Verification of an Intravenous Fluid Warmer: A Prospective, Two-Center Observational Trial

doi:10.21203/rs.3.rs-2121703/v1

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Verification of an Intravenous Fluid Warmer: A Prospective, Two-Center Observational Trial

https://doi.org/10.21203/rs.3.rs-2121703/v1

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Background

Avoiding inadvertent hypothermia during surgery is important. Intravenous fluid warmers used intraoperatively are critical for maintaining euthermia. We sought to prospectively evaluate the performance of the parylene-coated enFlow™ intravenous fluid warmer in patients undergoing surgery.

Methods

This was a prospective two-center observational clinical trial performed in inpatient surgical services of two large academic hospital systems. After informed consent, patients were enrolled in the study. All patients were adults scheduled for a surgery that was expected to last for at least 1 h with the administration of at least one liter of fluid warmed prior to infusion. Patient temperature was recorded in the preoperative unit, at the induction of anesthesia, and then every 15 or 30 minutes until the end of surgery. Temperature monitoring continued in the recovery unit. The parylene-coated enFlow™ intravenous fluid warmer was used in addition to the usual patient warming techniques. The primary outcome was the average core temperature, and secondary analyses assessed individual temperature measurements, temperature measurements during specific time periods, and rate of hypothermic events.

Results

Fifty patients (29 male) with a mean age of 64 years were included in the analysis. The mean surgical time was 195 minutes and patients received an average of 1142 ml of fluids. Core temperature dropped by only 0.3°C approximately 60 minutes after induction and recovered back to the baseline level approximately 60 minutes later. There was no correlation between flow rate and measured core body temperature.

Conclusions

The parylene-coated enFlow intravenous fluid warmer was able to warm fluids at all flow rates during prolonged surgery. The results showed that enFlow performed as expected.

Trial registration

The trial was registered prior to patient enrollment at clinicaltrials.gov (NCT04709627, Principal investigator: Mikko Lax, MD, Date of registration: 14 January 2021.)

Intravenous fluid warmer

hypothermia

surgery

anesthesia

prospective study.

The parylene-coated enFlow intravenous fluid warmer performed as expected in this prospective two-center clinical trial. Episodes of hypothermia were consistent with those reported for other devices, and there were no hyperthermic events.

Perioperative hypothermia is a well-known and well-studied risk factor associated with anesthesia and surgery. Current guidelines support the use of surgical techniques and devices to minimize core temperature fluctuations and avoid hypothermia.[1–6] During general anesthesia, normal vasoregulatory mechanisms are blunted, leading to a drop in the core temperature secondary to vasodilation. Hypothermia is more likely in a cold operating room environment, infusion of relatively cold intravenous fluids, and certain surgeries.[7] Perioperative hypothermia has been associated with delayed post-anesthetic recovery, increased blood loss during surgery with the need for transfusion, increased incidence of surgical wound infections, impairment of antibody- and cell-mediated immune defenses, and increased postoperative adverse myocardial events.[8–13] To reduce these events, current techniques to maintain normothermia include draping and covering the patient during surgery, active heating with forced air warming devices or heated water underbody pads, use of heated irrigation fluids in major body cavities, and warming of intravenous (IV) fluids as they are infused.[14] In particular, the use of warmed IV fluids is considered standard of care for avoidance of intraoperative hypothermia. Studies have shown that patients managed using fluid warmers maintained core body temperatures of 0.41°C to 0.74°C warmer using fluid warmers compared to other standard controls throughout the operative procedure with a relative risk of post-operative shivering of 0.39.[14]

The enFlow® (Vyaire Medical, Mettawa, IL, USA) is an active IV fluid warming system that attaches in series to the IV infusion line, which has a cartridge capable of heating fluids as they are infused into the patient. The enFlow cartridge recently underwent recall, redesign, and re-release secondary to concerns regarding the release of aluminium and other elements into the infusate.[15] The newer cartridge has been extensively tested in a bench environment for the release of aluminium, other potentially toxic elements, and organic molecules with favorable results.[16–22] Additional bench testing also confirmed that the newer parylene-coated enFlow design warmed fluids as efficiently as the previous design; however, the performance of the parylene-coated enFlow has not been evaluated in a clinical setting.[16]

