Paraclinical changes in continuous feeding and bolus feeding.
Conditions
Interventions
Intervention 1: Intervention group:Patients in this group received continuous enteral feeding with standard commercial solution of enterameal of karen group. After adding 11.3 g of powder to 50 cc of
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 85 Years
Inclusion criteria
Inclusion criteria: Patient with mechanical ventilation throught the endotracheal tube Feeding of Patient with NG tube Patient attendant satisfaction 18-85 years old
Exclusion criteria
Exclusion criteria: Patient with digestive Disease( diarrhea, ileus, obstruction, ostomy) Patient with renal failure
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Serum albumin level. Timepoint: Before the intervention and 7 days after the intervention. Method of measurement: Analysis by Bromocresol Green Pars Test Laboratory Kit.;Serum level of pre-albumin. Timepoint: Before the intervention and 2 days after the intervention. Method of measurement: Analysis by Nephlometry Laboratory Kit Brand Binding site.;Serum phosphate level. Timepoint: Before the intervention and 7 days after the intervention. Method of measurement: Photometric analysis uv test.;Serum lactate level. Timepoint: Before the intervention and 7 days after the intervention. Method of measurement: Enzymatic / colorimetric analysis kit by Fars Bayer Lab.;Frequency of defecation. Timepoint: During 7 days of intervention. Method of measurement: View and record in data log sheet.;Patient's blood sugar. Timepoint: Every six hours. Method of measurement: clever check Glucometer. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactJavad Seyyedi
Tehran University of Medical Sciences
Outcome results
None listed