Introduction
The prone decubitus (PD) or ventral decubitus position is an anatomical position of the human body characterized by lying face down keeping the patient’s head sideways and the neck in neutral position.
This position is commonly used in medical-surgical procedures, such as nephrolithotomy1, endoscopic retrograde cholangiopancreatography2, and in posterior fossa surgeries of the head, neck, vertebrae, retroperitoneum, and posterior body structures in case of plastic surgery3,4.
In intensive care units, the PD position has been used as part of adult respiratory distress syndrome (ARDS) treatment5-7. With this position, an improvement has been defined in oxygenation, pulmonary mechanics, pulmonary ventilation/perfusion (V/Q) ratio, and as a pulmonary protection maneuver in these patients5-7; the effect on mortality is still questioned, although a meta-analysis that included 12 works and 2129 patients showed a mortality decrease with the use of PD for more than 12 h8.
In ARDS, study and treatment have focused on the evaluation of pulmonary vascular damage, and the goals have been “lung opening” and arterial oxygen saturation optimization9.
With the new knowledge about pathophysiology in ARDS and with better non-invasive methods to assess the right ventricle (RV) as transthoracic echocardiography (TTE) does, hemodynamic aspects have acquired higher relevance, specifically the development of acute cor pulmonale10, which appears to be involved in mortality.
TTE assessment is usually carried out in dorsal decubitus (supine) or lateral position, since it does not interfere with the position of the transducer11,12; however, in the PD position, the anterior chest wall is obstructed and, therefore, having useful windows to carry out RV estimations appears to be limited.
Hence, in this work, as a first approach to the entity, we studied subjects without cardiopulmonary disease in PD position to know the feasibility of having adequate acoustic windows to determine RV parameters with TTE.
Methods
The work was carried out at the Postsurgical Cardiovascular Intensive Care Department (Postsurgical Therapy [PST]) of the Ignacio Chávez National Institute of Cardiology, from March 1, 2018, to December 31, 2018.
Study design
Pilot study, case series, and consecutive subjects who were admitted to the PST department and agreed to participate were studied.
Inclusion and exclusion criteria
Subjects of both genders, older than 18 years and without cardiopulmonary disease were included in the study. Subjects with acoustic window alterations were excluded from the study. Those with incomplete studies or studies of poor quality for analysis were censored.
To obtain partial oxygen saturation (SpO2), the same pulse oximeter was used in all subjects: Onyx® II Model 9550 (Nonin Medical INC., Plymouth, Minnesota, USA).
Systemic blood pressure (BP) was obtained with a Phillips® MP 70 pneumatic sphygmomanometer. Due to the slim build of all patients, the same standard bracelet was used on the right arm, with a 12 × 26-cm camera.
The echocardiography equipment used in all cases was the cardiovascular ultrasound system VIVID® E9, with M5S-D® sector heart probe (GE Vingmed Ultrasound A/S, Norten, Norway), with 1.5-4.6-MHz transducer, and images were obtained with tissue harmonic imaging. No echographic contrast medium was used to improve endocardial edges visualization.
All echocardiographic parameters were acquired by the same researcher (General Medical Council); the second evaluation, intended to establish intra-observer agreement with regard to parameters, was carried out 24 h after the first ones were estimated.
Echocardiographic parameters were quantified according to the guidelines published by the American Society of Echocardiography for assessment of the right heart11,12: tricuspid annular plane systolic excursion (TAPSE), calculated in M-mode in the four-chamber apical plane, measured in millimeters (Fig. 1A1 and A2); tricuspid S1-wave, lateral systolic tricuspid annular tissue velocity, using tissue Doppler in the four-chamber apical plane measured in cm/s, (Fig. 1B1 and B2); RV fractional area change (FAC, %), obtained from RV end-diastolic area in relation to RV systolic area in four-chamber projection, measured as a percentage; pulmonary artery systolic pressure (PAP-s) was calculated with the tricuspid insufficiency (TI) gradient using Bernoulli’s simplified equation: TI2 × 4 + RAP (right atrial pressure) inquired in a four-chamber projection with continuous Doppler, estimated in mmHg; RV/left ventricle (LV) ratio, quantified in four-chamber projection at diastole.
