Pre- and inter-transport
stabilization protocol for
patients with
hemorrhagic stroke
Arun Ranganath MD
David Seder MD, FCCP
Maine Medical Center
Department of Critical Care Services
ICH/IVH Aneurysmal SAH
Why do we need a
stabilization protocol?
• Multiple episodes of patients declining or dying
between initial ED presentation and arrival at
MMC
– Rebleeding (SAH) due to rerupture of aneurysm
– Hematoma expansion due to inadequate BP control
or coagulopathy
– Uncal or transtentorial herniation due to inadequate
treatment of mass effect and lack of attention to ICP
Goals of the protocol
• Provide simple but highly effective tools for
managing the most common preventable
causes of clinical decline in the CRITICAL
FIRST HOURS OF MANAGEMENT
• Facilitate and decrease delays in transfer
• Improve the statewide outcomes of patients
with hemorrhagic stroke
Where do the recommendations
come from?
Stabilization Protocol - Summary
• Transfer of appropriate patients within 1 hour of
presentation
• Protocolized BP management
• Protocolized reversal of warfarin
• Pre-transport Mannitol in selected patients
exhibiting a mechanism of injury, imaging, and exam
consistent with elevated ICP
• Appropriate oxygenation and ventilation
• Aminocaproic acid load for nontraumatic  SAH
• Fosphenytoin load for nontraumatic  SAH
1. Ultra-early transfer
• Rebleeding (SAH) and hematoma expansion
(ICH) are most likely in the very early hours after
a brain hemorrhage.
• Urgent surgical decompression, ventriculostomy
placement, and aneurysm repair save lives and
preserve neurological function.
• Dedicated care in a Neurological Intensive Care
Unit is associated with better patient outcomes.
1. How to connect for transfer
• Call MMC REMIS at 207-662-6632
• SAH: Ask for Neurosurgery attending
• ICH/IVH: Ask for Critical Care Medicine
attending
• If there is no ICU bed and the patient is in
trouble – we will bring to the MMC ED
2. Protocolized BP management
• ICH/IVH…or SAH!!
– Target SBP<140 mmHg within 20 minutes of
identifying bleed
– Nicardipine IV 5-15mg/hr – titrate q15m
– Labetalol IV 10-20mg IV push
– BP documentation q10 minutes
– Hydralazine is 3rd
line agent
• Do not allow hypotension
3. Protocolized warfarin reversal
• Reverse INR if > 1.5
• Vitamin K 10mg IV push
• PCC (Profilnine or Kcentra) push –
depending on INR…see next slide
• Do not wait for FFP to transfer!
Why PCC and not FFP?
• FFP is ineffective at rapidly reversing the INR
– Type and cross, Defrost, Rate of infusion
= HOURS OF DELAY
– Rare that adequate amount of FFP is infused
– 35% reversed at 24h prior to new MMC protocol
• PCC highly effective at reversing INR with
few AEs
– Inject and go…
• MMC PCC
experience:
– Initiated protocol
in 2009
– 18 months WA-
ICH after
implementation
compared to 36
months prior
– In-hospital
mortality declined
(45.1% vs 18.2%,
P=0.013)
Clin Neurol Neurosurg 2013;115(6):770-4
Crit Care Med 2011;39:S518
4. Pre-transport mannitol in
appropriate patients
• Large ICH with mass effect
• IVH with hydrocephalus
• SAH with hydrocephalus
• SAH with cerebral edema
• Any SAH with GCS<6
• Patients with a clinical exam suggesting
herniation
4. Pre-transport mannitol in
patients with elevated ICP
• 1gm/kg administered as fast as possible
• Keep the head of the bed at 30-45 degrees
during transport
• DO NOT HYPOVENTILATE
• DO NOT ALLOW MAP<80 mmHg
Mass effect – give mannitol Hydrocephalus – give mannitol if
GCS<8 or rapid decline
5. Appropriate oxygenation and
ventilation
• Keep the SpO2 > 94% but keep FiO2≤0.6
– Low (<60mmHg) and high (>300mmHg)
prehospital/ED PaO2 associated with WORSE
OUTCOMES
• Keep the ETCO2 between 30-40
– Hypoventilation causes increased ICP
– Hyperventilation causes decreased CBF
– Both are associated with WORSE OUTCOMES
6. Aminocaproic Acid for SAH
• Antifibrinolytic agent
– Decreases bleeding, increases clotting
• Decreases rebleeding: 11.4% to 2.7%
• Criteria
– Age < 65
– No prior history of MI, stroke, DVT, or PE
• 4g IV load then infuse at 1gm/hr
Stroke. 2008;39:2617
Cumulative rebleeding-free survival
according to antifibrinolytic group
• Significant decrease in
rebleeding in EACA-treated
patients (2.7%) versus non-
EACA patients (11.4%).
