Fluid Responsiveness in the Postoperative Patient: a Prospective Study

NCT ID: NCT02418663

Last Updated: 2015-05-15

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 245 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-06-30
• Study Completion Date: 2017-06-30

Brief Summary

The aim of this study is to determine the prevalence of Fluid Responsiveness (FR) (SV increases by at least 15% after Volume Expansion, VE) in postoperative patients admitted on a surgical ward after elective abdominal, thoracic and esophageal surgery

Detailed Description

Perioperative care

Preoperative Period

As per usual practice, the patient's staff surgeon will provide directives for preoperative fasting and fluid intake. These patients are encouraged to drink up to two hours before hospital admission, and also receive preoperative carbohydrate drinks the night before (100 grams), and the morning of surgery (50 grams) when indicated. Additionally, routine use of mechanical bowel preparation is avoided, and is prescribed only in selected cases. The patient's weight will be obtained upon arrival in the operating room.

Anesthetic and analgesic management

Anesthetic management and choice of postoperative analgesia will be as per usual care, at the discretion of the staff anesthesiologist in-charge of the case. An arterial line or central venous line may be inserted, and Goal Directed Fluid Therapy (GDFT) employed if deemed necessary.

Post-anesthesia Care Unit (PACU)

On arrival to the PACU, basic hemodynamic parameters, including heart rate (HR), blood pressure (BP), oxygen saturation, respiratory rate, temperature, and central venous pressure (CVP), if available, will be recorded according to standardized PACU protocol. A research assistant will then collect initial PACU values for these hemodynamic variables. Surgical time, estimated surgical blood loss, urine output, and intraoperative fluid and blood product administration will also be recorded. PACU care will be dictated by the treating staff anesthesiologists. Patients will be discharged from PACU according to standard institutional criteria.

Surgical floor

Postoperative care management, including the commencement of oral diet and fluid management, will be at the discretion of the surgical team. If required, VE (volume of the solution to be infused and type of the intravenous solution) will be decided case by case by the surgical team. The patient's weight will be obtained daily until hospital discharge. Patients will typically be discharged if afebrile, able to tolerate oral diet, pain is controlled (numeric rating scale (NRS) < 4), and they are able to ambulate.

Assessment of FR

A research assistant working in the department of Anesthesia will assess FR on two occasions:

1. When any VE is ordered by the treating team, either in PACU or on the surgical floor upon standard evaluation of hemodynamic parameters, urine output, surgical losses, and laboratory test abnormalities. FR will be assessed by measuring SV and Cardiac Output (CO) obtained by the ccNexfin system before 1 and 5 minute after VE. A patient will be considered a fluid responder if SV increases by at least 15% 1 minute after VE. A cut-off of 15% has been chosen as it represents the minimal clinical significant difference between two CO measurements obtained by thermodilution.

2. Upon arrival to the PACU, and every day before breakfast during the hospital stay. FR will be assessed by measuring SV and CO obtained by the ccNexfin system before and after 1 minute following 250 ml of Lactated Ringer's given as fluid challenge. A patient will be considered a fluid responder if SV increases by at least 15% after the fluid challenge.

Prediction of FR

A fluid challenge of 250 ml of Lactated Ringer's will be used to predict FR before the administration of any VE ordered by the treating team, either in PACU or on the surgical floor upon standard evaluation of hemodynamic parameters, urine output, surgical losses, and laboratory test abnormalities. A patient will be considered a fluid responder if SV increases by at least 15% 1 min after the end of a fluid challenge The utilization of fluid challenges has been shown to have high-accuracy (Receiver Operating Characteristic (ROC) curve of > 0.9) to predict FR in spontaneously breathing patients47. Furthermore, administration of fluid challenges to predict FR has already been described in several trials, including those with sick patient populations48 (ICU patients, patients undergoing major surgery, and patients with Ejection Fraction (EF) <40%).

