Evidence map›Paper›PMID 28856014›Full record

ArticleJournal of ultrasonography2017

Grayscale ultrasound characteristics of autosomal dominant polycystic kidney disease severity - an adult and pediatric cohort study.

Marcin Strzelczyk, Michał Podgórski, Susan Afshari, Marcin Tkaczyk, Monika Pawlak-Bratkowska, Piotr Grzelak

Open access · diamondAbstract read
In one paragraph

Article in Journal of ultrasonography, 2017. 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
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 93% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

6 authors at 1 institution in 1 country.

Marcin StrzelczykPolish Mother's Memorial Hospital Research Institute, Department of Diagnostic Imaging, Łódź, Poland.
Michał PodgórskiPolish Mother's Memorial Hospital Research Institute, Department of Diagnostic Imaging, Łódź, Poland.
Susan AfshariPolish Mother's Memorial Hospital Research Institute, Department of Pediatrics, Immunology and Nephrology, Łódź, Poland.
Marcin TkaczykPolish Mother's Memorial Hospital Research Institute, Department of Pediatrics, Immunology and Nephrology, Łódź, Poland.
Monika Pawlak-BratkowskaPolish Mother's Memorial Hospital Research Institute, Department of Pediatrics, Immunology and Nephrology, Łódź, Poland.
Piotr GrzelakPolish Mother's Memorial Hospital Research Institute, Department of Diagnostic Imaging, Łódź, Poland.
Polish Mother’s Memorial Hospital Research Institute · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe most common hereditary kidney condition is autosomal dominant polycystic kidney disease. It is the cause of 5-10% of end-stage renal disease. Its symptoms are generally late-onset, typically leading to development of hypertension and chronic kidney disease. Ultrasonography is the imaging modality of choice in its diagnosis and management. The aim of this study is to determine the diagnostic value of grayscale ultrasound imaging in evaluating disease severity. MATERIALS AND

methodsThe study group consisted of 81 patients diagnosed with autosomal dominant polycystic kidney disease, 35 adults and 46 children. Inclusion criterion for adults was the presence of at least 10 large cysts in each kidney; children included into the study had developed at least 1 large renal cyst in each kidney. The number of large cysts, echogenicity of kidney parenchyma, cortical thickness and presentation of cortex/medulla boundary were assessed with the use of Logiq E9 apparatus (GE Healthcare, Netherlands). Patients were divided into groups, based on these morphological parameters. Kidney function was assessed according to serum creatinine concentration and creatinine clearance. Statistical analysis was performed, with

resultsThe number of cysts and the degree of parenchymal dysfunction were the determinants of creatinine level and creatinine clearance, with the second predictor proving stronger.

conclusionsWe recommend that an ultrasound kidney examination in patients with polycystic kidney disease should include evaluating renal parenchyma and the number of cysts for better assessment of disease severity.

Indexed as

autosomal dominant polycystic kidney diseaseB-modechildrenultrasound

Identifiers

PMID28856014
PMCPMC5516076
OpenAlexW2724326914

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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.