Evidence map›Paper›PMID 38289075›Full record

ArticleAntimicrobial agents and chemotherapy2024

Effectiveness and safety of nirmatrelvir-ritonavir in kidney transplant recipients with severe kidney dysfunction infected with COVID-19.

Hui Yang, Xin Yu, Wenjing Hou, Xiangduan Liu, Jiaojiao Chen, Ying Zhang, Ying Wang, Ying Zhu, Qing Qian, Kuifen Ma and 1 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2024. 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
1.2field-weighted citation impact, top 25% 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, 3 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

11 authors at 5 institutions in 1 country.

Hui Yang *Department of Pharmacy, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.ORCID 0000-0002-1797-2215
Xin Yu *Department of Pharmacy, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Wenjing Hou *National Alliance of Transplant Pharmacists, Zhejiang, China.
Xiangduan Liu *National Alliance of Transplant Pharmacists, Zhejiang, China.
Jiaojiao Chen *Yantai Yuhuangding Hospital, Yantai, China.
Ying Zhang *Department of Pharmacy, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Ying WangDepartment of Pharmacy, Fifth Clinical College of Henan University of Traditional Chinese Medicine (Zhengzhou People's Hospital), Zhengzhou, China.
Ying ZhuDepartment of Pharmacy, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Qing Qian *National Alliance of Transplant Pharmacists, Zhejiang, China.ORCID 0000-0001-6019-9187
Kuifen Ma *National Alliance of Transplant Pharmacists, Zhejiang, China.ORCID 0000-0001-8547-4325
Zhuoling An *Department of Pharmacy, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.ORCID 0000-0002-7996-5002
Capital Medical University · CNHenan University of Traditional Chinese Medicine · CNFirst Affiliated Hospital Zhejiang University · CNThe First People's Hospital of Changzhou · CNYuhuangding Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transplant patients face an elevated risk of coronavirus disease 2019 (COVID-19) morbidity and mortality and commonly encounter renal dysfunction. Nirmatrelvir is primarily excreted through the kidneys. The dosage of nirmatrelvir/ritonavir (NR) needs to be adjusted according to the degree of renal function impairment. Nevertheless, NR is not recommended for patients with severe renal impairment (estimated glomerular filtration rate < 30 mL/min) due to a dearth of associated research. In this study, we focus on kidney transplant patients and document and analyze the experiences of using NR in individuals with severe kidney dysfunction. This was a retrospective multicenter study that included transplant recipients hospitalized for COVID-19 in five major tertiary hospitals in China from December 2022 to June 2023. The outcomes consisted of the disease progression rate by day 28, individual disease progression events, safety outcomes, information on adverse events (AEs), and the blood drug concentrations of immunosuppressants. Data were presented with descriptive statistics. All analyses were performed using SPSS version 22. In total, 40 patients were included in the analysis. Considering the potential interaction between drugs, all patients temporarily discontinued their immunosuppressants during the NR treatment. None of the 32 moderate patients experienced disease progression. However, among the eight patients with critical COVID-19, unfortunately, two of them died. During the medication period, four patients experienced a total of six AEs associated with NR. None of them experienced AEs with a maximum grade of ≥3. Blood drug concentrations of immunosuppressants were monitored in 22 of 40 patients, and the blood drug concentrations of immunosuppressants did not show a significant increase, but some patients experienced lower blood drug concentrations. Our findings supported the use of NR therapy for the treatment of COVID-19 in transplant patients with severe renal insufficiency. A modified dose of NR was well-tolerated.

Indexed as

COVID-19Kidney TransplantationRenal InsufficiencyAntiviral AgentsCOVID-19 Drug TreatmentDisease ProgressionHumansImmunosuppressive AgentsKidneyRitonavirTransplant RecipientsAntiviral AgentsImmunosuppressive AgentsRitonavirCOVID-19kidney transplantnirmatrelvir/ritonavirsevere kidney dysfunction

Identifiers

PMID38289075
PMCPMC10916375
OpenAlexW4391349263

What OpenQuestion holds

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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.