NORA_FC: EFFECT OF VASOPRESSORS ON FLUID CHALLENGE PERSISTENCE AN OBSERVATIONAL STUDY IN PATIENTS UNDERGOING LAPAROTOMY.

Sponsor
Humanitas Clinical and Research Center (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04934345
Collaborator
(none)
50
1
12
4.2

Study Details

Study Description

Brief Summary

The hemodynamic effect of the fluid challenge administration (FC) depends on different variables related to the interplay between cardiac function and vascular tone response.

In this context, the effect of adding a vasopressor to keep the arterial pressure between predefined ranges may impact on the persistence of stroke volume (SV) changes after FC administration. In fact, both the effect on arterial elastance and venous return may increase the persistence of SV increase, which is know to drop to baseline pre-FC values within fw minutes after FC administration.

This single-centre observational study, in elective patients scheduled for elective laparotomy, hypothesizes that intraoperative norepinephrine infusion would prolong the effect of FC administration.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Fluid challenge

Detailed Description

The appropriate fluid management in the perioperative period is an important, and still partially unclear, chapter of clinical practice for anaesthesiologists. Increasing evidence suggests that intraoperative fluid therapy should be tailored to individual patient's physiology with the purpose of targeting fluid administration to specific stroke volume (SV) responses, or its surrogates. For this reason, small repeated and fast boluses challenging the cardiovascular system should be preferred to continuous and prolonged infusions.

The fluid challenge (FC) is defined as a small amount of fluid given in a short period of time to assess whether the preload reserve of the patient can increase SV with further administration of fluids. A number of studies performed in the operating room evaluated the hemodynamic effects of FC solely considering the effect before and after the infusion. Recently, Aya demonstrated that at least 4 ml kg-1 should be infused to effectively challenge the preload, additionally showing that the hemodynamic effect of the FC is dissipated within 10 minutes, in both responders and in non-responders.

The approach of Aya et al. considers the FC as a drug evoking a systemic response on flow (i.e. SV) and pressure variables [i.e. systolic arterial pressure (SAP)]. Accordingly, the pharmacodynamic effect is evaluated by considering the magnitude (i.e. the maximal changes from baseline obtained for a specific variable), the global effect [i.e. considering the area under the curve (AUC) obtained by plotting the changes overtime] and the persistence of the hemodynamic response after the end of FC administration. The infusion time of FC administration, which ranges in the literature between 5 and 30 minutes, may influence the magnitude of SV response and, in turn, the amount of patients defined as fluid responders . Since several intraoperative pathways of hemodynamic optimization are based on the response to repeated FCs, a prolonged infusion time may potentially affect fluid responsiveness and, in turn, wrongly drive intraoperative fluid management and eventually affect postoperative outcomes.

Since FC is a test embedding at least three variables (i.e. the amount of fluid; the time needed to complete the administration and the SV change threshold used to define a positive response), the role of a one single component on the final outcome can be addressed only by keeping fixed the others. Our group recently investigated the role of the infusion rate in a multicentre study (under revision at the timing of writing this protocol) and our research is now focused on the assessment of the role of the vascular tone in the persistence of the FC effect overtime. The previous study demonstrated that the rate of infusion impact on FC response, however another crucial issue is related to the persistence of the effect of the FC on the SV. In fact, the SV is determined by the interplay between cardiac function and arterial load. Diastolic filling depends on venous return, which is determined by the "stressed volume" and venous compliance. Systolic cardiac function depends on both cardiac factors and arterial load and is predominantly determined by arterial elastance (Ea) and resistance. For this reason, the effect of a vasopressor (i.e. the norepinephrine, the most widely used) may impact on the persistence of the increase of the SV after FC administration.

This single-centre observational study, in elective patients scheduled for elective laparotomy, hypothesizes that intraoperative norepinephrine infusion would prolong the effect of FC administration.

Study Design

Study Type:
Observational
Anticipated Enrollment :
50 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
EFFECT OF VASOPRESSORS ON FLUID CHALLENGE PERSISTENCE: AN OBSERVATIONAL STUDY IN PATIENTS UNDERGOING LAPAROTOMY.
Anticipated Study Start Date :
Sep 1, 2021
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Sep 1, 2022

Arms and Interventions

Arm Intervention/Treatment
FC administration

All the patients receive crystalloids at 4 ml/kg/hour as maintenance fluid during surgery, according to standard practice. After the first episode of hypotension (MAP < 65 mmHg) the PPV is checked. PPV ≥ 13% - FC (4 ml/kg of crystalloids administered in 10') PPV < 13% - start norepinephrine (starting dose - 0.05 mcg/kg/min). In this group, the FC will be administered during an episode of intraoperative hypotension during NE infusion.

Diagnostic Test: Fluid challenge
The fluid challenge consists of a bolus of 4 ml/kg of crystalloids, administered over 10 minutes.

Outcome Measures

Primary Outcome Measures

  1. Stroke volume persistance [evaluated within 10 minutes after fluid challenge infusion]

    Stroke volume estimation with respect to baseline values

Secondary Outcome Measures

  1. Pharmakodynamic assesement of FC with and without NE [evaluated within 10 minutes after fluid challenge infusion]

    Area under the curve analysis

  2. dmax [evaluated within 10 minutes after fluid challenge infusion]

    the maximal percentage difference of the SV observed from baseline

  3. tmax [evaluated within 10 minutes after fluid challenge infusion]

    time when dmax maximal value was observed

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • adult patients, scheduled for elective laparotomy (>3h predicted) and requiring a FC.
Exclusion Criteria:
  • any recurrent cardiac arrhythmia;

  • reduced left (ejection fraction < 30%) or right (systolic peak velocity of tricuspid annular motion < 0.17 m/s) ventricular systolic function.

Once enrolled, the patient can be additionally excluded due to the occurrence of one of the following intraoperative conditions:

  1. significant bleeding (more than 500 ml in ½ hour)

  2. recurrent extrasystoles

  3. persistent low quality of the arterial signal affecting hemodynamic monitoring measurements

  4. intraoperative hemodynamic instability requiring the persistent use of vasopressors.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Humanitas Research Hospital Rozzano Milano Italy 20089

Sponsors and Collaborators

  • Humanitas Clinical and Research Center

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Humanitas Clinical and Research Center
ClinicalTrials.gov Identifier:
NCT04934345
Other Study ID Numbers:
  • NORA_FC
First Posted:
Jun 22, 2021
Last Update Posted:
Sep 9, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Sep 9, 2021