Evidence map›Paper›PMID 38606040›Full record

ArticleAnnals of clinical epidemiology2024

Treatment for patients with autosomal dominant polycystic kidney disease in the chronic kidney disease without kidney replacement therapy in real-world clinical practice: a descriptive retrospective cohort study.

Kazunori Sakoda, Kayoko Mizuno, Tomotsugu Seki, Kanna Shinkawa, Yuriko Kawai, Ayano Hayashi, Satomi Yoshida, Masato Takeuchi, Motoko Yanagita, Koji Kawakami

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical epidemiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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 at 2 institutions in 1 country.

Kazunori SakodaDepartment of Nephrology, Graduate School of Medicine, Kyoto University.
Kayoko MizunoDepartment of Pharmacoepidemiology, Graduate School of Medicine, Kyoto University.
Tomotsugu SekiDepartment of Cardiovascular Medicine, Kyoto Prefectural University of Medicine.
Kanna ShinkawaDepartment of Nephrology, Graduate School of Medicine, Kyoto University.
Yuriko KawaiDepartment of Nephrology, Graduate School of Medicine, Kyoto University.
Ayano HayashiDepartment of Nephrology, Graduate School of Medicine, Kyoto University.
Satomi YoshidaDepartment of Pharmacoepidemiology, Graduate School of Medicine, Kyoto University.
Masato TakeuchiDepartment of Pharmacoepidemiology, Graduate School of Medicine, Kyoto University.
Motoko YanagitaDepartment of Nephrology, Graduate School of Medicine, Kyoto University.
Koji KawakamiDepartment of Pharmacoepidemiology, Graduate School of Medicine, Kyoto University.
Kyoto University · JPKyoto Prefectural University of Medicine · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn real-world clinical practice, treatments selected for patients with autosomal dominant polycystic kidney disease (ADPKD) in the chronic kidney disease (CKD) without kidney replacement therapy (KRT) have not been reported. This study investigated the oral treatments used in these patients and the changes in their use in recent years. Additionally, we studied the factors affecting tolvaptan dose reduction or discontinuation.

methodsThis retrospective cohort study was conducted using the medical records of 160 hospitals in Japan. Patients with ADPKD or polycystic kidney disease registered on the database between January 2014 and December 2020 were selected. Changes in prescription proportions over time were assessed using the Cochran-Armitage test. We focused on patients prescribed with >15 mg of tolvaptan daily to identify the factors related to its dose reduction or discontinuation and used Multivariate Cox regression analysis to evaluate them.

resultsTolvaptan use in patients with ADPKD in the CKD without KRT stage has increased. As of 2020, 25% of patients were treated with tolvaptan. Overall, 3639 patients with ADPKD were enrolled in the database, of whom 156 were treated with tolvaptan. Of these, 64 patients (41%) reduced or discontinued tolvaptan during the observation period. The presence of an estimated glomerular filtration rate <60 mL/min/1.73 m

conclusionThe proportion of patients with ADPKD treated with high-dose tolvaptan is increasing. However, patients with late-stage CKD tended to reduce or discontinue tolvaptan.

Indexed as

Autosomal dominant polycystic kidney disease (ADPKD)chronic kidney disease (CKD)tolvaptan

Identifiers

PMID38606040
PMCPMC11006552
OpenAlexW4391213509

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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.