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Transfusion-Associated Circulatory Overload Best Eliminated With Lasix

Early Phase 1
Completed
Conditions
Transfusion-associated Circulatory Overload
Interventions
Drug: Normal Saline
Registration Number
NCT02802696
Lead Sponsor
Sunnybrook Health Sciences Centre
Brief Summary

This is a pilot double-blinded placebo-controlled randomized controlled trial (RCT) to evaluate the feasibility of conducting a multicenter, randomized, placebo-controlled trial to assess the efficacy of pre-transfusion furosemide in preventing transfusion-associated circulatory overload (TACO) in hemodynamically stable inpatients aged 65 years or older receiving a single unit red blood cell transfusion. Patients will be randomly allocated to receive either furosemide (20mg intravenous) or placebo (saline) within 60 minutes of starting a red blood cell (RBC) transfusion. Randomization will be stratified by centre and renal dysfunction (creatinine clearance ≥ 60 mL/min or \< 60 mL/min). This is a blinded trial: patients, care-providers (physicians and nurses), data collectors, outcome adjudicators, and data analysts will not be aware of group allocation.

Detailed Description

The investigators proposed this pilot study to assist us in determining the feasibility of conducting a definitive multicenter randomized trial across Canada.

Rationale:

The rationale for this study includes: (1) TACO is the leading cause of morbidity and mortality due to transfusion; (2) risk factors for TACO include older age, renal dysfunction and positive fluid balance; (3) furosemide is a diuretic commonly prescribed for fluid overload; (4) furosemide can decrease pulmonary artery pressures; and (5) clinical uncertainty as to the effect of furosemide in preventing TACO. The investigators will enroll 80 patients in this pilot study at two centers.

Hypothesis:

The investigators hypothesize that 80 patients can be enrolled in the trial within a 2-month period

Justification:

If pre-transfusion that furosemide decreases the rate of TACO with red blood cell transfusion, clinical practice worldwide would change. Over 800,000 patients in Canada receive a blood transfusion annually and many are at high risk for TACO and may benefit from this simple, low-cost intervention. This intervention could easily be generalizable worldwide. There are practical challenges related to patient recruitment, adherence to trial protocol and data collection, all of which the TACO-BEL Pilot Trial will seek to measure.

Objectives:

The primary outcome of this trial is to determine the feasibility of performing a large multi-centre, randomized, placebo-controlled trial with concealed allocation and blinded outcome assessment, adequately powered to determine a clinically significant effect of pre-transfusion furosemide on the incidence of transfusion-associated circulatory overload.

Primary outcome measure is the number of patients enrolled within a two-month period

Secondary feasibility outcome measures include:

1. Proportion of patients screened meeting eligibility criteria

2. Proportion of eligible patients consenting to participate

3. Proportion of consenting patients receiving the allocated treatment

4. Proportion of treated patients completing follow-up assessment

5. Proportion of patients in which blinding was maintained throughout study

Research Method:

Patients meeting inclusion criteria will be identified by reviewing transfusion orders received by the blood transfusion laboratory or by referral from ordering physicians; these patients will then be approached by study personnel to obtain pre-transfusion informed consent. Randomization will be performed by pharmacy at the time of drug preparation. The randomization code will be generated in random blocks of 4 to 6, stratified by center, and renal function at time of randomization (creatinine clearance \< 60 and ≥ 60 mL/min) using a computer based randomization program.

Intervention:

Patients will be administered a bolus dose of 20mg furosemide (20mg/2mL) intravenously within 60 minutes prior to the start of the red blood cell transfusion. Patients randomized to placebo will be administered an equal volume of normal saline intravenously immediately within 60 minutes prior to the start of the red blood cell transfusion.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
80
Inclusion Criteria
  • Age ≥ 65 years.
  • Receiving a single unit red blood cell transfusion
Exclusion Criteria
  • Active bleeding (active visible bleeding, required 2 or more RBC units in the preceding 24 hours, drop in Hb > 20 g/L in the preceding 24 hours);
  • Hemodynamically unstable (systolic blood pressure < 90 mmHg or on inotropes);
  • Anticipated major surgical procedure within 24 hours of enrolment;
  • Presence of hyponatremia (Na < 130 mmol/L);
  • Presence of hypokalemia (K < 3.5 mmol/L);
  • Dialysis or creatinine clearance < 30 mL/min;
  • Order for platelet or plasma transfusion at same time;
  • Allergy to furosemide;
  • Risk of withholding furosemide felt by attending physician to place patient at excessive risk of harm;
  • Previously enrolled in the study;
  • Plan for discharge on the day of randomization;
  • Unable to provide informed consent.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PlaceboNormal SalineNormal saline
FurosemideFurosemideDiuretic
Primary Outcome Measures
NameTimeMethod
Number of patients enrolled2 months period
Secondary Outcome Measures
NameTimeMethod
Proportion of patients screened meeting eligibility criteria2 months
Proportion of eligible patients consenting to participate2 months
Proportion of patient receiving the allocated treatment2 months
Proportion of treated patients completing follow-up assessment2 months
Proportion of patient in which blinding was maintained throughout study2 months
Vital SignsBaseline and 6 hours post transfusion

Change in vital signs immediately post-transfusion and at 6 hours post-transfusion

Positive end-expiratory pressureBaseline and 6 hours post transfusion

For patients on mechanical ventilation pre-transfusion, change in positive end-expiratory pressure

Inspiratory oxygenBaseline and 6 hours post transfusion

change in fraction of inspiratory oxygen at 6 hours post-transfusion

Incidence of TACO within 6 hours from completion of transfusionwithin 6 hours
Severity of TACO-graded as per the Public Health Agency of Canada's Transfusion Transmitted Injuries Surveillance Systemwithin 6 hours
Validation of TACO as per criteria adopted from the US Center for Disease Controlwithin 6 hours
Change in plasma brain natriuretic peptide(BNP)Baseline and Day 1
Net fluid balance at 24 hours from start of transfusion- all intravenously-administered fluids (including the transfused blood product and the study intervention)Within 24 hours
Proportion of patients developing hyponatremia or hypokalemia by Day 1By Day 1
Proportion of patients developing hypotensionWithin 24 hours
Proportion of patients developing acute kidney injuryWithin 24 hours
Need for increased supplemental oxygen is defined as any increase in oxygen flow ≥ 1 L/hr or (fraction of inspired oxygen)FiO2 ≥ 5% of 1 hour duration or longer, prompted by either patient symptoms or a fall in oxygen saturation(SpO2) ≥ 5%Within 24 hours
Need for inotropic support is defined as the initiation of a continuous infusion of dopamine, dobutamine, epinephrine, or norepinephrineWithin 24 hours
Need for additional diuretic or vasodilatory therapy is defined by the prescription of non-study furosemide, hydrochlorothiazide, metolazone, or either transdermal or intravenous nitroglycerinWithin 24 hours
Occurrence of acute coronary syndrome or new arrhythmiawithin 7 days
Mortality during hospital stayUpto 30 days
Length of hospital stayFrom date of admission until the date discharge from an acute care hospital or date of death from any cause, whichever came first, assessed up to 30 days.

Trial Locations

Locations (3)

Canadian Blood Services

🇨🇦

Toronto, Ontario, Canada

Sunnybrook Health Sciences Centre

🇨🇦

Toronto, Ontario, Canada

University Health Network

🇨🇦

Toronto, Ontario, Canada

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