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Analgesia-first Minimal Sedation for Spontaneous Intracerebral Hemorrhage Early Antihypertensive Treatment

Clinical Study of the Safety and Efficacy of Analgesia-first Minimal Sedation as an Early Antihypertensive Treatment for Spontaneous Intracerebral Hemorrhage

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03207100
Acronym
ASSICHH
Enrollment
338
Registered
2017-07-02
Start date
2017-12-06
Completion date
2021-05-15
Last updated
2023-12-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blood Pressure Variability, Duration of ICU Treatment and Mechanical Ventilation, Early Systolic Blood Pressure Control Rate, Healthcare Worker Satisfaction, Hematoma Growth

Keywords

Intracerebral hemorrhage, Early antihypertensive treatment, Analgesia-first, Sedation

Brief summary

This study evaluates safety and efficacy of analgesia-first minimal sedation as an early antihypertensive treatment for spontaneous intracerebral hemorrhage. The analgesia-first minimal sedation strategy relies on the remifentanil-mediated alleviation of pain-induced stress response and the antisympathetic activity of dexmedetomidine to restore the elevated blood pressure to normal level in patients with spontaneous intracerebral hemorrhage. This strategy allows rapid stabilization of blood pressure, and its use as a pre-treatment for patients on mechanical ventilation prior to painful procedures reduces blood pressure variability and thereby results in etiologic treatment. It is more effective in blood pressure control than conventional symptomatic antihypertensive treatment, reduces the incidence of early hematoma expansion and improves prognosis, ,lowers healthcare workers workload, increases patient adherence, and improves healthcare worker satisfaction.

Detailed description

Spontaneous intracerebral hemorrhage (ICH) is hemorrhage in the brain parenchyma caused by non-traumatic spontaneous rupture of cerebral artery, arteriole, vein and capillary in adults. ICH is a common problem, with subarachnoid hemorrhage. About 90% ICH patients have increased blood pressure (BP) that usually occurs immediately after disease onset. BP elevation in the acute phase of ICH is associated with poor prognosis, and its mechanism of action includes the local increase of initial hemorrhage, early hematoma expansion at hemorrhagic sites, the increased risk of early recurrent hemorrhage, serious cerebral edema, and recurrent stroke, this affects the most within the few hours following the onset of the disease. The current American Heart Association guidelines recommended early antihypertensive treatment and suggested that rapid decrease of BP to 140 mmHg is safe in ICH patients with no obvious antihypertensive contraindications. However, the significant differences between large studies conducted in recent years have led to great controversy on the effect of early antihypertensive treatment in acute ICH and disease prognosis. A meta-analysis of early antihypertensive treatment for ICH showed that differences in early BP control rate and BP increase variability are also the major causes of inconsistency between these studies. There is currently no consensus on the best antihypertensive regimen as it is difficult to reach the optimal BP level timely. Some studies have shown that stress response, pain, ICP increase and pre-onset BP elevation are factors that cause acute BP increase in ICH patients. In particular, restlessness, sleep deprivation, and stress due to intolerable pain can lead to dramatic BP and intracranial pressure (ICP) increases, further lead to secondary intracerebral hematoma expansion and subsequently cause neurologic degeneration and cerebral tissue damage. Therefore, the primary principles of ICH acute BP increase treatment are to keep quiet, restore BP to normal level, stably reduce BP, decrease BP variability, lower the chance of recurrent hemorrhage, and thereby improve long-term prognosis. Traditional antihypertensive treatment can only resolve the issue of BP elevation but not the root cause of disease. Analgesia and sedation is a critical component of and a global consensus in the clinical management of ICH patients. Remifentanil is a fentanyl μ-type opioid receptor agonist with strong and fast-acting analgesic effects, does not induce ICP elevation and can alleviate pain induced by sputum aspiration, body turning and back clapping in severe patients. A randomized trial on patients with craniocerebral injury has indicated that a remifentanil-based sedation strategy can significantly reduce the amount of sedative used and shorten the time of mechanical ventilation without affecting the functional assessment of the nervous system. Dexmedetomidine is an α2-adrenergic agonist that inhibits sympathetic activity by activating the pre-synaptic α2-receptor in the locus coeruleus, which in turn reduces norepinephrine release, that only slightly affects consciousness and breathing and helps patients with craniocerebral injury stay conscious while under sedation, allowing real-time functional assessment of the nervous system. Therefore, the research group developed a treatment strategy in which sufficient analgesia is applied in combination with a minimal sedation program as an effective and safe early an- tihypertensive treatment.We hypothesize that applying sufficient analgesia in combination with a minimal sedation program will involve the use of remifentanil for pain relief and dexmedetomidine for antisympathetic activity to restore elevated BP to normal levels in patients with spontaneous ICH, and we further hypothesize that this strategy will be more effective than conventional symptomatic antihypertensive treatment for controlling BP.

Interventions

COMBINATION_PRODUCTAnalgesia-first minimal sedation

Remifentanil will be administered by IV infusion and maintained at a dose of 0.025 μg/kg/min in non-mechanically ventilated patients and a dose of 0.05 μg/kg/min in mechanically ventilated patients. BP will be measured after 10 min of continuous infusion.If systolic BP is still ≥ 140 mmHg, then dexmedetomidine will be applied using an infusion pump at a dose of 0.2 μg/kg/h. BP will be measured again after 15 min of continuous infusion of dexmedetomidine. If systolic BP is still ≥ 140 mmHg, the dose of dexmedetomidine can be increased 0.1 μg/kg/h to the maximum of 0.6 μg/kg/h.If the maximum dose of dexmedetomidine does not lower blood pressure, use routine blood pressure reduction programs in each center to reduce blood pressure to the target range. Mechanically ventilated patients will be given a rapid remifentanil (0.5 μg/kg) infusion to reduce procedure-related pain.

