Paralytic Ileus
Conditions
Keywords
major abdominal surgery
Brief summary
Postoperative Ileus (POI) is considered as intolerance of oral intake due to disruption of the normal coordinated propulsive motor activity of the gastrointestinal (GI) tract following abdominal or non-abdominal surgery. Dexamethasone & Dexmedetomidine have been reported to attenuate the incidence of paralytic ileus after abdominal surgeries. Previous study has shown that a single dose of DM before induction of anesthesia may be beneficial to reduce ileus for IBD by alleviating the postoperative systemic inflammatory response. Perioperative dexmedetomidine in major abdominal surgeries significantly decreased the time to flatus, defecation, and resuming normal diet, shortened length of stay, and improved haemodynamic stability. The aim of this study is to compare the effect of preoperative intrathecal dexamethasone versus dexmedetomidine on paralytic ileus after major abdominal surgery.
Detailed description
Postoperative Ileus (POI) is considered as intolerance of oral intake due to disruption of the normal coordinated propulsive motor activity of the gastrointestinal (GI) tract following abdominal or non-abdominal surgery. Dexamethasone & Dexmedetomidine have been reported to attenuate the incidence of paralytic ileus after abdominal surgeries. Previous study has shown that a single dose of DM before induction of anesthesia may be beneficial to reduce ileus for IBD by alleviating the postoperative systemic inflammatory response. Perioperative dexmedetomidine in major abdominal surgeries significantly decreased the time to flatus, defecation, and resuming normal diet, shortened length of stay, and improved haemodynamic stability.
Interventions
DRUGDexamethasone
patients will receive intrathecal dexamethasone 8 mg in 3 ml volume.
DRUGDexmedetomidine
patients will receive intrathecal dexmedetomidine 0.5 µg/kg in 3 ml volume.
Sponsors
Assiut University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No
Inclusion criteria
* • Age: 18-60 years. * Sex: both males and females. * ASA physical status: I and II. * Operation: Open major abdominal surgery. * The surgery has to involve gastrointestinal resection and/or anastomosis.
Exclusion criteria
* • History of abnormal bowl habit or bowel obstruction * Allergy to dexamethasone or dexmedetomidine * Electrolyte disturbance * Patient who receive any drugs known to influence gastrointestinal motility. * Mental disorders or inability to cooperate * Morbid obesity (BMI \> 40), pregnancy, lactation * Diabetes * After neoadjuvant chemotherapy. * History of use of any steroids within the last 3 months * Previous abdominal surgery, herniorrhaphy or unplanned secondary surgery
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Incidence of postoperative vomiting | 24 hours | number of participants who had experienced vomiting on day 1. |
Contacts
Primary ContactAbdelrahman Mohamed Hamed, resident doctor
Outcome results
None listed