Evidence map›Paper›PMID 32276020›Full record

ArticleJournal of vascular surgery2020

Surgical management of pediatric renin-mediated hypertension secondary to renal artery occlusive disease and abdominal aortic coarctation.

Dawn M Coleman, Jonathan L Eliason, Robert Beaulieu, Tatum Jackson, Monita Karmakar, David B Kershaw, Zubin J Modi, Santhi K Ganesh, Minhaj S Khaja, David Williams and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of vascular surgery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
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  3. Endovascular salvage of renal artery bypass in pediatric a patient with neurofibromatosis type 1.Journal of vascular surgery cases and innovative techniques · 2025
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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

12 authors at 2 institutions in 1 country.

Dawn M ColemanSection of Vascular Surgery, Department of Surgery, University of Michigan, Ann Arbor, Mich. Electronic address: dawnbarn@med.umich.edu.
Jonathan L EliasonSection of Vascular Surgery, Department of Surgery, University of Michigan, Ann Arbor, Mich.
Robert BeaulieuSection of Vascular Surgery, Department of Surgery, University of Michigan, Ann Arbor, Mich.
Tatum JacksonSection of Vascular Surgery, Department of Surgery, University of Michigan, Ann Arbor, Mich.
Monita KarmakarDepartment of Surgery, University of Michigan, Ann Arbor, Mich.
David B KershawDivision of Pediatric Nephrology, Department of Pediatrics, University of Michigan, Ann Arbor, Mich.
Zubin J ModiDivision of Pediatric Nephrology, Department of Pediatrics, University of Michigan, Ann Arbor, Mich; Susan B. Meister Child Evaluation and Research Center, University of Michigan, Ann Arbor, Mich.
Santhi K GaneshDivision of Cardiovascular Medicine, Department of Medicine, University of Michigan, Ann Arbor, Mich; Department of Human Genetics, University of Michigan, Ann Arbor, Mich.
Minhaj S KhajaDivision of Vascular and Interventional Radiology, Department of Radiology, University of Michigan, Ann Arbor, Mich.
David WilliamsDivision of Vascular and Interventional Radiology, Department of Radiology, University of Michigan, Ann Arbor, Mich.
James C StanleySection of Vascular Surgery, Department of Surgery, University of Michigan, Ann Arbor, Mich.
University of Michigan Pediatric Renovascular Hypertension Center
University of Michigan–Ann Arbor · USMichigan Medicine · US

Funding

Genetic and Genomic Analysis of Arterial DysplasiaR01HL139672 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GANESH, SANTHI K · 2018 to 2021
$2.9M
NHLBI NIH HHS R01 HL139672
6 · The paper itself

Abstract

backgroundRenovascular hypertension (RVH) associated with renal artery and abdominal aortic narrowings is the third most common cause of pediatric hypertension. Untreated children may experience major cardiopulmonary complications, stroke, renal failure, and death. The impetus of this study was to describe the increasingly complex surgical practice for such patients with an emphasis on anatomic phenotype and contemporary outcomes after surgical management as a means of identifying those factors responsible for persistent or recurrent hypertension necessitating reoperation.

methodsA retrospective analysis was performed of consecutive pediatric patients with RVH undergoing open surgical procedures at the University of Michigan from 1991 to 2017. Anatomic phenotype and patient risk factors were analyzed to predict outcomes of blood pressure control and the need for secondary operations using ordered and binomial logistic multinomial regression models, respectively.

resultsThere were 169 children (76 girls, 93 boys) who underwent primary index operations at a median age of 8.3 years; 31 children (18%) had neurofibromatosis type 1, 76 (45%) had abdominal aortic coarctations, and 28 (17%) had a single functioning kidney. Before treatment at the University of Michigan, 51 children experienced failed previous open operations (15) or endovascular interventions (36) for RVH at other institutions. Primary surgical interventions (342) included main renal artery (136) and segmental renal artery (10) aortic reimplantation, renal artery bypass (55), segmental renal artery embolization (10), renal artery patch angioplasty (8), resection with reanastomosis (4), and partial or total nephrectomy (25). Non-renal artery procedures included patch aortoplasty (32), aortoaortic bypass (32), and splanchnic arterial revascularization (30). Nine patients required reoperation in the early postoperative period. During a mean follow-up of 49 months, secondary interventions were required in 35 children (21%), including both open surgical (37) and endovascular (14) interventions. Remedial intervention to preserve primary renal artery patency or a nephrectomy if such was impossible was required in 22 children (13%). The remaining secondary procedures were performed to treat previously untreated disease that became clinically evident during follow-up. Age at operation and abdominal aortic coarctation were independent predictors for reoperation. The overall experience revealed hypertension to be cured in 74 children (44%), improved in 78 (46%), and unchanged in 17 (10%). Children undergoing remedial operations were less likely (33%) to be cured of hypertension. There was no perioperative death or renal insufficiency requiring dialysis after either primary or secondary interventions.

conclusionsContemporary surgical treatment of pediatric RVH provides a sustainable overall benefit to 90% of children. Interventions in the very young (<3 years) and concurrent abdominal aortic coarctation increase the likelihood of reoperation. Patients undergoing remedial surgery after earlier operative failures are less likely to be cured of hypertension. Judicious postoperative surveillance is imperative in children surgically treated for RVH.

Indexed as

Blood PressureVascular Surgical ProceduresAdolescentAge FactorsAntihypertensive AgentsAorta, AbdominalAortic CoarctationChildChild, PreschoolFemaleHumansHypertension, RenovascularMaleRenal Artery ObstructionRetrospective StudiesTreatment OutcomeAntihypertensive AgentsAortic coarctationpediatricRenal artery stenosisRenovascular hypertension

Identifiers

PMID32276020
PMCPMC7541589
OpenAlexW3016115028

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.