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slow recruitment of patients
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Background:
One third of all ICH patients require intubation and mechanical ventilation and 1/3 of all ventilated patients require tracheostomy (i.e.≈10% of all ICH patients require tracheostomy). As shown previously, predisposing factors for tracheostomy are hematoma volume, hemorrhage location, presence of intraventricular hemorrhage (IVH), and occlusive hydrocephalus as well as presence of COPD (Huttner HB et al 2006 CVD).
Sustained restricted vigilance and impaired consciousness after ICH is likely to result in failure of extubation, raise in incidence of ventilator-associated pneumonia, increased amount of sedative drugs and prolonged duration of neurocritical care.
Hence an early tracheostomy may be beneficial in terms of reduced duration of mechanical ventilation.
Basic hypothesis:
Compared to patients with conventional ("late") tracheostomy between day 12 - 14, patients with "early" tracheostomy within 72h after admission will have:
Randomization:
Consecutive eligible patients are randomly assigned to Either "early" tracheostomy within 72h after hospital admission Or "late" tracheostomy (= control group; undergoing conventional tracheostomy between day 12 - 14 if extubation fails) Both groups receive plastic tracheostomy
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| early tracheostomy | Experimental | see study description |
|
| late tracheostomy | Active Comparator | Compared to the "early tracheostomy"-group, those patients who have been randomized to "late tracheostomy" will undergo conventional tracheostomy between day 12 - 14 if extubation fails |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Early tracheostomy | Procedure | Patients with supratentorial ICH who require mechanical ventilation, fulfill the inclusion criteria, and have been randomized to the "treatment arm" will receive an early tracheostomy within 72h after symptom onset. |
| Measure | Description | Time Frame |
|---|---|---|
| Cumulative time requiring mechanical ventilation and Overall duration of neurocritical care | Primary End-points:
| 30 days |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of respirator-associated pneumonia | 30 days | |
| Cumulative consumption of sedative drugs | 30 days | |
| Incidence of episodes with increased intracranial pressure |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Hagen B Huttner, MD | Department of Neurology, University of Erlangen-Nuremberg, Germany | Principal Investigator |
| Martin Köhrmann, MD | Department of Neurology, University of Erlangen, Germany | Study Director |
| Dimitre Staykov, MD | Department of Neurology, University of Erlangen, Germany | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University or Erlangen-Nuremberg | Erlangen | 91054 | Germany |
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| ID | Term |
|---|---|
| D002543 | Cerebral Hemorrhage |
| ID | Term |
|---|---|
| D020300 | Intracranial Hemorrhages |
| D002561 | Cerebrovascular Disorders |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
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| Late tracheostomy | Procedure | Compared to the "early tracheostomy"-group, those patients who have been randomized to "late tracheostomy" will undergo conventional tracheostomy between day 12 - 14 if extubation fails |
|
| 30 days |
| In-hospital mortality | 30 days |
| 3-months functional outcome (mRS) | functional outcome after 3 months using the modified Rankin Scale | 90 days |
| D009422 | Nervous System Diseases |
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| D006470 | Hemorrhage |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |