Evidence map›Paper›PMID 39103829›Full record

ArticleBMC infectious diseases2024

Nirmatrelvir/ritonavir treatment and the risk of post-COVID condition over 180 days in Malaysia.

Ee Vien Low, Mohan Dass Pathmanathan, Yi Yang Ten, Suresh Kumar Chidambaram, Wee Ric Kim, Wei Jia Lee, Zhi Wei Teh, Maheshwara Rao Appannan, Mastura Ismail, Azah Abdul Samad and 1 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2024. 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
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0citing papers in PubMed
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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.

Ee Vien LowInstitute for Clinical Research, National Institutes of Health, Ministry of Health Malaysia, No.1 Jalan Setia Murni U13/52, Seksyen U13, Shah Alam, Selangor, 40170, Malaysia. evienlow@gmail.com.
Mohan Dass PathmanathanInstitute for Clinical Research, National Institutes of Health, Ministry of Health Malaysia, No.1 Jalan Setia Murni U13/52, Seksyen U13, Shah Alam, Selangor, 40170, Malaysia.
Yi Yang TenInstitute for Clinical Research, National Institutes of Health, Ministry of Health Malaysia, No.1 Jalan Setia Murni U13/52, Seksyen U13, Shah Alam, Selangor, 40170, Malaysia.
Suresh Kumar ChidambaramDepartment of Medicine, Sungai Buloh Hospital, Sungai Buloh, Selangor, 47000, Malaysia.
Wee Ric KimDigital Health Division, Ministry of Health Malaysia, Block F1, Complex F, 62000, Putrajaya, Malaysia.
Wei Jia LeeDigital Health Division, Ministry of Health Malaysia, Block F1, Complex F, 62000, Putrajaya, Malaysia.
Zhi Wei TehDigital Health Division, Ministry of Health Malaysia, Block F1, Complex F, 62000, Putrajaya, Malaysia.
Maheshwara Rao AppannanDigital Health Division, Ministry of Health Malaysia, Block F1, Complex F, 62000, Putrajaya, Malaysia.
Mastura IsmailFamily Health Development Division, Ministry of Health Malaysia, Block E10, Complex E, Putrajaya, 62590, Malaysia.
Azah Abdul SamadSection 7 Health Clinic, No.2 Persiaran Kayangan, Seksyen 7, Shah Alam, Selangor, 40000, Malaysia.
Kalaiarasu M PeariasamyInstitute for Clinical Research, National Institutes of Health, Ministry of Health Malaysia, No.1 Jalan Setia Murni U13/52, Seksyen U13, Shah Alam, Selangor, 40170, Malaysia.

Funding

Ministry of Health Malaysia Research Grant NIH/800-3/2/2 Jilid 13 (182)
6 · The paper itself

Abstract

backgroundThe effect of nirmatrelvir/ritonavir on preventing post-COVID condition (PCC) in the BA4, BA5, and XBB Omicron predominant periods is not well understood. The purpose of this study was to assess how nirmatrelvir/ritonavir treatment affected both PCC and health-related quality of life.

methodsThis retrospective cohort study enrolled 2,524 adults aged 18 years and older who were eligible for nirmatrelvir/ritonavir between July 14 to November 14, 2022. All outcomes were observed from the patient's first visit to the primary health clinic, 1 week, 1 month, 3 months, and 6 months after testing positive for COVID-19. The primary outcome was the presence of PCC. Secondary outcomes included the effects on health-related quality of life, such as walking, bathing and dressing, activities, cause adverse emotions or signs that prevent individuals from leading normal lives over a 180-day observation period.

resultsThere were no significant differences observed between the nirmatrelvir/ritonavir and those not administered (control group) in terms of PCC symptoms at 3 months (OR 0.71 95% CI 0.31, 1.64) and 6 months (OR 1.30 95% CI 0.76, 2.21). At 3 months, the use of nirmatrelvir/ritonavir was associated with a 26% reduction in symptoms causing negative emotions (OR 0.74 95% CI 0.60, 0.92) and an increased likelihood of symptoms limiting walking (OR 1.58 95% CI 1.10, 2.27). However, there were no significant differences between the nirmatrelvir/ritonavir and the control group in terms of the impact of PCC on health-related quality of life at 6 months.

conclusionsOur study indicates that the administration of nirmatrelvir/ritonavir does not significantly reduce PCC after 3 months and 6 months in a population with high vaccination coverage.

Indexed as

COVID-19 Drug TreatmentQuality of LifeRitonavirAdultAgedAntiviral AgentsCOVID-19FemaleHumansMalaysiaMaleMiddle AgedRetrospective StudiesSARS-CoV-2Antiviral AgentsRitonavirLong COVIDMalaysiaNirmatrelvir/ritonavirpost-COVID condition

Identifiers

PMID39103829
PMCPMC11299408

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LicenceCC BY-NC-ND
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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.