Intussusception Clinical Trial
Official title:
Pneumatic Reduction For Intussusception In Children: A Retrospective Cohort Study In An Ultrahigh Volume Center
Verified date | April 2024 |
Source | National Children's Hospital, Vietnam |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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.
Status | Completed |
Enrollment | 3562 |
Est. completion date | April 2024 |
Est. primary completion date | December 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 2 Months to 30 Months |
Eligibility | 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. |
Country | Name | City | State |
---|---|---|---|
Vietnam | The National Hospital of Pediatrics | Hanoi | |
Vietnam | Vinmec Research Institute of Stem Cell and Gene Technology | Hanoi |
Lead Sponsor | Collaborator |
---|---|
National Children's Hospital, Vietnam | Vinmec Research Institute of Stem Cell and Gene Technology |
Vietnam,
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Complicated intussusception | Complications, including bowel perforation, occurred during FGAR | through study completion (2 years) | |
Primary | ICU admission | Clinically unstable patients post-FGAR that required ICU admission | through study completion (2 years) | |
Primary | Death | Mortality or severe morbidity noted post-FGAR | through study completion (2 years) | |
Primary | Failed FGAR | Unsuccessful reduction that requires transition to surgical intervention | through study completion (2 years) | |
Primary | Recurrence | Recurrence of intussusception during the follow-up period | through study completion (2 years) |
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