Evidence map›Paper›PMID 39649410›Full record

ArticleCurrent therapeutic research, clinical and experimental2024

US Real-World Effectiveness Study of Nirmatrelvir/Ritonavir in Preventing Hospitalization of High-Risk COVID-19 Patients.

Mark R Cullen, Xiaofeng Zhou, Scott P Kelly, Caihua Liang, Ling Li, Rongjun Shen, Heidi K Leister-Tebbe, Steven G Terra, Michael Gaffney, Leo Russo

Abstract read
In one paragraph

Article in Current therapeutic research, clinical and experimental, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. 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

10 authors.

Mark R CullenConsultant in Population Health Science, Los Altos Hills, California.
Xiaofeng ZhouGlobal Medical Epidemiology, Worldwide Medical and Safety, Pfizer Inc, New York, New York.
Scott P KellyGlobal Medical Epidemiology, Worldwide Medical and Safety, Pfizer Inc, New York, New York.
Caihua LiangGlobal Medical Epidemiology, Worldwide Medical and Safety, Pfizer Inc, New York, New York.
Ling LiGlobal Medical Epidemiology, Worldwide Medical and Safety, Pfizer Inc, New York, New York.
Rongjun ShenGlobal Medical Epidemiology, Worldwide Medical and Safety, Pfizer Inc, New York, New York.
Heidi K Leister-TebbeGlobal Product Development, Pfizer Inc, Collegeville, Pennsylvania.
Steven G TerraGlobal Product Development, Pfizer Inc, Andover, Massachusetts.
Michael GaffneyStatistical Research, Pfizer Inc, New York, New York.
Leo RussoGlobal Medical Epidemiology, Worldwide Medical and Safety, Pfizer Inc, Collegeville, Pennsylvania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: We describe nirmatrelvir/ritonavir (NMV/r) effectiveness in preventing hospitalization among COVID-19 patients at high risk of severe disease. Methods: An ongoing US population-based observational cohort study with retrospective and prospective collection of national electronic healthcare data collected from the US Optum® deidentified COVID-19 Electronic Health Record dataset during December 22, 2021-July 20, 2022. Participants were ≥12 years old; had a positive SARS-CoV-2 test, COVID-19 diagnosis, or NMV/r prescription; and were at high risk of severe COVID-19 based on demographic/clinical characteristics. Potential confounders between groups were balanced using propensity score matching. Immortal time bias was addressed. Hospitalization rates within 30 days from COVID-19 diagnosis were evaluated. Sensitivity analyses included 15-day hospitalization, chart review to investigate incidental hospitalization effects, and exclusion of patients identified as having COVID-19 based on NMV/r prescription alone. Outcomes were also evaluated by race, age, and COVID-19 vaccine status. Findings: Overall, 12,440 and 234,123 patients were included in the NMV/r and non-NMV/r groups, respectively. After propensity score matching, baseline characteristics were well balanced across groups (NMV/r, Implications: Real-world NMV/r effectiveness against hospitalization during Omicron predominance among COVID-19 patients at high risk of severe disease supports demonstrated clinical trial efficacy. Black patients underutilized NMV/r despite high effectiveness.

Indexed as

AntiviralCOVID-19Nirmatrelvir/ritonavirReal-worldSARS-CoV-2

Identifiers

PMID39649410
PMCPMC11625212

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.