• There was no difference in
ischemic complications
between cohorts.
• 8-fold increase in deep
venous thrombosis in the
EACA group but no increase
in pulmonary embolism.
• Nonsignificant 76%
reduction in mortality
attributable to rebleeding
• 13.3% increase in favorable
outcome in good-grade
EACA-treated patients and
6.8% increase in poor-grade
patients.
7. Prophylactic fosphenytoin
load for SAH
• A seizure would cause a surge in BP and re-
rupture of the aneurysm
– 15mg/kg IV fosphenytoin over 15 minutes or
levitiracetam 1000mg IV push
• Not recommended for ICH/IVH prophylaxis
• Appropriate in ICH/IVH if seizures occur
A few reminders…
• Transport should not be delayed for these
stabilization measures
• Sometimes patients will need transport prior
to completion of the stabilization bundle
• The Dx is not always obvious, and not every
patient will fit neatly into the stabilization
protocols – they should serve as a guideline
What quality measures will we
track?
• Adherence to protocol
– Delays to transfer, and why they occurred
– Warfarin reversal
– Maintenance of BP goals in ED/Transport
vehicle/MMC /ICU prior to securing the aneurysm
– Appropriate use of osmotherapy
– Aminocaproic acid and fosphenytoin use
• Adverse events
• Outcomes
Closing the loop, sharing
ownership
• Good outcomes in hemorrhagic stroke
require an outstanding system of care – we are
all part of it
• We will report back quality metrics on transfer
cases to the referring and primary care
physicians
• We will report back the MMC experience,
AEs, and outcome at hospital discharge
Discussion

Hemorrhagic stroke transfer protocol

  • 1.
    Pre- and inter-transport stabilizationprotocol for patients with hemorrhagic stroke Arun Ranganath MD David Seder MD, FCCP Maine Medical Center Department of Critical Care Services
  • 2.
  • 3.
    Why do weneed a stabilization protocol? • Multiple episodes of patients declining or dying between initial ED presentation and arrival at MMC – Rebleeding (SAH) due to rerupture of aneurysm – Hematoma expansion due to inadequate BP control or coagulopathy – Uncal or transtentorial herniation due to inadequate treatment of mass effect and lack of attention to ICP
  • 4.
    Goals of theprotocol • Provide simple but highly effective tools for managing the most common preventable causes of clinical decline in the CRITICAL FIRST HOURS OF MANAGEMENT • Facilitate and decrease delays in transfer • Improve the statewide outcomes of patients with hemorrhagic stroke
  • 5.
    Where do therecommendations come from?
  • 6.
    Stabilization Protocol -Summary • Transfer of appropriate patients within 1 hour of presentation • Protocolized BP management • Protocolized reversal of warfarin • Pre-transport Mannitol in selected patients exhibiting a mechanism of injury, imaging, and exam consistent with elevated ICP • Appropriate oxygenation and ventilation • Aminocaproic acid load for nontraumatic  SAH • Fosphenytoin load for nontraumatic  SAH
  • 7.
    1. Ultra-early transfer •Rebleeding (SAH) and hematoma expansion (ICH) are most likely in the very early hours after a brain hemorrhage. • Urgent surgical decompression, ventriculostomy placement, and aneurysm repair save lives and preserve neurological function. • Dedicated care in a Neurological Intensive Care Unit is associated with better patient outcomes.
  • 8.
    1. How toconnect for transfer • Call MMC REMIS at 207-662-6632 • SAH: Ask for Neurosurgery attending • ICH/IVH: Ask for Critical Care Medicine attending • If there is no ICU bed and the patient is in trouble – we will bring to the MMC ED
  • 9.
