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Neonatal Sepsis at Neonatal Intensive Care Units in Ghana

Primary Purpose

Neonatal SEPSIS

Status
Completed
Phase
Not Applicable
Locations
Ghana
Study Type
Interventional
Intervention
The WHO multimodal hand hygiene strategy
Sponsored by
Stephanie Bjerrum
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Neonatal SEPSIS focused on measuring Neonatal sepsis, Infection control, Hand hygiene, WHO multi modal

Eligibility Criteria

1 Minute - 48 Hours (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Admission NICU
  • Birth weight ≥750 Grams
  • ≤48 hours of age at time of enrolment
  • Consent to participate obtained from legal guardian

Exclusion Criteria:

  • Neonates with severe congenital malformations
  • Neonates who have undergone surgical procedure

Sites / Locations

  • Korle Bu Teaching Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Standard of care

Hand hygiene

Arm Description

Continuously monitoring of neonatal sepsis under standard of care at one site

The WHO multimodal hand hygiene strategy is implemented at one site

Outcomes

Primary Outcome Measures

Incidence of neonatal sepsis
Incidence of neonatal sepsis including clinical cases treated as sepsis and cases of neonatal sepsis with confirmed bloodstream infections per 1000 admissions.

Secondary Outcome Measures

Rate of hand hygiene compliance per opportunity
Hand hygiene events per opportunity for hand hygiene measured by direct observations
Rate of MDR Gram negative bacteria colonization among neonates
Prevalence of MDR Gram negative bacteria among admitted neonates
Length of admission in days
Days of admission
All-cause mortality
Mortality rates during admission

Full Information

First Posted
November 23, 2018
Last Updated
October 8, 2021
Sponsor
Stephanie Bjerrum
Collaborators
University of Copenhagen, Korle-Bu Teaching Hospital, Accra, Ghana, Rigshospitalet, Denmark, University of Ghana
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1. Study Identification

Unique Protocol Identification Number
NCT03755635
Brief Title
Neonatal Sepsis at Neonatal Intensive Care Units in Ghana
Official Title
Neonatal Sepsis at Neonatal Intensive Care Units of Two Major Referral Hospitals in Ghana
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
October 1, 2018 (Actual)
Primary Completion Date
September 30, 2019 (Actual)
Study Completion Date
September 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Stephanie Bjerrum
Collaborators
University of Copenhagen, Korle-Bu Teaching Hospital, Accra, Ghana, Rigshospitalet, Denmark, University of Ghana

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: Neonatal sepsis is a major contributor to global under five mortality. In developing countries a major proportion of neonatal sepsis is thought to emanate from the healthcare setting, due to challenges in infection prevention practices. Aim: To study the epidemiology of neonatal sepsis and evaluate the effect of multimodal infection control interventions on the incidence of neonatal sepsis; and colonization by multidrug resistant Gram negative bacteria (MDRGNB). Methods: A controlled before and after interventional trial comprising a 7 month pre- intervention phase, 5 month intervention phase and 7 month post-intervention phase. Neonates admitted at the Neonatal Intensive Care Unit (NICU) at Korle-Bu Teaching Hospital (KBTH) will be enrolled prospectively and followed up for diagnosis of sepsis and outcome of admission. This will be used to describe the epidemiology of neonatal sepsis. Swabs will be collected from a subpopulation of included neonates at intervention site (KBTH) and control site (37 Military Hospital) NICUs to assess colonization of neonates with MDRGNB. Environmental swabs will be collected from surfaces at the NICU to assess MDRGNB contamination of the environment. The intervention comprises infection prevention strategies including implementation of the WHO multimodal hand hygiene strategy. The primary endpoint is incidence of neonatal sepsis. Expected Outcome: This study will contribute to improved infection prevention practices in the participating NICUs and highlight lessons which other national and regional NICUs may learn from.
Detailed Description
Background In 2012, it was estimated that approximately 680,000 neonatal deaths in developing countries were due to bacterial infections, with an incidence risk of 7.6% and a case fatality risk of 9.8. A major proportion of neonatal infections are expected to be health-care associated, due to inadequate infrastructure and resources for infection control and prevention. Hospital acquired infections(HAIs) are associated with multi-drug resistant (MDR) bacteria, which increases the risk of therapeutic failure due to the limited choice of available antibiotics. HAIs also lead to extended duration of admission, increased medical costs, morbidity and mortality. Transmission of MDR bacteria in the hospital environment is thought to be due to unhygienic practices which occur during clinical invasive procedures, (e.g. artificial ventilation, catheter and intravenous line insertion). Neonatal infections may also be due to invasion by colonizing bacteria of the neonate, usually originating from maternal and environmental flora. According to the WHO, 50% of HAIs are preventable through implementation of infection control practices. The WHO has instituted a multimodal hand hygiene strategy that has been found to improve hand hygiene compliance and reduce the prevalence of HAIs. However, the effectiveness of this strategy in a neonatal intensive care unit (NICU) with high risk of colonization with environmental bacteria has not been studied. In fact, most studies that have examined the potential sources and mode of transmission of organisms that cause neonatal sepsis have been conducted in well-resourced countries. The hypothesis of the study is that the hospital environment serves as a source of MDR Gram negative bacteria responsible for neonatal colonization and sepsis among patients admitted at the NICU of the KBTH; and that implementation of the multimodal hand hygiene strategy will lead to a reduction in the incidence of neonatal sepsis and colonization by MDR Gram negative bacteria. Objective To determine the impact of multi-modal infection control interventions on the incidence of neonatal sepsis and colonization by MDR Gram negative bacteria. Method This study will evaluate the impact of WHO multimodal hand hygiene strategy on the incidence of neonatal sepsis and neonatal colonization by MDR Gram negative bacteria as well as pilot surveillance of neonatal sepsis at the participating sites. Study setting: Data will be collected at the NICU of the KBTH and the 37 Military Hospital, Accra, Ghana. Study Design: The study will be a controlled before and after interventional trial with one interventional site (KBTH) and a control site (37 Military hospital). Data will be collected over 19 months with a baseline phase of 7 months; an interventional phase of 5 months; and a post intervention phase of 7 months. Intervention: The WHO multimodal hand hygiene strategy comprises five essential elements; system change-availability of alcohol-based hand rub at the point of care and/ or access to safe continuous water supply and soap and towels; training and education of healthcare professionals; monitoring of hand hygiene practices and performance feedback; reminders in the workplace; and the creation of a handhygiene safety culture with the participation of both individual healthcare workers and senior hospital managers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neonatal SEPSIS
Keywords
Neonatal sepsis, Infection control, Hand hygiene, WHO multi modal

