Evaluating Ileostomy Hydration Protocol

Sponsor
The Guthrie Clinic (Other)
Overall Status
Recruiting
CT.gov ID
NCT04669964
Collaborator
(none)
100
1
48
2.1

Study Details

Study Description

Brief Summary

This is a prospective observational study on patients who undergo an ileostomy creation after implementing a hydration algorithm as routine care at Robert Packer Hospital. The Department of Surgery will be implementing a protocol to prevent dehydration for patients with high output ileostomies. Patients with high output ileostomies are at an increased risk for readmission for dehydration. By reviewing the data after applying this standardized hydration protocol, we can assess its efficacy on readmission rates and comorbidities stemming from dehydration.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Intravenous Hydration

Detailed Description

As of January 1, 2021, Robert Packer Hospital will implement a standardized hydration protocol for patients at high risk for readmission due to dehydration.

All postoperative ileostomy patients will be provided the following instructions at the bedside to ensure complete comprehension:

  1. Stoma maintenance education

  2. Hydration recommendations

  3. Intake and Output Worksheet education and trial

The colorectal surgeons standardized the postoperative medical management of ileostomy output.

Before discharge, the healthcare providers will complete a "Discharge Assessment Checklist".

On the day of discharge, patients will be categorized by the "Discharge Algorithm for Patients with Ileostomies." The algorithm will assign patients by their ileostomy output and determine their next management steps.

After discharge, all patients will record their fluid input and output using the "Daily Measurement of Intake/Output Worksheet" which will be used to monitor hydration over time. Patients who are high risk will receive outpatient intravenous hydration therapy. At each intravenous therapy appointment, the health care provider will review the Outpatient Intravenous Hydration Algorithm to determine the volume of fluid to distribute or if re-evaluation is necessary.

Data Collection After starting the standardized hydration protocol, researchers will prospectively collect data from monthly reports of patients who received an ileostomy creation.

Researchers will not mask the patients, care providers, investigators, and outcomes assessors.

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Evaluating the Efficacy of a Standardized Hydration Protocol After Ileostomy Creation
Actual Study Start Date :
Jan 1, 2021
Anticipated Primary Completion Date :
Jan 1, 2024
Anticipated Study Completion Date :
Jan 1, 2025

Arms and Interventions

Arm Intervention/Treatment
High-Risk For Dehydration

Patients with an Ileostomy output of >1L at discharge.

Procedure: Intravenous Hydration
Patients will receive daily intravenous hydration of normal saline based on their ileostomy output.

Outcome Measures

Primary Outcome Measures

  1. Readmission with 30 days [30 days after discharge for ileostomy creation]

    Unplanned hospital readmission within 30 days of ileostomy creation. Researchers will determine unplanned hospital readmissions through monthly generated patient reports and validated by chart review.

Secondary Outcome Measures

  1. Readmission [60 and 90 days after discharge for ileostomy creation]

    Unplanned hospital readmission within 60 and 90 days of surgery. Researchers will determine unplanned hospital readmissions through monthly generated patient reports and validated by chart review.

  2. Emergency Department Visits [30, 60, and 90 days after discharge for ileostomy creation]

    Emergency department visits within 30, 60, and 90 days of surgery. Researchers will determine emergency department visits through monthly generated patient reports and validated by chart review.

  3. Dehydration Events [30, 60, and 90 days after discharge for ileostomy creation]

    The number of clinically significant dehydration events within 30, 60, and 90 days of surgery. Researchers will determine the number of clinically significant dehydration events through monthly generated patient reports and validated by chart review.

  4. Reoperation [30, 60, and 90 days after discharge for ileostomy creation]

    The incidence of reoperation within 30, 60, and 90 days of surgery. Researchers will determine the incidence of reoperation through monthly generated patient reports and validated by chart review.

  5. Mortality [30, 60, and 90 days after discharge for ileostomy creation]

    Mortality rates within 30, 60, and 90 days of surgery. Researchers will determine mortality through monthly generated patient reports and validated by chart review

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients older than 18 years of age will be eligible for this study.

  • Patients who received emergent or elective end or loop ileostomy during the index admission will be eligible for this study.

Exclusion criteria:
  • Patients who have not received an ileostomy creation at Robert Packer Hospital will be ineligible.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Guthrie Robert Packer Hospital Sayre Pennsylvania United States 18840

Sponsors and Collaborators

  • The Guthrie Clinic

Investigators

  • Principal Investigator: Burt Cagir M FACS, Robert Packer Hospital

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
The Guthrie Clinic
ClinicalTrials.gov Identifier:
NCT04669964
Other Study ID Numbers:
  • 2011-73
First Posted:
Dec 17, 2020
Last Update Posted:
Aug 5, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by The Guthrie Clinic
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 5, 2022