Subject’s PD positioning required for him/her to remain lying face down with the head turned to the side and the neck in neutral position; in addition, the left arm was positioned in the upward direction (toward the head) and a 10-cm-height pillow was placed in the ventral infraclavicular region, which allowed for a better image to be obtained (Fig. 2). The transducer was placed between the 4th and 5th left intercostal space toward the anterior axillary line. With this position, the aforementioned variables could be obtained in the PD position. This position is a modification of the swimmer position used in an intensive care unit in case transesophageal echocardiography is not available13.
Maneuver
Once the study subject had been selected according to the inclusion criteria, he/she was placed in the dorsal decubitus (supine) position and the referred echocardiographic variables and vital signs were determined; then, 10 min later, the subject was placed in the PD position and the same images were obtained for echocardiographic analysis and recording of the same vital signs; finally, the subject returned to his/her final dorsal decubitus position and, 10 min later, all variables were estimated again. A third participant, blinded to the measurements, collected the results, and recorded them in the database.
Statistical analysis
Data are presented as averages ± standard deviation for numerical data, and as frequencies and percentages for nominal data. The analysis of between-group differences was performed using repeated measures ANOVA with Bonferroni’s adjustment. A p < 0.05 was considered statistically significant. Intra-subject agreement was analyzed for the estimated RV parameters with Bland-Altman’s statistic al method14, and its magnitude was calculated using the intraclass correlation coefficient15 with its 95% confidence interval (CI).
Since this was a pilot study to assess the feasibility of estimating parameters, a convenience sample of 50 subjects was used.
The study was approved by the Research and Ethics Committee of the Ignacio Chávez National Institute of Cardiology, and all subjects signed an informed consent letter before the echocardiography study.
Results
Fifty subjects without cardiopulmonary disease were studied. Average age was 30 ± 6 years, the male/female ratio was 44/6; weight, 77.33 ± 10.85 kg; height, 1.73 ± 0.07 m; body surface area, 1.91 ± 0.16 m2; and body mass index, 25.65 ± 2.71 kg/m2.
Vital signs behavior according to the inquired position is shown in table 1.
Dorsal decubitus X ± SD | Prone decubitus X ± SD | Dorsal decubitus X ± SD | p | |
---|---|---|---|---|
HR, bpm | 74 ± 9 | 77 ± 9 | 75 ± 8 | 1 vs. 2 = 0.014 2 vs. 3 = 0.45 1 vs. 3 = 0.789 |
RR, brpm | 14 ± 1 | 14 ± 1 | 14 ± 1 | 1 vs. 2 = 0.686 2 vs. 3 = 1.00 1 vs. 3 = 0.871 |
SpO2, % | 94.40 ± 1.70 | 96.64 ± 1.79 | 95.32 ± 1.36 | 1 vs. 2 = 0.001 2 vs. 3 = 0.001 1 vs. 3 = 0.001 |
SBP, mmHg | 124.12 ± 11.75 | 126 ± 11.24 | 123.88 ± 11.07 | 1 vs. 2 = 0.402 2 vs. 3 = 0.132 1 vs. 3 = 1.00 |
DBP, mmHg | 71.86 ± 8.23 | 74.06 ± 9.53 | 72 ± 7.70 | 1 vs. 2 = 0.154 2 vs. 3 = 0.099 1 vs. 3 = 1.00 |
MBP, mmHg | 65.33 ± 5.38 | 67.69 ± 6.31 | 65.29 ± 5.62 | 1 vs. 2 = 0.037 2 vs. 3 = 0.050 1 vs. 3 = 0.680 |
HR: heart ratio; bpm: beats per minute; RR: respiratory rate; brpm: breaths per minute; SBP: systolic blood pressure; DBP: diastolic blood pressure; M: mean; X: mean; SD: standard deviation; SpO2: partial oxygen saturation.
Echocardiographic variables in the dorsal and PD position are listed in table 2. The frequency at which acquiring the inquired variables were possible according to initial dorsal decubitus, supine decubitus and final dorsal decubitus position was, respectively: TAPSE 50 (100%), 50 (100%), 50 (100%); FAC: 50 (100%), 44 (88%), 50 (100%); RVDA 50 (100%), 44 (88%), and 49 (98%); RVSA: 50 (100%), 44 (88%), 49 (98%); PAP-s 35 (70%), 38 (76%), and 39 (78%); S’ wave: 50 (100%), 50 (100%), 50 (100%), and RV/LV ratio: 50 (100%), 46 (92%), and 50 (100%).
