Corticosteroid Treatment in the Acute Phase of Caustic Ingestion Management
- Conditions
- Caustic Esophageal InjuryEsophageal StenosisPharyngeal Stenosis
- Interventions
- Other: Placebo
- Registration Number
- NCT03760354
- Lead Sponsor
- Assistance Publique - Hôpitaux de Paris
- Brief Summary
The management of patients who have ingested a caustic product has changed since 2007. Whereas previously the lesion assessment and surgical indication were based on endoscopic data, the therapeutic algorithm is currently based solely on the results of a CT scan with contrast injection, performed 6 hours after ingestion. This examination makes it possible to reliably assess the viability of the esophageal and gastric walls and thus to indicate digestive resection. The therapeutic consequences of this new treatment are important because, by expanding the indications for conservative treatment after severe ingestion, it brings a significant gain in terms of survival, morbidity and functional outcome. In the absence of emergency digestive resection, however, the functional prognosis is often overshadowed by the formation of esophageal stenosis in the months following ingestion. Patients then require endoscopic dilation treatment. In the event of failure or impossibility of dilation, which defines refractory stenosis, esophageal reconstruction is necessary. In case of sequential pharyngeal stenosis following ingestion, esophageal and pharyngeal reconstruction is indicated as a first-line treatment, since these stenosis do not respond to endoscopic dilations. The expansion of the indications for conservative treatment after severe ingestion using CT scans has led to an increase in the incidence of after-effect stenosis.
We aim to develop a therapeutic approach that will prevent the development of refractory and pharyngeal esophageal stenosis. Indeed, there is currently no strategy that has proven effective in this regard in adults. The value of corticosteroid therapy for the prevention of caustic stenosis has only been evaluated in children and remains controversial.
The main objective is to evaluate the effect of early systemic corticosteroid therapy on the risk of refractory esophageal or pharyngeal stenosis within one year of ingestion of a caustic substance in a population of patients at high risk of stenosis, defined according to tomodensitometric criteria (grade IIb: severe lesions, absence of transparietal necrosis), and for whom there is no indication of urgent digestive resection.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 30
Not provided
- Indication of resection or surgical exploration in emergency
- History of caustic ingestion
- Corticosteroids taken at a dose greater than 20 mg prednisone within 7 days before randomization
- Contraindication to corticosteroid therapy:
- Any infectious condition that required antibiotic treatment within 7 days of randomization
- Any vaccine living within 7 days of randomization
- Hypersensitivity to one of the components
- Pregnancy in progress
- Breastfeeding in progress
- Co-intoxication involving vital prognosis and requiring, according to the patient's doctor, intensive care management
- Patient under guardianship or curatorship
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Placebo (no corticosteroid treatment) Placebo NaCl 0.9%, 100ml per day as a single slow intravenous administration over 60 minutes for a total treatment duration of 5 days Methylprednisolone Methylprednisolone Dose: 500mg/day for the first two days then 2mg/kg per day for three days. Dilution in 0.9% NaCl, 100 ml as a single slow intravenous administration over 60 minutes Total processing time of 5 days
- Primary Outcome Measures
Name Time Method Indication for esophageal or pharyngeal surgical reconstruction within 12 months post ingestion The primary outcome is the indication for esophageal or pharyngeal surgical reconstruction due to:
1. The occurrence of one or more esophageal stenosis refractory to endoscopic dilation within 12 months of ingestion, as defined by:
* The need for more than 5 sessions of esophageal endoscopic dilation
* Non-expandable stenosis or esophageal obstruction;
* An esophageal perforation that occurs during dilation, which contraindicates the continuation of dilation.
2. The occurrence of pharyngeal stenosis, defined by the need to perform pharyngoplasty.
- Secondary Outcome Measures
Name Time Method Delay in the occurrence of refractory stenosis or pharyngeal stenosis at 9 months Time between inclusion and occurrence of refractory stenosis or pharyngeal stenosis
Delay in the occurrence of refractory esophagal stenosis or pharyngeal stenosis at 12 months Time between inclusion and occurrence of refractory stenosis or pharyngeal stenosis
Distance of the stenosis at 12 months Distance between the stenosis and the dental arches (cm)
Number of stenosis at 12 months Number of stenosis will be evaluated by endoscopy
Length of stenosis at 12 months Length of each stenosis will be evaluated by endoscopy
Estimated diameter of stenosis at 12 months Diameter of each stenosis will be evaluated by endoscopy
Endoluminal inflammation at 12 months Importance of endoluminal inflammation during endoscopy performed for dilation (minimal, moderate, or severe)
Number of dilation sessions at 12 months Number of dilation sessions evaluated by endoscopy
Intervals between iterative dilations at 12 months Time between endoscopic dilatations if necessary iterative dilation
Extent of pharyngeal stenosis at 12 months Laryngeal stenosis associated with pharyngeal stenosis
Digestive perforations at 12 months Proportion of digestive perforations secondary to endoscopic dilation
Proportion of unanticipated adverse reactions at 12 months Unanticipated adverse reactions will be defined by the occurrence of death,cardiac arrest whatever the cause,unplanned admission to intensive care unit (ICU) or extended stay \> 24 ICU
Proportion of adverse reactions related to corticosteroid therapy within 7 days Adverse reactions related to corticosteroid therapy will be defined by the occurrence of infections needing antibiotic therapy or spontaneous digestive perforation or digestive bleeding or cardiac arrhythmias de novo or pulmonary edema requiring treatment (increased oxygen requirements and/or Diuretic and/or Vasodilator and/or non-invasive ventilation and/or invasive ventilation) or respiratory complications (High blood pressure requiring treatment - Metabolic alkalosis- Hypokalemia\<3.0mmol/l - Delirium- Decompensation of a psychiatric pathology)
C-Reactive Protein (CRP) at one month Inflammation markers
Tissue Growth Factor Beta (TGF beta) at one month Fibrosis markers
interleukin-6 (IL-6) at one month Inflammation markers
Tumour Necrosis Factor alpha (TNF alpha) at one month Inflammation markers
interleukin-1 (IL1) at one month Inflammation markers
Galectin 3 at one month Fibrosis markers