Effect of Early Versus Traditional Hospital Discharge on Maternal Outcome

March 16, 2018 updated by: Heba Saad, Ain Shams University

The Effect of Early Versus Traditional Hospital Discharge on Maternal Outcome for Women Undergoing Elective Cesarean Section

This study will investigate the effect of early hospital discharge versus traditional one on maternal outcome for women undergoing elective cesarean sections.

aim of the work is to assess rate of maternal hospital revisits after early hospital discharge at 8-12 hours following elective cesarean delivery compared to the current practice of discharge at 24-48 hours postoperatively.

Study Overview

Detailed Description

The effect of early versus traditional hospital discharge on maternal outcome for women undergoing elective cesarean section

Randomized clinical trial

Protocol of a thesis for partial fulfillment of master degree in obstetrics and gynecology

Postgraduate Student: Hebatallah Saad Sedky Mohamed Degree: M.B.B.Ch., faculty of medicine- Alexandria university (2013)

Co-DIRECTOR: Prof. Dr. Ahmed Hamdy Nagiub Abdulrahman Academic Position: professor of Obstetrics and Gynecology Department: faculty of medicine- Ain Shams University

Co-DIRECTOR: Dr. Mohamed Esmat Abbas Shawky Academic Position: Lecturer of Obstetrics and Gynecology Department: faculty of medicine- Ain Shams University

What is already known on this subject? What does this study add? The rate of cesarean delivery is increasing, in developing countries, its rate ranges from 13 to 47% of all cases of delivery (Gibbons et al 2010). Current practice is to discharge women from hospital 24-48 hours after cesarean delivery, however in some rural areas there is a common practice of earlier discharge. The effect of earlier discharge on women health is controversial. The present study will investigate the possibility of earlier discharge to reduce the cost of hospitalization and postoperative care, increase the turnover rate of obstetric hospitals and improve maternal outcome.

Many studies were concerned by early discharge of patients as there is evidence for colorectal surgery suggests that enhanced recovery programmes can reduce hospital stays by 0.5-3.5 days compared with conventional care (Fiona Paton et al 2014).

The average hospital stay following Cesarean delivery in most hospitals is 2 to 4 days (Tan et al 2012). Hospitalization allows close monitoring of women and early discovery and management of complication. Early discharge would, therefore, be a disadvantage and may delay identification and treatment of maternal and infant morbidity (National Institute of Health 2011). In contrast, several studies concluded that early discharge after Cesarean delivery is not associated with maternal readmissions (Brown et al 2011) and is associated with more maternal satisfaction and lesser cost (Umbeli et al 2010) and will decrease burden on medical facilities, increase turnover of obstetrics, reduce the cost of postoperative care, reduce rate of hospital acquired complications and Improve maternal neonatal relationship.

Study Type

Interventional

Enrollment (Anticipated)

156

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Egy 818
      • Cairo, Egy 818, Egypt, 11311
        • Recruiting
        • AinShams Maternity Hospital
        • Contact:
        • Contact:
        • Principal Investigator:
          • Heba S Sedky, M.B.B.Ch
    • Egy818
      • Cairo, Egy818, Egypt, 11311
        • Recruiting
        • AinShams Maternity Hospital
        • Contact:
        • Contact:
        • Principal Investigator:
          • Heba S Sedky, M.B.B.Ch

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 35 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Age between 20 and 35 years

    • Gestational age between 37-42 weeks
    • BMI less than 30 kg/m2
    • Have normal uncomplicated pregnancy
    • Planned lower uterine segment Cesarean section
    • Planned for primigravida or previous one or two Cesarean sections
    • Planned to have spinal anesthesia
    • Cesarean sections without intra-operative complications
    • Accepting to participate in the study

Exclusion Criteria:

  • • Emergency Cesarean section

    • Gestational age less than 37 or more than 42 weeks
    • BMI 30 kg/m2 or more.
    • Multiple pregnancies
    • Polyhydraminos
    • Abnormal placenta
    • Premature rupture of membranes
    • Previous abdominal surgeries or uterine surgeries
    • Not more than previous two Cesarean sections
    • Anemia: Hemoglobin level less than 10 g/dl
    • Cesarean section with intraoperative complications
    • General anesthesia
    • Fibroid uterus
    • RH incompatibility ( as there maybe delay of availability of anti-d immunoglobulins)
    • History of complicated pregnancy or delivery
    • Medical disorders(hypertension, diabetes mellitus, cardiac, pulmonary, renal, hepatic, endocrine and autoimmune disorders).
    • Women refusing participating in the study
    • Women having any contraindications or refusing spinal anesthesia

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: DIAGNOSTIC
  • Allocation: NA
  • Interventional Model: SINGLE_GROUP
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: early hospital discharge
women will be discharged early from hospital 12 hours postoperatively after elective cesarean sections.
early hospital discharge at 8-12 hours for women undergone elective cesarean section

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Rate of maternal hospital revisits
Time Frame: one week postoperatively
the aim is to reduce rate of maternal hospital revisits after discharge from the hospital which will be assessed by questionnaire
one week postoperatively

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maternal and family satisfaction,
Time Frame: one week postoperatively
the aim is to get the maximum satisfaction which will be assessed by questionnaire
one week postoperatively

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Hebatallah S Sedky, M.B.B.Ch, Ain Shams University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ANTICIPATED)

March 1, 2018

Primary Completion (ANTICIPATED)

September 1, 2018

Study Completion (ANTICIPATED)

December 1, 2018

Study Registration Dates

First Submitted

March 9, 2018

First Submitted That Met QC Criteria

March 16, 2018

First Posted (ACTUAL)

March 23, 2018

Study Record Updates

Last Update Posted (ACTUAL)

March 23, 2018

Last Update Submitted That Met QC Criteria

March 16, 2018

Last Verified

March 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • Early discharge

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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