Surgery Clinical Trial
Official title:
Influence of the End-inspiratory Pause on Mechanical Ventilation and Its Correlation With Electrical Impedance Tomography
This study evaluates the influence of two different end-inspiratory pause (EIP) times on respiratory mechanics and arterial gases of surgical patients when ventilated under an open lung approach (OLA) strategy. The investigators evaluate the impact of using EIP 10% versus 30% of the inspiratory time on a volume control model. The investigators also analyse the potential influence of these EIP on pulmonary gas distribution measured by electric impedance tomography.
Prolonging the EIP while maintaining an adequate expiratory time has shown benefits in terms
of improving alveolar effective ventilation and enhancing gas exchange in surgical and
intensive care patients. However, there are no published studies addressing the effects of
different EIP times on the respiratory mechanics and gas distribution of surgical patients
when associated with OLA strategies for ventilation.
Assuming the benefits of OLA, these investigators hypothesized about the potential effects of
increasing the EIP when ventilating patients in a volume control mode. In the present study
the investigators evaluated the influence of two different EIP (10% and 30% of the
inspiratory time) on the respiratory mechanics of patients submitted to scheduled abdominal
surgery under general anesthesia and ventilated with a protective lung strategy. The
investigators studied the influence of EIP on driving pressure (Pdriv), plateau pressure
(Pplat), respiratory static compliance (Crs) and open lung PEEP (OL-PEEP). We also assessed
gas distribution by means of electric impedance tomography and studied its influence on gas
exchange measured by means of serial gasometries.
Study protocol. A forced spirometry was performed in all patients after accepting their
inclusion.
On the day of surgery, standard monitoring was initiated on arrival in the theatre, including
electrocardiography, pulse oximetry, and noninvasive blood pressure monitoring. After light
sedation with 1-2 mg of midazolam, a thoracic epidural catheter was placed under local
anesthesia on anesthesiologist`s criteria. A remifentanil infusion 0.03 mcg/kg/min was
started before left radial artery catheterization under local anesthesia. After recording
basal data during full consciousness on 21% inspired oxygen, all participants were
preoxygenated via a facial mask for 5 min on spontaneous ventilation with fraction of
inspired oxygen (FiO2) of 0.7 and fresh gas flow of 6 L/min. After induction with propofol
((1-1.5 mg/kg of predicted body weight (PBW)), 0.8 mg/kg of PBW of rocuronium were
administered and proceeded with tracheal intubation. Patients were ventilated via a Primus
(Drager, Telford, PA, USA) using a tidal volume of 7 ml/kg of PBW; volume control mode
comprised an inspiration: expiration ratio of 1:2 and a respiratory rate of 12-14 breaths per
minute to maintain the etCO2 at 35-40 mmHg, with an initial PEEP of 5 cmH2O. EIP was
programmed according to randomization group. Fresh gas flow of 2 L/min with FiO2 of 0.7 was
used throughout the procedure. Anesthesia was maintained with remifentanil 0.03-0.1
mcg/kg/min and sevoflurane, with minimal alveolar concentration (MAC) of 0.7-1 adjusted for
patient´s age. Bispectral Index monitoring was used throughout the entire procedure (BIS
Quatro, Covidien Ilc, Mansfield, MA, USA). All ventilation parameters remained stable
throughout the study except the EIP (diverted in function of study protocol assignation) and
the PEEP, which was tailored according the principles of OLA ventilation previously
published. A central venous line was inserted in all cases and continuous cardiac output
monitoring, systemic vascular resistance and systolic volume variation were monitored
throught out all procedure by means of FloTrac sensor (Edwards Lifesciences, Irvine,
California, USA). Other monitoring included train of four (TOF) for neuromuscular relaxation.
Dräger Primus (Dräger Medical, Lübeck, Germany) was used for ventilation with continuous
monitoring of peak pressure (Ppk), Pplat, PEEP, Crs, FiO2, fraction of expired oxygen (FeO2),
end-tidal CO2 (etCO2). For blood gases an ABL90 FLEX PLUS analyzer (Radiometer Medical,
Copenhagen, Denmark) was used. If hemodynamic instability occurred during the ARM (fall> 20%
of the cardiac index or mean arterial pressure), maneuver was discontinued and ephedrine or
phenylephrine was administered and registered, restoring ARM on haemodynamics recovering.
Ventilatory management Data collection was made in five different moments (moment 0 to 4);
moment 0: after endotracheal intubation, on establishing mechanical ventilation and prior to
ARM, with the EIP assigned to each group and a standard PEEP of 5 cm H2O. Subsequently an ARM
was performed as previously described by Ferrando et al, with calculation of the optimal PEEP
by means of a decremental titration trial followed of a new AMR and establishment of a
tailored OL-PEEP, 2 cmH2O over optimal PEEP (moment 1). EIP was then crossed between groups
(30% in Group 1 and 10% in Group 2), moment 2. Another ARM was then performed with the
consequent re-assignation of a different OL-PEEP for each group (moment 3). Finally, EIP was
crossed again (moment 4). All data were collected 5 minutes after changes implementation.
