Publications by authors named "Aspirot A"

Background: To review the outcomes of premature patients with type C esophageal atresia (EA).

Methods: In this retrospective cohort study, charts of patients of type C EA patients were reviewed from 1992 to 2022. Outcomes of premature patients were compared to term patients.

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Background: The Canadian Association of Paediatric Surgeons launched a 10-year prospective assessment of the Canadian pediatric surgery workforce and training environment, beginning in 2013. The results of the first 5 years (2013-2017) were previously published. Here, we present the results of the last 5 years (2018-2022), and the cumulative results of the past decade.

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Introduction: Giant sacrococcygeal teratomas (GSCTs) involve severe deformation of the buttock region in addition to potential functional impacts. Little interest has been given to improving the aesthetic post-operative appearance in children with these tumours.

Methods: We describe a new technique for immediate reconstruction of GSCTs using buried dermal-fat flaps and a low transverse scar in the infragluteal fold.

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Article Synopsis
  • The study investigates the role of calretinin immunohistochemistry in defining the transition zone (TZ) for patients with short segment Hirschsprung disease (HSCR), a condition that affects nerve cells in the intestines.
  • Researchers analyzed surgical specimens from 51 HSCR patients using H&E staining and calretinin immunohistochemistry to identify the TZ borders.
  • Findings indicate that calretinin expression on mucosal nerve fibers is an early marker for the distal border of the TZ, while a maximum distance of 60 mm differentiates it from the proximal border defined by normal ganglion cell density.
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Purpose: Recent studies have identified transanastomotic tubes (TATs) as a risk factor for the development of anastomotic strictures after repair of esophageal atresia with tracheoesophageal fistula (EATEF). We further investigated these findings in a multicenter study.

Methods: We conducted a retrospective cohort study at three university-affiliated hospitals in the province of Quebec.

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Background & Aims: Hirschsprung disease (HSCR) is a life-threatening birth defect in which the distal colon is devoid of enteric neural ganglia. HSCR is treated by surgical removal of aganglionic bowel, but many children continue to have severe problems after surgery. We studied whether administration of glial cell derived neurotrophic factor (GDNF) induces enteric nervous system regeneration in mouse models of HSCR.

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Objectives: Esophageal dysmotility is common in patients with esophageal atresia (EA). High-resolution impedance manometry and pressure flow analysis (PFA) allow characterization of biomechanical events that drive bolus flow. The aims were to assess esophageal motility in children with EA, using PFA, and to test whether there is a correlation between PFA parameters and symptoms or endoscopic/histologic findings.

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Objective: To evaluate outcomes of patients with esophageal atresia (EA) on systematic treatment with proton pump inhibitors (PPI) since the neonatal period and to determine factors associated with successful discontinuation of PPI.

Study Design: Longitudinal cohort study with prospective data collection of 73 EA patients, over 11 years systematically treated with PPI. Outcome and predictive factors for discontinuation of PPI treatment were evaluated at study end in February 2017.

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Purpose: This study examines the impact of postoperative noninvasive ventilation strategies on outcomes in esophageal atresia-tracheoesophageal fistula (EA-TEF) patients.

Methods: A single center retrospective chart review was conducted on all neonates followed at the EA-TEF Clinic from 2005 to 2017. Primary outcomes were: survival, anastomotic leak, stricture, pneumothorax, and mediastinitis.

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Purpose: This study aims to characterize risk factors for Hirschsprung-associated enterocolitis (HAEC). We hypothesize that earlier pull-through surgery is associated with lower risks of developing postoperative HAEC.

Methods: A comparative study of 171 Hirschsprung patients treated from 1990 to 2017 was performed.

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Background: In 2014, a survey study of the Canadian pediatric surgery workforce predicted a need for 2 new pediatric surgeons/yr. in Canada. We sought to assess these predictions and evaluate the status of the workforce.

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Article Synopsis
  • The study investigates the frequency of esophageal complications (such as peptic esophagitis and eosinophilic esophagitis) in children who have undergone repair for esophageal atresia (EA) and tracheoesophageal fistula (TEF).
  • It involved a cohort of 77 children monitored through endoscopic examinations from 2005 to 2017, revealing that about 52% had histopathologically proven complications despite being treated with proton pump inhibitors (PPIs) or H2 receptor antagonists.
  • The research highlighted that a higher risk of complications was linked to children with recurrent anastomotic strictures, indicating a need for careful monitoring and potential early intervention for this group.
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Background: Necrotizing enterocolitis (NEC) is a serious complication of prematurity. Currently, there is limited evidence to guide investigation and treatment strategies.

