Evidence map›Paper›PMID 23381911›Full record

ReviewAmerican journal of cardiovascular drugs : drugs, devices, and other interventions2013

Drug treatment of acute ischemic stroke.

Sameer Bansal, Kiranpal S Sangha, Pooja Khatri

Open access · greenAbstract readReview
In one paragraph

Review in American journal of cardiovascular drugs : drugs, devices, and other interventions, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 3 pooled it
2.6field-weighted citation impact, top 10% 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

49 citing papers in PubMed, 3 syntheses or guidelines pooled it, 141 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Review
  6. Article
  7. Review
  8. HCNS neuroscience & therapeutics · 2025
    Article
  9. Review
  10. Review
  11. Investigating the Pharmacological Mechanisms of Total Flavonoids fromInternational journal of molecular sciences · 2024
    Article
  12. Stem cell therapy as a promising approach for ischemic stroke treatment.Current research in pharmacology and drug discovery · 2024
    Review
  13. Neuroprotective effect ofFrontiers in pharmacology · 2024
    Article
  14. Article
  15. Article
  16. Studying molecular signaling in major angiogenic diseases.Molecular and cellular biochemistry · 2022
    Review
  17. Article
  18. Integrative physiological assessment of cerebral hemodynamics and metabolism in acute ischemic stroke.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2022
    Review
  19. Article
  20. Article
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

3 authors at 2 institutions in 1 country.

Sameer BansalDepartment of Neurology, University of Cincinnati, College of Medicine, Cincinnati, OH 45267, USA.
Kiranpal S Sangha
Pooja Khatri
University of Cincinnati Medical Center · USUniversity of Colorado Health · US

Funding

The Significance of Intracranial Hemorrhage after Revascularization TherapyK23NS059843 · NINDS · UNIVERSITY OF CINCINNATI · PI KHATRI, POOJA · 2007 to 2011
$778k
NINDS NIH HHS K23 NS 059843NINDS NIH HHS K23 NS059843
6 · The paper itself

Abstract

Acute ischemic stroke (AIS) is the fourth leading cause of death and the leading cause of adult disability in the USA. AIS most commonly occurs when a blood vessel is obstructed leading to irreversible brain injury and subsequent focal neurologic deficits. Drug treatment of AIS involves intravenous thrombolysis with alteplase (recombinant tissue plasminogen activator [rtPA]). Intravenous alteplase promotes thrombolysis by hydrolyzing plasminogen to form the proteolytic enzyme plasmin. Plasmin targets the blood clot with limited systemic thrombolytic effects. Alteplase must be administered within a short time window to appropriate patients to optimize its therapeutic efficacy. Recent trials have shown this time window may be extended from 3 to 4.5 hours in select patients. Other acute supportive interventions for AIS include maintaining normoglycemia, euthermia and treating severe hypertension. Urgent anticoagulation for AIS has generally not shown benefits that exceed the hemorrhage risks in the acute setting. Urgent antiplatelet use for AIS has limited benefits and should only promptly be initiated if alteplase was not administered, or after 24 hours if alteplase was administered. The majority of AIS patients do not receive thrombolytic therapy due to late arrival to emergency departments and currently there is a paucity of acute interventions for them. Ongoing clinical trials may lead to further medical breakthroughs to limit the damage inflicted by this devastating disease.

Indexed as

AnimalsAntihypertensive AgentsBrain IschemiaClinical Trials as TopicFibrinolytic AgentsHumansStrokeThrombolytic TherapyTissue Plasminogen ActivatorTreatment OutcomeAntihypertensive AgentsFibrinolytic AgentsTissue Plasminogen Activator

Identifiers

PMID23381911
PMCPMC3840541
OpenAlexW2069170558

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

None linked

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.