Statistic analysis The investigators used the statistical software IBM SPSS Statistics for
Windows, version 24 (IBM Corp., Armonk, N.Y., USA) for data analysis. An exploratory analysis
of the data was performed using the mean and standard deviation or the median with
interquartile ranges for quantitative variables. The investigators used the percentages for
analysis of the qualitative variables. The investigators checked the normality of the
distribution of data with the Kolmogorov-Smirnov test, or with the Shaphiro-Wilk test for
variables with less than 50 records. The Student´s T test for paired samples was used to
analyse the difference in the means of quantitative paired variables (intra-group
differences), and the Student T test for independent samples to analyse the difference in the
means of quantitative variables between both groups (inter-group differences).
Finally, the investigators grouped records corresponding to the EIP applied after
recruitment, independently of the original assignation according to Group, In this sense,
investigators grouped data corresponding to Group 1 in moment 1 with Group 2 in moment 3
(EIP10% after recruitment) and data of Group 1 in moment 3 with Group 2 in moment 1 (EIP 30%
after recruitment), obtaining a sample of 32 registers in comparable paired conditions.
Calculation of the sample size Given the absence of previously published works with an
approach similar to the one proposed by investigators, the sample size was calculated based
on the data obtained in a pilot sample of 5 patients submitted to surgical and anesthesia
management similar to those of the protocol proposed. The investigators estimated the sample
size assuming the differences in Crs when changing from an EIP 10 % to 30% in a sequential
way (paired sample), determining an average difference 12 ml/cm H2O between both
interventions. Sample size was calculated to obtain a power of 80 % to detect differences in
the contrast of the null hypothesis h₀: μ₁ = μ₂ by means of a bilateral Student's T test for
two related samples, taking into account a level of significance is of 5 %, and assuming a
mean of the differences of 12 ± 20 units. Taking into account that the expected percentage of
dropouts was 20.00% it would be necessary to recruit 30 pairs of experimental units in the
study.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05583916 -
Same Day Discharge for Video-Assisted Thoracoscopic Surgery (VATS) Lung Surgery
|
N/A | |
Completed |
NCT04448041 -
CRANE Feasibility Study: Nutritional Intervention for Patients Undergoing Cancer Surgery in Low- and Middle-Income Countries
|
||
Completed |
NCT03213314 -
HepaT1ca: Quantifying Liver Health in Surgical Candidates for Liver Malignancies
|
N/A | |
Enrolling by invitation |
NCT05534490 -
Surgery and Functionality in Older Adults
|
N/A | |
Recruiting |
NCT04792983 -
Cognition and the Immunology of Postoperative Outcomes
|
||
Terminated |
NCT04612491 -
Pre-operative Consultation on Patient Anxiety and First-time Mohs Micrographic Surgery
|
||
Recruiting |
NCT06397287 -
PROM Project Urology
|
||
Recruiting |
NCT04444544 -
Quality of Life and High-Risk Abdominal Cancer Surgery
|
||
Completed |
NCT04204785 -
Noise in the OR at Induction: Patient and Anesthesiologists Perceptions
|
N/A | |
Completed |
NCT03432429 -
Real Time Tissue Characterisation Using Mass Spectrometry REI-EXCISE iKnife Study
|
||
Completed |
NCT04176822 -
Designing Animated Movie for Preoperative Period
|
N/A | |
Recruiting |
NCT05370404 -
Prescribing vs. Recommending Over-The-Counter (PROTECT) Analgesics for Patients With Postoperative Pain:
|
N/A | |
Not yet recruiting |
NCT05467319 -
Ferric Derisomaltose/Iron Isomaltoside and Outcomes in the Recovery of Gynecologic Oncology ERAS
|
Phase 3 | |
Recruiting |
NCT04602429 -
Children's Acute Surgical Abdomen Programme
|
||
Completed |
NCT03124901 -
Accuracy of Noninvasive Pulse Oximeter Measurement of Hemoglobin for Rainbow DCI Sensor
|
N/A | |
Completed |
NCT04595695 -
The Effect of Clear Masks in Improving Patient Relationships
|
N/A | |
Recruiting |
NCT06103136 -
Maestro 1.0 Post-Market Registry
|
||
Completed |
NCT05346588 -
THRIVE Feasibility Trial
|
Phase 3 | |
Completed |
NCT04059328 -
Novel Surgical Checklists for Gynecologic Laparoscopy in Haiti
|
||
Recruiting |
NCT03697278 -
Monitoring Postoperative Patient-controlled Analgesia (PCA)
|
N/A |