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Early Enteral Feeding After Intestinal Anastomosis

Not Applicable
Completed
Conditions
Intestinal Anastomosis
Interventions
Other: Early feeding
Other: late feeding after bowel sounds return
Registration Number
NCT00739271
Lead Sponsor
Christian Medical College and Hospital, Ludhiana, India
Brief Summary

The concept of starting the patient on early enteral nutrition has been a topic of much interest and research in the past decade. It is gaining widespread acceptance worldwide as more and more studies are being conducted proving early enteral nutrition to be more physiological, to prevent morphologic and functional trauma related alterations of the gut and to modulate immune and inflammatory responses, and as being less expensive than total parenteral nutrition. Early enteral nutrition is a major component of the recently introduced post operative rehabilitative regimens.

Early feeding has been shown to reduce the risk of any specific infection, mean length of hospital stay, anastomotic dehiscence, wound infection, pneumonia, intra abdominal abscesses. It leads to lower weight loss and early positive nitrogen balance. Hence, overall early enteral nutrition leads to reduced post operative morbidity and better patient outcome.

The objective of this study was to study and compare the effects of early enteral feeding with those of conventional management in patients undergoing intestinal anastomosis; the end points being return of bowel activity, incidence of septic complications, length of hospital stay, weight loss and post operative morbidity.

Detailed Description

Pre operatively, common parameters observed in both study and control groups were:

* Name

* Age

* Sex

* Date of admission

* Weight

* Indication of surgery

* Pre operative features of sepsis (whether present or not) which included temperature, pulse rate\& total leukocyte count.

Post operatively, the patients in the study group were kept nil per orally for the first forty eight hours. The nasogastric tube was removed on the first post operative day invariably.

After forty eight hours of surgery, subjects were started on sips of clear liquids orally; the amount was gradually increased as tolerated by the patient. The diet was stepped up to soft diet and to regular diet. A record was made of abdominal discomfort, pain or distension if experienced by the subject during feeding.

Record was made of the following:

* Site of anastomosis

* Type of anastomosis ( sutured / stapled )

* Time of removal of nasogastric tube

* Time of passage of flatus / stools post operatively

* Time of appearance of bowel sounds

* Features of sepsis which included temperature, pulse rate \& total leukocyte count

* Presence of wound infection

* Weight on the fifth day of surgery, at the time of discharge

* Date of discharge

* Length of hospital stay

Patients in the control group were kept on maintenance intravenous fluids containing dextrose and saline. Nasogastric tube was removed and feeds were started orally as decided by the operating surgeon depending on the clinical condition of the patient and presence of bowel activity. Post operative records were made of the same parameters as in the study group.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
82
Inclusion Criteria
  • All patients undergoing intestinal anastamosis on an elective or emergency basis
Exclusion Criteria
  • Re laparotomies
  • Patients who are immunosuppressed
  • Patients with renal failure
  • Patients with spinal injuries
  • Patients requiring critical care
  • Pediatric patients

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Study armEarly feedingEarly enteral feed 48 hours after abdominal surgery
Control armlate feeding after bowel sounds returnTraditional treatment where patient is kept on a nasogastric drainage for a few days after abdominal surgery, wait for bowel sounds to appear and then start enteral feeds.
Primary Outcome Measures
NameTimeMethod
To be able to tolerate early enteral feed48 hours
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Christian Medical College and Hospital

🇮🇳

Ludhiana, Punjab, India

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