Dorsal decubitus X ± SD | Prone decubitus X ± SD | Dorsal decubitus X ± SD | p | |
---|---|---|---|---|
TAPSE, mm | 19.74 ± 3.24 | 21.60 ± 2.97 | 19.44 ± 2.84 | 1 vs. 2 = 0.001 2 vs. 3 = 0.001 1 vs. 3 = 0.749 |
S’-wave, cm/s | 13.52 ± 1.87 | 15.02 ± 2.09 | 13.46 ± 1.55 | 1 vs. 2 = 0.001 2 vs. 3 = 0.001 1 vs. 3 = 1.00 |
RV FAC, % | 42.14 ± 5.78 | 45.73 ± 5.72 | 43.02 ± 4.66 | 1 vs. 2 = 0.001 2 vs. 3 = 0.004 1 vs. 3 = 0.188 |
RV area at diastole, cm2 | 17.25 ± 2.04 | 17.58 ± 2.18 | 17.09 ± 1.88 | 1 vs. 2 = 1.00 2 vs. 3 = 0.312 1 vs. 3 = 0.833 |
RV area at systole, cm2 | 9.98 ± 1.73 | 9.58 ± 1.63 | 9.74 ± 1.50 | 1 vs. 2 = 0.613 2 vs. 3 = 1.00 1 vs. 3 = 0.227 |
PASP mmHg | 16.40 ± 6.01 | 15.89 ± 5.24 | 15.74 ± 4.69 | 1 vs. 2 = 1.00 2 vs. 3 = 1.00 1 vs. 3 = 0.775 |
RV/LV | 0.74 ± 0.12 | 0.76 ± 0.11 | 0.75 ± 0.12 | 1 vs. 2 = 0.156 2 vs. 3 = 0.154 1 vs. 3 = 0.950 |
X: mean; SD: standard deviation; TAPSE: tricuspid annular plane systolic excursion; FAC: fractional area change; RV: right ventricle; LV: left ventricle; PASP: pulmonary artery systolic pressure; RV/LV: right ventricle-left ventricle ratio.
Intra-observer agreement for echocardiographic variables in the dorsal and supine position is shown in table 3. Fig. 3 shows TAPSE as the echocardiographic variable with the lowest variability in both positions.
Dorsal decubitus | Prone decubitus | |||
---|---|---|---|---|
Mean difference (bias) | ICC (95% CI) | Mean difference (bias) | ICC (95% CI) | |
TAPSE, mm | 0 (2, –2.0) | 0.976 (0.950, 0.988) | 0.1 (2, –1.9) | 0.974 (0.947, 0.987) |
S’-wave, cm/s | –0.46 (1.21, –2.14) | 0.954 (0.907, 0.968) | 0.2 (1.8, –1.4) | 0.963 (0.923, 0.982) |
RV FAC, % | 0.1 (6, –5.8) | 0.944 (0.882, 0.973) | 0.9 (8.3, –6.5) | 0.891 (0.757, 0.951) |
RV area at diastole, cm2 | 0.23 (1.44, –0.98) | 0.981 (0.959, 0.991) | 0.6 (3.9, –2.7) | 0.862 (0.691, 0.938) |
RV area at systole, cm2 | 0.17 (1.44, –1.11) | 0.973 (0.944, 0.987) | 0.4 (2.6, –1.9) | 0.884 (0.741, 0.948) |
PASP, mm Hg | –0.1 (5.3, –5.6) | 0.954 (0.892, 0.981) | –0.8 (5.2, –6.9) | 0.945 (0.878, 0.976) |
RV/LV | 0.01 (0.17, –0.14) | 0.856 (0.698, 0.932) | 0.02 (0.19, –0.15) | 0.796 (0.558, 0.905) |
ICC: intraclass correlation coefficient; CI: confidence interval; TAPSE: tricuspid annular plane systolic excursion; FAC: fractional area change; RV: right ventricle; PASP: pulmonary artery systolic pressure; RV/LV: right ventricle-left ventricle ratio.
