Pneumonia Research and Vaccine Impact League

NCT ID: NCT03900520

Last Updated: 2023-10-11

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 6004 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2020-10-13
• Study Completion Date: 2023-09-30

Brief Summary

The leading cause of severe respiratory disease and death in young children is Streptococcus pneumoniae (pneumococcus). An estimated one-fifth of global childhood pneumococcal-related deaths occurred in India. The pneumococcal conjugate vaccine (PCV) is a primary prevention tool against pneumococcal disease that is safe and effective and has been in use in many countries. In alignment with the Government of India's rollout of PCV sub-nationally in selected districts and states, this two-year observational study will use a non-interventional, observational prospective study design to evaluate the impact of PCV in 7 sites in India (5 hospitals and 2 community sites) by assessing clinical and serotype-specific outcomes that include hospitalized pneumonia and community pneumococcal carriage. A sub-study to assess the cost of illness of pneumonia will also be conducted. This study is anticipated to provide data to support sustainability of PCV expansion and disease surveillance in India.

Detailed Description

Streptococcus pneumoniae (pneumococcus) is the leading cause of severe respiratory disease and death in young children, and is also responsible for other serious diseases such as meningitis and sepsis. Global disease burden models for the year 2015, estimate that 20 percent of global childhood pneumococcal deaths occurred in India. Data from India indicate that available pneumococcal conjugate vaccines (PCV) include serotypes that account for 66 to 74 percent of invasive pneumococcal disease (IPD) in young children. The 2017 PCV launch into the national immunization schedule in selected high-burden states was poised to successfully combat the pneumococcal disease burden in the country once scale-up of vaccine coverage takes place. The Government of India has recommended robust evaluation of PCV impact to facilitate national rollout and sustained use of PCV.

This study aims to evaluate the impact of PCV introduction to the national immunization program. The investigators propose to quantify the impact of PCV on pneumonia and other acute respiratory infections resulting in hospitalization and on community carriage of pneumococci. Hereafter, in reference to the proposed study, the investigators use the term 'pneumonia' to denote to a group of physician-based diagnoses representing a range of acute respiratory illness including pneumonia. Specifically, the investigators propose to measure differences in the proportion of pneumonia hospitalizations in children 1-35 months colonized with vaccine-serotype (VT) pneumococcus, as well as differences in VT pneumococcal nasopharyngeal (NP) colonization in the community, comparing children enrolled at sites where PCV has been introduced (PCV sites) to children at sites where PCV has not yet been introduced (non-PCV sites). The health economic aims will consist of assessing the cost of illness of pneumococcal disease, and economic cost of pneumococcal disease and pneumonia hospitalization. The investigators have designed this portfolio of PCV impact evaluations within the context of PCV introduction and rollout in six selected states in India, mindful of the need for baseline data, the staggered plan for PCV roll-out, variance of cost-generating events, and the inherent biases of non-interventional studies with outcomes that are not specific for pneumococcal disease and that may be subject to secular trends and possible confounders. The study sites are located in New Delhi and within three of the six states that were included in the PCV rollout plan starting in 2017. The investigators plan this as a two-year study that will include data from both PCV sites and non-PCV sites, the comparison of which will allow an assessment of vaccine impact. Active study sites will be located in Delhi; Agra in Uttar Pradesh state (non-PCV-using); Bhopal in Madhya Pradesh state; and Jaipur in Rajasthan state (PCV-using). Community enrollment will take place in two demographic survey sites in Bhopal and Delhi, and economic assessment will take place in four hospital sites. Sites will use a common protocol to identify and recruit children, obtain nasopharyngeal swabs for colonization studies, and run validated laboratory tests. A reference laboratory will provide pneumococcal serotyping results, nasopharyngeal quantification of pneumococcus, and provide site laboratory oversight.

These data will provide evidence to policy makers on changes in pneumococcal disease burden in young children, pneumococcal community transmission changes as a result of PCV introduction, that can help policy makers support, optimize, and advocate for the expansion of the PCV immunization program in India and in other countries.

The primary objectives of PREVAIL are as follows:

1. Quantify the difference in the proportion of hospitalized pneumonia cases 1-35 months of age carrying a vaccine-type pneumococcus in the nasopharynx in cases enrolled at sites that have introduced PCV into the national immunization program compared to cases enrolled at sites that have not introduced PCV

2. Quantify the difference in the proportion of children in the community 1-35 months who are colonized with vaccine-type pneumococcus enrolled at a site that has introduced PCV into the national immunization program compared to the proportion of children colonized with vaccine-type pneumococcus enrolled at a site that has not introduced PCV

3. Determine the overall economic impact of PCV by: (i) Estimating the total cost of hospitalized pneumonia in children 1-35 months from the healthcare system and household perspectives; and (ii) Estimating the proportion of households facing catastrophic health spending and medical impoverishment from out-of-pocket health expenses due to hospitalized pneumonia in children 1-35 months.

Secondary objectives are evaluated within each of the four groups, and are;

1. Assess the difference in mortality and occurrence of illnesses within 3 months of hospital discharge among children aged 1-35 months presenting with pneumonia in PCV-using sites compared to children at non-PCV sites.

2. Quantify the difference in proportion among hospitalized cases aged 1-35 months with alveolar consolidation detected on radiography in PCV-using sites compared to children at non-PCV sites.

3. Quantify the difference in proportion among hospitalized cases aged 1-35 months with hypoxemia (oxygen saturation<90%) in PCV-using sites compared to children at non-PCV sites.

4. Quantify the difference in proportion of hospitalized cases aged 1-35 months that are vaccinated at PCV-using sites (indirect cohort method to assess vaccine effectiveness) between the following groups:

1. Carrying a VT vs. carrying a non-VT serotype

2. With vs. without alveolar consolidation

3. With vs. without hypoxemia

Conditions

Pneumonia

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Pneumonia group (PREVAIL-Pneumo)

Children aged 1-35 months with pneumonia or lower respiratory tract infection hospitalized or recommended for hospitalization

No interventions assigned to this group

Community group (PREVAIL-Community)

Children aged 1-35 years living in the community with no known systemic illness

No interventions assigned to this group

Economic group (PREVAIL-Econ)

PREVAIL-Pneumo-enrolled children hospitalized for pneumonia

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Age 1-35 months
• Admitting diagnosis is pneumonia or lower respiratory tract illness/infection Written informed consent obtained from parent or legally authorized representative

• Currently enrolled into the PREVAIL study

Exclusion Criteria

• Discharged as an PREVAIL case in the last 90 days

PREVAIL-Community:

• Written informed consent obtained from parent or legally authorized representative

• Known underlying serious disease (e.g., congenital heart diseases, immunodeficiency disorders, sickle cell anemia etc.) which may negatively influence the participant's ability to participate in the study

PREVAIL-Econ:

• Minimum Eligible Age: 1 Month
• Maximum Eligible Age: 35 Months
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Maulana Azad Medical College

OTHER

Sponsor Role: collaborator

Pfizer

INDUSTRY

Sponsor Role: collaborator

Johns Hopkins Bloomberg School of Public Health

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Anita Shet, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Johns Hopkins Bloomberg School of Public Health

Locations

Maulana Azad Medical College

New Delhi, , India

Countries

India

Other Identifiers

11740

Identifier Type: -

Identifier Source: org_study_id