Evidence map›Paper›PMID 36327795›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2023

Real-Time Whole Genome Sequencing to Guide Patient-Tailored Therapy of Severe Acute Respiratory Syndrome Coronavirus 2 Infection.

Luke B Snell, Adela Alcolea-Medina, Themoula Charalampous, Christopher Alder, Tom G S Williams, Flavia Flaviani, Rahul Batra, Prijay Bakrania, Rajeni Thangarajah, Stuart J D Neil and 6 more

Full text read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Commercial Immunoglobulin Products Contain Neutralizing Antibodies Against Severe Acute Respiratory Syndrome Coronavirus 2 Spike Protein.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
    Article
  6. Article
  7. Review
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

16 authors.

Luke B SnellDepartment of Infection, Guy's and St. Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0002-6263-9497
Adela Alcolea-MedinaDepartment of Infection, Guy's and St. Thomas' NHS Foundation Trust, London, UK.
Themoula CharalampousDepartment of Infection, Guy's and St. Thomas' NHS Foundation Trust, London, UK.
Christopher AlderDepartment of Infection, Guy's and St. Thomas' NHS Foundation Trust, London, UK.
Tom G S WilliamsDepartment of Infection, Guy's and St. Thomas' NHS Foundation Trust, London, UK.
Flavia FlavianiNational Institute for Health Research Biomedical Research Centre, Guy's and St. Thomas' NHS Foundation Trust, London, UK.
Rahul BatraDepartment of Infection, Guy's and St. Thomas' NHS Foundation Trust, London, UK.
Prijay BakraniaDepartment of Pharmacy, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Rajeni ThangarajahDepartment of Infection, Guy's and St. Thomas' NHS Foundation Trust, London, UK.
Stuart J D NeilDepartment of Infectious Diseases, King's College London, United Kingdom.
Claire van Nispen Tot PannerdenDepartment of Infection, Guy's and St. Thomas' NHS Foundation Trust, London, UK.
Alina BotgrosDepartment of Infection, Guy's and St. Thomas' NHS Foundation Trust, London, UK.
Emma AaronsDepartment of Infection, Guy's and St. Thomas' NHS Foundation Trust, London, UK.
Samuel T DouthwaiteDepartment of Infection, Guy's and St. Thomas' NHS Foundation Trust, London, UK.
Jonathan D EdgeworthDepartment of Infection, Guy's and St. Thomas' NHS Foundation Trust, London, UK.
Gaia NebbiaDepartment of Infection, Guy's and St. Thomas' NHS Foundation Trust, London, UK.

Funding

Medical Research Council MR/T005416/1Medical Research Council MR/W025140/1
6 · The paper itself

Abstract

The management of coronavirus disease 2019 has become more complex due to the expansion of available therapies. The presence of severe acute respiratory syndrome coronavirus 2 variants and mutations further complicates treatment due to their differing susceptibilities to therapies. Here we outline the use of real-time whole genome sequencing to detect persistent infection, evaluate for mutations confering resistance to treatments, and guide treatment decisions.

Indexed as

COVID-19HumansMutationSARS-CoV-2Whole Genome SequencingCOVID-19SARS-CoV-2whole genome sequencing

Identifiers

PMID36327795
PMCPMC10029986

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read2
Read underepoch 390

Registered trials

None linked

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.