Measurement of FR

1. Assessment of FR when VE is deemed necessary by the treating physician in PACU or on the surgical floor Prior to administration of a non-emergent fluid bolus (VE) ordered by the treating physician, nurses will additionally page the research assistant who will measure ccNexfin CO-Trek parameters as described earlier, and then administer a fluid challenge and measure FR. For simplicity, a single pager number will be used, and it will be affixed to the front of the chart of patients included in the study. A copy of the study protocol will also be given to nurses in the PACU and on the surgical floors for perusal.

The need for VE will be evaluated by the anesthetist in charge in PACU, or by the surgical team on the surgical ward. Hemodynamic variables triggering fluid administration will be decided based on standard evaluation of hemodynamic parameters, urine output, surgical losses, and laboratory test abnormalities. The type and amount of intravenous solution to be used will be decided by the anesthetist in charge or by the surgical team.

Before VE, hemodynamic variables including HR and BP will be measured by the research assistant. CVP will me measured in PACU if patients receive a central venous catheter. Then, the ccNexfin system will be applied in a standardized fashion according to manufacturer recommendations: an appropriately sized finger cuff will be selected and placed around the patient's middle finger. The wrist unit and heart reference sensor (HRS) will then be placed around the patient's wrist and ring finger respectively. The system will be zeroed, and the sensor end of the HRS will be placed at the level of the patient's heart, which allows for compensation for hydrostatic pressure differences between the finger and the heart. The ccNexfin will then calculate and display the values for an initial post-operative CO, Cardiac Index (CI), and SV. One and 5 minutes after the end of the VE, the same hemodynamic parameters will be measured. Should any further bolus of fluid be administered, FR and basic hemodynamic variables will be measured as above, upon administration of VE as ordered by the treating team.

2. Prediction of FR before the administration of any VE ordered by the treating team

A fluid challenge of 250 ml of Lactated Ringer's solution (Baxter, Lactated Ringer's Injection, USP, 1000 mL VIAFLEX Plastic Container) will be administered over 5 minutes by the research assistant before VE. One and 5 minutes following the end of the fluid challenge, basic hemodynamic values (as described above), as well as CO, CI, and SV obtained from the ccNexfin system, will again be recorded. An increase of SV by at least 15% 1 minute after the end of the fluid challenge will be considered clinically significant. Upon termination of a fluid challenge, the decision on weather to proceed with VE will be taken by the treating physician based only on standard signs and measures of hypovolemia and not on any of the ccNexfin SV and CO measurements obtained during the fluid challenge. The proportion of patients identified as fluid responsive after VE will be compared with the proportion of patients responding to the fluid challenge.

The research assistant will be available to measure FR from 6.30 AM to 7.30 PM every day during patient hospitalization. For patient safety, the research assistant must arrive at the bedside within ten minutes of being paged, in order to measure FR before VE. Intravenous fluids will be administered without measuring CO and administering a fluid challenge if:

1. the research assistant will not be able to arrive at the bedside within ten minutes;

2. the treating physician considers immediate administration of intravenous fluids necessary.

CO measurements will not be taken before administering blood products. Blood product administration (erythrocytes, platelets, fresh frozen plasma, or cryoprecipitate) will also be at the discretion of the staff anesthetist (in PACU) or at the discretion of the surgical team (surgical ward).

3. Daily assessment of FR

After surgery in PACU, and daily (before breakfast) for the duration of the patient's hospital stay a research assistant will administer a fluid challenge. As described above, CO, CI, and SV will be measured by the research assistant using the ccNexfin system, to assess for FR. A fluid challenge of 250 ml of Lactated Ringer's solution (Baxter, Lactated Ringer's Injection, USP, 1000 mL VIAFLEX Plastic Container) will then be administered over 5 minutes. One and 5 minutes following fluid challenge completion, basic hemodynamic values (as described above), as well as CO, CI, and SV obtained from the ccNexfin system, will again be recorded. An increase of SV by at least 15% 1 minute after the end of the fluid challenge will be considered clinically significant.

