Evidence map›Paper›PMID 32582581›Full record

ArticleFrontiers in pediatrics2020

Successful Treatment of Cyst Infection in an Infant With Autosomal Dominant Polycystic Kidney Disease Using Trimethoprim/Sulfamethoxazole.

Hiroki Yokoyama, Mayumi Sakaguchi, Yuko Yamada, Koichi Kitamoto, Shinichi Okada, Susumu Kanzaki, Noriyuki Namba

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in pediatrics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 40% 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 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Guideline
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

7 authors at 2 institutions in 1 country.

Hiroki YokoyamaDivision of Pediatrics and Perinatology, Faculty of Medicine, Tottori University, Yonago, Japan.
Mayumi SakaguchiDepartment of Pediatrics, Tottori Prefectural Central Hospital, Tottori, Japan.
Yuko YamadaDivision of Pediatrics and Perinatology, Faculty of Medicine, Tottori University, Yonago, Japan.
Koichi KitamotoDivision of Pediatrics and Perinatology, Faculty of Medicine, Tottori University, Yonago, Japan.
Shinichi OkadaDivision of Pediatrics and Perinatology, Faculty of Medicine, Tottori University, Yonago, Japan.
Susumu KanzakiAsahigawaso Rehabilitation and Medical Center, Okayama, Japan.
Noriyuki NambaDivision of Pediatrics and Perinatology, Faculty of Medicine, Tottori University, Yonago, Japan.
Tottori University · JPTottori Prefectural Central Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic disease causing renal cysts. Reports on kidney cyst infection in children are rare despite cyst infections being important complications of ADPKD. Here, we report a case of a child without any medical history who had a urinary tract infection with sepsis at 7 months. Leukocyturia persisted despite antibiotic therapy because the infection was treatment-resistant. Initial ultrasound and contrast computed tomography were inconclusive because cysts could not be detected clearly, and a family history of renal cysts was not determined. Subsequently, history of paternal renal cysts, thick walls in infectious cystic lesions on diffusion-weighted magnetic resonance imaging (MRI), and multiple small lesions with high signals on T2-weighted imaging in both kidneys became apparent. Upon diagnosis of ADPKD with cyst infection, antibiotic therapy was switched from cefotaxime to trimethoprim/sulfamethoxazole to achieve better cyst penetration, which successfully resolved the infection. In this patient, MRI was effective for clear visualization and diagnosis of infectious lesions and small cysts in undiagnosed ADPKD with cyst infection. Administering antibiotics with better cyst penetration is important. Trimethoprim/sulfamethoxazole is an option for use in children. This is the first case report that describes ADPKD with cyst infection in an infant in detail.

Indexed as

autosomal dominant polycystic kidney diseasecyst infectioninfantmagnetic resonance imagingtrimethoprim/sulfamethoxazole

Identifiers

PMID32582581
PMCPMC7280440
OpenAlexW3029520651

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.