Evidence map›Paper›PMID 21868742›Full record

ArticleStroke2011

Safety and tolerability of deferoxamine mesylate in patients with acute intracerebral hemorrhage.

Magdy Selim, Sharon Yeatts, Joshua N Goldstein, Joao Gomes, Steven Greenberg, Lewis B Morgenstern, Gottfried Schlaug, Michel Torbey, Bonnie Waldman, Guohua Xi and 2 more

3 registry-linked trialsOpen access · greenAbstract readClinical Trial, Phase IComparative StudyMulticenter Study
In one paragraph

Article in Stroke, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 84 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed, 3 pooled it
8.4field-weighted citation impact, top 2% 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.

NCT01662895 phase2terminatednot on this mapstarted 2013, after this paper: background citation

Futility Study of Deferoxamine in Intracerebral Hemorrhage

TypeinterventionalSponsorBeth Israel Deaconess Medical CenterRan2013 to 2018Enrolled42ConditionsIntracerebral HemorrhageArmsDeferoxamine, Normal saline
NCT02175225 phase2completednot on this mapstarted 2014, after this paper: background citation

Study of Deferoxamine Mesylate in Intracerebral Hemorrhage

TypeinterventionalSponsorBeth Israel Deaconess Medical CenterRan2014 to 2018Enrolled294ConditionsIntracerebral HemorrhageArmsDeferoxamine Mesylate, Placebo (for Deferoxamine Mesylate)
NCT02367248 phase1 / phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

Safety and Effectiveness Study of Deferoxamine and Xingnaojing Injection in Intracerebral Hemorrhage

TypeinterventionalSponsorCapital Medical UniversityRan2015 to 2016Enrolled180ConditionsIntracerebral HemorrhageArmsdeferoxamine, Xingnaojing injection, Normal saline
3 · Its place in the literature

Who cites it

84 citing papers in PubMed, 3 syntheses or guidelines pooled it, 143 citations in OpenAlex.

  1. Efficacy of desferrioxamine mesylate in intracerebral hematoma: a systemic review and meta-analysis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    Pooled it
  2. Iron chelators for acute stroke.The Cochrane database of systematic reviews · 2020
    Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Trial
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
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  14. Pathophysiology, Management, and Therapeutics in Subarachnoid Hemorrhage and Delayed Cerebral Ischemia: An Overview.Pathophysiology : the official journal of the International Society for Pathophysiology · 2023
    Review
  15. Article
  16. Review
  17. Article
  18. Role of Ferroptosis in Stroke.Cellular and molecular neurobiology · 2023
    Review
  19. Review
  20. Article

24 more citing papers are in PubMed but not listed here.

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 4 institutions in 1 country.

Magdy SelimDepartment of Neurology, Stroke Division, Beth Israel Deaconess Medical Center, Stroke Division, 330 Brookline Avenue-Palmer 127, Boston, MA 02215, USA. mselim@bidmc.harvard.edu
Sharon Yeatts
Joshua N Goldstein
Joao Gomes
Steven Greenberg
Lewis B Morgenstern
Gottfried Schlaug
Michel Torbey
Bonnie Waldman
Guohua Xi
Yuko Palesch
Deferoxamine Mesylate in Intracerebral Hemorrhage Investigators
Cleveland Clinic · USUniversity of Michigan–Ann Arbor · USMassachusetts General Hospital · USMedical University of South Carolina · US

Funding

Deferoxamine therapy for intracerebral hemorrhageU01NS052510 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI XI, GUOHUA · 2007 to 2010
$1.8M
Safety and Tolerability of Deferoxamine in Acute Cerebral HemorrhageR01NS057127 · NINDS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SELIM, MAGDY H · 2008 to 2010
$1.0M
NINDS NIH HHS 1R01-NS 057127NINDS NIH HHS R01 NS057127NINDS NIH HHS U01 NS052510
6 · The paper itself

Abstract

background and purposeTreatment with the iron chelator, deferoxamine mesylate (DFO), improves neurological recovery in animal models of intracerebral hemorrhage (ICH). We aimed to evaluate the feasibility, safety, and tolerability of varying dose-tiers of DFO in patients with spontaneous ICH, and to determine the maximum tolerated dose to be adopted in future efficacy studies.

methodsThis was a multicenter, phase-I, dose-finding study using the Continual Reassessment Method. DFO was administered by intravenous infusion for 3 consecutive days, starting within 18 hours of ICH onset. Subjects underwent repeated clinical assessments through 90 days, and computed tomography neuroimaging pre- and post-drug-administration.

resultsTwenty subjects were enrolled onto 5 dose tiers, starting with 7 mg/kg per day and ending with 62 mg/kg per day as the maximum tolerated dose. Median age was 68 years (range, 50-90); 60% were men; and median Glasgow Coma Scale and National Institutes of Health Stroke Scale scores on admission were 15 (5-15) and 9 (0-39), respectively. ICH location was lobar in 40%, deep in 50%, and brain stem in 10%; intraventricular hemorrhage was present in 15%. DFO was discontinued because of adverse events in 2 subjects (10%). Six subjects (30%) experienced 12 serious adverse events, none of which were drug-related. DFO infusions were associated with mild blood-pressure-lowering effects. Fifty percent of patients had modified Rankin scale scores ≤2, and 39% had modified Rankin scale scores of 4 to 6 on day 90; 15% died.

conclusionsConsecutive daily infusions of DFO after ICH are feasible, well-tolerated, and not associated with excessive serious adverse events or mortality. Our findings lay the groundwork for future studies to evaluate the efficacy of DFO in ICH.

Indexed as

Acute DiseaseAgedAged, 80 and overCerebral HemorrhageCohort StudiesDeferoxamineFemaleFollow-Up StudiesHumansHypotensionInfusions, IntravenousMaleMiddle AgedDeferoxamine

Identifiers

PMID21868742
PMCPMC3202043
OpenAlexW2094992383

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.