    2. Protocolized BPmanagement • ICH/IVH…or SAH!! – Target SBP<140 mmHg within 20 minutes of identifying bleed – Nicardipine IV 5-15mg/hr – titrate q15m – Labetalol IV 10-20mg IV push – BP documentation q10 minutes – Hydralazine is 3rd line agent • Do not allow hypotension
  • 10.
    3. Protocolized warfarinreversal • Reverse INR if > 1.5 • Vitamin K 10mg IV push • PCC (Profilnine or Kcentra) push – depending on INR…see next slide • Do not wait for FFP to transfer!
  • 12.
    Why PCC andnot FFP? • FFP is ineffective at rapidly reversing the INR – Type and cross, Defrost, Rate of infusion = HOURS OF DELAY – Rare that adequate amount of FFP is infused – 35% reversed at 24h prior to new MMC protocol • PCC highly effective at reversing INR with few AEs – Inject and go…
  • 13.
    • MMC PCC experience: –Initiated protocol in 2009 – 18 months WA- ICH after implementation compared to 36 months prior – In-hospital mortality declined (45.1% vs 18.2%, P=0.013) Clin Neurol Neurosurg 2013;115(6):770-4 Crit Care Med 2011;39:S518
  • 14.
    4. Pre-transport mannitolin appropriate patients • Large ICH with mass effect • IVH with hydrocephalus • SAH with hydrocephalus • SAH with cerebral edema • Any SAH with GCS<6 • Patients with a clinical exam suggesting herniation
  • 15.
    4. Pre-transport mannitolin patients with elevated ICP • 1gm/kg administered as fast as possible • Keep the head of the bed at 30-45 degrees during transport • DO NOT HYPOVENTILATE • DO NOT ALLOW MAP<80 mmHg
  • 16.
    Mass effect –give mannitol Hydrocephalus – give mannitol if GCS<8 or rapid decline
  • 17.
    5. Appropriate oxygenationand ventilation • Keep the SpO2 > 94% but keep FiO2≤0.6 – Low (<60mmHg) and high (>300mmHg) prehospital/ED PaO2 associated with WORSE OUTCOMES • Keep the ETCO2 between 30-40 – Hypoventilation causes increased ICP – Hyperventilation causes decreased CBF – Both are associated with WORSE OUTCOMES
  • 18.
    6. Aminocaproic Acidfor SAH • Antifibrinolytic agent – Decreases bleeding, increases clotting • Decreases rebleeding: 11.4% to 2.7% • Criteria – Age < 65 – No prior history of MI, stroke, DVT, or PE • 4g IV load then infuse at 1gm/hr
  • 19.
    Stroke. 2008;39:2617 Cumulative rebleeding-freesurvival according to antifibrinolytic group • Significant decrease in rebleeding in EACA-treated patients (2.7%) versus non- EACA patients (11.4%). • There was no difference in ischemic complications between cohorts. • 8-fold increase in deep venous thrombosis in the EACA group but no increase in pulmonary embolism. • Nonsignificant 76% reduction in mortality attributable to rebleeding • 13.3% increase in favorable outcome in good-grade EACA-treated patients and 6.8% increase in poor-grade patients.
  • 20.
    7. Prophylactic fosphenytoin loadfor SAH • A seizure would cause a surge in BP and re- rupture of the aneurysm – 15mg/kg IV fosphenytoin over 15 minutes or levitiracetam 1000mg IV push • Not recommended for ICH/IVH prophylaxis • Appropriate in ICH/IVH if seizures occur
  • 21.
    A few reminders… •Transport should not be delayed for these stabilization measures • Sometimes patients will need transport prior to completion of the stabilization bundle • The Dx is not always obvious, and not every patient will fit neatly into the stabilization protocols – they should serve as a guideline
  • 22.
    What quality measureswill we track? • Adherence to protocol – Delays to transfer, and why they occurred – Warfarin reversal – Maintenance of BP goals in ED/Transport vehicle/MMC /ICU prior to securing the aneurysm – Appropriate use of osmotherapy – Aminocaproic acid and fosphenytoin use • Adverse events • Outcomes
  • 23.
    Closing the loop,sharing ownership • Good outcomes in hemorrhagic stroke require an outstanding system of care – we are all part of it • We will report back quality metrics on transfer cases to the referring and primary care physicians • We will report back the MMC experience, AEs, and outcome at hospital discharge
  • 24.