To further assess this improved design in a clinical setting, this study evaluated the efficacy of the new parylene-coated enFlow IV fluid and blood warming system in maintaining normothermia in patients undergoing surgery. Our hypothesis was that the parylene-coated enFlow cartridge would provide adequate warming of the infusate during general anesthesia in adult patients for surgeries lasting over an hour and for patients receiving at least one liter of fluid. In this observational study, we evaluated the heating performance of the new enFlow at different flow rates and surgery durations. The primary outcome measure will be the mean of the temperature measurements taken during the course of surgery.

Ethics

Ethical approval

for this study was provided by the Ethics Committee of Helsinki and Uusimaa Hospital District (HUS/3206/2020) and the HUS Ethical Commission III, Helsinki, Finland (Chairperson Lauri Tammilehto) on 11 January 2021. The committee of 13 participants reviewed the clinical investigation plan, including amendments, the participant information leaflet, and informed consent. This study conforms to the STROBE statement.[23, 24] This study was conducted in accordance with the ethical principles in the Declaration of Helsinki. Written informed consent was obtained from all subjects participating in the trial. The trial was registered prior to patient enrollment at clinicaltrials.gov (NCT04709627, Principal investigator: Mikko Lax, MD, Date of registration: 14/01/2021.)

Study format

Subjects with scheduled surgeries were recruited for enrollment in the study consecutively from patients undergoing general anesthesia. The enrollment period was June 2021 through February 2022, when the number of qualifying cases was attained. Patients were enrolled if they were 18 years of age or older and required surgery for at least 1 h. Other inclusion criteria included an expectation of the perioperative need for at least one liter of infused fluids warmed during infusion, and the ability and willingness to provide informed consent. Exclusion criteria included pregnancy, a recent history of fever, or if the attending physician did not believe that participation of the patient would be in their best interest.

This was a noninterventional observational study. Participants were managed according to the routine care protocols of physicians and hospitals, receiving fluids warmed by the parylene-coated enFlow device. The device is packaged with a 7.5 cm extension set that is then connected via a 3-way stopcock connector to the patient (10 cm in length). Core temperature was monitored using a SpotOn™ forehead temperature monitor (3M Healthcare Division, St. Paul, MN, USA). For patients that had a urinary tract catheter placed for therapeutic reasons, bladder temperature measurements were also recorded at the same time points using the temperature sensor on the catheter. Surgical patients were also warmed using forced air warming, warming blankets, and control of the operating room temperature according to the hospital’s usual protocol. During the investigation period, a research operator acquired temperature measurements and collected data on the surgical and warming practices. Skin temperature measurements were taken at Baseline (i.e., 15 to 0 minutes prior to Induction), 15-, 30-, 60-, and 90-minutes post-induction, and then every 15 min until the end of surgery. A final measurement in the operating room was recorded at the end of surgery, followed by a reading upon arrival to the post-anesthesia care unit (PACU) and 30 min after arrival to the PACU. The level of and duration of high or low infusate temperatures were recorded for all patients. The levels of unacceptable infusate temperatures include: “Flashing Blue”: < 33°C, “Solid Blue”: ≥33°C and < 35°C, “Solid Yellow”: >42°C and ≤ 45°C, “Flashing Red”: >45°C.

This study was conducted at two hospital sites. The clinical data were recorded using an electronic data capture system and transferred to the research administrator for analysis. No treatment or control group analysis was performed, as non-use of an intravenous fluid warmer (i.e., a control group) would be unethical and a violation of these hospitals’ standard of care.

