Platelet transfusion limits haematoma growth and thus improves outcome in patients with intracerebral haemorrhage using anti-platelet therapy.
ID
Bron
Verkorte titel
Aandoening
Intracerebraal hematoom
CVA
Beroerte
Trombocyten transfusie
Intracerebral haemorrhage
Stroke
Platelet transfusion
Anti-platelet therapy
Ondersteuning
Sanquin
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Poor outcome defined as a modified Rankin Scale (mRS) score 4-6 after 3 months.
Achtergrond van het onderzoek
Platelet Transfusion in Cerebral Haemorrhage (PATCH)
Background
Stroke is a major cause of acquired disability in the Netherlands. After the care for children born with a handicap, the care for stroke patients consumes the largest portion of the total health care budget.
In recent years acute treatment in ischemic stroke improved significantly. Thrombolysis within 3 hours was shown to improve clinical outcome. However, for haemorrhagic stroke or intracerebral haemorrhage (ICH), which accounts for 15% of all stroke patients, no acute treatment option currently exists.
Haematoma volume is one of the most important outcome predictors in ICH. Because several studies have shown that haematoma volume increases during the first 6 hours after onset of ICH, reduction of this haematoma growth provides a promising target to improve outcome. Patients using platelet aggregation inhibitors (PAI) are especially at risk for haematoma growth and therefore platelet transfusion (PT) is an acute treatment option which should be investigated.
Objective
The objective of our study is to investigate whether platelet transfusion within 6 hours after onset of ICH can improve functional outcome by limiting haematoma growth in patients using PAI.
Study Design
Probe: Prospective, randomised, open treatment, blind end-point evaluation
Study Population
Patients with spontaneous ICH who were using PAI at least during the 7 days preceding haemorrhage.
Intervention
Patients are randomised to receive a single gift of platelets (5 or 10 donor units) within 6 hours after start of symptoms or standard care without platelet transfusion
Outcome
The primary endpoint is poor functional outcome as recorded on the modified Rankin Scale (mRS) at three months follow-up (mRS 4-6).
Secondary endpoints are complications of PT, haematoma enlargement on CT-scan, survival at three months, changes in outcome at three months (analysis of the mRS score as an ordinal scale ), poor outcome defined as mRS 3-6, disability assessed with the ALDS scale, cause of poor outcome, costs and predictive value of the CTA 'spot sign' and different laboratory measurements.
Sample Size
Poor outcome occurs in at least 70% of these patients. To detect a reduction of poor outcome from 70% to 50% with a two group Chi-square test with a 0.05 two-sided significance level and 80% power, 95 patients are needed in each group (190 patients in total).
Thirty centers are willing to participate in our study. If each center can randomize 3 to 4 patients each year, patient inclusion will be completed in 21 months. The last patient will then be assessed 2 years after the onset of the study.
Doel van het onderzoek
Platelet transfusion limits haematoma growth and thus improves outcome in patients with intracerebral haemorrhage using anti-platelet therapy.
Onderzoeksopzet
Primary outcome will be determined after 3 months.
Onderzoeksproduct en/of interventie
- 95 patients receive platelet transfusion as soon as possible within 6 hours after onset
- 95 patients receive standard care
Platelet transfusion consists of a single gift of 5 or 10 donor units depending on type of anti-platelet medication (only patients using clopidogrel receive 10 units).
Publiek
Academic Medical Center
University of Amsterdam
Irem Baharoglu
PO BOX 22660
Amsterdam 1100 DD
The Netherlands
m.i.baharoglu@amc.uva.nl
Wetenschappelijk
Academic Medical Center
University of Amsterdam
Irem Baharoglu
PO BOX 22660
Amsterdam 1100 DD
The Netherlands
m.i.baharoglu@amc.uva.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Age > 18 years
2. Non-traumatic, primary, supratentorial ICH
3. Haematoma volume > 150 cc
4. GCS score 8-15
5. Anti-platelet therapy for at least the previous 7 days
6. Transfusion can be started < 6 hrs after onset
7. Transfusion can be started < 1,5 hrs after CT
8. mRankin scale score before ICH 0 or 1
9. Informed consent obtained
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Bleeding pattern on CT suggestive of AVM or aneurysm
2. Haematoma evacuation planned < 24 hrs
3. Intraventricular haemorrhage (sedimentation in posterior horns is allowed)
4. Previous adverse reaction to platelet transfusion
5. Known use of vitamine K antagonists
6. Known thrombocytopenia < 100 x 109/l
7. History of coagulopathy
8. Previously legally incompetent adults prior to stroke
9. Death appears imminent
Opzet
Deelname
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Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL1257 |
NTR-old | NTR1303 |
CCMO | NL16450.018.08 |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |
OMON | NL-OMON31663 |