Evidence map›Paper›PMID 26900076›Full record

ArticleJournal of neuro-oncology2016

Posterior reversible encephalopathy syndrome in cancer patients: a single institution retrospective study.

Carlos Kamiya-Matsuoka, Asif M Paker, Linda Chi, Ayda Youssef, Sudhakar Tummala, Monica E Loghin

Abstract read
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In one paragraph

Article in Journal of neuro-oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 45 citations in OpenAlex.

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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 3 institutions in 2 countries.

Carlos Kamiya-MatsuokaDepartment of Neuro-Oncology, The University of Texas MD Anderson Cancer, 1400 Holcombe Blvd, Room FC7.3000, Unit 431, Houston, TX, 77030, USA. ckamiya@mdanderson.org.
Asif M PakerDepartment of Neuro-Oncology, The University of Texas MD Anderson Cancer, 1400 Holcombe Blvd, Room FC7.3000, Unit 431, Houston, TX, 77030, USA.
Linda ChiDepartment of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Unit 1459, Houston, TX, 77030, USA.
Ayda YoussefDepartment of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Unit 1459, Houston, TX, 77030, USA.
Sudhakar TummalaDepartment of Neuro-Oncology, The University of Texas MD Anderson Cancer, 1400 Holcombe Blvd, Room FC7.3000, Unit 431, Houston, TX, 77030, USA.
Monica E LoghinDepartment of Neuro-Oncology, The University of Texas MD Anderson Cancer, 1400 Holcombe Blvd, Room FC7.3000, Unit 431, Houston, TX, 77030, USA.
The University of Texas MD Anderson Cancer Center · USThe University of Texas Medical Branch at Galveston · USChildren Cancer Hospital · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Posterior reversible encephalopathy syndrome (PRES) is a clinico-radiologic entity. Its management and outcome in the oncology population is limited because it is still difficult to identify despite an increasingly recognized occurrence. This is the largest retrospective study of PRES in cancer patients reported from a single institution. We explore the clinical manifestations and radiologic features to comprehensively assess PRES in order to prevent permanent neurologic deficits and mortality. We retrospectively identified 69 patients with cancer who developed PRES at MDACC between 01/2006 to 06/2012. Clinical and radiographic data were abstracted from their records and reviewed for our analysis. Mean age at PRES onset was 52 ± 17.8 years. Fifty-two (75 %; p < 0.001) patients were women. Most common diagnoses were leukemia (30 %) and lymphoma (12 %). Forty-eight (70 %) patients were treated with chemotherapy, 21 (30 %) bone marrow transplant and 14 (20 %) tacrolimus. Most common clinical presentation was seizures (67 %). PRES was associated with hypertension in 62 (90 %) patients. On brain MRI, 33 (44 %) patients had some evidence of hemorrhage, 22 (73 %) of these were thrombocytopenic. Thirty-five (51 %) patients fully recovered and 19 (28 %) had permanent neurological deficits. Morbidity and mortality were associated with continuation with offending agent, thrombocytopenia, variations in mean arterial pressure ≥20 mmHg, electrographic seizures at onset, atypical MRI pattern and delay in diagnostic imaging (7.4 ± 4.8 days vs. 1.9 ± 1.8 days; p = 0.031) as half of them did not receive a prompt intervention. Special attention should be given to patients who present with high-risk factors in order to prevent development of PRES or decrease patient morbidity and mortality. Management of PRES should be guided by the radiographic findings. Overall, early recognition, discontinuation of the offending agents, correction of thrombocytopenia and blood pressure control are still the main strategies to manage PRES.

Indexed as

AdultAgedAntineoplastic AgentsBrainFemaleHumansKaplan-Meier EstimateMagnetic Resonance ImagingMaleMiddle AgedNeoplasmsPosterior Leukoencephalopathy SyndromeRetrospective StudiesRisk FactorsSeizuresAntineoplastic AgentsBone marrow transplantCancerChemotherapyNeurotoxicityPosterior reversible encephalopathy syndromeTacrolimus

Identifiers

PMID26900076
OpenAlexW2282113267

What OpenQuestion holds

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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.