Activity and Quality of Care Indicators' for a Sentinel Network Creation

There is no large-scale data in France or internationally, on the quality of care in gynecological emergencies, or the consequences of delay or misdiagnosis of women's health or on determinants of these delays or misdiagnosis. The creation of a sentinel network for gynecological emergencies could help quantify these links and test strategies to avoid the worst effects by implementing simple diagnostic tools from clinical research.

The network will be designed to promote research in women's health and the emergency reception by focusing on:

(i) Assessment of the quality and organization of care and professional practice for the management of gynecological emergencies.

(ii) The study of severe morbidity and its determinants (iii) comparison of organizational practices and health outcomes of women over time within the same department or between services having substantially the same recruitment (iv) Comparison of organization systems gynecological emergencies departement between different high resource francophone countries (France, Switzerland, Belgium).

(v) The assessment of new diagnostic strategies (sorting or diagnostic aid) or therapeutic derived from clinical research.

Completed

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Key information

Conditions

Obstetrics Gynecology Maternal Morbidity Quality

Sex eligibility

Female

Study type

Observational

Primary location

Poissy Saint Germain Hospital

Poissy, 78180, France

About this study

Objectives :

To measure the incidence of the potentially life-threatening gynaecological emergencies (G-PLE) and of the Cases of severe morbidity (SM)
To analyze the determinants of the SM,
To validate an objective score of quality

Criterias of evaluation:

Incidence of the G-PLE and SM cases during one month.
Reliability and validity of measurements of the indicators of quality of care.

Methodology:

Stage 1: Data acquisition (prospective) within 22 gynaecological emergencies departments.

Stage 2: Sampling and checking of files of patients included at stage 1

Calendar of the research project:

18 months:

6 months for the phase of preparation,
1 month for the investigation of incidence,
5 months for the phase of checking data,
6 months of statistical analysis

Statistical Analyzes:

Descriptive statistics of the data. Estimation of the incidence rate of the potentially life-threatening gynaecological emergencies (G-PLE) and of the cases of Severe morbidity (SM) among women consulting for acute pelvic pain.

To construct reliable quality indicators, principal components analysis and Cronbach's α statistics will be performed to determine the underlying dimensions. Construct validity of indicators will be assessed by testing predefined hypotheses about relationship between G-PLE and or SM and quality indicators.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

French-speaking gynaecological emergencies departments leaned with a public maternity volunteers to take part in the study.
Sample of files resulting from the principal centers recruiters

Exclusion criteria

Treatment and study plan

Primary outcomes

Incidence of the potentially life-threatening gynaecological emergencies (G-PLE )

Time frame: 1 year
Incidence of severe morbidity (SM) cases

Time frame: 1 year

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Official study title

Gynaecological Emergencies: Validation of Indicators of Activity and Quality of Care for Creation of a Network Sentinel

Acronym: URGO

Important dates

Study start: 2015
Primary completion: 2018
Study completion: 2018
First posted: Oct 24, 2014
Registry last updated: Mar 2, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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Completed