Critically-Ill Women Admitted to an Obstetric High Dependency Unit in a Resource-Limited Setting

Sponsor
Doctors with Africa - CUAMM (Other)
Overall Status
Completed
CT.gov ID
NCT04121234
Collaborator
(none)
523
1
17
30.8

Study Details

Study Description

Brief Summary

Sierra Leone faces the highest maternal mortality ratio in the world. Despite this extreme burden, the potential roles of obstetric critical care and high dependency units (HDUs) in this and other resource-limited settings remain scarcely explored. This study investigated epidemiology, clinical outcomes and risk factors for mortality in critically-ill parturients admitted to an obstetric HDU in a high volume, urban resource-limited maternity hospital.

Condition or Disease Intervention/Treatment Phase
  • Other: Exposure: " being admitted to HDU with a red code to OEWS"

Detailed Description

This is a retrospective observational study in women admitted to the HDU of Princess Christian Maternity Hospital (PCMH), Freetown, Sierra Leone, from 2nd October 2017 to 2nd October 2018. The study received ethical approval and waiver of informed consent from the Sierra Leone Ethics and Scientific Review Committee (18/12/18).

A set of predefined variables was assessed at hospital admission, HDU admission and at discharge from HDU. The primary data source was the HDU patient chart, with data crosschecked with the hospital patient charts and the HDU admission book for quality control purpose. Data of hospital deliveries, admissions and mortality were form the hospital register and the maternal mortality hospital database. Data were retrospectively collected by a study physician (CM) and included: patient demographics; admission date and source; main reason for admission in hospital; main reason for admission to the HDU (classified as: haemodynamic instability; sepsis; haemorrhage; acute renal failure; neurological impairment; respiratory distress; severe malaria; coagulopathy; other diagnoses). These are clinical diagnoses included in the hospital checklist to facilitate communication of referral to HDU and are thus based on the clinical assessment of the attending physician rather than on a strict research definitions.

Vital signs and treatments collected at admission included body temperature, heart rate, respiratory rate, neurological status according to the AVPU scale, systolic and diastolic blood pressure, transcutaneous saturation (SpO2). The ratio between SpO2 and fraction of inspired oxygen (SpO2/FiO2) was also measured. The obstetric modified early warning score (OEWS) was also calculated.

Specific treatments received at any point during HDU stay were extracted from the patient file and included: oxygen supplementation, use of vasopressors, blood transfusions, antibiotic therapy, activation of the magnesium protocol for eclamptic seizures prevention and hypotensive treatment protocol with hydralazine. Point of care laboratory parameters such as capillary lactates levels and haemoglobin were collected when available. Time from PCMH admission to HDU admission was calculated. Length of stay and patient outcomes (classified as death in HDU, discharge to ward, or transfer to other facility) were reported at discharge.

Study Design

Study Type:
Observational
Actual Enrollment :
523 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Pidemiology, Outcomes and Risk Factors for Mortality in Critically-Ill Women Admitted to an Obstetric High Dependency Unit in a Resource-Limited Setting
Actual Study Start Date :
May 1, 2018
Actual Primary Completion Date :
Jun 30, 2019
Actual Study Completion Date :
Sep 30, 2019

Outcome Measures

Primary Outcome Measures

  1. Morality in HDU [one year]

    The primary endpoint was the association between modifiable and non-modifiable factors and mortality during HDU stay. HDU death was defined as death during HDU stay, i.e. from referral to HDU to discharge from HDU.

Secondary Outcome Measures

  1. Hospital mortality [One year]

    Hospital mortality was death during the whole hospital stay.

  2. Lenght of stay [One year]

    Time between the hdu admission and the hdu discharge, in days.

  3. OEWS at the admission [one year]

    coded as: red, yellow, green

  4. reasons of admission [One Year]

    classified as: haemodynamic instability; sepsis; haemorrhage; acute renal failure; neurological impairment; respiratory distress; severe malaria; coagulopathy; other diagnoses

  5. Time of admission [One year]

    Night/day and Working days/weeknd

  6. Treatments received [One year]

    oxygen supplementation (yes/no), use of vasopressors (yes/no), blood transfusions (yes/no), antibiotic therapy (yes/no), activation of the magnesium protocol for eclamptic seizures prevention (yes/no) and hypotensive treatment protocol with hydralazine during the stay (yes/no).

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • All women admitted at HDU of the PCMH from the 2nd October 2017 to the 2nd October
Exclusion Criteria:
  • none

Contacts and Locations

Locations

Site City State Country Postal Code
1 Princess Christian Maternity Hospital Freetown Sierra Leone

Sponsors and Collaborators

  • Doctors with Africa - CUAMM

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Claudia Marotta, MD, MPH, Doctors with Africa - CUAMM
ClinicalTrials.gov Identifier:
NCT04121234
Other Study ID Numbers:
  • 070919CUAMM
First Posted:
Oct 9, 2019
Last Update Posted:
Oct 10, 2019
Last Verified:
Oct 1, 2019
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 Claudia Marotta, MD, MPH, Doctors with Africa - CUAMM
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 10, 2019