The Study of Pharmacokinetics and Pharmacodynamics of Cisatracurium
Märksõnad
Abstraktne
Kirjeldus
Neuromuscular blocking agents (NMBAs) are commonly used in critically ill patients, especially in adult respiratory distress syndrome (ARDS). Use of NMBAs to facilitate mechanical ventilation, to control patient/ventilator asynchrony and to reduce uncontrolled muscle tone in special conditions including tetanus, therapeutic hypothermia, and status epilepticus were increasingly found in current clinical practice.
Cisatracurium, 1Rcis-1'Rcis isomer of atracurium, is benzylisoquinolium nondepolarizing NMBAs which is three to five folds higher potency than atracurium besylate. The degradation of cisatracurium by hofmann elimination and ester hydrolysis in plasma generates laudanosine and a monoquaternary acrylate metabolite. Clinical practice guidelines for sustained neuromuscular blockade in the adult critically ill patient published in year 2016 strongly recommended cisatracurium due to a reduction in incidence of prolonged blockade, cardiovascular related adverse events and anaphylactic reactions. Moreover, recent evidence showed that early use of cisatracurium in early severe ARDS patients led to a significant reduction in mortality.
Regarding pharmacokinetics and pharmacodynamics of cisatracurium in critically ill patients, there were multiple factors affected cisatracurium blood concentration and neuromuscular blockade actions. Several reports demonstrated that pathophysiological changes, such as age, hypothermia/ hyperthermia, electrolyte imbalance and acid-base disturbances, had a significant impact on PK and PD of cisatracurium. Currently, there were an increasing data of slow response and less paralysis effect in critically ill patients receiving standard dose of cisatracurium. These may be explained by inadequate drug concentration at target organ, therefore, treatment failures regarding recommended dose of cisatracurium has been reported. Consequently, higher cisatracurium dose with higher drug concentration level might overcome a problem of inadequate level and therapeutic failure while receiving a standard dose of cisatracurium (a loading dose of 0.1-0.2 mg/kg, followed by a maintenance dose of 1-3 mcg/kg/min)
Kuupäevad
| Viimati kinnitatud: | 02/28/2019 |
| Esmalt esitatud: | 11/01/2017 |
| Hinnanguline registreerumine on esitatud: | 11/05/2017 |
| Esmalt postitatud: | 11/08/2017 |
| Viimane värskendus on esitatud: | 03/04/2019 |
| Viimati värskendus postitatud: | 03/05/2019 |
| Õppe tegelik alguskuupäev: | 12/14/2017 |
| Eeldatav esmane lõpetamise kuupäev: | 08/30/2018 |
| Eeldatav uuringu lõpetamise kuupäev: | 08/30/2018 |
Seisund või haigus
Sekkumine / ravi
Drug: Cisatracurium
Faas
Käerühmad
| Arm | Sekkumine / ravi |
|---|---|
| Experimental: Cisatracurium Patients who require paralysis with cisatracurium as part of their clinical care in ICU | Drug: Cisatracurium A single dose of 0.2 mg/kg intravenous bolus cisatracurium will be administered and blood samples will be taken before and at least 7 occasions post dose (at 1, 5, 10, 12, 15, 20, 30, and/or 60 minutes after a single bolus). |
Abikõlblikkuse kriteeriumid
| Õppimiseks sobivad vanused | 18 Years To 18 Years |
| Uuringuks kõlblikud sood | All |
| Võtab vastu tervislikke vabatahtlikke | Jah |
| Kriteeriumid | Inclusion Criteria: - Age greater than 18 years - Admission for ICU care - Require paralysis with cisatracurium as part of their clinical care - Patients or legal representatives who are able to understand and are willing and able to give their signed informed consent before any trial-related procedures are performed Exclusion Criteria: - Lactating women - Pregnancy women - Documented history of hypersensitivity to cisatracurium - Pre-existing neuromuscular disease - Patients with burn lesions - Currently diagnosed of hypothermia condition (tympanic body temperature ≤ 36 °C) - Patients currently receiving intravenous bolus or push of cisatracurium within 24 hours or receiving intravenous continuous infusion of cisatracurium within 48 hours prior to enrollment - Patients who have to receive intravenous continuous infusion of cisatracurium within 30 minutes after given intravenous bolus of 0.2 mg/ kg cisatracurium |
Tulemus
Esmased tulemusnäitajad
1. Total plasma concentration-time data [Pre-dose through 60 minutes post-dose]
2. Patient-ventilator asynchrony - time data [Pre-dose through 60 minutes post-dose]
3. The degree of neuromuscular block by train-of-four-watch monitor - time data [Pre-dose through 60 minutes post-dose]
Sekundaarsed tulemusmõõdud
1. Time to maximum concentration [Pre-dose through 60 minutes post-dose]
2. Half-life [Pre-dose through 60 minutes post-dose]
3. Clearance [Pre-dose through 60 minutes post-dose]
4. Elimination rate constant [Pre-dose through 60 minutes post-dose]
5. Time to maximum block [Pre-dose through 60 minutes post-dose]
6. Percentage of maximum block [Pre-dose through 60 minutes post-dose]
7. Time to patient-ventilator synchrony [Pre-dose through 60 minutes post-dose]
Muud tulemusmeetmed
1. Bispectral index (BIS) - time data [Pre-dose through 60 minutes post-dose]