Daily assessment of FR, regardless of whether patients will receive intravenous fluids, will determine if FR is associated with an increased risk of complications and/or prolonged hospital stay.

All ccNexfin values obtained before and after VE and any fluid challenge will be blinded to the treating anesthetist, the surgical team and the nursing team.

Conditions

Actual Impaired Fluid Volume

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: SCREENING
• Blinding Strategy: TRIPLE

Study Groups

Postoperative elective surgical patients

Patients undergoing major elective thoracic and abdominal, the latter group including upper gastrointestinal, esophageal, and colorectal procedures. In this group FR will predicted by administering a fluid challenge of 250 ml of Lactated Ringer's solution and measuring SV with the ccNexfin

Group Type: OTHER

Fluid challenge (250 ml Lactated Ringer's solution)

Intervention Type: DRUG

When VE is prescribed to a patient, a fluid challenge of 250mL Lactated Ringer's solution will first be administered. The ccNexfin system will be used to predict FR (SV increases by at least 15% in response to a fluid challenge). The remaining amount of fluid ordered by the treating team will then be administered, and SV will again be measured.

Additionally, a daily fluid challenge with 250mL of Lactated Ringer's will also be administered, with FR recorded as above

Interventions

Fluid challenge (250 ml Lactated Ringer's solution)

When VE is prescribed to a patient, a fluid challenge of 250mL Lactated Ringer's solution will first be administered. The ccNexfin system will be used to predict FR (SV increases by at least 15% in response to a fluid challenge). The remaining amount of fluid ordered by the treating team will then be administered, and SV will again be measured.

Additionally, a daily fluid challenge with 250mL of Lactated Ringer's will also be administered, with FR recorded as above

Intervention Type: DRUG

Other Intervention Names

Lactated Ringer's Injection

Eligibility Criteria

Inclusion Criteria

• Patients undergoing major elective thoracic and abdominal surgeries, the latter group including upper gastrointestinal, esophageal, and colorectal procedures,
• Patients treated with surgery-specific enhanced recovery programs (ERPs), implemented in 2010 at the Montreal General Hospital for colorectal surgery, and subsequently developed at the same institution for thoracic surgery

Exclusion Criteria

• Age <18 years
• Emergency surgery
• Patients who do not understand, read or communicate in either French or English
• Chronic kidney disease
• Congestive heart failure
• Severe aortic stenosis
• Patients not in sinus rhythm
• Patients requiring fluid restriction for any reason
• Known peripheral vascular disease or Raynaud's phenomenon
• Septic patients
• Acute circulatory shock

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

McGill University Health Centre/Research Institute of the McGill University Health Centre

OTHER

Sponsor Role: lead

Responsible Party

Gabriele Baldini, MD, MSc, Assistant Professor

Assistant Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Gabriele Baldini, MD, MSc

Role: PRINCIPAL_INVESTIGATOR

McGill University Health Centre/Research Institute of the McGill University Health Centre

Central Contacts

Gabriele Baldini, MD, MSc

Role: CONTACT

gabriele.baldini@mcgill.ca

514-934-1934 ext. 37012

References

Myles PS, Hunt JO, Nightingale CE, Fletcher H, Beh T, Tanil D, Nagy A, Rubinstein A, Ponsford JL. Development and psychometric testing of a quality of recovery score after general anesthesia and surgery in adults. Anesth Analg. 1999 Jan;88(1):83-90. doi: 10.1097/00000539-199901000-00016.

Reference Type: BACKGROUND

PMID: 9895071 (View on PubMed)

Charlson ME, Pompei P, Ales KL, MacKenzie CR. A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis. 1987;40(5):373-83. doi: 10.1016/0021-9681(87)90171-8.

Reference Type: BACKGROUND

PMID: 3558716 (View on PubMed)

Other Identifiers

14-452 SDR

Identifier Type: -

Identifier Source: org_study_id