Evidence map›Paper›PMID 40568344›Full record

ArticleThe Lancet regional health. Western Pacific2025

Capturing the complete clinical spectrum and incidence of severe acute Group A

Andrew Fox-Lewis, Kate Wong She, Emma Wong She, Avinash Sathiyaseelan, Anna Vesty, Sally A Roberts, Susan C Morpeth, Susan Taylor, Anneka Anderson, Julie Bennett and 2 more

Abstract read
In one paragraph

Article in The Lancet regional health. Western Pacific, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

12 authors.

Andrew Fox-LewisDivision of Infection and Immunity, Department of Molecular Medicine and Pathology, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Kate Wong SheAotearoa Clinical Trials, Middlemore Hospital, Auckland, New Zealand.
Emma Wong SheSchool of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Avinash SathiyaseelanSchool of Medicine, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Anna VestyDivision of Infection and Immunity, Department of Molecular Medicine and Pathology, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Sally A RobertsMicrobiology Department, LabPlus, Auckland City Hospital, Auckland, New Zealand.
Susan C MorpethMicrobiology Department, Middlemore Hospital, Auckland, New Zealand.
Susan TaylorMicrobiology Department, Middlemore Hospital, Auckland, New Zealand.
Anneka AndersonTe Kupenga Hauora Māori, University of Auckland, Auckland, New Zealand.
Julie BennettDivision of Infection and Immunity, Department of Molecular Medicine and Pathology, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Nicole J MorelandDivision of Infection and Immunity, Department of Molecular Medicine and Pathology, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Rachel WebbKidz First Children's Hospital, Middlemore Hospital, Auckland, New Zealand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The global health burden of Methods: This prospective population-based multicentre cross-sectional observational study utilized laboratory data and ARF notifications to capture all hospitalised GAS infections and toxin- and immune-mediated disease cases associated with hospitalisation in Auckland during 2023. The epidemiology, clinical features, incidence and hospitalisation costs of these cases are described. Findings: The complete clinical spectrum of severe acute GAS disease was observed, with 606 cases captured corresponding to 1:2000 people affected each year (52 cases/100,000 population/year). The burden is inequitably distributed across the population, greatest at the intersection of age, ethnicity and socioeconomic deprivation. In the most deprived areas, approximately 1:400 Pacific children <10-years and 1:200 Pacific adults ≥80-years are affected annually (261 and 483 cases/100,000 population/year, respectively). Direct hospitalisation costs exceeded $13·2 million New Zealand dollars. Interpretation: This study demonstrates that the complete clinical spectrum of severe acute GAS disease occurs in Auckland and is associated with a substantial health and economic burden. The high incidence and entire range of severe acute GAS disease present make Auckland an ideal location for future vaccine studies. Funding: Ministry of Health New Zealand, Health Research Council of New Zealand (HRC-NZ), Royal College of Pathologists of Australasia (RCPA) Foundation.

Indexed as

Burden of diseaseEpidemiologyGroup A StreptococcusStreptococcus pyogenesVaccine

Identifiers

PMID40568344
PMCPMC12192613

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.