A Study of Streptococcus Pneumonia Colonisation and Invasive Disease in Cambodian Children

Completed

• Conditions: Streptococcal Pneumonia
• Interventions: Other: Prospective study; Other: Cross-sectional surveys

• Registration Number: NCT03331952
• Lead Sponsor: University of Oxford

Brief Summary

Streptococcus pneumoniae (the pneumococcus) remains a leading cause of childhood mortality and morbidity. Between 2007 and 2012, Angkor Hospital for Children (AHC), Siem Reap, Cambodia documented that S. pneumoniae was responsible for around 10% of bloodstream infections in hospitalised children, with a case fatality rate of 15.6%.

The use of pneumococcal conjugate vaccines (PCV), covering between 7 and 13 of the \>90 pneumococcal serotypes, has resulted in significant declines in invasive pneumococcal disease (IPD) incidence in countries where they are included in routine childhood immunisation schedules. Paediatric radiologic pneumonia incidence is also reduced by PCV, but the impact on clinical pneumonia is minimal. The vaccines have had an effect on reducing the burden of drug resistant IPD, although this may not be sustained. Given the large number of serotypes not included in the current PCV formulations, it is not surprising that initial declines in overall IPD incidence have been eroded by, for the time being, small increases in IPD due to non-vaccine serotypes. To date most data on this serotype replacement disease has come from high-income countries. It less clear how much serotype replacement will occur in low and middle income countries, where pre-PCV disease incidence is generally higher and other factors, such as unregulated antimicrobial consumption, may play a role in encouraging non-vaccine serotype infections.

Nasopharyngeal colonisation by S. pneumoniae is common in childhood and is an essential prerequisite for invasive disease. Surveillance of pneumococcal colonisation can provide important data regarding serotype replacement and disease-associated serotypes, and may also allow prediction of likely IPD incidence changes post-vaccine introduction. A recent study of pneumococcal colonisation in children attending the AHC out-patients has documented an overall colonisation prevalence of approximately 65%.

In January 2015, Cambodia will introduce the 13-valent PCV (PCV13; serotypes covered 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19F, 19A, 23F). The vaccine will be rolled out nationally with a 3+0 dosing schedule (6, 10 and 14 weeks) and no catch up campaign. There is no robust national surveillance system in place to monitor the effects of PCV13 introduction.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2015-08-03
• Study First Submitted: 2017-11-01
• Study First Submitted QC: 2017-11-01
• Study First Posted: 2017-11-06
• Primary Completion: 2018-08-31
• Study Completion: 2018-10-19
• Status Verified: 2020-10
• Last Update Submitted: 2020-10-08
• Last Update Posted: 2020-10-09

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 4111

Inclusion Criteria

Not provided

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Exclusion Criteria

Not provided

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Invasive pneumococcal disease study (PCV-D)	Prospective study	Prospective study of children with invasive pneumococcal disease / probable bacterial meningitis (PCV-D) Clinical procedures At study enrolment: * Admission clinical findings / laboratory results will be recorded. * A questionnaire will be administered to the parent / guardian or caretaker to assess the child's immunisation status, household structure, environmental exposures, and recent antimicrobial use. Radiology procedures As part of routine clinical management at AHC, a digital chest radiograph (CXR) may be performed as part of a child's diagnostic work up. CXRs will be read and interpreted primarily by the AHC radiologists. All CXR will subsequently be re-read by two study clinicians and interpreted according to the WHO paediatric radiologic pneumonia criteria. Laboratory procedures • Residual routine clinical specimens further analysed as part of the study protocol: * Blood and cerebrospinal fluid culture specimens. * EDTA / serum specimens. * Urine.
Pneumonia study (PCV-P)	Prospective study	Prospective study of children hospitalised with clinical and/or radiologic pneumonia (PCV-P) Clinical procedures As described for PCV-D. Radiology procedures As part of routine clinical management at AHC, a digital chest radiograph (CXR) is performed on all children with an admission diagnosis of pneumonia. CXRs will be handled as described for PCV-D. Laboratory procedures * Study specific specimens: o Nasopharyngeal swab at enrolment. * Residual routine clinical specimens further analysed as part of the study protocol: * As described for PCV-D.
Pneumococcal colonisation study (PCV-C)	Cross-sectional surveys	Cross-sectional pneumococcal colonisation surveys in children attending the AHC out-patient department (PCV-C) Three annual surveys, enrolling 450 children each year, will be done to identify and characterise pneumococcal nasopharyngeal colonisation in AHC out-patient department (OPD) attendees. Clinical procedures • Subjects will be recruited from the OPD waiting area after nurse triage. A questionnaire will be administered to the parent / guardian or caretaker to assess the child's immunisation status (by review of the handheld immunisation card where possible), household structure, environmental exposures, and recent antimicrobial use. Laboratory procedures • Study specific specimens: o Nasopharyngeal swab at enrolment. A nasopharyngeal swab will be collected from each participant and these will be processed as described for PCV-P.

Primary Outcome Measures

Name	Time	Method
Invasive pneumococcal disease hospitalisation rates	3 years
Characteristics of invasive S. pneumoniae isolates in children <5 years of age admitted to Angkor Hospital for Children, in relation to national introduction of PCV13 in Cambodia	3 years

Secondary Outcome Measures

Name	Time	Method
Changes in pneumonia (both clinical and radiologic) hospitalisation rates in children <5 years of age, in relation to national introduction of PCV13 in Cambodia	3 years
Genotype in relation to national introduction of PCV13	3 years
Serotype in relation to national introduction of PCV13	3 years
Compare pneumococcal serotype colonisation in pneumonia cases with children attending the hospital out-patients for minor illnesses	3 years
Pneumococcal colonisation prevalence	3 years
Antimicrobial susceptibility profiles in relation to national introduction of PCV13	3 years

Trial Locations

Locations (1)

Angkor Hospital for Children; 🇰🇭 Siem Reap, Cambodia