Evidence map›Paper›PMID 37123886›Full record

ArticleInternational journal of general medicine2023

Post-Acute SARS-CoV-2 Symptoms are Fewer, Less Intense Over Time in People Treated with Mono-Clonal Antibodies for Acute Infection.

Jillian Kallman Price, Lynn H Gerber, Maria Stepanova, Leyla de Avila, Ali A Weinstein, Huong Pham, Fatema Nader, Mariam Afendy, Kathy Terra, Patrick Austin and 8 more

Open access · goldAbstract read
In one paragraph

Article in International journal of general medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 23% of its field
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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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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

18 authors at 3 institutions in 1 country.

Jillian Kallman PriceBetty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA, USA.ORCID 0000-0003-4150-2835
Lynn H GerberBetty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA, USA.
Maria StepanovaBetty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA, USA.
Leyla de AvilaBetty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA, USA.
Ali A WeinsteinDepartment of Global and Community Health, George Mason University, Fairfax, VA, USA.ORCID 0000-0002-3371-6086
Huong PhamBetty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA, USA.
Fatema NaderBetty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA, USA.
Mariam AfendyBetty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA, USA.
Kathy TerraCenter for Liver Disease, Department of Medicine, Inova Fairfax Medical Campus, Falls Church, VA, USA.
Patrick AustinBetty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA, USA.
Wisna'odom KeoBetty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA, USA.
Andrei RacilaBetty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA, USA.
James Michael EstepBetty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA, USA.
Suzannah GerberBetty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA, USA.
Manisha VermaBetty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA, USA.
Pegah GolabiBetty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA, USA.
Brian P LamBetty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA, USA.
Zobair YounossiBetty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA, USA.
Inova Health System · USGeorge Mason University · USInova Fairfax Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Many with post-acute SARS-CoV-2 (PASC) have persistent symptoms impacting physical and cognitive function, decreased health and health-related life quality. Monoclonal antibody (mAb) treatment was available to acutely infected patients which might improve these outcomes. Purpose: To compare patient perception of PASC symptoms for those receiving bamlanivimab or casirivimab and imdevimab (mAbs) to those not receiving this treatment (non-mAbs). To compare changes between these groups in symptoms, function and quality of life over a 6-month follow-up. Patients and Methods: Consented adults >28 days post-infection with positive SARS-CoV-2 qPCR or antigen test and SARS-CoV-2 infection between March of 2020 and July of 2022 were enrolled. This prospective, repeated measure observational study reports baseline through 6-month follow-up. Extensive sociodemographic data, detailed medical history, COVID-19 symptom history, and standardized measures of well-being, depression, anxiety, stigma, cognition, symptom assessment, distress, and health status were collected. Results: 323 participants [101 mAb, 221 non-mAb, 52.7±15.5 years, 47.7% male, body mass index (BMI) 31.4±8.4] were analyzed. Fewer symptoms at baseline were reported in mAb versus non-mAb participants (1.06±1.31 vs 1.78±2.15, respectively p=0.0177) 6 months: (0.911±1.276 mAb vs.1.75±2.22 non-mAb, p=0.0427). Both groups showed significant within-group decreases in symptom number (52 to 21 mAb, 126 to 63 non-mAb) and symptom burden (p=0.0088 mAb, p<0.00001 non-mAb). mAb patients had significantly shorter infection-to-baseline interval (days) (120.4±55.3 mAb vs 194.0±89.3 non-mAb, p<0.00001); less frequent history of myocardial infarction (0.0 vs 3.9%, p=0.0464); headache (2.0% vs.11.8%, p=0.0046), rash (3.1% vs 9.9%, p=0.0377), and miscellaneous muscle complaints (2.0% vs 12.3%, p=0.0035), plus significantly better 6-month mood. (2.2% vs 13.2%, p=0.0390). Conclusion: mAb treated participants had reduced symptom burden and consistently reported fewer symptoms than non-mAb at all time points despite less time since acute illness. Both groups reported a statistically significant decrease in symptoms by 6-month visit with no statistically significant differences between them at follow-up.

Indexed as

COVID-19monoclonal antibodiespatient-reported outcomesrecoverysymptom burden

Identifiers

PMID37123886
PMCPMC10145429
OpenAlexW4366831005

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.