Discussion
The purpose of the present work was to know, through TTE, the feasibility to estimate RV parameters related to its systolic function11,12 in the PD position in subjects without cardiopulmonary disease.
The study population had an average age of 30 years, were more frequently males and the body mass index was normal or overweight; with no cardiopulmonary disease.
Vital signs behavior in the study population was as follows: there were small differences in heart rate (HR) from ventral decubitus to PD position and returned to baseline HR when the subjects were moved back to the ventral decubitus position, p < 0.014 (Table 1).
As for respiratory rate (RR), there were no modifications with position changes, unlike SpO2, which increased when changing from ventral decubitus to PD position and returned to baseline level when the subject was returned to ventral decubitus position (p = 0.001) (Table 1).
There were no changes detected in systolic and diastolic BP; however, mean BP had discreet increases with the change from initial decubitus ventral to the PD position (p = 0.037) and from PD to ventral (p = 0.050), by means of which it equaled initial mean BP (Table 1).
Hemodynamic changes were associated with body position changes, as it has been previously referred in the field of anesthesia when adopting the PD position1-4,16,17. These changes reflect heart preload and afterload alterations.
Furthermore, these same body position changes cause differences in lung volumes and, therefore, in pulmonary V/Q, which is reflected in a better pulmonary V/Q ratio and its effect on gas exchange, which in our work was shown by a better SpO2 (better oxygen saturation).
This work was not designed to describe the pathophysiology of possible changes in vital signs or hemodynamics in the prone position; however, making some considerations about what could be occurring is possible. These vital signs discreet alterations appear to be related to the complex interaction that breath and circulation maintain18-20.
Changes have been described with breaths at normal tidal volume18 and not necessarily with the RR sole increase, which would support the lack of response in RR found in our results; in pathological states, this behavior can be more evident and deleterious19.
Changes in lung volume inspiratory/expiratory phases and intrathoracic pressure (ITP) during normal respiratory cycle alter right and left heart preload and afterload, whereupon they interact to vary cardiac output and BP with the respiratory cycle20.
During the inspiratory phase of respiration, while the alveoli are filled with air, ITP decreases, and favors systemic venous return toward the chest; the right heart fills up and blood is pumped into the pulmonary artery, which dilates to accommodate the flow. In two to three beats, blood reaches the LV and BP increases at the end of inspiration and beginning of expiration, whereupon BP slightly decreases at inspiration and increases during expiration; this effect can be enhanced or counteracted by the sudden increase of blood flow to the LV during inspiration18,21. In addition, mean BP transient increase with the PD position can be a reflection of the decrease in venous return (preload) induced by the position16,17.
In pathological conditions, these alterations can favor ventricular interdependence mechanisms18,19.
In the PD position, determining by TTE the parameters shown in table 2 was possible. This study also shows that it is possible to determine some parameters related to RV systolic function, which in theory would enable determining them in subjects with ARDS, which will be subject of another study.
Intra-subject variability with regard to the enquired indices is small, specifically for TAPSE and the S’-wave, and 100% of the time they could be measured; this small TAPSE variability has already been previously reported in another context22.
These RV echocardiographic parameters are modified according to position changes, specifically when adopting the PD position, and could be related to the preload alterations induced by position modification19-21.
Limitations
In this work, the purpose of knowing the feasibility of obtaining images for RV systolic function analysis was met. However, the estimation was carried out in subjects without cardiopulmonary disease and not on mechanical ventilation, as it occurs in patients with ARDS5,6. Furthermore, the sample was restricted to young patients, with the highest body mass index being overweight.
Nevertheless, this work shows that at least the PD position is not entirely a limitation to obtain these images and estimating RV echocardiographic parameters, which makes TTE a suitable, non-invasive tool to assess the moment when a patient with ARDS experiences cor pulmonale and opt for pronation; and conversely, also the moment the cor pulmonale disappears and the PD position is no longer required for patient improvement.
Conclusions
TTE is a useful tool for determining parameters related to RV systolic function. In the PD position, obtaining TTE images is possible to make a consistent and feasible analysis of RV systolic function.
Changes in vital signs and RV parameters estimated by TTE were associated with position changes.