Evidence map›Paper›PMID 41166017›Full record

SynthesisInternational urology and nephrology2026

Page kidney secondary to subcapsular hematoma in renal transplant recipients: a systematic review of reported cases.

Sundus Dadan, Wajahat Mirza, Mohammad Ayaz Khan

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in International urology and nephrology, 2026. 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
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Sundus DadanShifa International Hospital, Islamabad, Pakistan.
Wajahat MirzaShifa College of Medicine, Shifa Tameer-e-Millat University, Islamabad, Pakistan. wajahatmirza.clinicalresearch@gmail.com.ORCID http://orcid.org/0009-0001-9811-7754
Mohammad Ayaz KhanDepartment of Urology, Shifa International Hospital, Islamabad, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPage kidney secondary to subcapsular hematoma (SH) is a rare but serious complication in renal transplant recipients, typically occurring in the early postoperative period. This is caused by external graft compression, which impairs perfusion and leads to acute renal dysfunction. Prompt diagnosis and surgical intervention are essential for salvaging graft functions.

objectiveThis systematic review synthesizes available case-level evidence on Page kidney in transplant recipients, focusing on the timing of onset, clinical presentation, imaging characteristics, management strategies, and outcomes of Page kidney.

methodsA systematic search of the PubMed, Scopus, Embase, Web of Science, and Google Scholar databases was conducted until May 2024. Eligible studies included case reports and case series describing Page kidneys due to SH in renal transplant recipients. Data extraction included clinical features, imaging findings, interventions, and outcomes. The risk of bias was assessed using the Joanna Briggs Institute (JBI) Critical Appraisal Checklist. This review was registered with PROSPERO (CRD42024547165; University of York, UK).

resultsTen studies involving 15 patients were included in the analysis. Most patients (13/15) developed Page kidney within the first week after transplantation, while two cases presented > 6 months after transplantation. Common features included oliguria or anuria (86.7%), elevated resistive indices (RI ≥ 0.9), and crescentic subcapsular hematomas on Doppler ultrasound. Surgical evacuation was performed in 93.3% of the cases, with favorable renal recovery in 11 patients (73.3%). Late or missed diagnoses are correlated with irreversible graft losses. The risk of bias was low in all included studies.

conclusionPage kidney in transplant recipients, although rare, requires a high index of suspicion, particularly in the early postoperative period. Doppler ultrasonography remains central to diagnosis, while surgical decompression offers the best chance of graft salvage. Early recognition is critical given the narrow therapeutic window and high stakes of delayed intervention.

Indexed as

HematomaKidney DiseasesKidney TransplantationPostoperative ComplicationsHumansDoppler ultrasoundPage kidneyRenal transplantSubcapsular hematomaSurgical decompression

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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.