Incidence and risk factor for refeeding syndrome
Not Applicable
- Conditions
- Health Condition 1: E898- Other postprocedural endocrine andmetabolic complications and disorders
- Registration Number
- CTRI/2021/05/033773
- Lead Sponsor
- Chittaranjan National Cancer Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients greater than 18 years of age.
2.Patients with cancer of upper aero-digestive tract (Oral cavity, pharynx, larynx, oesophagus, stomach and periampullary cancers)
3.Moderate risk and high risk of refeeding syndrome according to ASPEN recommendations.
4.Receiving artificial nutrition in the postoperative period (nasogastric, nasojejunal and parenteral nutrition)
Exclusion Criteria
Patient on pre-operative artificial nutrition
Patient with dementia, renal impairment
Patient who are inoperable intraoperatively
Patient who refuses consent
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.To study the incidence of mild, moderate and severe refeeding syndrome using the ASPEN consensus among the study population.Timepoint: 7days
- Secondary Outcome Measures
Name Time Method To study the sensitivity and specificity of the NRS-2002 in identifying patients at risk of refeeding syndrome. <br/ ><br>To study the association of various pre-operative and post-operative factors with the development of refeeding syndrome <br/ ><br>To look for correlation between the severity of RS (lowest phosphate level) and calories received. <br/ ><br>To study the association of refeeding syndrome with post-operative morbidity. <br/ ><br>To investigate the clinical predictors of refeeding syndrome. <br/ ><br>Timepoint: 2 yrs