Does education intervention about adding HPI to standard practice alter clinician behaviour to the treatment of hypotension? As a secondary objective we assess whether incorporating HPI in a Goal-directed fluid therapy (GDFT) algorithm lowers the…
ID
Bron
Verkorte titel
Aandoening
Anesthesiology
Hypotension
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
A range of social-cognitive determinants of behaviour change including attitudes, self-efficacy, social norms, skills, as well as factors relating to the normalisation of technology into routine practice through qualitative data analysis.
Achtergrond van het onderzoek
Intraoperative hypotension has a high incidence in the perioperative population and is associated with an increase in postoperative complications and mortality. A MAP below 65 mmHg or a decrease of ƒ®20% from baseline increases the incidence of myocardial injury after non-cardiac surgery (MINS) and acute kidney injury (AKI). Recently, the FloTrac IQ algorithm (Edwards Lifesciences, Irvine, CA, USA) incorporating a hypotension predictability index (HPI), dynamic arterial elastance variable (Eadyn) and index assessment of left ventricular contractility (dP/dT) was developed which provides clinicians an early warning of an impending hypotensive episode as well as insight into its pathophysiology and thus buys time to take measures to prevent this hypotension from occurring. In addition, this algorithm also incorporates variables used in standard care such as pulse pressure variation (PPV), stroke volume variation and index (SVV and SVI) and cardiac index (CI). Whether clinicians find the new information acceptable to use, or that it confers clinical utility remains unknown and for this technology to become accepted, and in turn lead to a reduced incidence of hypotension, this would require a change in current behaviours including attitudes and skills. The underlying rationale is that by using the HPI and secondary information, intraoperative hypotension can be reduced and appropriately treated or even prevented. Alternatively, hypotension can also be avoided simply by requiring the treating clinician to keep the MAP >65 mmHg, although the treatments may be inappropriate in view of the underlying pathophysiology. Therefore, we aim to use education intervention on treatment of hypotension and incorporating HPI in this clinical treatment to alter clinician¡¦s behaviour.
Doel van het onderzoek
Does education intervention about adding HPI to standard practice alter clinician behaviour to the treatment of hypotension?
As a secondary objective we assess whether incorporating HPI in a Goal-directed fluid therapy (GDFT) algorithm lowers the incidence of intraoperative hypotension.
Onderzoeksopzet
- after cohort 1, before education: structured inteview about beliefs of clinicians (15-20) about costs and benefits of controlling hypertension.
- During cohort 2 and 3: questionnaires for clinicians attending cohort 2 and 3 about the perceived barriers for effective control of hypotension.
- 2 motnhs after training FlowTracIQ: questionnaires about usefulness en usibility of the FlowTracIQ and observations of 6-8 surgical procedures
- After phase 3; workshop with other clinicians focusing on likelihood of wider adoption.
Onderzoeksproduct en/of interventie
Patients:
Cohort 1 (first 50 patients): management of hypotension as usual.
Cohort 2 (second 50 patients): management of hypotension keeping the MAP >65.
Cohort 3 (third 50 patients): management of hypotonsion by using the FlowTrac IQ
Clinicians:
Between cohort 1 and 2, treating physicians receive education intervention regarding current evidence of intraoperative hypotension and adverse outcomes. Between cohort 2 and 3, treating physicians receive education intervention regarding how to use FlowTrac IQ and its parameters in the clinical management of hypotension.
On various time points, interviews and questionnaires measuring a range of social-cognitive determinants of behavior change will be performed.
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
• Patients due to undergo elective major abdominal, orthopedic, head and neck or vascular surgery requiring invasive arterial monitoring (decided at the discretion of the treating clinician) under general anesthesia with positive pressure ventilation, and with an expected duration of greater than 90 minutes, who will have goal directed fluid therapy performed as part of their standard care.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
• Requirement for an intentional intraoperative MAP of less than 65 mmHg as decided by the treating surgeon and/or anesthetist.
• A preoperative MAP of lower than 65 mmHg documented on 2 separate occasions at preoperative assessment clinic.
• Patients with significant right or left ventricular failure
• Patients with known intra cardiac shunt.
• Patients with known severe aortic stenosis (peak velocity greater than 4 meter per second and/or aortic valve area less than 1 cm2)
• Patients with known cardiac arrhythmias
• Planned positive pressure ventilation with tidal volume < 7 ml/kg
• Patients undergoing hepatic surgery
• Patients requiring dialysis.
• Patients who do not have the capacity to consent
• Patients aged less than 18 years of age.
Opzet
Deelname
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In overige registers
Register | ID |
---|---|
NTR-new | NL7091 |
NTR-old | NTR7289 |
Ander register | Research Register UMCG : 201800452 |