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Pneumatic Reduction For Intussusception In Children: A Retrospective Cohort Study

Completed
Conditions
Intussusception
Interventions
Procedure: Fluoroscopic-guided air-enema reduction (FGAR)
Registration Number
NCT06365333
Lead Sponsor
National Children's Hospital, Vietnam
Brief Summary

In pediatric patients, intussusception predominantly occurs in the ileocecal region, with over 90% of cases lacking identifiable causative factors, initiating through peristalsis-driven invagination of bowel segments leading to compromised blood flow and subsequent bowel edema. Persistent obstruction may progress to bowel ischemia and infarction. Vietnam exhibits a higher incidence of intussusception compared to other countries, albeit with similar clinical presentations and anatomical locations, hinting at shared pathophysiology. Despite evidence supporting the safety and efficacy of non-surgical reduction techniques, many medical centers in low- to middle-income countries (LMICs) have not adopted these methods, resulting in unnecessary surgical interventions. The Vietnam National Hospital of Pediatrics (NCH) has employed air enema reduction since the early 2000s but lacks a comprehensive study on fluoroscopic-guided air-enema reduction (FGAR) techniques or success rates. Thus, this study aims to evaluate the long-term outcomes of pneumatic reduction for intussusception at NCH, a high-volume institution in a lower-middle-income country.

Detailed Description

In pediatric patients, intussusception primarily occurs in the ileocecal region, with more than 90% of cases lacking identifiable causative factors. The invagination of bowel segments is propelled by peristalsis, leading to compromised blood flow. This venous occlusion precipitates bowel edema, and if the obstruction persists, it can progress to bowel ischemia and infarction. The incidence of intussusception in Vietnam exceeds that of any other country with available data on incidence rates. Despite variations in incidence rates, intussusception's clinical presentation and anatomical location remain largely consistent between Vietnam and other countries, suggesting a common underlying pathophysiology. Many medical centers in low- to middle-income countries (LMICs) have yet to adopt these non-surgical approaches, resulting in unnecessary surgical interventions for a significant portion of patients. At the Vietnam National Hospital of Pediatrics (NCH), air enema reduction has been a standard practice since the early 2000s. Nonetheless, there has been no comprehensive study delineating the technique of fluoroscopic-guided air-enema reduction (FGAR) at NCH, nor assessing its success rate.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
3562
Inclusion Criteria
  • All patients diagnosed with idiopathic intussusception, admitted to the National Children's Hospital between January 2016 and December 2017, exhibiting clinical signs and symptoms consistent with intussusception, and confirmed via ultrasound examination.
  • Fluoroscopy-guided pneumatic reduction was performed with a maximum of three attempts. Patients who did not respond to pneumatic reduction underwent minimally invasive surgical intervention, either laparoscopic reduction or trans-umbilical mini-open reduction.
Exclusion Criteria
  • Patients demonstrating clinical instability characterized by signs of peritonitis or intestinal perforation necessitating conventional laparotomy.
  • Patients deemed unsuitable for air enema reduction due to a grossly distended abdomen or compromised cardiopulmonary function.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
FGAR-treatedFluoroscopic-guided air-enema reduction (FGAR)Patients diagnosed with idiopathic intussusception, admitted to the National Children's Hospital between January 2016 and December 2017, exhibiting clinical signs and symptoms consistent with intussusception, and confirmed via ultrasound examination
Primary Outcome Measures
NameTimeMethod
Deaththrough study completion (2 years)

Mortality or severe morbidity noted post-FGAR

Failed FGARthrough study completion (2 years)

Unsuccessful reduction that requires transition to surgical intervention

Recurrencethrough study completion (2 years)

Recurrence of intussusception during the follow-up period

Complicated intussusceptionthrough study completion (2 years)

Complications, including bowel perforation, occurred during FGAR

ICU admissionthrough study completion (2 years)

Clinically unstable patients post-FGAR that required ICU admission

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (2)

The National Hospital of Pediatrics

🇻🇳

Hanoi, Vietnam

Vinmec Research Institute of Stem Cell and Gene Technology

🇻🇳

Hanoi, Vietnam

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