Statistical analysis

Sample size determination

The sample size for this study was determined based on the primary outcome of the average core temperature during surgery. We reviewed the related Cochrane Collaboration report of 209 subjects from nine studies with standard care practices.[14] We concluded that the core temperature during surgery could be expected to be maintained at 36.4°C (standard deviation [SD] 0.6°C). Assuming the same mean temperature and variation in this investigation, with 42 subjects, there would be a 99% chance that the control of the mean core temperature would be between 36.1 and 36.7°C. Our review also found that the mean core temperature (99% CI) among the studies was between 36.0 and 36.9°C, which is wider than the expected results of our investigation. Thus, our investigation was reasonably powered with 42 participants. To investigate the performance during longer surgeries, the protocol specified a total investigation size of 50 subjects, with at least 42 completing at least 60 minutes of surgery, and at least 12 subjects completed at least 120 minutes of surgery.

Data and statistical analyses

The primary endpoint for each subject was the mean and standard deviation of the core temperature SpotOn measurements taken during the surgery. To compare the performance of the enFlow device in this trial with previous studies, a noninferiority test was conducted to compare the mean patient temperature during surgery with the 209 patients compiled from nine studies in the Cochrane Collaboration report [14]. This test evaluated the null hypothesis that the difference in mean temperature in this study (µ₁) and the mean temperature from the Cochrane report (µ₂ = 36.4°C) is less than or equal to opposite of a predefined noninferiority margin (\({H}_{0}: {\mu }_{1}-{\mu }_{2}\le -\delta\)). The alternative hypothesis was that the difference in temperature is greater than the opposite of the noninferiority margin (\({H}_{a}: {\mu }_{1}-{\mu }_{2}> -\delta\)). Noninferiority will be established if the lower limit of the (1–2α)*100% confidence interval for the difference in the two means is above -δ. A noninferiority margin (δ) of 0.23°C was established based on the mean bias of SpotOn temperature compared to pulmonary artery temperature [25].

To visualize how temperature changed over the course of a surgery, the mean and 99% confidence intervals temperature across patients was calculated at each time point after the start of induction. Time points with less than 50% of the population were not included in the visualization. A repeated measures analysis of variance (ANOVA) with Dunnett’s test was conducted to compare mean temperatures at each time point to the Baseline temperature.

The study was subdivided into four predefined study periods, and the mean and standard deviation of measurements during periods were calculated: Baseline (i.e., 15 to 0 minutes prior to Induction), Induction period (i.e., 15-, 30-, 60-, and 90-minutes after start of induction) Post-Induction (i.e., additional measurements taken after 90 minutes after start of induction). A repeated measures ANOVA was performed to compare the mean temperatures at Baseline, Induction, Post-Induction, and PACU periods. Multiple comparison post-hoc tests were conducted for pairwise comparisons between periods if the ANOVA identified a significant difference between periods.

Hypothermic and hyperthermic events were identified for each patient during the entire surgery as well as separately during the Induction and Post-Induction periods. Hypothermia was defined as a patient temperature less than 36.0°C and hyperthermia as a temperature greater than 38.0°C. We quantified hypothermic and hyperthermic events using two different methods. The first method counted the total number of individual temperature measurements which were within the hypothermic or hyperthermic temperature ranges. The second method grouped hypothermic and hyperthermic episodes as continuous time periods where the temperature was within the hypothermic or hyperthermic ranges. These episodes were classified based on which study period they started in, and the duration of each event was calculated. The rate of these episodes was calculated as the number of episodes divided by the period duration. Finally, we quantified the proportion of patients that experienced at least one of these events during that study period.

To examine the relationship between the infusate flow rate and patient temperature, we examined the correlations between IV fluid flow rates and patient temperatures for measurements recorded during surgery. Robust linear regressions with bisquare weight functions and outliers removed (i.e., points greater than three standard deviations from the mean) were run for each relationship. For flow rates, we looked at the maximum and mean flow rates for each patient. For patient temperature, we included the minimum and mean temperatures during surgery for each patient. Furthermore, the same regressions were conducted looking at minimum and mean temperature versus change in patient temperature from their Baseline temperature. For these regressions, we included the largest decrease in temperature during surgery (i.e., minimum temperature – Baseline) and the mean change in temperature during surgery for each patient.

