WEANING-Study: "Weaning by Early Versus lAte Tracheostomy iN supratentorIal iNtracerebral Bleedings
- Conditions
- Intracerebral Hemorrhage
- Interventions
- Procedure: Early tracheostomyProcedure: Late tracheostomy
- Registration Number
- NCT01176214
- Lead Sponsor
- University of Erlangen-Nürnberg Medical School
- Brief Summary
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:
* shorter cumulative time of mechanical ventilation
* less incidence of ventilator-associated pneumonia
* less consumption of sedative drugs
* shorter duration of stay in neurocritical care unit
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
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 7
- Patients requiring intubation / mechanical ventilation
- Supratentorial intracerebral hemorrhage (including:)
- primary spontaneous ICH (lobar / deep)
- ICH related to anticoagulant therapy
- with or without intraventricular hemorrhage
- with or without occlusive and / or communicating hydrocephalus
- Hematoma volume >0 ml and <60 ml
- Age 18 - 85 years
- Informed consent (legal representative)
- Patients with elective intubation/ventilation for EVD placement
- Patients with "do not treat" / "do not resuscitate" orders, severe co- morbidity and life expectancy of less than 3 months
- Absent consent of relatives for invasive (neuro-)critical care
- Contraindication for tracheostomy
- Other than primary supratentorial ICH or supratentorial ICH related to oral anticoagulants
- Pre-existing COPD (known/treated)
- Pre-existing congestive heart failure (≥3 NYHA)
- Pre-existing modified Rankin Scale (≥4)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description early tracheostomy Early tracheostomy see study description late tracheostomy Late tracheostomy 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
- Primary Outcome Measures
Name Time Method Cumulative time requiring mechanical ventilation and Overall duration of neurocritical care 30 days Primary End-points:
* Cumulative time requiring mechanical ventilation
* Overall duration of neurocritical care
- Secondary Outcome Measures
Name Time Method Cumulative consumption of sedative drugs 30 days 3-months functional outcome (mRS) 90 days functional outcome after 3 months using the modified Rankin Scale
Incidence of respirator-associated pneumonia 30 days In-hospital mortality 30 days Incidence of episodes with increased intracranial pressure 30 days
Trial Locations
- Locations (1)
University or Erlangen-Nuremberg
🇩🇪Erlangen, Germany