Evidence map›Paper›PMID 40779307›Full record

ArticleJMIR research protocols2025

Establishing a Multicenter Active Adverse Events Following Immunization Sentinel Surveillance Network Across 22 Tertiary Care Hospitals in India: Protocol for a Prospective Observational Study.

Apoorva Sharan, Manoja Kumar Das, Akhil Pm, Ramesh Poluru, Neeraj Kumar Kashyap, Christian Burri, Jan Bonhoeffer, Satinder Aneja, Deepak Polpakara, Narendra Kumar Arora and 1 more

Abstract readClinical Trial Protocol
In one paragraph

Article in JMIR research protocols, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Apoorva SharanUniversity of Basel, Basel Switzerland, Swiss Tropical and Public Health Institute (Swiss TPH), Allschwil, Switzerland, Inclen Trust International, New Delhi, India.ORCID https://orcid.org/0000-0003-2166-401X
Manoja Kumar DasInclen Trust International, New Delhi, India.ORCID https://orcid.org/0000-0002-8559-5837
Akhil PmInclen Trust International, New Delhi, India.ORCID https://orcid.org/0009-0007-1052-9708
Ramesh PoluruInclen Trust International, New Delhi, India.ORCID https://orcid.org/0000-0002-7693-418X
Neeraj Kumar KashyapInclen Trust International, New Delhi, India.ORCID https://orcid.org/0000-0001-9374-6511
Christian BurriSwiss Tropical and Public Health Institute, University of Basel, Basel Switzerland, Allschwil, Switzerland.ORCID https://orcid.org/0000-0001-5418-1984
Jan BonhoefferUniversity of Basel Children's Hospital, University of Basel, Basel, Switzerland, Basel, Switzerland.ORCID https://orcid.org/0000-0001-9704-8315
Satinder AnejaSchool of Medical Sciences & Research, Sharda University, Greater Noida, India.ORCID https://orcid.org/0000-0001-9635-8792
Deepak PolpakaraJohn Snow India Private Limited, New Delhi, India.ORCID https://orcid.org/0009-0000-9250-3366
Narendra Kumar AroraInclen Trust International, New Delhi, India.ORCID https://orcid.org/0000-0003-3008-8616
MAASS Study GroupInclen Trust International, New Delhi, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe rapid evolution of immunization programs in low- and middle-income countries (LMICs) has necessitated an augmentation of capacity for postlicensure vaccine safety monitoring.

objectiveThis study describes the protocol for establishing a Multicenter Active Adverse Events Following Immunization Surveillance System (MAASS) network in India, which conducted prospective observational surveillance for 12 adverse pediatric outcomes between November 1, 2017, and March 20, 2020.

methodsA multistage site selection process was implemented, beginning with an initial screening survey followed by in-person visits to assess the suitability of potential tertiary care hospitals for inclusion in the network. We adopted a decentralized, collaborative approach to develop the study protocol, standardize case definitions, establish data collection procedures, and create a common data model for monitoring and analysis. Outcomes selected for surveillance included acute disseminated encephalomyelitis, anaphylaxis, aseptic meningitis, dengue, Guillain-Barré syndrome, Kawasaki disease, malaria, seizure, sepsis, thrombocytopenia, intussusception, and urinary tract infections. We screened all children aged 1-24 months who were hospitalized for more than 24 hours at participating sites to identify suspected or confirmed cases of these outcomes using a structured checklist. Written informed consent was obtained from the parent or legally authorized representative for inclusion in the study. Demographic, socioeconomic, and vaccine exposure information was collected for all included participants. Additional clinical information was gathered to assess the level of diagnostic certainty according to standardized case definitions. The study progressed through 3 distinct phases: network establishment (January-November 2017), active surveillance (November 2017-March 2020), and database analysis (April 2020-March 2024). The dissemination process is currently underway.

resultsA geographically representative data network was established across 15 public and 7 private tertiary care hospitals in 17 states and 1 union territory in India. During the study period, we screened 90,147 age-eligible admissions and confirmed 8362 cases with study outcomes. Using multiple analytic study designs, we generated a database of outcomes and exposures to investigate associations between vaccine-event pairs of interest.

conclusionsThe MAASS network is unprecedented in its scope and scale among LMICs. While the study is specific to India, the lessons learned in establishing and implementing the network offer valuable insights for developing active surveillance systems and strengthening capacity for benefit-risk evaluations of vaccines in resource-constrained settings. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): RR1-10.2196/64050.

Indexed as

Adverse Drug Reaction Reporting SystemsImmunizationSentinel SurveillanceChild, PreschoolFemaleHumansIndiaInfantMulticenter Studies as TopicObservational Studies as TopicProspective StudiesTertiary Care Centersactive surveillanceadverse events following immunizationlow- and middle-income countriesmulticenter studiespharmacovigilancepostlicensure safety surveillancevaccine safety

Identifiers

PMID40779307
PMCPMC12374136

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.