther
. 2023 Apr;
50(3):158-164.
PMID: 37088075
Introduction: Cloacal dysgenesis occurs from failure of embryological division of urogenital sinus and hindgut, leading to a single common perineal opening for genitourinary and gastrointestinal tracts. The prenatal diagnosis of...