Evidence map›Paper›PMID 37733097›Full record

ArticlePediatric nephrology (Berlin, Germany)2024

Nutcracker syndrome in pediatrics: initial findings and long-term follow-up results.

Iryna Akdemir, Ece Mekik Akar, Songül Yılmaz, Nilgün Çakar, Suat Fitöz, Zeynep Birsin Özçakar

Abstract read
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In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 3 citations in OpenAlex.

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  5. Nutcracker syndrome in pediatrics: a rare entity?Childhood kidney diseases · 2024
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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

6 authors at 1 institution in 1 country.

Iryna AkdemirDepartment of Pediatrics, Ankara University School of Medicine, Ankara, Turkey.
Ece Mekik AkarDivision of Pediatric Nephrology, Department of Pediatrics, Ankara University School of Medicine, Ankara, Turkey.
Songül YılmazDivision of Pediatric Nephrology, Department of Pediatrics, Ankara University School of Medicine, Ankara, Turkey.
Nilgün ÇakarDivision of Pediatric Nephrology, Department of Pediatrics, Ankara University School of Medicine, Ankara, Turkey.
Suat FitözDivision of Pediatric Radiology, Department of Radiology, Ankara University School of Medicine, Ankara, Turkey.
Zeynep Birsin ÖzçakarDivision of Pediatric Nephrology, Department of Pediatrics, Ankara University School of Medicine, Ankara, Turkey. zbozcakar@yahoo.com.ORCID 0000-0002-6376-9189
Ankara University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNutcracker syndrome (NCS) describes a set of symptoms and signs resulting from compression of the left renal vein (LRV). There is a lack of knowledge about its natural course, diagnosis, and management, especially in children. Herein, we present our single-center experience with a large number of patients who have long-term follow-up results.

methodsAll patients with NCS diagnosed between January 2011 and March 2021 were included and their data were obtained retrospectively.

resultsA total of 123 NCS patients (85 females) were included. The median age at the time of diagnosis was 12 (IQR 10-14) years, and BMI percentiles were below 5% in 38% of the cases. At the time of diagnosis, two-thirds of the patients were asymptomatic. The most common laboratory finding was nephritic proteinuria (98%), followed by microscopic hematuria (16%). Signs of LRV compression were significantly more evident in upright position Doppler ultrasonography (DUS) examination. All patients have been followed conservatively; hematuria and/or proteinuria resolved in 43 of the 108 patients (40%) within 35.8 ± 25.8 months of follow-up. Control DUS was performed in 52 patients after a mean period of 39.1 ± 21.3 months. The median peak velocity and diameter ratios of the LRV in the upright position were found to be decreased significantly when compared to the initial assessment (p < 0.05). Normal DUS findings were noted in 13 patients at the final evaluation.

conclusionsIn unexplained proteinuria and/or hematuria, NCS should be considered, especially in asthenic adolescents. Our results support conservative management in children as the first-line treatment approach.

Indexed as

HematuriaRenal Nutcracker SyndromeAdolescentChildFemaleFollow-Up StudiesHumansProteinuriaRenal VeinsRetrospective StudiesUltrasonographyDoppler ultrasonographyHematuriaLeft renal vein entrapmentNutcracker syndromeProteinuria

Identifiers

PMID37733097
OpenAlexW4386910457

What OpenQuestion holds

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Registered trials

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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.