For patients with bladder temperature measurements, a Bland-Altman analysis was conducted to compare time-aligned temperature measurement pairs from the SpotOn system with bladder temperature measurements.

To account for multiple comparisons, we used a significance level of α = 0.005 for each statistical test to maintain an overall Type I error of 5%.

A total of 54 patients were recruited for the study. Of the 54 patients, data from four patients were excluded because they did not meet the inclusion criteria. Therefore, 50 patients (29 male) completed the study and were included in the analysis. The mean surgical time was 195 (range: 64–434) minutes with all 50 included subjects having a surgical duration of at least 60 minutes and 38 subjects having a surgery lasting at least 120 minutes. Surgery started an average of 55 (SD 11) minutes after the start of induction. The mean age of the patients was 64 (SD 12) years with a mean body mass index (BMI) of 27.0 (SD 5.7) kg/m². The demographic characteristics of the patients and their summary statistics are shown in Table 1. The average ambient temperature in the surgical suites was 21.5°C (SD 1.0°C) at Baseline and 21.8°C (SD 1.1°C) at the end of surgery. The infusate temperature remained in the acceptable operating range (i.e., 35–42°C) for all patients and all times.

Table 1

Demographic characteristics and summary of results (N = 50 subjects); BMI: Body mass index, ASA: American Society of Anaesthesiologists.
Parameter	Mean or Count	SD	Range
Age (years) and range	64	12	(30–85)
Weight (kg)	78	16	(46–120)
Height (cm)	170	8	(158–183)
BMI (kg/m²) and range	27.0	5.7	(17–46)
Female/Males	21/29	-	-
ASA Physical Status (I/II/III/IV)	2/14/28/6	-	-
Duration of Surgery (minutes)	195	80	(64–434)
Surgery Duration (≥ 60 min / ≥120 min)	50/38
Ambient Temperature, Baseline (°C)	21.5	1.0	(19.6–26.0)
Ambient Temperature, Surgery End (°C)	21.8	1.1	(19.0-25.6)

Across the entire duration of surgery, patients received a mean total infusion volume of 1142 (SD 792) ml at an average rate of 343 (SD 125) ml/h (Table 2).

Table 2

Infusion flow rates and total volume infused during surgery (N = 50 subjects)
Parameter	Mean	SD	Range
Average Infusion Rate, Surgery (mL/h)	343	125	(189–923)
Maximum Infusion Rate, Surgery (mL/h)	649	455	(200–3200)
Total Infusion Volume, Surgery (mL)	1142	792	(358–4336)

As part of standard care, all patients were also warmed with one or more other additional methods of warming including forced-air patient warming, heated mattress, and alternative fluid warmers (Table 3).

Table 3

Forced-air Patient Warming (3M Bair Hugger System); Heated Mattress (Astopad); Fluid Warmer (HOTLINE Blood and Fluid Warmer or Level 1 H-1200 Fast Flow Fluid Warmer) (N = 50 subjects).
Warming Method	Count	Warming Duration, Mean (SD)
Forced-air Patient Warming	48	174 (88)
Heated Mattress	39	271 (73)
Fluid Warmer	8	247 (41)

During surgery, the mean temperature across all patients was 36.5 (99% confidence interval: 36.4, 36.7) °C. A noninferiority test established noninferiority of the enFlow to maintain patient temperature during surgery compared to previous clinical studies [14] with a noninferiority margin (δ) of 0.23°C. Specifically, the 99% confidence interval of the difference between the mean temperature in this study and those compiled from previous clinical studies was − 0.039 to 0.27°C. Noninferiority was established because the lower limit of this confidence interval is greater than -δ (i.e., -0.039 > -0.23).

