Pediatric Pertussis in Ambulatory Settings
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: non interventional study.
- Who it may be relevant to
- Registry conditions: Pertussis/Whooping Cough, Children, Only, Ambulatory. Basic parameters: 1 Day — 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
National Surveillance of Pediatric Pertussis in Ambulatory Settings
Overview
Since 2002, Whooping cough surveillance in pediatric private practice has been set up in France. The results of the first years, 2002-2006, have confirmed the effectiveness of the Pertussis whole-cell (Pw) vaccine and in particular the duration of protection of 9/10 years. After evaluating cases in children vaccinated with Pw vaccines, the study aims today to analyze cases in children vaccinated with Pertussis acellular (Pa) vaccines used since 2002/2003 and to assess, on an outpatient basis, the impact of new vaccine recommendations in France (in 2013, introduction of a 2 + 1 schedule - 8 weeks, 4 months and a 11-month recall - and a 6-year recall, and in 2014, update in the recommendations of exams to be prescribed based on the child's age and vaccination status).
Detailed description
The whooping cough surveillance objectives are :
* to follow the duration of protection of the Ca vaccines in the context of modifications of the vaccine recommendations * to describe the clinical characteristics of a population vaccinated with several boosters * to adapt complementary examinations for diagnostic purposes (culture, PCR, serology) according to the evolution of scientific knowledge * to monitor B. parapertussis infections * to train laboratories with nasopharyngeal aspiration * to monitor the evolution of the bacterial species All children aged 0-18 years, in whom the diagnosis of pertussis is mentioned and for which a biological check-up is requested, are included, except asymptomatic children with confirmed family case.
In case of suspected pertussis, real-time PCR and / or culture and / or (rarely) serology is / are still prescribed to the patient and / or his entourage.
Selected Pediatricians from the ACTIV group and the AFPA working in an outpatient clinic, located in different places in France, are participating in this network since 2001. The clinical evolution and the results of the examinations are transcribed on a case report form. The data are collected, firstly, during the visit where the diagnosis of whooping cough is suspected and a biological assessment requested (patient's medical history, clinical data, vaccination status and dates, as well as the search for a contaminated/contaminator) and secondly during the follow-up visit (results of the biological check-up and diagnosis, antibiotics potentially prescribed, and supplement data of the entourage, except in case of diagnosis of pertussis not retained).
All evaluations made by the pediatricians are regularly reviewed during meetings, and final diagnoses used are:
* biological pertussis * epidemiological pertussis * not evaluable * lost of follow up * no whooping cough
Interventions
- Other non interventional study
Primary outcome measures
- Duration of pertussis vaccines protection [Time frame: at inclusion]
Secondary outcome measures (1)
- Clinical characteristics of pertussis [Time frame: at inclusion]
Eligibility criteria
Inclusion criteria
- All children under 18 years old with a pertussis diagnosis is suspected and a biological exam is requested
Exclusion criteria
- children without symptoms with a household confirmed case
- cases for which the pertussis diagnosis was not suspected by the pediatrician
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Study design
- Observational model
- Cohort
Study locations
France · 1 center
- ACTIV — Créteil
Identifiers
NCT: NCT04807712 · ACT0606