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Controlled before and after interventional trial
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
5433 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard of care
Arm Type
No Intervention
Arm Description
Continuously monitoring of neonatal sepsis under standard of care at one site
Arm Title
Hand hygiene
Arm Type
Experimental
Arm Description
The WHO multimodal hand hygiene strategy is implemented at one site
Intervention Type
Combination Product
Intervention Name(s)
The WHO multimodal hand hygiene strategy
Other Intervention Name(s)
Hand hygiene
Intervention Description
Comprises five essential elements; system change-availability of alcohol-based hand rub at the point of care and/ or access to safe continuous water supply and soap and towels; training and education of healthcare professionals; monitoring of hand hygiene practices and performance feedback; reminders in the workplace; and the creation of a hand hygiene safety culture with the participation of both individual healthcare workers and senior hospital managers.
Primary Outcome Measure Information:
Title
Incidence of neonatal sepsis
Description
Incidence of neonatal sepsis including clinical cases treated as sepsis and cases of neonatal sepsis with confirmed bloodstream infections per 1000 admissions.
Time Frame
Post-intervention at 7 months
Secondary Outcome Measure Information:
Title
Rate of hand hygiene compliance per opportunity
Description
Hand hygiene events per opportunity for hand hygiene measured by direct observations
Time Frame
Post-intervention at 7 months
Title
Rate of MDR Gram negative bacteria colonization among neonates
Description
Prevalence of MDR Gram negative bacteria among admitted neonates
Time Frame
During intervention at 2 months and post-intervention at 7 months
Title
Length of admission in days
Description
Days of admission
Time Frame
Post-intervention at 7 months
Title
All-cause mortality
Description
Mortality rates during admission
Time Frame
Post-intervention at 7 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Minute
Maximum Age & Unit of Time
48 Hours
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Admission NICU Birth weight ≥750 Grams ≤48 hours of age at time of enrolment Consent to participate obtained from legal guardian Exclusion Criteria: Neonates with severe congenital malformations Neonates who have undergone surgical procedure
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Appiah Korang Labi, MD
Organizational Affiliation
Department of Int. Health and Immunlogy Microbiology, University og Copenhagen
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jørgen Kurtzhals, Professor
Organizational Affiliation
Department of Int. Health and Immunlogy Microbiology, University og Copenhagen
Official's Role
Study Director
Facility Information:
Facility Name
Korle Bu Teaching Hospital
City
Accra
Country
Ghana

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
34561387
Citation
Labi AK, Enweronu-Laryea CC, Nartey ET, Bjerrum S, Ayibor PK, Andersen LP, Newman MJ, Kurtzhals JAL. Bloodstream Infections at Two Neonatal Intensive Care Units in Ghana: Multidrug Resistant Enterobacterales Undermine the Usefulness of Standard Antibiotic Regimes. Pediatr Infect Dis J. 2021 Dec 1;40(12):1115-1121. doi: 10.1097/INF.0000000000003284.
Results Reference
derived

Learn more about this trial

Neonatal Sepsis at Neonatal Intensive Care Units in Ghana

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