Objectives: To evaluate the parameters used to diagnose or exclude NEC, and to identify differences between neonatologists and pediatric surgeons.

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Article Synopsis
  • Rumination syndrome involves the involuntary regurgitation of food shortly after eating, and this study focused on analyzing esophageal pressure patterns in affected children using high-resolution esophageal manometry (HREM).
  • The study evaluated 15 pediatric patients with rumination syndrome alongside 15 control subjects, identifying distinct types of rumination based on gastric pressure levels during episodes.
  • Results showed that HREM successfully identified rumination episodes in 80% of patients, highlighting its potential to confirm diagnosis and differentiate between types of rumination, though further research is needed to assess its impact on treatment.
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Article Synopsis
  • The study investigates the incidence of congenital vascular anomalies in patients with esophageal atresia (EA) and tracheoesophageal fistula (TEF), finding that 18% of patients had a vascular malformation.
  • Among these, aberrant right subclavian artery (ARSA) and right aortic arch (RAA) were the most common, with incidences of 12% and 6%, respectively.
  • The research also evaluates the effectiveness of esophagrams in diagnosing ARSA, revealing a sensitivity of 66% and a recommendation for computed tomography to better identify such anomalies before surgical interventions.
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After surgical correction of esophageal atresia with or without tracheoesophageal fistula, esophageal body motility dysfunction has been reported in nearly all patients. Using high-resolution esophageal manometry before surgical repair in 2 children with isolated tracheoesophageal fistula, we sought to determine whether dysmotility was present before any surgical insult to test the hypothesis that dysmotility associated with esophageal atresia with or without tracheoesophageal fistula is related to intrinsic primary factors linked to abnormal development of the esophagus. Both had an abnormal esophageal motility: one exhibited hypomotility with distal contraction, whereas the other showed a complete aperistalsis pattern.

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Background: There is significant lack of information regarding the Canadian pediatric surgery workforce.

Methods: An IRB-approved survey aimed at assessing workforce issues was administered to pediatric surgeons and pediatric surgery chiefs in Canada in 2012.

Results: The survey was completed by 98% of practicing surgeons and 13 of the 18 division chiefs.

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Congenital esophageal stenosis (CES) is a rare clinical condition but is frequently associated with esophageal atresia (EA). The aim of this study is to report the diagnosis, management, and outcome of CES associated with EA. Medical charts of CES-EA patients from Lille University Hospital, Sainte-Justine Hospital, and Montreal Children's Hospital were retrospectively reviewed.

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Introduction: Calretinin, a calcium-binding protein, has been reported to be an important new marker in Hirschsprung's disease (HD). The aim is to study the diagnostic value of Calretinin in total colonic aganglionosis (TA), prematurity, and superficial biopsy when nerve hyperplasia may not be accessed by ACE activity.

Methods: Records of patients diagnosed with HD at our institution from 1985 to 2010 were studied and patients with TA identified.

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Esophageal dysmotility is a considerable long-term issue in patients born with esophageal atresia (EA). To better characterize it, the normal esophageal motility is briefly reviewed with emphasis on the specific defects in EA. Multiple studies attempted to describe the dysmotility seen in patients with operated EA using esophageal manometry.

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Background: Esophageal dysmotility, a considerable issue following esophageal atresia (EA) repair, has been reported but has not been precisely described and characterized. Using high-resolution esophageal manometry (HREM), we characterized the esophageal motility patterns in children with repaired EA and compared these patterns of dysmotility with symptomatology.

Methods: HREM was performed as an outpatient procedure in patients with repaired EA.

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Aim: The aim of the present study was to evaluate the effect of amoxicillin/clavulanate (A/C) on gastrointestinal motility.

Methods: Twenty consecutive pediatric patients referred for antroduodenal manometry received 20 mg/kg of A/C into the small bowel lumen. In 10 patients (group A), A/C was given 1 hour after and in 10 (group B), 1 hour before ingestion of a meal.

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Background: Open transumbilical pyloromyotomy (UMBP) and laparoscopic pyloromyotomy (LAP) have been compared on different outcomes, but postoperative pain as a primary end point had never been assessed. The aim of this study was to compare the use of analgesia in UMBP and LAP patients.

Methods: Infants with hypertrophic pyloric stenosis treated by UMBP in 2008-2009 were matched with LAP-treated infants.

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Background/purpose: The management of asymptomatic congenital lung lesions is controversial. Some centers recommend resection in infancy, and others prefer observation. Our objective was to evaluate the pulmonary function of children who underwent lung resection at 12 months or younger.

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