Feasibility Study Comparing Enteral vs Parenteral Nutritional Outcomes in Autologous Stem Cell Transplant Patients
Malignant Hematologic Neoplasm
About this trial
This is an interventional treatment trial for Malignant Hematologic Neoplasm focused on measuring Non- Hodgkin's Lymphoma, Hodgkin's Lymphoma, Multiple Myeloma, AHSCT
Eligibility Criteria
Inclusion Criteria:
- All adult patients aged 18 to 75 years.
- Patients admitted to Victoria Hospital undergoing AHSCT on C7 unit.
- Patient consented to participate in the study
- Patients diagnosed with the following conditions: Non- Hodgkin's Lymphoma (all types), Hodgkin's Lymphoma (all subtypes) and Multiple Myeloma
- Patients receiving any of the following: Conditioning chemotherapy: Melphalan, Etoposide/Melphalan, or Carmustine, Etoposide, Cytarabine, Melphalan
- Have a functional Gastrointestinal tract
Exclusion Criteria:
- Intestinal obstruction
- Patients with nasal deformities, tumors of nasal tracts or upper nare obstruction.
- Patients with active bacteremia while proceeding with transplant
- Patients with active malignancy of Upper GI tract, not in remission as evidenced by recent imaging studies (< 4 weeks)
- Patients with any GI bleeding, paralytic ileus, obstruction, or any other GI condition which excludes use of the GI system for nutritional support as these patients will require PN feeding only and cannot be randomized
Sites / Locations
- London Health Sciences Centre-Victoria HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Parenteral Nutrition
Enteral Nutrition
Patients who have been randomized to receive PN will be started on day 5 post AHSCT. This will be if patient intake is < 80% of usual oral intake at that time. The central venous catheter required for PN administration will be already in place for AHSCT treatment, prior to admission and pre-transplant evaluation. Nutritional support will continue until oral intake is >50% or until the patient is ready for discharge if intake remains < 50% of recommendations.
Patients who have been randomized to receive EN will have a Nasogastric tube (NGT) inserted on day 5 post AHSCT, prior to start of Enteral feeds. This would be a polyurethane tube, 8-10 French, which will be inserted by physician or Nurse Practitioner with position confirmed by radiological examination. This will be if patient intake is < 80% of usual oral intake at that time. Nutritional support will continue until oral intake is >50% or until the patient is ready for discharge if intake remains < 50% of recommendations.