Figure 1 shows the mean and 99% confidence intervals for SpotOn temperature measurements obtained before, during, and after the surgery. There were statistically significant decreases in the core temperature from Baseline at 30-, 60-, 90-, and 105-minutes after the start of induction (p ≤ 0.0002). Temperature reached a minimum at 60- and 90- minutes after start of induction, with a temperature 0.3°C below the Baseline temperature. Core temperature then recovered back to the Baseline temperature for the remainder of the surgery and into the PACU.

Table 4 summarizes patient temperatures for each of the four study periods. Patient temperature dropped significant from Baseline (36.6°C) during the Induction phase (36.4°C, p = 0.0001) and then rebounded back during the Post-Induction phase (36.6°C, p = 0.78) which continued into the PACU (36.5°C, p = 0.041).

Table 4

Descriptive statistics of average patient temperatures during four study periods. PACU: Post-Anesthesia Care Unit.
Study Period	Mean	SD	Range
Baseline (°C)	36.6	0.4	(35.4–37.6)
Induction (°C)	36.4	0.4	(35.1–37.2)
Post-Induction (°C)	36.6	0.4	(35.3–37.2)
PACU (°C)	36.5	0.5	(35.1–37.5)

There were 819 SpotOn temperature readings recorded during this study. Of the 819 temperature readings recorded, there were 81 (10%) below the hypothermic threshold of 36.0°C and zero were above the hyperthermic threshold of 38.0°C (Table 5). The minimum single temperature measurement during surgery was 35.1°C, and the maximum single temperature measurement was 37.5°C.

Table 5

Number of hypothermic and hyperthermic temperature measurements by study period.
Study Period	< 36°C	36°C – 38°C	Total
Induction	37 (13%)	257 (87%)	294
Post-Induction	44 (8%)	481 (91%)	525
Entire Surgery	81 (10%)	738 (90%)	819

Grouping consecutive temperature measurements below the hypothermic threshold into continuous episodes, a total of 19 hypothermic episodes were experience in 16 (32%) patients. Thirteen of these episodes started during the Induction study phase while six started in the Post-Induction study phase. During surgery, patients experienced an average of 0.09 hypothermic episodes per hour (i.e., 1 episode every 11.1 hours) (Table 6). These hypothermic events lasted for a median duration of 15 minutes with a minimum duration of 0 minutes (i.e., single temperature measurement) and maximum duration of 210 minutes.

Table 6

Summary population statistics of hypothermic episodes commencing during the Induction and Post-Induction periods.
Parameter	Entire Surgery	Induction	Post-Induction
Hypothermic Episodes Median (25th, 75th percentile)	0 (0, 1)	0 (0, 1)	0 (0, 0)
Hyperthermic Episodes Per Hour	0.09	0.17	0.04
Percent of Patients with at Least One Hypothermic Episode	32%	26%	10%

To examine the relationship between infusate flow rate and patient temperature, we ran linear regressions between IV fluid flow rates and patient temperatures for measurements recorded during surgery (Fig. 2). The linear regressions revealed no association between fluid flow rates and patient temperature (p ≥ 0.37).

As an additional analysis, we explored the correlation between IV fluid flow rate and change in patient temperature from their Baseline temperature recorded prior to surgery (Fig. 3). These linear regressions also revealed no association between fluid flow rates and change in temperature from Baseline (p ≥ 0.12).

The Bland-Altman analysis comparing time-coincident temperature measurements by the SpotOn and bladder temperature patients showed good agreement between the two measurement techniques (Fig. 4). SpotOn temperatures were on average 0.21°C higher (95% limits of agreement: -0.79°C to 1.19°C) than bladder temperature measurements for the 400 measurement pairs from the 22 patients with a urinary tract catheter.

Two adverse events were identified through the study, both unrelated to the study device. Specifically, one consented patient was tachycardic with weakening vitals and the procedure was cancelled. In the second patient, the cannula broke the patient’s vein, resulting in solution flowing into tissue and a swollen arm.