COMBINATION_PRODUCTAntihypertensive treatment

Routine antihypertensive treatment will be performed in accordance with the protocol of each respective research center. Urapidil, nicardipine, and labetalol will be used in this group. Urapidil will be used as follows: a slow IV injection of 10-15 mg and then IV pumping for maintenance at an initial rate of 2 mg/min, adjusted according to BP to a maximum of 9 mg/min. Nicardipine will be used as follows: IV pumping at 0.5μg/kg/min adjusted according to BP to a maximum of 6μg/kg/min. Labetalol will be used as follows: IV infusion for maintenance at 1-4 mg/min until the aim is reached.The mechanically ventilated patients in the control group will be administered a rapid physiological saline infusion as a controlled pretreatment.

Sponsors

Xuanwu Hospital, Beijing
CollaboratorOTHER
Qilu Hospital of Shandong University
CollaboratorOTHER
First Affiliated Hospital of Kunming Medical University
CollaboratorOTHER
First Affiliated Hospital of Xinjiang Medical University
CollaboratorOTHER
Second Affiliated Hospital of Third Military Medical University
CollaboratorOTHER
Henan Provincial People's Hospital
CollaboratorOTHER
The Second Hospital University of South China
CollaboratorOTHER
Shenzhen Second People's Hospital
CollaboratorOTHER
People's Hospital of Guangxi Zhuang Autonomous Region
CollaboratorOTHER
Department of Biostatistics, Southern Medical University
CollaboratorUNKNOWN
LanZhou University
CollaboratorOTHER
The First Affiliated Hospital of HuNan University of Medicine
CollaboratorUNKNOWN
Guangdong 999 Brain Hospital
CollaboratorOTHER
Maoming People's Hospital
CollaboratorOTHER
The Fifth Affiliated Hospital of Southern Medical University
CollaboratorOTHER
Zhongshan People's Hospital, Guangdong, China
CollaboratorOTHER
Fifth Affiliated Hospital, Sun Yat-Sen University
CollaboratorOTHER
Hong Yang
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

This study uses a single-blinded design in which only the investigators and not the subjects know the method of intervention.

Intervention model description

Subjects are grouped into the analgesia-first minimal sedation group (experimental group) or antihypertensive drug treatment group (control group) using the central randomization system upon enrollment. Antihypertensive intervention is performed on the subjects in accordance to the protocol of each group.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Definitive diagnosis of ICH-induced acute brain injury by CT; 2. Systolic BP ≥150 mmHg for at least twice; 3. \>18 years old; 4. Feasible for emergency antihypertensive treatment and real-time BP monitoring; 5. Disease onset is within 24h; 6. ICU or stroke unit admission within 24h.

Exclusion criteria

1. Subject has contraindications for emergency intensified antihypertensive treatment; 2. Intracranial hemorrhage secondary to intracranial tumor, recent trauma, cerebral infarction and thrombolytic therapy; 3. History of ischemic stroke within 30 days before disease onset; 4. Clinical or imaging examination reveals an expected high mortality in subject within the next 24h; 5. Presence of dementia or significant post-stroke disability; 6. Coagulation disorder caused by drugs or hematologic diseases; 7. Allergy to opioids; 8. Interference test result, assessment and follow-up of comorbidity; 9. Presence of sinus arrest, borderline rhythm, grade II and above atrioventricular block and malignant arrhythmia; 10. Individual is pregnant or lactating; 11. Currently participating in other drug studies or clinical trials; 12. Subject or guardian is unwilling to provide his/her informed consent form, or subject is highly unable to persist with the study and follow-up; 13. Subject's participation in the study will increase his/her study-related risk, and other reasons that make the subject unsuitable for the study as determined by the investigator.

Design outcomes

Primary

MeasureTime frameDescription
Systolic BP control rate at 1h post-treatment initiation1h post-treatment initiationThe number of patients who systolic BP decreased to \<140 mmHg at 1h post-treatment initiation compared to the total number of each group.

Secondary

MeasureTime frameDescription
Hematoma growth at 24 h24h of treatmentHead CT re-examination is required for the subjects after 24h of treatment.Hematoma expansion is defined as V2-V1≥12.5 cm³ or (V2-V1)/V1\>33% (V1 and V2 represent the hematoma volume in the two CT scans, respectively).
BP variabilityUp to 7 daysBPs are also recorded every hour from hour 2 to 24 post-treatment, and monitored on d2-d7 of treatment of recorded every 6h daily (4 times per day); BP Coefficient of Variation (CV) = (standard deviation of BP/mean of systolic BP).
Neurologic functionUp to 7 daysAssessed once every morning using the National Institutes of Health Stroke Scale (NIHSS), Glasgow Coma Scale scores (GCS), Richmond Agitation-Sedation Scale (RASS), Nonverbal Adult Pain Assessment Scale (NVPS), Reaction Level Scale (RLS).
Duration of ICU treatment and mechanical ventilationUp to 7 daysDuration of ICU treatment and mechanical ventilation
cerebral tissue oxygenation index (TOI)Up to 7 days and around sputum aspirationAssess changes in the TOI after sputum aspiration in mechanical ventilation patients
28-day mortality and disability rate28 daysUsing a binary indicator of the patient's death or dependency at 28 days, with dependency being defined by a score of 3 to 5 on the modified Rankin Score (mRS)
90-day mortality and disability rate90 daysUsing a binary indicator of the patient's death or dependency at 90 days, with dependency being defined by a score of 3 to 5 on the modified Rankin Score (mRS)
Healthcare worker satisfaction7 day or discharge from ICU (if patients discharge from ICU in 7 days)Questionnaire is designed based on the Copenhagen Psychosocial Questionnaire, with a parameter for self-assessed workload.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026