In this clinical observational study, core patient temperature dropped by an average of 0.3°C approximately 60 minutes after the start of induction of general anesthesia for patients receiving warmed flows with the enFlow fluid warmer. Patient temperature returned to baseline levels approximately 60 minutes later. This magnitude drop in temperature is consistent with prior studies and noninferiority was established compared with compiled results from nine clinical studies.[14] In a study from 1993 using healthy volunteers undergoing general anesthesia without the use of active warming techniques or application of heating blankets, core body temperature decreased by approximately 1.5°C within one hour.[10] A drop in core body temperature to this extent has been shown to lead to significant adverse clinical events, including a two-fold increase in cardiac events[8], delayed wound healing with increased risk of infection[11], and an increase in surgical blood loss and use of perioperative blood product transfusions, even with smaller drops in core temperature.[12, 26] In a Cochrane Review of the effect of intravenous fluid warmers, Campbell et al.[14] found that, with a fluid warmer, core temperature was about half a degree higher compared to patients not given warmed fluids. This suggests a typical decrease in core temperature of 1.0°C using other methods of warming fluids.[14] The results of this study show an average decrease in core temperature of only 0.3°C (Fig. 1), indicating success in mitigating the risk of incidental hypothermia associated with surgery and anesthesia. Only 32% of patients experienced any temperatures below the hypothermic threshold (Table 6). Furthermore, these episodes typically quickly resolved with a median duration of 15 minutes.

The exact degree to which warmed intravenous fluids prevent hypothermia or warm patient core temperatures is subject to discussion, but several researchers have attempted to quantify such therapies. Sari et al. demonstrated that up to 79% of patients experienced incidental hypothermia when no active fluid-warming systems were employed, with a significant increase in post-operative shivering in patients who experienced intra-operative hypothermia.[27] While these results are particularly important during high-risk abdominal and cardiac surgery, they also translate into lesser-risk ambulatory and sedation procedures, even when more modest infusion volumes are expected (< 1 L). Kim et al. evaluated ambulatory urologic procedures under monitored anesthesia care and showed a significantly reduced drop in core temperature after induction, at the end of the procedure, and in recovery compared with patients who did not receive warmed IV fluids (p = 0.004, p = 0.02, and p = 0.008, respectively).[28] Hasankhani showed similar results in ambulatory orthopedic surgery, where the final core temperature averaged 36.4°C when IV fluids were warmed compared to 35.9°C in controls (p = 0.001).[29] This aligns with the results of a meta-analysis of literature covering the use of warmed IV fluids during anesthesia, showing a mean core temperature of 0.41°C to 0.79°C warmer in patients who received warmed IV fluids compared to controls.[14]

Active fluid warming systems have significant limitations in the amount of heating they can produce alone, as there is a ceiling limit on how warm the infusate can be without causing cellular or organ injury. As such, it is agreed that the main contribution of active fluid warming perioperatively is to reduce the effects of heat loss to the environment rather than true heating of a hypothermic patient, converse to active cooling of a patient where infusate temperatures may be given at 30–40°C lower than body temperature.[30] Mathematical thermodynamic models have been created to predict core temperature variations based on the temperature of the infusate and the baseline temperature of the patient. Barthel and Blumenberg separately designed models that predict that the average adult core temperature is likely to decrease by approximately 0.3–0.4°C with every liter of room temperature IV fluid, whereas the rise in core temperature using the same volume of warmed infusate is calculated at 0.1°C.[30, 31]

Our results corroborated these predicted outcomes. Not only did the patients in this study demonstrate a less significant decrease in core temperature after induction of anesthesia and throughout surgery compared with historical data of non-warmed IV fluids, but the degree to which temperature dropped in these patients mirrors data previously described with other active fluid warming devices and in the proposed mathematical models.

Overall, patients in this study experienced a modest decrease in core temperature compared to baseline upon induction of anesthesia (approximately 0.3°C), with recovery of core temperature back to baseline within 3 hours. Compared with other published data and mathematical models predicting patient body temperature changes with infused fluids, our results suggest that the enFlow fluid warming system was successful in reducing the degree of change in body temperature associated with anesthesia and surgery and the incidence of hypothermia during anesthesia, along with a more rapid return of core body temperature to baseline.

This study has several limitations. This was an uncontrolled and unblinded study design and there was no control group of patients not receiving warmed intravenous fluids as this would represent a violation of ethics given it would expose patients to undue risk. This was also not a comparison study to see if enFlow with its parylene coating worked better than any other intravenous fluid warmer, so there was no comparator group. All patients were co-managed with force-air warming and warming blankets, measures which weren’t controlled by the research protocol. Clearly these measures contributed to the avoidance of hypothermia. However, the previously mentioned studies also utilized ancillary warming devices but without intravenous fluid warming, and marked decreases in core body temperature were measured. In addition, Campbell et al showed that warmed IV fluids vs. room temperature IV fluids increased core temperature by 0.5 °C independent from other temperature management factors.[14] Core temperature in this study was estimated using the SpotOn temperature measurement system. This measurement technique has been validated against pulmonary artery catheter measurements with a mean error of -0.23°C [25]. Furthermore, we showed good agreement between SpotOn temperatures and bladder temperature measurements in the subset of patients with a unitary tract catheter (Fig. 4). We considered adding temperature sensors at each end of the warming cartridge to evaluate the impact of the device. However, the specifications of the device state that the output fluid temperature is 40 ± 2 °C. The enFlow heater has a temperature sensor which monitors the output fluid temperature and alarms if it is outside of the range. This project did not seek to confirm that the device performs within the technical specifications. Finally, the study was not adequately powered to fully clarify overall safety of the device nor the correlation between infusate flow rate and core body temperature.

Combined with previous lab-based bench studies demonstrating the efficacy of the newer-designed enFlow system compared to its historical design in warm-infused fluids, this study provides substantial evidence that the parylene-coated enFlow system operates as intended in living patients undergoing surgery and anesthesia and should be considered when actively warming patients at risk for hypothermia.

In this prospective multicenter study, the newly designed parylene-coated enFlow IV fluid warming system provided active warming to patients undergoing surgery and anesthesia consistent with previous studies of similar devices across a wide range of infusate flow rates. Even with the new parylene coating on the heating blocks, the enFlow system performs as intended.

ANOVA – Analysis of variance

ASA – American Society of Anesthesiologists

BMI – Body mass index

IV – Intravenous

LoA – Limit of agreement

PACU – Post-anesthesia care unit

SD – Standard deviation

STROBE – Strengthening the Reporting of Observational Studies in Epidemiology

Ethics approval and consent to participate

Ethical approval for this study was provided by the Ethics Committee of Helsinki and Uusimaa Hospital District (HUS/3206/2020) and the HUS Ethical Commission III, Helsinki, Finland (Chairperson Lauri Tammilehto) on 11 January 2021. The committee of 13 participants reviewed the clinical investigation plan, including amendments, the participant information leaflet, and informed consent. This study conforms to the STROBE statement. This study was conducted in accordance with the ethical principles in the Declaration of Helsinki. Written informed consent was obtained from all subjects participating in the trial.

Consent for publication

Not applicable

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Competing interests

ML, SM, KR, JJ, and VK have no competing interests. DB, ER, HG, and AW are Vyaire Medical employees. SC is a consultant working with Vyaire Medical.

Funding

None. Departmental funding only.

Authors' contributions

ML, SM, and AW contributed to design of the work, drafting the manuscript, and final approval of the version to be published, and agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. KR, JJ, DB, VK, SC, ER, and HG contributed to the collection and analysis of the data, drafting the manuscript, and final approval of the version to be published, and agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Acknowledgements

None

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Competing interest reported. ML, SM, KR, JJ, and VK have no competing interests. DB, ER, HG, and AW are Vyaire Medical employees. SC is a consultant working with Vyaire Medical.

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Verification of an Intravenous Fluid Warmer: A Prospective, Two-Center Observational Trial

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